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Items: 1 to 20 of 184

1.

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.

Lindsay EA, Vitelli F, Su H, Morishima M, Huynh T, Pramparo T, Jurecic V, Ogunrinu G, Sutherland HF, Scambler PJ, Bradley A, Baldini A.

Nature. 2001 Mar 1;410(6824):97-101.

PMID:
11242049
2.

A genetic link between Tbx1 and fibroblast growth factor signaling.

Vitelli F, Taddei I, Morishima M, Meyers EN, Lindsay EA, Baldini A.

Development. 2002 Oct;129(19):4605-11.

3.

Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage.

Liao J, Kochilas L, Nowotschin S, Arnold JS, Aggarwal VS, Epstein JA, Brown MC, Adams J, Morrow BE.

Hum Mol Genet. 2004 Aug 1;13(15):1577-85. Epub 2004 Jun 9.

4.

Congenital heart disease in mice deficient for the DiGeorge syndrome region.

Lindsay EA, Botta A, Jurecic V, Carattini-Rivera S, Cheah YC, Rosenblatt HM, Bradley A, Baldini A.

Nature. 1999 Sep 23;401(6751):379-83.

PMID:
10517636
5.

Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development.

Zhang Z, Cerrato F, Xu H, Vitelli F, Morishima M, Vincentz J, Furuta Y, Ma L, Martin JF, Baldini A, Lindsay E.

Development. 2005 Dec;132(23):5307-15. Erratum in: Development. 2005;132(24):5614.

6.

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.

Merscher S, Funke B, Epstein JA, Heyer J, Puech A, Lu MM, Xavier RJ, Demay MB, Russell RG, Factor S, Tokooya K, Jore BS, Lopez M, Pandita RK, Lia M, Carrion D, Xu H, Schorle H, Kobler JB, Scambler P, Wynshaw-Boris A, Skoultchi AI, Morrow BE, Kucherlapati R.

Cell. 2001 Feb 23;104(4):619-29.

7.

22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development.

Scambler PJ.

Pediatr Cardiol. 2010 Apr;31(3):378-90. doi: 10.1007/s00246-009-9613-0. Review.

PMID:
20054531
8.

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

Jerome LA, Papaioannou VE.

Nat Genet. 2001 Mar;27(3):286-91.

PMID:
11242110
9.

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.

10.

Beta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1.

Huh SH, Ornitz DM.

Development. 2010 Apr;137(7):1137-47. doi: 10.1242/dev.045534.

11.

Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene.

Chieffo C, Garvey N, Gong W, Roe B, Zhang G, Silver L, Emanuel BS, Budarf ML.

Genomics. 1997 Aug 1;43(3):267-77.

PMID:
9268629
12.

Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis.

Morishima M, Yanagisawa H, Yanagisawa M, Baldini A.

Dev Dyn. 2003 Sep;228(1):95-104.

13.

Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy.

Aggarwal VS, Liao J, Bondarev A, Schimmang T, Lewandoski M, Locker J, Shanske A, Campione M, Morrow BE.

Hum Mol Genet. 2006 Nov 1;15(21):3219-28. Epub 2006 Sep 25.

14.

The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning.

Fagman H, Liao J, Westerlund J, Andersson L, Morrow BE, Nilsson M.

Hum Mol Genet. 2007 Feb 1;16(3):276-85. Epub 2006 Dec 12.

15.

DiGeorge syndrome: an update.

Baldini A.

Curr Opin Cardiol. 2004 May;19(3):201-4. Review.

PMID:
15096950
16.

VEGF: a modifier of the del22q11 (DiGeorge) syndrome?

Stalmans I, Lambrechts D, De Smet F, Jansen S, Wang J, Maity S, Kneer P, von der Ohe M, Swillen A, Maes C, Gewillig M, Molin DG, Hellings P, Boetel T, Haardt M, Compernolle V, Dewerchin M, Plaisance S, Vlietinck R, Emanuel B, Gittenberger-de Groot AC, Scambler P, Morrow B, Driscol DA, Moons L, Esguerra CV, Carmeliet G, Behn-Krappa A, Devriendt K, Collen D, Conway SJ, Carmeliet P.

Nat Med. 2003 Feb;9(2):173-82. Epub 2003 Jan 21.

PMID:
12539040
17.

The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis.

Kelly RG, Jerome-Majewska LA, Papaioannou VE.

Hum Mol Genet. 2004 Nov 15;13(22):2829-40. Epub 2004 Sep 22.

18.

Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer.

Yamagishi H, Maeda J, Hu T, McAnally J, Conway SJ, Kume T, Meyers EN, Yamagishi C, Srivastava D.

Genes Dev. 2003 Jan 15;17(2):269-81.

19.

Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome.

Prescott K, Ivins S, Hubank M, Lindsay E, Baldini A, Scambler P.

Hum Genet. 2005 May;116(6):486-96. Epub 2005 Mar 19.

PMID:
15778864
20.

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;133(5):977-87. Epub 2006 Feb 1.

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