US20040014051A1
(en)
*
|
2002-07-18 |
2004-01-22 |
Isis Pharmaceuticals Inc. |
Antisense modulation of breast cancer-1 expression
|
US7812149B2
(en)
|
1996-06-06 |
2010-10-12 |
Isis Pharmaceuticals, Inc. |
2′-Fluoro substituted oligomeric compounds and compositions for use in gene modulations
|
US5898031A
(en)
|
1996-06-06 |
1999-04-27 |
Isis Pharmaceuticals, Inc. |
Oligoribonucleotides for cleaving RNA
|
US9096636B2
(en)
|
1996-06-06 |
2015-08-04 |
Isis Pharmaceuticals, Inc. |
Chimeric oligomeric compounds and their use in gene modulation
|
US7425545B2
(en)
|
2001-07-25 |
2008-09-16 |
Isis Pharmaceuticals, Inc. |
Modulation of C-reactive protein expression
|
US7199107B2
(en)
|
2002-05-23 |
2007-04-03 |
Isis Pharmaceuticals, Inc. |
Antisense modulation of kinesin-like 1 expression
|
WO2004031350A2
(en)
|
2002-09-26 |
2004-04-15 |
Amgen, Inc. |
Modulation of forkhead box o1a expression
|
WO2004044138A2
(en)
|
2002-11-05 |
2004-05-27 |
Isis Pharmaceuticals, Inc. |
Chimeric oligomeric compounds and their use in gene modulation
|
WO2004044132A2
(en)
|
2002-11-05 |
2004-05-27 |
Isis Pharmaceuticals, Inc. |
Modified oligonucleotides for use in rna interference
|
US7144999B2
(en)
|
2002-11-23 |
2006-12-05 |
Isis Pharmaceuticals, Inc. |
Modulation of hypoxia-inducible factor 1 alpha expression
|
WO2004072284A1
(en)
|
2003-02-11 |
2004-08-26 |
Antisense Therapeutics Ltd |
Modulation of insulin like growth factor i receptor expression
|
US7803781B2
(en)
|
2003-02-28 |
2010-09-28 |
Isis Pharmaceuticals, Inc. |
Modulation of growth hormone receptor expression and insulin-like growth factor expression
|
US20040185559A1
(en)
|
2003-03-21 |
2004-09-23 |
Isis Pharmaceuticals Inc. |
Modulation of diacylglycerol acyltransferase 1 expression
|
US7598227B2
(en)
|
2003-04-16 |
2009-10-06 |
Isis Pharmaceuticals Inc. |
Modulation of apolipoprotein C-III expression
|
US7399853B2
(en)
|
2003-04-28 |
2008-07-15 |
Isis Pharmaceuticals |
Modulation of glucagon receptor expression
|
WO2005013901A2
(en)
|
2003-07-31 |
2005-02-17 |
Isis Pharmaceuticals, Inc. |
Oligomeric compounds and compositions for use in modulation of small non-coding rnas
|
US7825235B2
(en)
|
2003-08-18 |
2010-11-02 |
Isis Pharmaceuticals, Inc. |
Modulation of diacylglycerol acyltransferase 2 expression
|
NZ576775A
(en)
|
2003-09-18 |
2010-12-24 |
Isis Pharmaceuticals Inc |
Modulation of eIF4E expression
|
WO2005027962A1
(en)
|
2003-09-18 |
2005-03-31 |
Isis Pharmaceuticals, Inc. |
4’-thionucleosides and oligomeric compounds
|
EP1678194B1
(en)
|
2003-10-10 |
2013-06-26 |
Alchemia Oncology Pty Limited |
The modulation of hyaluronan synthesis and degradation in the treatment of disease
|
US20050191653A1
(en)
|
2003-11-03 |
2005-09-01 |
Freier Susan M. |
Modulation of SGLT2 expression
|
WO2005056825A1
(en)
*
|
2003-12-05 |
2005-06-23 |
Board Of Regents, The University Of Texas System |
Screening for modulators of mekk2 and mekk3
|
EP2363480A3
(en)
|
2004-01-20 |
2015-10-07 |
Isis Pharmaceuticals, Inc. |
Modulation of glucocorticoid receptor expression
|
US7468431B2
(en)
|
2004-01-22 |
2008-12-23 |
Isis Pharmaceuticals, Inc. |
Modulation of eIF4E-BP2 expression
|
US8778900B2
(en)
*
|
2004-01-22 |
2014-07-15 |
Isis Pharmaceuticals, Inc. |
Modulation of eIF4E-BP1 expression
|
US8569474B2
(en)
|
2004-03-09 |
2013-10-29 |
Isis Pharmaceuticals, Inc. |
Double stranded constructs comprising one or more short strands hybridized to a longer strand
|
EP1730309B1
(en)
|
2004-03-15 |
2016-05-04 |
Ionis Pharmaceuticals, Inc. |
Compositions and methods for optimizing cleavage of rna by rnase h
|
US20050244869A1
(en)
|
2004-04-05 |
2005-11-03 |
Brown-Driver Vickie L |
Modulation of transthyretin expression
|
US8394947B2
(en)
|
2004-06-03 |
2013-03-12 |
Isis Pharmaceuticals, Inc. |
Positionally modified siRNA constructs
|
US7884086B2
(en)
|
2004-09-08 |
2011-02-08 |
Isis Pharmaceuticals, Inc. |
Conjugates for use in hepatocyte free uptake assays
|
WO2006086667A2
(en)
|
2005-02-09 |
2006-08-17 |
Avi Bio Pharma, Inc. |
Antisense composition and method for treating muscle atrophy
|
US8252756B2
(en)
|
2005-06-14 |
2012-08-28 |
Northwestern University |
Nucleic acid functionalized nanoparticles for therapeutic applications
|
AU2006318194B2
(en)
|
2005-11-21 |
2012-08-09 |
Isis Pharmaceuticals, Inc. |
Modulation of eiF4E-BP2 expression
|
PL3210633T3
(en)
|
2006-01-26 |
2019-12-31 |
Ionis Pharmaceuticals, Inc. |
Compositions and their uses directed to huntingtin
|
JP2009535383A
(en)
|
2006-05-03 |
2009-10-01 |
バルティック テクロノジー デヴェロプメント,リミテッド |
Antisense agents combining oligonucleotides modified with strongly bound bases and artificial nucleases
|
US8198253B2
(en)
|
2006-07-19 |
2012-06-12 |
Isis Pharmaceuticals, Inc. |
Compositions and their uses directed to HBXIP
|
US20080293053A1
(en)
*
|
2006-12-28 |
2008-11-27 |
The Regents Of The University Of Michigan |
shRNA Materials and Methods of Using Same for Inhibition of DKK-1
|
MX2009008470A
(en)
|
2007-02-09 |
2009-11-26 |
Univ Northwestern |
Particles for detecting intracellular targets.
|
DK2826863T3
(en)
|
2007-05-30 |
2017-12-04 |
Univ Northwestern |
NUCLEIC ACID FUNCTIONALIZED NANOPARTICLES FOR THERAPEUTIC APPLICATIONS
|
US20100280098A1
(en)
*
|
2007-10-05 |
2010-11-04 |
Juliano Rudolph L |
Receptor targeted oligonucleotides
|
WO2009143390A2
(en)
|
2008-05-22 |
2009-11-26 |
Isis Pharmaceuticals, Inc. |
Methods for modulating expression of rbp4
|
WO2009143391A2
(en)
*
|
2008-05-22 |
2009-11-26 |
Isis Pharmaceuticals, Inc |
Methods for modulation expression of creb
|
EP2310507A4
(en)
|
2008-07-08 |
2013-03-20 |
David Gladstone Inst |
Methods and compositions for modulating angiogenesis
|
CA2737661C
(en)
|
2008-09-23 |
2019-08-20 |
Alnylam Pharmaceuticals, Inc. |
Chemical modifications of monomers and oligonucleotides with cycloaddition
|
US9732324B2
(en)
|
2008-10-23 |
2017-08-15 |
Cornell University |
Anti-viral method
|
CA2744207C
(en)
|
2008-11-24 |
2019-05-28 |
Northwestern University |
Polyvalent rna-nanoparticle compositions
|
CN102317458B
(en)
|
2008-12-04 |
2018-01-02 |
库尔纳公司 |
Pass through treatment of the suppression of erythropoietin(EPO) (EPO) natural antisense transcript to EPO relevant diseases
|
CN102307997B
(en)
|
2008-12-04 |
2018-03-30 |
库尔纳公司 |
By suppressing to treat the related disease of Sirtuin 1 (SIRT1) for the natural antisense transcript of Sirtuin 1
|
KR101866152B1
(en)
|
2008-12-04 |
2018-06-08 |
큐알엔에이, 인크. |
Treatment of tumor suppressor gene related diseases by inhibition of natural antisense transcript to the gene
|
US20100233270A1
(en)
|
2009-01-08 |
2010-09-16 |
Northwestern University |
Delivery of Oligonucleotide-Functionalized Nanoparticles
|
EP2396408B1
(en)
|
2009-02-12 |
2017-09-20 |
CuRNA, Inc. |
Treatment of glial cell derived neurotrophic factor (gdnf) related diseases by inhibition of natural antisense transcript to gdnf
|
HUE026280T2
(en)
|
2009-02-12 |
2016-06-28 |
Curna Inc |
Treatment of brain derived neurotrophic factor (bdnf) related diseases by inhibition of natural antisense transcript to bdnf
|
US20110319317A1
(en)
|
2009-03-04 |
2011-12-29 |
Opko Curna, Llc |
Treatment of sirtuin 1 (sirt1) related diseases by inhibition of natural antisense transcript to sirt1
|
WO2010107733A2
(en)
|
2009-03-16 |
2010-09-23 |
Curna, Inc. |
Treatment of nuclear factor (erythroid-derived 2)-like 2 (nrf2) related diseases by inhibition of natural antisense transcript to nrf2
|
JP5904935B2
(en)
|
2009-03-17 |
2016-04-20 |
クルナ・インコーポレーテッド |
Treatment of DLK1-related diseases by suppression of natural antisense transcripts against Delta-like 1 homolog (DLK1)
|
ES2661787T3
(en)
|
2009-05-01 |
2018-04-04 |
Curna, Inc. |
Treatment of hemoglobin-related diseases (hbf / hbg) by inhibition of natural antisense transcript for hbf / hbg
|
CA2761152A1
(en)
|
2009-05-06 |
2010-11-11 |
Opko Curna, Llc |
Treatment of lipid transport and metabolism gene related diseases by inhibition of natural antisense transcript to a lipid transport and metabolism gene
|
ES2609655T3
(en)
|
2009-05-06 |
2017-04-21 |
Curna, Inc. |
Treatment of diseases related to tristetraproline (TTP) by inhibition of natural antisense transcript for TTP
|
US8957037B2
(en)
|
2009-05-18 |
2015-02-17 |
Curna, Inc. |
Treatment of reprogramming factor related diseases by inhibition of natural antisense transcript to a reprogramming factor
|
CN102549158B
(en)
|
2009-05-22 |
2017-09-26 |
库尔纳公司 |
By suppressing to treat the disease that TFE3 is related to IRS albumen 2 (IRS2) for transcription factor E3 (TFE3) natural antisense transcript
|
EP2435571B1
(en)
|
2009-05-28 |
2016-12-14 |
CuRNA, Inc. |
Treatment of antiviral gene related diseases by inhibition of natural antisense transcript to an antiviral gene
|
KR101702689B1
(en)
|
2009-06-16 |
2017-02-06 |
큐알엔에이, 인크. |
Treatment of paraoxonase 1 (pon1) related diseases by inhibition of natural antisense transcript to pon1
|
CN102695797B
(en)
|
2009-06-16 |
2018-05-25 |
库尔纳公司 |
By inhibiting to treat the relevant disease of glue protogene for the natural antisense transcript of glue protogene
|
CA2765889A1
(en)
|
2009-06-24 |
2010-12-29 |
Opko Curna, Llc |
Treatment of tumor necrosis factor receptor 2 (tnfr2) related diseases by inhibition of natural antisense transcript to tnfr2
|
EP2446037B1
(en)
|
2009-06-26 |
2016-04-20 |
CuRNA, Inc. |
Treatment of down syndrome gene related diseases by inhibition of natural antisense transcript to a down syndrome gene
|
CN102762731B
(en)
|
2009-08-05 |
2018-06-22 |
库尔纳公司 |
By inhibiting to treat insulin gene (INS) relevant disease for the natural antisense transcript of insulin gene (INS)
|
US9023822B2
(en)
|
2009-08-25 |
2015-05-05 |
Curna, Inc. |
Treatment of 'IQ motif containing GTPase activating protein' (IQGAP) related diseases by inhibition of natural antisense transcript to IQGAP
|
CA2779099C
(en)
|
2009-10-30 |
2021-08-10 |
Northwestern University |
Templated nanoconjugates
|
US8236570B2
(en)
|
2009-11-03 |
2012-08-07 |
Infoscitex |
Methods for identifying nucleic acid ligands
|
US8841429B2
(en)
|
2009-11-03 |
2014-09-23 |
Vivonics, Inc. |
Nucleic acid ligands against infectious prions
|
MX2012006580A
(en)
|
2009-12-11 |
2012-09-28 |
Genecode As |
Methods of facilitating neural cell survival using gdnf family ligand (gfl) mimetics or ret signaling pathway activators.
|
CN102712927B
(en)
|
2009-12-16 |
2017-12-01 |
库尔纳公司 |
By suppressing film combination transcription factor peptase, the natural antisense transcript of site 1 (MBTPS1) treats MBTPS1 relevant diseases
|
CN102869776B
(en)
|
2009-12-23 |
2017-06-23 |
库尔纳公司 |
HGF relevant diseases are treated by suppressing the natural antisense transcript of HGF (HGF)
|
CN102781480B
(en)
|
2009-12-23 |
2018-07-27 |
库尔纳公司 |
UCP2 relevant diseases are treated by inhibiting the natural antisense transcript of uncoupling protein-3 (UCP2)
|
CN102770540B
(en)
|
2009-12-29 |
2017-06-23 |
库尔纳公司 |
P63 relevant diseases are treated by suppressing the natural antisense transcript of oncoprotein 63 (p63)
|
EP2519633B1
(en)
|
2009-12-29 |
2017-10-25 |
CuRNA, Inc. |
Treatment of nuclear respiratory factor 1 (nrf1) related diseases by inhibition of natural antisense transcript to nrf1
|
CN102906264B
(en)
|
2010-01-04 |
2017-08-04 |
库尔纳公司 |
IRF8 relevant diseases are treated by suppressing the natural antisense transcript of interferon regulatory factor 8 (IRF8)
|
CN102822342B
(en)
|
2010-01-06 |
2017-05-10 |
库尔纳公司 |
Treatment of pancreatic developmental gene related diseases by inhibition of natural antisense transcript to a pancreatic developmental gene
|
JP6027893B2
(en)
|
2010-01-11 |
2016-11-16 |
カッパーアールエヌエー,インコーポレイテッド |
Treatment of sex hormone binding globulin (SHBG) related diseases by inhibition of natural antisense transcripts against sex hormone binding globulin (SHBG)
|
NO2529015T3
(en)
|
2010-01-25 |
2018-04-14 |
|
|
US9198972B2
(en)
|
2010-01-28 |
2015-12-01 |
Alnylam Pharmaceuticals, Inc. |
Monomers and oligonucleotides comprising cycloaddition adduct(s)
|
WO2011094580A2
(en)
|
2010-01-28 |
2011-08-04 |
Alnylam Pharmaceuticals, Inc. |
Chelated copper for use in the preparation of conjugated oligonucleotides
|
US8962586B2
(en)
|
2010-02-22 |
2015-02-24 |
Curna, Inc. |
Treatment of pyrroline-5-carboxylate reductase 1 (PYCR1) related diseases by inhibition of natural antisense transcript to PYCR1
|
WO2011112732A2
(en)
|
2010-03-12 |
2011-09-15 |
The Brigham And Women's Hospital, Inc. |
Methods of treating vascular inflammatory disorders
|
KR101900962B1
(en)
|
2010-04-09 |
2018-09-20 |
큐알엔에이, 인크. |
Treatment of fibroblast growth factor 21 (fgf21) related diseases by inhibition of natural antisense transcript to fgf21
|
WO2011139917A1
(en)
|
2010-04-29 |
2011-11-10 |
Isis Pharmaceuticals, Inc. |
Modulation of transthyretin expression
|
CA2798218A1
(en)
|
2010-05-03 |
2011-11-10 |
Curna, Inc. |
Treatment of sirtuin (sirt) related diseases by inhibition of natural antisense transcript to a sirtuin (sirt)
|
EP2569328B1
(en)
|
2010-05-11 |
2016-12-14 |
The U.S.A. As Represented By The Secretary, Department Of Health And Human Services |
Programmable self-assembled nanostructures based on sidechain-modified pna for the multivalent display of ligands
|
TWI531370B
(en)
|
2010-05-14 |
2016-05-01 |
可娜公司 |
Treatment of par4 related diseases by inhibition of natural antisense transcript to par4
|
US8980858B2
(en)
|
2010-05-26 |
2015-03-17 |
Curna, Inc. |
Treatment of methionine sulfoxide reductase a (MSRA) related diseases by inhibition of natural antisense transcript to MSRA
|
NO2576783T3
(en)
|
2010-05-26 |
2018-04-28 |
|
|
WO2011163069A2
(en)
|
2010-06-21 |
2011-12-29 |
The Trustees Of The University Of Pennsylvania |
Protease triggered release of molecules from hydrogels
|
ES2663598T3
(en)
|
2010-07-14 |
2018-04-16 |
Curna, Inc. |
Treatment of diseases related to the large disc homolog (dlg) by inhibiting the natural antisense transcript to dlg
|
WO2012021942A1
(en)
|
2010-08-19 |
2012-02-23 |
Howard Florey Institute |
Tam receptors and tam receptor ligands in detection and modulation of neuropathological disease
|
KR101886457B1
(en)
|
2010-10-06 |
2018-08-07 |
큐알엔에이, 인크. |
Treatment of sialidase 4 (neu4) related diseases by inhibition of natural antisense transcript to neu4
|
US20140031250A1
(en)
|
2010-10-07 |
2014-01-30 |
David Tsai Ting |
Biomarkers of Cancer
|
EP2630241B1
(en)
|
2010-10-22 |
2018-10-17 |
CuRNA, Inc. |
Treatment of alpha-l-iduronidase (idua) related diseases by inhibition of natural antisense transcript to idua
|
DK2633052T3
(en)
|
2010-10-27 |
2018-07-16 |
Curna Inc |
TREATMENT OF INTERFERON-RELATED DEVELOPMENT REGULATOR 1 (IFRD1) -RELATED DISEASES BY INHIBITION OF NATURAL ANTISENCE TRANSCRIPT TO IFRD1
|
EP3702460A1
(en)
|
2010-11-12 |
2020-09-02 |
The General Hospital Corporation |
Polycomb-associated non-coding rnas
|
KR102010598B1
(en)
|
2010-11-23 |
2019-08-13 |
큐알엔에이, 인크. |
Treatment of nanog related diseases by inhibition of natural antisense transcript to nanog
|
EP2663323B1
(en)
|
2011-01-14 |
2017-08-16 |
The General Hospital Corporation |
Methods targeting mir-128 for regulating cholesterol/lipid metabolism
|
EP2697244B1
(en)
|
2011-04-13 |
2017-05-17 |
Ionis Pharmaceuticals, Inc. |
Antisense modulation of ptp1b expression
|
US9593330B2
(en)
|
2011-06-09 |
2017-03-14 |
Curna, Inc. |
Treatment of frataxin (FXN) related diseases by inhibition of natural antisense transcript to FXN
|
WO2012174476A2
(en)
|
2011-06-16 |
2012-12-20 |
Isis Pharmaceuticals, Inc. |
Antisense modulation of fibroblast growth factor receptor 4 expression
|
AU2012308320C1
(en)
|
2011-09-14 |
2018-08-23 |
Translate Bio Ma, Inc. |
Multimeric oligonucleotide compounds
|
ES2856091T3
(en)
|
2011-09-14 |
2021-09-27 |
Univ Northwestern |
Nanoconjugates capable of crossing the blood-brain barrier
|
EP2758533B1
(en)
|
2011-09-20 |
2018-04-11 |
Ionis Pharmaceuticals, Inc. |
Antisense modulation of gcgr expression
|
US20130085139A1
(en)
|
2011-10-04 |
2013-04-04 |
Royal Holloway And Bedford New College |
Oligomers
|
US10184151B2
(en)
|
2011-10-11 |
2019-01-22 |
The Brigham And Women's Hospital, Inc. |
Micrornas in neurodegenerative disorders
|
RU2014119787A
(en)
|
2011-10-25 |
2015-12-10 |
Айсис Фармасьютикалс, Инк. |
GCCR ANTI-SENSE REGULATION
|
EP2790736B1
(en)
|
2011-12-12 |
2018-01-31 |
Oncoimmunin, Inc. |
In vivo delivery of oligonucleotides
|
HUE040179T2
(en)
|
2012-03-15 |
2019-02-28 |
Curna Inc |
Treatment of brain derived neurotrophic factor (bdnf) related diseases by inhibition of natural antisense transcript to bdnf
|
WO2013163628A2
(en)
|
2012-04-27 |
2013-10-31 |
Duke University |
Genetic correction of mutated genes
|
DK2850186T3
(en)
|
2012-05-16 |
2019-04-08 |
Translate Bio Ma Inc |
COMPOSITIONS AND PROCEDURES FOR MODULATING SMN GENFAMILY EXPRESSION
|
WO2013173652A1
(en)
|
2012-05-16 |
2013-11-21 |
Rana Therapeutics, Inc. |
Compositions and methods for modulating gene expression
|
WO2013184209A1
(en)
|
2012-06-04 |
2013-12-12 |
Ludwig Institute For Cancer Research Ltd. |
Mif for use in methods of treating subjects with a neurodegenerative disorder
|
EP2943194A1
(en)
|
2012-09-17 |
2015-11-18 |
Chemedest Ltd. |
Treatment of peripheral neuropathy using gfr(alpha)3 type receptor agonists
|
ES2862125T3
(en)
|
2013-06-13 |
2021-10-07 |
Antisense Therapeutics Ltd |
Combination therapy for acromegaly
|
WO2014210041A1
(en)
|
2013-06-25 |
2014-12-31 |
The United States Of America, As Represented By The Secretary, Department Of Health & Human Service |
Glucan-encapsulated sirna for treating type 2 diabetes mellitus
|
JP6618910B2
(en)
|
2013-09-05 |
2019-12-11 |
サレプタ セラピューティクス,インコーポレイテッド |
Inclusion of antisense-induced exon 2 in acid α-glucosidase
|
EP3047023B1
(en)
|
2013-09-19 |
2019-09-04 |
The United States Of America, As Represented By The Secretary, Department Of Health And Human Services |
Compositions and methods for inhibiting jc virus (jcv)
|
US9963705B2
(en)
|
2013-11-12 |
2018-05-08 |
New England Biolabs, Inc. |
DNMT inhibitors
|
CA2844640A1
(en)
|
2013-12-06 |
2015-06-06 |
The University Of British Columbia |
Method for treatment of castration-resistant prostate cancer
|
WO2015112438A1
(en)
|
2014-01-21 |
2015-07-30 |
The United States Of America, As Represented By The Secretary, Department Of Health And Human Services |
cGAP-PNA MULTIVALENT PEPTIDE NUCLEIC ACID LIGAND DISPLAY
|
WO2015171918A2
(en)
|
2014-05-07 |
2015-11-12 |
Louisiana State University And Agricultural And Mechanical College |
Compositions and uses for treatment thereof
|
WO2015190922A1
(en)
|
2014-06-10 |
2015-12-17 |
Erasmus University Medical Center Rotterdam |
Antisense oligonucleotides useful in treatment of pompe disease
|
EP3483179B1
(en)
|
2014-06-18 |
2020-09-16 |
Albert Einstein College of Medicine |
Syntac polypeptides and uses thereof
|
EP3760208B1
(en)
|
2014-06-25 |
2024-05-29 |
The General Hospital Corporation |
Targeting human satellite ii (hsatii)
|
CA2966044A1
(en)
|
2014-10-30 |
2016-05-06 |
The General Hospital Corporation |
Methods for modulating atrx-dependent gene repression
|
AU2015349680A1
(en)
|
2014-11-21 |
2017-06-08 |
Northwestern University |
The sequence-specific cellular uptake of spherical nucleic acid nanoparticle conjugates
|
JP6929791B2
(en)
|
2015-02-09 |
2021-09-01 |
デューク ユニバーシティ |
Compositions and methods for epigenome editing
|
US20180200387A1
(en)
|
2015-02-23 |
2018-07-19 |
Crispr Therapeutics Ag |
Materials and methods for treatment of human genetic diseases including hemoglobinopathies
|
MA41795A
(en)
|
2015-03-18 |
2018-01-23 |
Sarepta Therapeutics Inc |
EXCLUSION OF AN EXON INDUCED BY ANTISENSE COMPOUNDS IN MYOSTATIN
|
US10961532B2
(en)
|
2015-04-07 |
2021-03-30 |
The General Hospital Corporation |
Methods for reactivating genes on the inactive X chromosome
|
EP3294889B1
(en)
|
2015-05-11 |
2021-01-06 |
Murdoch University |
Multiple sclerosis treatment
|
US10849917B2
(en)
|
2015-06-01 |
2020-12-01 |
Sarepta Therapeutics, Inc. |
Antisense-induced exon exclusion in type VII collagen
|
JP2018524588A
(en)
|
2015-06-26 |
2018-08-30 |
ベス・イスラエル・ディーコネス・メディカル・センター,インコーポレイテッド |
Cancer therapy targeting tetraspanin 33 (Tspan33) in bone marrow-derived suppressor cells
|
WO2017023861A1
(en)
|
2015-08-03 |
2017-02-09 |
The Regents Of The University Of California |
Compositions and methods for modulating abhd2 activity
|
JP2018532402A
(en)
|
2015-09-24 |
2018-11-08 |
クリスパー セラピューティクス アーゲー |
Novel families of RNA programmable endonucleases and their use in genome editing and other applications
|
CN108699555A
(en)
|
2015-10-09 |
2018-10-23 |
萨勒普塔医疗公司 |
Composition for treating Duchenne's dystrophy and associated disease and method
|
WO2017066497A2
(en)
|
2015-10-13 |
2017-04-20 |
Duke University |
Genome engineering with type i crispr systems in eukaryotic cells
|
CA3000931A1
(en)
|
2015-10-28 |
2017-05-04 |
Crispr Therapeutics Ag |
Materials and methods for treatment of duchenne muscular dystrophy
|
EP3370734B1
(en)
|
2015-11-05 |
2023-01-04 |
Children's Hospital Los Angeles |
Antisense oligo for use in treating acute myeloid leukemia
|
MX2018005332A
(en)
|
2015-11-06 |
2018-11-09 |
Crispr Therapeutics Ag |
Materials and methods for treatment of glycogen storage disease type 1a.
|
CA3005878A1
(en)
|
2015-11-19 |
2017-05-26 |
The Brigham And Women's Hospital, Inc. |
Lymphocyte antigen cd5-like (cd5l)-interleukin 12b (p40) heterodimers in immunity
|
EP3384024B1
(en)
|
2015-12-01 |
2022-02-02 |
CRISPR Therapeutics AG |
Materials and methods for treatment of alpha-1 antitrypsin deficiency
|
CA3007152A1
(en)
|
2015-12-07 |
2017-06-15 |
Erasmus University Medical Center Rotterdam |
Enzymatic replacement therapy and antisense therapy for pompe disease
|
MX2018007840A
(en)
|
2015-12-23 |
2019-05-02 |
Crispr Therapeutics Ag |
Materials and methods for treatment of amyotrophic lateral sclerosis and/or frontal temporal lobular degeneration.
|
JP7412079B2
(en)
|
2015-12-23 |
2024-01-12 |
レプルカ プロプライアタリー リミティド |
Nucleic acid oligomers and their uses
|
EP3411078A1
(en)
|
2016-02-02 |
2018-12-12 |
Crispr Therapeutics AG |
Materials and methods for treatment of severe combined immunodeficiency (scid) or omenn syndrome
|
US20190112353A1
(en)
|
2016-02-18 |
2019-04-18 |
Crispr Therapeutics Ag |
Materials and methods for treatment of severe combined immunodeficiency (scid) or omenn syndrome
|
WO2017147087A1
(en)
|
2016-02-25 |
2017-08-31 |
The Brigham And Women's Hospital, Inc. |
Treatment methods for fibrosis targeting smoc2
|
EP3429632B1
(en)
|
2016-03-16 |
2023-01-04 |
CRISPR Therapeutics AG |
Materials and methods for treatment of hereditary haemochromatosis
|
EA201892366A1
(en)
|
2016-04-18 |
2019-03-29 |
Сарепта Терапьютикс, Инк. |
ANTISMINAL OLIGOMERS AND METHODS OF THEIR APPLICATION FOR THE TREATMENT OF DISEASES ASSOCIATED WITH THE GENE OF THE ACID ALPHA-GLUCOSIDASE
|
US20200330609A1
(en)
|
2016-04-18 |
2020-10-22 |
Crispr Therapeutics Ag |
Materials and methods for treatment of hemoglobinopathies
|
WO2017191503A1
(en)
|
2016-05-05 |
2017-11-09 |
Crispr Therapeutics Ag |
Materials and methods for treatment of hemoglobinopathies
|
WO2017201210A1
(en)
|
2016-05-18 |
2017-11-23 |
Cue Biopharma, Inc. |
T-cell modulatory multimeric polypeptides and methods of use thereof
|
US11339201B2
(en)
|
2016-05-18 |
2022-05-24 |
Albert Einstein College Of Medicine |
Variant PD-L1 polypeptides, T-cell modulatory multimeric polypeptides, and methods of use thereof
|
WO2018002762A1
(en)
|
2016-06-29 |
2018-01-04 |
Crispr Therapeutics Ag |
Materials and methods for treatment of amyotrophic lateral sclerosis (als) and other related disorders
|
EP3478828B1
(en)
|
2016-06-29 |
2024-09-04 |
CRISPR Therapeutics AG |
Materials and methods for treatment of friedreich ataxia and other related disorders
|
EP3478829A1
(en)
|
2016-06-29 |
2019-05-08 |
Crispr Therapeutics AG |
Materials and methods for treatment of myotonic dystrophy type 1 (dm1) and other related disorders
|
AU2017292169B2
(en)
|
2016-07-06 |
2021-12-23 |
Vertex Pharmaceuticals Incorporated |
Materials and methods for treatment of pain related disorders
|
CN109843914B
(en)
|
2016-07-06 |
2024-03-15 |
沃泰克斯药物股份有限公司 |
Materials and methods for treating pain-related disorders
|
WO2018007871A1
(en)
|
2016-07-08 |
2018-01-11 |
Crispr Therapeutics Ag |
Materials and methods for treatment of transthyretin amyloidosis
|
WO2018013525A1
(en)
|
2016-07-11 |
2018-01-18 |
Translate Bio Ma, Inc. |
Nucleic acid conjugates and uses thereof
|
WO2018020323A2
(en)
|
2016-07-25 |
2018-02-01 |
Crispr Therapeutics Ag |
Materials and methods for treatment of fatty acid disorders
|
NL2017295B1
(en)
|
2016-08-05 |
2018-02-14 |
Univ Erasmus Med Ct Rotterdam |
Antisense oligomeric compound for Pompe disease
|
NL2017294B1
(en)
|
2016-08-05 |
2018-02-14 |
Univ Erasmus Med Ct Rotterdam |
Natural cryptic exon removal by pairs of antisense oligonucleotides.
|
EP3532638A4
(en)
|
2016-10-31 |
2020-07-29 |
University of Massachusetts |
Targeting microrna-101-3p in cancer therapy
|
CN110191955B
(en)
|
2016-12-13 |
2024-05-31 |
西雅图儿童医院(Dba西雅图儿童研究所) |
Method for exogenous drug activation of chemical-induced signaling complexes expressed in engineered cells in vitro and in vivo
|
AU2017379900A1
(en)
|
2016-12-22 |
2019-06-13 |
Cue Biopharma, Inc. |
T-cell modulatory multimeric polypeptides and methods of use thereof
|
EP3565829A4
(en)
|
2017-01-09 |
2021-01-27 |
Cue Biopharma, Inc. |
T-cell modulatory multimeric polypeptides and methods of use thereof
|
EP3577224A4
(en)
|
2017-02-03 |
2020-11-25 |
The University Of Western Australia |
Novel treatment for neat1 associated disease
|
WO2018154439A1
(en)
|
2017-02-22 |
2018-08-30 |
Crispr Therapeutics Ag |
Materials and methods for treatment of spinocerebellar ataxia type 1 (sca1) and other spinocerebellar ataxia type 1 protein (atxn1) gene related conditions or disorders
|
EP3585899A1
(en)
|
2017-02-22 |
2020-01-01 |
CRISPR Therapeutics AG |
Materials and methods for treatment of primary hyperoxaluria type 1 (ph1) and other alanine-glyoxylate aminotransferase (agxt) gene related conditions or disorders
|
EP3585900B1
(en)
|
2017-02-22 |
2022-12-21 |
CRISPR Therapeutics AG |
Materials and methods for treatment of spinocerebellar ataxia type 2 (sca2) and other spinocerebellar ataxia type 2 protein (atxn2) gene related conditions or disorders
|
CA3054031A1
(en)
|
2017-02-22 |
2018-08-30 |
Crispr Therapeutics Ag |
Compositions and methods for gene editing
|
WO2018154418A1
(en)
|
2017-02-22 |
2018-08-30 |
Crispr Therapeutics Ag |
Materials and methods for treatment of early onset parkinson's disease (park1) and other synuclein, alpha (snca) gene related conditions or disorders
|
EP3596118B1
(en)
|
2017-03-15 |
2024-08-21 |
Cue Biopharma, Inc. |
Combination of multimeric fusion polypeptides and immune checkpoint inhibitor for treating hpv-associated cancer
|
EP3612232A1
(en)
|
2017-04-21 |
2020-02-26 |
The Broad Institute, Inc. |
Targeted delivery to beta cells
|
WO2018209270A1
(en)
|
2017-05-11 |
2018-11-15 |
Northwestern University |
Adoptive cell therapy using spherical nucleic acids (snas)
|
IL270415B2
(en)
|
2017-05-12 |
2024-08-01 |
Crispr Therapeutics Ag |
Materials and methods for engineering cells and uses thereof in immuno-oncology
|
CA3074839A1
(en)
|
2017-09-07 |
2019-03-14 |
Cue Biopharma, Inc. |
T-cell modulatory multimeric polypeptide with conjugation sites and methods of use thereof
|
CA3079172A1
(en)
|
2017-10-17 |
2019-04-25 |
Crispr Therapeutics Ag |
Compositions and methods for gene editing for hemophilia a
|
JP7394753B2
(en)
|
2017-10-18 |
2023-12-08 |
サレプタ セラピューティクス, インコーポレイテッド |
antisense oligomer compounds
|
MA50849A
(en)
|
2017-10-26 |
2020-09-02 |
Vertex Pharma |
SUBSTANCES AND METHODS FOR THE TREATMENT OF HEMOGLOBINOPATHIES
|
EP3707155A2
(en)
|
2017-11-09 |
2020-09-16 |
Vertex Pharmaceuticals Incorporated |
Crispr/cas systems for treatment of dmd
|
EP3714055A1
(en)
|
2017-11-21 |
2020-09-30 |
CRISPR Therapeutics AG |
Materials and methods for treatment of autosomal dominant retinitis pigmentosa
|
BR112020011255A2
(en)
|
2017-12-05 |
2020-11-24 |
Vertex Pharmaceuticals Incorporated |
human cd34 + hematopoietic stem cells and progenitors modified by crispr-cas9 and uses thereof
|
AU2018386301A1
(en)
|
2017-12-14 |
2020-06-18 |
Bayer Healthcare Llc |
Novel RNA-programmable endonuclease systems and their use in genome editing and other applications
|
WO2019123429A1
(en)
|
2017-12-21 |
2019-06-27 |
Casebia Therapeutics Llp |
Materials and methods for treatment of usher syndrome type 2a
|
WO2019139896A1
(en)
|
2018-01-09 |
2019-07-18 |
Cue Biopharma, Inc. |
Multimeric t-cell modulatory polypeptides and methods of use thereof
|
CA3088180A1
(en)
|
2018-01-12 |
2019-07-18 |
Crispr Therapeutics Ag |
Compositions and methods for gene editing by targeting transferrin
|
EP3749768A1
(en)
|
2018-02-05 |
2020-12-16 |
Vertex Pharmaceuticals Incorporated |
Materials and methods for treatment of hemoglobinopathies
|
US11566236B2
(en)
|
2018-02-05 |
2023-01-31 |
Vertex Pharmaceuticals Incorporated |
Materials and methods for treatment of hemoglobinopathies
|
AU2019217875A1
(en)
|
2018-02-06 |
2020-08-20 |
Icahn School Of Medicine At Mount Sinai |
Repeat RNA as biomarkers of tumor immune response
|
US20210130824A1
(en)
|
2018-02-16 |
2021-05-06 |
Crispr Therapeutics Ag |
Compositions and methods for gene editing by targeting fibrinogen-alpha
|
CA3092497A1
(en)
|
2018-03-19 |
2019-09-26 |
Crispr Therapeutics Ag |
Novel rna-programmable endonuclease systems and uses thereof
|
WO2019204668A1
(en)
|
2018-04-18 |
2019-10-24 |
Casebia Therapeutics Limited Liability Partnership |
Compositions and methods for knockdown of apo(a) by gene editing for treatment of cardiovascular disease
|
KR20210016353A
(en)
|
2018-04-27 |
2021-02-15 |
시애틀 칠드런즈 호스피탈 디/비/에이 시애틀 칠드런즈 리서치 인스티튜트 |
Rapamycin-resistant cells
|
WO2019217997A1
(en)
|
2018-05-14 |
2019-11-21 |
Murdoch University |
Methods for treating vegf-related conditions
|
US20210292766A1
(en)
|
2018-08-29 |
2021-09-23 |
University Of Massachusetts |
Inhibition of Protein Kinases to Treat Friedreich Ataxia
|
WO2020081843A1
(en)
|
2018-10-17 |
2020-04-23 |
Casebia Therapeutics Limited Liability Partnership |
Compositions and methods for delivering transgenes
|
AU2019404285A1
(en)
|
2018-12-19 |
2021-07-22 |
Cue Biopharma, Inc. |
Multimeric T-cell modulatory polypeptides and methods of use thereof
|
SG11202108357PA
(en)
|
2019-02-15 |
2021-08-30 |
Crispr Therapeutics Ag |
Gene editing for hemophilia a with improved factor viii expression
|
WO2020171889A1
(en)
|
2019-02-19 |
2020-08-27 |
University Of Rochester |
Blocking lipid accumulation or inflammation in thyroid eye disease
|
JP2022522405A
(en)
|
2019-03-06 |
2022-04-19 |
キュー バイオファーマ, インコーポレイテッド |
T cell regulatory multimeric polypeptide and its usage
|
WO2020186059A2
(en)
|
2019-03-12 |
2020-09-17 |
Crispr Therapeutics Ag |
Novel high fidelity rna-programmable endonuclease systems and uses thereof
|
MX2021013858A
(en)
|
2019-05-14 |
2022-03-22 |
Univ Monash |
Modulators and modulation of the receptor for advanced glycation end-products rna.
|
BR112022007749A2
(en)
|
2019-10-23 |
2022-07-05 |
Cue Biopharma Inc |
TGF-B, MASKED CONSTRUCTION, TGF-B COMPLEX, MASKED TGF-B COMPLEX HETERODIMER, ONE OR MORE NUCLEIC ACIDS, USE OF ONE OR MORE MASKED TGF-B CONSTRUCTS OR COMPLEXES, COMPOSITION, METHOD OF PRODUCTION OF A MASKED TGF-B CONSTRUCTION OR COMPLEX AND PHARMACEUTICAL COMPOSITION
|
WO2021122944A1
(en)
|
2019-12-18 |
2021-06-24 |
Alia Therapeutics Srl |
Compositions and methods for treating retinitis pigmentosa
|
US20220290136A1
(en)
|
2020-09-30 |
2022-09-15 |
Crispr Therapeutics Ag |
Materials and methods for treatment of amyotrophic lateral sclerosis
|
JP2023550935A
(en)
|
2020-11-18 |
2023-12-06 |
レンバ・ベーフェー |
UMLILO antisense transcription inhibitor
|
US20240209371A1
(en)
|
2021-04-22 |
2024-06-27 |
Dana-Farber Cancer Institute, Inc. |
Compositions and methods for treating cancer
|
EP4352214A1
(en)
|
2021-06-11 |
2024-04-17 |
Bayer AG |
Type v rna programmable endonuclease systems
|
EP4101928A1
(en)
|
2021-06-11 |
2022-12-14 |
Bayer AG |
Type v rna programmable endonuclease systems
|
WO2023285431A1
(en)
|
2021-07-12 |
2023-01-19 |
Alia Therapeutics Srl |
Compositions and methods for allele specific treatment of retinitis pigmentosa
|
EP4144841A1
(en)
|
2021-09-07 |
2023-03-08 |
Bayer AG |
Novel small rna programmable endonuclease systems with impoved pam specificity and uses thereof
|
WO2023118349A1
(en)
|
2021-12-21 |
2023-06-29 |
Alia Therapeutics Srl |
Type ii cas proteins and applications thereof
|
WO2023118068A1
(en)
|
2021-12-23 |
2023-06-29 |
Bayer Aktiengesellschaft |
Novel small type v rna programmable endonuclease systems
|
WO2023166425A1
(en)
|
2022-03-01 |
2023-09-07 |
Crispr Therapeutics Ag |
Methods and compositions for treating angiopoietin-like 3 (angptl3) related conditions
|
WO2023194359A1
(en)
|
2022-04-04 |
2023-10-12 |
Alia Therapeutics Srl |
Compositions and methods for treatment of usher syndrome type 2a
|
WO2023237587A1
(en)
|
2022-06-10 |
2023-12-14 |
Bayer Aktiengesellschaft |
Novel small type v rna programmable endonuclease systems
|
WO2024056880A2
(en)
|
2022-09-16 |
2024-03-21 |
Alia Therapeutics Srl |
Enqp type ii cas proteins and applications thereof
|
WO2024105162A1
(en)
|
2022-11-16 |
2024-05-23 |
Alia Therapeutics Srl |
Type ii cas proteins and applications thereof
|
WO2024129743A2
(en)
|
2022-12-13 |
2024-06-20 |
Bluerock Therapeutics Lp |
Engineered type v rna programmable endonucleases and their uses
|
WO2024149810A2
(en)
|
2023-01-11 |
2024-07-18 |
Alia Therapeutics Srl |
Type ii cas proteins and applications thereof
|