Nakano Noritsugu | Department of Molecular Pathogenesis, Division of Medical Science, Medical Research Institute, Tokyo

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著作論文

PJ-574 A Novel Missense Mutation (R2401H) in the Human Cardiac Ryanodine Receptor Gene (RyR2) in Patient with Catecholaminergic Polymorphic Ventricular Tachycardia(Arrhythmia, Basic and Diagnosis/Pathophysiology/EPS (A) : PJ96)(Poster Session (Japanese))
OJ-083 KCNQ1 Mutation Causing Defective Channel Trafficking and Dominant-Negative Suppression Underlie Severe Phenotype of Congenital Long QT Syndrome(Arrhythmia, Basic 1 (A) : OJ10)(Oral Presentation (Japanese))
A Novel Disease Genes for Cardiomyopathy : Identification of a CAV3 Mutation and Its Functional Alteration
Microarray-Based Identification of Three Candidate Genes for Human Heart Failure : From Dahl Rat Model to Human Genome
Novel HERG mutations in long QT syndrome in Japan
Genetic risk factors for myocardial infarction in Japanese
Identification of caveolin-3 mutation in familial cardiomyopathy
IS160 P27kip1 Downregulation Precedes the Cyclin-E Associated Kinase Activation During Neointimal VSMC Proliferation.

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