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Journal Abstract Search

269 related items for PubMed ID: 17047027

  • 21. Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development.
    Moraes F, Nóvoa A, Jerome-Majewska LA, Papaioannou VE, Mallo M.
    Mech Dev; 2005 Feb; 122(2):199-212. PubMed ID: 15652707
    [Abstract] [Full Text] [Related]

  • 22. Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1.
    Ivins S, Lammerts van Beuren K, Roberts C, James C, Lindsay E, Baldini A, Ataliotis P, Scambler PJ.
    Dev Biol; 2005 Sep 15; 285(2):554-69. PubMed ID: 16109395
    [Abstract] [Full Text] [Related]

  • 23. R115866 inhibits all-trans-retinoic acid metabolism and exerts retinoidal effects in rodents.
    Stoppie P, Borgers M, Borghgraef P, Dillen L, Goossens J, Sanz G, Szel H, Van Hove C, Van Nyen G, Nobels G, Vanden Bossche H, Venet M, Willemsens G, Van Wauwe J.
    J Pharmacol Exp Ther; 2000 Apr 15; 293(1):304-12. PubMed ID: 10734183
    [Abstract] [Full Text] [Related]

  • 24. Complementary domains of retinoic acid production and degradation in the early chick embryo.
    Swindell EC, Thaller C, Sockanathan S, Petkovich M, Jessell TM, Eichele G.
    Dev Biol; 1999 Dec 01; 216(1):282-96. PubMed ID: 10588879
    [Abstract] [Full Text] [Related]

  • 25. CYP26 inhibitor R115866 increases retinoid signaling in intimal smooth muscle cells.
    Ocaya P, Gidlöf AC, Olofsson PS, Törmä H, Sirsjö A.
    Arterioscler Thromb Vasc Biol; 2007 Jul 01; 27(7):1542-8. PubMed ID: 17510468
    [Abstract] [Full Text] [Related]

  • 26. Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis.
    Morishima M, Yanagisawa H, Yanagisawa M, Baldini A.
    Dev Dyn; 2003 Sep 01; 228(1):95-104. PubMed ID: 12950083
    [Abstract] [Full Text] [Related]

  • 27. Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations.
    Arnold JS, Werling U, Braunstein EM, Liao J, Nowotschin S, Edelmann W, Hebert JM, Morrow BE.
    Development; 2006 Mar 01; 133(5):977-87. PubMed ID: 16452092
    [Abstract] [Full Text] [Related]

  • 28. The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures.
    Abu-Abed S, Dollé P, Metzger D, Beckett B, Chambon P, Petkovich M.
    Genes Dev; 2001 Jan 15; 15(2):226-40. PubMed ID: 11157778
    [Abstract] [Full Text] [Related]

  • 29. Inhibition of the all-trans Retinoic Acid (atRA) Hydroxylases CYP26A1 and CYP26B1 Results in Dynamic, Tissue-Specific Changes in Endogenous atRA Signaling.
    Stevison F, Hogarth C, Tripathy S, Kent T, Isoherranen N.
    Drug Metab Dispos; 2017 Jul 15; 45(7):846-854. PubMed ID: 28446509
    [Abstract] [Full Text] [Related]

  • 30. Generating gradients of retinoic acid in the chick embryo: Cyp26C1 expression and a comparative analysis of the Cyp26 enzymes.
    Reijntjes S, Gale E, Maden M.
    Dev Dyn; 2004 Jul 15; 230(3):509-17. PubMed ID: 15188435
    [Abstract] [Full Text] [Related]

  • 31. Embryonic expression of Tbx1, a DiGeorge syndrome candidate gene, in the lamprey Lampetra fluviatilis.
    Sauka-Spengler T, Le Mentec C, Lepage M, Mazan S.
    Gene Expr Patterns; 2002 Nov 15; 2(1-2):99-103. PubMed ID: 12617845
    [Abstract] [Full Text] [Related]

  • 32. Tbx1 genetically interacts with the transforming growth factor-β/bone morphogenetic protein inhibitor Smad7 during great vessel remodeling.
    Papangeli I, Scambler PJ.
    Circ Res; 2013 Jan 04; 112(1):90-102. PubMed ID: 23011393
    [Abstract] [Full Text] [Related]

  • 33. Inactivation of Bmp4 from the Tbx1 expression domain causes abnormal pharyngeal arch artery and cardiac outflow tract remodeling.
    Nie X, Brown CB, Wang Q, Jiao K.
    Cells Tissues Organs; 2011 Jan 04; 193(6):393-403. PubMed ID: 21123999
    [Abstract] [Full Text] [Related]

  • 34. Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways.
    Vitelli F, Morishima M, Taddei I, Lindsay EA, Baldini A.
    Hum Mol Genet; 2002 Apr 15; 11(8):915-22. PubMed ID: 11971873
    [Abstract] [Full Text] [Related]

  • 35. Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome.
    Racedo SE, Hasten E, Lin M, Devakanmalai GS, Guo T, Ozbudak EM, Cai CL, Zheng D, Morrow BE.
    PLoS Genet; 2017 Mar 15; 13(3):e1006687. PubMed ID: 28346476
    [Abstract] [Full Text] [Related]

  • 36. Functional properties and substrate characterization of human CYP26A1, CYP26B1, and CYP26C1 expressed by recombinant baculovirus in insect cells.
    Helvig C, Taimi M, Cameron D, Jones G, Petkovich M.
    J Pharmacol Toxicol Methods; 2011 Mar 15; 64(3):258-63. PubMed ID: 21906690
    [Abstract] [Full Text] [Related]

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  • 39. Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice.
    Mastromoro G, Calcagni G, Versacci P, Putotto C, Chinali M, Lambiase C, Unolt M, Pelliccione E, Anaclerio S, Caprio C, Cioffi S, Bilio M, Baban A, Drago F, Digilio MC, Marino B, Baldini A.
    PLoS One; 2019 Mar 15; 14(4):e0211170. PubMed ID: 30933971
    [Abstract] [Full Text] [Related]

  • 40. Identification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear development.
    Monks DC, Morrow BE.
    Dev Dyn; 2012 Mar 15; 241(3):563-73. PubMed ID: 22275070
    [Abstract] [Full Text] [Related]

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