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Results: 1 to 20 of 56

1.

Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma.

Zsurka G, Baron M, Stewart JD, Kornblum C, Bös M, Sassen R, Taylor RW, Elger CE, Chinnery PF, Kunz WS.

J Neuropathol Exp Neurol. 2008 Sep;67(9):857-66. doi: 10.1097/NEN.0b013e3181839b2d.

PMID:
18716558
[PubMed - indexed for MEDLINE]
2.

Mitochondrial DNA polymerase-gamma and human disease.

Hudson G, Chinnery PF.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R244-52. Review.

PMID:
16987890
[PubMed - indexed for MEDLINE]
Free Article
3.

The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders.

Cohen BH, Naviaux RK.

Methods. 2010 Aug;51(4):364-73. doi: 10.1016/j.ymeth.2010.05.008. Epub 2010 Jun 15. Review.

PMID:
20558295
[PubMed - indexed for MEDLINE]
4.

Polymerase gamma 1 mutations: clinical correlations.

Milone M, Massie R.

Neurologist. 2010 Mar;16(2):84-91. doi: 10.1097/NRL.0b013e3181c78a89. Review.

PMID:
20220442
[PubMed - indexed for MEDLINE]
5.

Mitochondrial genomic contribution to mitochondrial dysfunction in Alzheimer's disease.

Onyango I, Khan S, Miller B, Swerdlow R, Trimmer P, Bennett P Jr.

J Alzheimers Dis. 2006 Jul;9(2):183-93. Review.

PMID:
16873965
[PubMed - indexed for MEDLINE]
6.

DNA polymerase gamma and mitochondrial disease: understanding the consequence of POLG mutations.

Chan SS, Copeland WC.

Biochim Biophys Acta. 2009 May;1787(5):312-9. doi: 10.1016/j.bbabio.2008.10.007. Epub 2008 Oct 29. Review.

PMID:
19010300
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Mutations in DNA polymerase gamma cause error prone DNA synthesis in human mitochondrial disorders.

Copeland WC, Ponamarev MV, Nguyen D, Kunkel TA, Longley MJ.

Acta Biochim Pol. 2003;50(1):155-67. Review.

PMID:
12673356
[PubMed - indexed for MEDLINE]
Free Article
8.

Mitochondrial DNA analysis in clinical laboratory diagnostics.

Wong LJ, Boles RG.

Clin Chim Acta. 2005 Apr;354(1-2):1-20. Epub 2005 Jan 27. Review.

PMID:
15748595
[PubMed - indexed for MEDLINE]
9.

Consequences of mutations in human DNA polymerase gamma.

Longley MJ, Graziewicz MA, Bienstock RJ, Copeland WC.

Gene. 2005 Jul 18;354:125-31. Review.

PMID:
15913923
[PubMed - indexed for MEDLINE]
10.

Autosomal disorders of mitochondrial DNA maintenance.

Van Goethem G.

Acta Neurol Belg. 2006 Jun;106(2):66-72. Review.

PMID:
16898256
[PubMed - indexed for MEDLINE]
11.

Mitochondrial respiratory chain disorders and the liver.

Morris AA.

Liver. 1999 Oct;19(5):357-68. Review.

PMID:
10533792
[PubMed - indexed for MEDLINE]
12.

Mitochondrial diseases.

Vu TH, Hirano M, DiMauro S.

Neurol Clin. 2002 Aug;20(3):809-39, vii-viii. Review.

PMID:
12432831
[PubMed - indexed for MEDLINE]
13.

Respiratory function decline and DNA mutation in mitochondria, oxidative stress and altered gene expression during aging.

Wei YH, Wu SB, Ma YS, Lee HC.

Chang Gung Med J. 2009 Mar-Apr;32(2):113-32. Review.

PMID:
19403001
[PubMed - indexed for MEDLINE]
Free Article
14.

[Inherited and acquired disorders of mitochondrial DNA].

Walker UA.

Praxis (Bern 1994). 2002 Dec 4;91(49):2129-38. Review. German.

PMID:
12523180
[PubMed - indexed for MEDLINE]
15.

Analysis of potential cancer biomarkers in mitochondrial DNA.

Jakupciak JP, Dakubo GD, Maragh S, Parr RL.

Curr Opin Mol Ther. 2006 Dec;8(6):500-6. Review.

PMID:
17243485
[PubMed - indexed for MEDLINE]
16.

Mitochondrial DNA copy number and mitochondrial DNA deletion in adult and senescent rats.

Gadaleta MN, Rainaldi G, Lezza AM, Milella F, Fracasso F, Cantatore P.

Mutat Res. 1992 Sep;275(3-6):181-93. Review.

PMID:
1383760
[PubMed - indexed for MEDLINE]
17.

Mitochondrial DNA mutation associated with aging and degenerative disease.

Nagley P, Mackay IR, Baumer A, Maxwell RJ, Vaillant F, Wang ZX, Zhang C, Linnane AW.

Ann N Y Acad Sci. 1992 Dec 26;673:92-102. Review.

PMID:
1485738
[PubMed - indexed for MEDLINE]
18.

Alpers syndrome: progressive neuronal degeneration of children with liver disease.

Gordon N.

Dev Med Child Neurol. 2006 Dec;48(12):1001-3. Review.

PMID:
17109792
[PubMed - indexed for MEDLINE]
19.

Mitochondrial abnormalities in inclusion-body myositis.

Oldfors A, Moslemi AR, Jonasson L, Ohlsson M, Kollberg G, Lindberg C.

Neurology. 2006 Jan 24;66(2 Suppl 1):S49-55. Review.

PMID:
16432145
[PubMed - indexed for MEDLINE]
20.

Neuropathologic aspects of cytochrome C oxidase deficiency.

Tanji K, Bonilla E.

Brain Pathol. 2000 Jul;10(3):422-30. Review.

PMID:
10885661
[PubMed - indexed for MEDLINE]

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