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English
From a DNA helicase to brittle hair
scientific article published on 01 October 1998
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
title
From a DNA helicase to brittle hair
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
author
Sebastiaan Winkler
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
author name string
Hoeijmakers JH
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
publication date
1 October 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
volume
20
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
page(s)
106-107
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
exact match
https://scigraph.springernature.com/pub.10.1038/2396
0 references
cites work
Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F2396
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F2396
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F2396
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mechanism of open complex and dual incision formation by human nucleotide excision repair factors
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F2396
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA repair. Engagement with transcription
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F2396
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Three Unusual Repair Deficiencies Associated with Transcription Factor BTF2(TFIIH): Evidence for the Existence of a Transcription Syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F2396
retrieved
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/10.1038%2F2396
retrieved
7 January 2021
based on heuristic
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/10.1038%2F2396
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/2396
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
PubMed publication ID
9771695
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9771695
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9771695%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
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