Cardiac malformations in Pdgfrα mutant embryos are associated with increased expression of WT1 and Nkx2.5 in the second heart field-Reference-Cited by-同舟云学术

Cardiac malformations in Pdgfrα mutant embryos are associated with increased expression of WT1 and Nkx2.5 in the second heart field

Published:2010-07-14 Issue:8 Volume:239 Page:2307-2317
ISSN:1058-8388
Container-title:Developmental Dynamics
language:en
Short-container-title:Dev. Dyn.

Author:

Bax Noortje A.M.,Bleyl Steven B.,Gallini Radiosa,Wisse Lambertus J.,Hunter Jennifer,Van Oorschot Angelique A.M.,Mahtab Edris A.F.,Lie-Venema Heleen,Goumans Marie-Jose,Betsholtz Christer,Gittenberger-de Groot Adriana C.

Publisher

Wiley

Subject

Developmental Biology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/dvdy.22363/fullpdf

Reference42 articles.

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2. Targeted mutation reveals essential functions of the homeodomain transcription factor Shox2 in sinoatrial and pacemaking development;Blaschke;Circulation,2007

3. Dysregulation of the PDGFRA gene causes inflow tract anomalies including TAPVR: integrating evidence from human genetics and model organisms;Bleyl;Hum Mol Genet,2010

4. Deficiency of the vestibular spine in atrioventricular septal defects in human fetuses with down syndrome;Blom;Am J Cardiol,2003

5. Formation of the venous pole of the heart from an Nkx2-5-negative precursor population requires Tbx18;Christoffels;Circ Res,2006

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