スポンサーリンク
Department Of Molecular Pathogenesis Division Of Adult Diseases | 論文
- Mutational Analysis of Fukutin Gene in Dilated Cardiomyopathy and Hypertrophic Cardiomyopathy(Molecular Cardiology)
- 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)
- 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)
- FRS-090 Identification of a Novel Disease Gene for Hypertrophic Cardiomyopathy(FRS19,Genetic Abnormalities in Cardiac Hypertrophy and Cardiomyopathy (M),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Soc
- 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 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
- 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
- FRS-032 Testicular hormone accelerates the develoment and progress of dilated cardiomyopathy in an animal model(Molecular Determinants for the Development of Cardiomyopathy(M),Featured Research Session,The 72nd Annual Scientific Meeting of the Japanese Ci
- FRS-065 Overexpression of Cardiac Myosin Light Chain Phosphatase Small Subunit (hHS-M21) Lead to Hypertrophic Cardiomyopathy(Heart Failure, Cardiac Remodeling and Cardiomyopathy 1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- 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
スポンサーリンク