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Naoki Nishida

Showing results (121-130 of 144) with videos related to

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International Journal of Legal Medicine|April 3, 2013
Identification and characterization of a novel genetic mutation with prolonged QT syndrome in an unexplained postoperative deathYukiko Hata, Hisashi Mori, Ayumi Tanaka, et al.
Journal of Cardiology|February 25, 2016
Anomalous origin of the right coronary artery evaluated with multidetector computed tomography and its clinical relevanceKeiichi Hirono, Yukiko Hata, Naruaki Miyao, et al.
Pathology International|January 19, 2024
Enterocolic granulomatous phlebitis associated with epidermal growth factor-containing fibulin-like extracellular matrix protein 1 deposition and focal amyloid properties: A case reportShojiro Ichimata, Akane Aikawa, Naonori Sugishita, et al.
Neuropathology and Applied Neurobiology|April 18, 2024
Revisiting the relevance of Hirano bodies in neurodegenerative diseasesKoji Yoshida, Shelley L Forrest, Shojiro Ichimata, et al.
Journal of Clinical Medicine|March 19, 2020
Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart FailureKeiichi Hirono, Yukiko Hata, Nariaki Miyao, et al.
Biochemical and Biophysical Research Communications|September 28, 2013
Characterization of a novel mutant KCNQ1 channel subunit lacking a large part of the C-terminal domainKatsuya Kimoto, Koshi Kinoshita, Tomoki Yokoyama, et al.
Journal of Cardiovascular Electrophysiology|July 7, 2012
A novel missense mutation causing a G487R substitution in the S2-S3 loop of human ether-à-go-go-related gene channelKoshi Kinoshita, Yoshiaki Yamaguchi, Kohki Nishide, et al.
Heart Rhythm|January 19, 2016
SCN5A(K817E), a novel Brugada syndrome-associated mutation that alters the activation gating of NaV1.5 channelKoshi Kinoshita, Hiroyuki Takahashi, Yukiko Hata, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|January 15, 2014
Glycine/Serine polymorphism at position 38 influences KCNE1 subunit's modulatory actions on rapid and slow delayed rectifier K+ currentsYoshiaki Yamaguchi, Kohki Nishide, Mario Kato, et al.
Journal of the American Heart Association|September 1, 2017
A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular NoncompactionCe Wang, Yukiko Hata, Keiichi Hirono, et al.
Pageof 15

Showing results (121-130 of 144) with videos related to

Sort By:
Pageof 15
International Journal of Legal Medicine|April 3, 2013
Identification and characterization of a novel genetic mutation with prolonged QT syndrome in an unexplained postoperative deathYukiko Hata, Hisashi Mori, Ayumi Tanaka, et al.
Journal of Cardiology|February 25, 2016
Anomalous origin of the right coronary artery evaluated with multidetector computed tomography and its clinical relevanceKeiichi Hirono, Yukiko Hata, Naruaki Miyao, et al.
Pathology International|January 19, 2024
Enterocolic granulomatous phlebitis associated with epidermal growth factor-containing fibulin-like extracellular matrix protein 1 deposition and focal amyloid properties: A case reportShojiro Ichimata, Akane Aikawa, Naonori Sugishita, et al.
Neuropathology and Applied Neurobiology|April 18, 2024
Revisiting the relevance of Hirano bodies in neurodegenerative diseasesKoji Yoshida, Shelley L Forrest, Shojiro Ichimata, et al.
Journal of Clinical Medicine|March 19, 2020
Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart FailureKeiichi Hirono, Yukiko Hata, Nariaki Miyao, et al.
Biochemical and Biophysical Research Communications|September 28, 2013
Characterization of a novel mutant KCNQ1 channel subunit lacking a large part of the C-terminal domainKatsuya Kimoto, Koshi Kinoshita, Tomoki Yokoyama, et al.
Journal of Cardiovascular Electrophysiology|July 7, 2012
A novel missense mutation causing a G487R substitution in the S2-S3 loop of human ether-à-go-go-related gene channelKoshi Kinoshita, Yoshiaki Yamaguchi, Kohki Nishide, et al.
Heart Rhythm|January 19, 2016
SCN5A(K817E), a novel Brugada syndrome-associated mutation that alters the activation gating of NaV1.5 channelKoshi Kinoshita, Hiroyuki Takahashi, Yukiko Hata, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|January 15, 2014
Glycine/Serine polymorphism at position 38 influences KCNE1 subunit's modulatory actions on rapid and slow delayed rectifier K+ currentsYoshiaki Yamaguchi, Kohki Nishide, Mario Kato, et al.
Journal of the American Heart Association|September 1, 2017
A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular NoncompactionCe Wang, Yukiko Hata, Keiichi Hirono, et al.
Pageof 15