AP815A - An obesity (ob) polypeptide capable of modulating body weight, nucleic acids therefore, and diagnostic and therapeutic use thereof. - Google Patents
An obesity (ob) polypeptide capable of modulating body weight, nucleic acids therefore, and diagnostic and therapeutic use thereof. Download PDFInfo
- Publication number
- AP815A AP815A APAP/P/1997/000919A AP9700919A AP815A AP 815 A AP815 A AP 815A AP 9700919 A AP9700919 A AP 9700919A AP 815 A AP815 A AP 815A
- Authority
- AP
- ARIPO
- Prior art keywords
- seq
- body weight
- polypeptide
- protein
- sequence
- Prior art date
Links
- 230000037396 body weight Effects 0.000 title abstract description 33
- 150000007523 nucleic acids Chemical class 0.000 title abstract description 33
- 108020004707 nucleic acids Proteins 0.000 title abstract description 27
- 102000039446 nucleic acids Human genes 0.000 title abstract description 27
- 230000001225 therapeutic effect Effects 0.000 title abstract description 12
- 208000008589 Obesity Diseases 0.000 title description 89
- 235000020824 obesity Nutrition 0.000 title description 89
- 102000004196 processed proteins & peptides Human genes 0.000 title description 87
- 108090000765 processed proteins & peptides Proteins 0.000 title description 87
- 229920001184 polypeptide Polymers 0.000 title description 85
- 108090000623 proteins and genes Proteins 0.000 abstract description 48
- 102000004169 proteins and genes Human genes 0.000 abstract description 29
- 241001465754 Metazoa Species 0.000 abstract description 26
- 239000002773 nucleotide Substances 0.000 abstract description 23
- 125000003729 nucleotide group Chemical group 0.000 abstract description 23
- 101001063991 Homo sapiens Leptin Proteins 0.000 abstract description 17
- 241000124008 Mammalia Species 0.000 abstract description 14
- 102000049953 human LEP Human genes 0.000 abstract description 12
- 238000006243 chemical reaction Methods 0.000 abstract description 11
- 239000013604 expression vector Substances 0.000 abstract description 8
- 239000000463 material Substances 0.000 abstract description 8
- 230000001580 bacterial effect Effects 0.000 abstract description 7
- 238000002360 preparation method Methods 0.000 abstract description 5
- 241000238631 Hexapoda Species 0.000 abstract description 4
- 210000004962 mammalian cell Anatomy 0.000 abstract description 4
- 241000282412 Homo Species 0.000 abstract description 3
- 230000003321 amplification Effects 0.000 abstract description 2
- 230000006583 body weight regulation Effects 0.000 abstract description 2
- 239000013599 cloning vector Substances 0.000 abstract description 2
- 229940088597 hormone Drugs 0.000 abstract description 2
- 239000005556 hormone Substances 0.000 abstract description 2
- 239000003068 molecular probe Substances 0.000 abstract description 2
- 238000003199 nucleic acid amplification method Methods 0.000 abstract description 2
- 101150102573 PCR1 gene Proteins 0.000 abstract 1
- 150000001413 amino acids Chemical class 0.000 description 51
- 241000699670 Mus sp. Species 0.000 description 48
- 108020004414 DNA Proteins 0.000 description 35
- 235000001014 amino acid Nutrition 0.000 description 32
- 229940024606 amino acid Drugs 0.000 description 32
- 235000018102 proteins Nutrition 0.000 description 27
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 25
- 241000699666 Mus <mouse, genus> Species 0.000 description 23
- 239000000523 sample Substances 0.000 description 21
- 102000016267 Leptin Human genes 0.000 description 20
- 230000000694 effects Effects 0.000 description 20
- 241000282414 Homo sapiens Species 0.000 description 17
- 108010092277 Leptin Proteins 0.000 description 17
- 210000004027 cell Anatomy 0.000 description 16
- 239000012634 fragment Substances 0.000 description 15
- 230000000875 corresponding effect Effects 0.000 description 13
- 238000000034 method Methods 0.000 description 13
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 12
- 210000000577 adipose tissue Anatomy 0.000 description 12
- 230000035772 mutation Effects 0.000 description 12
- 108010076504 Protein Sorting Signals Proteins 0.000 description 11
- 210000001789 adipocyte Anatomy 0.000 description 11
- 239000002299 complementary DNA Substances 0.000 description 11
- 238000003752 polymerase chain reaction Methods 0.000 description 11
- 108091028043 Nucleic acid sequence Proteins 0.000 description 10
- 238000003776 cleavage reaction Methods 0.000 description 10
- 239000013615 primer Substances 0.000 description 10
- 230000007017 scission Effects 0.000 description 10
- 241001529936 Murinae Species 0.000 description 9
- 241000235648 Pichia Species 0.000 description 9
- 241000700159 Rattus Species 0.000 description 9
- 238000000338 in vitro Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 102000007056 Recombinant Fusion Proteins Human genes 0.000 description 8
- 108010008281 Recombinant Fusion Proteins Proteins 0.000 description 8
- 238000004458 analytical method Methods 0.000 description 8
- 206010012601 diabetes mellitus Diseases 0.000 description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 8
- 230000002068 genetic effect Effects 0.000 description 8
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Chemical group OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 8
- 235000004554 glutamine Nutrition 0.000 description 8
- 108020004999 messenger RNA Proteins 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 238000013519 translation Methods 0.000 description 8
- 208000001072 type 2 diabetes mellitus Diseases 0.000 description 8
- 238000001262 western blot Methods 0.000 description 8
- 239000005557 antagonist Substances 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 239000013598 vector Substances 0.000 description 7
- 108020004705 Codon Proteins 0.000 description 6
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Chemical group CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 description 6
- 239000002537 cosmetic Substances 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 239000000499 gel Substances 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- 239000012528 membrane Substances 0.000 description 6
- 235000006109 methionine Nutrition 0.000 description 6
- 238000003757 reverse transcription PCR Methods 0.000 description 6
- 238000002560 therapeutic procedure Methods 0.000 description 6
- 102000053602 DNA Human genes 0.000 description 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 5
- 108091092724 Noncoding DNA Proteins 0.000 description 5
- 235000004279 alanine Nutrition 0.000 description 5
- 210000000349 chromosome Anatomy 0.000 description 5
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Chemical group SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 5
- 235000018417 cysteine Nutrition 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 5
- 230000007547 defect Effects 0.000 description 5
- 201000010099 disease Diseases 0.000 description 5
- 239000000284 extract Substances 0.000 description 5
- 210000004185 liver Anatomy 0.000 description 5
- 229930182817 methionine Chemical group 0.000 description 5
- 239000008194 pharmaceutical composition Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 241000894007 species Species 0.000 description 5
- 210000001519 tissue Anatomy 0.000 description 5
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 description 4
- 102000007469 Actins Human genes 0.000 description 4
- 108010085238 Actins Proteins 0.000 description 4
- 239000004471 Glycine Substances 0.000 description 4
- 102000003839 Human Proteins Human genes 0.000 description 4
- 108090000144 Human Proteins Proteins 0.000 description 4
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical group SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 4
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 4
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical group CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 4
- 101100181592 Mus musculus Lep gene Proteins 0.000 description 4
- 108091034117 Oligonucleotide Proteins 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 210000000593 adipose tissue white Anatomy 0.000 description 4
- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 description 4
- 230000000692 anti-sense effect Effects 0.000 description 4
- 239000012472 biological sample Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- ATDGTVJJHBUTRL-UHFFFAOYSA-N cyanogen bromide Chemical compound BrC#N ATDGTVJJHBUTRL-UHFFFAOYSA-N 0.000 description 4
- ZMMJGEGLRURXTF-UHFFFAOYSA-N ethidium bromide Chemical compound [Br-].C12=CC(N)=CC=C2C2=CC=C(N)C=C2[N+](CC)=C1C1=CC=CC=C1 ZMMJGEGLRURXTF-UHFFFAOYSA-N 0.000 description 4
- 229960005542 ethidium bromide Drugs 0.000 description 4
- 230000037406 food intake Effects 0.000 description 4
- 235000012631 food intake Nutrition 0.000 description 4
- 230000004927 fusion Effects 0.000 description 4
- 238000009396 hybridization Methods 0.000 description 4
- 238000001597 immobilized metal affinity chromatography Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 150000003384 small molecules Chemical class 0.000 description 4
- 229920000936 Agarose Polymers 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- 108091026890 Coding region Proteins 0.000 description 3
- 238000002965 ELISA Methods 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Chemical group OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 3
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical group C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 3
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical group CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 3
- 108090000143 Mouse Proteins Proteins 0.000 description 3
- 108020004485 Nonsense Codon Proteins 0.000 description 3
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Chemical group CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 3
- 239000004473 Threonine Chemical group 0.000 description 3
- 239000011543 agarose gel Substances 0.000 description 3
- 125000000637 arginyl group Chemical group N[C@@H](CCCNC(N)=N)C(=O)* 0.000 description 3
- 230000004071 biological effect Effects 0.000 description 3
- 238000010367 cloning Methods 0.000 description 3
- 208000035475 disorder Diseases 0.000 description 3
- 239000003937 drug carrier Substances 0.000 description 3
- 102000037865 fusion proteins Human genes 0.000 description 3
- 108020001507 fusion proteins Proteins 0.000 description 3
- 235000013922 glutamic acid Nutrition 0.000 description 3
- 239000004220 glutamic acid Chemical group 0.000 description 3
- 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 description 3
- 238000001114 immunoprecipitation Methods 0.000 description 3
- 229940039781 leptin Drugs 0.000 description 3
- NRYBAZVQPHGZNS-ZSOCWYAHSA-N leptin Chemical compound O=C([C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CC(C)C)CCSC)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CS)C(O)=O NRYBAZVQPHGZNS-ZSOCWYAHSA-N 0.000 description 3
- 125000001360 methionine group Chemical group N[C@@H](CCSC)C(=O)* 0.000 description 3
- 230000003228 microsomal effect Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 235000008521 threonine Nutrition 0.000 description 3
- 238000011144 upstream manufacturing Methods 0.000 description 3
- 239000004474 valine Chemical group 0.000 description 3
- 235000014393 valine Nutrition 0.000 description 3
- 208000016261 weight loss Diseases 0.000 description 3
- SBKVPJHMSUXZTA-MEJXFZFPSA-N (2S)-2-[[(2S)-2-[[(2S)-1-[(2S)-5-amino-2-[[2-[[(2S)-1-[(2S)-6-amino-2-[[(2S)-2-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-3-(1H-indol-3-yl)propanoyl]amino]-3-(1H-imidazol-4-yl)propanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-4-methylpentanoyl]amino]-5-oxopentanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]acetyl]amino]-5-oxopentanoyl]pyrrolidine-2-carbonyl]amino]-4-methylsulfanylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoic acid Chemical group C([C@@H](C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(O)=O)NC(=O)[C@@H](N)CC=1C2=CC=CC=C2NC=1)C1=CNC=N1 SBKVPJHMSUXZTA-MEJXFZFPSA-N 0.000 description 2
- 108020005065 3' Flanking Region Proteins 0.000 description 2
- 108020005029 5' Flanking Region Proteins 0.000 description 2
- 238000011752 CBA/J (JAX™ mouse strain) Methods 0.000 description 2
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 206010020772 Hypertension Diseases 0.000 description 2
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical group OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical group OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Chemical group NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
- 239000004472 Lysine Chemical group 0.000 description 2
- 108010038049 Mating Factor Proteins 0.000 description 2
- 101100351017 Mus musculus Pax4 gene Proteins 0.000 description 2
- 125000001429 N-terminal alpha-amino-acid group Chemical group 0.000 description 2
- 108700026244 Open Reading Frames Proteins 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000004365 Protease Substances 0.000 description 2
- 108020004511 Recombinant DNA Proteins 0.000 description 2
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 2
- 229920002684 Sepharose Polymers 0.000 description 2
- 238000002105 Southern blotting Methods 0.000 description 2
- 108090000190 Thrombin Proteins 0.000 description 2
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 description 2
- 210000003486 adipose tissue brown Anatomy 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 230000004075 alteration Effects 0.000 description 2
- 238000003556 assay Methods 0.000 description 2
- 210000000227 basophil cell of anterior lobe of hypophysis Anatomy 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- 239000012531 culture fluid Substances 0.000 description 2
- 230000009089 cytolysis Effects 0.000 description 2
- 238000012217 deletion Methods 0.000 description 2
- 230000037430 deletion Effects 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000029087 digestion Effects 0.000 description 2
- 229940088598 enzyme Drugs 0.000 description 2
- 201000010063 epididymitis Diseases 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000002523 gelfiltration Methods 0.000 description 2
- 238000001415 gene therapy Methods 0.000 description 2
- 125000000404 glutamine group Chemical group N[C@@H](CCC(N)=O)C(=O)* 0.000 description 2
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Chemical group OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 2
- 235000014304 histidine Nutrition 0.000 description 2
- 210000003016 hypothalamus Anatomy 0.000 description 2
- 239000012133 immunoprecipitate Substances 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 210000003000 inclusion body Anatomy 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- 235000018977 lysine Nutrition 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000002503 metabolic effect Effects 0.000 description 2
- 210000001589 microsome Anatomy 0.000 description 2
- 230000003278 mimic effect Effects 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 108091027963 non-coding RNA Proteins 0.000 description 2
- 102000042567 non-coding RNA Human genes 0.000 description 2
- 230000037434 nonsense mutation Effects 0.000 description 2
- 235000016709 nutrition Nutrition 0.000 description 2
- 230000001575 pathological effect Effects 0.000 description 2
- 239000013612 plasmid Substances 0.000 description 2
- 238000002264 polyacrylamide gel electrophoresis Methods 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 235000019419 proteases Nutrition 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 108091008146 restriction endonucleases Proteins 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 239000012723 sample buffer Substances 0.000 description 2
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229960004072 thrombin Drugs 0.000 description 2
- 238000004260 weight control Methods 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical group OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- 102000040650 (ribonucleotides)n+m Human genes 0.000 description 1
- OSBLTNPMIGYQGY-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetic acid;boric acid Chemical compound OB(O)O.OCC(N)(CO)CO.OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O OSBLTNPMIGYQGY-UHFFFAOYSA-N 0.000 description 1
- KAAUTWNXDOZQPH-NVSRRLLLSA-N 2-aminoacetic acid (2S)-2-amino-3-hydroxypropanoic acid (2S)-2-amino-3-(1H-imidazol-5-yl)propanoic acid (2S)-2-amino-4-methylsulfanylbutanoic acid Chemical group NCC(O)=O.OC[C@H](N)C(O)=O.CSCC[C@H](N)C(O)=O.OC(=O)[C@@H](N)CC1=CNC=N1 KAAUTWNXDOZQPH-NVSRRLLLSA-N 0.000 description 1
- NOFBOJZLPLKNHT-WSTBAARBSA-N 2-aminoacetic acid;(2s)-2-amino-3-hydroxypropanoic acid;(2s)-pyrrolidine-2-carboxylic acid Chemical group NCC(O)=O.OC[C@H](N)C(O)=O.OC(=O)[C@@H]1CCCN1 NOFBOJZLPLKNHT-WSTBAARBSA-N 0.000 description 1
- CZMRCDWAGMRECN-UHFFFAOYSA-N 2-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound OCC1OC(CO)(OC2OC(CO)C(O)C(O)C2O)C(O)C1O CZMRCDWAGMRECN-UHFFFAOYSA-N 0.000 description 1
- 208000030507 AIDS Diseases 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 208000007848 Alcoholism Diseases 0.000 description 1
- 108700028369 Alleles Proteins 0.000 description 1
- 208000000103 Anorexia Nervosa Diseases 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 description 1
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 206010003694 Atrophy Diseases 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- 108010077805 Bacterial Proteins Proteins 0.000 description 1
- 206010006895 Cachexia Diseases 0.000 description 1
- 241000282465 Canis Species 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 102000014914 Carrier Proteins Human genes 0.000 description 1
- 108010078791 Carrier Proteins Proteins 0.000 description 1
- 102000029816 Collagenase Human genes 0.000 description 1
- 108060005980 Collagenase Proteins 0.000 description 1
- 239000003155 DNA primer Substances 0.000 description 1
- 239000003298 DNA probe Substances 0.000 description 1
- SHIBSTMRCDJXLN-UHFFFAOYSA-N Digoxigenin Natural products C1CC(C2C(C3(C)CCC(O)CC3CC2)CC2O)(O)C2(C)C1C1=CC(=O)OC1 SHIBSTMRCDJXLN-UHFFFAOYSA-N 0.000 description 1
- 108010067770 Endopeptidase K Proteins 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 208000004930 Fatty Liver Diseases 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 108010058643 Fungal Proteins Proteins 0.000 description 1
- 206010064571 Gene mutation Diseases 0.000 description 1
- 206010019708 Hepatic steatosis Diseases 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 206010020880 Hypertrophy Diseases 0.000 description 1
- 206010022491 Insulin resistant diabetes Diseases 0.000 description 1
- 102100034343 Integrase Human genes 0.000 description 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical group OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 1
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical group OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical group OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical group NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 1
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical group OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 1
- 108091026898 Leader sequence (mRNA) Proteins 0.000 description 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
- 101100102907 Mus musculus Wdtc1 gene Proteins 0.000 description 1
- 125000000729 N-terminal amino-acid group Chemical group 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 238000000636 Northern blotting Methods 0.000 description 1
- 238000012408 PCR amplification Methods 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Chemical group OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 108010092799 RNA-directed DNA polymerase Proteins 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- 241000235070 Saccharomyces Species 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Chemical group OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- 241000187747 Streptomyces Species 0.000 description 1
- 239000008051 TBE buffer Substances 0.000 description 1
- 108091036066 Three prime untranslated region Proteins 0.000 description 1
- 108700009124 Transcription Initiation Site Proteins 0.000 description 1
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 1
- 241000251539 Vertebrata <Metazoa> Species 0.000 description 1
- 230000003187 abdominal effect Effects 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 239000000556 agonist Substances 0.000 description 1
- 201000007930 alcohol dependence Diseases 0.000 description 1
- 125000000539 amino acid group Chemical group 0.000 description 1
- 230000000890 antigenic effect Effects 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 235000009582 asparagine Nutrition 0.000 description 1
- 229960001230 asparagine Drugs 0.000 description 1
- 125000000613 asparagine group Chemical group N[C@@H](CC(N)=O)C(=O)* 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 230000037444 atrophy Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000003542 behavioural effect Effects 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Chemical group OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 239000012148 binding buffer Substances 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 210000004899 c-terminal region Anatomy 0.000 description 1
- 238000010804 cDNA synthesis Methods 0.000 description 1
- 235000019577 caloric intake Nutrition 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 230000023852 carbohydrate metabolic process Effects 0.000 description 1
- 235000021256 carbohydrate metabolism Nutrition 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 230000002759 chromosomal effect Effects 0.000 description 1
- 229960002424 collagenase Drugs 0.000 description 1
- 238000004590 computer program Methods 0.000 description 1
- 230000001268 conjugating effect Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 description 1
- 210000000805 cytoplasm Anatomy 0.000 description 1
- 230000001086 cytosolic effect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000000378 dietary effect Effects 0.000 description 1
- QONQRTHLHBTMGP-UHFFFAOYSA-N digitoxigenin Natural products CC12CCC(C3(CCC(O)CC3CC3)C)C3C11OC1CC2C1=CC(=O)OC1 QONQRTHLHBTMGP-UHFFFAOYSA-N 0.000 description 1
- SHIBSTMRCDJXLN-KCZCNTNESA-N digoxigenin Chemical compound C1([C@@H]2[C@@]3([C@@](CC2)(O)[C@H]2[C@@H]([C@@]4(C)CC[C@H](O)C[C@H]4CC2)C[C@H]3O)C)=CC(=O)OC1 SHIBSTMRCDJXLN-KCZCNTNESA-N 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000004064 dysfunction Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001400 expression cloning Methods 0.000 description 1
- 208000010706 fatty liver disease Diseases 0.000 description 1
- 230000008713 feedback mechanism Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000012252 genetic analysis Methods 0.000 description 1
- 125000000291 glutamic acid group Chemical group N[C@@H](CCC(O)=O)C(=O)* 0.000 description 1
- 229960004198 guanidine Drugs 0.000 description 1
- PJJJBBJSCAKJQF-UHFFFAOYSA-N guanidinium chloride Chemical compound [Cl-].NC(N)=[NH2+] PJJJBBJSCAKJQF-UHFFFAOYSA-N 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 125000000487 histidyl group Chemical group [H]N([H])C(C(=O)O*)C([H])([H])C1=C([H])N([H])C([H])=N1 0.000 description 1
- 230000003284 homeostatic effect Effects 0.000 description 1
- 230000009097 homeostatic mechanism Effects 0.000 description 1
- 230000003054 hormonal effect Effects 0.000 description 1
- 210000005260 human cell Anatomy 0.000 description 1
- 210000003917 human chromosome Anatomy 0.000 description 1
- 230000001127 hyperphagic effect Effects 0.000 description 1
- 230000002806 hypometabolic effect Effects 0.000 description 1
- 230000003053 immunization Effects 0.000 description 1
- 238000003018 immunoassay Methods 0.000 description 1
- 230000002163 immunogen Effects 0.000 description 1
- 238000007901 in situ hybridization Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000001361 intraarterial administration Methods 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000000741 isoleucyl group Chemical group [H]N([H])C(C(C([H])([H])[H])C([H])([H])C([H])([H])[H])C(=O)O* 0.000 description 1
- BPHPUYQFMNQIOC-NXRLNHOXSA-N isopropyl beta-D-thiogalactopyranoside Chemical compound CC(C)S[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O BPHPUYQFMNQIOC-NXRLNHOXSA-N 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 125000001909 leucine group Chemical group [H]N(*)C(C(*)=O)C([H])([H])C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 1
- 238000013507 mapping Methods 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000004066 metabolic change Effects 0.000 description 1
- 230000009456 molecular mechanism Effects 0.000 description 1
- 230000017074 necrotic cell death Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 230000008823 permeabilization Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- COLNVLDHVKWLRT-QMMMGPOBSA-N phenylalanine group Chemical group N[C@@H](CC1=CC=CC=C1)C(=O)O COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 230000036470 plasma concentration Effects 0.000 description 1
- 229920002704 polyhistidine Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 210000004896 polypeptide structure Anatomy 0.000 description 1
- 210000000229 preadipocyte Anatomy 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000004393 prognosis Methods 0.000 description 1
- 235000013930 proline Nutrition 0.000 description 1
- 230000017854 proteolysis Effects 0.000 description 1
- 230000002685 pulmonary effect Effects 0.000 description 1
- 238000003127 radioimmunoassay Methods 0.000 description 1
- 238000003259 recombinant expression Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007894 restriction fragment length polymorphism technique Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000011808 rodent model Methods 0.000 description 1
- 230000036186 satiety Effects 0.000 description 1
- 235000019627 satiety Nutrition 0.000 description 1
- 201000000980 schizophrenia Diseases 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 235000004400 serine Nutrition 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 1
- 210000000952 spleen Anatomy 0.000 description 1
- 231100000240 steatosis hepatitis Toxicity 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 238000011285 therapeutic regimen Methods 0.000 description 1
- -1 thiophosphate Chemical class 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 241001515965 unidentified phage Species 0.000 description 1
- 210000003934 vacuole Anatomy 0.000 description 1
- 125000002987 valine group Chemical group [H]N([H])C([H])(C(*)=O)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 210000005253 yeast cell Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/26—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against hormones ; against hormone releasing or inhibiting factors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/06—Preparations for care of the skin for countering cellulitis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/5759—Products of obesity genes, e.g. leptin, obese (OB), tub, fat
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K2217/00—Genetically modified animals
- A01K2217/05—Animals comprising random inserted nucleic acids (transgenic)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/34—Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/158—Expression markers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Medicinal Chemistry (AREA)
- Genetics & Genomics (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Obesity (AREA)
- Zoology (AREA)
- Diabetes (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Endocrinology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Wood Science & Technology (AREA)
- Analytical Chemistry (AREA)
- Child & Adolescent Psychology (AREA)
- Physics & Mathematics (AREA)
- Toxicology (AREA)
- Biotechnology (AREA)
- Gastroenterology & Hepatology (AREA)
- Microbiology (AREA)
- Pathology (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- General Engineering & Computer Science (AREA)
- Cardiology (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/292,345 US6001968A (en) | 1994-08-17 | 1994-08-17 | OB polypeptides, modified forms and compositions |
| US08/347,563 US5935810A (en) | 1994-08-17 | 1994-11-30 | Mammalian ob polypeptides capable of modulating body weight, corresponding nucleic acids, and diagnostic and therapeutic uses thereof |
| US08/438,431 US6429290B1 (en) | 1994-08-17 | 1995-05-10 | OB polypeptides, modified forms and derivatives |
| US08/483,211 US6309853B1 (en) | 1994-08-17 | 1995-06-07 | Modulators of body weight, corresponding nucleic acids and proteins, and diagnostic and therapeutic uses thereof |
| PCT/US1995/010479 WO1996005309A2 (fr) | 1994-08-17 | 1995-08-17 | Modulateurs de masse corporelle, proteines et acides nucleiques correspondants, et utilisations a des fins therapeutiques et diagnostiques |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AP9700919A0 AP9700919A0 (en) | 1997-01-31 |
| AP815A true AP815A (en) | 2000-03-10 |
Family
ID=27501568
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| APAP/P/1997/000919A AP815A (en) | 1994-08-17 | 1995-08-17 | An obesity (ob) polypeptide capable of modulating body weight, nucleic acids therefore, and diagnostic and therapeutic use thereof. |
Country Status (32)
| Country | Link |
|---|---|
| US (1) | US6309853B1 (fr) |
| EP (1) | EP0777732B1 (fr) |
| JP (1) | JP3479080B2 (fr) |
| CN (1) | CN1162978B (fr) |
| AP (1) | AP815A (fr) |
| BG (1) | BG64710B1 (fr) |
| BR (1) | BR9508596A (fr) |
| CA (1) | CA2195955C (fr) |
| CZ (1) | CZ295018B6 (fr) |
| DE (2) | DE777732T1 (fr) |
| EE (1) | EE04377B1 (fr) |
| ES (1) | ES2108663T3 (fr) |
| FI (1) | FI121709B (fr) |
| GB (1) | GB2292382B (fr) |
| GE (1) | GEP20022701B (fr) |
| GR (1) | GR970300021T1 (fr) |
| HK (1) | HK1001495A1 (fr) |
| HU (1) | HU223563B1 (fr) |
| IL (2) | IL114987A (fr) |
| IS (1) | IS4416A (fr) |
| LV (1) | LV11868B (fr) |
| MD (1) | MD2311G2 (fr) |
| MX (1) | MX9701200A (fr) |
| NO (2) | NO323847B1 (fr) |
| NZ (1) | NZ291689A (fr) |
| OA (1) | OA10596A (fr) |
| PL (1) | PL183352B1 (fr) |
| RO (1) | RO121036B1 (fr) |
| SI (1) | SI9520090A (fr) |
| SK (1) | SK287191B6 (fr) |
| TR (1) | TR199501021A2 (fr) |
| WO (1) | WO1996005309A2 (fr) |
Families Citing this family (346)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6310034B1 (en) | 1993-05-21 | 2001-10-30 | Ut-Battelle, Llc | Agouti polypeptide compositions |
| US6350730B1 (en) | 1994-08-17 | 2002-02-26 | The Rockefeller University | OB polypeptides and modified forms as modulators of body weight |
| US6471956B1 (en) | 1994-08-17 | 2002-10-29 | The Rockefeller University | Ob polypeptides, modified forms and compositions thereto |
| US6429290B1 (en) | 1994-08-17 | 2002-08-06 | The Rockefeller University | OB polypeptides, modified forms and derivatives |
| US6001968A (en) | 1994-08-17 | 1999-12-14 | The Rockefeller University | OB polypeptides, modified forms and compositions |
| US5858967A (en) * | 1995-01-20 | 1999-01-12 | University Of Washington | Appetite supression factor and related methods |
| US5827734A (en) * | 1995-01-20 | 1998-10-27 | University Of Washington | Materials and methods for determining ob protein in a biological sample |
| US5580954A (en) * | 1995-01-31 | 1996-12-03 | Eli Lilly And Company | Anti-obesity proteins |
| US5691309A (en) * | 1995-01-31 | 1997-11-25 | Eli Lilly And Company | Anti-obesity proteins |
| US5605886A (en) * | 1995-01-31 | 1997-02-25 | Eli Lilly And Company | Anti-obesity proteins |
| US5594104A (en) * | 1995-01-31 | 1997-01-14 | Eli Lilly And Company | Anti-obesity proteins |
| US5563244A (en) * | 1995-01-31 | 1996-10-08 | Eli Lilly And Company | Anti-obesity proteins |
| US5563245A (en) * | 1995-01-31 | 1996-10-08 | Eli Lilly And Company | Anti-obesity proteins |
| US5569743A (en) * | 1995-01-31 | 1996-10-29 | Eli Lilly And Company | Anti-obesity proteins |
| WO1996023515A1 (fr) * | 1995-01-31 | 1996-08-08 | Eli Lilly And Company | Proteines anti-obesite |
| US5559208A (en) * | 1995-01-31 | 1996-09-24 | Eli Lilly And Company | Anti-obesity proteins |
| US5567678A (en) * | 1995-01-31 | 1996-10-22 | Eli Lilly And Company | Anti-obesity proteins |
| US5552523A (en) * | 1995-01-31 | 1996-09-03 | Eli Lilly And Company | Anti-obesity proteins |
| US5552522A (en) * | 1995-01-31 | 1996-09-03 | Eli Lilly And Company | Anti-obesity proteins |
| US5554727A (en) * | 1995-01-31 | 1996-09-10 | Eli Lilly And Company | Anti-obesity proteins |
| US5563243A (en) * | 1995-01-31 | 1996-10-08 | Eli Lilly And Company | Anti-obesity proteins |
| US5567803A (en) * | 1995-01-31 | 1996-10-22 | Eli Lilly And Company | Anti-obesity proteins |
| US5574133A (en) * | 1995-01-31 | 1996-11-12 | Eli Lilly And Company | Anti-obesity proteins |
| US5594101A (en) * | 1995-03-03 | 1997-01-14 | Eli Lilly And Company | Anti-obesity proteins |
| US5719266A (en) * | 1995-03-17 | 1998-02-17 | Eli Lilly And Company | Anti-obesity proteins |
| EP0736599A3 (fr) * | 1995-04-03 | 1996-12-11 | Takeda Chemical Industries Ltd | Le gène d'obésité de rat, son produit génique et sa production |
| AU5098396A (en) * | 1995-04-07 | 1996-10-23 | Kuyus-Stiftung | Cosmetic composition for treating cellulite |
| US5840517A (en) * | 1995-04-26 | 1998-11-24 | Eli Lilly And Company | Process for preparing obesity protein analogs |
| US5614379A (en) * | 1995-04-26 | 1997-03-25 | Eli Lilly And Company | Process for preparing anti-obesity protein |
| GB9509164D0 (en) * | 1995-05-05 | 1995-06-28 | Smithkline Beecham Plc | Novel compounds |
| DE741187T1 (de) * | 1995-05-05 | 1997-04-30 | Hoffmann La Roche | Rekombinante Obesitäts-(OB)-Proteine |
| ZA963530B (en) * | 1995-05-05 | 1996-11-05 | Hoffmann La Roche | Recombinant obese (ob) proteins |
| WO1996035787A1 (fr) * | 1995-05-08 | 1996-11-14 | Chiron Corporation | Acides nucleiques pour traiter l'obesite |
| CA2221303A1 (fr) * | 1995-05-19 | 1996-11-21 | Dennis Paul Smith | Produit du gene de l'obesite |
| AU5800696A (en) * | 1995-05-26 | 1996-12-11 | Eli Lilly And Company | Rhesus ob protein and dna |
| US6395509B1 (en) | 1995-05-26 | 2002-05-28 | Eli Lilly And Company | DNA encoding Rhesus ob protein |
| AU6028396A (en) * | 1995-06-07 | 1996-12-30 | Amgen, Inc. | Ob protein compositions and method |
| GB9511935D0 (en) * | 1995-06-13 | 1995-08-09 | Smithkline Beecham Plc | Novel compound |
| EP0833835A4 (fr) * | 1995-06-22 | 1999-05-26 | Lilly Co Eli | Intermediaires de proteines contre l'obesite, leur preparation et leur utilisation |
| ZA965346B (en) * | 1995-06-30 | 1997-12-24 | Lilly Co Eli | Methods of treating neuropeptide Y-associated conditions. |
| EP0759441A3 (fr) * | 1995-06-30 | 1999-06-30 | Eli Lilly And Company | Procédés de traitement des pathologies associées aux peptides neuropeptide Y |
| AU695934B2 (en) * | 1995-06-30 | 1998-08-27 | Eli Lilly And Company | Methods for treating diabetes |
| JP4173913B2 (ja) * | 1995-08-17 | 2008-10-29 | アムジエン・インコーポレーテツド | Ｏｂタンパク質組成物を用いて血中脂質レベルを減少させ又は減少した血中脂質レベルを維持する方法 |
| WO1997011192A1 (fr) * | 1995-09-19 | 1997-03-27 | Eli Lilly And Company | Adn codant des proteines medicinales |
| WO1997016550A1 (fr) * | 1995-11-02 | 1997-05-09 | Bristol-Myers Squibb Company | Fragments polypeptides derives du produit genique obese |
| US6936439B2 (en) | 1995-11-22 | 2005-08-30 | Amgen Inc. | OB fusion protein compositions and methods |
| US20030040467A1 (en) | 1998-06-15 | 2003-02-27 | Mary Ann Pelleymounter | Ig/ob fusions and uses thereof. |
| EP1285664B1 (fr) * | 1995-11-22 | 2010-01-20 | Amgen Inc. | Procédés permettant d'accroitre la masse tissulaire maigre à l'aide de compositions à base de proteine ob |
| US6225446B1 (en) | 1995-12-06 | 2001-05-01 | Schering Corporation | Mutational variants of mammalian proteins |
| AU1406497A (en) * | 1995-12-06 | 1997-06-27 | Schering Corporation | Mutational variants of mammalian ob gene proteins |
| US7632922B1 (en) | 1995-12-22 | 2009-12-15 | Amgen, Inc. | Osteoprotegerin |
| US6369027B1 (en) * | 1995-12-22 | 2002-04-09 | Amgen Inc. | Osteoprotegerin |
| US6620413B1 (en) | 1995-12-27 | 2003-09-16 | Genentech, Inc. | OB protein-polymer chimeras |
| DE69632546T2 (de) * | 1995-12-27 | 2005-06-30 | Genentech, Inc., South San Francisco | Ob proteinderivate mit verlängerter halbwertzeit |
| US6541604B1 (en) | 1996-01-08 | 2003-04-01 | Genentech, Inc. | Leptin receptor having a WSX motif |
| US20050019325A1 (en) | 1996-01-08 | 2005-01-27 | Carter Paul J. | WSX receptor agonist antibodies |
| US7074397B1 (en) | 1996-01-08 | 2006-07-11 | Genentech, Inc. | Method for enhancing proliferation or differentiation of a cell using ob protein |
| US6087129A (en) | 1996-01-19 | 2000-07-11 | Betagene, Inc. | Recombinant expression of proteins from secretory cell lines |
| US6110707A (en) * | 1996-01-19 | 2000-08-29 | Board Of Regents, The University Of Texas System | Recombinant expression of proteins from secretory cell lines |
| US5831017A (en) * | 1996-01-25 | 1998-11-03 | Eli Lilly And Company | Obesity protein analog compounds and formulations thereof |
| HUP0000280A3 (en) * | 1996-03-01 | 2002-09-30 | Amgen Inc Thousand Oaks | Canine ob protein compositions and methods |
| JP2000509018A (ja) * | 1996-03-26 | 2000-07-18 | イーライ・リリー・アンド・カンパニー | 肥満タンパク質製剤 |
| EP0917469A1 (fr) * | 1996-04-19 | 1999-05-26 | ZymoGenetics, Inc. | Procedes permettant d'induire la formation osseuse |
| US6007998A (en) * | 1996-04-22 | 1999-12-28 | Merck & Co., Inc. | Leptin assay |
| US6025324A (en) * | 1996-05-15 | 2000-02-15 | Hoffmann-La Roche Inc. | Pegylated obese (ob) protein compositions |
| DK0929310T3 (da) * | 1996-06-04 | 2007-12-10 | Scripps Research Inst | Diagnostiske og terapeutiske metoder relateret til regulering af energimobilisering med OB-protein og OB-antistoffer |
| CN1221426A (zh) * | 1996-06-06 | 1999-06-30 | 史密丝克莱恩比彻姆有限公司 | 来普亭(鄂毕肽)片段 |
| WO1997048419A1 (fr) * | 1996-06-20 | 1997-12-24 | Merck & Co., Inc. | Therapie genique de l'obesite |
| US6001816A (en) * | 1996-06-20 | 1999-12-14 | Merck & Co., Inc. | Gene therapy for leptin deficiency |
| WO1997048806A1 (fr) * | 1996-06-20 | 1997-12-24 | Merck & Co., Inc. | Therapie genique pour le traitement de l'obesite |
| US6630346B1 (en) * | 1996-06-20 | 2003-10-07 | Merck & Co., Inc. | Gene therapy for obesity |
| US5869037A (en) * | 1996-06-26 | 1999-02-09 | Cornell Research Foundation, Inc. | Adenoviral-mediated gene transfer to adipocytes |
| US20020110857A1 (en) * | 1996-07-31 | 2002-08-15 | Spurlock Michael E. | Bovine leptin protein, antisense and antibody |
| US6277592B1 (en) * | 1996-07-31 | 2001-08-21 | Purina Mills, Inc. | Porcine leptin protein, nucleic acid sequences coding therefor and uses thereof |
| WO1998008512A1 (fr) * | 1996-08-30 | 1998-03-05 | Amgen Inc. | Methodes pour accroitre la sensibilite d'un individu a la proteine ob par accroissement de l'affinite du recepteur de la proteine ob |
| CA2266585A1 (fr) * | 1996-09-20 | 1998-03-26 | Hoechst Aktiengesellschaft | Utilisation d'antagonistes de la leptine pour le traitement de la resistance insulinique dans les diabetes non insulino-dependants |
| SE520392C2 (sv) * | 1996-09-27 | 2003-07-01 | Creative Peptides Sweden Ab C | Specifika peptider för behandling av diabetes mellitus |
| WO1998016545A1 (fr) * | 1996-10-11 | 1998-04-23 | Eli Lilly And Company | Proteines therapeutiques |
| UA65549C2 (uk) | 1996-11-05 | 2004-04-15 | Елі Ліллі Енд Компані | Спосіб регулювання ожиріння шляхом периферійного введення аналогів та похідних glp-1 (варіанти) та фармацевтична композиція |
| NL1004559C2 (nl) * | 1996-11-18 | 1998-05-19 | Unilife | Boter. |
| AU5654998A (en) * | 1996-12-06 | 1998-06-29 | F. Hoffmann-La Roche Ag | Muteins of obese protein |
| CA2217698A1 (fr) * | 1996-12-20 | 1998-06-20 | Eli Lilly And Company | Proteines contre l'obesite |
| WO1998028414A1 (fr) * | 1996-12-20 | 1998-07-02 | Eli Lilly And Company | Proteines anti-obesite |
| KR100937550B1 (ko) * | 1996-12-20 | 2010-01-19 | 암젠 인코포레이티드 | Ｏｂ 융합 단백질 조성물과 이 단백질의 제조 방법 |
| CN101239089A (zh) * | 1997-04-15 | 2008-08-13 | Csir公司 | 具有食欲抑制剂活性的药物组合物 |
| US20020019352A1 (en) * | 1997-04-17 | 2002-02-14 | David N. Brems | Stable, active, human ob protein compositions and methods |
| WO1998055139A1 (fr) * | 1997-06-06 | 1998-12-10 | Smithkline Beecham Plc | Utilisation d'antagonistes de leptine pour traiter le diabete |
| US6017876A (en) | 1997-08-15 | 2000-01-25 | Amgen Inc. | Chemical modification of granulocyte-colony stimulating factor (G-CSF) bioactivity |
| WO1999029732A2 (fr) | 1997-12-08 | 1999-06-17 | Lexigen Pharmaceuticals Corporation | Proteines de fusion heterodymeres utiles en therapie immune ciblee et a une stimulation immune generale |
| US5866547A (en) | 1998-01-20 | 1999-02-02 | Beth Israel Deaconess Medical Center | Methods of neuroendocrine regulation of affective disorders |
| EP0950417A3 (fr) | 1998-02-23 | 2000-02-23 | Pfizer Products Inc. | Traitement d' anomalies du squelette |
| US6541033B1 (en) | 1998-06-30 | 2003-04-01 | Amgen Inc. | Thermosensitive biodegradable hydrogels for sustained delivery of leptin |
| US6210924B1 (en) | 1998-08-11 | 2001-04-03 | Amgen Inc. | Overexpressing cyclin D 1 in a eukaryotic cell line |
| ATE230796T1 (de) * | 1998-08-12 | 2003-01-15 | Medical Res Council | Obesitätsphänotyp erzeugendes gen |
| US7208572B2 (en) | 1998-08-21 | 2007-04-24 | Albany Medical College | Leptin-related peptides |
| US6777388B1 (en) | 1998-08-21 | 2004-08-17 | Clf Medical Technology Acceleration Program, Inc. | Leptin-related peptides |
| US7056504B1 (en) | 1998-08-27 | 2006-06-06 | Massachusetts Institute Of Technology | Rationally designed heparinases derived from heparinase I and II |
| CA2341412A1 (fr) * | 1998-08-27 | 2000-03-09 | Massachusetts Institute Of Technology | Heparinases a conception rationnelle derivees de l'heparinase i et ii |
| US6420339B1 (en) | 1998-10-14 | 2002-07-16 | Amgen Inc. | Site-directed dual pegylation of proteins for improved bioactivity and biocompatibility |
| ATE348163T1 (de) | 1998-10-23 | 2007-01-15 | Amgen Inc | Thrombopoietin substitute |
| US6660843B1 (en) † | 1998-10-23 | 2003-12-09 | Amgen Inc. | Modified peptides as therapeutic agents |
| US7488590B2 (en) | 1998-10-23 | 2009-02-10 | Amgen Inc. | Modified peptides as therapeutic agents |
| US6245740B1 (en) | 1998-12-23 | 2001-06-12 | Amgen Inc. | Polyol:oil suspensions for the sustained release of proteins |
| AU2221600A (en) | 1998-12-31 | 2000-07-31 | Chiron Corporation | Improved expression of hiv polypeptides and production of virus-like particles |
| CZ20012406A3 (cs) * | 1999-01-07 | 2002-03-13 | Lexigen Pharmaceuticals, Corp. | Exprese a export proteinů působících proti obezitě jako Fc fúzních proteinů |
| CA2359840C (fr) * | 1999-02-12 | 2012-10-23 | Amgen Inc. | Compositions glycosylees de leptine et procedes correspondants |
| WO2000056903A2 (fr) * | 1999-03-22 | 2000-09-28 | Zymogenetics, Inc. | Methodes ameliorees de production de proteines dans la pichia transformee |
| US20050272652A1 (en) | 1999-03-29 | 2005-12-08 | Gault Victor A | Peptide analogues of GIP for treatment of diabetes, insulin resistance and obesity |
| EP1190364A2 (fr) | 1999-04-23 | 2002-03-27 | Massachusetts Institute Of Technology | Systeme et procede de notation de polymeres |
| US7067110B1 (en) | 1999-07-21 | 2006-06-27 | Emd Lexigen Research Center Corp. | Fc fusion proteins for enhancing the immunogenicity of protein and peptide antigens |
| SK782002A3 (en) | 1999-07-21 | 2003-08-05 | Lexigen Pharm Corp | FC fusion proteins for enhancing the immunogenicity of protein and peptide antigens |
| WO2001010912A1 (fr) | 1999-08-09 | 2001-02-15 | Lexigen Pharmaceuticals Corp. | Complexes d'anticorps contenant plusieurs cytokines |
| US8106098B2 (en) | 1999-08-09 | 2012-01-31 | The General Hospital Corporation | Protein conjugates with a water-soluble biocompatible, biodegradable polymer |
| GB2396815B (en) * | 1999-10-27 | 2004-09-08 | Phytopharm Plc | A composition comprising a pregnenone derivative and an NSAID |
| JP2003514552A (ja) | 1999-11-12 | 2003-04-22 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフトング | 改善された性質を有するエリトロポエチンの形態 |
| WO2001058957A2 (fr) | 2000-02-11 | 2001-08-16 | Lexigen Pharmaceuticals Corp. | Amelioration de la demi-vie circulante de proteines de fusion a base d'anticorps |
| EP1266013B1 (fr) * | 2000-03-08 | 2014-10-15 | Massachusetts Institute Of Technology | Heparinase iii et ses utilisations |
| US6743778B2 (en) | 2000-04-21 | 2004-06-01 | Amgen Inc. | Apo-AI/AII peptide derivatives |
| US6677136B2 (en) | 2000-05-03 | 2004-01-13 | Amgen Inc. | Glucagon antagonists |
| US7517526B2 (en) | 2000-06-29 | 2009-04-14 | Merck Patent Gmbh | Enhancement of antibody-cytokine fusion protein mediated immune responses by combined treatment with immunocytokine uptake enhancing agents |
| GB2363985B (en) * | 2000-06-30 | 2004-09-29 | Phytopharm Plc | Extracts,compounds & pharmaceutical compositions having anti-diabetic activity and their use |
| US6443013B1 (en) * | 2000-08-04 | 2002-09-03 | Samsung Electronics Co., Ltd. | Rotary test fixture |
| CN1231262C (zh) * | 2000-09-04 | 2005-12-14 | 金晓骏 | 载脂蛋白b－100表位的模拟肽、其多联体和修饰肽,以及含有这些肽的疫苗组合物 |
| ATE426805T1 (de) | 2000-09-12 | 2009-04-15 | Massachusetts Inst Technology | Verfahren und produkte, die mit niedermolekularem heparin assoziiert sind |
| EP1328260A2 (fr) | 2000-10-18 | 2003-07-23 | Massachusetts Institute Of Technology | Procedes et produits associes a l'administration pulmonaires de polysaccharides |
| US7054758B2 (en) | 2001-01-30 | 2006-05-30 | Sciona Limited | Computer-assisted means for assessing lifestyle risk factors |
| JP4279554B2 (ja) | 2001-02-19 | 2009-06-17 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ｔ細胞エピトープの識別方法および低減された免疫原性を有する分子の製造方法 |
| EP1366067B1 (fr) | 2001-03-07 | 2012-09-26 | Merck Patent GmbH | Technique d'expression pour des proteines contenant un fragment d'anticorps isotype chimerique |
| WO2002079415A2 (fr) | 2001-03-30 | 2002-10-10 | Lexigen Pharmaceuticals Corp. | Reduction de l'immunogenicite de proteines de fusion |
| DE60239454D1 (de) | 2001-05-03 | 2011-04-28 | Merck Patent Gmbh | Rekombinanter, tumorspezifischer antikörper und dessen verwendung |
| CN1970077A (zh) | 2001-05-11 | 2007-05-30 | 安姆根有限公司 | 与tall－1结合的肽和相关分子 |
| US20030083286A1 (en) * | 2001-08-22 | 2003-05-01 | Ching-Leou Teng | Bioadhesive compositions and methods for enhanced intestinal drug absorption |
| US20030124196A1 (en) * | 2001-08-22 | 2003-07-03 | Susan Weinbach | Pulsatile release compositions and methods for enhanced intestinal drug absorption |
| DE10145553B4 (de) * | 2001-09-16 | 2006-06-08 | Gene Architects Ag | Nukleinsäure für einen Klonierungsvektor |
| US9969980B2 (en) | 2001-09-21 | 2018-05-15 | Garnet Biotherapeutics | Cell populations which co-express CD49c and CD90 |
| US7138370B2 (en) | 2001-10-11 | 2006-11-21 | Amgen Inc. | Specific binding agents of human angiopoietin-2 |
| JP2005506994A (ja) * | 2001-10-22 | 2005-03-10 | アムジェン インコーポレイテッド | ヒト脂肪組織萎縮症を処置するためのレプチンの使用および該処置のための素因決定方法 |
| JP4547152B2 (ja) | 2001-10-23 | 2010-09-22 | オクラホマ メディカル リサーチ ファウンデーション | β−セクレターゼ阻害剤および使用方法 |
| ATE542137T1 (de) | 2001-12-04 | 2012-02-15 | Merck Patent Gmbh | Immunocytokine mit modulierter selektivität |
| EP1468036B1 (fr) | 2002-01-14 | 2008-10-08 | The General Hospital Corporation | Polymeres de polycetal biodegradables et procedes de preparation et d'utilisation associes |
| US20030191056A1 (en) | 2002-04-04 | 2003-10-09 | Kenneth Walker | Use of transthyretin peptide/protein fusions to increase the serum half-life of pharmacologically active peptides/proteins |
| CA2387003A1 (fr) * | 2002-05-21 | 2003-11-21 | 984012 Alberta Ltd. | Methode d'amelioration de la productivite de l'elevage d'animaux de boucherie |
| WO2004009082A1 (fr) | 2002-07-19 | 2004-01-29 | The General Hospital Corporation | Conjugues d'oxime et leur procedes de formation et leur utilisation |
| AU2003256613A1 (en) | 2002-07-19 | 2004-02-09 | Amgen Inc. | Protein conjugates with a water-soluble biocompatible, biogradable polymer |
| JP2006508056A (ja) | 2002-08-28 | 2006-03-09 | イミュネックス・コーポレーション | 心臓血管疾患を治療するための組成物および方法 |
| BRPI0317376B8 (pt) | 2002-12-17 | 2021-05-25 | Merck Patent Gmbh | proteína de fusão de anticorpo-il2 designada como hu14.18-il2, usos da mesma, vetor e composição farmacêutica |
| US8491883B2 (en) | 2003-06-27 | 2013-07-23 | Advanced Technologies And Regenerative Medicine, Llc | Treatment of amyotrophic lateral sclerosis using umbilical derived cells |
| US8790637B2 (en) | 2003-06-27 | 2014-07-29 | DePuy Synthes Products, LLC | Repair and regeneration of ocular tissue using postpartum-derived cells |
| US9592258B2 (en) | 2003-06-27 | 2017-03-14 | DePuy Synthes Products, Inc. | Treatment of neurological injury by administration of human umbilical cord tissue-derived cells |
| US9572840B2 (en) | 2003-06-27 | 2017-02-21 | DePuy Synthes Products, Inc. | Regeneration and repair of neural tissue using postpartum-derived cells |
| ES2568463T3 (es) | 2003-06-27 | 2016-04-29 | DePuy Synthes Products, Inc. | Regeneración y reparación de tejido neural usando células del postparto derivadas del cordon umbilical |
| US7875272B2 (en) | 2003-06-27 | 2011-01-25 | Ethicon, Incorporated | Treatment of stroke and other acute neuraldegenerative disorders using postpartum derived cells |
| EP1648935A2 (fr) | 2003-07-25 | 2006-04-26 | Amgen Inc. | Antagonistes et agonistes de ldcam et procedes d'utilisation |
| JP4585186B2 (ja) * | 2003-07-31 | 2010-11-24 | 杏林製薬株式会社 | 肥満、糖尿病及び脂質代謝異常の新規な予防又は治療剤 |
| DE602004032553D1 (de) | 2003-09-05 | 2011-06-16 | Gen Hospital Corp | Polyacetal-arzneimittelkonjugate als freisetzungssystem |
| US7897639B2 (en) | 2003-10-21 | 2011-03-01 | Colucid Pharmaceuticals, Inc. | Carbamoyl esters that inhibit cholinesterase and release pharmacologically active agents |
| DE10352510A1 (de) * | 2003-11-07 | 2005-06-23 | Forschungsinstitut Für Die Biologie Landwirtschaftlicher Nutztiere | Verfahren zur Identifizierung von Wirkstoffen zur Beeinflussung der Körpermasse und des Fettansatzes |
| US20060003008A1 (en) | 2003-12-30 | 2006-01-05 | Gibson John W | Polymeric devices for controlled release of active agents |
| EP2417980A1 (fr) | 2004-02-11 | 2012-02-15 | Amylin Pharmaceuticals Inc. | Polypeptides hybrides présentant des propriétés pouvant être choisies |
| US8076288B2 (en) | 2004-02-11 | 2011-12-13 | Amylin Pharmaceuticals, Inc. | Hybrid polypeptides having glucose lowering activity |
| CA2572765C (fr) | 2004-07-08 | 2013-05-21 | Amgen Inc. | Peptides therapeutiques |
| US20090233986A1 (en) * | 2004-07-27 | 2009-09-17 | Mount Sinai School Of Medicine | Methods and compositions for using sax2 |
| JP2008513497A (ja) | 2004-09-17 | 2008-05-01 | コメンティス，インコーポレーテッド | メマプシン２βセクレターゼ活性を阻害するアミノ含有化合物およびその使用方法 |
| US20090029912A1 (en) | 2004-09-24 | 2009-01-29 | Stan Gronthos | Method of enhancing proliferation and/or survival of mesenchymal precursor cells (mpc) |
| US7442778B2 (en) | 2004-09-24 | 2008-10-28 | Amgen Inc. | Modified Fc molecules |
| WO2006032092A1 (fr) | 2004-09-24 | 2006-03-30 | Angioblast Systems, Inc. | Descendance cellulaire de précurseurs mésenchymateux développés multipotents (memp) et son utilisation |
| US8394765B2 (en) | 2004-11-01 | 2013-03-12 | Amylin Pharmaceuticals Llc | Methods of treating obesity with two different anti-obesity agents |
| US20090156474A1 (en) | 2004-11-01 | 2009-06-18 | Amylin Pharmaceuticals, Inc. | Methods for treating obesity and obesity related diseases and disorders |
| WO2006053883A1 (fr) | 2004-11-18 | 2006-05-26 | Vib Vzw | Domaine de fibronectine iii servant d'antagonistes de recepteurs de la leptine |
| US7307142B2 (en) * | 2004-11-26 | 2007-12-11 | Yissum Research And Development Company Of The Hebrew University Of Jerusalem | Leptin antagonists |
| EP1833496B1 (fr) | 2004-12-23 | 2013-07-31 | Ethicon, Incorporated | Traitement de l'ictus cerebral et d'autres troubles neurodegeneratifs aigus a base de cellules tirees de tissus puerperaux |
| BRPI0606992A2 (pt) | 2005-02-11 | 2009-07-28 | Amylin Pharmaceuticals Inc | análogo e polipeptìdeos hìbridos de gip com propriedades selecionáveis |
| US8263545B2 (en) | 2005-02-11 | 2012-09-11 | Amylin Pharmaceuticals, Inc. | GIP analog and hybrid polypeptides with selectable properties |
| WO2006110668A1 (fr) | 2005-04-08 | 2006-10-19 | Comentis, Inc. | Composes inhibant l'activite beta-secretase et leurs methodes d'utilisation |
| KR101446634B1 (ko) | 2005-04-12 | 2014-10-16 | 메소블라스트, 아이엔씨. | 조직 비특이적인 알카리 포스파타제에 의한 다분화성 성체세포의 분리 |
| US7833979B2 (en) | 2005-04-22 | 2010-11-16 | Amgen Inc. | Toxin peptide therapeutic agents |
| EP2330124B1 (fr) | 2005-08-11 | 2015-02-25 | Amylin Pharmaceuticals, LLC | Polypeptides hybrides ayant des propriétés sélectionnables |
| BRPI0614649A2 (pt) | 2005-08-11 | 2011-04-12 | Amylin Pharmaceuticals Inc | polipeptìdeos hìbridos com propriedades selecionáveis |
| US8008453B2 (en) | 2005-08-12 | 2011-08-30 | Amgen Inc. | Modified Fc molecules |
| US8227408B2 (en) * | 2005-09-07 | 2012-07-24 | Neurotez, Inc. | Leptin as an anti-amyloidogenic biologic and methods for delaying the onset and reducing Alzheimer's disease-like pathology |
| US8642543B2 (en) * | 2005-09-07 | 2014-02-04 | Neurotez, Inc. | Methods for treating progressive cognitive disorders related to neurofibrillary tangles |
| KR20080074120A (ko) | 2005-10-13 | 2008-08-12 | 휴먼 게놈 사이언시즈, 인코포레이티드 | 자가항체 양성 질환 환자의 치료에 유용한 방법 및 조성물 |
| TW200736277A (en) | 2005-11-14 | 2007-10-01 | Amgen Inc | RANKL antibody-PTH/PTHrP chimeric molecules |
| PL1971681T3 (pl) | 2005-12-16 | 2018-01-31 | Depuy Synthes Products Inc | Kompozycje oraz sposoby do hamowania niepożądanej odpowiedzi immunologicznej w przypadku transplantacji z brakiem zgodności tkankowej |
| US9125906B2 (en) | 2005-12-28 | 2015-09-08 | DePuy Synthes Products, Inc. | Treatment of peripheral vascular disease using umbilical cord tissue-derived cells |
| US20070224205A1 (en) | 2006-03-07 | 2007-09-27 | Powell Thomas J | Compositions that include hemagglutinin, methods of making and methods of use thereof |
| US9283260B2 (en) | 2006-04-21 | 2016-03-15 | Amgen Inc. | Lyophilized therapeutic peptibody formulations |
| EP2032600A2 (fr) | 2006-05-19 | 2009-03-11 | Glycofi, Inc. | Compositions d'érythropoïétine |
| ES2376396T3 (es) | 2006-06-26 | 2012-03-13 | Amgen Inc. | Método para tratar aterosclerosis. |
| CN101541783B (zh) | 2006-06-30 | 2014-10-01 | 苏尼西斯制药有限公司 | 吡啶酮基pdk1抑制剂 |
| US8497240B2 (en) | 2006-08-17 | 2013-07-30 | Amylin Pharmaceuticals, Llc | DPP-IV resistant GIP hybrid polypeptides with selectable properties |
| US7803769B2 (en) | 2006-10-25 | 2010-09-28 | Amgen Inc. | OSK1 peptide analogs and pharmaceutical compositions |
| EP2083811B1 (fr) | 2006-11-22 | 2016-10-26 | Clinical Research Associates, LLC | Procédés de traitement du syndrome de down, du syndrome de l'x fragile et de l'autisme |
| JP5591691B2 (ja) | 2007-05-22 | 2014-09-17 | アムジエン・インコーポレーテツド | 生物活性を有する融合タンパク質を作製するための組成物及び方法 |
| DK2170283T3 (en) | 2007-06-22 | 2019-04-15 | Univ Texas | CREATION OF STABLE SUBMICRON Peptide OR PROTEIN PARTICLES BY THIN FILM FREEZING |
| SI2489731T1 (sl) | 2007-07-26 | 2014-12-31 | Amgen Inc. Patent Operations, M/S 28-2-C | Modificirani encimi lecitin-holesterol aciltransferaze |
| KR20100059919A (ko) | 2007-09-24 | 2010-06-04 | 코멘티스, 인코포레이티드 | 치료를 위한 베타-세크레타제 억제제로서 (3-히드록시-4-아미노-부탄-2일)-3-(2-티아졸-2-일-피롤리딘-1-카르보닐) 벤즈아미드 유도체 및 관련 화합물 |
| SG190562A1 (en) | 2008-04-18 | 2013-06-28 | Vaxinnate Corp | Deletion mutants of flagellin and methods of use |
| ES2600469T3 (es) | 2008-05-23 | 2017-02-09 | National Jewish Health | Un compuesto para su uso en el tratamiento de lesiones asociadas con la exposición al gas fosgeno o al gas de cloro |
| WO2009149379A2 (fr) | 2008-06-05 | 2009-12-10 | Regents Of The University Of Michigan | Utilisation de leptine pour le traitement de maladies et affections de stéatose hépatique |
| AU2009262199B2 (en) | 2008-06-27 | 2012-08-09 | Amgen Inc. | Ang-2 inhibition to treat multiple sclerosis |
| JP6144873B2 (ja) | 2008-09-15 | 2017-06-07 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | Ｉｒｅ１、ｓｒｃ、及びａｂｌ活性を調節するための方法及び組成物 |
| JP4966434B2 (ja) | 2008-10-15 | 2012-07-04 | バクスター・インターナショナル・インコーポレイテッド | 結合抗体の存在下における組換え血液凝固因子のｐｅｇ化 |
| CN102281865B (zh) | 2008-10-15 | 2017-04-05 | 精达制药公司 | 高浓缩药物颗粒、制剂、混悬剂及其应用 |
| WO2010054017A1 (fr) * | 2008-11-04 | 2010-05-14 | Nikolaos Tezapsidis | Compositions à base de leptine et méthodes de traitement de troubles évolutifs de la fonction cognitive provoqués par une accumulation d’enchevêtrements neurofibrillaires et de bêta-amyloïde |
| WO2010068759A1 (fr) | 2008-12-10 | 2010-06-17 | Mersana Therapeutics, Inc. | Formules pharmaceutiques de conjugués camptothécine-polymère biodégradables et biocompatibles |
| DK2379087T3 (da) | 2008-12-19 | 2014-11-10 | Depuy Synthes Products Llc | Celler, der stammer fra navlestrengsvæv, til behandling af neuropatisk smerte og spasticitet |
| US10179900B2 (en) | 2008-12-19 | 2019-01-15 | DePuy Synthes Products, Inc. | Conditioned media and methods of making a conditioned media |
| CA2747794C (fr) | 2008-12-19 | 2018-10-30 | Advanced Technologies And Regenerative Medicine, Llc | Traitement des poumons et des maladies et troubles pulmonaires |
| CN108530543B (zh) | 2009-02-03 | 2023-06-23 | 阿穆尼克斯制药公司 | 延伸重组多肽和包含该延伸重组多肽的组合物 |
| CN102498204B (zh) | 2009-03-26 | 2015-02-04 | 德普伊新特斯产品有限责任公司 | 人脐带组织细胞作为用于阿尔茨海默病的疗法 |
| EP2416797A4 (fr) | 2009-04-10 | 2013-04-24 | Amylin Pharmaceuticals Llc | Composés agonistes de l'amyline pour mammifères ayant une carence en strogènes |
| CN102647998A (zh) | 2009-06-19 | 2012-08-22 | 医学免疫有限责任公司 | 蛋白酶变体 |
| NZ713361A (en) | 2009-08-17 | 2017-06-30 | Memorial Sloan Kettering Cancer Center | Heat shock protein binding compounds, compositions, and methods for making and using same |
| US9029359B2 (en) | 2009-09-04 | 2015-05-12 | Biogen Idec Ma, Inc. | Heteroaryl Btk inhibitors |
| PL2473049T3 (pl) | 2009-09-04 | 2019-07-31 | Biogen Ma Inc. | Inhibitory kinazy tyrozynowej brutona |
| RU2615130C2 (ru) | 2009-10-06 | 2017-04-04 | Милленниум Фармасьютикалз, Инк | Гетероциклические соединения, используемые в качестве ингибиторов pdk1 |
| JP2013510088A (ja) | 2009-11-05 | 2013-03-21 | ブラウン ユニバーシティ | ｍＴＯＲのシグナル伝達の増強を処置する方法 |
| US20110136728A1 (en) * | 2009-12-09 | 2011-06-09 | Patricia Grasso | Methods of increasing bone formation using leptin-related peptides |
| HUE027199T2 (en) | 2009-12-10 | 2016-08-29 | Univ California | Amyloid binding agents |
| CN110269856A (zh) | 2010-03-30 | 2019-09-24 | 维颂公司 | 多取代芳族化合物作为凝血酶的抑制剂 |
| CN101812450B (zh) * | 2010-04-28 | 2012-01-11 | 中国农业大学 | 辅助鉴定具有不同体重性状鸡的方法及其专用引物 |
| ES2630031T3 (es) | 2010-09-28 | 2017-08-17 | Aegerion Pharmaceuticals, Inc. | Un polipéptido de leptina pinnípedo-humano quimérico con solubilidad aumentada |
| US9273028B2 (en) | 2010-10-29 | 2016-03-01 | Biogen Ma Inc. | Heterocyclic tyrosine kinase inhibitors |
| BR112013020719B1 (pt) | 2011-02-14 | 2018-04-17 | Allergan, Inc. | Composições de derivados de bimatoprost tipo éster e métodos |
| US9580427B2 (en) | 2011-05-17 | 2017-02-28 | The Regents Of The University Of California | Kinase inhibitors |
| JP2014521594A (ja) | 2011-05-25 | 2014-08-28 | アミリン・ファーマシューティカルズ，リミテッド・ライアビリティ・カンパニー | 長持続期間デュアルホルモンコンジュゲート |
| WO2012174484A2 (fr) * | 2011-06-15 | 2012-12-20 | Nse Products, Inc. | Identification de marqueurs de restriction calorique et mimétiques de restriction calorique |
| ES2732475T3 (es) | 2011-07-08 | 2019-11-22 | Aegerion Pharmaceuticals Inc | Polipéptidos modificados por ingeniería genética que tienen una duración potenciada de la acción y una inmunogenicidad reducida |
| BR112014003071A2 (pt) | 2011-08-10 | 2017-02-21 | Depuy Synthes Products Llc | tratamento de doença vascular periférica com o uso de células derivadas do tecido do cordão umbilical |
| WO2013077921A2 (fr) | 2011-09-02 | 2013-05-30 | The Regents Of The University Of California | Pyrazolo[3,4-d]pyrimidines substituées et utilisations de celles-ci |
| CA2853729A1 (fr) | 2011-10-28 | 2013-05-02 | Board Of Regents, The University Of Texas System | Nouvelles compositions et procedes pour traiter le cancer |
| CN104837987B (zh) | 2011-12-23 | 2018-10-02 | 德普伊新特斯产品公司 | 人脐带组织来源的细胞的检测 |
| EP2836482B1 (fr) | 2012-04-10 | 2019-12-25 | The Regents of The University of California | Compositions et méthodes pour le traitement du cancer |
| US9353087B2 (en) | 2012-06-08 | 2016-05-31 | Biogen Ma Inc. | Inhibitors of Bruton's tyrosine kinase |
| AR091273A1 (es) | 2012-06-08 | 2015-01-21 | Biogen Idec Inc | Inhibidores de pirimidinil tirosina quinasa |
| CA2913736A1 (fr) | 2012-06-11 | 2013-12-19 | The Regents Of The University Of California | Composes et procedes de traitement du cancer |
| US9090595B2 (en) | 2012-08-27 | 2015-07-28 | Allergan, Inc. | Reduced central corneal thickening by use of hydrophilic ester prodrugs of beta-chlorocyclopentanes |
| KR20200110820A (ko) | 2012-08-27 | 2020-09-25 | 알레간 인코포레이티드 | 베타-클로로시클로펜탄의 친수성 에스테르 전구약물의 이용에 의한 감소된 중심 각막 비후 |
| US8932598B2 (en) | 2012-08-28 | 2015-01-13 | Vaxinnate Corporation | Fusion proteins and methods of use |
| WO2014052669A1 (fr) | 2012-09-26 | 2014-04-03 | The Regents Of The University Of California | Modulation de ire1 |
| CN111529535A (zh) | 2012-09-27 | 2020-08-14 | 儿童医学中心公司 | 用于治疗肥胖症的化合物和其使用方法 |
| US9364462B2 (en) | 2012-10-30 | 2016-06-14 | The Regents Of The University Of California | Alpha-1-adrenergic receptor agonist therapy |
| AU2013204922B2 (en) | 2012-12-20 | 2015-05-14 | Celgene Corporation | Chimeric antigen receptors |
| CN105101803A (zh) | 2013-02-06 | 2015-11-25 | 人类起源公司 | 具有改进特异性的修饰的t淋巴细胞 |
| EP2968215B1 (fr) | 2013-03-14 | 2021-05-05 | The Regents of the University of California | Agents mucolytiques thiosaccharidiques |
| CA2901529A1 (fr) | 2013-03-15 | 2014-09-18 | Allergan, Inc. | Bimatoprost pour l'amelioration de la production de leptine |
| CN105246902B (zh) | 2013-03-15 | 2018-05-04 | 加利福尼亚大学董事会 | 无环核苷膦酸二酯 |
| EP3831840A1 (fr) | 2013-03-15 | 2021-06-09 | Celgene Corporation | Lymphocytes t modifiés |
| CA2902431A1 (fr) | 2013-03-15 | 2014-09-25 | Kevin Michael Short | Halogenopyrazoles en tant qu'inhibiteurs de la thrombine |
| BR112015022340A2 (pt) | 2013-03-15 | 2017-07-18 | Verseon Corp | método para tratamento ou prevenção de uma doença ou distúrbio relacionado à calicreína em um sujeito, composto, e, composição farmacêutica |
| UY35464A (es) | 2013-03-15 | 2014-10-31 | Araxes Pharma Llc | Inhibidores covalentes de kras g12c. |
| WO2015009742A2 (fr) | 2013-07-15 | 2015-01-22 | Board Of Regents, The University Of Texas System | Composés et méthodes pour le traitement du cancer, des troubles neurologiques, du sevrage de l'éthanol, de l'anxiété, de la dépression, et de la douleur neuropathique |
| LT3035926T (lt) | 2013-08-19 | 2020-11-25 | The Regents Of The University Of California | Junginiai ir būdai, skirti epileptinio sutrikimo gydymui |
| WO2015031799A1 (fr) | 2013-08-30 | 2015-03-05 | The Regents Of The University Of California, A California Corporation | Compositions contenant des nanocristaux scintillateurs et leurs procédés d'utilisation |
| JO3805B1 (ar) | 2013-10-10 | 2021-01-31 | Araxes Pharma Llc | مثبطات كراس جي12سي |
| PL3074033T3 (pl) | 2013-11-26 | 2019-08-30 | The Children's Medical Center Corporation | Związki do leczenia otyłości i sposoby ich zastosowania |
| WO2015089327A1 (fr) | 2013-12-11 | 2015-06-18 | Biogen Idec Ma Inc. | Composés biaryliques utiles pour le traitement de maladies humaines en oncologie, neurologie et immunologie |
| AR098721A1 (es) | 2013-12-11 | 2016-06-08 | Biogen Idec Inc | Inhibidores de biarilo de tirosina quinasa de bruton |
| JP6491214B2 (ja) | 2013-12-23 | 2019-03-27 | メモリアル スローン ケタリング キャンサー センター | 放射性標識のための方法および試薬 |
| AU2015206570A1 (en) | 2014-01-15 | 2016-07-14 | Medimmune, Llc | RSV-specific antibodies and functional parts thereof |
| KR20160124835A (ko) | 2014-02-20 | 2016-10-28 | 알러간, 인코포레이티드 | 베타-클로로시클로펜탄의 친수성 에스테르 프로드럭의 사용에 의해 감소된 중앙 각막 비후 |
| US20170209408A1 (en) | 2014-04-03 | 2017-07-27 | The Children's Medical Center Corporation | Hsp90 inhibitors for the treatment of obesity and methods of use thereof |
| KR102461419B1 (ko) | 2014-05-13 | 2022-11-02 | 메모리얼 슬로안 케터링 캔서 센터 | Hsp70 조정물질 및 이의 제조 및 이용 방법 |
| US10414814B2 (en) | 2014-07-03 | 2019-09-17 | City Of Hope | Tumor-selective CTLA-4 antagonists |
| NZ729046A (en) | 2014-08-12 | 2022-07-29 | Celgene Corp | Car-t lymphocytes engineered to home to lymph node b cell zone, skin, or gastrointestinal tract |
| CN111808136B (zh) | 2014-09-15 | 2024-06-11 | 加利福尼亚大学董事会 | 核苷酸类似物 |
| CN106687445A (zh) | 2014-09-17 | 2017-05-17 | 维颂公司 | 作为丝氨酸蛋白酶抑制剂的吡唑基取代的吡啶酮化合物 |
| JO3556B1 (ar) | 2014-09-18 | 2020-07-05 | Araxes Pharma Llc | علاجات مدمجة لمعالجة السرطان |
| US9862701B2 (en) | 2014-09-25 | 2018-01-09 | Araxes Pharma Llc | Inhibitors of KRAS G12C mutant proteins |
| US10011600B2 (en) | 2014-09-25 | 2018-07-03 | Araxes Pharma Llc | Methods and compositions for inhibition of Ras |
| ES2757798T3 (es) | 2014-10-02 | 2020-04-30 | Allergan Inc | Profármacos de éster de gamma-lactamas y su uso |
| ES2789351T3 (es) | 2015-01-13 | 2020-10-26 | Hope City | Máscaras de enlace peptídico de proteínas de unión a CTLA4 |
| WO2016138138A1 (fr) | 2015-02-25 | 2016-09-01 | The Regents Of The University Of California | Agonistes de récepteur 5ht pour le traitement de troubles |
| RU2017131562A (ru) | 2015-02-27 | 2019-03-27 | Версеон Корпорейшн | Замещенные пиразольные соединения как ингибиторы сериновых протеаз |
| US11072592B2 (en) | 2015-02-27 | 2021-07-27 | The Regents Of The University Of California | Small molecules that enable cartilage rejuvenation |
| MX382355B (es) | 2015-04-10 | 2025-03-13 | Araxes Pharma Llc | Compuestos de quinazolina sustituidos y métodos de uso de los mismos. |
| MX2017013275A (es) | 2015-04-15 | 2018-01-26 | Araxes Pharma Llc | Inhibidores triciclicos fusionados de kras y metodos de uso de los mismos. |
| AU2016247858B2 (en) | 2015-04-17 | 2020-10-15 | Ludwig Institute For Cancer Research Ltd. | PLK4 inhibitors |
| US20180282310A1 (en) | 2015-06-10 | 2018-10-04 | Biogen Ma Inc. | Forms and compositions of biaryl inhibitors of bruton's tyrosine kinase |
| US10144724B2 (en) | 2015-07-22 | 2018-12-04 | Araxes Pharma Llc | Substituted quinazoline compounds and methods of use thereof |
| MX2021006326A (es) | 2015-09-17 | 2022-12-16 | Inhibidores de pcna. | |
| CN105132566A (zh) * | 2015-09-21 | 2015-12-09 | 上海中优生物高科技有限责任公司 | 毒素堆积型肥胖基因个体化干预饮品的制备方法及其系统 |
| US10730867B2 (en) | 2015-09-28 | 2020-08-04 | Araxes Pharma Llc | Inhibitors of KRAS G12C mutant proteins |
| US10647703B2 (en) | 2015-09-28 | 2020-05-12 | Araxes Pharma Llc | Inhibitors of KRAS G12C mutant proteins |
| WO2017058792A1 (fr) | 2015-09-28 | 2017-04-06 | Araxes Pharma Llc | Inhibiteurs de protéines kras portant la mutation g12c |
| WO2017058728A1 (fr) | 2015-09-28 | 2017-04-06 | Araxes Pharma Llc | Inhibiteurs de protéines kras portant la mutation g12c |
| WO2017058902A1 (fr) | 2015-09-28 | 2017-04-06 | Araxes Pharma Llc | Inhibiteurs de protéines mutantes kras g12c |
| WO2017058915A1 (fr) | 2015-09-28 | 2017-04-06 | Araxes Pharma Llc | Inhibiteurs de protéines mutantes kras g12c |
| WO2017058807A1 (fr) | 2015-09-28 | 2017-04-06 | Araxes Pharma Llc | Inhibiteurs de protéines kras portant la mutation g12c |
| AU2016335563B2 (en) | 2015-10-08 | 2022-10-27 | Neurona Therapeutics Inc. | Neural precursor cell populations and uses thereof |
| TWI824372B (zh) | 2015-10-12 | 2023-12-01 | 美商再生元醫藥公司 | 活化瘦素受體的抗原結合蛋白 |
| WO2017070256A2 (fr) | 2015-10-19 | 2017-04-27 | Araxes Pharma Llc | Méthode de criblage d'inhibiteurs de ras |
| WO2017070565A1 (fr) | 2015-10-23 | 2017-04-27 | Sunesis Pharmaceuticals, Inc. | Inhibiteurs de pdk1 hétérocycliques destinés à être utilisés pour traiter le cancer |
| CN119241632A (zh) | 2015-10-23 | 2025-01-03 | Erx制药股份有限公司 | 雷公藤红素的类似物 |
| KR20180081596A (ko) | 2015-11-16 | 2018-07-16 | 아락세스 파마 엘엘씨 | 치환된 헤테로사이클릭 그룹을 포함하는 2-치환된 퀴나졸린 화합물 및 이의 사용 방법 |
| WO2017100546A1 (fr) | 2015-12-09 | 2017-06-15 | Araxes Pharma Llc | Procédés de préparation de dérivés de quinazoléine |
| JP6938510B2 (ja) | 2015-12-24 | 2021-09-22 | ザ・リージエンツ・オブ・ザ・ユニバーシテイー・オブ・カリフオルニア | Ｃｆｔｒ制御因子及びこの使用方法 |
| BR112018012934B1 (pt) | 2015-12-24 | 2023-11-07 | The Regents Of The University Of California | Reguladores cftr e métodos de uso dos mesmos |
| CN109310709A (zh) | 2015-12-30 | 2019-02-05 | 细胞基因公司 | T淋巴细胞生产方法和由此产生的t淋巴细胞 |
| US10822312B2 (en) | 2016-03-30 | 2020-11-03 | Araxes Pharma Llc | Substituted quinazoline compounds and methods of use |
| MA45047A (fr) | 2016-04-25 | 2019-03-27 | Forma Therapeutics Inc | Procédés d'utilisation d'inhibiteurs de fasn |
| US20210323913A1 (en) | 2016-04-29 | 2021-10-21 | Board Of Regents, The University Of Texas System | Sigma receptor binders |
| EA034415B1 (ru) | 2016-05-12 | 2020-02-05 | Анакор Фармасьютикалс, Инк. | Оксабороловые сложные эфиры и их применения |
| US10646488B2 (en) | 2016-07-13 | 2020-05-12 | Araxes Pharma Llc | Conjugates of cereblon binding compounds and G12C mutant KRAS, HRAS or NRAS protein modulating compounds and methods of use thereof |
| WO2018017153A1 (fr) | 2016-07-21 | 2018-01-25 | Biogen Ma Inc. | Formes de succinate et compositions d'inhibiteurs de tyrosine kinase de bruton |
| EP3491008A2 (fr) | 2016-07-26 | 2019-06-05 | BioMarin Pharmaceutical Inc. | Nouvelles protéines de capside de virus adéno-associés |
| US11542261B2 (en) | 2016-08-17 | 2023-01-03 | Children's Hospital Medical Center | Substituted Imidazo[1,2-a]-pyridines as IRAK 1/4 and FLT3 inhibitors |
| US11254667B2 (en) | 2016-08-17 | 2022-02-22 | Children's Hospital Medical Center | Substituted imidazo[1,2-A]pyridines as IRAK 1/4 and flt3 inhibitors |
| US10775386B2 (en) | 2016-09-12 | 2020-09-15 | Aegerion Pharmaceuticals, Inc. | Methods of detecting anti-leptin neutralizing antibodies |
| JP2019529484A (ja) | 2016-09-29 | 2019-10-17 | アラクセス ファーマ エルエルシー | Ｋｒａｓ ｇ１２ｃ変異体タンパク質の阻害剤 |
| US10377743B2 (en) | 2016-10-07 | 2019-08-13 | Araxes Pharma Llc | Inhibitors of RAS and methods of use thereof |
| JP7100028B2 (ja) | 2016-10-20 | 2022-07-12 | セルジーン コーポレイション | セレブロン系のヘテロ二量体化可能なキメラ抗原受容体 |
| EP3555077B1 (fr) | 2016-12-15 | 2023-04-19 | The Regents of The University of California | Compositions et procédés pour le traitement du cancer |
| EP3573964A1 (fr) | 2017-01-26 | 2019-12-04 | Araxes Pharma LLC | Composés à base de benzothiophène et de benzothiazole et leurs procédés d'utilisation |
| WO2018140600A1 (fr) | 2017-01-26 | 2018-08-02 | Araxes Pharma Llc | Composés hétéro-hétéro-bicycliques fusionnés et leurs procédés d'utilisation |
| WO2018140514A1 (fr) | 2017-01-26 | 2018-08-02 | Araxes Pharma Llc | Dérivés de 1-(6-(3-hydroxynaphtalen-1-yl)quinazolin-2-yl)azétidin-1-yl)prop-2-en-1-one et composés similaires utilisés en tant qu'inhibiteurs de kras g12c pour le traitement du cancer |
| EP3573954A1 (fr) | 2017-01-26 | 2019-12-04 | Araxes Pharma LLC | Composés benzohétéroaromatiques bicycliques fusionnés et leurs procédés d'utilisation |
| US11279689B2 (en) | 2017-01-26 | 2022-03-22 | Araxes Pharma Llc | 1-(3-(6-(3-hydroxynaphthalen-1-yl)benzofuran-2-yl)azetidin-1 yl)prop-2-en-1-one derivatives and similar compounds as KRAS G12C modulators for treating cancer |
| CN110869357A (zh) | 2017-05-25 | 2020-03-06 | 亚瑞克西斯制药公司 | 化合物及其用于治疗癌症的使用方法 |
| US11639346B2 (en) | 2017-05-25 | 2023-05-02 | Araxes Pharma Llc | Quinazoline derivatives as modulators of mutant KRAS, HRAS or NRAS |
| KR20200010306A (ko) | 2017-05-25 | 2020-01-30 | 아락세스 파마 엘엘씨 | Kras의 공유적 억제제 |
| CN107385020A (zh) * | 2017-06-23 | 2017-11-24 | 西安医学院 | 瘦素在人重组fgf21蛋白活性检测中的应用 |
| WO2019070917A1 (fr) | 2017-10-03 | 2019-04-11 | The Schepens Eye Research Institute, Inc. | Composés et compositions pour inhiber la dégénérescence de l'épithélium pigmentaire rétinien et procédés les utilisant |
| US11040981B2 (en) | 2017-10-10 | 2021-06-22 | Syros Pharmaceuticals, Inc. | Pyrrolotriazine compounds and methods of inhibiting TAM kinases |
| WO2019143719A1 (fr) | 2018-01-16 | 2019-07-25 | Syros Pharmaceuticals, Inc. | Inhibiteurs de la kinase cycline-dépendante 7 (cdk7) |
| JP7590183B2 (ja) | 2018-03-13 | 2024-11-26 | 武田薬品工業株式会社 | 血漿カリクレインのインヒビターとしての置換されたイミダゾピリジン及びその使用 |
| US11608381B2 (en) | 2018-04-06 | 2023-03-21 | Regeneron Pharmaceuticals, Inc. | Methods of treatment using a leptin receptor agonist antibody |
| AU2019265560A1 (en) | 2018-05-09 | 2020-11-26 | Biomarin Pharmaceutical Inc. | Methods of treating phenylketonuria |
| TW202005978A (zh) | 2018-05-14 | 2020-02-01 | 美商拜奧馬林製藥公司 | 新穎肝靶向腺相關病毒載體 |
| US12134620B2 (en) | 2018-08-01 | 2024-11-05 | Araxes Pharma Llc | Heterocyclic spiro compounds and methods of use thereof for the treatment of cancer |
| AU2019340387C1 (en) | 2018-09-10 | 2025-06-19 | The Regents Of The University Of California | Dithiolsaccharide mucolytic agents and uses thereof |
| EP4516300A3 (fr) | 2019-06-14 | 2025-08-06 | Children's Hospital Medical Center | Ciblage thérapeutique rationnel d'états de signalisation immunitaire oncogènes dans des tumeurs malignes myéloïdes par l'intermédiaire de l'enzyme de conjugaison d'ubiquitine ube2n |
| EP4031245A1 (fr) | 2019-09-18 | 2022-07-27 | Takeda Pharmaceutical Company Limited | Inhibiteurs hétéroaryles de la kallicréine plasmatique |
| EP4477220A3 (fr) | 2019-09-18 | 2025-02-26 | Takeda Pharmaceutical Company Limited | Inhibiteurs de la kallicréine plasmatique et leurs utilisations |
| WO2021211938A1 (fr) | 2020-04-17 | 2021-10-21 | Shire Human Genetic Therapies, Inc. | Formes solides d'inhibiteurs de la kallicréine plasmatique |
| WO2021211930A1 (fr) | 2020-04-17 | 2021-10-21 | Shire Human Genetic Therapies, Inc. | Formes et composition d'inhibiteurs de la kallicréine plasmatique |
| CN117355523A (zh) | 2021-03-17 | 2024-01-05 | 武田药品工业株式会社 | 血浆激肽释放酶的多环抑制剂 |
| EP4308229A1 (fr) | 2021-03-17 | 2024-01-24 | Takeda Pharmaceutical Company Limited | Inhibiteurs de la kallicréine plasmatique |
| CN117396474A (zh) | 2021-03-17 | 2024-01-12 | 武田药品工业株式会社 | 血浆激肽释放酶抑制剂 |
| AU2022240596A1 (en) | 2021-03-17 | 2023-10-19 | Takeda Pharmaceutical Company Limited | Heteroaryl inhibitors of plasma kallikrein |
| EP4308227A1 (fr) | 2021-03-17 | 2024-01-24 | Takeda Pharmaceutical Company Limited | Inhibiteurs imidazopyridinyle de la kallicréine plasmatique |
| CA3223636A1 (fr) | 2021-08-06 | 2023-02-09 | Christopher Walton CARROLL | Compositions et procedes de degradation selective de proteines modifiees |
| AU2023310177A1 (en) | 2022-07-21 | 2025-03-06 | Antiva Biosciences, Inc. | Compositions and dosage forms for treatment of hpv infection and hpv-induced neoplasia |
| WO2024040241A1 (fr) | 2022-08-19 | 2024-02-22 | Viracta Therapeutics, Inc. | Formulations pharmaceutiques, processus de préparation et méthodes d'utilisation |
| EP4587434A1 (fr) | 2022-09-15 | 2025-07-23 | Takeda Pharmaceutical Company Limited | Dérivés de n-((isoquinolin-6-yl)méthyl)-1 h-pyrazole-4-carboxamide en tant qu' inhibiteurs de la kallicréine plasmatique pour le traitement de l'angioedème héréditaire |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0566410A2 (fr) * | 1992-04-17 | 1993-10-20 | Sankyo Company Limited | Dérivés du facteur inhibiteur de l'adipogenèse, leur préparation et leur utilisation |
| WO1994000558A1 (fr) * | 1992-06-19 | 1994-01-06 | Joslin Diabetes Center, Inc. | Rad diabetogene: un gene specifique au diabete de type ii |
Family Cites Families (89)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE31006E (en) | 1968-09-24 | 1982-08-03 | Akzona Incorporated | Process for the demonstration and determination of reaction components having specific binding affinity for each other |
| US3654090A (en) | 1968-09-24 | 1972-04-04 | Organon | Method for the determination of antigens and antibodies |
| US3650090A (en) | 1970-06-19 | 1972-03-21 | Phillips Petroleum Co | Analysis of gaseous mixtures |
| NL154598B (nl) | 1970-11-10 | 1977-09-15 | Organon Nv | Werkwijze voor het aantonen en bepalen van laagmoleculire verbindingen en van eiwitten die deze verbindingen specifiek kunnen binden, alsmede testverpakking. |
| US4179337A (en) | 1973-07-20 | 1979-12-18 | Davis Frank F | Non-immunogenic polypeptides |
| US4016043A (en) | 1975-09-04 | 1977-04-05 | Akzona Incorporated | Enzymatic immunological method for the determination of antigens and antibodies |
| US4491632A (en) | 1979-10-22 | 1985-01-01 | The Massachusetts General Hospital | Process for producing antibodies to hepatitis virus and cell lines therefor |
| US4444887A (en) | 1979-12-10 | 1984-04-24 | Sloan-Kettering Institute | Process for making human antibody producing B-lymphocytes |
| US4342566A (en) | 1980-02-22 | 1982-08-03 | Scripps Clinic & Research Foundation | Solid phase anti-C3 assay for detection of immune complexes |
| DE3167442D1 (en) | 1980-07-07 | 1985-01-10 | Nat Res Dev | Improvements in or relating to cell lines |
| US4341761A (en) | 1980-07-25 | 1982-07-27 | E. I. Du Pont De Nemours And Company | Antibodies to immunogenic peptides and their use to purify human fibroblast interferon |
| US4466917A (en) | 1981-02-12 | 1984-08-21 | New York University | Malaria vaccine |
| US4493890A (en) | 1981-03-23 | 1985-01-15 | Miles Laboratories, Inc. | Activated apoglucose oxidase and its use in specific binding assays |
| US4451570A (en) | 1981-03-26 | 1984-05-29 | The Regents Of The University Of California | Immunoglobulin-secreting human hybridomas from a cultured human lymphoblastoid cell line |
| US4399121A (en) | 1981-11-04 | 1983-08-16 | Miles Laboratories, Inc. | Iodothyronine immunogens and antibodies |
| US4427783A (en) | 1981-12-14 | 1984-01-24 | Hoffmann-La Roche Inc. | Immunoassay of thymosin α1 |
| US6936694B1 (en) | 1982-05-06 | 2005-08-30 | Intermune, Inc. | Manufacture and expression of large structural genes |
| US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
| US4650764A (en) | 1983-04-12 | 1987-03-17 | Wisconsin Alumni Research Foundation | Helper cell |
| US4631211A (en) | 1985-03-25 | 1986-12-23 | Scripps Clinic & Research Foundation | Means for sequential solid phase organic synthesis and methods using the same |
| JP2876058B2 (ja) | 1986-08-18 | 1999-03-31 | エミスフィア・テクノロジーズ・インコーポレイテッド | 薬物送達システム |
| US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
| US5071773A (en) | 1986-10-24 | 1991-12-10 | The Salk Institute For Biological Studies | Hormone receptor-related bioassays |
| US4980289A (en) | 1987-04-27 | 1990-12-25 | Wisconsin Alumni Research Foundation | Promoter deficient retroviral vector |
| US4981784A (en) | 1987-12-02 | 1991-01-01 | The Salk Institute For Biological Studies | Retinoic acid receptor method |
| US5010175A (en) | 1988-05-02 | 1991-04-23 | The Regents Of The University Of California | General method for producing and selecting peptides with specific properties |
| KR0133561B1 (ko) | 1988-05-13 | 1998-04-21 | 스티븐 엠. 오드레 | 과립구 군체 자극인자의 정제방법 |
| JPH04501662A (ja) | 1988-09-26 | 1992-03-26 | ザ・サルク・インスティチュート・バイオテクノロジー／インダストリアル・アソシエイツ・インコーポレーテッド | 混合給送組換え酵母発酵 |
| US5102789A (en) | 1989-03-15 | 1992-04-07 | The Salk Institute Biotechnology/Industrial Associates, Inc. | Production of epideramal growth factor in pichia pastoris yeast cells |
| DE68925966T2 (de) | 1988-12-22 | 1996-08-29 | Kirin Amgen Inc | Chemisch modifizierte granulocytenkolonie erregender faktor |
| US5124263A (en) | 1989-01-12 | 1992-06-23 | Wisconsin Alumni Research Foundation | Recombination resistant retroviral helper cell and products produced thereby |
| US5098833A (en) | 1989-02-23 | 1992-03-24 | Genentech, Inc. | DNA sequence encoding a functional domain of a lymphocyte homing receptor |
| US5116964A (en) | 1989-02-23 | 1992-05-26 | Genentech, Inc. | Hybrid immunoglobulins |
| US5225538A (en) | 1989-02-23 | 1993-07-06 | Genentech, Inc. | Lymphocyte homing receptor/immunoglobulin fusion proteins |
| US5354844A (en) | 1989-03-16 | 1994-10-11 | Boehringer Ingelheim International Gmbh | Protein-polycation conjugates |
| WO1990014092A1 (fr) | 1989-05-18 | 1990-11-29 | Cell Genesys, Inc. | Utilisation d'oligonucleotides mono-brins pour la modification axee sur le site de genes mammiferes in vivo |
| US5399346A (en) | 1989-06-14 | 1995-03-21 | The United States Of America As Represented By The Department Of Health And Human Services | Gene therapy |
| US5073627A (en) | 1989-08-22 | 1991-12-17 | Immunex Corporation | Fusion proteins comprising GM-CSF and IL-3 |
| US5013556A (en) | 1989-10-20 | 1991-05-07 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
| AU635844B2 (en) | 1989-11-06 | 1993-04-01 | Cell Genesys, Inc. | Production of proteins using homologous recombination |
| DK0505500T3 (da) | 1989-12-22 | 1997-08-25 | Applied Research Systems | Modificering af endogen genekspression med regulatorisk element ved hjælp af homolog rekombination |
| US5139749A (en) | 1990-06-22 | 1992-08-18 | Tas, Inc. | Fluidized calcining process |
| WO1992016192A1 (fr) | 1991-03-15 | 1992-10-01 | Amgen Inc. | Administration pulmonaire d'un facteur de stimulation des populations de granulocytes |
| ZA924674B (en) | 1991-07-02 | 1993-04-28 | Imclone Systems Inc | Cysteine depleted il-6 mutein |
| US5447851B1 (en) | 1992-04-02 | 1999-07-06 | Univ Texas System Board Of | Dna encoding a chimeric polypeptide comprising the extracellular domain of tnf receptor fused to igg vectors and host cells |
| CA2131003A1 (fr) | 1992-05-26 | 1993-12-09 | Raymond G. Goodwin | Nouvelle cytokine liant le cd30 |
| CA2148484A1 (fr) | 1992-11-13 | 1994-05-26 | Stewart Lyman | Nouvelle cytokine appelee ligand elk |
| US5574018A (en) | 1994-07-29 | 1996-11-12 | Amgen Inc. | Conjugates of vitamin B12 and proteins |
| US5643748A (en) | 1994-09-14 | 1997-07-01 | Progenitor, Inc. | HU-B1.219, a novel human hematopoietin receptor |
| US5827734A (en) | 1995-01-20 | 1998-10-27 | University Of Washington | Materials and methods for determining ob protein in a biological sample |
| US5580954A (en) | 1995-01-31 | 1996-12-03 | Eli Lilly And Company | Anti-obesity proteins |
| US5569743A (en) | 1995-01-31 | 1996-10-29 | Eli Lilly And Company | Anti-obesity proteins |
| US5567803A (en) | 1995-01-31 | 1996-10-22 | Eli Lilly And Company | Anti-obesity proteins |
| US5574133A (en) | 1995-01-31 | 1996-11-12 | Eli Lilly And Company | Anti-obesity proteins |
| US5605886A (en) | 1995-01-31 | 1997-02-25 | Eli Lilly And Company | Anti-obesity proteins |
| US5563244A (en) | 1995-01-31 | 1996-10-08 | Eli Lilly And Company | Anti-obesity proteins |
| US5554727A (en) | 1995-01-31 | 1996-09-10 | Eli Lilly And Company | Anti-obesity proteins |
| US5691309A (en) | 1995-01-31 | 1997-11-25 | Eli Lilly And Company | Anti-obesity proteins |
| US5569744A (en) | 1995-01-31 | 1996-10-29 | Eli Lilly And Company | Anti-obesity proteins |
| US5552523A (en) | 1995-01-31 | 1996-09-03 | Eli Lilly And Company | Anti-obesity proteins |
| US5563245A (en) | 1995-01-31 | 1996-10-08 | Eli Lilly And Company | Anti-obesity proteins |
| US5552522A (en) | 1995-01-31 | 1996-09-03 | Eli Lilly And Company | Anti-obesity proteins |
| US5521283A (en) | 1995-01-31 | 1996-05-28 | Eli Lilly And Company | Anti-obesity proteins |
| US5552524A (en) | 1995-01-31 | 1996-09-03 | Eli Lilly And Company | Anti-obesity proteins |
| US5594104A (en) | 1995-01-31 | 1997-01-14 | Eli Lilly And Company | Anti-obesity proteins |
| US5563243A (en) | 1995-01-31 | 1996-10-08 | Eli Lilly And Company | Anti-obesity proteins |
| US5525705A (en) | 1995-01-31 | 1996-06-11 | Eli Lilly And Company | Anti-obesity proteins |
| WO1996023515A1 (fr) | 1995-01-31 | 1996-08-08 | Eli Lilly And Company | Proteines anti-obesite |
| US5532336A (en) | 1995-01-31 | 1996-07-02 | Eli Lilly And Company | Anti-obesity proteins |
| US5559208A (en) | 1995-01-31 | 1996-09-24 | Eli Lilly And Company | Anti-obesity proteins |
| US5567678A (en) | 1995-01-31 | 1996-10-22 | Eli Lilly And Company | Anti-obesity proteins |
| US5594101A (en) | 1995-03-03 | 1997-01-14 | Eli Lilly And Company | Anti-obesity proteins |
| US5719266A (en) | 1995-03-17 | 1998-02-17 | Eli Lilly And Company | Anti-obesity proteins |
| EP0736599A3 (fr) | 1995-04-03 | 1996-12-11 | Takeda Chemical Industries Ltd | Le gène d'obésité de rat, son produit génique et sa production |
| JPH08333394A (ja) | 1995-04-03 | 1996-12-17 | Takeda Chem Ind Ltd | ラット肥満遺伝子、その遺伝子産物およびその製造法 |
| US5739277A (en) | 1995-04-14 | 1998-04-14 | Genentech Inc. | Altered polypeptides with increased half-life |
| US5614379A (en) | 1995-04-26 | 1997-03-25 | Eli Lilly And Company | Process for preparing anti-obesity protein |
| DE741187T1 (de) | 1995-05-05 | 1997-04-30 | Hoffmann La Roche | Rekombinante Obesitäts-(OB)-Proteine |
| CA2221303A1 (fr) | 1995-05-19 | 1996-11-21 | Dennis Paul Smith | Produit du gene de l'obesite |
| AU5800696A (en) | 1995-05-26 | 1996-12-11 | Eli Lilly And Company | Rhesus ob protein and dna |
| EP0759441A3 (fr) | 1995-06-30 | 1999-06-30 | Eli Lilly And Company | Procédés de traitement des pathologies associées aux peptides neuropeptide Y |
| AU695934B2 (en) | 1995-06-30 | 1998-08-27 | Eli Lilly And Company | Methods for treating diabetes |
| WO1997011192A1 (fr) | 1995-09-19 | 1997-03-27 | Eli Lilly And Company | Adn codant des proteines medicinales |
| US5698389A (en) | 1995-11-16 | 1997-12-16 | Tularik, Inc. | Transcriptional promoter of the murine obesity gene |
| AU1705197A (en) | 1996-01-19 | 1997-08-11 | Eli Lilly And Company | Obesity protein formulations |
| AU2243997A (en) | 1996-01-19 | 1997-08-11 | Eli Lilly And Company | Obesity protein formulations |
| EP0784982A3 (fr) | 1996-01-19 | 1999-08-18 | Eli Lilly And Company | Préparation des protéines contre l'obésité |
| JP2000504319A (ja) | 1996-01-19 | 2000-04-11 | イーライ・リリー・アンド・カンパニー | 肥満症タンパク質製剤 |
| JP2000509018A (ja) | 1996-03-26 | 2000-07-18 | イーライ・リリー・アンド・カンパニー | 肥満タンパク質製剤 |
-
1995
- 1995-06-07 US US08/483,211 patent/US6309853B1/en not_active Expired - Lifetime
- 1995-08-17 GE GEAP19953625A patent/GEP20022701B/en unknown
- 1995-08-17 BR BR9508596A patent/BR9508596A/pt not_active IP Right Cessation
- 1995-08-17 JP JP50761896A patent/JP3479080B2/ja not_active Expired - Lifetime
- 1995-08-17 DE DE0777732T patent/DE777732T1/de active Pending
- 1995-08-17 EE EE9700030A patent/EE04377B1/xx unknown
- 1995-08-17 IL IL11498795A patent/IL114987A/en not_active IP Right Cessation
- 1995-08-17 MX MX9701200A patent/MX9701200A/es active IP Right Grant
- 1995-08-17 CA CA2195955A patent/CA2195955C/fr not_active Expired - Lifetime
- 1995-08-17 WO PCT/US1995/010479 patent/WO1996005309A2/fr not_active Ceased
- 1995-08-17 CN CN951956752A patent/CN1162978B/zh not_active Expired - Lifetime
- 1995-08-17 AP APAP/P/1997/000919A patent/AP815A/en active
- 1995-08-17 NZ NZ291689A patent/NZ291689A/xx not_active IP Right Cessation
- 1995-08-17 SK SK221-97A patent/SK287191B6/sk not_active IP Right Cessation
- 1995-08-17 MD MD97-0100A patent/MD2311G2/ro not_active IP Right Cessation
- 1995-08-17 DE DE19531931A patent/DE19531931A1/de not_active Ceased
- 1995-08-17 TR TR95/01021A patent/TR199501021A2/xx unknown
- 1995-08-17 SI SI9520090A patent/SI9520090A/sl not_active IP Right Cessation
- 1995-08-17 ES ES95929591T patent/ES2108663T3/es not_active Expired - Lifetime
- 1995-08-17 EP EP95929591A patent/EP0777732B1/fr not_active Expired - Lifetime
- 1995-08-17 GB GB9516947A patent/GB2292382B/en not_active Expired - Lifetime
- 1995-08-17 RO RO97-00311A patent/RO121036B1/ro unknown
- 1995-08-17 HU HU9901249A patent/HU223563B1/hu active IP Right Grant
- 1995-08-17 CZ CZ1997460A patent/CZ295018B6/cs not_active IP Right Cessation
- 1995-08-17 PL PL95319021A patent/PL183352B1/pl unknown
-
1997
- 1997-01-17 IS IS4416A patent/IS4416A/is unknown
- 1997-02-06 OA OA60960A patent/OA10596A/en unknown
- 1997-02-12 BG BG101228A patent/BG64710B1/bg unknown
- 1997-02-14 NO NO19970683A patent/NO323847B1/no not_active IP Right Cessation
- 1997-02-17 FI FI970656A patent/FI121709B/fi not_active IP Right Cessation
- 1997-03-17 LV LVP-97-42A patent/LV11868B/en unknown
- 1997-07-30 GR GR970300021T patent/GR970300021T1/el unknown
-
1998
- 1998-01-16 HK HK98100386A patent/HK1001495A1/xx not_active IP Right Cessation
-
2004
- 2004-05-20 IL IL16209304A patent/IL162093A0/xx active IP Right Grant
-
2006
- 2006-11-17 NO NO20065287A patent/NO326376B1/no not_active IP Right Cessation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0566410A2 (fr) * | 1992-04-17 | 1993-10-20 | Sankyo Company Limited | Dérivés du facteur inhibiteur de l'adipogenèse, leur préparation et leur utilisation |
| WO1994000558A1 (fr) * | 1992-06-19 | 1994-01-06 | Joslin Diabetes Center, Inc. | Rad diabetogene: un gene specifique au diabete de type ii |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AP815A (en) | An obesity (ob) polypeptide capable of modulating body weight, nucleic acids therefore, and diagnostic and therapeutic use thereof. | |
| US7063958B1 (en) | Nucleic acids db, the receptor for leptin | |
| US6124439A (en) | OB polypeptide antibodies and method of making | |
| US7544492B1 (en) | OB polypeptides, modified forms and derivatives | |
| US6048837A (en) | OB polypeptides as modulators of body weight | |
| US20040213763A1 (en) | Modulators of body weight, corresponding nucleic acids and proteins, and diagnostic and therapeutic uses thereof | |
| US6350730B1 (en) | OB polypeptides and modified forms as modulators of body weight | |
| US6471956B1 (en) | Ob polypeptides, modified forms and compositions thereto | |
| RU2273645C9 (ru) | Полипептид ожирения (ов)(варианты), его аналог (варианты) и слитый белок (варианты), изолированная молекула нуклеиновой кислоты, молекула днк, рекомбинантный вектор клонирования, рекомбинантный вектор экспрессии, фармацевтическая композиция, моноклональное и поликлональное антитело | |
| AU2004201496B2 (en) | DB the receptor for leptin nucleic acids encoding the receptor, and uses thereof | |
| US6124448A (en) | Nucleic acid primers and probes for the mammalian OB gene | |
| US7084252B1 (en) | DB, the receptor for leptin | |
| US7148004B1 (en) | Oligonucleotides of the OB-R isoforms and methods of diagnosing body weight | |
| US7619079B2 (en) | Db, the receptor for leptin, nucleic acids encoding the receptor, and uses thereof | |
| KR100584177B1 (ko) | 체중 변조물질,상응하는 핵산 및 단백질,및 이들의 진단 및 치료학적 용도 | |
| US6821945B1 (en) | Modulators of body weight, corresponding nucleic acids and proteins, and diagnostic and therapeutic uses thereof | |
| AU738966B2 (en) | Modulators of body weight, corresponding nucleic acids and proteins, and diagnostic and therapeutic uses thereof | |
| JP2001157591A (ja) | 体重のモジュレーター、対応する核酸およびタンパク質、ならびにそれらの診断および治療用途 |