位置：成果数据库 > 期刊 > 期刊详情页
Molecular basis for genistein-induced inhibition of Kir2.3 currents
  • ISSN号：0031-6768
  • 期刊名称：Pflugers Archiv-European Journal of Physiology
  • 时间：0
  • 页码：413-423
  • 语言：英文
  • 相关项目：细胞膜受体调节M/KCNQ钾离子通道功能的分子机制的研究
作者： Jia, Zhanfeng|Liu, Boyi|Zhang, Guohong|Zhang, Hailin|Zhao, Zhiying|Jia, Qingzhong|Geng, Xian|
同期刊论文项目
细胞膜受体调节M/KCNQ钾离子通道功能的分子机制的研究
期刊论文 28 会议论文 16
同项目期刊论文
Regulation of CCL5 Expression in Smooth Muscle Cells Following Arterial Injury
脂筏在细胞信号特异性调节钾离子通道功能中的作用
细胞膜磷脂酰肌醇4,5-二磷酸对TRP通道功能的调节作用
The acute nociceptive signals induced by bradykinin in rat sensory neurons are mediated by inhibitio
Depolarization Increases Phosphatidylinositol (PI) 4,5-Bisphosphate Level and KCNQ Currents through
Activation of ATP-sensitive potassium channels antagonize nociceptive behavior and hyperexcitability
Characteristics and molecular basis of celecoxib modulation on K(v)7 potassium channels
Membrane depolarization increases membrane PtdIns(4,5)P2 levels through mechanisms involving PKC &be
Activation of KCNQ2/3 potassium channels by novel pyrazolo[1,5-a]pyrimidin-7(4H)-one derivatives.
水杨酸钠对大鼠颞皮层神经元延迟整流钾通道的抑制作用
不同日龄大鼠颈上交感神经节神经元电转染方法
TMEM16A:钙激活氯通道研究进展
新型钾通道开放剂(QO-58)在大鼠体内组织分布研究
Design, synthesis and biological activity of pyrazolo[1,5-a]pyrimidin-7(4H)-ones as novel Kv7/KCNQ p
EGF enhances the migration of cancer cells by up-regulation of TRPM7.
Genistein inhibits voltage-gated sodium currents in SCG neurons through protein tyrosine kinase-depe
Phosphatidylinositol 4,5-bisphosphate hydrolysis mediates histamine-induced KCNQ/M current inhibitio
Arachidonic acid activates Kir2.3 channels by enhancing channel-phosphatidyl-inositol 4,5-bisphospha
Antihistamine mepyramine directly inhibits KCNQ/M channel and depolarizes rat superior cervical gang
NGF inhibits M/KCNQ currents and selectively alters neuronal excitability in subsets of sympathetic
缓激肽、离子通道与炎症性疼痛
Specificity of G beta gamma Signaling Depends on G alpha Subunit Coupling with G-Protein-Sensitive K
蛋白激酶C对内向整流钾离子通道的调节机制
蛋白激酶C和磷脂酰肌醇4,5二磷酸之间相互调节作用的研究进展
瑞替加滨的合成