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公开(公告)号：US20150363558A1
公开(公告)日：2015-12-17
申请号：US13603284
申请日：2012-09-04
CPC分类号： C12Q1/6883 , C12Q2600/118 , C12Q2600/156 , G16B20/00 , G16B40/00
摘要： The present invention relates to novel genetic markers associated with endometriosis and risk of developing endometriosis, and methods and materials for determining whether a human subject has endometriosis or is at risk of developing endometriosis and the use of such risk information in selectively administering a treatment that at least partially prevents or compensates for an endometriosis related symptom.
摘要翻译： 本发明涉及与子宫内膜异位症和子宫内膜异位症发生风险相关的新型遗传标记，以及用于确定人受试者是否具有子宫内膜异位症或处于发展子宫内膜异位症风险的方法和材料，以及使用这种风险信息来选择性地施用治疗 至少部分预防或补偿子宫内膜异位症相关症状。
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公开(公告)号：US20150368714A1
公开(公告)日：2015-12-24
申请号：US13789082
申请日：2013-03-07
申请人： Kenneth Ward , Rakesh N. Chettier , Hans Albertsen
发明人： Kenneth Ward , Rakesh N. Chettier , Hans Albertsen
IPC分类号： C12Q1/68
CPC分类号： A61K31/566 , C12Q1/6883 , C12Q2600/156
摘要： The present invention relates to novel genetic markers associated with endometriosis and risk of developing endometriosis, and methods and materials for determining whether a human subject has endometriosis or is at risk of developing endometriosis and the use of such risk information in selectively administering a treatment that at least partially prevents or compensates for an endometriosis related symptom.
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公开(公告)号：US08932993B1
公开(公告)日：2015-01-13
申请号：US13788913
申请日：2013-03-07
申请人： Kenneth Ward , Rakesh N. Chettier , Hans Albertsen
发明人： Kenneth Ward , Rakesh N. Chettier , Hans Albertsen
CPC分类号： C12Q1/6883 , C12Q2600/106 , C12Q2600/156 , C12Q2600/172
摘要： The present invention relates to novel genetic markers associated with endometriosis and risk of developing endometriosis, and methods and materials for determining whether a human subject has endometriosis or is at risk of developing endometriosis and the use of such risk information in selectively administering a treatment that at least partially prevents or compensates for an endometriosis related symptom.
摘要翻译： 本发明涉及与子宫内膜异位症和子宫内膜异位症发生风险相关的新型遗传标记，以及用于确定人受试者是否具有子宫内膜异位症或处于发展子宫内膜异位症风险的方法和材料，以及使用这种风险信息来选择性地施用治疗 至少部分预防或补偿子宫内膜异位症相关症状。
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公开(公告)号：US09434991B2
公开(公告)日：2016-09-06
申请号：US13789082
申请日：2013-03-07
申请人： Kenneth Ward , Rakesh N. Chettier , Hans Albertsen
发明人： Kenneth Ward , Rakesh N. Chettier , Hans Albertsen
IPC分类号： C12Q1/68
CPC分类号： A61K31/566 , C12Q1/6883 , C12Q2600/156
摘要： The present invention relates to novel genetic markers associated with endometriosis and risk of developing endometriosis, and methods and materials for determining whether a human subject has endometriosis or is at risk of developing endometriosis and the use of such risk information in selectively administering a treatment that at least partially prevents or compensates for an endometriosis related symptom.
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5.发明申请公开(公告)号：US20150337373A1
公开(公告)日：2015-11-26
申请号：US13364378
申请日：2012-02-02
IPC分类号： C12Q1/68 , C12N15/113 , C07K16/18
CPC分类号： C12Q1/6883 , C12Q2600/106 , C12Q2600/156 , C12Q2600/172
摘要： The present invention relates to novel genetic markers associated with degenerative disc disease (DDD), risk of developing DDD and risk of DDD progression, and methods and materials for determining whether a human subject has DDD, is at risk of developing DDD or is at risk of DDD progression.
摘要翻译： 本发明涉及与退行性椎间盘疾病（DDD）相关的新型遗传标记，发展DDD的风险和DDD进展的风险以及用于确定人类受试者是否具有DDD的方法和材料是否具有发展DDD或处于危险中的风险 的DDD进展。
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公开(公告)号：US20130310261A1
公开(公告)日：2013-11-21
申请号：US13848772
申请日：2013-03-22
CPC分类号： C12Q1/6883 , C12Q2600/118 , C12Q2600/156 , C12Q2600/172 , G16H50/30
摘要： The present invention relates to novel genetic markers associated with scoliosis, risk of developing scoliosis and risk of scoliosis curve progression, and simplified methods and materials for determining whether a human subject has scoliosis, is at risk of developing scoliosis or is at risk of scoliosis curve progression.
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公开(公告)号：US20130288913A1
公开(公告)日：2013-10-31
申请号：US13852932
申请日：2013-03-28
IPC分类号： C12Q1/68
CPC分类号： C12Q1/6876 , C12Q1/68 , C12Q1/6883 , C12Q2600/156 , C40B30/04 , G16Z99/00
摘要： The present invention relates to novel genetic markers associated with scoliosis, risk of developing scoliosis and risk of scoliosis curve progression, and simplified methods and materials for determining whether a human subject has scoliosis, is at risk of developing scoliosis or is at risk of scoliosis curve progression.
摘要翻译： 本发明涉及与脊柱侧凸相关的新型遗传标记，发生脊柱侧弯的风险和脊柱侧弯曲线进展的风险，以及用于确定人类受试者是否患有脊柱侧弯的简化方法和材料是否处于发生脊柱侧凸的风险或处于脊柱侧凸的风险中 进步。
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公开(公告)号：US20120258884A1
公开(公告)日：2012-10-11
申请号：US13526876
申请日：2012-06-19
CPC分类号： C12Q1/6876 , C12Q1/68 , C12Q1/6883 , C12Q2600/156 , C40B30/04 , G16Z99/00
摘要： The present invention relates to novel genetic markers associated with scoliosis, risk of developing scoliosis and risk of scoliosis curve progression, and simplified methods and materials for determining whether a human subject has scoliosis, is at risk of developing scoliosis or is at risk of scoliosis curve progression.
摘要翻译： 本发明涉及与脊柱侧凸相关的新型遗传标记，发生脊柱侧弯的风险和脊柱侧弯曲线进展的风险，以及用于确定人类受试者是否患有脊柱侧弯的简化方法和材料是否处于发生脊柱侧凸的风险或处于脊柱侧凸的风险中 进步。
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公开(公告)号：US20150361494A1
公开(公告)日：2015-12-17
申请号：US13159132
申请日：2011-06-13
IPC分类号： C40B30/04 , A61K38/02 , G06F19/24 , A61K39/395 , A61K31/7088 , A61P15/00 , A61K48/00
CPC分类号： C12Q1/6883 , C12Q2600/106 , C12Q2600/156
摘要： The present invention relates to novel genetic markers associated with endometriosis and risk of developing endometriosis, and methods and materials for determining whether a human subject has endometriosis or is at risk of developing endometriosis and the use of such risk information in selectively administering a treatment that at least partially prevents or compensates for an endometriosis related symptom.
摘要翻译： 本发明涉及与子宫内膜异位症和子宫内膜异位症发生风险相关的新型遗传标记，以及用于确定人受试者是否具有子宫内膜异位症或处于发展子宫内膜异位症风险的方法和材料，以及使用这种风险信息来选择性地施用治疗 至少部分预防或补偿子宫内膜异位症相关症状。
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10.发明申请公开(公告)号：US20100003691A1
公开(公告)日：2010-01-07
申请号：US12496642
申请日：2009-07-01
CPC分类号： C12Q1/6883 , C12Q2600/106 , C12Q2600/156 , C12Q2600/172
摘要： The present invention relates to novel genetic markers associated with degenerative disc disease (DDD), risk of developing DDD and risk of DDD progression, and methods and materials for determining whether a human subject has DDD, is at risk of developing DDD or is at risk of DDD progression.
摘要翻译： 本发明涉及与退行性椎间盘疾病（DDD）相关的新型遗传标记，发展DDD的风险和DDD进展的风险以及用于确定人类受试者是否具有DDD的方法和材料是否具有发展DDD或处于危险中的风险 的DDD进展。
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