KR19990082528A - 단백질 카이나제 씨 발현을 조절하기 위한 메톡시에톡시 올리고뉴클레오티드 - Google Patents

단백질 카이나제 씨 발현을 조절하기 위한 메톡시에톡시 올리고뉴클레오티드 Download PDF

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KR19990082528A
KR19990082528A KR1019980706264A KR19980706264A KR19990082528A KR 19990082528 A KR19990082528 A KR 19990082528A KR 1019980706264 A KR1019980706264 A KR 1019980706264A KR 19980706264 A KR19980706264 A KR 19980706264A KR 19990082528 A KR19990082528 A KR 19990082528A
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South Korea
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pkc
oligonucleotides
oligonucleotide
isis
expression
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Abandoned
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KR1019980706264A
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Korean (ko)
Inventor
니콜라스 엠. 딘
피에르 마틴
칼 하인즈 알트만
Original Assignee
한스 루돌프 하우스, 아네트 와너
노바르티스 아게
파샬 비. 린네
아이시스 파마수티컬즈 인코포레이티드
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Publication of KR19990082528A publication Critical patent/KR19990082528A/ko
Abandoned legal-status Critical Current

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    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1137Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against enzymes
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    • C07H21/04Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
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    • C12Y207/00Transferases transferring phosphorus-containing groups (2.7)
    • C12Y207/11Protein-serine/threonine kinases (2.7.11)
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    • C12N2310/341Gapmers, i.e. of the type ===---===
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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KR1019980706264A 1996-02-14 1997-02-13 단백질 카이나제 씨 발현을 조절하기 위한 메톡시에톡시 올리고뉴클레오티드 Abandoned KR19990082528A (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US8/601,269 1996-02-14
US08/601,269 US5948898A (en) 1992-03-16 1996-02-14 Methoxyethoxy oligonucleotides for modulation of protein kinase C expression

Publications (1)

Publication Number Publication Date
KR19990082528A true KR19990082528A (ko) 1999-11-25

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KR1019980706264A Abandoned KR19990082528A (ko) 1996-02-14 1997-02-13 단백질 카이나제 씨 발현을 조절하기 위한 메톡시에톡시 올리고뉴클레오티드

Country Status (11)

Country Link
US (1) US5948898A (enExample)
EP (1) EP0881914B1 (enExample)
JP (1) JP2000506382A (enExample)
KR (1) KR19990082528A (enExample)
AT (1) ATE273718T1 (enExample)
AU (1) AU715760B2 (enExample)
CA (1) CA2246230A1 (enExample)
DE (1) DE69730315D1 (enExample)
NO (1) NO983716L (enExample)
NZ (1) NZ331358A (enExample)
WO (1) WO1997029780A1 (enExample)

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KR100906153B1 (ko) * 2007-07-04 2009-07-03 재단법인 한국원자력의학원 프로테인 카이네즈 씨 활성 저해용 단백질 및 이를포함하는 약제학적 조성물

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US8153602B1 (en) * 1991-11-19 2012-04-10 Isis Pharmaceuticals, Inc. Composition and methods for the pulmonary delivery of nucleic acids
US6153599A (en) * 1992-03-16 2000-11-28 Isis Pharmaceuticals, Inc. Methoxyethoxy oligonucleotides for modulation of protein kinase C expression
US6117847A (en) * 1992-03-16 2000-09-12 Isis Pharmaceuticals, Inc. Oligonucleotides for enhanced modulation of protein kinase C expression
US6537973B1 (en) * 1992-03-16 2003-03-25 Isis Pharmaceuticals, Inc. Oligonucleotide inhibition of protein kinase C
US6608035B1 (en) * 1994-10-25 2003-08-19 Hybridon, Inc. Method of down-regulating gene expression
BR9707529A (pt) * 1996-02-14 2000-01-04 Isis Pharmaceuticals Inc Oligunucleotìdeo especificamente hibridizável com dna ou rna.
CA2286396C (en) * 1997-04-30 2010-07-06 Isis Pharmaceuticals Inc. Oligonucleotides for enhanced bioavailability
EP1012331B1 (en) 1997-07-01 2006-03-29 Isis Pharmaceuticals, Inc. Compositions and methods for the delivery of oligonucleotides via the alimentary canal
AU745880B2 (en) 1998-05-21 2002-04-11 Isis Pharmaceuticals, Inc. Compositions and methods for non-parenteral delivery of oligonucleotides
US6300320B1 (en) * 1999-01-05 2001-10-09 Isis Pharmaceuticals, Inc. Modulation of c-jun using inhibitors of protein kinase C
US6465628B1 (en) 1999-02-04 2002-10-15 Isis Pharmaceuticals, Inc. Process for the synthesis of oligomeric compounds
US20060258562A1 (en) * 2000-07-31 2006-11-16 Healor Ltd. Methods and pharmaceutical compositions for healing wounds
RU2491952C2 (ru) * 2003-07-15 2013-09-10 Бар-Илан Юнивесити Способы и фармакологические композиции для заживления ран
US8258105B2 (en) 2003-10-07 2012-09-04 Isis Pharmaceuticals, Inc. Antisense oligonucleotides optimized for kidney targeting
US20050191653A1 (en) 2003-11-03 2005-09-01 Freier Susan M. Modulation of SGLT2 expression
JO2660B1 (en) 2006-01-20 2012-06-17 نوفارتيس ايه جي Pi-3 inhibitors and methods of use
AR060358A1 (es) 2006-04-06 2008-06-11 Novartis Vaccines & Diagnostic Quinazolinas para la inhibicion de pdk 1
BRPI0820722A2 (pt) 2007-12-20 2015-06-16 Novartis Ag Derivados de tiazol usados como inibidores de pi 3 cinases
CN102325789A (zh) * 2009-02-24 2012-01-18 希尔洛有限公司 用于治疗痤疮和其它病症的内脂素治疗药物
US8293753B2 (en) 2009-07-02 2012-10-23 Novartis Ag Substituted 2-carboxamide cycloamino ureas
JP2013516500A (ja) * 2010-01-11 2013-05-13 ヒールオア・リミテッド 炎症性疾患および障害を治療するための方法
AR082418A1 (es) 2010-08-02 2012-12-05 Novartis Ag Formas cristalinas de 1-(4-metil-5-[2-(2,2,2-trifluoro-1,1-dimetil-etil)-piridin-4-il]-tiazol-2-il)-amida de 2-amida del acido (s)-pirrolidin-1,2-dicarboxilico
MX343706B (es) 2011-01-31 2016-11-18 Novartis Ag Derivados heterocíclicos novedosos.
BR112014009890A2 (pt) 2011-10-28 2020-10-27 Novartis Ag derivados de purina e seu uso no tratamento de doença
BR112014028420A2 (pt) 2012-05-16 2017-09-19 Novartis Ag regime de dosagem para um inibidor de quinase pi-3
PL3076969T3 (pl) 2013-12-06 2022-01-17 Novartis Ag Schemat dawkowania selektywnego inhibitora 3-kinazy fosfatydynozytolu alfa-izoformy
MX2018005298A (es) 2015-11-02 2018-06-22 Novartis Ag Regimen de dosificacion para un inhibidor de fosfatidilinositol 3-quinasa.
WO2018060833A1 (en) 2016-09-27 2018-04-05 Novartis Ag Dosage regimen for alpha-isoform selective phosphatidylinositol 3-kinase inhibitor alpelisib

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US5034506A (en) * 1985-03-15 1991-07-23 Anti-Gene Development Group Uncharged morpholino-based polymers having achiral intersubunit linkages
US5264423A (en) * 1987-03-25 1993-11-23 The United States Of America As Represented By The Department Of Health And Human Services Inhibitors for replication of retroviruses and for the expression of oncogene products
US5225326A (en) * 1988-08-31 1993-07-06 Research Development Foundation One step in situ hybridization assay
US5098890A (en) * 1988-11-07 1992-03-24 Temple University-Of The Commonwealth System Of Higher Education Antisence oligonucleotides to c-myb proto-oncogene and uses thereof
US5087617A (en) * 1989-02-15 1992-02-11 Board Of Regents, The University Of Texas System Methods and compositions for treatment of cancer using oligonucleotides
US5135917A (en) * 1990-07-12 1992-08-04 Nova Pharmaceutical Corporation Interleukin receptor expression inhibiting antisense oligonucleotides
US5138045A (en) * 1990-07-27 1992-08-11 Isis Pharmaceuticals Polyamine conjugated oligonucleotides
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US5681747A (en) * 1992-03-16 1997-10-28 Isis Pharmaceuticals, Inc. Nucleic acid sequences encoding protein kinase C and antisense inhibition of expression thereof
JPH06508154A (ja) * 1992-04-06 1994-09-14 グラクソ、ソシエダッド、アノニマ ペプチド
US5585479A (en) * 1992-07-24 1996-12-17 The United States Of America As Represented By The Secretary Of The Navy Antisense oligonucleotides directed against human ELAM-I RNA
FR2706484B1 (fr) * 1993-06-11 1995-09-01 Inst Nat Sante Rech Med Polypeptide mutant de la protéine kinase C, séquences d'acides nucléiques codant pour ledit polypeptide et leurs utilisations.

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100906153B1 (ko) * 2007-07-04 2009-07-03 재단법인 한국원자력의학원 프로테인 카이네즈 씨 활성 저해용 단백질 및 이를포함하는 약제학적 조성물

Also Published As

Publication number Publication date
EP0881914A1 (en) 1998-12-09
NO983716L (no) 1998-10-06
EP0881914B1 (en) 2004-08-18
NZ331358A (en) 2000-01-28
CA2246230A1 (en) 1997-08-21
NO983716D0 (no) 1998-08-13
EP0881914A4 (enExample) 1999-01-07
WO1997029780A1 (en) 1997-08-21
ATE273718T1 (de) 2004-09-15
DE69730315D1 (de) 2004-09-23
AU715760B2 (en) 2000-02-10
US5948898A (en) 1999-09-07
JP2000506382A (ja) 2000-05-30
AU2119297A (en) 1997-09-02

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