Purification and Comparative Assay of the Human Mitochondrial Replicative DNA Helicase

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Purification and Comparative Assay of the Human Mitochondrial Replicative DNA Helicase

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-my

2016年学术文章

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2016年學術文章

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2016年學術文章

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2016年學術文章

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Purification and Comparative Assay of the Human Mitochondrial Replicative DNA Helicase

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Purification and Comparative Assay of the Human Mitochondrial Replicative DNA Helicase

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Purification and Comparative Assay of the Human Mitochondrial Replicative DNA Helicase

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Purification and Comparative Assay of the Human Mitochondrial Replicative DNA Helicase

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Purification and Comparative Assay of the Human Mitochondrial Replicative DNA Helicase

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Purification and Comparative Assay of the Human Mitochondrial Replicative DNA Helicase

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P1476

Purification and Comparative Assay of the Human Mitochondrial Replicative DNA Helicase

@en

P2093

Fernando A Rosado-Ruiz

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Laurie S Kaguni

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Minyoung So

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P2860

TWINKLE Has 5' -> 3' DNA helicase activity and is specifically stimulated by mitochondrial single-stranded DNA-binding protein

Modular architecture of the hexameric human mitochondrial DNA helicase

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

Functional roles of the N- and C-terminal regions of the human mitochondrial single-stranded DNA-binding protein

Dynamic effects of cofactors and DNA on the oligomeric state of human mitochondrial DNA helicase.

Defects in mitochondrial DNA replication and human disease

Modeling pathogenic mutations of human twinkle in Drosophila suggests an apoptosis role in response to mitochondrial defects.

Reduced stimulation of recombinant DNA polymerase γ and mitochondrial DNA (mtDNA) helicase by variants of mitochondrial single-stranded DNA-binding protein (mtSSB) correlates with defects in mtDNA replication in animal cells.

Differential phenotypes of active site and human autosomal dominant progressive external ophthalmoplegia mutations in Drosophila mitochondrial DNA helicase expressed in Schneider cells.

Functional importance of the conserved N-terminal domain of the mitochondrial replicative DNA helicase

P304

185-198

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P31

scholarly article

P356

10.1007/978-1-4939-3040-1_14

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P407

English

P478

1351

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P577

2016-01-01T00:00:00Z

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P698

26530683

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P932

4703107

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