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Environmental Science and Pollution Research International
|
December 19, 2012
Polychlorinated biphenyl (118) activates osteoclasts and induces bone resorption in goldfish
Koji Yachiguchi, Noriko Matsumoto, Yuki Haga, et al.
Heart Rhythm
|
August 25, 2022
Disrupted Ca<sub>V</sub>1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model
Asami Kashiwa, Takeru Makiyama, Hirohiko Kohjitani, et al.
Circulation. Arrhythmia and Electrophysiology
|
August 7, 2020
Cardiac Emerinopathy: A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction
Taisuke Ishikawa, Hiroyuki Mishima, Julien Barc, et al.
Nature Genetics
|
April 3, 2012
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair
Yuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake, et al.
Cardiovascular Research
|
August 4, 2025
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants
Taisuke Ishikawa, Hiroki Kimoto, Akiko Seki, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 20, 2011
Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome
Kazuhiko Arima, Akira Kinoshita, Hiroyuki Mishima, et al.
European Heart Journal
|
July 5, 2021
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome
Taisuke Ishikawa, Hiroki Kimoto, Hiroyuki Mishima, et al.
Journal of the American College of Cardiology
|
July 15, 2017
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation
Akiko Seki, Taisuke Ishikawa, Xavier Daumy, et al.
Plos One
|
December 3, 2024
Correction: Targeted deep sequencing analyses of long QT syndrome in a Japanese population
Yuki Nagata, Ryo Watanabe, Christian Eichhorn, et al.
Nature Communications
|
November 25, 2021
Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency
Nobuo Kanazawa, Hiroaki Hemmi, Noriko Kinjo, et al.
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Showing results (101-110 of 114) with videos related to
Sort By:
Page
of 12
Environmental Science and Pollution Research International
|
December 19, 2012
Polychlorinated biphenyl (118) activates osteoclasts and induces bone resorption in goldfish
Koji Yachiguchi, Noriko Matsumoto, Yuki Haga, et al.
Heart Rhythm
|
August 25, 2022
Disrupted Ca<sub>V</sub>1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model
Asami Kashiwa, Takeru Makiyama, Hirohiko Kohjitani, et al.
Circulation. Arrhythmia and Electrophysiology
|
August 7, 2020
Cardiac Emerinopathy: A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction
Taisuke Ishikawa, Hiroyuki Mishima, Julien Barc, et al.
Nature Genetics
|
April 3, 2012
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair
Yuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake, et al.
Cardiovascular Research
|
August 4, 2025
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants
Taisuke Ishikawa, Hiroki Kimoto, Akiko Seki, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 20, 2011
Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome
Kazuhiko Arima, Akira Kinoshita, Hiroyuki Mishima, et al.
European Heart Journal
|
July 5, 2021
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome
Taisuke Ishikawa, Hiroki Kimoto, Hiroyuki Mishima, et al.
Journal of the American College of Cardiology
|
July 15, 2017
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation
Akiko Seki, Taisuke Ishikawa, Xavier Daumy, et al.
Plos One
|
December 3, 2024
Correction: Targeted deep sequencing analyses of long QT syndrome in a Japanese population
Yuki Nagata, Ryo Watanabe, Christian Eichhorn, et al.
Nature Communications
|
November 25, 2021
Heterozygous missense variant of the proteasome subunit β-type 9 causes neonatal-onset autoinflammation and immunodeficiency
Nobuo Kanazawa, Hiroaki Hemmi, Noriko Kinjo, et al.
Page
of 12