专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

1. 发明授权

US06180337B2 Diagnosis of the fragile X syndrome 失效
标题翻译：诊断脆性X综合征
公开(公告)号：US06180337B2
公开(公告)日：2001-01-30
申请号：US07751891
申请日：1991-08-29
申请人： C. Thomas Caskey , David L. Nelson , Maura Pieretti , Stephen T. Warren , Ben A. Oostra , Ying-hui Fu
发明人： C. Thomas Caskey , David L. Nelson , Maura Pieretti , Stephen T. Warren , Ben A. Oostra , Ying-hui Fu
IPC分类号： C12Q168
CPC分类号： C12Q1/683 , C12Q1/6841 , C12Q1/6883 , C12Q2600/154 , C12Q2600/156 , C12Q2600/158
摘要： A sequence of the FMR-1 gene is disclosed. This sequence and related probes, cosmids and unique repeats are used to detect X-linked diseases and especially the fragile X syndrome. Also, methods using methylation-sensitive restriction endonuclease and PCR primer probes were used to detect X-linked disease.
摘要翻译：公开了FMR-1基因的序列。该序列和相关探针，粘粒和独特重复用于检测X连锁疾病，特别是脆性X综合征。此外，使用甲基化敏感性限制性内切核酸酶和PCR引物探针的方法检测X连锁疾病。

2. 发明申请

US20050175995A1 Methods for assessing risk for cardiac dysrythmia in a human subject 有权
标题翻译：评估人类受试者心脏失血风险的方法
公开(公告)号：US20050175995A1
公开(公告)日：2005-08-11
申请号：US10475452
申请日：2002-04-22
申请人： Louis Ptacek , Ying-Hui Fu
发明人： Louis Ptacek , Ying-Hui Fu
IPC分类号： C12Q1/68
CPC分类号： C12Q1/6883 , C12Q2600/156
摘要： The present invention relates to methods for assessing the risk of a patient for developing a potentially fatal cardiac dysrhythmia and for diagnosing Andersen's Syndrome. A tissue sample from a patient is obtained and the DNA or proteins of the sample isolated. From the DNA and protein isolates the sequence of the KCNJ2 gene or the Kir2.1 polypeptide can be obtained. The KCNJ2 gene or the Kir2.1 can be screened for alteration as compared to the wile-type sequence. An alteration in a copy of the KCNJ2 gene or a Kir2.1 polypeptide indicates that the patient has a high risk for developing a cardiac dysrhythmia and can be diagnosed with Andersen's Syndrome. The invention also related to isolated nucleic acid molecules with one or more alterations as compared to the wild-type sequence.
摘要翻译：本发明涉及用于评估患者发展潜在致命性心脏心律失常并用于诊断安徒生综合征的风险的方法。获得来自患者的组织样品，并分离样品的DNA或蛋白质。从DNA和蛋白质分离中可以获得KCNJ2基因或Kir2.1多肽的序列。与Wile型序列相比，可以筛选KCNJ2基因或Kir2.1，以进行改变。 KCNJ2基因或Kir2.1多肽拷贝的改变表明患者发生心脏性心律失常的风险很高，可以诊断为安徒生综合征。与野生型序列相比，本发明还涉及具有一个或多个改变的分离的核酸分子。

3. 发明授权

US06794187B2 Mass1 gene, a target for anticonvulsant drug development 失效
标题翻译： Mass1基因，抗惊厥药物开发的目标
公开(公告)号：US06794187B2
公开(公告)日：2004-09-21
申请号：US10220587
申请日：2002-09-03
申请人： Louis J. Ptacek , H. Steve White , Ying-Hui Fu , Shana Skradski
发明人： Louis J. Ptacek , H. Steve White , Ying-Hui Fu , Shana Skradski
IPC分类号： C12N516
CPC分类号： C07K14/47 , A01K2217/05 , A01K2217/075 , C12N2517/02
摘要： The present invention relates to a novel gene which is associated with audiogenic seizures in mice. The gene is known as the Monogenic Audiogenic Seizure-susceptible gene or mass1. The product of the mass1 gene is designated MASS1. Nucleic acid molecules that encode for MASS1 have been identified and purified. The sequence of murine mass1 can be found at SEQ ID NO: 1, and the sequence of human mass1 can be found at SEQ ID NO: 3. Mammalian genes encoding a MASS1 protein are also provided. The invention also provides recombinant vectors comprising nucleic acid molecules that code for a MASS1 protein. These vectors can be plasmids. In certain embodiments, the vectors are prokaryotic or eukaryotic expression vectors. The nucleic acid coding for MASS1 can be linked to a heterologous promoter. The invention also relates to transgenic animals in which one or both alleles of the endogenous mass1 gene is mutated.
摘要翻译：本发明涉及与小鼠中的听觉发作相关的新基因。该基因被称为单因子感觉性发作敏感基因或质量1。 mass1基因的产物命名为MASS1。编码MASS1的核酸分子已被鉴定和纯化。鼠群1的序列可以在SEQ ID NO：1中找到，并且人质粒1的序列可以在SEQ ID NO：3中找到。还提供了编码MASS1蛋白的哺乳动物基因。本发明还提供了包含编码MASS1蛋白的核酸分子的重组载体。这些载体可以是质粒。在某些实施方案中，载体是原核或真核表达载体。编码MASS1的核酸可以与异源启动子连接。本发明还涉及转基因动物，其中内源mass1基因的一个或两个等位基因被突变。

4. 发明授权

US07306911B2 Methods for assessing risk for cardiac dysrythmia in a human subject 有权
标题翻译：评估人类受试者心脏失血风险的方法
公开(公告)号：US07306911B2
公开(公告)日：2007-12-11
申请号：US10475452
申请日：2002-04-22
申请人： Louis Ptacek , Ying-Hui Fu
发明人： Louis Ptacek , Ying-Hui Fu
IPC分类号： C12Q1/68 , C12P19/34 , C07H21/02 , C07H21/04
CPC分类号： C12Q1/6883 , C12Q2600/156
摘要： The present invention relates to methods for assessing the risk of a patient for developing a potentially fatal cardiac dysrhythmia and for diagnosing Andersen's Syndrome. A tissue sample from a patient is obtained and the DNA or proteins of the sample isolated. From the DNA and protein isolates the sequence of the KCNJ2 gene or the Kir2.1 polypeptide can be obtained. The KCNJ2 gene or the Kir2.1 can be screened for alteration as compared to the wile-type sequence. An alteration in a copy of the KCNJ2 gene or a Kir2.1 polypeptide indicates that the patient has a high risk for developing a cardiac dysrhythmia and can be diagnosed with Andersen's Syndrome. The invention also related to isolated nucleic acid molecules with one or more alterations as compared to the wild-type sequence.
摘要翻译：本发明涉及用于评估患者发展潜在致命性心脏心律失常并用于诊断安徒生综合征的风险的方法。获得来自患者的组织样品，并分离样品的DNA或蛋白质。从DNA和蛋白质分离物可以获得KCNJ2基因或Kir2.1多肽的序列。与Wile型序列相比，可以筛选KCNJ2基因或Kir2.1，以进行改变。 KCNJ2基因或Kir2.1多肽拷贝的改变表明患者发生心脏性心律失常的风险很高，可以诊断为安徒生综合征。与野生型序列相比，本发明还涉及具有一个或多个改变的分离的核酸分子。

5. 发明授权

US5552282A Diagnosis of myotonic muscular dystrophy 失效
标题翻译：诊断肌强直性肌营养不良症
公开(公告)号：US5552282A
公开(公告)日：1996-09-03
申请号：US484044
申请日：1993-06-06
申请人： C. Thomas Caskey , Ying-Hui Fu , David L. Friedman , Antonio Pizzuti , Raymond G. Fenwick
发明人： C. Thomas Caskey , Ying-Hui Fu , David L. Friedman , Antonio Pizzuti , Raymond G. Fenwick
IPC分类号： C07K14/47 , C12Q1/68 , C07H21/04 , C12N15/00 , C12P19/34
CPC分类号： C12Q1/6883 , C07K14/471 , C12Q2600/156
摘要： The present invention includes a DNA clone from the myotonic muscular dystrophy gene, a cosmid probe to the myotonic dystrophy site, as well as methods of detecting myotonic muscular dystrophy using RFLP. The method involves the steps of digesting DNA from an individual to be tested with a restriction endonuclease and detecting the restriction fragment length polymorphism with hybridization to probes within the myotonic muscular locus and southern blot analysis. Alternatively, the myotonic muscular dystrophy gene can be measured by determining the amount of mRNA or measuring the amount of protein with an antibody. Further, the myotonic muscular dystrophy gene defect can be detected using either fluorescence in situ hybridization or pulsed field gel electrophoresis using the probes described herein.
摘要翻译：本发明包括来自肌强直性营养不良基因的DNA克隆，对肌强直营养不良位点的粘粒探针，以及使用RFLP检测肌强直性营养不良的方法。该方法包括用限制性内切核酸酶消化来自待测个体的DNA的步骤，并通过与强直肌肌肉轨迹内的探针杂交和Southern印迹分析检测限制性片段长度多态性。或者，可以通过测定mRNA的量或用抗体测量蛋白质的量来测量肌强直性肌营养不良基因。此外，使用本文所述的探针，可以使用荧光原位杂交或脉冲场凝胶电泳检测肌强直性肌营养不良基因缺陷。

6. 发明授权

US6090620A Genes and gene products related to Werner's syndrome 失效
标题翻译：与维纳综合征相关的基因和基因产物
公开(公告)号：US6090620A
公开(公告)日：2000-07-18
申请号：US781891
申请日：1996-12-27
申请人： Ying-Hui Fu , Chang-En Yu , Junko Oshima , John T. Mulligan , Gerard D. Schellenberg
发明人： Ying-Hui Fu , Chang-En Yu , Junko Oshima , John T. Mulligan , Gerard D. Schellenberg
IPC分类号： A01K67/027 , A01K67/00 , C07H21/04 , C07K14/00 , C07K14/47 , C07K16/18 , C12N5/10 , C12N9/64 , C12N9/90 , C12N15/09 , C12N15/861 , C12N15/867 , C12P21/08 , C12Q1/68 , C12N5/00 , C12N15/00 , C12N15/63
CPC分类号： C07K14/47 , C12N9/90 , A01K2217/05 , C12N2799/021
摘要： The present invention discloses nucleic acid molecules encoding WRN gene products, expresion vectors, viral vectors, and host cells suitable for expressing such products.
摘要翻译：本发明公开了编码WRN基因产物，表达载体，病毒载体和适于表达该产物的宿主细胞的核酸分子。

7. 发明申请

US20080220430A1 Methods for assessing risk for cardiac dysrythmia in a human subject 审中-公开
标题翻译：评估人类受试者心脏失血风险的方法
公开(公告)号：US20080220430A1
公开(公告)日：2008-09-11
申请号：US11981388
申请日：2007-10-30
申请人： Louis Ptacek , Ying-Hui Fu
发明人： Louis Ptacek , Ying-Hui Fu
IPC分类号： C12Q1/68
CPC分类号： C12Q1/6883 , C12Q2600/156
摘要： The present invention relates to methods for assessing the risk of a patient for developing a potentially fatal cardiac dysrhythmia and for diagnosing Andersen's Syndrome. A tissue sample from a patient is obtained and the DNA or proteins of the sample isolated. From the DNA and protein isolates the sequence of the KCNJ2 gene or the Kir2.1 polypeptide can be obtained. The KCNJ2 gene or the Kir2.1 can be screened for alteration as compared to the wile-type sequence. An alteration in a copy of the KCNJ2 gene or a Kir2.1 polypeptide indicates that the patient has a high risk for developing a cardiac dysrhythmia and can be diagnosed with Andersen's Syndrome. The invention also related to isolated nucleic acid molecules with one or more alterations as compared to the wild-type sequence.
摘要翻译：本发明涉及用于评估患者发展潜在致命性心脏心律失常并用于诊断安徒生综合征的风险的方法。获得来自患者的组织样品，并分离样品的DNA或蛋白质。从DNA和蛋白质分离物可以获得KCNJ2基因或Kir2.1多肽的序列。与Wile型序列相比，可以筛选KCNJ2基因或Kir2.1，以进行改变。 KCNJ2基因或Kir2.1多肽拷贝的改变表明患者发生心脏性心律失常的风险很高，可以诊断为安徒生综合征。与野生型序列相比，本发明还涉及具有一个或多个改变的分离的核酸分子。

8. 发明授权

US07285641B2 Antibodies against gene products related to Werner's Syndrome 失效
标题翻译：抗Werner综合征基因产物抗体
公开(公告)号：US07285641B2
公开(公告)日：2007-10-23
申请号：US10374077
申请日：2003-02-25
申请人： Ying-Hui Fu , Chang-En Yu , Junko Oshima , John T Mulligan , Gerard D Schellenberg
发明人： Ying-Hui Fu , Chang-En Yu , Junko Oshima , John T Mulligan , Gerard D Schellenberg
IPC分类号： C07K16/00
CPC分类号： C07K14/47 , A01K2217/05 , C12N9/90 , C12N2799/021
摘要： The present invention discloses antibodies that specifically bind to a WRN gene product or a portion thereof.
摘要翻译：本发明公开了特异性结合WRN基因产物或其一部分的抗体。

9. 发明申请

US20050015822A1 Mass 1 gene, a target for anticonvulsant drug development 审中-公开
标题翻译： Mass 1基因，抗惊厥药物开发的目标
公开(公告)号：US20050015822A1
公开(公告)日：2005-01-20
申请号：US10912280
申请日：2004-08-04
申请人： Louis Ptacek , H. White , Ying-Hui Fu , Shana Skradski
发明人： Louis Ptacek , H. White , Ying-Hui Fu , Shana Skradski
IPC分类号： C07K14/47 , C12P21/04 , A01K67/027 , C12N5/06
CPC分类号： C07K14/47 , A01K2217/05 , A01K2217/075 , C12N2517/02
摘要： The present invention relates to a novel gene which is associated with audiogenic seizures in mice. The gene is known as the Monogenic Audiogenic Seizure-susceptible gene or mass1. The product of the mass1 gene is designated MASS1. Nucleic acid molecules that encode for MASS1 have been identified and purified. The sequence of murine mass1 can be found at SEQ ID NO: 1, and the sequence of human mass1 can be found at SEQ ID NO: 3. Mammalian genes encoding a MASS1 protein are also provided. The invention also provides recombinant vectors comprising nucleic acid molecules that code for a MASS1 protein. These vectors can be plasmids. In certain embodiments, the vectors are prokaryotic or eukaryotic expression vectors. The nucleic acid coding for MASS1 can be linked to a heterologous promoter. The invention also relates to transgenic animals in which one or both alleles of the endogenous mass1 gene is mutated.
摘要翻译：本发明涉及与小鼠中的听觉发作相关的新基因。该基因被称为单因子感觉性发作敏感基因或质量1。 mass1基因的产物命名为MASS1。编码MASS1的核酸分子已被鉴定和纯化。鼠群1的序列可以在SEQ ID NO：1中找到，并且人质粒1的序列可以在SEQ ID NO：3中找到。还提供了编码MASS1蛋白的哺乳动物基因。本发明还提供了包含编码MASS1蛋白的核酸分子的重组载体。这些载体可以是质粒。在某些实施方案中，载体是原核或真核表达载体。编码MASS1的核酸可以与异源启动子连接。本发明还涉及转基因动物，其中内源mass1基因的一个或两个等位基因被突变。

10. 发明授权

US06583112B1 Gene products related to werner's syndrome 失效
标题翻译：与维纳综合征相关的基因产物
公开(公告)号：US06583112B1
公开(公告)日：2003-06-24
申请号：US09618166
申请日：2000-07-17
申请人： Ying-Hui Fu , Chang-En Yu , Junko Oshima , John T. Mulligan , Gerard D. Schellenberg
发明人： Ying-Hui Fu , Chang-En Yu , Junko Oshima , John T. Mulligan , Gerard D. Schellenberg
IPC分类号： C07K1400
CPC分类号： C07K14/47 , A01K2217/05 , C12N9/90 , C12N2799/021
摘要： The present invention discloses nucleic acid molecules encoding WRN gene products, expression vectors and host cells suitable for expressing such products.
摘要翻译：本发明公开了编码WRN基因产物，表达载体和适于表达这些产物的宿主细胞的核酸分子。

你已经成功收藏专利！

检索式保存成功!

IPRDB

热门服务

关于我们

友情链接

联系方式