Compositions and Methods for Treating Multiple Sclerosis
    1.
    发明申请
    Compositions and Methods for Treating Multiple Sclerosis 有权
    治疗多发性硬化的组合物和方法

    公开(公告)号:US20140378387A1

    公开(公告)日:2014-12-25

    申请号:US14370515

    申请日:2013-01-04

    Inventor: Fang Liu

    Abstract: Disclosed are polypeptides, compositions and methods for the treatment or prophylaxis of multiple sclerosis. The method involves the steps of administering a polypeptide, or nucleic acid encoding the polypeptide, comprising the GluR2 NTa1-3-2 (Y142-K172) amino acid sequence as shown by SEQ ID NO:1 or SEQ ID NO:5 to a subject in need of the treatment.

    Abstract translation: 公开了用于治疗或预防多发性硬化的多肽,组合物和方法。 该方法包括将如SEQ ID NO:1或SEQ ID NO:5所示的GluR2 NTa1-3-2(Y142-K172)氨基酸序列的多肽或编码该多肽的核酸给予受试者的步骤 需要治疗。

    Compositions and methods for treating multiple sclerosis
    4.
    发明授权
    Compositions and methods for treating multiple sclerosis 有权
    用于治疗多发性硬化的组合物和方法

    公开(公告)号:US09518104B2

    公开(公告)日:2016-12-13

    申请号:US14370515

    申请日:2013-01-04

    Inventor: Fang Liu

    Abstract: Disclosed are polypeptides, compositions and methods for the treatment or prophylaxis of multiple sclerosis. The method involves the steps of administering a polypeptide, or nucleic acid encoding the polypeptide, comprising the GluR2 NTal-3-2 (Y142-K172) amino acid sequence as shown by SEQ ID NO:1 or SEQ ID NO:5 to a subject in need of the treatment.

    Abstract translation: 公开了用于治疗或预防多发性硬化的多肽,组合物和方法。 该方法包括以下步骤:将如SEQ ID NO:1或SEQ ID NO:5所示的包含GluR2 NTal-3-2(Y142-K172)氨基酸序列的多肽或编码该多肽的核酸给予受试者 需要治疗。

    Polypeptides and Methods For Modulating D1-D2 Dopamine Receptor Interaction and Function
    5.
    发明申请
    Polypeptides and Methods For Modulating D1-D2 Dopamine Receptor Interaction and Function 审中-公开
    多肽和调节D1-D2多巴胺受体相互作用和功能的方法

    公开(公告)号:US20160237138A1

    公开(公告)日:2016-08-18

    申请号:US14996354

    申请日:2016-01-15

    Inventor: Fang Liu Lin Pei

    Abstract: The present invention provides for prevention and/or treatment of neurological or neuropsychiatric disorders involving abnormal D1-D2 dopamine receptor coupling and/or activation. Methods and agents are provided for modulating dopamine receptor function arising from D1-D2 coupling and/or activation. Agents of the present invention include fragments of D2 receptor or D1 receptor that can disrupt D1-D2 coupling.

    Abstract translation: 本发明提供预防和/或治疗涉及D1-D2多巴胺受体偶联和/或活化异常的神经或神经精神障碍。 提供了用于调节由D1-D2偶联和/或激活产生的多巴胺受体功能的方法和试剂。 本发明的药剂包括可以破坏D1-D2偶联的D2受体或D1受体的片段。

    Methods for modulating D1-D2 dopamine receptor coupling and function
    6.
    发明授权
    Methods for modulating D1-D2 dopamine receptor coupling and function 有权
    调节D1-D2多巴胺受体偶联和功能的方法

    公开(公告)号:US09266954B2

    公开(公告)日:2016-02-23

    申请号:US13862010

    申请日:2013-04-12

    Inventor: Fang Liu Lin Pei

    Abstract: The present invention provides for prevention and/or treatment of neurological or neuropsychiatric disorders involving abnormal D1-D2 dopamine receptor coupling and/or activation. Methods and agents are provided for modulating dopamine receptor function arising from D1-D2 coupling and/or activation. Agents of the present invention include fragments of D2 receptor or D1 receptor that can disrupt D1-D2 coupling.

    Abstract translation: 本发明提供预防和/或治疗涉及D1-D2多巴胺受体偶联和/或活化异常的神经或神经精神障碍。 提供了用于调节由D1-D2偶联和/或激活产生的多巴胺受体功能的方法和试剂。 本发明的药剂包括可以破坏D1-D2偶联的D2受体或D1受体的片段。

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