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424 related items for PubMed ID: 12782567

  • 1. Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.
    Arad M, Moskowitz IP, Patel VV, Ahmad F, Perez-Atayde AR, Sawyer DB, Walter M, Li GH, Burgon PG, Maguire CT, Stapleton D, Schmitt JP, Guo XX, Pizard A, Kupershmidt S, Roden DM, Berul CI, Seidman CE, Seidman JG.
    Circulation; 2003 Jun 10; 107(22):2850-6. PubMed ID: 12782567
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  • 3. Glycogen storage diseases presenting as hypertrophic cardiomyopathy.
    Arad M, Maron BJ, Gorham JM, Johnson WH, Saul JP, Perez-Atayde AR, Spirito P, Wright GB, Kanter RJ, Seidman CE, Seidman JG.
    N Engl J Med; 2005 Jan 27; 352(4):362-72. PubMed ID: 15673802
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  • 4. Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome.
    Patel VV, Arad M, Moskowitz IP, Maguire CT, Branco D, Seidman JG, Seidman CE, Berul CI.
    J Am Coll Cardiol; 2003 Sep 03; 42(5):942-51. PubMed ID: 12957447
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  • 5. Familial Wolff-Parkinson-White Syndrome: a disease of glycogen storage or ion channel dysfunction?
    Light PE.
    J Cardiovasc Electrophysiol; 2006 May 03; 17 Suppl 1():S158-S161. PubMed ID: 16686673
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  • 9. N488I mutation of the gamma2-subunit results in bidirectional changes in AMP-activated protein kinase activity.
    Zou L, Shen M, Arad M, He H, Løfgren B, Ingwall JS, Seidman CE, Seidman JG, Tian R.
    Circ Res; 2005 Aug 19; 97(4):323-8. PubMed ID: 16051890
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  • 12. Increased glycogen stores due to gamma-AMPK overexpression protects against ischemia and reperfusion damage.
    Ofir M, Arad M, Porat E, Freimark D, Chepurko Y, Vidne BA, Seidman CE, Seidman JG, Kemp BE, Hochhauser E.
    Biochem Pharmacol; 2008 Apr 01; 75(7):1482-91. PubMed ID: 18261713
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  • 16. Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy.
    Gollob MH, Seger JJ, Gollob TN, Tapscott T, Gonzales O, Bachinski L, Roberts R.
    Circulation; 2001 Dec 18; 104(25):3030-3. PubMed ID: 11748095
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  • 17. Fatal congenital heart glycogenosis caused by a recurrent activating R531Q mutation in the gamma 2-subunit of AMP-activated protein kinase (PRKAG2), not by phosphorylase kinase deficiency.
    Burwinkel B, Scott JW, Bührer C, van Landeghem FK, Cox GF, Wilson CJ, Grahame Hardie D, Kilimann MW.
    Am J Hum Genet; 2005 Jun 18; 76(6):1034-49. PubMed ID: 15877279
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  • 18. Mutation in the γ2-subunit of AMP-activated protein kinase stimulates cardiomyocyte proliferation and hypertrophy independent of glycogen storage.
    Kim M, Hunter RW, Garcia-Menendez L, Gong G, Yang YY, Kolwicz SC, Xu J, Sakamoto K, Wang W, Tian R.
    Circ Res; 2014 Mar 14; 114(6):966-75. PubMed ID: 24503893
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