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Items: 1 to 20 of 176

1.

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.

2.

Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse.

Abu-Issa R, Smyth G, Smoak I, Yamamura K, Meyers EN.

Development. 2002 Oct;129(19):4613-25.

3.

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.

PMID:
17000704
4.

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.

5.

Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors.

Hu T, Yamagishi H, Maeda J, McAnally J, Yamagishi C, Srivastava D.

Development. 2004 Nov;131(21):5491-502. Epub 2004 Oct 6.

6.

Cre-mediated excision of Fgf8 in the Tbx1 expression domain reveals a critical role for Fgf8 in cardiovascular development in the mouse.

Brown CB, Wenning JM, Lu MM, Epstein DJ, Meyers EN, Epstein JA.

Dev Biol. 2004 Mar 1;267(1):190-202. Erratum in: Dev Biol. 2004 Jul 1;271(1):223.

7.

Fgf15 is required for proper morphogenesis of the mouse cardiac outflow tract.

Vincentz JW, McWhirter JR, Murre C, Baldini A, Furuta Y.

Genesis. 2005 Apr;41(4):192-201.

PMID:
15789410
8.

Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants.

Vitelli F, Zhang Z, Huynh T, Sobotka A, Mupo A, Baldini A.

Dev Biol. 2006 Jul 15;295(2):559-70. Epub 2006 Apr 4.

9.

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
10.

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.

PMID:
11971873
11.

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.

12.

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.

PMID:
15385444
13.

An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.

Frank DU, Fotheringham LK, Brewer JA, Muglia LJ, Tristani-Firouzi M, Capecchi MR, Moon AM.

Development. 2002 Oct;129(19):4591-603.

14.

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
15.

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.

16.

Retinoid signaling is essential for patterning the endoderm of the third and fourth pharyngeal arches.

Wendling O, Dennefeld C, Chambon P, Mark M.

Development. 2000 Apr;127(8):1553-62.

17.

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.

18.
19.

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.

20.

Zebrafish fgf24 functions with fgf8 to promote posterior mesodermal development.

Draper BW, Stock DW, Kimmel CB.

Development. 2003 Oct;130(19):4639-54.

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