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公开(公告)号:US08067389B2
公开(公告)日:2011-11-29
申请号:US12505911
申请日:2009-07-20
CPC分类号: C12N15/1138 , C12N2310/14
摘要: The present application is directed to siRNA-based silencing of the type II receptor of TGFβ. siRNAs that target this receptor abrogate the receptor protein and transcript, TGFβ-mediated processes such as fibronectin assembly and cell migration also are inhibited and the molecules of the invention are efficacious in reducing the inflammatory response and matrix deposition. These findings show that siRNAs can be successfully delivered both in vitro and in vivo to regulate the TGFβ type II receptor level and modulate wound response. Methods and compositions exploiting the findings of the present invention have a wide-ranging application, extending from treatment of disorders of the eye to other organs and tissues throughout the body.
摘要翻译: 本申请涉及TGF-bgr的II型受体的基于siRNA的沉默。 靶向该受体的siRNA消除受体蛋白和转录物,TGFβb介导的过程如纤连蛋白装配和细胞迁移也受到抑制,本发明的分子有效降低炎症反应和基质沉积。 这些研究结果表明,siRNA可以在体外和体内成功传递,以调节TGF-bgr; II型受体水平和调节伤口反应。 利用本发明的发现的方法和组合物具有广泛的应用,从眼睛疾病的治疗延伸到整个身体的其他器官和组织。
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公开(公告)号:US07662924B2
公开(公告)日:2010-02-16
申请号:US11267986
申请日:2005-11-07
申请人: Oscar Colamonici , Shahid Siddiqui
发明人: Oscar Colamonici , Shahid Siddiqui
CPC分类号: C07K16/30 , C07K14/4747 , G01N33/5011 , G01N2510/00
摘要: The present invention provides β-subunit-Associated Regulator of Apoptosis, or BARA, polypeptides and nucleic acid molecules encoding the same. The invention also provides selective binding agents, vectors, host cells, non-human transgenic animals, devices and methods for producing BARA polypeptides. The invention further provides compositions comprising BARA nucleic acids, polypeptides, and fusions or derivatives thereof. The invention further provides methods for treating, preventing, or ameliorating a medical disease, condition, or disorder comprising administering BARA or BARA compositions, as well as methods of diagnosing a pathological condition related to BARA. Still further, the invention provides methods of modulating levels of BARA expression and methods of determining whether a compound stimulates or inhibits BARA polypeptide activity or BARA polypeptide production.
摘要翻译: 本发明提供了β亚单位相关的细胞凋亡调控因子或BARA多肽和编码该调控因子的核酸分子。 本发明还提供选择性结合剂,载体,宿主细胞,非人转基因动物,用于产生BARA多肽的装置和方法。 本发明还提供了包含BARA核酸,多肽及其融合物或衍生物的组合物。 本发明还提供了治疗,预防或改善包括施用BARA或BARA组合物的医学疾病,病症或病症的方法,以及诊断与BARA相关的病理状况的方法。 此外,本发明提供了调节BARA表达水平的方法以及确定化合物是否刺激或抑制BARA多肽活性或BARA多肽生产的方法。
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公开(公告)号:US20090318537A1
公开(公告)日:2009-12-24
申请号:US12505911
申请日:2009-07-20
IPC分类号: A61K31/7105 , C07H21/02
CPC分类号: C12N15/1138 , C12N2310/14
摘要: The present application is directed to siRNA-based silencing of the type II receptor of TGFβ. siRNAs that target this receptor abrogate the receptor protein and transcript, TGFβ-mediated processes such as fibronectin assembly and cell migration also are inhibited and the molecules of the invention are efficacious in reducing the inflammatory response and matrix deposition. These findings show that siRNAs can be successfully delivered both in vitro and in vivo to regulate the TGFβ type II receptor level and modulate wound response. Methods and compositions exploiting the findings of the present invention have a wide-ranging application, extending from treatment of disorders of the eye to other organs and tissues throughout the body.
摘要翻译: 本申请涉及TGFbeta的II型受体的基于siRNA的沉默。 靶向该受体的siRNA消除受体蛋白和转录物,TGFβ介导的过程如纤连蛋白装配和细胞迁移也受到抑制,本发明的分子有效降低炎症反应和基质沉积。 这些研究结果表明siRNA可以在体外和体内成功递送,以调节TGFbeta II型受体水平并调节伤口应答。 利用本发明的发现的方法和组合物具有广泛的应用,从眼睛疾病的治疗延伸到整个身体的其他器官和组织。
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公开(公告)号:US07490000B2
公开(公告)日:2009-02-10
申请号:US11511560
申请日:2006-08-29
申请人: Shahid Siddiqui , Allen Duan , Vijay Garg , Joseph Stanek , Elaine Chen , Ramakrishna Raju , Steven Schondorf , Floyd Cadwell , George Dolan , Jeffrey Boismier
发明人: Shahid Siddiqui , Allen Duan , Vijay Garg , Joseph Stanek , Elaine Chen , Ramakrishna Raju , Steven Schondorf , Floyd Cadwell , George Dolan , Jeffrey Boismier
CPC分类号: B60W20/00 , B60K6/32 , B60K6/445 , B60L11/123 , B60L11/14 , B60L11/1881 , B60L15/2045 , B60W10/28 , B60W50/082 , Y02T10/52 , Y02T10/6217 , Y02T10/6239 , Y02T10/645 , Y02T10/7005 , Y02T10/7077 , Y02T10/7283 , Y02T10/84 , Y02T90/16 , Y02T90/34
摘要: An alternative fuel vehicle having a fuel economy control module with associated logic that allows the vehicle to operate in a fuel economy mode based on a desired fuel economy preference. The fuel economy control logic is in electrical communication with a vehicle system controller (VSC) and may be integrally formed as a sub-module within the VSC. A fuel economy control switch controlled by the fuel economy control logic toggles between an on and an off position to enable or disable a fuel economy mode. A fuel economy control selector allows a user to select a desired fuel economy mode preference once the fuel economy control switch is on. The fuel economy mode selected represents a predefined desired fuel economy preference such as a distance per amount of fuel consumed, or alternatively, a percentage of a balance between a fuel economy operation and a fuel performance operation.
摘要翻译: 具有燃料经济性控制模块的替代燃料车辆具有相关联的逻辑,其允许车辆基于期望的燃料经济性偏好以燃料经济模式运行。 燃料经济性控制逻辑与车辆系统控制器(VSC)电连通,并且可以一体地形成为VSC内的子模块。 由燃油经济性控制逻辑控制的燃料经济性控制开关在打开和关闭位置之间切换以启用或禁用燃料经济性模式。 燃油经济性控制选择器允许用户在燃料经济性控制开关打开时选择期望的燃料经济性模式偏好。 选择的燃料经济性模式表示预定的期望的燃料经济性偏好,例如每消耗的燃料量的距离,或者燃料经济性操作和燃料性能操作之间的平衡百分比。
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公开(公告)号:US20080059035A1
公开(公告)日:2008-03-06
申请号:US11511560
申请日:2006-08-29
申请人: Shahid Siddiqui , Zhihui Duan , Vijay Garg , Joseph Stanek , Elaine Chen , Ramakrishna Raju , Steven Schondorf , Floyd Cadwell , George Dolan , Jeffrey Boismier
发明人: Shahid Siddiqui , Zhihui Duan , Vijay Garg , Joseph Stanek , Elaine Chen , Ramakrishna Raju , Steven Schondorf , Floyd Cadwell , George Dolan , Jeffrey Boismier
CPC分类号: B60W20/00 , B60K6/32 , B60K6/445 , B60L11/123 , B60L11/14 , B60L11/1881 , B60L15/2045 , B60W10/28 , B60W50/082 , Y02T10/52 , Y02T10/6217 , Y02T10/6239 , Y02T10/645 , Y02T10/7005 , Y02T10/7077 , Y02T10/7283 , Y02T10/84 , Y02T90/16 , Y02T90/34
摘要: An alternative fuel vehicle having a fuel economy control module with associated logic that allows the vehicle to operate in a fuel economy mode based on a desired fuel economy preference. The fuel economy control logic is in electrical communication with a vehicle system controller (VSC) and may be integrally formed as a sub-module within the VSC. A fuel economy control switch controlled by the fuel economy control logic toggles between an on and an off position to enable or disable a fuel economy mode. A fuel economy control selector allows a user to select a desired fuel economy mode preference once the fuel economy control switch is on. The fuel economy mode selected represents a predefined desired fuel economy preference such as a distance per amount of fuel consumed, or alternatively, a percentage of a balance between a fuel economy operation and a fuel performance operation.
摘要翻译: 具有燃料经济性控制模块的替代燃料车辆具有相关联的逻辑,其允许车辆基于期望的燃料经济性偏好以燃料经济模式运行。 燃料经济性控制逻辑与车辆系统控制器(VSC)电连通,并且可以一体地形成为VSC内的子模块。 由燃油经济性控制逻辑控制的燃料经济性控制开关在打开和关闭位置之间切换以启用或禁用燃料经济性模式。 燃油经济性控制选择器允许用户在燃料经济性控制开关打开时选择期望的燃料经济性模式偏好。 选择的燃料经济性模式表示预定的期望的燃料经济性偏好,例如每消耗的燃料量的距离,或者燃料经济性操作和燃料性能操作之间的平衡百分比。
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公开(公告)号:US20060229266A1
公开(公告)日:2006-10-12
申请号:US10567958
申请日:2004-08-10
申请人: Nalin Kumar , Beatrice Yue , Shahid Siddiqui , Asrar Malik , Jose Pulido
发明人: Nalin Kumar , Beatrice Yue , Shahid Siddiqui , Asrar Malik , Jose Pulido
CPC分类号: C12N15/1138 , C12N2310/14
摘要: The present application is directed to siRNA-based silencing of the type II receptor of TGFβ. siRNAs that target this receptor abrogate the receptor protein and transcript, TGFβ-mediated processes such as fibronectin assembly and cell migration also are inhibited and the molecules of the invention are efficacious in reducing the inflammatory response and matrix deposition. These findings show that siRNAs can be successfully delivered both in vitro and in vivo to regulate the TGFβ type II receptor level and modulate wound response. Methods and compositions exploiting the findings of the present invention have a wide-ranging application, extending from treatment of disorders of the eye to other organs and tissues throughout the body.
摘要翻译: 本申请涉及TGFbeta的II型受体的基于siRNA的沉默。 靶向该受体的siRNA消除受体蛋白和转录物,TGFβ介导的过程如纤连蛋白装配和细胞迁移也受到抑制,本发明的分子有效降低炎症反应和基质沉积。 这些研究结果表明siRNA可以在体外和体内成功递送,以调节TGFbeta II型受体水平并调节伤口应答。 利用本发明的发现的方法和组合物具有广泛的应用,从眼睛疾病的治疗延伸到整个身体的其他器官和组织。
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公开(公告)号:US20060121505A1
公开(公告)日:2006-06-08
申请号:US11267986
申请日:2005-11-07
申请人: Oscar Colamonici , Shahid Siddiqui
发明人: Oscar Colamonici , Shahid Siddiqui
CPC分类号: C07K16/30 , C07K14/4747 , G01N33/5011 , G01N2510/00
摘要: The present invention provides β-subunit-Associated Regulator of Apoptosis, or BARA, polypeptides and nucleic acid molecules encoding the same. The invention also provides selective binding agents, vectors, host cells, non-human transgenic animals, devices and methods for producing BARA polypeptides. The invention further provides compositions comprising BARA nucleic acids, polypeptides, and fusions or derivatives thereof. The invention further provides methods for treating, preventing, or ameliorating a medical disease, condition, or disorder comprising administering BARA or BARA compositions, as well as methods of diagnosing a pathological condition related to BARA. Still further, the invention provides methods of modulating levels of BARA expression and methods of determining whether a compound stimulates or inhibits BARA polypeptide activity or BARA polypeptide production.
摘要翻译: 本发明提供了β亚单位相关的细胞凋亡调控因子或BARA多肽和编码该调控因子的核酸分子。 本发明还提供选择性结合剂,载体,宿主细胞,非人转基因动物,用于产生BARA多肽的装置和方法。 本发明还提供了包含BARA核酸,多肽及其融合物或衍生物的组合物。 本发明还提供了治疗,预防或改善包括施用BARA或BARA组合物的医学疾病,病症或病症的方法,以及诊断与BARA相关的病理状况的方法。 此外,本发明提供了调节BARA表达水平的方法以及确定化合物是否刺激或抑制BARA多肽活性或BARA多肽生产的方法。
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