515 results on '"Itoh, Hideki"'
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102. A Common Mutation of Long QT Syndrome Type 1 in Japan
103. A type 2 ryanodine receptor variant associated with reduced Ca2+ release and short-coupled torsades de pointes ventricular arrhythmia.
104. Abstract 16509: Young Long QT Syndrome Patients With KCNH2 Mutations Have Late Onset but Severe Symptoms
105. Abstract 12704: The Prognosis of Andersen-Tawil Syndrome is Not So Benign as Ever Thought
106. A rare KCNE1 polymorphism, D85N, as a genetic modifier of long QT syndrome
107. BOTH GAIN- AND LOSS-OF-FUNCTION SCN5A MUTATIONS ASSOCIATED WITH INFANTILE FATAL VENTRICULAR ARRHYTHMIAS
108. Nonsense-mediated mRNA decay due to a CACNA1C splicing mutation in a patient with Brugada syndrome
109. Long-term Pharmacological Therapy of Brugada Syndrome: Is J-wave Attenuation a Marker of Drug Efficacy?
110. A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels
111. Thermal Activation of Cardiac Thin Filaments Induces Contraction without Intracellular Ca2+ Changes: Studies with Cardiomyocytes and an In Vitro Motility Assay
112. Bleb Formation in a Hela Cell Induced by Temperature Gradient
113. Microscopic heat pulse-induced calcium dynamics in single WI-38 fibroblasts
114. 3P230 Ca2+-burst in rat hippocampal neurons induced by microscopic heat pulses(Neuroscience & Sensory systems,Poster,The 52th Annual Meeting of the Biophysical Society of Japan(BSJ2014))
115. A novel KCNH2 mutation as a modifier for short QT interval
116. Cardiac Channelopathies Associated with Infantile Fatal Ventricular Arrhythmias: From the Cradle to the Bench
117. Trans-Resectoscope Stimulation Predicts the Need to Block Adductor Response During Bladder Tumor Resection
118. Identification of a KCNQ1 Polymorphism Acting as a Protective Modifier Against Arrhythmic Risk in Long-QT Syndrome
119. Microscopic Heat Pulses Induce Ca2+-Independent Contraction of Cardiomyocytes
120. L-Type Calcium Channel Mutations in Japanese Patients With Inherited Arrhythmias
121. Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan
122. 3P292 Mapping of thermal conductivity in single living cells(27. Bioimaging,Poster)
123. Phenotype Variability in Patients Carrying KCNJ2 Mutations
124. Microscopic Analysis of Calcium Dynamics in Single Migrant Cells in Response to a Heat Pulse
125. 290 The KCNQ1 rs2074238 polymorphism is a genetic modifier of cardiac risk in long QT syndrome
126. 2H1510 Ca^<2+>-independent on-off regulation of a cardiomyocyte by microscopic heat pulses(Muscle,Oral Presentation,The 50th Annual Meeting of the Biophysical Society of Japan)
127. Microscopic heat pulses induce contraction of cardiomyocytes without calcium transients
128. Clinical and electrocardiographic characteristics of patients with short QT interval in a large hospital-based population
129. Seasonal and Circadian Distributions of Cardiac Events in Genotyped Patients With Congenital Long QT Syndrome
130. Impact of ABCB1, ABCG2, and CYP3A5polymorphisms on plasma trough concentrations of apixaban in Japanese patients with atrial fibrillation
131. KCNE5 ( KCNE1L ) Variants Are Novel Modulators of Brugada Syndrome and Idiopathic Ventricular Fibrillation
132. KCNE5 Variants Are Novel Modulators of Brugada Syndrome and Idiopathic Ventricular Fibrillation
133. Site-Specific Arrhythmogenesis in Structurally Normal Heart of Non-Brugada Patients with Ventricular Arrhythmias Originating from Ventricular Outflow Tract
134. Intrathecally administered Sema3A protein attenuates neuropathic pain behavior in rats with chronic constriction injury of the sciatic nerve
135. 3L1358 Sensitivity of Ca^<2+> dynamics to the heat pulse in migrant cells at various temperatures(Cell biology 5,The 49th Annual Meeting of the Biophysical Society of Japan)
136. Mutations of the Cardiac Ryanodine Recepter (RyR2) Gene in Catecholaminergic Polymorphic Ventricular Tachycardia
137. Long QT Syndromes Are Heterogeneous Disease Entities Presenting not only QT Prolongation but Multiple Phenotypes—Cases with Compound Heterozygous Mutations
138. Long QT syndrome with compound mutations is associated with a more severe phenotype: A Japanese multicenter study
139. Atrioventricular Block-Induced Torsades de Pointes With Clinical and Molecular Backgrounds Similar to Congenital Long QT Syndrome
140. Japanese Journal of Electrocardiology
141. Japanese Journal of Electrocardiology
142. 2P212 Ca^<2+> response to microscopic heat pulses in a migrant cell(The 48th Annual Meeting of the Biophysical Society of Japan)
143. 1P335 1J1435 High-speed imaging of heat transfer in single living cells.(Bioimaging,Oral Presentations,The 48th Annual Meeting of the Biophysical Society of Japan)
144. Aortopulmonary Artery Dissection
145. Latent Genetic Backgrounds and Molecular Pathogenesis in Drug-Induced Long-QT Syndrome
146. D85N, a KCNE1 Polymorphism, Is a Disease-Causing Gene Variant in Long QT Syndrome
147. Drug-induced Brugada ECG Changes Associated With A Novel SCN5A Mutation In A Patient With Atrial Arrhythmias
148. Dynamic Change in ST-Segment and Spontaneous Occurrence of Ventricular Fibrillation in Brugada Syndrome With a Novel Nonsense Mutation in the SCN5A Gene During Long-Term Follow-up
149. Abstract 1523: A Novel SCN5A Gain-of-Function Mutation M1875T Associated with Familial Atrial Fibrillation
150. Hydroxyzine, a First Generation H1-Receptor Antagonist, Inhibits Human Ether-a-go-go–Related Gene (HERG) Current and Causes Syncope in a Patient With the HERG Mutation
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