Furutani Michiko | Tokyo Women's Medical University

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著作論文

A Common Mitochondrial 16189 DNA Variant Associated with Left Ventricular Hypertrophy in Type 2 Diabetes Mellitus
FRS-059 Phenotypic and Genotypic Analysis in Familial Atrial Septal Defect(Oxidative Stress, Autonomic Function and Peripheral Vascular Diseases (H) : FRS7)(Featured Research Session (English))
Implications of Mutations of Activin Receptor-Like Kinase 1 Gene (ALK1) in Addition to Bone Morphogenetic Protein Receptor II Gene (BMPR2) in Children With Pulmonary Arterial Hypertension
PJ-735 The Same Mutations in the Cardiac Troponin T Gene Show Various Prognoses in Japanese Patients with Hypertrophic Cardiomyopathy(Cardiac hypertrophy, basic/clinical-4 (M) PJ125,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting
Genotype and Phenotype of Cardiovascular Diseases (del22q11.2, Williams and Brugada syndromes)
IS052 A mitochondrial DNA is responsible for the pathogenesis of congenital long QT syndrome
IS091 Electrophysiological properties of the mutant HERG channel (G601S) expressed in mammalian cells
0720 Genetic analysis of familial long QT Syndrome : Missense mutation in HERG in LQT2 family
Genetic Analysis of Essential Cardiac Transcription Factors in 256 Patients With Non-Syndromic Congenital Heart Defects

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