PubMed (cited) for id: 590050

Year	Number of Results
1990	2
1991	4
1992	7
1993	6
1994	4
1995	6
1996	5
1997	5
1998	6
1999	7
2000	4
2001	11
2003	3
2004	4
2005	3
2006	4
2007	4
2008	4
2009	2
2010	4
2012	1
2013	1
2016	1
2024	0

1

The phenotypic spectrum of fifty Czech m.3243A>G carriers.

Dvorakova V, Kolarova H, Magner M, Tesarova M, Hansikova H, Zeman J, Honzik T. Dvorakova V, et al. Mol Genet Metab. 2016 Aug;118(4):288-95. doi: 10.1016/j.ymgme.2016.06.003. Epub 2016 Jun 6. Mol Genet Metab. 2016. PMID: 27296531

2

High risk of severe cardiac adverse events in patients with mitochondrial m.3243A>G mutation.

Malfatti E, Laforêt P, Jardel C, Stojkovic T, Behin A, Eymard B, Lombès A, Benmalek A, Bécane HM, Berber N, Meune C, Duboc D, Wahbi K. Malfatti E, et al. Neurology. 2013 Jan 1;80(1):100-5. doi: 10.1212/WNL.0b013e31827b1a2f. Epub 2012 Dec 12. Neurology. 2013. PMID: 23243073

3

Autonomic symptoms in carriers of the m.3243A>G mitochondrial DNA mutation.

Parsons T, Weimer L, Engelstad K, Linker A, Battista V, Wei Y, Hirano M, Dimauro S, De Vivo DC, Kaufmann P. Parsons T, et al. Arch Neurol. 2010 Aug;67(8):976-9. doi: 10.1001/archneurol.2010.174. Arch Neurol. 2010. PMID: 20697048 Free PMC article.

4

MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.

Nakamura M, Yabe I, Sudo A, Hosoki K, Yaguchi H, Saitoh S, Sasaki H. Nakamura M, et al. J Med Genet. 2010 Oct;47(10):659-64. doi: 10.1136/jmg.2009.072058. Epub 2010 Jul 7. J Med Genet. 2010. PMID: 20610441 Free article.

5

Helix unwinding and base flipping enable human MTERF1 to terminate mitochondrial transcription.

Yakubovskaya E, Mejia E, Byrnes J, Hambardjieva E, Garcia-Diaz M. Yakubovskaya E, et al. Cell. 2010 Jun 11;141(6):982-93. doi: 10.1016/j.cell.2010.05.018. Cell. 2010. PMID: 20550934 Free PMC article.

6

Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetes.

Li R, Guan MX. Li R, et al. Mol Cell Biol. 2010 May;30(9):2147-54. doi: 10.1128/MCB.01614-09. Epub 2010 Mar 1. Mol Cell Biol. 2010. PMID: 20194621 Free PMC article.

7

Efficacy of lamotrigine in disabling myoclonus in a patient with an mtDNA A3243G mutation.

Costello DJ, Sims KB. Costello DJ, et al. Neurology. 2009 Apr 7;72(14):1279-80. doi: 10.1212/01.wnl.0000345663.71421.1d. Neurology. 2009. PMID: 19349610 No abstract available.

8

Protean phenotypic features of the A3243G mitochondrial DNA mutation.

Kaufmann P, Engelstad K, Wei Y, Kulikova R, Oskoui M, Battista V, Koenigsberger DY, Pascual JM, Sano M, Hirano M, DiMauro S, Shungu DC, Mao X, De Vivo DC. Kaufmann P, et al. Arch Neurol. 2009 Jan;66(1):85-91. doi: 10.1001/archneurol.2008.526. Arch Neurol. 2009. PMID: 19139304 Free PMC article.

9

The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2.

Sasarman F, Antonicka H, Shoubridge EA. Sasarman F, et al. Hum Mol Genet. 2008 Dec 1;17(23):3697-707. doi: 10.1093/hmg/ddn265. Epub 2008 Aug 27. Hum Mol Genet. 2008. PMID: 18753147

10

Pathogenic mitochondrial DNA mutations are common in the general population.

Elliott HR, Samuels DC, Eden JA, Relton CL, Chinnery PF. Elliott HR, et al. Am J Hum Genet. 2008 Aug;83(2):254-60. doi: 10.1016/j.ajhg.2008.07.004. Am J Hum Genet. 2008. PMID: 18674747 Free PMC article.

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