A Novel SCN5A Gain-of-Function Mutation M1875T Associated With Familial Atrial Fibrillation

Takeru Makiyama, Masaharu Akao, Satoshi Shizuta, +10

Journal of the American College of Cardiology

Genetic DisorderGeneticsFamilial Atrial FibrillationMolecular BiologyMolecular Genetics +2

High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5AGene Mutations

Takeru Makiyama, Masaharu Akao, Keiko Tsuji, +13

Journal of the American College of Cardiology

Genetic DisorderGeneticsGenetic EpidemiologyCongenital Heart DefectCongenital Heart Anomaly +6

Novel <b> <i>KCNJ2</i> </b> Mutation in Familial Periodic Paralysis With Ventricular Dysrhythmia

Tomohiko Ai, Yuichiro Fujiwara, Keiko Tsuji, +4

Circulation

Immunomodulating effect of vitamin D3 derivatives on type-1 cellular immunity

Ikuo Imazeki, Junko Matsuzaki, Keiko Tsuji, +1

Biomedical Research

Molecular Characterization of Heat Shock-Like Factor Encoded on the Human Y Chromosome, and Implications for Male Infertility1

Toshikatstu Shinka, Yoko Sato, Gang Chen, +7

Biology of Reproduction

FertilityCytogeneticsGeneticsGenomic MechanismGynecology +18

Genotype-phenotype correlations ofKCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome

Yoshisumi Haruna, Atsushi Kobori, Takeru Makiyama, +18

Human Mutation

Significance of hydrogen burst from growing cultures of Desulfovibrio vulgaris, Miyazaki, and the role of hydrogenase and cytochrome c3 in energy production system

Keiko Tsuji, Tatsuhiko Yagi

Archives of Microbiology

BiologyHydrogen BurstHydrogen ProductionEngineeringBiochemistry +11

Characterization and Subcellular Localization of KCNQ1 with a Heterozygous Mutation in the C Terminus

Minoru Horie, Tomoyuki Kubota, Hidetada Yoshida, +11

Journal of Molecular and Cellular Cardiology

Heterozygous MutationSignal TransductionHyperpolarization (Biology)Natural SciencesSubcellular Localization +8

N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome

Seiko Ohno, Dimitar P. Zankov, Hidetada Yoshida, +7

Heart Rhythm

Long Qt SyndromeSignal TransductionDistinct PhenotypesGenetic DisorderGenetics +3

The properties of the Kir6.1–6.2 tandem channel co-expressed with SUR2A

Yutaka Kono, Minoru Horie, Makoto Takano, +5

Pflügers Archiv - European Journal of Physiology

BiochemistryNatural SciencesMolecular BiologyIon ChannelsKir6.1–6.2 Tandem Channel