Benson DW - Search Results

1

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways.

Benson DW, Silberbach GM, Kavanaugh-McHugh A, Cottrill C, Zhang Y, Riggs S, Smalls O, Johnson MC, Watson MS, Seidman JG, Seidman CE, Plowden J, Kugler JD. Benson DW, et al. J Clin Invest. 1999 Dec;104(11):1567-73. doi: 10.1172/JCI8154. J Clin Invest. 1999. PMID: 10587520 Free PMC article.

2

Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease.

Kasahara H, Lee B, Schott JJ, Benson DW, Seidman JG, Seidman CE, Izumo S. Kasahara H, et al. Among authors: benson dw. J Clin Invest. 2000 Jul;106(2):299-308. doi: 10.1172/JCI9860. J Clin Invest. 2000. PMID: 10903346 Free PMC article.

3

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy.

Arad M, Benson DW, Perez-Atayde AR, McKenna WJ, Sparks EA, Kanter RJ, McGarry K, Seidman JG, Seidman CE. Arad M, et al. Among authors: benson dw. J Clin Invest. 2002 Feb;109(3):357-62. doi: 10.1172/JCI14571. J Clin Invest. 2002. PMID: 11827995 Free PMC article.

4

Congenital heart disease caused by mutations in the transcription factor NKX2-5.

Schott JJ, Benson DW, Basson CT, Pease W, Silberbach GM, Moak JP, Maron BJ, Seidman CE, Seidman JG. Schott JJ, et al. Among authors: benson dw. Science. 1998 Jul 3;281(5373):108-11. doi: 10.1126/science.281.5373.108. Science. 1998. PMID: 9651244

5

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

Siu BL, Niimura H, Osborne JA, Fatkin D, MacRae C, Solomon S, Benson DW, Seidman JG, Seidman CE. Siu BL, et al. Among authors: benson dw. Circulation. 1999 Mar 2;99(8):1022-6. doi: 10.1161/01.cir.99.8.1022. Circulation. 1999. PMID: 10051295

6

Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome.

Mehdirad AA, Fatkin D, DiMarco JP, MacRae CA, Wase A, Seidman JG, Seidman CE, Benson DW. Mehdirad AA, et al. Among authors: benson dw. J Cardiovasc Electrophysiol. 1999 May;10(5):629-35. doi: 10.1111/j.1540-8167.1999.tb00239.x. J Cardiovasc Electrophysiol. 1999. PMID: 10355918

7

Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects.

Benson DW, Sharkey A, Fatkin D, Lang P, Basson CT, McDonough B, Strauss AW, Seidman JG, Seidman CE. Benson DW, et al. Circulation. 1998 May 26;97(20):2043-8. doi: 10.1161/01.cir.97.20.2043. Circulation. 1998. PMID: 9610535

8

Missense mutation in the pore region of HERG causes familial long QT syndrome.

Benson DW, MacRae CA, Vesely MR, Walsh EP, Seidman JG, Seidman CE, Satler CA. Benson DW, et al. Circulation. 1996 May 15;93(10):1791-5. doi: 10.1161/01.cir.93.10.1791. Circulation. 1996. PMID: 8635257

9

NKX2.5 mutations in patients with tetralogy of fallot.

Goldmuntz E, Geiger E, Benson DW. Goldmuntz E, et al. Among authors: benson dw. Circulation. 2001 Nov 20;104(21):2565-8. doi: 10.1161/hc4601.098427. Circulation. 2001. PMID: 11714651

10

A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation.

Ashraf H, Pradhan L, Chang EI, Terada R, Ryan NJ, Briggs LE, Chowdhury R, Zárate MA, Sugi Y, Nam HJ, Benson DW, Anderson RH, Kasahara H. Ashraf H, et al. Among authors: benson dw. Circ Cardiovasc Genet. 2014 Aug;7(4):423-433. doi: 10.1161/CIRCGENETICS.113.000281. Epub 2014 Jul 15. Circ Cardiovasc Genet. 2014. PMID: 25028484 Free PMC article.

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