UV-induced skin carcinogenesis in xeroderma pigmentosum group A (XPA) gene-knockout mice with nucleotide excision repair-deficiency (Q30670975)

26 June 2017

title

UV-induced skin carcinogenesis in xeroderma pigmentosum group A (XPA) gene-knockout mice with nucleotide excision repair-deficiency (English)

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xeroderma pigmentosum group A

26 June 2017

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xeroderma pigmentosum

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based on heuristic

inferred from title

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Tanaka K

1

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26 June 2017

Kamiuchi S

2

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26 June 2017

Ren Y

3

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26 June 2017

Yonemasu R

4

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26 June 2017

Ichikawa M

5

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26 June 2017

Murai H

6

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26 June 2017

Yoshino M

7

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26 June 2017

Takeuchi S

8

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26 June 2017

Saijo M

9

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26 June 2017

Nakatsu Y

10

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26 June 2017

Miyauchi-Hashimoto H

11

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26 June 2017

Horio T

12

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26 June 2017

language of work or name

English

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publication date

1 June 2001

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26 June 2017

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26 June 2017

volume

477

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26 June 2017

issue

1-2

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26 June 2017

page(s)

31-40

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Effect of DNA lesions on transcription elongation

26 June 2017

cites work

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Molecular mechanism of nucleotide excision repair.

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High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A gene

7 January 2021

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Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain

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Molecular cloning of human XPAC gene homologs from chicken, Xenopus laevis and Drosophila melanogaster

7 January 2021

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DNA repair protein XPA binds replication protein A (RPA).

7 January 2021

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RPA involvement in the damage-recognition and incision steps of nucleotide excision repair

7 January 2021

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Sequential binding of DNA repair proteins RPA and ERCC1 to XPA in vitro

7 January 2021

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An interaction between the DNA repair factor XPA and replication protein A appears essential for nucleotide excision repair

7 January 2021

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Solution structure of the DNA- and RPA-binding domain of the human repair factor XPA

7 January 2021

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Resonance assignments, solution structure, and backbone dynamics of the DNA- and RPA-binding domain of human repair factor XPA.

7 January 2021

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7 January 2021

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Formation of a ternary complex by human XPA, ERCC1, and ERCC4(XPF) excision repair proteins

7 January 2021

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Isolation of human complexes proficient in nucleotide excision repair

7 January 2021

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

7 January 2021

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DNA damage recognition by XPA protein promotes efficient recruitment of transcription factor II H.

7 January 2021

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Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein

7 January 2021

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DNA-binding polarity of human replication protein A positions nucleases in nucleotide excision repair

7 January 2021

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Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair

7 January 2021

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Order of assembly of human DNA repair excision nuclease

7 January 2021

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Open complex formation around a lesion during nucleotide excision repair provides a structure for cleavage by human XPG protein

7 January 2021

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

7 January 2021

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The non-catalytic function of XPG protein during dual incision in human nucleotide excision repair.

7 January 2021

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Assembly, subunit composition, and footprint of human DNA repair excision nuclease

7 January 2021

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

7 January 2021

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Human DNA repair excision nuclease. Analysis of the roles of the subunits involved in dual incisions by using anti-XPG and anti-ERCC1 antibodies

7 January 2021

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Mutational analysis of a function of xeroderma pigmentosum group A (XPA) protein in strand-specific DNA repair

7 January 2021

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A novel cytoplasmic GTPase XAB1 interacts with DNA repair protein XPA

7 January 2021

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XAB2, a novel tetratricopeptide repeat protein involved in transcription-coupled DNA repair and transcription

7 January 2021

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Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA.

7 January 2021

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High susceptibility to ultraviolet-induced carcinogenesis in mice lacking XPC.

7 January 2021

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7 January 2021

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Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Decreased UV sensitivity, mismatch repair activity and abnormal cell cycle checkpoints in skin cancer cell lines derived from UVB-irradiated XPA-deficient mice

7 January 2021

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7 January 2021

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Ultraviolet radiation-induced suppression of natural killer cell activity is enhanced in xeroderma pigmentosum group A (XPA) model mice

7 January 2021

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ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

7 January 2021

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Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II

7 January 2021

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Biochemical and biological characterization of wild-type and ATPase-deficient Cockayne syndrome B repair protein.

7 January 2021

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Cockayne syndrome group B protein enhances elongation by RNA polymerase II

7 January 2021

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Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes

7 January 2021

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RNA polymerase II elongation complexes containing the Cockayne syndrome group B protein interact with a molecular complex containing the transcription factor IIH components xeroderma pigmentosum B and p62

7 January 2021

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The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex

7 January 2021

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UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells

7 January 2021

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The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH

7 January 2021

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10.1016/S0027-5107(01)00093-8

7 January 2021

Identifiers

DOI

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26 June 2017

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