Kimura Akinori | Medical Research Institute Tokyo Medical And Dental University

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著作論文

17-Year Follow-up Study of a Patient With Obstructive Hypertrophic Cardiomyopathy With a Deletion Mutation in the Cardiac Myosin Binding Protein C Gene
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))
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))
The role of a common TNNT2 polymorphism in cardiac hypertrophy
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)
Identification of a Novel Disease Gene for Dilated Cardiomyopathy ; an ; αβ-crystallin Mutation Affecting the Interaction with Titin (Cardiac Hypertrophy/Cardiomyopathy 2 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
An SCN5A Mutation Associated With Idiopathic Ventricular Fibrillation Alters The Na^+ Channel Pore Structure And Responses To Antiarrhythmic Drugs
OJ-032 Protein Tyrosine Kinase, c-Src, Regulates Gating Properties and Membrane Trafficking of the HERG Channel via Different Mechanisms(Arrhythmia, basic-2 (A) OJ6,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanes
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
FRS-026 HERG potassium channel regulated by phosphotyrosine kinase(Arrhythmia-Basic : Molecular and Genetic : Basis (A) : FRS4)(Featured Research Session (English))
PJ-201 A Compound Heterozygous Mutation in KCNQ1 Associated with Long QT Syndrome(Arrhythmia, basic(05)(A),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations
FRS-051 Identification of a Novel Disease Gene for Restrictive Cardiomyopathy(Frontier of Cardiomyopathy Research-1 (M) FRS11,Featured Research Session,The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
OE-020 Genetic Screening and Compound Mutations in Patients with Hypertrophic Cardiomyopathy(OE04,Cardiomyopathy/Hypertrophy (Clinical) (M),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
IS034 Frequency and geographic distribution of mutations in the HCM genes found in Oriental familial hypertrophic cardiomyopathy
OJ-447 Heart-specific growth factor-like gene may be involved in the development of hypertensive heart disease.(Heart Failure, Basic 3 (M) : OJ54)(Oral Presentation (Japanese))
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
Genomic structure and eight novel exonic polymorphisms of the human N-cadherin gene
IS109 Clinical significance of dual isotope myocardial perfusion imaging with iodine-123 BMIPP and thallium-201 in hypertrophic cardiomyopathy
Mutation of ZASP causes alteration in the affinity to protein kinase C subtypes and associates with familial dilated cardiomyopathy
Molecular Etiology of Idiopathic Cardiomyopathy in Asian Populations
A frameshift deletion mutation in the cardiac myosin-binding protein C gene associated with dilated phase of hypertrophic cardiomyopathy and dilated cardiomyopathy
Prevalence and Distribution of Sarcomeric Gene Mutations in Japanese Patients With Familial Hypertrophic Cardiomyopathy
Genetic Screening and Double Mutation in Japanese Patients With Hypertrophic Cardiomyopathy
Role of HCN4 channel in preventing ventricular arrhythmia
HLA-DPB1 and NFKBIL1 may confer the susceptibility to chronic thromboembolic pulmonary hypertension in the absence of deep vein thrombosis
Validation of eight genetic risk factors in East Asian populations replicated the association of BRAP with coronary artery disease
Validation of the association between AGTRL1 polymorphism and coronary artery disease in the Japanese and Korean populations
Replication studies for the association of PSMA6 polymorphism with coronary artery disease in East Asian populations
Complex divergence at a microsatellite marker C1_2_5 in the lineage of HLA-Cw/-B haplotype
Hunting for genes for hypertension : the Millennium Genome Project for Hypertension

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