Associated Papers
Connexin Mutations and Hereditary Diseases.
Qiu Y et al.
International Journal of Molecular Sciences, 2022
Atrial Fibrillation: Focus on Myocardial Connexins and Gap Junctions.
Guo YH et al.
Biology, 2022
Cytoskeletal Protein Variants Driving Atrial Fibrillation: Potential Mechanisms of Action.
van Wijk SW et al.
Cells, 2022
Functional Characterization of Novel Atrial Fibrillation-Linked GJA5 (Cx40) Mutants.
Noureldin M et al.
International Journal of Molecular Sciences, 2018
Mechanisms linking connexin mutations to human diseases.
Kelly JJ et al.
Cell and Tissue Research, 2015
Degradation of a connexin40 mutant linked to atrial fibrillation is accelerated.
Gemel J et al.
Journal of Molecular and Cellular Cardiology, 2014
An atrial-fibrillation-linked connexin40 mutant is retained in the endoplasmic reticulum and impairs the function of atrial gap-junction channels.
Sun Y et al.
Disease Models & Mechanisms, 2014
Atrial fibrillation-linked GJA5/connexin40 mutants impaired gap junctions via different mechanisms.
Bai D
Febs Letters, 2014
Atrial fibrillation-linked germline GJA5/connexin40 mutants showed an increased hemichannel function.
Sun Y et al.
Plos One, 2014
Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation.
Shi HF et al.
Molecular Medicine Reports, 2013
[Genetic predictors of sick sinus node syndrome].
Chernova AA et al.
Kardiologiia, 2013
Novel connexin40 missense mutations in patients with familial atrial fibrillation.
Yang YQ et al.
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, 2010
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