(Q24304166)

3'-5' DNA helicase activity

GOA release 2020-03-11

1 reference

Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome

GOA release 2020-03-11

author

Jean-Marc Egly

series ordinal

3

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Valentyn Oksenych

object named as

Valentyn Oksenych

series ordinal

2

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Frédéric Coin

object named as

Frédéric Coin

series ordinal

1

0 references

language of work or name

English

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publication date

27 April 2007

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published in

Molecular Cell

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volume

26

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page(s)

245-56

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issue

2

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Purification of the transcription/repair factor TFIIH and evaluation of its associated activities in vitro

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

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

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

p8/TTD-A as a repair-specific TFIIH subunit

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Conserved XPB core structure and motifs for DNA unwinding: implications for pathway selection of transcription or excision repair

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

XPD mutations prevent TFIIH-dependent transactivation by nuclear receptors and phosphorylation of RARalpha

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Reconstitution of the transcription factor TFIIH: assignment of functions for the three enzymatic subunits, XPB, XPD, and cdk7

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Sequential assembly of the nucleotide excision repair factors in vivo

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Transcriptional activators stimulate DNA repair.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Basal transcription defect discriminates between xeroderma pigmentosum and trichothiodystrophy in XPD patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

DNA repair. Engagement with transcription

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

RAD25 is a DNA helicase required for DNA repair and RNA polymerase II transcription

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

XPG endonuclease makes the 3' incision in human DNA nucleotide excision repair

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

TFIIH XPB mutants suggest a unified bacterial-like mechanism for promoter opening but not escape

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Phosphorylation of XPB helicase regulates TFIIH nucleotide excision repair activity

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Helicase Motif III in SecA is essential for coupling preprotein binding to translocation ATPase.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

p52 Mediates XPB function within the transcription/repair factor TFIIH.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Ordered conformational changes in damaged DNA induced by nucleotide excision repair factors

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

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%2FJ.MOLCEL.2007.03.009

7 January 2021

Substrate specificity of the cdk-activating kinase (CAK) is altered upon association with TFIIH

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

The comings and goings of nucleotide excision repair factors on damaged DNA

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Unraveling DNA helicases. Motif, structure, mechanism and function

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

DNA repair and transcriptional deficiencies caused by mutations in the Drosophila p52 subunit of TFIIH generate developmental defects and chromosome fragility.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021

Dynamic interaction of TTDA with TFIIH is stabilized by nucleotide excision repair in living cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLCEL.2007.03.009

7 January 2021