Screening for the Genetic Defect Causing Tibial Hemimelia in Bovines
    1.
    发明申请
    Screening for the Genetic Defect Causing Tibial Hemimelia in Bovines 失效
    筛选引起胫骨半纤维的遗传缺陷

    公开(公告)号:US20090239212A1

    公开(公告)日:2009-09-24

    申请号:US11549888

    申请日:2006-10-16

    IPC分类号: C12Q1/68

    摘要: The invention provides methods, materials and kits for analyzing DNA samples from bovine to determine whether the animal is a recessive carrier of a genetic mutation that is associated with tibial hemimelia. DNA-containing samples are analyzed by genetic testing to determine whether or not a deletion mutation is present in one of the alleles that encodes Aristaless-like4 (ALX4) protein, wherein the deletion mutation is associated with tibial hemimelia.

    摘要翻译: 本发明提供用于分析来自牛的DNA样品的方法,材料和试剂盒,以确定动物是否是与胫骨半纤维相关的遗传突变的隐性载体。 通过遗传测试分析含DNA的样品,以确定编码无亚型4(ALX4)蛋白的等位基因之一中是否存在缺失突变,其中缺失突变与胫骨半纤维相关。

    Screening for Arthrogryposis Multiplex in Bovines
    2.
    发明申请
    Screening for Arthrogryposis Multiplex in Bovines 失效
    筛查牛肉中的关节炎综合征

    公开(公告)号:US20110151440A1

    公开(公告)日:2011-06-23

    申请号:US12642028

    申请日:2009-12-18

    IPC分类号: C12Q1/68 C07H21/04

    CPC分类号: C12Q1/6883 C12Q2600/124

    摘要: Provided are methods, materials and kits for analyzing DNA samples from bovine to determine whether the animal is a recessive carrier of a genetic mutation that is associated with arthrogryposis multiplex (AM). DNA-containing samples are analyzed by genetic testing to determine whether or not a deletion mutation is present in one of the alleles that are responsible for the AM genetic mutation. In an aspect the deletion encompasses the entirety of the ISG15 ubiquitin-like modifier (ISG15) gene. In an aspect the deletion further encompasses one or both of the 5′ regulatory region of the hairy and enhancer split 4 (HES4) and of the agrin (AGRN) gene and of the first two exons of the AGRN gene.

    摘要翻译: 提供了用于分析来自牛的DNA样品的方法,材料和试剂盒,以确定动物是否是与关节病综合征(AM)相关的遗传突变的隐性载体。 通过遗传测试分析含DNA样品,以确定在负责AM基因突变的一个等位基因中是否存在缺失突变。 在一方面,缺失包括整个ISG15泛素样修饰(ISG15)基因。 在一方面,缺失进一步包括毛发和增强子分裂4(HES4)和集聚蛋白(AGRN)基因的5'调节区和AGRN基因的前两个外显子中的一个或两个。

    Screening for arthrogryposis multiplex in bovines
    3.
    发明授权
    Screening for arthrogryposis multiplex in bovines 失效
    在牛中筛查关节痛综合征

    公开(公告)号:US08431346B2

    公开(公告)日:2013-04-30

    申请号:US12642028

    申请日:2009-12-18

    IPC分类号: C12Q1/68 C12P19/34

    CPC分类号: C12Q1/6883 C12Q2600/124

    摘要: Provided are methods, materials and kits for analyzing DNA samples from bovine to determine whether the animal is a recessive carrier of a genetic mutation that is associated with arthrogryposis multiplex (AM). DNA-containing samples are analyzed by genetic testing to determine whether or not a deletion mutation is present in one of the alleles that are responsible for the AM genetic mutation. In an aspect the deletion encompasses the entirety of the ISG15 ubiquitin-like modifier (ISG15) gene. In an aspect the deletion further encompasses one or both of the 5′ regulatory region of the hairy and enhancer split 4 (HES4) and of the agrin (AGRN) gene and of the first two exons of the AGRN gene.

    摘要翻译: 提供了用于分析来自牛的DNA样品的方法,材料和试剂盒,以确定动物是否是与关节病综合征(AM)相关的遗传突变的隐性载体。 通过遗传测试分析含DNA样品,以确定在负责AM基因突变的一个等位基因中是否存在缺失突变。 在一方面,缺失包括整个ISG15泛素样修饰(ISG15)基因。 在一方面,缺失进一步包括毛发和增强子分裂4(HES4)和集聚蛋白(AGRN)基因的5'调节区和AGRN基因的前两个外显子中的一个或两个。

    Screening for the genetic defect causing tibial hemimelia in bovines
    4.
    发明授权
    Screening for the genetic defect causing tibial hemimelia in bovines 失效
    筛选引起胫骨hemimelia的遗传缺陷

    公开(公告)号:US08158356B2

    公开(公告)日:2012-04-17

    申请号:US11549888

    申请日:2006-10-16

    IPC分类号: C12Q1/68

    摘要: The invention provides methods, materials and kits for analyzing DNA samples from bovine to determine whether the animal is a recessive carrier of a genetic mutation that is associated with tibial hemimelia. DNA-containing samples are analyzed by genetic testing to determine whether or not a deletion mutation is present in one of the alleles that encodes Aristaless-like4 (ALX4) protein, wherein the deletion mutation is associated with tibial hemimelia.

    摘要翻译: 本发明提供用于分析来自牛的DNA样品的方法,材料和试剂盒,以确定动物是否是与胫骨半纤维相关的遗传突变的隐性载体。 通过遗传测试分析含DNA的样品,以确定编码无亚型4(ALX4)蛋白的等位基因之一中是否存在缺失突变,其中缺失突变与胫骨半纤维相关。