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公开(公告)号:US07528118B2
公开(公告)日:2009-05-05
申请号:US11235385
申请日:2005-09-26
CPC分类号: C12N15/113 , A61K31/7105 , A61K31/718 , C12N2310/14 , C12N2310/315 , C12N2310/321 , C12N2310/3515 , C12N2310/3521
摘要: The invention relates to compositions and methods for modulating the expression of apolipoprotein B, and more particularly to the downregulation of apolipoprotein B by chemically modified oligonucleotides.
摘要翻译: 本发明涉及用于调节载脂蛋白B的表达的组合物和方法,更具体地涉及通过化学修饰的寡核苷酸下载载脂蛋白B的方法。
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公开(公告)号:US20080194512A1
公开(公告)日:2008-08-14
申请号:US11959936
申请日:2007-12-19
CPC分类号: C12N15/1131 , C12N2310/14 , C12N2310/53
摘要: The present invention relates to a double-stranded ribonucleic acid (dsRNA) having a nucleotide sequence which is less that 30 nucleotides in length and which is substantially identical to at least a part of a 3′-untranslated region (3′-UTR) of a (+) strand RNA virus, such as HCV, as well as pharmaceutical compositions comprising the dsRNA, together with a pharmaceutically acceptable carrier. The pharmaceutical compositions are useful for treating infections and diseases caused by the replication or activity of the (+) strand RNA virus, as well as methods for inhibiting viral replication.
摘要翻译: 本发明涉及具有长度小于30个核苷酸的核苷酸序列的双链核糖核酸(dsRNA),并且其基本上与3'非翻译区(3'-UTR)的至少一部分相同 (+)链RNA病毒,例如HCV,以及包含dsRNA的药物组合物,以及药学上可接受的载体。 药物组合物可用于治疗由(+)链RNA病毒的复制或活性引起的感染和疾病以及用于抑制病毒复制的方法。
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公开(公告)号:US07361752B2
公开(公告)日:2008-04-22
申请号:US11303367
申请日:2005-12-14
IPC分类号: C07H21/04
CPC分类号: C12N15/1135 , C12N2310/14
摘要: The invention relates to compositions and methods for modulating the expression of the MLL-AF4 fusion gene, and more particularly to the downregulation of MLL-AF4 by chemically modified oligonucleotides.
摘要翻译: 本发明涉及用于调节MLL-AF4融合基因表达的组合物和方法,更具体地涉及化学修饰寡核苷酸对MLL-AF4的下调。
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公开(公告)号:US07348314B2
公开(公告)日:2008-03-25
申请号:US10384512
申请日:2003-03-07
CPC分类号: C12N15/1131 , C12N2310/14 , C12N2310/53
摘要: The present invention relates to a double-stranded ribonucleic acid (dsRNA) having a nucleotide sequence which is less that 30 nucleotides in length and which is substantially identical to at least a part of a 3′-untranslated region (3′-UTR) of a (+) strand RNA virus, such as HCV, as well as pharmaceutical compositions comprising the dsRNA, together with a pharmaceutically acceptable carrier. The pharmaceutical compositions are useful for treating infections and diseases caused by the replication or activity of the (+) strand RNA virus, as well as methods for inhibiting viral replication.
摘要翻译: 本发明涉及具有长度小于30个核苷酸的核苷酸序列的双链核糖核酸(dsRNA),并且其基本上与3'非翻译区(3'-UTR)的至少一部分相同 (+)链RNA病毒,例如HCV,以及包含dsRNA的药物组合物,以及药学上可接受的载体。 药物组合物可用于治疗由(+)链RNA病毒的复制或活性引起的感染和疾病以及用于抑制病毒复制的方法。
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公开(公告)号:US20120142757A1
公开(公告)日:2012-06-07
申请号:US13343426
申请日:2012-01-04
IPC分类号: A61K31/713 , A61P35/00 , C12N15/63 , C12N5/10 , C12N5/02 , C12N15/113 , A61P11/00
CPC分类号: C12N15/113 , C12N2310/14 , C12N2310/3515
摘要: The invention relates to a double-stranded ribonucleic acid (dsRNA) for inhibiting the expression of an Aha gene (Aha1 gene), comprising an antisense strand having a nucleotide sequence which is less that 30 nucleotides in length, generally 19-25 nucleotides in length, and which is substantially complementary to at least a part of an Aha gene. The invention also relates to a pharmaceutical composition comprising the dsRNA together with a pharmaceutically acceptable carrier; methods for treating diseases caused by Aha1 expression and the expression of an Aha gene using the pharmaceutical composition; and methods for inhibiting the expression of an Aha gene in a cell.
摘要翻译: 本发明涉及用于抑制Aha基因(Aha1基因)表达的双链核糖核酸(dsRNA),其包含长度小于30个核苷酸的核苷酸序列的反义链,其长度通常为19-25个核苷酸 并且其与Aha基因的至少一部分基本上互补。 本发明还涉及包含dsRNA与药学上可接受的载体的药物组合物; 用于治疗由Aha1表达引起的疾病和使用该药物组合物表达Aha基因的方法; 以及抑制细胞中Aha基因表达的方法。
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公开(公告)号:US07928217B2
公开(公告)日:2011-04-19
申请号:US11139089
申请日:2005-05-27
申请人: Hans-Peter Vornlocher , Ingo Roehl , Philipp Hadwiger , Tracy Stage Zimmermann , Muthiah Manoharan , Kallanthottathil G. Rajeev , Akin Akinc
发明人: Hans-Peter Vornlocher , Ingo Roehl , Philipp Hadwiger , Tracy Stage Zimmermann , Muthiah Manoharan , Kallanthottathil G. Rajeev , Akin Akinc
CPC分类号: C07H21/02 , C12N15/111 , C12N15/113 , C12N2310/14 , C12N2310/315 , C12N2310/318 , C12N2310/321 , C12N2310/322 , C12N2310/323 , C12N2310/3231 , C12N2310/53 , C12N2320/51 , C12N2310/3521 , C12N2310/3525 , C12N2310/3527
摘要: This invention relates to modified double-stranded oligoribonucleic acid (dsRNA) having improved stability in cells and biological fluids, and methods of making and identifying dsRNA having improved stability, and of using the dsRNA to inhibit the expression or function of a target gene.
摘要翻译: 本发明涉及在细胞和生物流体中具有改善的稳定性的修饰的双链寡核糖核酸(dsRNA),以及制备和鉴定具有改善的稳定性的dsRNA的方法,以及使用dsRNA抑制靶基因的表达或功能。
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公开(公告)号:US20110071209A1
公开(公告)日:2011-03-24
申请号:US12847958
申请日:2010-07-30
IPC分类号: A61K31/713 , A61P25/00 , C07H21/04
CPC分类号: C12N15/113 , C12N2310/14 , C12N2310/315 , C12N2310/321 , C12N2310/346 , C12N2310/3515 , C12N2310/3521
摘要: The invention relates to compositions and methods for modulating the expression of the RhoA gene, and more particularly to the downregulation of RhoA by chemically modified oligonucleotides.
摘要翻译: 本发明涉及用于调节RhoA基因表达的组合物和方法,更具体地说涉及通过化学修饰的寡核苷酸下调RhoA。
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48.
公开(公告)号:US07902168B2
公开(公告)日:2011-03-08
申请号:US12487605
申请日:2009-06-18
申请人: Dinah Wen-Yee Sah , Maria Frank-Kamenetsky , Anke Geick , Philipp Hadwiger , Ingo Roehl , Pamela Tan , Hans-Peter Vornlocher
发明人: Dinah Wen-Yee Sah , Maria Frank-Kamenetsky , Anke Geick , Philipp Hadwiger , Ingo Roehl , Pamela Tan , Hans-Peter Vornlocher
CPC分类号: C12N15/1138 , C12N2310/14 , C12N2310/315 , C12N2310/321 , C12N2310/322 , C12N2310/3515 , C12N2310/3521
摘要: The invention relates to a double-stranded ribonucleic acid (dsRNA) for inhibiting the expression of the Nav1.8 gene (Nav1.8 gene), comprising an antisense strand having a nucleotide sequence which is less that 25 nucleotides in length and which is substantially complementary to at least a part of the Nav1.8 gene. The invention also relates to a pharmaceutical composition comprising the dsRNA together with a pharmaceutically acceptable carrier; methods for treating diseases caused by the expression of the Nav1.8 gene using the pharmaceutical composition; and methods for inhibiting the expression of the Nav1.8 gene gene in a cell.
摘要翻译: 本发明涉及用于抑制Nav1.8基因(Nav1.8基因)表达的双链核糖核酸(dsRNA),其包含具有长度小于25个核苷酸的核苷酸序列的反义链,其基本上 与Nav1.8基因的至少一部分互补。 本发明还涉及包含dsRNA与药学上可接受的载体的药物组合物; 用于治疗由使用该药物组合物的Nav1.8基因表达引起的疾病的方法; 以及抑制细胞中Nav1.8基因表达的方法。
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公开(公告)号:US07846908B2
公开(公告)日:2010-12-07
申请号:US11724790
申请日:2007-03-15
CPC分类号: C12N15/1136 , C12N2310/14 , C12N2310/321 , C12N2310/3521
摘要: The present invention concerns methods of treatment using transforming growth factor beta (TGF-beta) modulators. More specifically, the invention concerns methods of treating disorders associated with undesirable TGF-beta signaling, by administering short interfering RNA which down-regulate the expression of TGF-beta, and agents useful therein.
摘要翻译: 本发明涉及使用转化生长因子β(TGF-β)调节剂的治疗方法。 更具体地,本发明涉及通过施用下调TGF-β表达的短干扰RNA以及其中有用的试剂来治疗与不期望的TGF-β信号传导相关的病症的方法。
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50.
公开(公告)号:US20100234446A1
公开(公告)日:2010-09-16
申请号:US12510128
申请日:2009-07-27
IPC分类号: A61K31/7105 , C07H21/02 , A61P35/00
CPC分类号: C12N15/1135 , C12N2310/14 , C12N2310/315 , C12N2310/32 , C12N2310/33
摘要: The invention relates to compositions and methods for modulating the expression of Bcr-Abl, and more particularly to the down-regulation of Bcr-Abl mRNA and Bcr-Abl protein levels by oligonucleotides via RNA interference, e.g., chemically modified oligonucleotides.
摘要翻译: 本发明涉及用于调节Bcr-Abl表达的组合物和方法,更具体地涉及通过RNA干扰的寡核苷酸(例如化学修饰的寡核苷酸)对Bcr-Abl mRNA和Bcr-Abl蛋白水平的下调。
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