Similar articles for PMID: 20031621

Year	Number of Results
2001	2
2002	1
2003	4
2004	3
2005	9
2006	8
2007	8
2008	5
2009	6
2010	8
2011	2
2012	1
2013	5
2014	3
2015	1
2016	6
2017	5
2018	7
2020	4
2021	1
2022	2

1

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. 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

2

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. Arad M, et al. Circulation. 2003 Jun 10;107(22):2850-6. doi: 10.1161/01.CIR.0000075270.13497.2B. Epub 2003 Jun 2. Circulation. 2003. PMID: 12782567

3

Identification and functional analysis of a novel PRKAG2 mutation responsible for Chinese PRKAG2 cardiac syndrome reveal an important role of non-CBS domains in regulating the AMPK pathway.

Zhang BL, Xu RL, Zhang J, Zhao XX, Wu H, Ma LP, Hu JQ, Zhang JL, Ye Z, Zheng X, Qin YW. Zhang BL, et al. J Cardiol. 2013 Oct;62(4):241-8. doi: 10.1016/j.jjcc.2013.04.010. Epub 2013 Jun 15. J Cardiol. 2013. PMID: 23778007 Free article.

4

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. J Clin Invest. 2002 Feb;109(3):357-62. doi: 10.1172/JCI14571. J Clin Invest. 2002. PMID: 11827995 Free PMC article.

5

Gain-of-function R225W mutation in human AMPKgamma(3) causing increased glycogen and decreased triglyceride in skeletal muscle.

Costford SR, Kavaslar N, Ahituv N, Chaudhry SN, Schackwitz WS, Dent R, Pennacchio LA, McPherson R, Harper ME. Costford SR, et al. PLoS One. 2007 Sep 19;2(9):e903. doi: 10.1371/journal.pone.0000903. PLoS One. 2007. PMID: 17878938 Free PMC article.

6

Establishment of a PRKAG2 cardiac syndrome disease model and mechanism study using human induced pluripotent stem cells.

Zhan Y, Sun X, Li B, Cai H, Xu C, Liang Q, Lu C, Qian R, Chen S, Yin L, Sheng W, Huang G, Sun A, Ge J, Sun N. Zhan Y, et al. J Mol Cell Cardiol. 2018 Apr;117:49-61. doi: 10.1016/j.yjmcc.2018.02.007. Epub 2018 Feb 13. J Mol Cell Cardiol. 2018. PMID: 29452156

7

CRISPR correction of the PRKAG2 gene mutation in the patient's induced pluripotent stem cell-derived cardiomyocytes eliminates electrophysiological and structural abnormalities.

Ben Jehuda R, Eisen B, Shemer Y, Mekies LN, Szantai A, Reiter I, Cui H, Guan K, Haron-Khun S, Freimark D, Sperling SR, Gherghiceanu M, Arad M, Binah O. Ben Jehuda R, et al. Heart Rhythm. 2018 Feb;15(2):267-276. doi: 10.1016/j.hrthm.2017.09.024. Epub 2017 Sep 14. Heart Rhythm. 2018. PMID: 28917552

8

A PRKAG2 mutation causes biphasic changes in myocardial AMPK activity and does not protect against ischemia.

Banerjee SK, Ramani R, Saba S, Rager J, Tian R, Mathier MA, Ahmad F. Banerjee SK, et al. Biochem Biophys Res Commun. 2007 Aug 24;360(2):381-7. doi: 10.1016/j.bbrc.2007.06.067. Epub 2007 Jun 19. Biochem Biophys Res Commun. 2007. PMID: 17597581

9

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. Ofir M, et al. Biochem Pharmacol. 2008 Apr 1;75(7):1482-91. doi: 10.1016/j.bcp.2007.12.011. Epub 2008 Jan 5. Biochem Pharmacol. 2008. PMID: 18261713

10

Overexpression of G100S mutation in PRKAG2 causes Wolff-Parkinson-White syndrome in zebrafish.

Zhang BL, Ye Z, Xu RL, You XH, Qin YW, Wu H, Cao J, Zhang JL, Zheng X, Zhao XX. Zhang BL, et al. Clin Genet. 2014 Sep;86(3):287-91. doi: 10.1111/cge.12267. Epub 2013 Oct 25. Clin Genet. 2014. PMID: 23992123

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