Related references
Note: Only part of the references are listed.Gatecholaminergic polymorphic ventricular tachycardia-related mutations R33Q and L167H alter calcium sensitivity of human cardiac calsequestrin
Giorgia Valle et al.
BIOCHEMICAL JOURNAL (2008)
Luminal Ca2+ regulation of single cardiac ryanodine receptors:: Insights provided by calsequestrin and its mutants
Jia Qin et al.
JOURNAL OF GENERAL PHYSIOLOGY (2008)
Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardia
Marina Cerrone et al.
CIRCULATION RESEARCH (2007)
Characterization of human cardiac calsequestrin and its deleterious mutants
EunJung Kim et al.
JOURNAL OF MOLECULAR BIOLOGY (2007)
Modest reductions of cardiac calsequestrin increase sarcoplasmic reticulum Ca2+ leak independent of luminal Ca2+ and trigger ventricular arrhythmias in mice
Nagesh Chopra et al.
CIRCULATION RESEARCH (2007)
Comparison of the profiles of postoperative systemic Hemodynamics and oxygen transport in Neonates after the hybrid or the norwood procedure - A pilot study
Jia Li et al.
CIRCULATION (2007)
Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia
Lei Song et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Different endoplasmic reticulum trafficking and processing pathways for calsequestrin (CSQ) and epitope-tagged CSQ
Timothy D. Houle et al.
EXPERIMENTAL CELL RESEARCH (2006)
Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia
Marina Raffaele di Barletta et al.
CIRCULATION (2006)
Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia - Insights from a RyR2 R4496C knock-in mouse model
Nian Liu et al.
CIRCULATION RESEARCH (2006)
Abnormal interactions of calsequestrin with the ryanodine receptor calcium release channel complex linked to exercise-induced sudden cardiac death
Dmitry Terentyev et al.
CIRCULATION RESEARCH (2006)
Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor
M Cerrone et al.
CIRCULATION RESEARCH (2005)
Navigating the signalling network in mouse cardiac myocytes
GR Sambrano et al.
NATURE (2002)
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia
AV Postma et al.
CIRCULATION RESEARCH (2002)
Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia
SG Priori et al.
CIRCULATION (2002)
Electroanatomic mapping of arrhythmogenic right ventricular dysplasia
N Boulos et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2001)
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel
H Lahat et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Share Paper
