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Elife|December 13, 2019
<i>Straightjacket/α2δ3</i> deregulation is associated with cardiac conduction defects in myotonic dystrophy type 1Emilie Auxerre-Plantié, Masayuki Nakamori, Yoan Renaud, et al.
Developmental Biology|October 11, 2003
Cortical and retinal defects caused by dosage-dependent reductions in VEGF-A paracrine signalingJody J Haigh, Paula I Morelli, Holger Gerhardt, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 1, 2016
14-3-3epsilon controls multiple developmental processes in the mouse heartAdriana C Gittenberger-de Groot, Tamara Hoppenbrouwers, Lucile Miquerol, et al.
Developmental Biology|January 26, 2007
Nkx2.5 cell-autonomous gene function is required for the postnatal formation of the peripheral ventricular conduction systemSonia Meysen, Laurine Marger, Kenneth W Hewett, et al.
Circulation|October 6, 2005
Discontinuous conduction in mouse bundle branches is caused by bundle-branch architectureToon A B van Veen, Harold V M van Rijen, Marjan J A van Kempen, et al.
Circulation|August 15, 2020
A Notch3-Marked Subpopulation of Vascular Smooth Muscle Cells Is the Cell of Origin for Occlusive Pulmonary Vascular LesionsLea C Steffes, Alexis A Froistad, Adam Andruska, et al.
Development (Cambridge, England)|July 26, 2018
Embryonic Tbx3<sup>+</sup> cardiomyocytes form the mature cardiac conduction system by progressive fate restrictionRajiv A Mohan, Mathilda T M Mommersteeg, Jorge N Domínguez, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 30, 2016
Interaction Between ALK1 Signaling and Connexin40 in the Development of Arteriovenous MalformationsKonstantinos Gkatzis, Jérémy Thalgott, Damien Dos-Santos-Luis, et al.
Plos Genetics|July 7, 2018
Deletion of Nkx2-5 in trabecular myocardium reveals the developmental origins of pathological heterogeneity associated with ventricular non-compaction cardiomyopathyCaroline Choquet, Thi Hong Minh Nguyen, Pierre Sicard, et al.
Circulation Research|June 1, 2012
Epistatic rescue of Nkx2.5 adult cardiac conduction disease phenotypes by prospero-related homeobox protein 1 and HDAC3Catherine A Risebro, Louisa K Petchey, Nicola Smart, et al.
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