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Journal Abstract Search


148 related items for PubMed ID: 38749189

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  • 3. Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome.
    Ryckebüsch L, Bertrand N, Mesbah K, Bajolle F, Niederreither K, Kelly RG, Zaffran S.
    Circ Res; 2010 Mar 05; 106(4):686-94. PubMed ID: 20110535
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  • 8. 22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development.
    Scambler PJ.
    Pediatr Cardiol; 2010 Apr 05; 31(3):378-90. PubMed ID: 20054531
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  • 13. Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.
    Xu H, Morishima M, Wylie JN, Schwartz RJ, Bruneau BG, Lindsay EA, Baldini A.
    Development; 2004 Jul 05; 131(13):3217-27. PubMed ID: 15175244
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  • 17. Endothelial neuropilin disruption in mice causes DiGeorge syndrome-like malformations via mechanisms distinct to those caused by loss of Tbx1.
    Zhou J, Pashmforoush M, Sucov HM.
    PLoS One; 2012 Jul 05; 7(3):e32429. PubMed ID: 22396765
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  • 20. Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: genetic evidence of impaired tissue response to Fgf8.
    Vitelli F, Lania G, Huynh T, Baldini A.
    J Mol Cell Cardiol; 2010 Nov 05; 49(5):836-40. PubMed ID: 20807544
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