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Results: 13

Related Articles by Review for PubMed (Select 15917273)

1.

Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome.

Luoma PT, Luo N, Löscher WN, Farr CL, Horvath R, Wanschitz J, Kiechl S, Kaguni LS, Suomalainen A.

Hum Mol Genet. 2005 Jul 15;14(14):1907-20. Epub 2005 May 25.

2.

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
3.

Mitochondrial DNA polymerase-gamma and human disease.

Hudson G, Chinnery PF.

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

4.

Mitochondrial DNA replication and disease: insights from DNA polymerase γ mutations.

Stumpf JD, Copeland WC.

Cell Mol Life Sci. 2011 Jan;68(2):219-33. doi: 10.1007/s00018-010-0530-4. Epub 2010 Oct 8. Review.

5.

Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial replicase, Pol γ.

Euro L, Farnum GA, Palin E, Suomalainen A, Kaguni LS.

Nucleic Acids Res. 2011 Nov;39(21):9072-84. doi: 10.1093/nar/gkr618. Epub 2011 Aug 8. Review.

6.

Purification and functional characterization of human mitochondrial DNA polymerase gamma harboring disease mutations.

Kasiviswanathan R, Longley MJ, Young MJ, Copeland WC.

Methods. 2010 Aug;51(4):379-84. doi: 10.1016/j.ymeth.2010.02.015. Epub 2010 Feb 20. Review.

7.

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.

8.

Polymerase gamma disease through the ages.

Saneto RP, Naviaux RK.

Dev Disabil Res Rev. 2010;16(2):163-74. doi: 10.1002/ddrr.105. Review.

PMID:
20818731
9.

Defects of mitochondrial DNA replication.

Copeland WC.

J Child Neurol. 2014 Sep;29(9):1216-24. doi: 10.1177/0883073814537380. Epub 2014 Jun 30. Review.

PMID:
24985751
10.

[Molecular biology of defects in the mitochondrial electron-transfer complexes].

Tanaka M.

Seikagaku. 1991 Mar;63(3):169-87. Review. Japanese. No abstract available.

PMID:
2071965
11.

Mitochondrial myopathies: genetic defects.

Harding AE, Holt IJ, Cooper JM, Schapira AH, Sweeney M, Clark JB, Morgan-Hughes JA.

Biochem Soc Trans. 1990 Aug;18(4):519-22. Review. No abstract available.

PMID:
2276422
12.

DNA polymerase γ and disease: what we have learned from yeast.

Lodi T, Dallabona C, Nolli C, Goffrini P, Donnini C, Baruffini E.

Front Genet. 2015 Mar 17;6:106. doi: 10.3389/fgene.2015.00106. eCollection 2015. Review.

13.

[Molecular mechanisms for the nontargeted mutations induced by chemical mutagens].

Yu YN, Yang J.

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2003 Oct;32(5):369-74. Review. Chinese. No abstract available.

PMID:
14610732
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