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    Schizophrenia associated genes, proteins and biallelic markers
    2.
    发明授权
    Schizophrenia associated genes, proteins and biallelic markers 失效
    精神分裂症相关基因，蛋白质和双重标记物

    公开(公告)号：US06476208B1

    公开(公告)日：2002-11-05

    申请号：US09539333

    申请日：2000-03-30

    申请人： Daniel Cohen ,  Marta Blumenfeld ,  Ilya Chumakov ,  Lydie Bougueleret ,  Bernard Bihain ,  Laurent Essioux

    发明人： Daniel Cohen ,  Marta Blumenfeld ,  Ilya Chumakov ,  Lydie Bougueleret ,  Bernard Bihain ,  Laurent Essioux

    IPC分类号： C07M2102

    CPC分类号： C07K14/47 ,  A01K2217/075 ,  C12Q1/6883 ,  C12Q2600/156

    摘要： The invention concerns the human sbg1, g34665, sbg2, g35017 and g35018 genes, polynucleotides, polypeptides biallelic markers, and human chromosome 13q31-q33 biallelic markers. The invention also concerns the association established between schizophrenia and bipolar disorder and the biallelic markers and the sbg1, g34665, sbg2, g35017 and g35018 genes and nucleotide sequences. The invention provides means to identify compounds useful in the treatment of schizophrenia, bipolar disorder and related diseases, means to determine the predisposition of individuals to said disease as well as means for the disease diagnosis and prognosis.

    摘要翻译： 本发明涉及人sbg1，g34665，sbg2，g35017和g35018基因，多核苷酸，多肽双重标记和人染色体13q31-q33双重标记。 本发明还涉及精神分裂症和双相情感障碍与双重标记和sbg1，g34665，sbg2，g35017和g35018基因和核苷酸序列之间建立的关联。 本发明提供了鉴定用于治疗精神分裂症，双相性精神障碍和相关疾病的化合物的方法，用于确定个体对所述疾病的倾向以及疾病诊断和预后的手段。

    Schizophrenia associated gene, proteins and biallelic markers
    3.
    发明授权
    Schizophrenia associated gene, proteins and biallelic markers 失效
    精神分裂症相关基因，蛋白质和双重标记物

    公开(公告)号：US06555316B1

    公开(公告)日：2003-04-29

    申请号：US09679409

    申请日：2000-10-03

    申请人： Daniel Cohen ,  Marta Blumenfeld ,  Ilya Chumakov ,  Lydie Bougueleret ,  Laurent Essioux

    发明人： Daniel Cohen ,  Marta Blumenfeld ,  Ilya Chumakov ,  Lydie Bougueleret ,  Laurent Essioux

    IPC分类号： C12Q168

    CPC分类号： C12Q1/6883 ,  C07K14/47 ,  C07K16/18 ,  C12Q2600/156 ,  C12Q2600/172

    摘要： The invention concerns the human g35030 gene, polynucleotides, polypeptides biallelic markers, and human chromosome 13q31-q33 biallelic markers. The invention also concerns the association established between schizophrenia and bipolar disorder and the biallelic markers and the g35030 gene and nucleotide sequences. The invention provides means to identify compounds useful in the treatment of schizophrenia, bipolar disorder and related diseases, means to determine the predisposition of individuals to said disease as well as means for the disease diagnosis and prognosis.

    摘要翻译： 本发明涉及人g35030基因，多核苷酸，多肽双向标记和人染色体13q31-q33双重标记。 本发明还涉及精神分裂症和双相障碍与双重标记和g35030基因和核苷酸序列之间的关联。 本发明提供了鉴定用于治疗精神分裂症，双相性精神障碍和相关疾病的化合物的方法，用于确定个体对所述疾病的易感性以及疾病诊断和预后的手段。

    Prostate cancer gene
    6.
    发明授权
    Prostate cancer gene 失效
    前列腺癌基因

    公开(公告)号：US06265546B1

    公开(公告)日：2001-07-24

    申请号：US09338907

    申请日：1999-06-23

    申请人： Daniel Cohen ,  Marta Blumenfeld ,  Ilya Chumakov ,  Lydie Bougueleret

    发明人： Daniel Cohen ,  Marta Blumenfeld ,  Ilya Chumakov ,  Lydie Bougueleret

    IPC分类号： C07K100

    CPC分类号： C12N9/6445 ,  A01K2217/05 ,  A61K38/00 ,  C07K14/47 ,  C12Q1/6827 ,  C12Q1/6886 ,  C12Q2600/106 ,  C12Q2600/136 ,  C12Q2600/156 ,  C12Q2600/172

    摘要： The present invention relates to PG1, a gene associated with prostate cancer. The invention provides polynucleotides including biallelic markers derived from PG1 and from flanking genomic regions. Primers hybridizing to these biallelic markers and regions flanking are also provided. This invention provides polynucleotides and methods suitable for genotyping a nucleic acid containing sample for one or more biallelic markers of the invention. Further, the invention provides methods to detect a statistical correlation between a biallelic marker allele and prostate cancer and between a haplotype and prostate cancer. The invention also relates to diagnostic methods of determining whether an individual is at risk for developing prostate cancer, and whether an individual suffers from prostate cancer as a result of a mutation in the PG1 gene.

    摘要翻译： 本发明涉及与前列腺癌相关的基因PG1。 本发明提供了多核苷酸，其包括衍生自PG1和来自侧翼基因组区域的双重标记。 还提供了与这些双重标记和侧翼区域杂交的引物。 本发明提供了适用于对本发明的一种或多种双重标记的含有核酸的样品进行基因分型的多核苷酸和方法。 此外，本发明提供了检测双重标记等位基因与前列腺癌之间以及单倍型与前列腺癌之间的统计学相关性的方法。 本发明还涉及确定个体是否处于发展中的前列腺癌风险的诊断方法以及PG1基因突变导致个体患有前列腺癌的诊断方法。

    Prostate cancer gene
    7.
    发明授权
    Prostate cancer gene 失效
    前列腺癌基因

    公开(公告)号：US07189833B2

    公开(公告)日：2007-03-13

    申请号：US09901484

    申请日：2001-07-09

    申请人： Daniel Cohen ,  Marta Blumenfeld ,  Ilya Chumakov ,  Lydie Bougueleret

    发明人： Daniel Cohen ,  Marta Blumenfeld ,  Ilya Chumakov ,  Lydie Bougueleret

    IPC分类号： C07H21/02

    CPC分类号： C12N9/6445 ,  A01K2217/05 ,  A61K38/00 ,  C07K14/47 ,  C12Q1/6827 ,  C12Q1/6886 ,  C12Q2600/136 ,  C12Q2600/156 ,  C12Q2600/172

    摘要： The present invention relates to PG1, a gene associated with prostate cancer. The invention provides polynucleotides including biallelic markers derived from PG1 and from flanking genomic regions. Primers hybridizing to these biallelic markers and regions flanking are also provided. This invention provides polynucleotides and methods suitable for genotyping a nucleic acid containing sample for one or more biallelic markers of the invention. Further, the invention provides methods to detect a statistical correlation between a biallelic marker allele and prostate cancer and between a haplotype and prostate cancer. The invention also relates to diagnostic methods of determining whether an individual is at risk for developing prostate cancer, and whether an individual suffers from prostate cancer as a result of a mutation in the PG1 gene.

    摘要翻译： 本发明涉及与前列腺癌相关的基因PG1。 本发明提供了多核苷酸，其包括衍生自PG1和来自侧翼基因组区域的双重标记。 还提供了与这些双重标记和侧翼区域杂交的引物。 本发明提供了适用于对本发明的一种或多种双重标记的含有核酸的样品进行基因分型的多核苷酸和方法。 此外，本发明提供了检测双重标记等位基因与前列腺癌之间以及单倍型与前列腺癌之间的统计学相关性的方法。 本发明还涉及确定个体是否处于发展中的前列腺癌风险的诊断方法以及PG1基因突变导致个体患有前列腺癌的诊断方法。

    Prostate cancer gene
    8.
    发明授权
    Prostate cancer gene 失效
    前列腺癌基因

    公开(公告)号：US06346381B1

    公开(公告)日：2002-02-12

    申请号：US09218207

    申请日：1998-12-22

    申请人： Daniel Cohen ,  Marta Blumenfeld ,  Ilya Chumakov ,  Lydie Bougueleret

    发明人： Daniel Cohen ,  Marta Blumenfeld ,  Ilya Chumakov ,  Lydie Bougueleret

    IPC分类号： C12Q168

    CPC分类号： C07K14/47 ,  A01K2217/05 ,  A61K38/00 ,  C12Q1/6827 ,  C12Q1/6886 ,  C12Q2600/136 ,  C12Q2600/172

    摘要： The present invention relates to PG1, a gene associated with prostate cancer. The invention provides polynucleotides including biallelic markers derived from PG1 and from flanking genomic regions. Primers hybridizing to these biallelic markers and regions flanking are also provided. This invention provides polynucleotides and methods suitable for genotyping a nucleic acid containing sample for one or more biallelic markers of the invention. Further, the invention provides methods to detect a statistical correlation between a biallelic marker allele and prostate cancer and between a haplotype and prostate cancer. The invention also relates to diagnostic methods of determining whether an individual is at risk for developing prostate cancer, and whether an individual suffers from prostate cancer as a result of a mutation in the PG1 gene.

    摘要翻译： 本发明涉及与前列腺癌相关的基因PG1。 本发明提供了多核苷酸，其包括衍生自PG1和来自侧翼基因组区域的双重标记。 还提供了与这些双重标记和侧翼区域杂交的引物。 本发明提供了适用于对本发明的一种或多种双重标记的含有核酸的样品进行基因分型的多核苷酸和方法。 此外，本发明提供了检测双重标记等位基因与前列腺癌之间以及单倍型与前列腺癌之间的统计学相关性的方法。 本发明还涉及确定个体是否处于发展中的前列腺癌风险的诊断方法以及PG1基因突变导致个体患有前列腺癌的诊断方法。

    Methods, software and apparati for identifying genomic regions harboring a gene associated with a detectable trait
    10.
    发明申请
    Methods, software and apparati for identifying genomic regions harboring a gene associated with a detectable trait 审中-公开
    方法，软件和装置，用于鉴定携带可检测性状相关基因的基因组区域

    公开(公告)号：US20050158788A1

    公开(公告)日：2005-07-21

    申请号：US11048148

    申请日：2005-02-01

    申请人： Nicholas Schork ,  Laurent Essioux ,  Annick Cohen-Akenine ,  Marta Blumenfeld ,  Daniel Cohen

    发明人： Nicholas Schork ,  Laurent Essioux ,  Annick Cohen-Akenine ,  Marta Blumenfeld ,  Daniel Cohen

    IPC分类号： G01N33/53 ,  C12N15/09 ,  C12Q1/68 ,  G01N33/566 ,  G06F17/30 ,  G06F19/18 ,  G06F19/22 ,  G06F19/24 ,  G06F19/00 ,  G01N33/48 ,  G01N33/50

    CPC分类号： C12Q1/6827 ,  G16B20/00 ,  G16B30/00 ,  G16B40/00

    摘要： The present invention relates to methods, software, and apparati for determining whether a genomic region harbors a gene associated with a detectable trait. In one embodiment, the present invention relates to a method of confirming that a genomic region harbors a gene associated with a detectable trait comprising the steps of identifying a candidate genomic region suspected of harboring the gene associated with the detectable trait, constructing a trait-associated distribution of association values using the biallelic markers in the candidate genomic region, identifying a plurality of biallelic markers in random genomic regions which are not suspected of harboring the gene associated with the detectable trait, constructing a random distribution of association values using the biallelic markers in the random genomic regions, comparing the trait-associated distribution of association values to the random distribution of association values, and determining whether the trait-associated distribution of association values and the random distribution of association values are significantly different from one another. In other embodiments, the present invention comprises software for performing the above method and devices comprising the software in a retrievable form.

    摘要翻译： 本发明涉及用于确定基因组区域是否包含与可检测特征相关的基因的方法，软件和装置。 在一个实施方案中，本发明涉及一种确认基因组区域包含与可检测性状相关的基因的方法，其包括以下步骤：鉴定疑似携带可检测性状相关基因的候选基因组区域，构建与性状相关 在候选基因组区域中使用双重标记的关联值的分布，鉴定不怀疑携带与可检测性状相关的基因的随机基因组区域中的多个双重标记，使用双重标记物建立关联值的随机分布 随机基因组区域，将关联值的性状相关分布与关联值的随机分布进行比较，以及确定关联值的性状相关分布和关联值的随机分布是否彼此显着不同。 在其他实施例中，本发明包括用于执行上述方法的软件和包括可检索形式的软件的装置。