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Journal of Molecular and Cellular Cardiology
Volume 49, Issue 5
, Pages 836-840
, November 2010
Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: Genetic evidence of impaired tissue response to Fgf8
References
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- . A genetic link between Tbx1 and fibroblast growth factor signaling. Development. 2002;129:4605–4611
- . Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants. Dev. Biol. 2006;295:559–570
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- . Frs2alpha-deficiency in cardiac progenitors disrupts a subset of FGF signals required for outflow tract morphogenesis. Development. 2008;135:3611–3622
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PII: S0022-2828(10)00326-3
doi: 10.1016/j.yjmcc.2010.08.023
© 2010 Elsevier Ltd. All rights reserved.
« Previous
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Journal of Molecular and Cellular Cardiology
Volume 49, Issue 5
, Pages 836-840
, November 2010
