Neurological disorders associated with DNA strand-break processing enzymes. - Test2 - elhamkhani - TriplyDB

Neurological disorders associated with DNA strand-break processing enzymes.

Neurological disorders associated with DNA strand-break processing enzymes.

http://www.wikidata.org/entity/Q34535722

about

Characterization of DNA Substrate Binding to the Phosphatase Domain of the DNA Repair Enzyme Polynucleotide Kinase/Phosphatase Tyrosyl-DNA phosphodiesterases: rescuing the genome from the risks of relaxation.Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.Tdp1 processes chromate-induced single-strand DNA breaks that collapse replication forks

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Neurological disorders associated with DNA strand-break processing enzymes.

http://www.wikidata.org/entity/Q34535722

description

2016 nî lūn-bûn

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2016 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

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name

Neurological disorders associated with DNA strand-break processing enzymes.

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Neurological disorders associated with DNA strand-break processing enzymes.

@en

Neurological disorders associated with DNA strand-break processing enzymes.

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type

label

Neurological disorders associated with DNA strand-break processing enzymes.

@ast

Neurological disorders associated with DNA strand-break processing enzymes.

@en

Neurological disorders associated with DNA strand-break processing enzymes.

@nl

prefLabel

Neurological disorders associated with DNA strand-break processing enzymes.

@ast

Neurological disorders associated with DNA strand-break processing enzymes.

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Neurological disorders associated with DNA strand-break processing enzymes.

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J.MAD.2016.07.009

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Mechanisms of Ageing and Development

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Neurological disorders associated with DNA strand-break processing enzymes.

@en

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Bingcheng Jiang

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J N Mark Glover

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Michael Weinfeld

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P2860

CK2 phosphorylation-dependent interaction between aprataxin and MDC1 in the DNA damage response

Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3'-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damage

Molecular characterization of a human DNA kinase

Actions of aprataxin in multiple DNA repair pathways

Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1

Conversion of phosphoglycolate to phosphate termini on 3' overhangs of DNA double strand breaks by the human tyrosyl-DNA phosphodiesterase hTdp1

Spinocerebellar ataxia with axonal neuropathy: consequence of a Tdp1 recessive neomorphic mutation?

The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates

The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4

Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3'-phosphate and 3'-phosphoglycolate ends

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130-140

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scholarly article

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10.1016/J.MAD.2016.07.009

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Pt A

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161

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2016-07-25T00:00:00Z

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27470939

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5266678

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