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Department Of Molecular Pathogenesis Division Of Adult Diseases Medical Research Institute Tokyo Med | 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))
- Long-term Observation on the Clinical Course of Myocardial Infarction with Special Reference to Recurence
- 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))
- 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)
- 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
- Hepatitis C Virus Infection and Heart Diseases : A Multicenter Study in Japan
- 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)
- Genetic Analysis of Dilated Cardiomyopathy : HLA and immunoglobulin genes may confer susceptibility : MOLECULAR ANALYSIS OF THE PATHOPHYSIOLOGY OF CARDIOMYPATHY
- 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)
- 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
- DNA TYPING OF HLA CLASS II GENES IN DILATED CARDIOMYOPATHY
- THE ANALYSIS OF THE CARDIAC β MYOSIN HEAVY CHAIN GENE IN JAPANESE 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
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