Dysmyelination not demyelination causes neurological symptoms in preweaned mice in a murine model of Cockayne syndrome. (Q35849782)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22393014 AND SRC:MED&resulttype=core&format=json

25 January 2020

title

Dysmyelination not demyelination causes neurological symptoms in preweaned mice in a murine model of Cockayne syndrome (English)

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25 January 2020

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4

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author name string

Ingrid Revet

1

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25 January 2020

Luzviminda Feeney

2

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25 January 2020

Amy A Tang

3

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25 January 2020

James E Cleaver

5

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25 January 2020

language of work or name

English

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publication date

5 March 2012

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Proceedings of the National Academy of Sciences of the United States of America

25 January 2020

published in

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25 January 2020

volume

109

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25 January 2020

issue

12

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25 January 2020

page(s)

4627-4632

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25 January 2020

1 reference

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Premature aging and cancer in nucleotide excision repair-disorders

11 July 2018

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Functional relevance of the histone gammaH2Ax in the response to DNA damaging agents.

11 July 2018

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Proteins of nucleotide and base excision repair pathways interact in mitochondria to protect from loss of subcutaneous fat, a hallmark of aging

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11 July 2018

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

11 July 2018

1 reference

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

11 July 2018

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Accumulation of (5'S)-8,5'-cyclo-2'-deoxyadenosine in organs of Cockayne syndrome complementation group B gene knockout mice

11 July 2018

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11 July 2018

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A neurological phenotype in mice with DNA repair gene Ercc1 deficiency

11 July 2018

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

11 July 2018

1 reference

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Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH

11 July 2018

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p53 suppression overwhelms DNA polymerase eta deficiency in determining the cellular UV DNA damage response

11 July 2018

1 reference

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

11 July 2018

1 reference

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XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients

11 July 2018

1 reference

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Impaired genome maintenance suppresses the growth hormone--insulin-like growth factor 1 axis in mice with Cockayne syndrome

11 July 2018

1 reference

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The role of CSA in the response to oxidative DNA damage in human cells

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3311387

Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3311387

Increased apoptosis, p53 up-regulation, and cerebellar neuronal degeneration in repair-deficient Cockayne syndrome mice

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3311387

Retinal degeneration and ionizing radiation hypersensitivity in a mouse model for Cockayne syndrome

11 July 2018

1 reference

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Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo

11 July 2018

1 reference

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An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria

11 July 2018

1 reference

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Cockayne syndrome group B protein (CSB) plays a general role in chromatin maintenance and remodeling

11 July 2018

1 reference

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11 July 2018

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11 July 2018

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Oxidative nucleotide damage and superoxide dismutase expression in the brains of xeroderma pigmentosum group A and Cockayne syndrome

11 July 2018

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11 July 2018

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

11 July 2018

1 reference

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

11 July 2018

1 reference

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11 July 2018

1 reference

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11 July 2018

1 reference

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The transcriptional response after oxidative stress is defective in Cockayne syndrome group B cells

11 July 2018

1 reference

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11 July 2018

1 reference

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11 July 2018

1 reference

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Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes

11 July 2018

1 reference

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11 July 2018

1 reference

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11 July 2018

1 reference

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Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosum

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3311387

Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome

11 July 2018

1 reference

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Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition

11 July 2018

1 reference

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11 July 2018

1 reference

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High susceptibility to ultraviolet-induced carcinogenesis in mice lacking XPC

11 July 2018

1 reference

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UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I.

11 July 2018

1 reference

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11 July 2018

1 reference

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Abnormal kinetics of DNA synthesis in ultraviolet light-irradiated cells from patients with Cockayne's syndrome

11 July 2018

1 reference

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

11 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073/PNAS.1202621109

Structural and molecular hair abnormalities in trichothiodystrophy.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073/PNAS.1202621109

A New Human Photosensitive Subject with a Defect in the Recovery of DNA Synthesis after Ultraviolet-light Irradiation

21 January 2018

1 reference

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Blockage of RNA polymerase as a possible trigger for u.v. light-induced apoptosis

14 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22393014

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Direct restart of a replication fork stalled by a head-on RNA polymerase

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22393014

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.1202621109

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22393014 AND SRC:MED&resulttype=core&format=json

25 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22393014 AND SRC:MED&resulttype=core&format=json

25 January 2020

PubMed publication ID

22393014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22393014 AND SRC:MED&resulttype=core&format=json