User profiles for J. D. Steimle

Jeffrey D Steimle

Baylor College of Medicine
Verified email at bcm.edu
Cited by 637

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 …

[HTML][HTML] De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects

…, S Reddy, D Bernstein, T Burns, JD Steimle… - PLoS …, 2016 - journals.plos.org
Congenital heart disease (CHD) has a complex genetic etiology, and recent studies suggest
that high penetrance de novo mutations may account for only a small fraction of disease. In …

[HTML][HTML] Foxf Genes Integrate Tbx5 and Hedgehog Pathways in the Second Heart Field for Cardiac Septation

…, JD Bosman, X Ren, JD Steimle… - PLoS …, 2014 - journals.plos.org
The Second Heart Field (SHF) has been implicated in several forms of congenital heart
disease (CHD), including atrioventricular septal defects (AVSDs). Identifying the SHF gene …

[PDF][PDF] The cardiac TBX5 interactome reveals a chromatin remodeling network essential for cardiac septation

L Waldron, JD Steimle, TM Greco, NC Gomez… - Developmental cell, 2016 - cell.com
Human mutations in the cardiac transcription factor gene TBX5 cause congenital heart
disease (CHD), although the underlying mechanism is unknown. We report characterization of …

Evolutionarily conserved Tbx5Wnt2/2b pathway orchestrates cardiopulmonary development

JD Steimle, SA Rankin, CE Slagle… - Proceedings of the …, 2018 - National Acad Sciences
Codevelopment of the lungs and heart underlies key evolutionary innovations in the transition
to terrestrial life. Cardiac specializations that support pulmonary circulation, including the …

Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms

O Burnicka-Turek, JD Steimle, W Huang… - Human molecular …, 2016 - academic.oup.com
Atrioventricular septal defects (AVSDs) are a common severe form of congenital heart
disease (CHD). In this study we identified deleterious non-synonymous mutations in two cilia …

Tbx5 drives Aldh1a2 expression to regulate a RA-Hedgehog-Wnt gene regulatory network coordinating cardiopulmonary development

SA Rankin, JD Steimle, XH Yang, AB Rydeen… - Elife, 2021 - elifesciences.org
… are essential for both heart and lung development (Steimle et al., 2018). Endodermal Hh
signals … - dissected cardiopulmonary progenitor (CPP) tissue based on bulk RNA- seq (Steimle

Transcriptional dysregulation underlies both monogenic arrhythmia syndrome and common modifiers of cardiac repolarization

…, AT Hale, DO Kryshtal, K Kim, JD Steimle, JD Brown… - Circulation, 2023 - Am Heart Assoc
… Drs Bersell and Parikh, and JD Steimle are supported by the National Heart, Lung, and …
Hale AT CB, York JD. Metabolic labeling of inositol phosphates and phosphatidylinositols in …

Transcriptional patterning of the ventricular cardiac conduction system

O Burnicka-Turek, MT Broman, JD Steimle… - Circulation …, 2020 - Am Heart Assoc
Rationale: The heartbeat is organized by the cardiac conduction system (CCS), a specialized
network of cardiomyocytes. Patterning of the CCS into atrial node versus ventricular …

[HTML][HTML] Decoding the PITX2-controlled genetic network in atrial fibrillation

JD Steimle, FJG Canozo, M Park, ZA Kadow… - Jci Insight, 2022 - ncbi.nlm.nih.gov
Atrial fibrillation (AF), the most common sustained cardiac arrhythmia and a major risk factor
for stroke, often arises through ectopic electrical impulses derived from the pulmonary veins (…