TBX5: a key regulator of heart development

JD Steimle, IP Moskowitz - Current topics in developmental biology, 2017 - Elsevier
TBX5 is a member of the T-box transcription factor family and is primarily known for its role in
cardiac and forelimb development. Human patients with dominant mutations in TBX5 are …

Overview of high throughput sequencing technologies to elucidate molecular pathways in cardiovascular diseases

JM Churko, GL Mantalas, MP Snyder, JC Wu - Circulation research, 2013 - Am Heart Assoc
High throughput sequencing technologies have become essential in studies on genomics,
epigenomics, and transcriptomics. Although sequencing information has traditionally been …

Genomic analyses implicate noncoding de novo variants in congenital heart disease

F Richter, SU Morton, SW Kim, A Kitaygorodsky… - Nature …, 2020 - nature.com
A genetic etiology is identified for one-third of patients with congenital heart disease (CHD),
with 8% of cases attributable to coding de novo variants (DNVs). To assess the contribution …

Negative regulation of ABA signaling by WRKY33 is critical for Arabidopsis immunity towards Botrytis cinerea 2100

S Liu, B Kracher, J Ziegler, RP Birkenbihl, IE Somssich - elife, 2015 - elifesciences.org
The Arabidopsis mutant wrky33 is highly susceptible to Botrytis cinerea. We identified> 1680
Botrytis-induced WRKY33 binding sites associated with 1576 Arabidopsis genes …

PRDM16 is a compact myocardium-enriched transcription factor required to maintain compact myocardial cardiomyocyte identity in left ventricle

T Wu, Z Liang, Z Zhang, C Liu, L Zhang, Y Gu… - Circulation, 2022 - Am Heart Assoc
Background: Left ventricular noncompaction cardiomyopathy (LVNC) was discovered half a
century ago as a cardiomyopathy with excessive trabeculation and a thin ventricular wall. In …

Complex interdependence regulates heterotypic transcription factor distribution and coordinates cardiogenesis

L Luna-Zurita, CU Stirnimann, S Glatt, BL Kaynak… - Cell, 2016 - cell.com
Transcription factors (TFs) are thought to function with partners to achieve specificity and
precise quantitative outputs. In the developing heart, heterotypic TF interactions, such as …

A promoter interaction map for cardiovascular disease genetics

LE Montefiori, DR Sobreira, NJ Sakabe, I Aneas… - Elife, 2018 - elifesciences.org
Over 500 genetic loci have been associated with risk of cardiovascular diseases (CVDs);
however, most loci are located in gene-distal non-coding regions and their target genes are …

A common genetic variant within SCN10A modulates cardiac SCN5A expression

M Van Den Boogaard, S Smemo… - The Journal of …, 2014 - Am Soc Clin Investig
Variants in SCN10A, which encodes a voltage-gated sodium channel, are associated with
alterations of cardiac conduction parameters and the cardiac rhythm disorder Brugada …

iPSC-derived cardiomyocytes reveal abnormal TGF-β signalling in left ventricular non-compaction cardiomyopathy

K Kodo, SG Ong, F Jahanbani, V Termglinchan… - Nature cell …, 2016 - nature.com
Left ventricular non-compaction (LVNC) is the third most prevalent cardiomyopathy in
children and its pathogenesis has been associated with the developmental defect of the …

Overexpression of Tbx20 in adult cardiomyocytes promotes proliferation and improves cardiac function after myocardial infarction

F Xiang, M Guo, KE Yutzey - Circulation, 2016 - Am Heart Assoc
Background—Adult mammalian cardiomyocytes (CMs) have the potential to proliferate, but
this is not sufficient to generate adequate CMs after myocardial infarction (MI). The …