Search research articles
Contact Us
Filters
Showing results (81-90 of 117) with videos related to
Page
of 12
Sort By:
Journal of Cardiology
|
November 18, 2017
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome
Daisuke Fukumoto, Wei-Guang Ding, Yuko Wada, et al.
Heart Rhythm
|
March 9, 2010
High prevalence of early repolarization in short QT syndrome
Hiroshi Watanabe, Takeru Makiyama, Taku Koyama, et al.
Frontiers in Physiology
|
August 5, 2024
Novel <i>KCNQ1</i> Q234K variant, identified in patients with long QT syndrome and epileptiform activity, induces both gain- and loss-of-function of slowly activating delayed rectifier potassium currents
Tadashi Nakajima, Shuntaro Tamura, Reika Kawabata-Iwakawa, 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 mutations
Jie Wu, Yuka Mizusawa, Seiko Ohno, et al.
Journal of the American Heart Association
|
August 20, 2020
Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1
Hideki Itoh, Takashi Hisamatsu, Takuhisa Tamura, et al.
Nature Communications
|
November 28, 2019
Neonatal Wnt-dependent Lgr5 positive stem cells are essential for uterine gland development
Ryo Seishima, Carly Leung, Swathi Yada, et al.
Journal of Cardiovascular Electrophysiology
|
January 10, 2014
Gain-of-function KCNH2 mutations in patients with Brugada syndrome
Q I Wang, Seiko Ohno, Wei-Guang Ding, et al.
The Journal of General Physiology
|
May 19, 2020
Single-cell temperature mapping with fluorescent thermometer nanosheets
Kotaro Oyama, Mizuho Gotoh, Yuji Hosaka, et al.
JACC. Clinical Electrophysiology
|
May 17, 2018
Impact of Updated Diagnostic Criteria for Long QT Syndrome on Clinical Detection of Diseased Patients: Results From a Study of Patients Carrying Gene Mutations
Kenshi Hayashi, Tetsuo Konno, Noboru Fujino, et al.
Journal of Cardiology
|
November 7, 2016
Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote
Yusuke Fujii, Yuichi Matsumoto, Kenshi Hayashi, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 117) with videos related to
Sort By:
Page
of 12
Journal of Cardiology
|
November 18, 2017
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome
Daisuke Fukumoto, Wei-Guang Ding, Yuko Wada, et al.
Heart Rhythm
|
March 9, 2010
High prevalence of early repolarization in short QT syndrome
Hiroshi Watanabe, Takeru Makiyama, Taku Koyama, et al.
Frontiers in Physiology
|
August 5, 2024
Novel <i>KCNQ1</i> Q234K variant, identified in patients with long QT syndrome and epileptiform activity, induces both gain- and loss-of-function of slowly activating delayed rectifier potassium currents
Tadashi Nakajima, Shuntaro Tamura, Reika Kawabata-Iwakawa, 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 mutations
Jie Wu, Yuka Mizusawa, Seiko Ohno, et al.
Journal of the American Heart Association
|
August 20, 2020
Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1
Hideki Itoh, Takashi Hisamatsu, Takuhisa Tamura, et al.
Nature Communications
|
November 28, 2019
Neonatal Wnt-dependent Lgr5 positive stem cells are essential for uterine gland development
Ryo Seishima, Carly Leung, Swathi Yada, et al.
Journal of Cardiovascular Electrophysiology
|
January 10, 2014
Gain-of-function KCNH2 mutations in patients with Brugada syndrome
Q I Wang, Seiko Ohno, Wei-Guang Ding, et al.
The Journal of General Physiology
|
May 19, 2020
Single-cell temperature mapping with fluorescent thermometer nanosheets
Kotaro Oyama, Mizuho Gotoh, Yuji Hosaka, et al.
JACC. Clinical Electrophysiology
|
May 17, 2018
Impact of Updated Diagnostic Criteria for Long QT Syndrome on Clinical Detection of Diseased Patients: Results From a Study of Patients Carrying Gene Mutations
Kenshi Hayashi, Tetsuo Konno, Noboru Fujino, et al.
Journal of Cardiology
|
November 7, 2016
Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote
Yusuke Fujii, Yuichi Matsumoto, Kenshi Hayashi, et al.
Page
of 12