Similar articles for PMID: 7669057

Year	Number of Results
1988	1
1990	3
1991	6
1992	8
1993	11
1994	13
1995	27
1996	21
1997	14
1998	12
1999	15
2000	10
2001	12
2002	13
2003	3
2004	15
2005	9
2006	8
2007	10
2008	14
2009	6
2010	7
2011	9
2012	13
2013	8
2014	10
2015	6
2016	7
2017	6
2018	7
2019	13
2020	11
2021	6
2022	3
2023	1
2024	0

1

A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome.

Nakamura M, Nakano S, Goto Y, Ozawa M, Nagahama Y, Fukuyama H, Akiguchi I, Kaji R, Kimura J. Nakamura M, et al. Biochem Biophys Res Commun. 1995 Sep 5;214(1):86-93. doi: 10.1006/bbrc.1995.2260. Biochem Biophys Res Commun. 1995. PMID: 7669057

2

Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.

Du W, Li W, Chen G, Cao H, Tang H, Tang X, Jin Q, Sun Z, Zhao H, Zhou W, He S, Lv Y, Zhao J, Zhang X. Du W, et al. Biosens Bioelectron. 2009 Apr 15;24(8):2371-6. doi: 10.1016/j.bios.2008.12.008. Epub 2008 Dec 9. Biosens Bioelectron. 2009. PMID: 19155171

3

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.

4

The molecular genetics of mitochondrial cytopathies: the Melbourne experience.

Thyagarajan D, Byrne E, Dennet X, Marzuki S. Thyagarajan D, et al. Clin Exp Neurol. 1992;29:172-81. Clin Exp Neurol. 1992. PMID: 1343860

5

A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.

Seibel P, Flierl A, Kottlors M, Reichmann H. Seibel P, et al. Biochem Biophys Res Commun. 1994 Apr 29;200(2):938-42. doi: 10.1006/bbrc.1994.1540. Biochem Biophys Res Commun. 1994. PMID: 8179630

6

MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation.

Mongini T, Doriguzzi C, Chiadò-Piat L, Silvestri G, Servidei S, Palmucci L. Mongini T, et al. Clin Neuropathol. 2002 Mar-Apr;21(2):72-6. Clin Neuropathol. 2002. PMID: 12005255

7

A new mechanism for mtDNA pathogenesis: impairment of post-transcriptional maturation leads to severe depletion of mitochondrial tRNASer(UCN) caused by T7512C and G7497A point mutations.

Möllers M, Maniura-Weber K, Kiseljakovic E, Bust M, Hayrapetyan A, Jaksch M, Helm M, Wiesner RJ, von Kleist-Retzow JC. Möllers M, et al. Nucleic Acids Res. 2005 Sep 30;33(17):5647-58. doi: 10.1093/nar/gki876. Print 2005. Nucleic Acids Res. 2005. PMID: 16199753 Free PMC article.

8

A novel mutation in the mitochondrial tRNA(Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency.

Wong LJ, Yim D, Bai RK, Kwon H, Vacek MM, Zane J, Hoppel CL, Kerr DS. Wong LJ, et al. J Med Genet. 2006 Sep;43(9):e46. doi: 10.1136/jmg.2005.040626. J Med Genet. 2006. PMID: 16950817 Free PMC article.

9

A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss.

Cardaioli E, Da Pozzo P, Gallus GN, Malandrini A, Gambelli S, Gaudiano C, Malfatti E, Viscomi C, Zicari E, Berti G, Serni G, Dotti MT, Federico A. Cardaioli E, et al. Neuromuscul Disord. 2007 Oct;17(9-10):681-3. doi: 10.1016/j.nmd.2007.05.001. Epub 2007 Jul 5. Neuromuscul Disord. 2007. PMID: 17614276

10

Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.

Liu CS, Cheng WL, Lee CF, Ma YS, Lin CY, Huang CC, Wei YH. Liu CS, et al. Acta Neurol Scand. 2006 May;113(5):334-41. doi: 10.1111/j.1600-0404.2006.00586.x. Acta Neurol Scand. 2006. PMID: 16629770

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