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A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
9651581
retrieved
31 January 2017
title
A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy
(English)
1 reference
stated in
PubMed
PubMed ID
9651581
retrieved
31 January 2017
main subject
Excision repair cross-complementing rodent repair deficiency, complementation group 2
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GOA release 2020-03-11
trichothiodystrophy
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inferred from title
author
Jan Hoeijmakers
series ordinal
9
object named as
J. H. Hoeijmakers
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PubMed
PubMed ID
9651581
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31 January 2017
author name string
J. de Boer
series ordinal
1
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PubMed
PubMed ID
9651581
retrieved
31 January 2017
J. de Wit
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2
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PubMed
PubMed ID
9651581
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31 January 2017
H. van Steeg
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3
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PubMed
PubMed ID
9651581
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31 January 2017
R. J. Berg
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4
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PubMed
PubMed ID
9651581
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31 January 2017
H. Morreau
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5
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PubMed
PubMed ID
9651581
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31 January 2017
P. Visser
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6
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PubMed
PubMed ID
9651581
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31 January 2017
A. R. Lehmann
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7
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PubMed
PubMed ID
9651581
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31 January 2017
M. Duran
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PubMed
PubMed ID
9651581
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31 January 2017
G. Weeda
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10
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PubMed
PubMed ID
9651581
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31 January 2017
language of work or name
English
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publication date
1 June 1998
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PubMed
PubMed ID
9651581
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31 January 2017
published in
Molecular Cell
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PubMed
PubMed ID
9651581
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31 January 2017
volume
1
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PubMed
PubMed ID
9651581
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31 January 2017
page(s)
981–990
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PubMed
PubMed ID
9651581
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31 January 2017
issue
7
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PubMed
PubMed ID
9651581
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31 January 2017
cites work
DNA repair. Engagement with transcription
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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The primary structure of the alpha subunit of human elongation factor 1. Structural aspects of guanine-nucleotide-binding sites
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy
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Crossref
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA.
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Mechanism of open complex and dual incision formation by human nucleotide excision repair factors
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Structural and mutational analysis of the xeroderma pigmentosum group D (XPD) gene
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reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Keratins and the skin
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Characterization of the human spr2 promoter: induction after UV irradiation or TPA treatment and regulation during differentiation of cultured primary keratinocytes
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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A comparison of the proteins of normal and trichothiodystrophic human hair
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Crossref
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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Introduction of a subtle mutation into the Hox-2.6 locus in embryonic stem cells
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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TFIIH: a key component in multiple DNA transactions
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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The small proline-rich proteins constitute a multigene family of differentially regulated cornified cell envelope precursor proteins
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Intermittent hair loss in a child with PIBI(D)S syndrome and trichothiodystrophy with defective DNA repair-xeroderma pigmentosum group D.
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Simplified mammalian DNA isolation procedure
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7 January 2021
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Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes
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Comparison of samples of human hair by two-dimensional electrophoresis
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LCR/MEL: a versatile system for high-level expression of heterologous proteins in erythroid cells
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Buffalo rat liver cells produce a diffusible activity which inhibits the differentiation of murine embryonal carcinoma and embryonic stem cells
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Competent transcription initiation by RNA polymerase II in cell-free extracts from xeroderma pigmentosum groups B and D in an optimized RNA transcription assay
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Crossref
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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Use of double-replacement gene targeting to replace the murine alpha-lactalbumin gene with its human counterpart in embryonic stem cells and mice.
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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DNA repair investigations in nine Italian patients affected by trichothiodystrophy.
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Crossref
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells
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Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980098-2
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7 January 2021
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Identifiers
DOI
10.1016/S1097-2765(00)80098-2
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1803214
OpenCitations bibliographic resource ID
1803214
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1803214
PubMed ID
9651581
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1803214
ResearchGate publication ID
13632362
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