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151. Functional Characterization of Alternative Splicing in the C Terminus of L-type CaV1.3 Channels.

152. Differential splicing patterns of L-Type calcium channel Cav1.2 subunit in hearts of Spontaneously Hypertensive Rats and Wistar Kyoto rats

153. Comparative genomics of the human and Fugu voltage-gated calcium channel α1-subunit gene family reveals greater diversity in Fugu

154. Alternative Splicing of P/Q-Type Ca2+ Channels Shapes Presynaptic Plasticity

155. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

156. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

157. Enhanced isradipine sensitivity in vascular smooth muscle cells due to hypoxia-induced Ca v 1.2 splicing and RbFox1/Fox2 downregulation.

159. Characterization of Ca V 1.2 exon 33 heterozygous knockout mice and negative correlation between Rbfox1 and Ca V 1.2 exon 33 expressions in human heart failure.

160. Alternative Splicing of L-type Ca V 1.2 Calcium Channels: Implications in Cardiovascular Diseases.

161. Substance P induces plasticity and synaptic tagging/capture in rat hippocampal area CA2.

162. Transgenic Mice Overexpressing the Divalent Metal Transporter 1 Exhibit Iron Accumulation and Enhanced Parkin Expression in the Brain.

163. Metaplasticity mechanisms restore plasticity and associativity in an animal model of Alzheimer's disease.

164. Exclusion of alternative exon 33 of Ca V 1.2 calcium channels in heart is proarrhythmogenic.

165. Aberrant Splicing Promotes Proteasomal Degradation of L-type Ca V 1.2 Calcium Channels by Competitive Binding for Ca V β Subunits in Cardiac Hypertrophy.

166. Histamine resets the circadian clock in the suprachiasmatic nucleus through the H1R-CaV 1.3-RyR pathway in the mouse.

167. TRPM4 inhibition promotes angiogenesis after ischemic stroke.

168. Splice variant specific modulation of CaV1.2 calcium channel by galectin-1 regulates arterial constriction.

169. Neurodegenerative diseases: exercising toward neurogenesis and neuroregeneration.

170. CaV1.2 channelopathies: from arrhythmias to autism, bipolar disorder, and immunodeficiency.

171. Understanding alternative splicing of Cav1.2 calcium channels for a new approach towards individualized medicine.

172. Molecular alteration of Ca(v)1.2 calcium channel in chronic myocardial infarction.

173. Alternative splicing of voltage-gated calcium channels: from molecular biology to disease.

174. Separate locations of urocortin and its receptors in mouse testis: function in male reproduction and the relevant mechanisms.

175. Alternative splicing of the Ca(v)1.3 channel IQ domain, a molecular switch for Ca2+-dependent inactivation within auditory hair cells.

176. Comparative genomics of the human and Fugu voltage-gated calcium channel alpha1-subunit gene family reveals greater diversity in Fugu.

177. Urocortin II inhibits the apoptosis of mesenteric arterial smooth muscle cells via L-type calcium channels in spontaneously hypertensive rats.

178. Splicing for alternative structures of Cav1.2 Ca2+ channels in cardiac and smooth muscles.

179. Transcript scanning reveals novel and extensive splice variations in human l-type voltage-gated calcium channel, Cav1.2 alpha1 subunit.

180. Alternative splicing as a molecular switch for Ca2+/calmodulin-dependent facilitation of P/Q-type Ca2+ channels.

181. Systematic identification of splice variants in human P/Q-type channel alpha1(2.1) subunits: implications for current density and Ca2+-dependent inactivation.

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