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Items: 1 to 20 of 157

1.

Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes.

Pauws E, Hoshino A, Bentley L, Prajapati S, Keller C, Hammond P, Martinez-Barbera JP, Moore GE, Stanier P.

Hum Mol Genet. 2009 Nov 1;18(21):4171-9. doi: 10.1093/hmg/ddp368. Epub 2009 Jul 31. Erratum in: Hum Mol Genet. 2010 Aug 1;19(15):3103.

2.

Tbx22 expressions during palatal development in fetuses with glucocorticoid-/alcohol-induced C57BL/6N cleft palates.

Kim SM, Lee JH, Jabaiti S, Lee SK, Choi JY.

J Craniofac Surg. 2009 Sep;20(5):1316-26. doi: 10.1097/SCS.0b013e3181ae6686.

PMID:
19816249
3.

Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.

Braybrook C, Lisgo S, Doudney K, Henderson D, Marçano AC, Strachan T, Patton MA, Villard L, Moore GE, Stanier P, Lindsay S.

Hum Mol Genet. 2002 Oct 15;11(22):2793-804.

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A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia.

Pauws E, Moore GE, Stanier P.

J Med Genet. 2009 Aug;46(8):555-61. doi: 10.1136/jmg.2009.066902.

PMID:
19648124
6.
7.

Expression of mouse Tbx22 supports its role in palatogenesis and glossogenesis.

Herr A, Meunier D, Müller I, Rump A, Fundele R, Ropers HH, Nuber UA.

Dev Dyn. 2003 Apr;226(4):579-86.

8.

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

Braybrook C, Doudney K, Marçano AC, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P.

Nat Genet. 2001 Oct;29(2):179-83.

PMID:
11559848
9.

Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations.

Kantaputra PN, Paramee M, Kaewkhampa A, Hoshino A, Lees M, McEntagart M, Masrour N, Moore GE, Pauws E, Stanier P.

J Dent Res. 2011 Apr;90(4):450-5. doi: 10.1177/0022034510391052. Epub 2011 Jan 19.

PMID:
21248356
10.

Expression and requirement of T-box transcription factors Tbx2 and Tbx3 during secondary palate development in the mouse.

Zirzow S, Lüdtke TH, Brons JF, Petry M, Christoffels VM, Kispert A.

Dev Biol. 2009 Dec 15;336(2):145-55. doi: 10.1016/j.ydbio.2009.09.020. Epub 2009 Sep 19.

11.

Regulation of Tbx22 during facial and palatal development.

Fuchs A, Inthal A, Herrmann D, Cheng S, Nakatomi M, Peters H, Neubüser A.

Dev Dyn. 2010 Nov;239(11):2860-74. doi: 10.1002/dvdy.22421.

12.

TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression.

Andreou AM, Pauws E, Jones MC, Singh MK, Bussen M, Doudney K, Moore GE, Kispert A, Brosens JJ, Stanier P.

Am J Hum Genet. 2007 Oct;81(4):700-12. Epub 2007 Aug 16.

13.

X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations.

Pauws E, Peskett E, Boissin C, Hoshino A, Mengrelis K, Carta E, Abruzzo MA, Lees M, Moore GE, Erickson RP, Stanier P.

Clin Genet. 2013 Apr;83(4):352-8. doi: 10.1111/j.1399-0004.2012.01930.x. Epub 2012 Aug 7.

PMID:
22784330
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16.

The Mn1 transcription factor acts upstream of Tbx22 and preferentially regulates posterior palate growth in mice.

Liu W, Lan Y, Pauws E, Meester-Smoor MA, Stanier P, Zwarthoff EC, Jiang R.

Development. 2008 Dec;135(23):3959-68. doi: 10.1242/dev.025304. Epub 2008 Oct 23.

17.

Patterning of palatal rugae through sequential addition reveals an anterior/posterior boundary in palatal development.

Pantalacci S, Prochazka J, Martin A, Rothova M, Lambert A, Bernard L, Charles C, Viriot L, Peterkova R, Laudet V.

BMC Dev Biol. 2008 Dec 16;8:116. doi: 10.1186/1471-213X-8-116.

18.

Loss-of-function mutation in the X-linked TBX22 promoter disrupts an ETS-1 binding site and leads to cleft palate.

Fu X, Cheng Y, Yuan J, Huang C, Cheng H, Zhou R.

Hum Genet. 2015 Feb;134(2):147-58. doi: 10.1007/s00439-014-1503-8. Epub 2014 Nov 6.

PMID:
25373698
19.

TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population.

Suphapeetiporn K, Tongkobpetch S, Siriwan P, Shotelersuk V.

Clin Genet. 2007 Nov;72(5):478-83. Epub 2007 Sep 14.

PMID:
17868388
20.

Isolated cleft palate in mice with a targeted mutation of the LIM homeobox gene lhx8.

Zhao Y, Guo YJ, Tomac AC, Taylor NR, Grinberg A, Lee EJ, Huang S, Westphal H.

Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):15002-6.

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