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公开(公告)号:US08148089B2
公开(公告)日:2012-04-03
申请号:US12702201
申请日:2010-02-08
申请人: John P. Anderson , Kelly Banducci , Guriqbal S. Basi , David Chereau , Tamie J. Chilcote , Normand L. Frigon, Jr. , Jason Goldstein , Irene Griswold
发明人: John P. Anderson , Kelly Banducci , Guriqbal S. Basi , David Chereau , Tamie J. Chilcote , Normand L. Frigon, Jr. , Jason Goldstein , Irene Griswold
IPC分类号: G01N33/53
CPC分类号: C12Q1/6883 , C12N15/1137 , C12N15/86 , C12N2310/11 , C12N2310/14 , C12N2740/15043 , C12Q1/485 , C12Q2600/136 , C12Q2600/158 , C12Y207/11016 , C12Y207/11021 , G01N2500/04 , G01N2800/28
摘要: The invention provides agents and methods for treatment of diseases associated with Lewy body diseases (LBDs) in the brain of a patient. Preferred agents include inhibitors of PLK2 kinase.
摘要翻译: 本发明提供了用于治疗与患者脑中的路易体疾病(LBD)相关的疾病的药剂和方法。 优选的试剂包括PLK2激酶的抑制剂。
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公开(公告)号:US20110207796A1
公开(公告)日:2011-08-25
申请号:US12865857
申请日:2009-02-13
申请人: John P. Anderson , Kelly Banducci , Guriqbal S. Basi , David Chereau , Tamie J. Chilcote , Normand L. Frigon, JR. , Jason Goldstein , Irene Griswold-Prenner
发明人: John P. Anderson , Kelly Banducci , Guriqbal S. Basi , David Chereau , Tamie J. Chilcote , Normand L. Frigon, JR. , Jason Goldstein , Irene Griswold-Prenner
IPC分类号: C12Q1/48 , C12N5/071 , A61K31/7105 , A61P25/28
CPC分类号: C12Q1/485 , C12N15/1137 , C12N2310/14 , G01N2500/04 , G01N2800/2835
摘要: Agents and methods for treatment of diseases associated with Lewy body diseases (LBDs) in the brain of a patient are provided. Preferred agents include inhibitors of PLK2 kinase.
摘要翻译: 提供了用于治疗与患者脑中路易体疾病(LBD)相关的疾病的药剂和方法。 优选的试剂包括PLK2激酶的抑制剂。
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公开(公告)号:US20080300206A1
公开(公告)日:2008-12-04
申请号:US12030849
申请日:2008-02-13
申请人: John P. Anderson , Kelly Banducci , Guriqbal S. Basi , David Chereau , Tamie J. Chilcote , Normand L. Frigon, JR. , Jason Goldstein , Irene Griswold-Prenner
发明人: John P. Anderson , Kelly Banducci , Guriqbal S. Basi , David Chereau , Tamie J. Chilcote , Normand L. Frigon, JR. , Jason Goldstein , Irene Griswold-Prenner
IPC分类号: A61K31/70 , C12N5/06 , A61K31/44 , A61K31/415 , A61K31/47 , A61K31/40 , C12Q1/48 , A01K67/027 , A61P25/00
CPC分类号: C12Q1/6883 , C12N15/1137 , C12N15/86 , C12N2310/11 , C12N2310/14 , C12N2740/15043 , C12Q1/485 , C12Q2600/136 , C12Q2600/158 , C12Y207/11016 , C12Y207/11021 , G01N2500/04 , G01N2800/28
摘要: The invention provides agents and methods for treatment of diseases associated with Lewy body diseases (LBDs) in the brain of a patient. Preferred agents include inhibitors of PLK2 kinase.
摘要翻译: 本发明提供了用于治疗与患者脑中的路易体疾病(LBD)相关的疾病的药剂和方法。 优选的试剂包括PLK2激酶的抑制剂。
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公开(公告)号:US07553639B2
公开(公告)日:2009-06-30
申请号:US11669093
申请日:2007-01-30
申请人: Tami J. Chilcote , Kelly Banducci , Normand L. Frigon, Jr. , Guriqbal S. Basi , John P. Anderson , Jason Goldstein , Irene Griswold-Prenner , David Chereau
发明人: Tami J. Chilcote , Kelly Banducci , Normand L. Frigon, Jr. , Guriqbal S. Basi , John P. Anderson , Jason Goldstein , Irene Griswold-Prenner , David Chereau
CPC分类号: C12Q1/6883 , C12N15/1137 , C12N15/86 , C12N2310/11 , C12N2310/14 , C12N2740/15043 , C12Q1/485 , C12Q2600/136 , C12Q2600/158 , C12Y207/11016 , C12Y207/11021 , G01N2500/04 , G01N2800/28
摘要: The invention provides agents and methods for treatment of diseases associated with Lewy body diseases (LBDs) in the brain of a patient. Preferred agents include inhibitors of PLK2 and GRK6 kinases.
摘要翻译: 本发明提供了用于治疗与患者脑中的路易体疾病(LBD)相关的疾病的药剂和方法。 优选的试剂包括PLK2和GRK6激酶的抑制剂。
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公开(公告)号:US20080160011A1
公开(公告)日:2008-07-03
申请号:US11669093
申请日:2007-01-30
申请人: Tami J. Chilcote , Kelly Banducci , Normand L. Frigon , Guriqbal S. Basi , John P. Anderson , Jason Goldstein , Irene Griswold-Prenner , David Chereau
发明人: Tami J. Chilcote , Kelly Banducci , Normand L. Frigon , Guriqbal S. Basi , John P. Anderson , Jason Goldstein , Irene Griswold-Prenner , David Chereau
CPC分类号: C12Q1/6883 , C12N15/1137 , C12N15/86 , C12N2310/11 , C12N2310/14 , C12N2740/15043 , C12Q1/485 , C12Q2600/136 , C12Q2600/158 , C12Y207/11016 , C12Y207/11021 , G01N2500/04 , G01N2800/28
摘要: The invention provides agents and methods for treatment of diseases associated with Lewy body diseases (LBDs) in the brain of a patient. Preferred agents include inhibitors of PLK2 and GRK6 kinases.
摘要翻译: 本发明提供了用于治疗与患者脑中的路易体疾病(LBD)相关的疾病的药剂和方法。 优选的试剂包括PLK2和GRK6激酶的抑制剂。
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公开(公告)号:US20090035217A1
公开(公告)日:2009-02-05
申请号:US12040739
申请日:2008-02-29
IPC分类号: A61K49/00 , G01N33/00 , A01K67/027 , A61K38/00 , C12N9/50 , A61P25/00 , A61K39/395 , C12Q1/02 , C07K16/18
CPC分类号: C07K16/18 , A01K67/0275 , A01K2217/05 , A01K2227/105 , A01K2227/706 , A01K2267/0356 , A61K38/00 , C07K2317/33 , C07K2317/34 , C12N15/8509 , C12Q1/6883 , C12Q2600/156 , G01N33/6896 , G01N2800/28 , G01N2800/2814 , G01N2800/2821 , G01N2800/2835
摘要: The application identifies novel fragments of alpha-synuclein in patients with Lewy Body Disease (LBD) and transgenic animal models thereof. These diseases are characterized by aggregations of alpha-synuclein. The fragments have a truncated C-terminus relative to full-length alpha-synuclein. Some fragments are characterized by a molecular weight of about 12 kDa as determined by SDS gel electrophoresis in tricine buffer and a truncation of at least ten contiguous amino acids from the C-terminus of natural alpha-synuclein. The site of cleavage preferably occurs after residue 117 and before residue 126 of natural alpha-synuclein. The identification of these novel fragments of alpha-synuclein has a number of application in for example, drug discovery, diagnostics, therapeutics, and transgenic animals.
摘要翻译: 该应用鉴定了路易体病(LBD)患者和其转基因动物模型中的α-突触核蛋白的新片段。 这些疾病的特征在于α-突触核蛋白的聚集。 片段相对于全长α-突触核蛋白具有截短的C-末端。 一些片段的特征在于分子量约12kDa,通过SDS胶体电泳在三氯缓冲液中测定,并从天然α-突触核蛋白的C末端截断至少十个相邻的氨基酸。 切割位点优选在残基117之后和天然α-突触核蛋白的残基126之前发生。 这些新型α-突触核蛋白片段的鉴定在药物发现,诊断,治疗和转基因动物中有许多应用。
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公开(公告)号:US09879071B2
公开(公告)日:2018-01-30
申请号:US13604441
申请日:2012-09-05
IPC分类号: A61K39/395 , C07K16/00 , A61K39/00 , C07K16/18 , A01K67/027 , C12N15/85 , C12Q1/68 , G01N33/68 , A61K38/00
CPC分类号: C07K16/18 , A01K67/0275 , A01K2217/05 , A01K2227/105 , A01K2227/706 , A01K2267/0356 , A61K38/00 , C07K2317/33 , C07K2317/34 , C12N15/8509 , C12Q1/6883 , C12Q2600/156 , G01N33/6896 , G01N2800/28 , G01N2800/2814 , G01N2800/2821 , G01N2800/2835
摘要: The application identifies novel fragments of alpha-synuclein in patients with Lewy Body Disease (LBD) and transgenic animal models thereof. These diseases are characterized by aggregations of alpha-synuclein. The fragments have a truncated C-terminus relative to full-length alpha-synuclein. Some fragments are characterized by a molecular weight of about 12 kDa as determined by SDS gel electrophoresis in tricine buffer and a truncation of at least ten contiguous amino acids from the C-terminus of natural alpha-synuclein. The site of cleavage preferably occurs after residue 117 and before residue 126 of natural alpha-synuclein. The identification of these novel fragments of alpha-synuclein has a number of application in for example, drug discovery, diagnostics, therapeutics, and transgenic animals.
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公开(公告)号:US20130072663A1
公开(公告)日:2013-03-21
申请号:US13604441
申请日:2012-09-05
IPC分类号: C07K16/18
CPC分类号: C07K16/18 , A01K67/0275 , A01K2217/05 , A01K2227/105 , A01K2227/706 , A01K2267/0356 , A61K38/00 , C07K2317/33 , C07K2317/34 , C12N15/8509 , C12Q1/6883 , C12Q2600/156 , G01N33/6896 , G01N2800/28 , G01N2800/2814 , G01N2800/2821 , G01N2800/2835
摘要: The application identifies novel fragments of alpha-synuclein in patients with Lewy Body Disease (LBD) and transgenic animal models thereof. These diseases are characterized by aggregations of alpha-synuclein. The fragments have a truncated C-terminus relative to full-length alpha-synuclein. Some fragments are characterized by a molecular weight of about 12 kDa as determined by SDS gel electrophoresis in tricine buffer and a truncation of at least ten contiguous amino acids from the C-terminus of natural alpha-synuclein. The site of cleavage preferably occurs after residue 117 and before residue 126 of natural alpha-synuclein. The identification of these novel fragments of alpha-synuclein has a number of application in for example, drug discovery, diagnostics, therapeutics, and transgenic animals.
摘要翻译: 该应用鉴定了路易体病(LBD)患者和其转基因动物模型中的α-突触核蛋白的新片段。 这些疾病的特征在于α-突触核蛋白的聚集。 片段相对于全长α-突触核蛋白具有截短的C-末端。 一些片段的特征在于分子量约12kDa,通过SDS胶体电泳在三氯缓冲液中测定,并从天然α-突触核蛋白的C末端截断至少十个相邻的氨基酸。 切割位点优选在残基117之后和天然α-突触核蛋白的残基126之前发生。 这些新型α-突触核蛋白片段的鉴定在药物发现,诊断,治疗和转基因动物中有许多应用。
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公开(公告)号:US07358331B2
公开(公告)日:2008-04-15
申请号:US11194115
申请日:2005-07-29
CPC分类号: C07K16/18 , A01K67/0275 , A01K2217/05 , A01K2227/105 , A01K2227/706 , A01K2267/0356 , A61K38/00 , C07K2317/33 , C07K2317/34 , C12N15/8509 , C12Q1/6883 , C12Q2600/156 , G01N33/6896 , G01N2800/28 , G01N2800/2814 , G01N2800/2821 , G01N2800/2835
摘要: The application identifies novel fragments of alpha-synuclein in patients with Lewy Body Disease (LBD) and transgenic animal models thereof. These diseases are characterized by aggregations of alpha-synuclein. The fragments have a truncated C-terminus relative to full-length alpha-synuclein. Some fragments are characterized by a molecular weight of about 12 kDa as determined by SDS gel electrophoresis in tricine buffer and a truncation of at least ten contiguous amino acids from the C-terminus of natural alpha-synuclein. The site of cleavage preferably occurs after residue 117 and before residue 126 of natural alpha-synuclein. The identification of these novel fragments of alpha-synuclein has a number of application in for example, drug discovery, diagnostics, therapeutics, and transgenic animals.
摘要翻译: 该应用鉴定了路易体病(LBD)患者和其转基因动物模型中的α-突触核蛋白的新片段。 这些疾病的特征在于α-突触核蛋白的聚集。 片段相对于全长α-突触核蛋白具有截短的C-末端。 一些片段的特征在于分子量约12kDa,通过SDS胶体电泳在三氯缓冲液中测定,并从天然α-突触核蛋白的C末端截断至少十个相邻的氨基酸。 切割位点优选在残基117之后和天然α-突触核蛋白的残基126之前发生。 这些新型α-突触核蛋白片段的鉴定在药物发现,诊断,治疗和转基因动物中有许多应用。
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公开(公告)号:US07306945B2
公开(公告)日:2007-12-11
申请号:US10969335
申请日:2004-10-19
CPC分类号: A01K67/027 , C07K14/47 , C12N15/10 , C12N15/1096 , C12Q1/68
摘要: The application identifies fragments of alpha-synuclein in patients with Lewy Body Disease (LBD) and transgenic animal models thereof. These diseases are characterized by aggregations of alpha-synuclein. The fragments have a truncated C-terminus relative to full-length alpha-synuclein. Some fragments are characterized by a molecular weight of about 12 kDa as determined by SDS gel electrophoresis in tricine buffer and a truncation of at least ten contiguous amino acids from the C-terminus of natural alpha-synuclein. The site of cleavage preferably occurs after residue 117 and before residue 126 of natural alpha-synuclein. The identification of these novel fragments of alpha-synuclein has a number of application in for example, drug discovery, diagnostics, therapeutics, and transgenic animals.
摘要翻译: 该应用程序识别路易体病(LBD)患者和其转基因动物模型中α-突触核蛋白的片段。 这些疾病的特征在于α-突触核蛋白的聚集。 片段相对于全长α-突触核蛋白具有截短的C-末端。 一些片段的特征在于分子量约12kDa,通过SDS胶体电泳在三氯缓冲液中测定,并从天然α-突触核蛋白的C末端截断至少十个相邻的氨基酸。 切割位点优选在残基117之后和天然α-突触核蛋白的残基126之前发生。 这些新型α-突触核蛋白片段的鉴定在药物发现,诊断,治疗和转基因动物中有许多应用。
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