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)

スポンサーリンク

概要

• 論文の詳細を見る
• 社団法人日本循環器学会の論文
• 2005-03-01

著者

• YAMASHINA Akira

  Tokyo Medical University

• Tashiro Misako

  新潟大学 1内

• Yamashina Akira

  Tokyo Ccu Network Scientific Committee

• Kimura Akinori

  Department Of Molecular Pathogenesis Medical Research Institute Tokyo Medical And Dental University

• Ueda Kazuo

  Pathogenesis Medical Research Institute Tokyo Medical And Dental University

• Kimura Akinori

  東京医科歯科大学難治疾患研究所 分子病態分野

• Inagaki Natsuko

  Tokyo Medical University

• Hayashi Takeharu

  Tokyo Medical and Dental University

• Ueda Kazuo

  Tokyo Medical and Dental University

• Takahashi Megumi

  Tokyo Medical and Dental University

• Teraoka Kunihiko

  Tokyo Medical University

• Chikamori Taishirou

  Tokyo Medical University

• Yasunami Michio

  Tokyo Medical and Dental University

• Kimura Akinori

  Tokyo Medical and Dental University

• Yasunami Michio

  Laboratory Of Genome Diversity School Of Biomedical Science Tokyo Medical And Dental University

• Kimura Akinori

  Medical Research Institute Tokyo Medical And Dental University

• Hayashi Takeharu

  Department Of Molecular Pathogenesis Medical Research Institute Tokyo Medical And Dental University

• Inagaki Natsuko

  Department Of Molecular Pathogenesis Medical Research Institute Tokyo Medical And Dental University

• Takahashi Megumi

  Department Of Molecular Pathogenesis Medical Research Institute Tokyo Medical And Dental University

• Kimura Akinori

  Department Of Molecular Pathogenesis Division Of Medical Science Medical Research Institute Tokyo Me

• Kimura Akinori

  Department Of Molecular Pathogenesis Division Of Adult Diseases Medical Research Institute Tokyo Med

• Takahashi Megumi

  Department Of Molecular Pathogenesis Division Of Medical Science Medical Research Institute Tokyo Me

• Ueda Kazuo

  Department Of Molecular Pathogenesis Division Of Medical Science Medical Research Institute Tokyo Medical And Dental University

関連論文

• The Japanese Society of Hypertension Committee for Guidelines for the Management of Hypertension
• OE-115 Current State of Emergency Cardiovascular Care Requiring CCU Admission in Tokyo Metropolitan District : From Tokyo CCU Network Annual Survey(OE20,ACS/AMI (Clinical/Diagnosis) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of T
• 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))
• OE-115 Current State of Emergency Cardiovascular Care Requiring CCU Admission in Tokyo Metropolitan District : From Tokyo CCU Network Annual Survey(OE20,ACS/AMI (Clinical/Diagnosis) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of T
• A Theoretical Consideration of T Wave Generation : An Experimental and Clinical Study
• Studies on the Regulation of Circulatory and Respiratory Systems (XVI)
• Studies on the Vectorcardiogram (Report III) The Direction of the QRS and T Loops
• 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))
• 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)
• 1 Diagnostic Imaging of Vulnerable Plaque on IVUS with Pressure Wire(Imaging of Vulnerable Plaque,Meet the Expert 8 (ME8) (I),The 70th Anniversary 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))
• 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
• -0837-MECHANISM OF RIGHT VENTRICULAR DYDKINESIS (RVD) ASSOCIATED WITH ACUTE ENTERIOR MYOCARDIAL INFARCTION : THE 54th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
• 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
• Prevention against Sudden Cardiac Death in Patients with Highly-risked Cardiac Disease : Tokyo Coronary Care Home Defibrillation Program(Emergency Care 1 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
• 37. A Study of Experimental Fusion Beats: with Special Reference to the Ventricular Complex of WPW Syndrome and Atrioventricular Conduction Time
• IS034 Frequency and geographic distribution of mutations in the HCM genes found in Oriental familial hypertrophic cardiomyopathy
• 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
• 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
• Role of HCN4 channel in preventing ventricular arrhythmia
• Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia
• 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
• -0031-GENETIC ANALYSIS OF DILATED CARDIOMYOPATHY (DCM) : IGLV GENE POLYMORPHISM IN DCM
• GENETIC ANALYSIS OF FAMILIAL HYPERTROPHIC CARDIOMYOPATHY (HCM) : 2ND REPORT : Cardiomyopathy, Myocarditis : 53 Annual Scientific Meeting, Japanese Circulation Society
• On the F Wave in Artial Fibrillation
• Usefulness of the Thrombolysis Therapy for the Treatment of Acute Myocardial Infarction Using the Rescue^ Catheter
• A frameshift deletion mutation in the cardiac myosin-binding protein C gene associated with dilated phase of hypertrophic cardiomyopathy and dilated cardiomyopathy
• Molecular Etiologies of Cardiomyopathies(Clinical Approach to Personalized Medicine in Cardiovascular disease, The 69th 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
• 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
• HLA and CTLA4 polymorphisms may confer a synergistic risk in the susceptibility to Graves' disease
• Hunting for genes for hypertension : the Millennium Genome Project for Hypertension
• Association Study of CD14 Polymorphism With Myocardial Infarction in a Japanese Population

もっと見る 閉じる

スポンサーリンク