Novel connexin40 missense mutations in patients with familial atrial fibrillation.
about
Emerging directions in the genetics of atrial fibrillationTargeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.A contemporary review on the genetic basis of atrial fibrillation.Degradation of a connexin40 mutant linked to atrial fibrillation is accelerated.Mutations in cardiovascular connexin genes.Low prevalence of connexin-40 gene variants in atrial tissues and blood from atrial fibrillation subjectsConnexin40 abnormalities and atrial fibrillation in the human heartAtrial fibrillation-linked germline GJA5/connexin40 mutants showed an increased hemichannel functionMolecular mechanisms regulating formation, trafficking and processing of annular gap junctions.Association of angiotensin-converting enzyme gene I/D and CYP11B2 gene -344T/C polymorphisms with lone atrial fibrillation and its recurrence after catheter ablationA variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot.Genetic mechanisms of atrial fibrillation: impact on response to treatmentThe presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability.Atrial fibrillation: the role of common and rare genetic variants.Interfering amino terminal peptides and functional implications for heteromeric gap junction formation.Atrial fibrillation-linked GJA5/connexin40 mutants impaired gap junctions via different mechanisms.Genetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice.Connexin Remodeling Contributes to Atrial Fibrillation.Atrial fibrillation-associated connexin40 mutants make hemichannels and synergistically form gap junction channels with novel properties.Genotype influence in responses to therapy for atrial fibrillation.An atrial-fibrillation-linked connexin40 mutant is retained in the endoplasmic reticulum and impairs the function of atrial gap-junction channelsHuman diseases associated with connexin mutations.Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation.Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation FamilyConnexins in Cardiovascular and Neurovascular Health and Disease: Pharmacological Implications.Role of Non-Myocyte Gap Junctions and Connexin Hemichannels in Cardiovascular Health and Disease: Novel Therapeutic Targets?Functional Characterization of Novel Atrial Fibrillation-Linked GJA5 (Cx40) Mutants.Familial clustering of atrial fibrillation and comparative longitudinal outcomes of familial and non-familial atrial fibrillation
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P2860
Novel connexin40 missense mutations in patients with familial atrial fibrillation.
description
2010 nî lūn-bûn
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2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
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2010年學術文章
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name
Novel connexin40 missense mutations in patients with familial atrial fibrillation.
@en
Novel connexin40 missense mutations in patients with familial atrial fibrillation.
@nl
type
label
Novel connexin40 missense mutations in patients with familial atrial fibrillation.
@en
Novel connexin40 missense mutations in patients with familial atrial fibrillation.
@nl
prefLabel
Novel connexin40 missense mutations in patients with familial atrial fibrillation.
@en
Novel connexin40 missense mutations in patients with familial atrial fibrillation.
@nl
P2093
P2860
P356
P1433
P1476
Novel connexin40 missense mutations in patients with familial atrial fibrillation.
@en
P2093
Hai-Feng Shi
Hong-Wei Tan
Wei-Feng Jiang
Wei-Yi Fang
Xian-Ling Zhang
Xin-Hua Wang
Yi-Qing Yang
P2860
P304
P356
10.1093/EUROPACE/EUQ274
P577
2010-07-21T00:00:00Z