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Results: 1 to 20 of 162

Similar articles for PubMed (Select 16691575)

1.

Using the TBX5 transcription factor to grow and sculpt the heart.

Hatcher CJ, McDermott DA.

Am J Med Genet A. 2006 Jul 1;140(13):1414-8. Review.

PMID:
16691575
2.

TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed.

Mori AD, Bruneau BG.

Curr Opin Cardiol. 2004 May;19(3):211-5. Review.

PMID:
15096952
3.

TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts.

Reamon-Buettner SM, Borlak J.

Hum Mutat. 2004 Jul;24(1):104.

PMID:
15221798
4.

Novel TBX5 mutations in patients with Holt-Oram syndrome.

Debeer P, Race V, Gewillig M, Devriendt K, Frijns JP.

Clin Orthop Relat Res. 2007 Sep;462:20-6.

PMID:
17534187
5.

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease.

Bruneau BG, Nemer G, Schmitt JP, Charron F, Robitaille L, Caron S, Conner DA, Gessler M, Nemer M, Seidman CE, Seidman JG.

Cell. 2001 Sep 21;106(6):709-21.

6.

TBX5, a gene mutated in Holt-Oram syndrome, is regulated through a GC box and T-box binding elements (TBEs).

Sun G, Lewis LE, Huang X, Nguyen Q, Price C, Huang T.

J Cell Biochem. 2004 May 1;92(1):189-99. Erratum in: J Cell Biochem. 2004 Jul 1;92(4):864.

PMID:
15095414
7.

Expanding the spectrum of TBX5 mutations in Holt-Oram syndrome: detection of two intragenic deletions by quantitative real time PCR, and report of eight novel point mutations.

Borozdin W, Bravo Ferrer Acosta AM, Bamshad MJ, Botzenhart EM, Froster UG, Lemke J, Schinzel A, Spranger S, McGaughran J, Wand D, Chrzanowska KH, Kohlhase J.

Hum Mutat. 2006 Sep;27(9):975-6.

PMID:
16917909
8.

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.

Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE.

Nat Genet. 1997 Jan;15(1):30-5. Erratum in: Nat Genet 1997 Apr;15(4):411.

PMID:
8988165
9.

Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation.

Hiroi Y, Kudoh S, Monzen K, Ikeda Y, Yazaki Y, Nagai R, Komuro I.

Nat Genet. 2001 Jul;28(3):276-80.

PMID:
11431700
10.

Current advances in Holt-Oram syndrome.

Huang T.

Curr Opin Pediatr. 2002 Dec;14(6):691-5. Review.

PMID:
12436037
11.

Preimplantation genetic diagnosis of human congenital heart malformation and Holt-Oram syndrome.

He J, McDermott DA, Song Y, Gilbert F, Kligman I, Basson CT.

Am J Med Genet A. 2004 Apr 1;126A(1):93-8.

PMID:
15039979
12.

TBX5 transcription factor regulates cell proliferation during cardiogenesis.

Hatcher CJ, Kim MS, Mah CS, Goldstein MM, Wong B, Mikawa T, Basson CT.

Dev Biol. 2001 Feb 15;230(2):177-88.

13.

Three novel TBX5 mutations in Chinese patients with Holt-Oram syndrome.

Yang J, Hu D, Xia J, Yang Y, Ying B, Hu J, Zhou X.

Am J Med Genet. 2000 Jun 5;92(4):237-40.

PMID:
10842287
14.

Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesis.

Mori AD, Zhu Y, Vahora I, Nieman B, Koshiba-Takeuchi K, Davidson L, Pizard A, Seidman JG, Seidman CE, Chen XJ, Henkelman RM, Bruneau BG.

Dev Biol. 2006 Sep 15;297(2):566-86. Epub 2006 May 24. Erratum in: Dev Biol. 2007 Sep 15;309(2):386.

15.

Identification of the TBX5 transactivating domain and the nuclear localization signal.

Zaragoza MV, Lewis LE, Sun G, Wang E, Li L, Said-Salman I, Feucht L, Huang T.

Gene. 2004 Apr 14;330:9-18.

PMID:
15087119
16.

A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation.

Postma AV, van de Meerakker JB, Mathijssen IB, Barnett P, Christoffels VM, Ilgun A, Lam J, Wilde AA, Lekanne Deprez RH, Moorman AF.

Circ Res. 2008 Jun 6;102(11):1433-42. doi: 10.1161/CIRCRESAHA.107.168294. Epub 2008 May 1.

17.

TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome.

McDermott DA, Bressan MC, He J, Lee JS, Aftimos S, Brueckner M, Gilbert F, Graham GE, Hannibal MC, Innis JW, Pierpont ME, Raas-Rothschild A, Shanske AL, Smith WE, Spencer RH, St John-Sutton MG, van Maldergem L, Waggoner DJ, Weber M, Basson CT.

Pediatr Res. 2005 Nov;58(5):981-6. Epub 2005 Sep 23.

PMID:
16183809
18.

Microarray analysis of Tbx5-induced genes expressed in the developing heart.

Plageman TF Jr, Yutzey KE.

Dev Dyn. 2006 Oct;235(10):2868-80.

19.

Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations.

Basson CT, Huang T, Lin RC, Bachinsky DR, Weremowicz S, Vaglio A, Bruzzone R, Quadrelli R, Lerone M, Romeo G, Silengo M, Pereira A, Krieger J, Mesquita SF, Kamisago M, Morton CC, Pierpont ME, Müller CW, Seidman JG, Seidman CE.

Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):2919-24.

20.

Holt-Oram syndrome: a new mutation in the TBX5 gene in two unrelated families.

Gruenauer-Kloevekorn C, Froster UG.

Ann Genet. 2003 Jan-Mar;46(1):19-23.

PMID:
12818525
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