METHODS FOR THE REPAIR AND/OR REGENERATION OF DAMAGED MYOCARDIUM USING VARIANTS OF HEPATOCYTE GROWTH FACTOR
    3.
    发明申请
    METHODS FOR THE REPAIR AND/OR REGENERATION OF DAMAGED MYOCARDIUM USING VARIANTS OF HEPATOCYTE GROWTH FACTOR 审中-公开
    使用肝细胞生长因子变量修复和/或再生损伤的心肌细胞的方法

    公开(公告)号:WO2009062143A3

    公开(公告)日:2010-01-07

    申请号:PCT/US2008082967

    申请日:2008-11-10

    发明人: ANVERSA PIERO

    摘要: Methods for repairing damaged myocardium and/or myocardial cells including the administration of variants of hepatocyte growth factor or activated cardiac stem cells are disclosed and claimed. In addition, methods for forming coronary vasculature including the administration of variants of hepatocyte growth factor or activated cardiac stem cells are described. In particular, administration of variants of hepatocyte growth factor, such as NK1, 1K1, and HP11, are useful for the repair and/or regeneration of damaged myocardium or formation of coronary vasculature. Methods of activating cardiac stem cells in vitro are also disclosed.

    摘要翻译: 公开并要求保护用于修复损伤的心肌和/或心肌细胞的方法,包括给予肝细胞生长因子或活化的心脏干细胞的变体。 此外,描述了形成冠状动脉脉管系统的方法,包括给予肝细胞生长因子或活化的心脏干细胞的变体。 特别地,肝细胞生长因子(例如NK1,1K1和HP11)的变体的施用可用于损伤心肌的修复和/或再生或冠状动脉脉管系统的形成。 还公开了体外激活心脏干细胞的方法。

    METHODS AND COMPOSITIONS FOR THE REPAIR AND/OR REGENERATION OF DAMAGED MYOCARDIUM USING CYTOKINES AND VARIANTS THEREOF
    4.
    发明申请
    METHODS AND COMPOSITIONS FOR THE REPAIR AND/OR REGENERATION OF DAMAGED MYOCARDIUM USING CYTOKINES AND VARIANTS THEREOF 审中-公开
    使用细胞因子及其变体修复和/或再生损伤的心肌细胞的方法和组合物

    公开(公告)号:WO2009062143A2

    公开(公告)日:2009-05-14

    申请号:PCT/US2008/082967

    申请日:2008-11-10

    发明人: ANVERSA, Piero

    摘要: Methods, compositions, and kits for repairing damaged myocardium and/or myocardial cells including the administration of cytokines, variants of cytokines, cardiac stem cells, or combinations thereof are disclosed and claimed. In addition, methods, compositions, and kits for forming coronary vasculature including the administration of cytokines, variants of cytokines, cardiac stem cells, or combinations thereof are described. In particular, administration of variants of hepatocyte growth factor, such as NK1, 1K1, and HP11, are useful for the repair and/or regeneration of damaged myocardium or formation of coronary vasculature. Methods of activating cardiac stem cells in vitro are also disclosed.

    摘要翻译: 公开和要求保护用于修复损伤的心肌和/或心肌细胞的方法,组合物和试剂盒,包括细胞因子的施用,细胞因子的变体,心脏干细胞或其组合。 此外,描述了用于形成冠状动脉脉管系统的方法,组合物和试剂盒,包括细胞因子的施用,细胞因子的变体,心脏干细胞或其组合。 特别地,肝细胞生长因子(例如NK1,1K1和HP11)的变体的施用可用于损伤心肌的修复和/或再生或冠状动脉脉管系统的形成。 还公开了体外激活心脏干细胞的方法。

    SMOOTH MUSCLE RELAXATION
    6.
    发明申请
    SMOOTH MUSCLE RELAXATION 审中-公开
    平滑肌肉放松

    公开(公告)号:WO2007126653A3

    公开(公告)日:2008-10-23

    申请号:PCT/US2007007008

    申请日:2007-03-21

    发明人: WOLIN MICHAEL

    IPC分类号: A61K38/16 A61K31/195

    CPC分类号: A61K31/195

    摘要: The invention relates to methods of inducing smooth muscle relaxation, for example, a method of inducing relaxation of a vascular or a non-vascular muscle or a method of inducing relaxation of the microvasculature, in a subject in need thereof by promoting the accumulation of protoporphyrin IX in the smooth muscle.

    摘要翻译: 本发明涉及通过促进原卟啉的积累来诱导平滑肌松弛的方法,例如诱导血管或非血管肌松弛的方法或诱导微血管松弛的方法 IX在平滑​​肌中。

    PURINES ARE SELF-RENEWAL SIGNALS FOR NEURAL STEM CELLS, AND PURINE RECEPTOR ANTAGONISTS PROMOTE NEURONAL AND GLIAL DIFFERENTIATION THEREFROM
    7.
    发明申请
    PURINES ARE SELF-RENEWAL SIGNALS FOR NEURAL STEM CELLS, AND PURINE RECEPTOR ANTAGONISTS PROMOTE NEURONAL AND GLIAL DIFFERENTIATION THEREFROM 审中-公开
    产品是神经干细胞的自我更新信号,以及嘌呤受体拮抗剂促进神经元和神经元的分化

    公开(公告)号:WO2005079250A3

    公开(公告)日:2008-06-19

    申请号:PCT/US2005004017

    申请日:2005-02-10

    摘要: The present invention relates to a method of inhibiting differentiation of a population of neural stem cells by contacting a purinergic receptor agonist and a population of neural stem cells under conditions effective to inhibit differentiation of the population of neural stem cells. Another aspect of the present invention relates to a method of producing neurons and/or glial cells from a population of neural stem cells by culturing a population of neural stem cells with a purinergic receptor antagonist under conditions effective to cause the neural stem cells to differentiate into neurons and/or glial cells. The purinergic receptor agonist can also be used in a method of inducing proliferation and self-renewal of neural stem cells in a subject and a method of treating a neurological disease or neurodegenerative condition in a subject. The purinergic receptor antagonist can also be used in treating a neoplastic disease of the brain or spinal cord in a subject.

    摘要翻译: 本发明涉及通过在有效抑制神经干细胞群分化的条件下使嘌呤能受体激动剂和神经干细胞群接触来抑制神经干细胞群体的分化的方法。 本发明的另一方面涉及通过在有效地使神经干细胞分化成为的神经干细胞的条件下用嘌呤能受体拮抗剂培养一群神经干细胞来从神经干细胞群体产生神经元和/或神经胶质细胞的方法 神经元和/或神经胶质细胞。 嘌呤能受体激动剂也可以用于诱导受试者神经干细胞的增殖和自我更新的方法以及治疗受试者的神经疾病或神经变性病症的方法。 嘌呤能受体拮抗剂也可用于治疗受试者中脑或脊髓的肿瘤性疾病。

    PURINE RECEPTOR INHIBITION AS A THERAPEUTIC STRATEGY IN SPINAL CORD AND BRAIN
    9.
    发明申请
    PURINE RECEPTOR INHIBITION AS A THERAPEUTIC STRATEGY IN SPINAL CORD AND BRAIN 审中-公开
    嘌呤受体抑制作为脊髓和脑的治疗策略

    公开(公告)号:WO2005041892A3

    公开(公告)日:2005-08-11

    申请号:PCT/US2004036355

    申请日:2004-11-02

    CPC分类号: A61K31/33 A61K31/47

    摘要: The present invention is directed to a method of treating a subject with acute spinal cord injury by administering a purine receptor antagonist to the subject under conditions effective to treat spinal cord injury. The purine receptor antagonist inhibits P2X purine receptor activation. The inhibition of P2X purine receptor activation can also be used in conjunction with methods of treating a subject with spinal cord ischemia resulting from stroke or vascular insult, interruption, or mechanical injury, treating a subject with ischemic or traumatic insults of brain tissue in regions expressing P2X receptors, and for inhibiting ATP-triggered brain or spinal cord cell death.

    摘要翻译: 本发明涉及通过在有效治疗脊髓损伤的条件下向受试者施用嘌呤受体拮抗剂来治疗患有急性脊髓损伤的受试者的方法。 嘌呤受体拮抗剂抑制P2X嘌呤受体激活。 P2X嘌呤受体激活的抑制还可以与治疗患有中风或血管损伤,中断或机械损伤引起的脊髓缺血的受试者的方法联合使用,治疗患有缺血性或创伤性脑组织缺血性或创伤性损伤的受试者 P2X受体,并用于抑制ATP引发的脑或脊髓细胞死亡。

    PURINE RECEPTOR INHIBITION AS A THERAPEUTIC STRATEGY IN SPINAL CORD AND BRAIN
    10.
    发明申请
    PURINE RECEPTOR INHIBITION AS A THERAPEUTIC STRATEGY IN SPINAL CORD AND BRAIN 审中-公开
    嘌呤受体抑制作为脊髓和脑中的治疗策略

    公开(公告)号:WO2005041892A2

    公开(公告)日:2005-05-12

    申请号:PCT/US2004/036355

    申请日:2004-11-02

    IPC分类号: A61K

    CPC分类号: A61K31/33 A61K31/47

    摘要: The present invention is directed to a method of treating a subject with acute spinal cord injury by administering a purine receptor antagonist to the subject under conditions effective to treat spinal cord injury. The purine receptor antagonist inhibits P2X purine receptor activation. The inhibition of P2X purine receptor activation can also be used in conjunction with methods of treating a subject with spinal cord ischemia resulting from stroke or vascular insult, interruption, or mechanical injury, treating a subject with ischemic or traumatic insults of brain tissue in regions expressing P2X receptors, and for inhibiting ATP-triggered brain or spinal cord cell death.

    摘要翻译: 本发明涉及通过在有效治疗脊髓损伤的条件下向受试者施用嘌呤受体拮抗剂来治疗患有急性脊髓损伤的受试者的方法。 嘌呤受体拮抗剂抑制P2X嘌呤受体活化。 P2X嘌呤受体活化的抑制也可以与由中风或血管损伤,中断或机械损伤引起的脊髓缺血治疗受试者的方法一起使用,在表达的区域中治疗脑组织的缺血性或创伤性损伤的受试者 P2X受体,并用于抑制ATP触发的脑或脊髓细胞死亡。