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Items: 1 to 20 of 237


Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development.

Garg V, Yamagishi C, Hu T, Kathiriya IS, Yamagishi H, Srivastava D.

Dev Biol. 2001 Jul 1;235(1):62-73.


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.


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.


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.


[Effect of external retinoic acid on Tbx1 gene during zebrafish embryogenesis].

Zhang LF, Gui YH, Zhong T, Wang YX, Qian LX, Dong YX, Jiang Q, Sun SN, Song HY.

Zhonghua Er Ke Za Zhi. 2007 Apr;45(4):267-71. Chinese.


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;2(1-2):99-103.


The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans.

Piotrowski T, Ahn DG, Schilling TF, Nair S, Ruvinsky I, Geisler R, Rauch GJ, Haffter P, Zon LI, Zhou Y, Foott H, Dawid IB, Ho RK.

Development. 2003 Oct;130(20):5043-52.


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.


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.


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 1;15(23):3394-410. Epub 2006 Oct 17.


The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.

Wilming LG, Snoeren CA, van Rijswijk A, Grosveld F, Meijers C.

Hum Mol Genet. 1997 Feb;6(2):247-58.


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.


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.


TBX1, a DiGeorge syndrome candidate gene, is inhibited by retinoic acid.

Zhang L, Zhong T, Wang Y, Jiang Q, Song H, Gui Y.

Int J Dev Biol. 2006;50(1):55-61.


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.


Cloning and characterization of zebrafish tbx1.

Kochilas LK, Potluri V, Gitler A, Balasubramanian K, Chin AJ.

Gene Expr Patterns. 2003 Oct;3(5):645-51.


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.


Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.

Berti L, Mittler G, Przemeck GK, Stelzer G, Günzler B, Amati F, Conti E, Dallapiccola B, Hrabé de Angelis M, Novelli G, Meisterernst M.

Genomics. 2001 Jun 15;74(3):320-32.

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