Xeroderma Pigmentosum Group C Protein Complex Is the Initiator of Global Genome Nucleotide Excision Repair (Q24312736)

https://api.crossref.org/works/10.1016/S1097-2765(00)80132-X

RAD23 homolog B, nucleotide excision repair protein

8 January 2025

main subject

1 reference

XPC complex subunit, DNA damage recognition and repair factor

GOA release 2020-03-11

1 reference

nucleotide-excision repair

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

xeroderma pigmentosum

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xeroderma pigmentosum group C

inferred from title

1 reference

1 reference

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9

J H Hoeijmakers

J H

Hoeijmakers

1 reference

PubMed

9 December 2023

5

P. J. van der Spek

1 reference

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author name string

K. Sugasawa

1

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J. M. Ng

2

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C. Masutani

3

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S. Iwai

4

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A. P. Eker

6

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F. Hanaoka

7

1 reference

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D. Bootsma

8

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J. H. Hoeijmakers

9

1 reference

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http://www.cell.com/article/S109727650080132X/pdf

8 January 2025

publication date

August 1998

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language of work or name

English

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work available at URL

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https://api.elsevier.com/content/article/PII:S109727650080132X?httpAccept=text/xml

8 January 2025

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8 January 2025

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2

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issue

2

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page(s)

223-32

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The XPA protein is a zinc metalloprotein with an ability to recognize various kinds of DNA damage

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DNA repair in an active gene: removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall

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Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G

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

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

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Purification and characterization of a human protein that binds to damaged DNA.

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Preferential binding of the xeroderma pigmentosum group A complementing protein to damaged DNA.

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Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome

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Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C

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Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23

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Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene

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The relative cytotoxicity of (6-4) photoproducts and cyclobutane dimers in mammalian cells

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Implications of the zinc-finger motif found in the DNA-binding domain of the human XPA protein

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Model for XPC-independent transcription-coupled repair of pyrimidine dimers in humans

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Reconstitution of human DNA repair excision nuclease in a highly defined system

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Molecular mechanism of transcription-repair coupling

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Proliferating cell nuclear antigen is required for DNA excision repair

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HHR23B, a human Rad23 homolog, stimulates XPC protein in nucleotide excision repair in vitro

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Two Human Homologs of Rad23 Are Functionally Interchangeable in Complex Formation and Stimulation of XPC Repair Activity

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The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA

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Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes

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Complementation of the xeroderma pigmentosum DNA repair defect in cell-free extracts

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Comparative analysis of binding of human damaged DNA-binding protein (XPE) and Escherichia coli damage recognition protein (UvrA) to the major ultraviolet photoproducts: T[c,s]T, T[t,s]T, T[6-4]T, and T[Dewar]T.

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Uvr excision repair protein complex of Escherichia coli binds to the convex side of a cisplatin-induced kink in the DNA.

8 January 2025

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Repair of O6-methylguanine by ABC excinuclease of Escherichia coli in vitro

8 January 2025

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8 January 2025

Identifiers

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9734359

release_yosagcghqzhybednwzjhcfavua

8 January 2025

Fatcat ID

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OpenCitations bibliographic resource ID

625493

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OpenCitations Corpus

1 reference

National Center for Biotechnology Information