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Laboratory Of Genome Diversity School Of Biomedical Science Tokyo Medical And Dental University | 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)
- 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
- Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations
- 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
- Mutation of ZASP causes alteration in the affinity to protein kinase C subtypes and associates with familial dilated cardiomyopathy
- 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
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