Pitx2 modulates a Tbx5-dependent gene regulatory network to maintain atrial rhythm

RD Nadadur, MT Broman, B Boukens… - Science translational …, 2016 - science.org
Cardiac rhythm is extremely robust, generating 2 billion contraction cycles during the
average human life span. Transcriptional control of cardiac rhythm is poorly understood. We …

[HTML][HTML] The role of transcription factors in atrial fibrillation

M Zhou, Y Liao, X Tu - Journal of thoracic disease, 2015 - ncbi.nlm.nih.gov
Atrial fibrillation (AF) is a complex disease that results from genetic and environmental
factors and their interactions. In recent years, genome-wide association studies (GWAS) and …

Atrial fibrillation risk loci interact to modulate Ca2+-dependent atrial rhythm homeostasis

B Laforest, W Dai, L Tyan, S Lazarevic… - The Journal of …, 2019 - Am Soc Clin Investig
Atrial fibrillation (AF), defined by disorganized atrial cardiac rhythm, is the most prevalent
cardiac arrhythmia worldwide. Recent genetic studies have highlighted a major heritable …

[HTML][HTML] TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy

XL Zhang, XB Qiu, F Yuan, J Wang, CM Zhao… - Biochemical and …, 2015 - Elsevier
The cardiac T-box transcription factor TBX5 is crucial for proper cardiovascular
development, and mutations in TBX5 have been associated with various congenital heart …

TBX5 mutations contribute to early-onset atrial fibrillation in Chinese and Caucasians

JF Ma, F Yang, SN Mahida, L Zhao… - Cardiovascular …, 2016 - academic.oup.com
Aims Atrial fibrillation (AF) is a common arrhythmia with an important heritable aspect. The
genetic factors underlying AF have not been fully elucidated. Methods and results We …

Mog1 knockout causes cardiac hypertrophy and heart failure by downregulating tbx5‐cryab‐hspb2 signalling in zebrafish

D Gou, J Zhou, Q Song, Z Wang, X Bai… - Acta …, 2021 - Wiley Online Library
Aims MOG1 is a small protein that can bind to small GTPase RAN and regulate transport of
RNA and proteins between the cytoplasm and nucleus. However, the in vivo physiological …

[HTML][HTML] TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome

DF Guo, RG Li, F Yuan, HY Shi… - Molecular …, 2016 - spandidos-publications.com
Previous genome-wide association studies have demonstrated that single nucleotide
polymorphisms in T‑box (TBX) 5 are associated with increased susceptibility to atrial …

Ionic and cellular mechanisms underlying TBX5/PITX2 insufficiency-induced atrial fibrillation: Insights from mathematical models of human atrial cells

J Bai, PA Gladding, MK Stiles, VV Fedorov, J Zhao - Scientific reports, 2018 - nature.com
Transcription factors TBX5 and PITX2 involve in the regulation of gene expression of ion
channels and are closely associated with atrial fibrillation (AF), the most common cardiac …

A TBX5 3′ UTR variant increases the risk of congenital heart disease in the Han Chinese population

F Wang, D Liu, RR Zhang, LW Yu, JY Zhao, XY Yang… - Cell discovery, 2017 - nature.com
TBX5 is a vital transcription factor involved in cardiac development in a dosage-dependent
manner. But little is known about the potential association of TBX5 3′ untranslated region …

Pathophysiology of idiopathic atrial fibrillation-prognostic and treatment implications

B Weijs, U Schotten, H Crijns - Current pharmaceutical design, 2015 - ingentaconnect.com
The term idiopathic or lone atrial fibrillation (AF) is commonly used in the young and
apparently healthy individual who suffers from AF. Although there is conflicting evidence …