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Journal Abstract Search

218 related items for PubMed ID: 15917203

  • 41. Tbx1: Transcriptional and Developmental Functions.
    Baldini A, Fulcoli FG, Illingworth E.
    Curr Top Dev Biol; 2017; 122():223-243. PubMed ID: 28057265
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  • 48. Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndrome.
    Gao S, Li X, Amendt BA.
    Curr Allergy Asthma Rep; 2013 Dec; 13(6):613-21. PubMed ID: 23996541
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  • 49. Microduplication 22q11.2: a new chromosomal syndrome.
    Portnoï MF.
    Eur J Med Genet; 2009 Dec; 52(2-3):88-93. PubMed ID: 19254783
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  • 52. Significant improvement of cardiac outflow tract septation defects in a DiGeorge syndrome model after minoxidil treatment.
    Aurigemma I, Ferrentino R, Krishnan VP, Lanzetta O, Angelini C, Illingworth E, Baldini A.
    Biochem Biophys Res Commun; 2024 Aug 06; 720():150104. PubMed ID: 38749189
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  • 55. Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes.
    Taddei I, Morishima M, Huynh T, Lindsay EA.
    Proc Natl Acad Sci U S A; 2001 Sep 25; 98(20):11428-31. PubMed ID: 11562466
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  • 56. Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick.
    Roberts C, Ivins S, Cook AC, Baldini A, Scambler PJ.
    Hum Mol Genet; 2006 Dec 01; 15(23):3394-410. PubMed ID: 17047027
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  • 60. Molecular and genetic aspects of DiGeorge/velocardiofacial syndrome.
    Driscoll DA.
    Methods Mol Med; 2006 Dec 01; 126():43-55. PubMed ID: 16930005
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