(Q39622327)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21143350%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

Mutant Cockayne syndrome group B protein inhibits repair of DNA topoisomerase I-DNA covalent complex (English)

1 reference

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17 January 2020

1 reference

5

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17 January 2020

author name string

Katsuyoshi Horibata

1

1 reference

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17 January 2020

Masafumi Saijo

2

1 reference

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17 January 2020

Mui N Bay

3

1 reference

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17 January 2020

Li Lan

4

1 reference

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17 January 2020

Philip J Brooks

6

1 reference

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17 January 2020

Masamitsu Honma

7

1 reference

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17 January 2020

Takehiko Nohmi

8

1 reference

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17 January 2020

Akira Yasui

9

1 reference

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17 January 2020

Kiyoji Tanaka

10

1 reference

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17 January 2020

publication date

9 December 2010

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17 January 2020

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17 January 2020

volume

16

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17 January 2020

issue

1

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17 January 2020

page(s)

101-114

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Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage?

17 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

DNA topoisomerases: structure, function, and mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Transcription-dependent degradation of topoisomerase I-DNA covalent complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

ATM, the Mre11/Rad50/Nbs1 complex, and topoisomerase I are concentrated in the nucleus of Purkinje neurons in the juvenile human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Transcription-coupled DNA repair: two decades of progress and surprises

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

DNA single-strand break repair and spinocerebellar ataxia with axonal neuropathy-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Deletion of 5' sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Mechanistic links between nonsense-mediated mRNA decay and pre-mRNA splicing in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Human DNA topoisomerase I: relaxation, roles, and damage control

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Hereditary ataxia SCAN1 cells are defective for the repair of transcription-dependent topoisomerase I cleavage complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Cockayne syndrome: Review of 140 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

An abundant evolutionarily conserved CSB-PiggyBac fusion protein expressed in Cockayne syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

DNA Topoisomerase I Inhibitors: Chemistry, Biology, and Interfacial Inhibition

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Topoisomerase I-mediated DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Three novel mutations responsible for Cockayne syndrome group A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Hyperphosphorylation of RNA polymerase II in response to topoisomerase I cleavage complexes and its association with transcription- and BRCA1-dependent degradation of topoisomerase I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Host cell reactivation of plasmids containing oxidative DNA lesions is defective in Cockayne syndrome but normal in UV-sensitive syndrome fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Ultraviolet-sensitive syndrome cells are defective in transcription-coupled repair of cyclobutane pyrimidine dimers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Cooperation of the Cockayne syndrome group B protein and poly(ADP-ribose) polymerase 1 in the response to oxidative stress.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Deficiency of the Cockayne syndrome B (CSB) gene aggravates the genomic instability caused by endogenous oxidative DNA base damage in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Primary fibroblasts of Cockayne syndrome patients are defective in cellular repair of 8-hydroxyguanine and 8-hydroxyadenine resulting from oxidative stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Different effects of CSA and CSB deficiency on sensitivity to oxidative DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X

Neuropathology of Cockayne syndrome: Evidence for impaired development, premature aging, and neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2010.01467.X