Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice
By E. Lindsay, F. Vitelli, H. Su, M. Morishima, Tuong Huynh, T. Pramparo, V. Jurecic, George Ogunrinu, H. Sutherland, P. Scambler and 2 more. Nature, 2001
1,000 citations recorded by the source corpus.
Subfields: Epidemiology, Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/3d9210072ce4283d155326a7787a5b49aac06534
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Citations in the corpus
- Essential Role for ADAM19 in Cardiovascular Morphogenesis (2004, background): “It will now be interesting to further explore potential functional connections between ADAM19 and these proteins as well as other molecules that are implicated in endocardial cushion transformation and/or conotruncal defects, such as RXR, smad6, and TBX1 (14, 16, 21, 31 , 35).”
- Recent advances in craniofacial morphogenesis (2006, background): “Tbx-1 mutant mice show failure to form caudal pouches, whereas the first pharyngeal pouch develops normally (Jerome and Papaioannou, 2001; Lindsay et al., 2001).”