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T-box factors determine cardiac design.
Hoogaars WM, Barnett P, Moorman AF, Christoffels VM. Hoogaars WM, et al. Among authors: barnett p. Cell Mol Life Sci. 2007 Mar;64(6):646-60. doi: 10.1007/s00018-007-6518-z. Cell Mol Life Sci. 2007. PMID: 17380306 Free PMC article. Review.
Msx1 and Msx2 are functional interacting partners of T-box factors in the regulation of Connexin43.
Boogerd KJ, Wong LY, Christoffels VM, Klarenbeek M, Ruijter JM, Moorman AF, Barnett P. Boogerd KJ, et al. Among authors: barnett p. Cardiovasc Res. 2008 Jun 1;78(3):485-93. doi: 10.1093/cvr/cvn049. Epub 2008 Feb 19. Cardiovasc Res. 2008. PMID: 18285513
A large permissive regulatory domain exclusively controls Tbx3 expression in the cardiac conduction system.
van Weerd JH, Badi I, van den Boogaard M, Stefanovic S, van de Werken HJ, Gomez-Velazquez M, Badia-Careaga C, Manzanares M, de Laat W, Barnett P, Christoffels VM. van Weerd JH, et al. Among authors: barnett p. Circ Res. 2014 Aug 1;115(4):432-41. doi: 10.1161/CIRCRESAHA.115.303591. Epub 2014 Jun 24. Circ Res. 2014. PMID: 24963028
Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer.
van den Boogaard M, Wong LY, Tessadori F, Bakker ML, Dreizehnter LK, Wakker V, Bezzina CR, 't Hoen PA, Bakkers J, Barnett P, Christoffels VM. van den Boogaard M, et al. Among authors: barnett p. J Clin Invest. 2012 Jul;122(7):2519-30. doi: 10.1172/JCI62613. Epub 2012 Jun 18. J Clin Invest. 2012. PMID: 22706305 Free PMC article.
Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome.
Boogerd CJ, Dooijes D, Ilgun A, Mathijssen IB, Hordijk R, van de Laar IM, Rump P, Veenstra-Knol HE, Moorman AF, Barnett P, Postma AV. Boogerd CJ, et al. Among authors: barnett p. Cardiovasc Res. 2010 Oct 1;88(1):130-9. doi: 10.1093/cvr/cvq178. Epub 2010 Jun 2. Cardiovasc Res. 2010. PMID: 20519243
Two out of the five mutations are peculiar: one, p.H220del, is associated with additional extra-cardiac defects, perhaps by interfering with other T-box dependant pathways, and another, p.I106V, leads to limb defects only, which is supported by its normal interactio …
Two out of the five mutations are peculiar: one, p.H220del, is associated with additional extra-cardiac defects, perhaps by interferi …
Expression of muscle segment homeobox genes in the developing myocardium.
Boogerd CJ, Moorman AF, Barnett P. Boogerd CJ, et al. Among authors: barnett p. Anat Rec (Hoboken). 2010 Jun;293(6):998-1001. doi: 10.1002/ar.21112. Anat Rec (Hoboken). 2010. PMID: 20225205
Protein interactions at the heart of cardiac chamber formation.
Boogerd CJ, Moorman AF, Barnett P. Boogerd CJ, et al. Among authors: barnett p. Ann Anat. 2009 Dec;191(6):505-17. doi: 10.1016/j.aanat.2009.06.004. Epub 2009 Jul 2. Ann Anat. 2009. PMID: 19647421 Review.
Epicardium and myocardium separate from a common precursor pool by crosstalk between bone morphogenetic protein- and fibroblast growth factor-signaling pathways.
van Wijk B, van den Berg G, Abu-Issa R, Barnett P, van der Velden S, Schmidt M, Ruijter JM, Kirby ML, Moorman AF, van den Hoff MJ. van Wijk B, et al. Among authors: barnett p. Circ Res. 2009 Aug 28;105(5):431-41. doi: 10.1161/CIRCRESAHA.109.203083. Epub 2009 Jul 23. Circ Res. 2009. PMID: 19628790 Free PMC article.
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. Postma AV, et al. Among authors: barnett p. Circ Res. 2008 Jun 6;102(11):1433-42. doi: 10.1161/CIRCRESAHA.107.168294. Epub 2008 May 1. Circ Res. 2008. PMID: 18451335
Sequencing of TBX5 revealed a novel mutation, c.373G>A, resulting in the missense mutation p.Gly125Arg, in all investigated affected family members, cosegregating with the disease. ...Thus, contrary to previously published HOS mutations, the p.G125R TBX5 mutation …
Sequencing of TBX5 revealed a novel mutation, c.373G>A, resulting in the missense mutation p.Gly125Arg, in all investigated affect …
Tbx3 controls the sinoatrial node gene program and imposes pacemaker function on the atria.
Hoogaars WM, Engel A, Brons JF, Verkerk AO, de Lange FJ, Wong LY, Bakker ML, Clout DE, Wakker V, Barnett P, Ravesloot JH, Moorman AF, Verheijck EE, Christoffels VM. Hoogaars WM, et al. Among authors: barnett p. Genes Dev. 2007 May 1;21(9):1098-112. doi: 10.1101/gad.416007. Genes Dev. 2007. PMID: 17473172 Free PMC article.
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