HUMAN DIACYLGLYCEROL ACYLTRANSFERASE 2 (DGAT2) FAMILY MEMBERS AND USES THEREFOR
    41.
    发明申请
    HUMAN DIACYLGLYCEROL ACYLTRANSFERASE 2 (DGAT2) FAMILY MEMBERS AND USES THEREFOR 审中-公开
    人类胆固醇ACYLTRANSFERASE 2(DGAT2)家族成员及其用途

    公开(公告)号:US20070166748A1

    公开(公告)日:2007-07-19

    申请号:US11684365

    申请日:2007-03-09

    摘要: The present invention relates to compositions and methods for the diagnosis and treatment of obesity and related metabolic disorders. The invention provides isolated nucleic acids molecules, designated DGAT2 family member nucleic acid molecules, which encode diacylglycerol acyltransferase family members. The invention also provides recombinant expression vectors containing DGAT2 family member nucleic acid molecules, host cells into which the expression vectors have been introduced, and nonhuman transgenic animals in which a DGAT2 family member gene has been introduced or disrupted. The invention still further provides isolated DGAT2 family member proteins, fusion proteins, antigenic peptides and anti-DGAT2 family member antibodies. Methods of use of the provided DGAT2 family member compositions for screening, diagnostic and therapeutic methods in connection, with obesity disorders are also disclosed.

    摘要翻译: 本发明涉及用于诊断和治疗肥胖症及相关代谢紊乱的组合物和方法。 本发明提供编码二酰基甘油酰基转移酶家族成员的分离的核酸分子,称为DGAT2家族成员核酸分子。 本发明还提供了含有DGAT2家族成员核酸分子的重组表达载体,已引入表达载体的宿主细胞,以及导入或破坏了DGAT2家族成员基因的非人类转基因动物。 本发明还进一步提供分离的DGAT2家族成员蛋白,融合蛋白,抗原肽和抗DGAT2家族成员抗体。 还公开了所提供的DGAT2家族成员组合物用于与肥胖症有关的筛选,诊断和治疗方法的方法。

    2786, a novel human aminopeptidase
    43.
    发明授权
    2786, a novel human aminopeptidase 失效
    2786,一种新型人氨基肽酶

    公开(公告)号:US07235634B2

    公开(公告)日:2007-06-26

    申请号:US10767308

    申请日:2004-01-29

    IPC分类号: C07K14/00

    CPC分类号: C12N9/48

    摘要: The present invention relates to a newly identified human aminopeptidase. The invention also relates to polynucleotides encoding the aminopeptidase. The invention further relates to methods using the aminopeptidase polypeptides and polynucleotides as a target for diagnosis and treatment in aminopeptidase-related disorders. The invention further relates to drug-screening methods using the aminopeptidase polypeptides and polynucleotides to identify agonists and antagonists for diagnosis and treatment. The invention further encompasses agonists and antagonists based on the aminopeptidase polypeptides and polynucleotides. The invention further relates to procedures for producing the aminopeptidase polypeptides and polynucleotides.

    摘要翻译: 本发明涉及新鉴定的人类氨基肽酶。 本发明还涉及编码氨基肽酶的多核苷酸。 本发明还涉及使用氨基肽酶多肽和多核苷酸作为在氨基肽酶相关疾病中进行诊断和治疗的靶标的方法。 本发明还涉及使用氨基肽酶多肽和多核苷酸鉴定用于诊断和治疗的激动剂和拮抗剂的药物筛选方法。 本发明还包括基于氨基肽酶多肽和多核苷酸的激动剂和拮抗剂。 本发明还涉及生产氨基肽酶多肽和多核苷酸的方法。

    Human protein kinase, phosphatase, and protease family members and uses thereof
    44.
    发明授权
    Human protein kinase, phosphatase, and protease family members and uses thereof 失效
    人蛋白激酶,磷酸酶和蛋白酶家族成员及其用途

    公开(公告)号:US07070947B2

    公开(公告)日:2006-07-04

    申请号:US10170789

    申请日:2002-06-13

    摘要: The invention provides isolated nucleic acids molecules, designated 2504, 15977, 14760, 53070, 15985, 50365, 26583, 21953, m32404, 14089, and 23436 nucleic acid molecules, which encode novel human protein kinase family members, serine/threonine protein kinase family members, hexokinase family members, serine/threonine phosphatase family members, prolyl oligopeptidase family members, trypsin family members, trypsin serine protease family members, and ubiquitin protease family members. The invention also provides antisense nucleic acid molecules, recombinant expression vectors containing 2504, 15977, 14760, 53070, 15985, 50365, 26583, 21953, m32404, 14089, or 23436 nucleic acid molecules, host cells into which the expression vectors have been introduced, and nonhuman transgenic animals in which a 2504, 15977, 14760, 53070, 15985, 50365, 26583, 21953, m32404, 14089, or 23436 gene has been introduced or disrupted. The invention still further provides isolated 2504, 15977, 14760, 53070, 15985, 50365, 26583, 21953, m32404, 14089, or 23436 proteins, fusion proteins, antigenic peptides and anti-2504, 15977, 14760, 53070, 15985, 50365, 26583, 21953, m32404, 14089, or 23436 antibodies. Diagnostic methods utilizing compositions of the invention are also provided.

    摘要翻译: 本发明提供编码新的人蛋白激酶家族成员,丝氨酸/苏氨酸蛋白激酶家族的分离的核酸分子,命名为2504,15977,14760,53070,15985,5042,56583,21953,m32404,14089和23436核酸分子 成员,己糖激酶家族成员,丝氨酸/苏氨酸磷酸酶家族成员,脯氨酰寡肽酶家族成员,胰蛋白酶家族成员,胰蛋白酶丝氨酸蛋白酶家族成员和泛素蛋白酶家族成员。 本发明还提供了反义核酸分子,含有2504,15977,14760,53070,15985,5042,26583,21953,m32404,14089或23436核酸分子的重组表达载体,已经引入表达载体的宿主细胞, 和非人类转基因动物,其中引入或破坏了2504,15977,14760,53070,15985,550365,26583,21953,m32404,14089或23436基因。 本发明还进一步提供分离的2504,15977,14760,53070,15985,5038,26583,21953,m32404,14089或23436蛋白,融合蛋白,抗原肽和抗2504,15977,14760,53070,15985,50365, 26583,21953,m32404,14089或23436抗体。 还提供了利用本发明组合物的诊断方法。

    ACTR-1 a novel human acyltransferase and uses thereof
    45.
    发明授权
    ACTR-1 a novel human acyltransferase and uses thereof 有权
    ACTR-1是一种新的人类酰基转移酶及其用途

    公开(公告)号:US07052888B2

    公开(公告)日:2006-05-30

    申请号:US09935290

    申请日:2001-08-21

    IPC分类号: C12N9/10 C07H21/04

    摘要: The invention provides isolated nucleic acid molecules, designated ACTR-1 nucleic acid molecules, which encode novel acyltransferase family members. The invention also provides antisense nucleic acid molecules, recombinant expression vectors containing ACTR-1 nucleic acid molecules, host cells into which the expression vectors have been introduced, and nonhuman transgenic animals in which an ACTR-1 gene has been introduced or disrupted. The invention still further provides isolated ACTR-1 proteins, fusion proteins, antigenic peptides and anti-ACTR-1 antibodies. Diagnostic methods utilizing compositions of the invention are also provided.

    摘要翻译: 本发明提供编码新的酰基转移酶家族成员的分离的核酸分子,命名为ACTR-1核酸分子。 本发明还提供了反义核酸分子,含有ACTR-1核酸分子的重组表达载体,其中引入了表达载体的宿主细胞和其中引入或破坏了ACTR-1基因的非人类转基因动物。 本发明还进一步提供了分离的ACTR-1蛋白,融合蛋白,抗原肽和抗ACTR-1抗体。 还提供了利用本发明组合物的诊断方法。

    47174, a novel human glycosyltransferase and uses thereof
    46.
    发明授权
    47174, a novel human glycosyltransferase and uses thereof 失效
    47174,一种新的人类糖基转移酶及其用途

    公开(公告)号:US06703230B2

    公开(公告)日:2004-03-09

    申请号:US09973457

    申请日:2001-10-09

    IPC分类号: C12Q300

    摘要: The invention provides isolated nucleic acids molecules, designated 47174 nucleic acid molecules, which encode novel glycosyltransferase family members. The invention also provides antisense nucleic acid molecules, recombinant expression vectors containing 47174 nucleic acid molecules, host cells into which the expression vectors have been introduced, and nonhuman transgenic animals in which a 47174 gene has been introduced or disrupted. The invention still further provides isolated 47174 proteins, fusion proteins, antigenic peptides and anti-47174 antibodies. Diagnostic methods utilizing compositions of the invention are also provided. The invention also provides methods of modulating pain or pain related disorders utilizing the compositions of the invention. Accordingly, methods of treating, preventing and/or diagnosing neurological disorders are disclosed.

    摘要翻译: 本发明提供编码新的糖基转移酶家族成员的分离的核酸分子,命名为47174核酸分子。 本发明还提供了反义核酸分子,含有47174个核酸分子的重组表达载体,其中引入了表达载体的宿主细胞,以及47174基因导入或破坏的非人转基因动物。 本发明还进一步提供分离的47174蛋白,融合蛋白,抗原肽和抗-47174抗体。 还提供了利用本发明组合物的诊断方法。 本发明还提供利用本发明组合物调节疼痛或疼痛相关疾病的方法。 因此,公开了治疗,预防和/或诊断神经障碍的方法。

    21529, a novel adenylate cyclase
    47.
    发明授权

    公开(公告)号:US06607892B2

    公开(公告)日:2003-08-19

    申请号:US10121911

    申请日:2002-04-12

    IPC分类号: G01N3353

    CPC分类号: C12N9/88

    摘要: Novel adenylate cyclase polypeptides, proteins, and nucleic acid molecules are disclosed. In addition to isolated, full-length adenylate cyclase proteins, the invention further provides isolated adenylate cyclase fusion proteins, antigenic peptides, and anti-adenylate cyclase antibodies. The invention also provides adenylate cyclase nucleic acid molecules, recombinant expression vectors containing a nucleic acid molecule of the invention, host cells into which the expression vectors have been introduced, and nonhuman transgenic animals in which an adenylate cyclase gene has been introduced or disrupted. Diagnostic, screening, and therapeutic methods utilizing compositions of the invention are also provided.

    Human aminopeptidase
    48.
    发明授权
    Human aminopeptidase 失效
    人类氨基肽酶

    公开(公告)号:US06444802B1

    公开(公告)日:2002-09-03

    申请号:US09409180

    申请日:1999-09-30

    IPC分类号: C07H2104

    摘要: The present invention relates to a newly identified human aminopeptidase. The invention also relates to polynucleotides encoding the aminopeptidase. The invention further relates to methods using the aminopeptidase polypeptides and polynucleotides as a target for diagnosis and treatment in aminopeptidase-related disorders. The invention further relates to drug-screening methods using the aminopeptidase polypeptides and polynucleotides to identify agonists and antagonists for diagnosis and treatment. The invention further encompasses agonists and antagonists based on the aminopeptidase polypeptides and polynucleotides. The invention further relates to procedures for producing the aminopeptidase polypeptides and polynucleotides.

    摘要翻译: 本发明涉及新鉴定的人类氨基肽酶。 本发明还涉及编码氨基肽酶的多核苷酸。 本发明还涉及使用氨基肽酶多肽和多核苷酸作为在氨基肽酶相关疾病中进行诊断和治疗的靶标的方法。 本发明还涉及使用氨基肽酶多肽和多核苷酸鉴定用于诊断和治疗的激动剂和拮抗剂的药物筛选方法。 本发明还包括基于氨基肽酶多肽和多核苷酸的激动剂和拮抗剂。 本发明还涉及生产氨基肽酶多肽和多核苷酸的方法。

    21529, a novel adenylate cyclase
    49.
    发明授权

    公开(公告)号:US06403358B1

    公开(公告)日:2002-06-11

    申请号:US09412210

    申请日:1999-10-05

    IPC分类号: C12N988

    CPC分类号: C12N9/88

    摘要: Novel adenylate cyclase polypeptides, proteins, and nucleic acid molecules are disclosed. In addition to isolated, full-length adenylate cyclase proteins, the invention further provides isolated adenylate cyclase fusion proteins, antigenic peptides, and anti-adenylate cyclase antibodies. The invention also provides adenylate cyclase nucleic acid molecules, recombinant expression vectors containing a nucleic acid molecule of the invention, host cells into which the expression vectors have been introduced, and nonhuman transgenic animals in which an adenylate cyclase gene has been introduced or disrupted. Diagnostic, screening, and therapeutic methods utilizing compositions of the invention are also provided.