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Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.
Gollob MH, Green MS, Tang AS, Gollob T, Karibe A, Ali Hassan AS, Ahmad F, Lozado R, Shah G, Fananapazir L, Bachinski LL, Roberts R. Gollob MH, et al. Among authors: roberts r. N Engl J Med. 2001 Jun 14;344(24):1823-31. doi: 10.1056/NEJM200106143442403. N Engl J Med. 2001. PMID: 11407343 Free article.
Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome.
Sidhu JS, Rajawat YS, Rami TG, Gollob MH, Wang Z, Yuan R, Marian AJ, DeMayo FJ, Weilbacher D, Taffet GE, Davies JK, Carling D, Khoury DS, Roberts R. Sidhu JS, et al. Among authors: roberts r. Circulation. 2005 Jan 4;111(1):21-9. doi: 10.1161/01.CIR.0000151291.32974.D5. Epub 2004 Dec 20. Circulation. 2005. PMID: 15611370 Free PMC article.
Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogen.
Folmes KD, Chan AY, Koonen DP, Pulinilkunnil TC, Baczkó I, Hunter BE, Thorn S, Allard MF, Roberts R, Gollob MH, Light PE, Dyck JR. Folmes KD, et al. Among authors: roberts r. Circ Cardiovasc Genet. 2009 Oct;2(5):457-66. doi: 10.1161/CIRCGENETICS.108.834564. Epub 2009 Jul 15. Circ Cardiovasc Genet. 2009. PMID: 20031621
5,887 results