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Ageing: repair and transcription keep us from premature ageing
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12194834
retrieved
27 June 2017
title
Ageing: repair and transcription keep us from premature ageing
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12194834
retrieved
27 June 2017
author name string
Alan Lehmann
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12194834
retrieved
27 June 2017
language of work or name
English
0 references
publication date
1 August 2002
1 reference
stated in
Europe PubMed Central
PubMed ID
12194834
retrieved
27 June 2017
published in
Current Biology
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stated in
Europe PubMed Central
PubMed ID
12194834
retrieved
27 June 2017
volume
12
1 reference
stated in
Europe PubMed Central
PubMed ID
12194834
retrieved
27 June 2017
issue
16
1 reference
stated in
Europe PubMed Central
PubMed ID
12194834
retrieved
27 June 2017
page(s)
R550-1
1 reference
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Europe PubMed Central
PubMed ID
12194834
retrieved
27 June 2017
cites work
Genome maintenance mechanisms for preventing cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
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7 January 2021
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inferred from DOI database lookup
Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
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7 January 2021
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inferred from DOI database lookup
A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Premature aging in mice deficient in DNA repair and transcription
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
TFIIH: a key component in multiple DNA transactions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA repair. Engagement with transcription
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cockayne syndrome: Review of 140 cases
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cockayne syndrome: defective repair of transcription?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2802%2901050-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0960-9822(02)01050-3
1 reference
stated in
Europe PubMed Central
PubMed ID
12194834
retrieved
27 June 2017
PubMed ID
12194834
1 reference
stated in
Europe PubMed Central
PubMed ID
12194834
retrieved
27 June 2017
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