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公开(公告)号:US20110014208A1
公开(公告)日:2011-01-20
申请号:US12888751
申请日:2010-09-23
申请人: LYNN MACDONALD , RICHARD TORRES , MARC R. MORRA , JOEL H. MARTIN , JOEL C. REINHARDT , PAUL TISEO
发明人: LYNN MACDONALD , RICHARD TORRES , MARC R. MORRA , JOEL H. MARTIN , JOEL C. REINHARDT , PAUL TISEO
IPC分类号: A61K39/395 , A61P19/02
CPC分类号: C07K16/22 , A61K9/0019 , A61K39/3955 , A61K45/06 , A61K2039/505 , A61K2039/545 , C07K2317/56 , C07K2317/565 , C07K2317/76
摘要: Methods are disclosed for treating osteoarthritis in a human subject in need thereof, comprising administering to the subject a therapeutically effective amount of an anti-human NGF antibody, or antigen-binding fragment thereof, wherein at least one symptom associated with osteoarthritis is prevented, ameliorated or improved.
摘要翻译: 公开了用于治疗有需要的人类受试者骨关节炎的方法,其包括向受试者施用治疗有效量的抗人NGF抗体或其抗原结合片段,其中至少一种与骨关节炎有关的症状被预防,改善 或改进。
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公开(公告)号:US20140033336A1
公开(公告)日:2014-01-30
申请号:US14046285
申请日:2013-10-04
IPC分类号: A01K67/027
摘要: A method for engineering and utilizing large DNA vectors to target, via homologous recombination, and modify, in any desirable fashion, endogenous genes and chromosomal loci in eukaryotic cells. These large DNA targeting vectors for eukaryotic cells, termed LTVECs, are derived from fragments of cloned genomic DNA larger than those typically used by other approaches intended to perform homologous targeting in eukaryotic cells. Also provided is a rapid and convenient method of detecting eukaryotic cells in which the LTVEC has correctly targeted and modified the desired endogenous gene(s) or chromosomal locus (loci) as well as the use of these cells to generate organisms bearing the genetic modification.
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公开(公告)号:US20140017229A1
公开(公告)日:2014-01-16
申请号:US14036530
申请日:2013-09-25
IPC分类号: C07K16/00
CPC分类号: C12P21/00 , A01K67/0275 , A01K67/0278 , A01K2207/15 , A01K2217/05 , A01K2227/105 , A01K2267/01 , C07K16/00 , C07K16/28 , C07K16/462 , C07K2317/10 , C07K2317/21 , C07K2317/24 , C07K2317/51 , C07K2317/515 , C07K2317/56 , C12N15/67 , C12N15/85 , C12N15/8509 , C12N15/902 , C12N15/907 , C12N2800/204
摘要: A method for engineering and utilizing large DNA vectors to target, via homologous recombination, and modify, in any desirable fashion, endogenous genes and chromosomal loci in eukaryotic cells. These large DNA targeting vectors for eukaryotic cells, termed LTVECs, are derived from fragments of cloned genomic DNA larger than those typically used by other approaches intended to perform homologous targeting in eukaryotic cells. Also provided is a rapid and convenient method of detecting eukaryotic cells in which the LTVEC has correctly targeted and modified the desired endogenous gene(s) or chromosomal locus (loci) as well as the use of these cells to generate organisms bearing the genetic modification.
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公开(公告)号:US20140073010A1
公开(公告)日:2014-03-13
申请号:US14080114
申请日:2013-11-14
IPC分类号: C12P21/00
CPC分类号: C12P21/00 , A01K67/0275 , A01K67/0278 , A01K2207/15 , A01K2217/05 , A01K2227/105 , A01K2267/01 , C07K16/00 , C07K16/28 , C07K16/462 , C07K2317/10 , C07K2317/21 , C07K2317/24 , C07K2317/51 , C07K2317/515 , C07K2317/56 , C12N15/67 , C12N15/85 , C12N15/8509 , C12N15/902 , C12N15/907 , C12N2800/204
摘要: A method for engineering and utilizing large DNA vectors to target, via homologous recombination, and modify, in any desirable fashion, endogenous genes and chromosomal loci in eukaryotic cells. These large DNA targeting vectors for eukaryotic cells, termed LTVECs, are derived from fragments of cloned genomic DNA larger than those typically used by other approaches intended to perform homologous targeting in eukaryotic cells. Also provided is a rapid and convenient method of detecting eukaryotic cells in which the LTVEC has correctly targeted and modified the desired endogenous gene(s) or chromosomal locus (loci) as well as the use of these cells to generate organisms bearing the genetic modification.
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公开(公告)号:US20140041068A1
公开(公告)日:2014-02-06
申请号:US14046291
申请日:2013-10-04
IPC分类号: A01K67/027
摘要: A method for engineering and utilizing large DNA vectors to target, via homologous recombination, and modify, in any desirable fashion, endogenous genes and chromosomal loci in eukaryotic cells. These large DNA targeting vectors for eukaryotic cells, termed LTVECs, are derived from fragments of cloned genomic DNA larger than those typically used by other approaches intended to perform homologous targeting in eukaryotic cells. Also provided is a rapid and convenient method of detecting eukaryotic cells in which the LTVEC has correctly targeted and modified the desired endogenous gene(s) or chromosomal locus (loci) as well as the use of these cells to generate organisms bearing the genetic modification.
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公开(公告)号:US20140018522A1
公开(公告)日:2014-01-16
申请号:US14036892
申请日:2013-09-25
IPC分类号: C07K16/28
CPC分类号: C12P21/00 , A01K67/0275 , A01K67/0278 , A01K2207/15 , A01K2217/05 , A01K2227/105 , A01K2267/01 , C07K16/00 , C07K16/28 , C07K16/462 , C07K2317/10 , C07K2317/21 , C07K2317/24 , C07K2317/51 , C07K2317/515 , C07K2317/56 , C12N15/67 , C12N15/85 , C12N15/8509 , C12N15/902 , C12N15/907 , C12N2800/204
摘要: A method for engineering and utilizing large DNA vectors to target, via homologous recombination, and modify, in any desirable fashion, endogenous genes and chromosomal loci in eukaryotic cells. These large DNA targeting vectors for eukaryotic cells, termed LTVECs, are derived from fragments of cloned genomic DNA larger than those typically used by other approaches intended to perform homologous targeting in eukaryotic cells. Also provided is a rapid and convenient method of detecting eukaryotic cells in which the LTVEC has correctly targeted and modified the desired endogenous gene(s) or chromosomal locus (loci) as well as the use of these cells to generate organisms bearing the genetic modification.
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公开(公告)号:US20110195454A1
公开(公告)日:2011-08-11
申请号:US13022759
申请日:2011-02-08
申请人: JOHN MCWHIRTER , LYNN MACDONALD , SEAN STEVENS , SAMUEL DAVIS , DAVID R. BUCKLER , ANDREW J. MURPHY
发明人: JOHN MCWHIRTER , LYNN MACDONALD , SEAN STEVENS , SAMUEL DAVIS , DAVID R. BUCKLER , ANDREW J. MURPHY
IPC分类号: C12P21/02 , A01K67/027
CPC分类号: C07K16/22 , A01K67/0278 , A01K2207/15 , A01K2217/072 , A01K2217/15 , A01K2227/105 , A01K2267/01 , C07K16/00 , C07K2317/21 , C07K2317/24 , C07K2317/515 , C07K2317/565 , C07K2317/567 , C07K2317/76 , C07K2317/92 , C07K2319/30 , C12N15/8509 , C12N2800/204
摘要: A genetically modified mouse is provided, wherein the mouse is incapable of rearranging and expressing an endogenous mouse immunoglobulin light chain variable sequence, wherein the mouse expresses only one or two human light chain variable domains encoded by human immunoglobulin sequences operably linked to the mouse kappa (κ) constant gene at the endogenous mouse κ locus, wherein the mouse expresses a reverse chimeric antibody having a light chain variable domain derived from one of only two human light chain variable region gene segments and a mouse κ constant domain, and a human heavy chain variable domain and a mouse heavy chain constant domain, from an endogenous mouse heavy chain locus. Bispecific epitope-binding proteins that are fully human are provided, comprising two different heavy chains that associate with an identical light chain that comprises a variable domain derived from one of two different human light chain variable region gene segments.
摘要翻译: 提供遗传修饰的小鼠,其中小鼠不能重新排列并表达内源性小鼠免疫球蛋白轻链可变序列,其中小鼠仅表达由人免疫球蛋白序列编码的一个或两个可操作地连接到小鼠κ的人轻链可变结构域( &kgr;)内源性小鼠的恒定基因 基因座,其中小鼠表达具有仅来自两个人轻链可变区基因片段之一的轻链可变结构域和小鼠kgr的逆嵌合抗体; 恒定结构域,以及来自内源小鼠重链基因座的人重链可变结构域和小鼠重链恒定结构域。 提供了完全人的双特异性表位结合蛋白,其包含两个不同的重链,所述重链与相同的轻链相关,其包含衍生自两个不同人轻链可变区基因片段之一的可变结构域。
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