DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

By Loydie A. Jerome, V. Papaioannou. Nature Genetics, 2001

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Transcriptional mechanisms regulating skeletal muscle differentiation, growth and homeostasis (2011, background): “TBX1 mutants also suffer from impaired myogenesis in the first branchial arch and lack the muscles that normally originate from other arches owing to severe malformations of these structure”
Fiber types in mammalian skeletal muscles. (2011, background): “Pitx2 null embryos lack EOMs (248, 415), and branchial arch myogenesis is impaired in Tbx1 mutants (380, 403).”
Building the mammalian heart from two sources of myocardial cells (2005, neutral): “fcgi?db=gene&cmd=Retrieve&dopt=full_report&list_uids=21380"> Tbx1 (T-box 1) mutant mic”
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).”