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Results: 1 to 20 of 99

Similar articles for PubMed (Select 24675841)

1.

TBX3 regulates splicing in vivo: a novel molecular mechanism for Ulnar-mammary syndrome.

Kumar P P, Franklin S, Emechebe U, Hu H, Moore B, Lehman C, Yandell M, Moon AM.

PLoS Genet. 2014 Mar 27;10(3):e1004247. doi: 10.1371/journal.pgen.1004247. eCollection 2014 Mar.

2.

The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome.

Bamshad M, Le T, Watkins WS, Dixon ME, Kramer BE, Roeder AD, Carey JC, Root S, Schinzel A, Van Maldergem L, Gardner RJ, Lin RC, Seidman CE, Seidman JG, Wallerstein R, Moran E, Sutphen R, Campbell CE, Jorde LB.

Am J Hum Genet. 1999 Jun;64(6):1550-62.

3.

Mouse TBX3 mutants suggest novel molecular mechanisms for Ulnar-mammary syndrome.

Frank DU, Emechebe U, Thomas KR, Moon AM.

PLoS One. 2013 Jul 2;8(7):e67841. doi: 10.1371/journal.pone.0067841. Print 2013.

5.

The ulnar-mammary syndrome gene, Tbx3, is a direct target of the retinoic acid signaling pathway, which regulates its expression during mouse limb development.

Ballim RD, Mendelsohn C, Papaioannou VE, Prince S.

Mol Biol Cell. 2012 Jun;23(12):2362-72. doi: 10.1091/mbc.E11-09-0790. Epub 2012 Apr 25.

6.

TBX3, the gene mutated in ulnar-mammary syndrome, promotes growth of mammary epithelial cells via repression of p19ARF, independently of p53.

Platonova N, Scotti M, Babich P, Bertoli G, Mento E, Meneghini V, Egeo A, Zucchi I, Merlo GR.

Cell Tissue Res. 2007 May;328(2):301-16. Epub 2007 Jan 30.

PMID:
17265068
7.

Phenotype of a patient with contiguous deletion of TBX5 and TBX3: expanding the disease spectrum.

Bogarapu S, Bleyl SB, Calhoun A, Viskochil D, Saarel EV, Everitt MD, Frank DU.

Am J Med Genet A. 2014 May;164A(5):1304-9. doi: 10.1002/ajmg.a.36447. Epub 2014 Mar 24.

PMID:
24664963
8.

The face of Ulnar Mammary syndrome?

Joss S, Kini U, Fisher R, Mundlos S, Prescott K, Newbury-Ecob R, Tolmie J.

Eur J Med Genet. 2011 May-Jun;54(3):301-5. doi: 10.1016/j.ejmg.2010.12.010. Epub 2011 Jan 1.

PMID:
21199695
9.

Diverse functional networks of Tbx3 in development and disease.

Washkowitz AJ, Gavrilov S, Begum S, Papaioannou VE.

Wiley Interdiscip Rev Syst Biol Med. 2012 May-Jun;4(3):273-83. doi: 10.1002/wsbm.1162. Epub 2012 Feb 14.

10.

Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome.

He Ml, Wen L, Campbell CE, Wu JY, Rao Y.

Proc Natl Acad Sci U S A. 1999 Aug 31;96(18):10212-7. Erratum in: Proc Natl Acad Sci U S A 1999 Nov 9;96(23):13589.

11.

Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene.

Klopocki E, Neumann LM, Tönnies H, Ropers HH, Mundlos S, Ullmann R.

Eur J Hum Genet. 2006 Dec;14(12):1274-9. Epub 2006 Aug 9.

12.

Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of Holt-Oram and ulnar-mammary syndromes.

Alby C, Bessieres B, Bieth E, Attie-Bitach T, Fermont L, Citony I, Razavi F, Vekemans M, Escande F, Manouvrier S, Malan V, Amiel J.

Am J Med Genet A. 2013 Jul;161A(7):1797-802. doi: 10.1002/ajmg.a.36054. Epub 2013 May 24.

PMID:
23713051
14.

Lethal arrhythmias in Tbx3-deficient mice reveal extreme dosage sensitivity of cardiac conduction system function and homeostasis.

Frank DU, Carter KL, Thomas KR, Burr RM, Bakker ML, Coetzee WA, Tristani-Firouzi M, Bamshad MJ, Christoffels VM, Moon AM.

Proc Natl Acad Sci U S A. 2012 Jan 17;109(3):E154-63. doi: 10.1073/pnas.1115165109. Epub 2011 Dec 27.

15.

Novel mutation of TBX3 in a Japanese family with ulnar-mammary syndrome: implication for impaired sex development.

Sasaki G, Ogata T, Ishii T, Hasegawa T, Sato S, Matsuo N.

Am J Med Genet. 2002 Jul 15;110(4):365-9.

PMID:
12116211
16.

The T-box transcription factors TBX2 and TBX3 in mammary gland development and breast cancer.

Douglas NC, Papaioannou VE.

J Mammary Gland Biol Neoplasia. 2013 Jun;18(2):143-7. doi: 10.1007/s10911-013-9282-8. Epub 2013 Apr 28. Review.

17.

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome.

Bamshad M, Lin RC, Law DJ, Watkins WC, Krakowiak PA, Moore ME, Franceschini P, Lala R, Holmes LB, Gebuhr TC, Bruneau BG, Schinzel A, Seidman JG, Seidman CE, Jorde LB.

Nat Genet. 1997 Jul;16(3):311-5. Erratum in: Nat Genet 1998 May;19(1):102.

PMID:
9207801
18.

TBX3 and its splice variant TBX3 + exon 2a are functionally similar.

Hoogaars WM, Barnett P, Rodriguez M, Clout DE, Moorman AF, Goding CR, Christoffels VM.

Pigment Cell Melanoma Res. 2008 Jun;21(3):379-87. doi: 10.1111/j.1755-148X.2008.00461.x. Epub 2008 Apr 26.

PMID:
18444963
19.

Ulnar mammary syndrome.

Ramirez RN, Kozin SH.

J Hand Surg Am. 2014 Apr;39(4):803-5. doi: 10.1016/j.jhsa.2014.01.024. No abstract available.

PMID:
24679913
20.

Functional role of transcriptional factor TBX5 in pre-mRNA splicing and Holt-Oram syndrome via association with SC35.

Fan C, Chen Q, Wang QK.

J Biol Chem. 2009 Sep 18;284(38):25653-63. doi: 10.1074/jbc.M109.041368. Epub 2009 Jul 31.

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