Nucleotide excision repair genes are expressed at low levels and are not detectably inducible in Caenorhabditis elegans somatic tissues, but their function is required for normal adult life after UVC exposure (Q33514210)

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English	Nucleotide excision repair genes are expressed at low levels and are not detectably inducible in Caenorhabditis elegans somatic tissues, but their function is required for normal adult life after UVC exposure	scientific article

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11 February 2020

Nucleotide excision repair genes are expressed at low levels and are not detectably inducible in Caenorhabditis elegans somatic tissues, but their function is required for normal adult life after UVC exposure (English)

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11 February 2020

Caenorhabditis elegans

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Human XPA (Xeroderma pigmentosum comp grp A) related CELE_K07G5.2

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GOA release 2020-03-11

1

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11 February 2020

Maxwell C K Leung

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11 February 2020

8

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11 February 2020

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Tracey L Crocker

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Ana M Rodriguez

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D Wade Lehmann

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Jonathan H Freedman

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Ben Van Houten

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1 January 2010

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11 February 2020

Mutation Research

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11 February 2020

683

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1-2

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57-67

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describes a project that uses

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A discrete time model for the analysis of medium-throughput C. elegans growth data

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DNA repair in mammalian cells : Nucleotide excision repair: variations on versatility

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Transcriptional profiling in C. elegans suggests DNA damage dependent apoptosis as an ancient function of the p53 family

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Caenorhabditis elegans: an emerging model in biomedical and environmental toxicology.

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Longevity and resistance to stress correlate with DNA repair capacity in Caenorhabditis elegans

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Nucleotide excision repair and the degradation of RNA pol II by the Caenorhabditis elegans XPA and Rsp5 orthologues, RAD-3 and WWP-1.

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Decline of nucleotide excision repair capacity in aging Caenorhabditis elegans

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Checkpoint proteins control survival of the postmitotic cells in Caenorhabditis elegans

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Checkpoint silencing during the DNA damage response in Caenorhabditis elegans embryos

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Regulation of growth by ploidy in Caenorhabditis elegans

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Prokaryotic nucleotide excision repair: the UvrABC system.

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21 June 2018

Nucleotide excision repair

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The eukaryotic nucleotide excision repair pathway

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Functional characterization of global genomic DNA repair and its implications for cancer.

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Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegans

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Subpathways of nucleotide excision repair and their regulation

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Xeroderma pigmentosum and related disorders: defects in DNA repair and transcription

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Measuring gene-specific nucleotide excision repair in human cells using quantitative amplification of long targets from nanogram quantities of DNA.

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Genomic heterogeneity of nucleotide excision repair

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Induction of the SOS response increases the efficiency of global nucleotide excision repair of cyclobutane pyrimidine dimers, but not 6-4 photoproducts, in UV-irradiated Escherichia coli.

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Radiation effects on life span in Caenorhabditis elegans

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A yeast excision-repair gene is inducible by DNA damaging agents

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DNA damage induced nucleotide excision repair in Saccharomyces cerevisiae.

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UV-induced de novo protein synthesis enhances nucleotide excision repair efficiency in a transcription-dependent manner in S. cerevisiae

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Participation of stress-inducible systems and enzymes involved in BER and NER in the protection of Escherichia coli against cumene hydroperoxide

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UV irradiation of wild type and radiation-sensitive mutants of the nematode Caenorhabditis elegans: fertilities, survival, and parental effects

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https://pubmed.ncbi.nlm.nih.gov/19879883

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Ultraviolet mutagenesis of radiation-sensitive (rad) mutants of the nematode Caenorhabditis elegans

1 reference

https://pubmed.ncbi.nlm.nih.gov/19879883

12 December 2020

based on heuristic

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Inducible nucleotide excision repair (NER) of UV-induced cyclobutane pyrimidine dimers in the cell cycle of the budding yeast Saccharomyces cerevisiae: evidence that inducible NER is confined to the G1 phase of the mitotic cell cycle

1 reference

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12 December 2020

based on heuristic

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Quantitative PCR-based measurement of nuclear and mitochondrial DNA damage and repair in mammalian cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19879883

12 December 2020

based on heuristic

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Identifiers

10.1016/J.MRFMMM.2009.10.008

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11 February 2020

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11 February 2020

1 reference

Europe PubMed Central

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11 February 2020

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