JP2010537958A5 - - Google Patents

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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Withdrawn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)
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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Withdrawn legal-status Critical Current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JP2010522397A 2007-08-30 2008-08-29 Fabp4/ap2を調節するためのrnaアンタゴニスト化合物 Withdrawn JP2010537958A (ja)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 (enExample) 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JP2010522397A Withdrawn JP2010537958A (ja) 2007-08-30 2008-08-29 Fabp4/ap2を調節するためのrnaアンタゴニスト化合物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 (enExample)
EP (1) EP2198024A2 (enExample)
JP (1) JP2010537958A (enExample)
AU (1) AU2008292091A1 (enExample)
CA (1) CA2697970A1 (enExample)
WO (1) WO2009027527A2 (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2408919B1 (en) * 2009-03-16 2017-10-18 CuRNA, Inc. Treatment of nuclear factor (erythroid-derived 2)-like 2 (nrf2) related diseases by inhibition of natural antisense transcript to nrf2
JP6128848B2 (ja) * 2009-08-05 2017-05-17 クルナ・インコーポレーテッド インスリン遺伝子(ins)に対する天然アンチセンス転写物の抑制によるインスリン遺伝子(ins)関連疾患の治療
US9255154B2 (en) 2012-05-08 2016-02-09 Alderbio Holdings, Llc Anti-PCSK9 antibodies and use thereof
EP3010514B1 (en) 2013-06-16 2021-01-20 National University Corporation Tokyo Medical and Dental University Double-stranded antisense nucleic acid with exon-skipping effect
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
US4914210A (en) * 1987-10-02 1990-04-03 Cetus Corporation Oligonucleotide functionalizing reagents
US4962029A (en) * 1987-10-02 1990-10-09 Cetus Corporation Covalent oligonucleotide-horseradish peroxidase conjugate
US6433159B1 (en) * 1992-09-10 2002-08-13 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
CA2143678A1 (en) * 1992-09-10 1994-03-17 Kevin P. Anderson 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)
TR199901180T2 (xx) * 1996-11-27 1999-08-23 Pfizer Inc. Apo B-Salg�lama/MTP inhibit�r amidler.
AU726374B2 (en) * 1997-03-05 2000-11-02 University Of Washington Novel screening methods to identify agents that selectively inhibit hepatitis C virus replication
WO2004014852A2 (en) * 2002-08-12 2004-02-19 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
EP2530157B1 (en) * 2003-07-31 2016-09-28 Regulus Therapeutics Inc. Oligomeric compounds and compositions for use in modulation of miRNAs
DK1786472T3 (da) * 2004-08-10 2013-04-15 Genzyme Corp Antisense-modulering af apolipoprotein B-ekspression
EP2076597A2 (en) * 2006-10-09 2009-07-08 Santaris Pharma A/S Rna antagonist compounds for the modulation of pcsk9

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