Inhomogeneous Current Distribution in Ag/Bi2223 Tape

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概要

• 論文の詳細を見る
• Japan Institute of Metalsの論文

著者

• Osamura Kozo

  Department Of Metallurgy Kyoto University

• SAKAI Akira

  Mesoscopic Materials Research Center, Kyoto University

• Itoh Hideki

  Department Of Anesthesiology And Critical Care Medicine Yokohama City University Graduate School Of

• Itoh Hideki

  Department Of Materials Science And Engineering Kyoto University

• MATSUNO Ken-ichi

  Department of Materials Science and Engineering, Kyoto University

• Matsuno Ken-ichi

  Department Of Materials Science And Engineering Kyoto University

• Osamura Kozo

  Department Of Materials Science And Engineering Kyoto University

• Sakai Akira

  Mesoscopic Materials Research Center Kyoto University

• Sakai Akira

  Mesoscopic Materials Research Center

関連論文

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• PE-106 SCN5A and Lamin A/C Gene Mutations are Highly Prevalent in Patients with Familial Bradyarrhythmic Disorders(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulat
• A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation
• Heterogeneous Structure of Amorphous Materials
• OJ-012 Mutation Analysis for the Human Cardiac Ryanodine Receptor Gene (RyR2) in Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)(Arrhythmia, diagnosis/pathophysiology/EPS-03, The 71st Annual Scientific Meeting of the Japanese Circulation Soci
• PE-104 Severer Phenotypes of Long QT Syndrome are Associated with Compound Mutations : A Multicenter Study(PE018,Arrhythmia, Others (Clinical/Pathophysiology) (A),Poster Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Soci
• 2 Latent Genetic Backgrounds and Molecular Pathogenesis of Drug-induced Long QT Syndrome(Proarrhythmic Risk of Drugs and Their Evaluation,Symposium 7 (SY-07) (I),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
• 1 A Novel Genetic Marker for Potential Risk of QT Prolongation and Cardiac Sudden Death : KCNE1-D85N Polymorphism(Biomarkers, Genetic Polymorphism, and Risk Estimation,Symposium 1 (SY-01) (H),The 73rd Annual Scientific Meeting of The Japanese Circulation
• Dynamic Change in ST-Segment and Spontaneous Occurrence of Ventricular Fibrillation in Brugada Syndrome With a Novel Nonsense Mutation in the SCN5A Gene During Long-Term Follow-up
• Mutation Site Dependent Variability of Cardiac Events in Japanese LQT2 Form of Congenital Long-QT Syndrome
• OJ-009 A Common KCNE1 Polymorphism, D85N, is a Genetic Modifier of Long QT Syndrome(Arrhythmia, diagnosis/ Pathophysiology/ EPS(03)(A),Oral Presentation(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
• OE-391 Cardiac sodium channel gene mutations are prevalent in Japanese patients with familial sick sinus syndrome(Arrhythmia, diagnosis/Pathophysiology/EPS(02)(A),Oral Presentation(English),The 72nd Annual Scientific Meeting of the Japanese Circulation So
• FRS-109 A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation(New Horizon in Diagnosis and Pathophysiology of Arrhythmia(A),Featured Research Session,The 72nd Annual Scientific Meeting of the Japanese Circulation Soci
• OJ-009 N- And C-terminal KCNE1 Mutations Cause Distinct Phenotypes of Long QT Syndrome(Arrhythmia, diagnosis/pathophysiology/EPS-03, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
• 1 Brugada Syndrome and Diverse Phenotypes of Cardiac Sodium Channelopathies(Symposium 5 (SY-05) (A) New Findings of Mechanism and Therapeutic Strategies of Idiopathic Ventricular Fibrillation,Special Program,The 72nd Annual Scientific Meeting of the Japan
• PJ-043 Clinical Characteristics for Japanese Patients with Genotyped Long-QT Syndrome(Arrhythmia, diagnosis/pathophysiology/EPS-10, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
• Conductance in Breaking Nanocontacts of Some Transition Metals
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• OJ-007 Variable Genetic Backgrounds Between Congenital and Acquired Long-QT Syndromes(Arrhythmia, diagnosis/pathophysiology/EPS-03, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
• PJ-190 A KCNE1 Single Nucleotide Polymorphism, D85N, Serves as a Modifier in Forme-fruste Type of Long QT syndrome(Genetics/Genetically engineered models/Gene therapy-3 (M) PJ32,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of t
• OJ-349 High Incidence of Cardiac Events for Long-QT Syndrome with Compound Mutations(Arrhythmia, diagnosis/pathophysiology/EPS-4 (A) OJ59,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
• OJ-064 Age-Related Triggers for Life-Threatening Arrhythmia in Genotyped Long-QT Syndrome(Arrhythmia, diagnosis/pathophysiology/EPS-3 (A) OJ11,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
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• PJ-602 Clinical Characteristics Associated with Mutation Sites in LQT2 Form of Congenital Long-QT Syndrome(Arrhythmia, basic-5 (A) PJ101,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
• Fracture Toughness Measurements of Ba_2YCu_3O_ Superconducting Oxide by Means of Indentation Technique : Electrical Properties of Condensed Matter
• Observations of Mixed-Phase Y-Ba-Cu-O Superconductors with a Scanning Electron Microscope at Low Temperatures : Electrical Properties of Condensed Matter
• Quantized Conductance in Pt Nanocontacts
• Serum Levels of NCC-ST-439 in Dukes' C Colorectal Cancer Patients: A Preliminary Report
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• Arrhythmogenesis in the Short-QT Syndrome Associated With Combined HERG Channel Gating Defects : A Simulation Study
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• Improvement of Critical Current Density in YBa_2Cu_3O_ Superconductor by Sn Addition
• Precise Study of Vortex Structures in Nb by Small-Angle Neutron Scattering
• A Novel Synthesis of α,β,γ,δ-Unsaturated Selenoamides by Using [3,3] Sigmatropic Rearrangement of Alkynyl Propargyl Selenides in the Presence of Diethylamine
• Crystal Structures of α-anaβ-Indium Selenide, In_2Se_3
• Atrioventricular Block-Induced Torsades de Pointes With Clinical and Molecular Backgrounds Similar to Congenital Long QT Syndrome
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• Nonstoichiometry of Superconducting Ba_2YCu_3O_ at Temperatures between 870 and 1180 K : Electrical Properties of Condensed Matter
• Effect of Zincate Treatment on Adhesion of Electroless Nickel-Phosphorus Coating for Commercial Pure Aluminum
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• Clinical and Electrophysiological Characteristics of Brugada Syndrome Caused by a Missense Mutation in the S5-pore site of SCN5A(Arrhythmia, Diagnosis/Pathophysiology/EPS 5 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
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• FRS-144 A Novel Missense Mutation of SCN5A Gene Associated with Brugada Syndrome by Bidirectional Effects on Blocking Actions of Antiarrhythmic Drugs(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
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• SCN5A Mutations in the S5-S6 Region Cause Brugada Syndromeand Cardiac Conduction Disturbances
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• Inhomogeneous Current Distribution in Ag/Bi2223 Tape
• Lattice Parameter and Thermal Expansion Measurements of a LiF(001)Surface by He-Atom Beam Diffraction Method
• Phase Diagram of GaAs -GaP Quasi-Binary System
• Free Carrier Absorption in n-GaAs
• Phase Transition and Crystal Structure of Ba_2CuO_x Oxide
• Local Atomic Arrangement in an In_Ga_As Quasi-Binary Alloy Grown by Liquid-Phase Epitaxy
• Barrier-Height Imaging of Oxygen-Adsorbed Si(111) 7×7 Surfaces ( Scanning Tunneling Microscopy)
• Crystal Structure of Ternary Ba_8YCu_4O Phase
• Relative Integrated Intensity of the X-Ray Diffraction and Effective Charge in GaAs_P_x Compounds
• Scanning Tunneling Microscopy Barrier-Height Imaging of Shockley Dislocations on a Au(111) Reconstructed Surface
• Seasonal and Circadian Distributions of Cardiac Events in Genotyped Patients With Congenital Long QT Syndrome
• Carvedilol, a Non-Selective β-with α_1-Blocker is Effective in Long QT Syndrome Type 2
• Barrier-Height Imaging of Si(001) 2 × n
• Mutations of the Cardiac Ryanodine Recepter (RyR2) Gene in Catecholaminergic Polymorphic Ventricular Tachycardia
• Observation of Mesoscopic Structures in NdBa2Cu3O7-δ by Small-Angle Neutron Scattering
• KCNE5 Variants Are Novel Modulators of Brugada Syndrome and Idiopathic Ventricular Fibrillation
• Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia
• L-Type Calcium Channel Mutations in Japanese Patients With Inherited Arrhythmias
• Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan
• Hydroxyzine, a First Generation H1-Receptor Antagonist, Inhibits Human Ether-a-go-go-Related Gene (HERG) Current and Causes Syncope in a Patient With the HERG Mutation
• Anisotropy and Lorentz-Force Dependences of Critical Current Density in $C$-Axis-Oriented YBa2Cu3O7-δ Thin Film
• Precise Study of Vortex Structures in Nb by Small-Angle Neutron Scattering
• Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan
• L-Type Calcium Channel Mutations in Japanese Patients With Inherited Arrhythmias

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