Related references
Note: Only part of the references are listed.RyR2 regulates Cx43 hemichannel intracellular Ca2+-dependent activation in cardiomyocytes
Alessio Lissoni et al.
CARDIOVASCULAR RESEARCH (2021)
Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction disease
Ruo-Gu Li et al.
HEART RHYTHM (2021)
KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy
Ning Li et al.
GENES (2021)
PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation
Xiao-Juan Guo et al.
JOURNAL OF THE AMERICAN HEART ASSOCIATION (2021)
Remodeling of Cardiac Gap Junctional Cell-Cell Coupling
Stefan Dhein et al.
CELLS (2021)
Metastable Atrial State Underlies the Primary Genetic Substrate for MYL4 Mutation-Associated Atrial Fibrillation
Zaniar Ghazizadeh et al.
CIRCULATION (2020)
EHD1 Modulates Cx43 Gap Junction Remodeling Associated With Cardiac Diseases
Tania Martins-Marques et al.
CIRCULATION RESEARCH (2020)
ISL1 loss-of-function variation causes familial atrial fibrillation
Shao-Hui Wu et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2020)
Genetics and Epigenetics of Atrial Fibrillation
Estefania Lozano-Velasco et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2020)
Cardiac β-adrenergic receptor activation mediates distinct and cell type-dependent changes in the expression and distribution of connexin 43
Yi Zhang et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2020)
Golgi Fragmentation in Human Patients with Chronic Atrial Fibrillation: A New Aspect of Remodeling
Luisa Jungk et al.
THORACIC AND CARDIOVASCULAR SURGEON (2019)
Heart Disease and Stroke Statistics-2019 Update A Report From the American Heart Association
Emelia J. Benjamin et al.
CIRCULATION (2019)
Mutation in NPPA causes atrial fibrillation by activating inflammation and cardiac fibrosis in a knock-in rat model
Chen Cheng et al.
FASEB JOURNAL (2019)
Mechanisms of atrial fibrillation
Rohan S. Wijesurendra et al.
HEART (2019)
A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation
Asma Mechakra et al.
AMERICAN JOURNAL OF CARDIOLOGY (2019)
Lamin A mutation impairs interaction with nucleoporin NUP155 and disrupts nucleocytoplasmic transport in atrial fibrillation
Meng Han et al.
HUMAN MUTATION (2019)
Gap junction gene and protein families: Connexins, innexins, and pannexins
Eric C. Beyer et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2018)
Functional Characterization of Novel Atrial Fibrillation-Linked GJA5 (Cx40) Mutants
Mahmoud Noureldin et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2018)
Differential Association of Cx37 and Cx40 Genetic Variants in Atrial Fibrillation with and without Underlying Structural Heart Disease
Sebastian Carballo et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2018)
A SHOX2 loss-of-function mutation underlying familial atrial fibrillation
Ning Li et al.
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES (2018)
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation
Akiko Seki et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2017)
Intercalated disc in failing hearts from patients with dilated cardiomyopathy: Its role in the depressed left ventricular function
Ana Ortega et al.
PLOS ONE (2017)
Cardiac Cx43, Cx40 and Cx45 co-assembling: involvement of connexins epitopes in formation of hemichannels and Gap junction channels
Thomas Desplantez
BMC CELL BIOLOGY (2017)
Atrial Fibrillation Epidemiology, Pathophysiology, and Clinical Outcomes
Laila Staerk et al.
CIRCULATION RESEARCH (2017)
TBX5 mutations contribute to early-onset atrial fibrillation in Chinese and Caucasians
Ji-Fang Ma et al.
CARDIOVASCULAR RESEARCH (2016)
TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome
Dong-Feng Guo et al.
MOLECULAR MEDICINE REPORTS (2016)
A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation
Nathan Orr et al.
NATURE COMMUNICATIONS (2016)
Genetic basis of atrial fibrillation
Oscar Campuzano et al.
GENES & DISEASES (2016)
Combining Foxc2 and Connexin37 deletions in mice leads to severe defects in lymphatic vascular growth and remodeling
John D. Kanady et al.
DEVELOPMENTAL BIOLOGY (2015)
Mutations in cardiovascular connexin genes
Filippo Molica et al.
BIOLOGY OF THE CELL (2014)
2014 AHA/ACC/HRS Guideline for the Management of Patients With Atrial Fibrillation A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the Heart Rhythm Society
Craig T. January et al.
CIRCULATION (2014)
An atrial-fibrillation-linked connexin40 mutant is retained in the endoplasmic reticulum and impairs the function of atrial gap-junction channels
Yiguo Sun et al.
DISEASE MODELS & MECHANISMS (2014)
A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation
Jun Wang et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2014)
Association of Connexin37 C1019T with myocardial infarction and coronary artery disease: a meta-analysis
Dan Wen et al.
EXPERIMENTAL GERONTOLOGY (2014)
Hunting for connexin hemichannels
Juan C. Saez et al.
FEBS LETTERS (2014)
Cx37 C1019T Polymorphism May Contribute to the Pathogenesis of Coronary Heart Disease
Long Zhao et al.
GENETIC TESTING AND MOLECULAR BIOMARKERS (2014)
Connexin40 abnormalities and atrial fibrillation in the human heart
Joanna Gemel et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2014)
Atrial Fibrillation-Linked Germline GJA5/Connexin40 Mutants Showed an Increased Hemichannel Function
Yiguo Sun et al.
PLOS ONE (2014)
Regulation of connexin expression by transcription factors and epigenetic mechanisms
Masahito Oyamada et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2013)
Rare Variants in GJA5 Are Associated With Early-Onset Lone Atrial Fibrillation
Ingrid E. Christophersen et al.
CANADIAN JOURNAL OF CARDIOLOGY (2013)
c-Jun N-terminal kinase activation contributes to reduced connexin43 and development of atrial arrhythmias
Jiajie Yan et al.
CARDIOVASCULAR RESEARCH (2013)
Absence of venous valves in mice lacking Connexin37
Stephanie J. Munger et al.
DEVELOPMENTAL BIOLOGY (2013)
The Connexin40A96S mutation from a patient with atrial fibrillation causes decreased atrial conduction velocities and sustained episodes of induced atrial fibrillation in mice
Indra Luebkemeier et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2013)
Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation
Hai-Feng Shi et al.
MOLECULAR MEDICINE REPORTS (2013)
Association between C1019T polymorphism of the connexin37 gene and coronary heart disease in patients with in-stent restenosis
Su-Xia Guo et al.
EXPERIMENTAL AND THERAPEUTIC MEDICINE (2013)
Connexins and Atrial Fibrillation Filling in the Gaps
Takeshi Kato et al.
CIRCULATION (2012)
Connexin Gene Transfer Preserves Conduction Velocity and Prevents Atrial Fibrillation
Tomonori Igarashi et al.
CIRCULATION (2012)
Connexin45 Provides Optimal Atrioventricular Nodal Conduction in the Adult Mouse Heart
Marina Frank et al.
CIRCULATION RESEARCH (2012)
Cardiac connexins, mutations and arrhythmias
Mario Delmar et al.
CURRENT OPINION IN CARDIOLOGY (2012)
On the different roles of AT1 and AT2 receptors in stretch-induced changes of connexin43 expression and localisation
Aida Salameh et al.
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2012)
Genetic variants of connexin37 are associated with carotid intima-medial thickness and future onset of ischemic stroke
Hsin-Bang Leu et al.
ATHEROSCLEROSIS (2011)
Effects of metoprolol therapy on cardiac gap junction remodelling and conduction in human chronic atrial fibrillation
S. Dhein et al.
BRITISH JOURNAL OF PHARMACOLOGY (2011)
2011 ACCF/AHA/HRS Focused Updates Incorporated into the ACC/AHA/ESC 2006 Guidelines for the Management of Patients with Atrial Fibrillation
Valentin Fuster et al.
CIRCULATION (2011)
A Peptide Mimetic of the Connexin43 Carboxyl Terminus Reduces Gap Junction Remodeling and Induced Arrhythmia Following Ventricular Injury
Michael P. O'Quinn et al.
CIRCULATION RESEARCH (2011)
A Common Connexin-40 Gene Promoter Variant Affects Connexin-40 Expression in Human Atria and Is Associated With Atrial Fibrillation
Robert C. Wirka et al.
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY (2011)
Paradigm of Genetic Mosaicism and Lone Atrial Fibrillation Physiological Characterization of a Connexin 43-Deletion Mutant Identified From Atrial Tissue
Isabelle L. Thibodeau et al.
CIRCULATION (2010)
Novel connexin40 missense mutations in patients with familial atrial fibrillation
Yi-Qing Yang et al.
EUROPACE (2010)
Connexin40 nonsense mutation in familial atrial fibrillation
Yi-Qing Yang et al.
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE (2010)
The role of connexin40 in atrial fibrillation
Sevasti-Maria Chaldoupi et al.
CARDIOVASCULAR RESEARCH (2009)
Association Between the Connexin37 Polymorphism and Peripheral Arterial Disease in Subjects With Type 2 Diabetes
N. Katakami et al.
DIABETES CARE (2009)
Functional differences between human Cx37 polymorphic hemichannels
Jean-Paul Derouette et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2009)
Gap Junctions
Daniel A. Goodenough et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2009)
Molecular basis of cardiac action potential repolarization
Yoram Rudy
CONTROL AND REGULATION OF TRANSPORT PHENOMENA IN THE CARDIAC SYSTEM (2008)
Remodelling of gap junctions and connexin expression in diseased myocardium
Nicholas J. Severs et al.
CARDIOVASCULAR RESEARCH (2008)
Is there a role for remodeled connexins in AF? No simple answers
Heather S. Duffy et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2008)
Dynamic ATP signalling and neural development
Nicholas Dale
JOURNAL OF PHYSIOLOGY-LONDON (2008)
The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans
Radoslaw Dobrowolski et al.
HUMAN MOLECULAR GENETICS (2008)
Myocardial Gap Junctions: Targets for Novel Approaches in the Prevention of Life-Threatening Cardiac Arrhythmias
N. Tribulova et al.
PHYSIOLOGICAL RESEARCH (2008)
Gap junction remodeling and cardiac arrhythmogenesis in a murine model of oculodentodigital dysplasia
Nellie Kalcheva et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Gating properties of heterotypic gap junction channels formed of connexins 40, 43, 45
Mindaugas Rackauskas et al.
BIOPHYSICAL JOURNAL (2007)
The association of human connexin 40 genetic polymorphisms with atrial fibrillation
Jyh-Ming Juang et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2007)
Model-dependent effects of the gap junction conduction-enhancing antiarrhythmic peptide rotigaptide (ZP123) on experimental atrial fibrillation in dogs
Akiko Shiroshita-Takeshita et al.
CIRCULATION (2007)
Do allelic variants of the connexin37 1019 gene polymorphism differentially predict for coronary artery disease and myocardial infarction?
Cindy W. Wong et al.
ATHEROSCLEROSIS (2007)
Connexin37 1019 gene polymorphism in myocardial infarction patients and centenarians
Florinda Listi et al.
ATHEROSCLEROSIS (2007)
Chronic hemodynamic overload of the atria is an important factor for gap junction remodeling in human and rat hearts
Catherine Rucker-Martin et al.
CARDIOVASCULAR RESEARCH (2006)
Connexin37 protects against atherosclerosis by regulating monocyte adhesion
Cindy W. Wong et al.
NATURE MEDICINE (2006)
Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation
Michael H. Gollob et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Cardiac connexins as candidate genes for idiopathic atrial fibrillation
Michael H. Gollob
CURRENT OPINION IN CARDIOLOGY (2006)
Expression of connexins 40 and 43 in human left atrium in atrial fibrillation of different aetiologies
U Wetzel et al.
HEART (2005)
Basic mechanisms of cardiac impulse propagation and associated arrhythmias
AG Kléber et al.
PHYSIOLOGICAL REVIEWS (2004)
Relationship between connexins and atrial activation during human atrial fibrillation
P Kanagaratnam et al.
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY (2004)
Connexin 48.5 is required for normal cardiovascular function and lens development in zebrafish embryos
SH Cheng et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation
M Firouzi et al.
CIRCULATION RESEARCH (2004)
Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring
CS Fox et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2004)
Gap junction alterations in human cardiac disease
NJ Severs et al.
CARDIOVASCULAR RESEARCH (2004)
Role of gap junctions in the propagation of the cardiac action potential
S Rohr
CARDIOVASCULAR RESEARCH (2004)
Pharmacological characterization of the new stable antiarrhythmic peptide analog Ac-D-Tyr-D-Pro-D-Hyp-Gly-D-Ala-Gly-NH2 (ZP123):: In vivo and in vitro studies
AL Kjolbye et al.
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS (2003)
High incidence of cardiac malformations in connexin40-deficient mice
H Gu et al.
CIRCULATION RESEARCH (2003)
Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia
WA Paznekas et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Cardiac gap junctions and connexins: their role in atrial fibrillation and potential as therapeutic targets
HMW van der Velden et al.
CARDIOVASCULAR RESEARCH (2002)
Structural correlate of atrial fibrillation in human patients
S Kostin et al.
CARDIOVASCULAR RESEARCH (2002)
Gap junction channels formed by coexpressed connexin40 and connexin43
V Valiunas et al.
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY (2001)
Heterogeneous expression of gap junction channels in the heart leads to conduction defects and ventricular dysfunction
DE Gutstein et al.
CIRCULATION (2001)
Effects of chronic atrial fibrillation on gap junction distribution in human and rat atria
L Polontchouk et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2001)
Prevalence of diagnosed atrial fibrillation in adults - National implications for rhythm management and stroke prevention: the AnTicoagulation and Risk Factors in Atrial Fibrillation (ATRIA) study
AS Go et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2001)
Functional expression and biophysical properties of polymorphic variants of the human gap junction protein connexin37
SS Kumari et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2000)
Share Paper
