Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Futoshi Toyoda

Showing results (41-50 of 55) with videos related to

Pageof 6
Sort By:
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|April 15, 2014
Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypesMegumi Fukuyama, Qi Wang, Koichi Kato, et al.
Heart Rhythm|October 8, 2013
A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channelsKanae Hasegawa, Seiko Ohno, Takashi Ashihara, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 29, 2025
Afadin Promotes Vascular Smooth Muscle Cell Contraction by Interacting With Phospholipase C to Enhance Ca<sup>2+</sup> Signaling for Blood Pressure RegulationMd Mahbubur Rahman Khan, Akira Sato, Akio Shimizu, et al.
Scientific Reports|November 9, 2022
Gradient-based parameter optimization method to determine membrane ionic current composition in human induced pluripotent stem cell-derived cardiomyocytesHirohiko Kohjitani, Shigeya Koda, Yukiko Himeno, et al.
Japanese Journal of Ophthalmology|April 5, 2016
Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsiaKazuki Kuniyoshi, Sanae Muraki-Oda, Hisao Ueyama, et al.
Scientific Reports|February 17, 2018
A hERG mutation E1039X produced a synergistic lesion on I<sub>Ks</sub> together with KCNQ1-R174C mutation in a LQTS family with three compound mutationsJie Wu, Yuka Mizusawa, Seiko Ohno, et al.
Human Mutation|March 24, 2009
Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndromeSeiko Ohno, Futoshi Toyoda, Dimitar P Zankov, et al.
Circulation Research|December 25, 2010
Reciprocal control of hERG stability by Hsp70 and Hsc70 with implication for restoration of LQT2 mutant stabilityPeili Li, Haruaki Ninomiya, Yasutaka Kurata, et al.
Journal of the American College of Cardiology|August 22, 2009
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndromeYukiko Nishio, Takeru Makiyama, Hideki Itoh, et al.
The Journal of General Physiology|July 17, 2013
The G-protein-gated K+ channel, IKACh, is required for regulation of pacemaker activity and recovery of resting heart rate after sympathetic stimulationPietro Mesirca, Laurine Marger, Futoshi Toyoda, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|April 15, 2014
Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypesMegumi Fukuyama, Qi Wang, Koichi Kato, et al.
Heart Rhythm|October 8, 2013
A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channelsKanae Hasegawa, Seiko Ohno, Takashi Ashihara, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 29, 2025
Afadin Promotes Vascular Smooth Muscle Cell Contraction by Interacting With Phospholipase C to Enhance Ca<sup>2+</sup> Signaling for Blood Pressure RegulationMd Mahbubur Rahman Khan, Akira Sato, Akio Shimizu, et al.
Scientific Reports|November 9, 2022
Gradient-based parameter optimization method to determine membrane ionic current composition in human induced pluripotent stem cell-derived cardiomyocytesHirohiko Kohjitani, Shigeya Koda, Yukiko Himeno, et al.
Japanese Journal of Ophthalmology|April 5, 2016
Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsiaKazuki Kuniyoshi, Sanae Muraki-Oda, Hisao Ueyama, et al.
Scientific Reports|February 17, 2018
A hERG mutation E1039X produced a synergistic lesion on I<sub>Ks</sub> together with KCNQ1-R174C mutation in a LQTS family with three compound mutationsJie Wu, Yuka Mizusawa, Seiko Ohno, et al.
Human Mutation|March 24, 2009
Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndromeSeiko Ohno, Futoshi Toyoda, Dimitar P Zankov, et al.
Circulation Research|December 25, 2010
Reciprocal control of hERG stability by Hsp70 and Hsc70 with implication for restoration of LQT2 mutant stabilityPeili Li, Haruaki Ninomiya, Yasutaka Kurata, et al.
Journal of the American College of Cardiology|August 22, 2009
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndromeYukiko Nishio, Takeru Makiyama, Hideki Itoh, et al.
The Journal of General Physiology|July 17, 2013
The G-protein-gated K+ channel, IKACh, is required for regulation of pacemaker activity and recovery of resting heart rate after sympathetic stimulationPietro Mesirca, Laurine Marger, Futoshi Toyoda, et al.
Pageof 6