A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy (Q28593147)

31 January 2017

title

A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy (English)

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Excision repair cross-complementing rodent repair deficiency, complementation group 2

31 January 2017

main subject

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GOA release 2020-03-11

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9

J. H. Hoeijmakers

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31 January 2017

J. de Boer

1

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31 January 2017

J. de Wit

2

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31 January 2017

H. van Steeg

3

1 reference

31 January 2017

R. J. Berg

4

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31 January 2017

H. Morreau

5

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31 January 2017

P. Visser

6

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31 January 2017

A. R. Lehmann

7

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31 January 2017

M. Duran

8

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31 January 2017

G. Weeda

10

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31 January 2017

language of work or name

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1 June 1998

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31 January 2017

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31 January 2017

volume

1

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31 January 2017

issue

7

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31 January 2017

page(s)

981–990

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DNA repair. Engagement with transcription

31 January 2017

cites work

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7 January 2021

The primary structure of the alpha subunit of human elongation factor 1. Structural aspects of guanine-nucleotide-binding sites

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7 January 2021

Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy

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https://api.crossref.org/works/10.1016/S1097-2765(00)80098-2

7 January 2021

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/S1097-2765(00)80098-2

7 January 2021

Mechanism of open complex and dual incision formation by human nucleotide excision repair factors

1 reference

https://api.crossref.org/works/10.1016/S1097-2765(00)80098-2

7 January 2021

Structural and mutational analysis of the xeroderma pigmentosum group D (XPD) gene

1 reference

https://api.crossref.org/works/10.1016/S1097-2765(00)80098-2

7 January 2021

Keratins and the skin

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https://api.crossref.org/works/10.1016/S1097-2765(00)80098-2

7 January 2021

Characterization of the human spr2 promoter: induction after UV irradiation or TPA treatment and regulation during differentiation of cultured primary keratinocytes

1 reference

https://api.crossref.org/works/10.1016/S1097-2765(00)80098-2

7 January 2021

A comparison of the proteins of normal and trichothiodystrophic human hair

1 reference

https://api.crossref.org/works/10.1016/S1097-2765(00)80098-2

7 January 2021

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/S1097-2765(00)80098-2

7 January 2021

TFIIH: a key component in multiple DNA transactions

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7 January 2021

The small proline-rich proteins constitute a multigene family of differentially regulated cornified cell envelope precursor proteins

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7 January 2021

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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7 January 2021

Simplified mammalian DNA isolation procedure

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7 January 2021

Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes

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7 January 2021

Comparison of samples of human hair by two-dimensional electrophoresis

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7 January 2021

LCR/MEL: a versatile system for high-level expression of heterologous proteins in erythroid cells

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7 January 2021

DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor

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7 January 2021

Buffalo rat liver cells produce a diffusible activity which inhibits the differentiation of murine embryonal carcinoma and embryonic stem cells

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7 January 2021

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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7 January 2021

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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7 January 2021

DNA repair investigations in nine Italian patients affected by trichothiodystrophy.

1 reference

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7 January 2021

Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.

1 reference

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7 January 2021

Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Three Unusual Repair Deficiencies Associated with Transcription Factor BTF2(TFIIH): Evidence for the Existence of a Transcription Syndrome

1 reference

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7 January 2021

A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome

1 reference

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7 January 2021