Yasunami Michio | Department Of Immunogenetics Institute Of Tropical Medicine (nekken) Nagasaki University

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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-504 Functional alterations of TCAP mutations found in hypertrophic cardiomyopathy and dilated cardiomyopathy(Cardiomyopathy, Basic (M) : OJ62)(Oral Presentation (Japanese))
Mutations in a Hyperpolarization-activated Channel as the Molecular Basis of Ventricular Arrhythmia(Arrhythmia, Basic 4 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Mutational Analysis of Cardiac Ryanodine Receptor Genes (RyR2) in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Arrhythmogenic Right Ventricular Cardiomyopathy(Arrhythmia, Basic 2 (A), The 69th Annual Scientific Meeting of the Ja
A Novel Frameshift Mutation in C-Terminal Region of HERG
Chromosome-Wide Association Study of Disease-Related Polymorphisms for Myocardial Infarction
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
Identification of a novel HLA-linked susceptibility gene to Takayasu's arteritis
Genetic risk factors for myocardial infarction in Japanese
Identification of caveolin-3 mutation in familial cardiomyopathy
Mutation of ZASP causes alteration in the affinity to protein kinase C subtypes and associates with familial dilated cardiomyopathy
Microfluorometric assay for quantification of anti-erythrocytic antibody level in sera of Plasmodium berghei ANKA infected semi-immune mice
HLA-DPB1 and NFKBIL1 may confer the susceptibility to chronic thromboembolic pulmonary hypertension in the absence of deep vein thrombosis
Association Study of CD14 Polymorphism With Myocardial Infarction in a Japanese Population

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