JP2010537958A5 - - Google Patents

Download PDF

Info

Publication number
JP2010537958A5
JP2010537958A5 JP2010522397A JP2010522397A JP2010537958A5 JP 2010537958 A5 JP2010537958 A5 JP 2010537958A5 JP 2010522397 A JP2010522397 A JP 2010522397A JP 2010522397 A JP2010522397 A JP 2010522397A JP 2010537958 A5 JP2010537958 A5 JP 2010537958A5
Authority
JP
Japan
Prior art keywords
oligomer
oligomer according
nucleotide analogues
nucleotide
nucleobase
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP2010522397A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010537958A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2008/061432 external-priority patent/WO2009027527A2/en
Publication of JP2010537958A publication Critical patent/JP2010537958A/ja
Publication of JP2010537958A5 publication Critical patent/JP2010537958A5/ja
Withdrawn legal-status Critical Current

Links

JP2010522397A 2007-08-30 2008-08-29 Fabp4/ap2を調節するためのrnaアンタゴニスト化合物 Withdrawn JP2010537958A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US96901607P 2007-08-30 2007-08-30
PCT/EP2008/061432 WO2009027527A2 (en) 2007-08-30 2008-08-29 Rna antagonist compounds for the modulation of fabp4/ap2

Publications (2)

Publication Number Publication Date
JP2010537958A JP2010537958A (ja) 2010-12-09
JP2010537958A5 true JP2010537958A5 (OSRAM) 2011-10-13

Family

ID=40228054

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010522397A Withdrawn JP2010537958A (ja) 2007-08-30 2008-08-29 Fabp4/ap2を調節するためのrnaアンタゴニスト化合物

Country Status (6)

Country Link
US (1) US20110054011A1 (OSRAM)
EP (1) EP2198024A2 (OSRAM)
JP (1) JP2010537958A (OSRAM)
AU (1) AU2008292091A1 (OSRAM)
CA (1) CA2697970A1 (OSRAM)
WO (1) WO2009027527A2 (OSRAM)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102482677B (zh) * 2009-03-16 2017-10-17 库尔纳公司 通过抑制nrf2的天然反义转录物治疗核因子(红细胞衍生2)‑样2(nrf2)相关疾病
EP2462229B1 (en) * 2009-08-05 2016-05-11 CuRNA, Inc. Treatment of insulin gene (ins) related diseases by inhibition of natural antisense transcript to an insulin gene (ins)
US9255154B2 (en) 2012-05-08 2016-02-09 Alderbio Holdings, Llc Anti-PCSK9 antibodies and use thereof
CN105324119A (zh) 2013-06-16 2016-02-10 国立大学法人东京医科齿科大学 具有外显子跳跃效应的双链反义核酸
WO2015009544A1 (en) * 2013-07-11 2015-01-22 Texas Heart Institute Rna interference of fabp4 for the treatment of atherosclerosis

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4962029A (en) * 1987-10-02 1990-10-09 Cetus Corporation Covalent oligonucleotide-horseradish peroxidase conjugate
US4914210A (en) * 1987-10-02 1990-04-03 Cetus Corporation Oligonucleotide functionalizing reagents
US6433159B1 (en) * 1992-09-10 2002-08-13 Isis Pharmaceuticals, Inc. Compositions and methods for treatment of Hepatitis C virus associated diseases
AU680435B2 (en) * 1992-09-10 1997-07-31 Isis Pharmaceuticals, Inc. Compositions and methods for treatment of hepatitis C virus-associated diseases
US6423489B1 (en) * 1992-09-10 2002-07-23 Isis Pharmaceuticals, Inc. Compositions and methods for treatment of Hepatitis C virus-associated diseases
DK0832069T3 (da) * 1995-06-07 2003-04-22 Pfizer Biphenyl-2-carboxylsyre-tetrahydroisoquinolin-6-ylamidderivater, deres fremstilling og deres anvendelse som inhibitorer af sekretion af mikrosomalt triglyceridoverførselsprotein og/eller apolipoprotein B (Apo B)
EP0944602A1 (en) * 1996-11-27 1999-09-29 Pfizer Inc. Apo b-secretion/mtp inhibitory amides
PL335721A1 (en) * 1997-03-05 2000-05-08 Ribogene Novel methods of screening serving the purpose of identifying the factors of selective hepatitis c virus replication inhibition
US7183302B2 (en) * 2002-08-12 2007-02-27 Bristol-Myers Squibb Company Iminothiazolidinones as inhibitors of HCV replication
UA79300C2 (en) * 2002-08-12 2007-06-11 Janssen Pharmaceutica Nv N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion
US7087229B2 (en) * 2003-05-30 2006-08-08 Enzon Pharmaceuticals, Inc. Releasable polymeric conjugates based on aliphatic biodegradable linkers
FR2848572B1 (fr) * 2002-12-12 2005-12-09 Univ Joseph Fourier Molecules inhibitrices de la synthese proteique du virus de l'hepatite c et procede de criblage desdites molecules inhibitrices
DE10300861A1 (de) * 2003-01-10 2004-07-22 Metagen Pharmaceuticals Gmbh Verwendung von an FABP4 bindenden Substanzen zur Diagnose und Behandlung des Harnblasenkarzinoms
WO2004076614A2 (de) * 2003-02-27 2004-09-10 Bernd Hinzmann Humane nukleinsäuresequenzen aus prostatakarzinomen
EP1648914A4 (en) * 2003-07-31 2009-12-16 Regulus Therapeutics Inc OLIGOMERIC COMPOUNDS AND COMPOSITIONS USEFUL FOR MODULATING SMALL NON-CODING RNA
ES2663810T3 (es) * 2004-08-10 2018-04-17 Kastle Therapeutics, Llc Métodos para modular los niveles de lipoproteínas y colesterol en humanos
CA2666191C (en) * 2006-10-09 2017-07-11 Santaris Pharma A/S Rna antagonist compounds for the modulation of pcsk9

Similar Documents

Publication Publication Date Title
JP2010505432A5 (OSRAM)
JP2016520310A5 (OSRAM)
JP2009532392A5 (OSRAM)
IL300119A (en) Oligonucleotides for inducing paternal ube3a expression
JP2012510297A5 (OSRAM)
JP2008510019A5 (OSRAM)
JP2015514418A5 (OSRAM)
JP2015518712A5 (OSRAM)
JP2015523853A5 (OSRAM)
JP2014527401A5 (OSRAM)
JP2015523855A5 (OSRAM)
JP2015518710A5 (OSRAM)
RU2015155332A (ru) Олигонуклеотидные модуляторы в-клеточной cll/лимфомы 11а (bcl11а) и их применение
JP2016522674A5 (OSRAM)
JP2018507711A5 (OSRAM)
JP2016116520A5 (OSRAM)
JP2009532044A5 (OSRAM)
HRP20201200T1 (hr) OLIGONUKLEOTIDNI SPOJEVI ZA CILJANJE HUNTINGTIN mRNK
JP2013535212A5 (OSRAM)
JP2011500858A5 (OSRAM)
JP2018529732A5 (OSRAM)
JP2015519057A5 (OSRAM)
JP2014511686A5 (OSRAM)
JP2015532097A5 (OSRAM)
WO2007112753A8 (en) Pharmaceutical composition comprising anti-mirna antisense oligonucleotides