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    • 4. 发明申请
    • ISOLATED POLYNUCLEOTIDES AND NUCLEIC ACID CONSTRUCTS FOR DIRECTING EXPRESSION OF A GENE-OF-INTEREST IN CELLS
    • 用于指导细胞中基因表达的分离的多核苷酸和核酸构建体
    • WO2012052878A1
    • 2012-04-26
    • PCT/IB2011/054493
    • 2011-10-12
    • VASCULAR BIOGENICS LTD.FEIGE, ErezGERSHGOREN, TalBANGIO, LivnatBREITBART, Eyal
    • FEIGE, ErezGERSHGOREN, TalBANGIO, LivnatBREITBART, Eyal
    • C07K14/575
    • C07K14/57536C07K2319/00C07K2319/02
    • Isolated polynucleotides comprising at least 14 nucleotides of SEQ ID NO:6 of a pre-proendothelin promoter which comprise at least 2 consecutive sequences being positioned next to at least one nucleotide position selected from the group consisting of at least one nucleotide of SEQ ID NO:46, 47, 52, 49, 50, 53 and 54, which is mutated as compared to SEQ ID NO:6 such that when the isolated polynucleotide is integrated into the PPE-1 promoter and placed upstream of a luciferase coding sequence the expression level of the luciferase coding sequence is upregulated or downregulated as compared to when SEQ ID NO:6 is similarly integrated into the PPE-1 promoter and placed upstream of the luciferase coding sequence. Also provided are nucleic acid constructs comprising same, methods of using same and pharmaceutical compositions comprising same for increasing or decreasing expression of a polynucleotide of interest in endothelial and non-endothelial cells.
    • 包含前内皮素启动子的SEQ ID NO:6至少14个核苷酸的分离的多核苷酸,其包含至少两个连续序列,位于选自SEQ ID NO:6的至少一个核苷酸的至少一个核苷酸位置旁边。 46,47,52,49,50,53和54,其与SEQ ID NO:6相比突变,使得当分离的多核苷酸整合到PPE-1启动子中并置于萤光素酶编码序列的上游时,其表达水平 与SEQ ID NO:6类似地整合到PPE-1启动子中并置于荧光素酶编码序列上游的荧光素酶编码序列的上调或下调。 还提供了包含其的核酸构建体,使用它们的方法和包含其的药物组合物,用于增加或减少内皮和非内皮细胞中感兴趣的多核苷酸的表达。
    • 10. 发明申请
    • COMBINED TREATMENT UTILIZING VB-201
    • 使用VB-201的组合治疗
    • WO2011083467A1
    • 2011-07-14
    • PCT/IL2011/000010
    • 2011-01-05
    • VASCULAR BIOGENICS LTD.COHEN, YaelYACOV, NivaBREITBART, Eyal
    • COHEN, YaelYACOV, NivaBREITBART, Eyal
    • A61K45/00
    • A61K31/685A61K31/198A61K31/366A61K31/40A61K31/505A61K31/683A61K38/02A61K45/06Y02A50/414
    • Methods of treatment which utilize co-administration of the oxidized lipid VB-201 with an additional therapeutically active agent are described herein. Methods of treating a cardiovascular disease are described herein, comprising co-administration of VB-201 and a statin to a subject who is not fully responsive to the statin, as well as methods of treating an inflammatory disease or disorder, comprising co-administration of VB-201 and glatiramer acetate. A pharmaceutical composition comprising VB-201, identified for use in combination with glatiramer acetate, is also described herein. Methods of determining a therapeutically effective amount of VB-201 in a subject and of determining a therapeutically effective amount of VB-201 for co-administration with an additional therapeutically active agent are also described. Novel unit dosage forms of VB-201 and methods utilizing same are also disclosed.
    • 本文描述了利用氧化脂质VB-201与另外的治疗活性剂共同给药的治疗方法。 本文描述了治疗心血管疾病的方法,包括将VB-201和他汀类药物共同给予对他汀类药物不完全反应的受试者以及治疗炎性疾病或病症的方法,包括共同给予 VB-201和醋酸格拉默。 本文还描述了一种包含鉴定为与醋酸格拉默组合使用的VB-201的药物组合物。 还描述了确定受试者中治疗有效量的VB-201和确定治疗有效量的用于与另外的治疗活性剂共同施用的VB-201的方法。 还公开了VB-201的新型单位剂型及其利用方法。