Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial replicase, Pol γ-Reference-Cited by-同舟云学术

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

Published:2011-08-08 Issue:21 Volume:39 Page:9072-9084
ISSN:1362-4962
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Euro Liliya,Farnum Gregory A.,Palin Eino,Suomalainen Anu,Kaguni Laurie S.

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/39/21/9072/16778916/gkr618.pdf

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3. Functional human mitochondrial DNA polymerase gamma forms a heterotrimer;Yakubovskaya;J. Biol. Chem.,2006

4. Identification of 5′-deoxyribose phosphate lyase activity in human DNA polymerase gamma and its role in mitochondrial base excision repair in vitro;Longley;Proc. Natl Acad. Sci. USA,1998

5. A novel processive mechanism for DNA synthesis revealed by structure, modeling and mutagenesis of the accessory subunit of human mitochondrial DNA polymerase;Fan;J. Mol. Biol.,2006

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