首页> 外国专利> ADENOSINE A1 AND A3 RECEPTOR GENE SEQUENCE VARIATIONS FOR PREDICTING DISEASE OUTCOME AND TREATMENT OUTCOME

ADENOSINE A1 AND A3 RECEPTOR GENE SEQUENCE VARIATIONS FOR PREDICTING DISEASE OUTCOME AND TREATMENT OUTCOME

机译:腺苷A1和A3受体基因序列变异用于预测疾病结果和治疗结果

摘要

The present invention relates to methods for identify subjects for responsiveness to adenosine agonist treatment. Another aspect of the present invention relates to methods to predict a relative infarct size in response to ischemia reperfusion injury. In particular, the present invention relates to methods for to identify responsiveness to adenosine agonist treatment and/or relative infarct size by identifying a sequence differences such as mutations and/or polymorphisms in the human A1 adenosine receptor (A1-AR) gene that alters the stability of the A1-AR mRNA. Other aspect of the present invention relates to methods to identify responsiveness to adenosine agonist treatment and/or relative infarct size by identifying a sequence differences, such as mutations and/or polymorphisms in the human A3 adenosine receptor (A3-AR) gene that alters the A3-AR protein function. Other aspect of the present invention also relate to kits and assays to detect sequence differences in the human A1 adenosine receptor (A1-AR) gene and/or A3 adenosine receptor (A3-AR) gene.
机译:本发明涉及鉴定受试者对腺苷激动剂治疗的反应性的方法。本发明的另一方面涉及预测响应于缺血再灌注损伤的相对梗塞大小的方法。特别地,本发明涉及用于通过鉴定改变人A1腺苷受体(A1-AR)基因的序列差异例如突变和/或多态性来鉴定对腺苷激动剂治疗和/或相对梗塞大小的反应性的方法。 A1-AR mRNA的稳定性。本发明的另一方面涉及通过鉴定序列差异(例如改变人A3腺苷受体(A3-AR)基因中的突变和/或多态性)来鉴定​​对腺苷激动剂治疗的反应性和/或相对梗塞大小的方法。 A3-AR蛋白功能。本发明的另一方面还涉及试剂盒和测定法,以检测人A1腺苷受体(A1-AR)基因和/或A3腺苷受体(A3-AR)基因中的序列差异。

著录项

  • 公开/公告号US2010047798A1

    专利类型

  • 公开/公告日2010-02-25

    原文格式PDF

  • 申请/专利权人 ARTHUR M. FELDMAN;ZHONG TANG;

    申请/专利号US20070514031

  • 发明设计人 ARTHUR M. FELDMAN;ZHONG TANG;

    申请日2007-11-08

  • 分类号C12Q1/68;C07H21/04;C07K2/00;C07K16/00;G06F19/00;

  • 国家 US

  • 入库时间 2022-08-21 18:52:16

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