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公开(公告)号:EP3463439B1
公开(公告)日:2022-08-03
申请号:EP17740138.7
申请日:2017-06-02
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12.
公开(公告)号:EP3582674B1
公开(公告)日:2022-05-04
申请号:EP18710943.4
申请日:2018-02-16
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公开(公告)号:EP3636778B1
公开(公告)日:2022-01-12
申请号:EP19190336.8
申请日:2011-08-18
发明人: SNIDER, Lauren , VAN DER MAAREL, Silvère M. , TAPSCOTT, Stephen J. , TAWIL, Rabi , LEMMERS, Richard J.L.F. , GENG, Linda
IPC分类号: C12Q1/6883 , C12N15/11 , A61K48/00 , G01N33/68
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公开(公告)号:EP3033108B1
公开(公告)日:2021-03-24
申请号:EP14836047.2
申请日:2014-08-18
IPC分类号: A61K39/395 , A61K31/7088 , A61K38/10
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公开(公告)号:EP3034083B1
公开(公告)日:2020-12-09
申请号:EP15186785.0
申请日:2007-09-21
发明人: Thornton, Charles A. , Wheeler, Thurman , Sobezak, Krzysztof , Osborne, Robert , Miller, Jill , Swanson, Maurice
IPC分类号: A61K31/7036 , G01N33/50 , G01N33/68 , A61K38/00 , A61K47/54 , A61P21/00 , A61P21/04 , A61P43/00 , C12N15/113
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16.
公开(公告)号:EP3688406A1
公开(公告)日:2020-08-05
申请号:EP18797514.9
申请日:2018-10-23
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公开(公告)号:EP3636778A1
公开(公告)日:2020-04-15
申请号:EP19190336.8
申请日:2011-08-18
申请人: Fred Hutchinson Cancer Research Center , Leiden University Medical Center , University of Rochester
发明人: SNIDER, Lauren , VAN DER MAAREL, Silvère M. , TAPSCOTT, Stephen J. , TAWIL, Rabi , LEMMERS, Richard J.L.F. , GENG, Linda
IPC分类号: C12Q1/6883 , C12N15/11 , A61K48/00 , G01N33/68
摘要: In one aspect, the invention provides a method of screening a human subject to determine if said subject has a genetic predisposition to develop, or is suffering from Facioscapulohumeral Dystrophy (FSHD), said method comprising: (a) providing a biological sample comprising genomic DNA from the subject; and (b) analyzing the portion of the genomic DNA in the sample corresponding to the distal D4Z4-pLAM region on chromosome 4 and determining the presence or absence of a polymorphism resulting in a functional polyadenylation sequence operationally linked to exon 3 of the DUX4 gene, wherein a determination of the absence of a functional polyadenylation sequence operationally linked to exon 3 of the DUX4 gene indicates that the subject does not have a genetic predisposition to develop, and is not suffering from FSHD, and/or wherein a determination of the presence of a functional polyadenylation sequence operationally linked to exon 3 of the DUX4 gene indicates that the subject has a genetic predisposition to develop, or is suffering from Facioscapulohumeral Dystrophy (FSHD).
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公开(公告)号:EP3154534B1
公开(公告)日:2020-02-12
申请号:EP15735770.8
申请日:2015-06-12
IPC分类号: A61K31/00 , A61K31/357 , A61K31/365 , A61K31/366 , A61K31/381 , A61K31/41 , A61K31/4178 , A61K31/426 , A61K31/427 , A61K31/4409 , A61K31/4422 , A61K31/47 , A61K31/546 , A61K31/63 , A61K31/635 , A61P31/04
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公开(公告)号:EP3595677A1
公开(公告)日:2020-01-22
申请号:EP18714931.5
申请日:2018-03-14
IPC分类号: A61K31/733 , A61K9/20 , A61K9/48 , A61P19/02
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