Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease (Q28238547)

Disruption of mouse Slx4, a regulator of structure-specific nucleases, phenocopies Fanconi anemia

Europe PubMed Central

title

Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease (English)

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Siobhán Q Gregg

1

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Andria Rasile Robinson

series ordinal

2

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Laura J Niedernhofer

series ordinal

3

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language of work or name

English

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publication date

15 July 2011

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published in

DNA Repair

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volume

10

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issue

7

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page(s)

781-91

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cites work

1 reference

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Mutations of the SLX4 gene in Fanconi anemia

20 March 2017

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Human SLX4 is a Holliday junction resolvase subunit that binds multiple DNA repair/recombination endonucleases

20 March 2017

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Mammalian BTBD12/SLX4 assembles a Holliday junction resolvase and is required for DNA repair

20 March 2017

1 reference

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Drosophila MUS312 and the vertebrate ortholog BTBD12 interact with DNA structure-specific endonucleases in DNA repair and recombination

20 March 2017

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Coordination of structure-specific nucleases by human SLX4/BTBD12 is required for DNA repair

20 March 2017

1 reference

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Mouse models of Fanconi anemia

20 March 2017

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Human XPF controls TRF2 and telomere length maintenance through distinctive mechanisms

20 March 2017

1 reference

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Delayed and accelerated aging share common longevity assurance mechanisms

20 March 2017

1 reference

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ERCC1-XPF endonuclease facilitates DNA double-strand break repair

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

XPD helicase structures and activities: insights into the cancer and aging phenotypes from XPD mutations

20 March 2017

1 reference

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The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Structural basis for the recruitment of ERCC1-XPF to nucleotide excision repair complexes by XPA

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure

20 March 2017

1 reference

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A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis

20 March 2017

1 reference

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Crystal structure and DNA binding functions of ERCC1, a subunit of the DNA structure-specific endonuclease XPF-ERCC1

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

ERCC1/XPF removes the 3' overhang from uncapped telomeres and represses formation of telomeric DNA-containing double minute chromosomes

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

The structure-specific endonuclease Ercc1-Xpf is required for targeted gene replacement in embryonic stem cells

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Control of human telomere length by TRF1 and TRF2

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Mapping of interaction domains between human repair proteins ERCC1 and XPF

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Retracted: A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function

20 March 2017

1 reference

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Repair of site-specific double-strand breaks in a mammalian chromosome by homologous and illegitimate recombination

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Mutational analysis of the human nucleotide excision repair gene ERCC1

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Specific association between the human DNA repair proteins XPA and ERCC1

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Specific cleavage of model recombination and repair intermediates by the yeast Rad1-Rad10 DNA endonuclease

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

RAD1 and RAD10, but not other excision repair genes, are required for double-strand break-induced recombination in Saccharomyces cerevisiae

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Purification and characterization of the XPF-ERCC1 complex of human DNA repair excision nuclease

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Molecular cloning of a human DNA repair gene

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

RAD10, an excision repair gene of Saccharomyces cerevisiae, is involved in the RAD1 pathway of mitotic recombination

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Removal of nonhomologous DNA ends in double-strand break recombination: the role of the yeast ultraviolet repair gene RAD1

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Deletion of genes implicated in protecting the integrity of male germ cells has differential effects on the incidence of DNA breaks and germ cell loss

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Mice with skin-specific DNA repair gene (Ercc1) inactivation are hypersensitive to ultraviolet irradiation-induced skin cancer and show more rapid actinic progression

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Reduced hematopoietic reserves in DNA interstrand crosslink repair-deficient Ercc1-/- mice

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Deletion of the nucleotide excision repair gene Ercc1 reduces immunoglobulin class switching and alters mutations near switch recombination junctions

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Nucleotide excision repair gene (ERCC1) deficiency causes G(2) arrest in hepatocytes and a reduction in liver binucleation: the role of p53 and p21

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Retinal degeneration and ionizing radiation hypersensitivity in a mouse model for Cockayne syndrome

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

The structure-specific endonuclease Ercc1-Xpf is required to resolve DNA interstrand cross-link-induced double-strand breaks

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Growth retardation, early death, and DNA repair defects in mice deficient for the nucleotide excision repair enzyme XPF

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

DNA repair gene Ercc1 is essential for normal spermatogenesis and oogenesis and for functional integrity of germ cell DNA in the mouse

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Mice with DNA repair gene (ERCC-1) deficiency have elevated levels of p53, liver nuclear abnormalities and die before weaning

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endings

20 March 2017

1 reference

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Accelerated aging of intervertebral discs in a mouse model of progeria.

7 April 2017

1 reference

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Hyper telomere recombination accelerates replicative senescence and may promote premature aging

29 September 2017

1 reference

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Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patients

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

XPF-ERCC1 participates in the Fanconi anemia pathway of cross-link repair.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Fanconi anemia and its diagnosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

29 September 2017

1 reference

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TRF1 controls telomere length and mitotic fidelity in epithelial homeostasis.

29 September 2017

1 reference

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Non-homologous end joining in class switch recombination: the beginning of the end

29 September 2017

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29 September 2017

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29 September 2017

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A review of ageing and an examination of clinical methods in the assessment of ageing skin. Part I: Cellular and molecular perspectives of skin ageing

29 September 2017

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Mechanism of replication-coupled DNA interstrand crosslink repair

29 September 2017

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A neurological phenotype in mice with DNA repair gene Ercc1 deficiency

29 September 2017

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The Utilization during Mitotic Cell Division of Loci Controlling Meiotic Recombination and Disjunction in DROSOPHILA MELANOGASTER.

29 September 2017

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Increased genomic instability is not a prerequisite for shortened lifespan in DNA repair deficient mice

29 September 2017

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The structure of the human ERCC1/XPF interaction domains reveals a complementary role for the two proteins in nucleotide excision repair

29 September 2017

1 reference

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Movement disorders in the older patient: differential diagnosis and general management

29 September 2017

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Role of oxidative stress in age-associated chronic kidney pathologies

29 September 2017

1 reference

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Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage

29 September 2017

1 reference

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Biology of intervertebral disc aging and degeneration: involvement of the extracellular matrix

29 September 2017

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

29 September 2017

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Yeast Mre11 and Rad1 proteins define a Ku-independent mechanism to repair double-strand breaks lacking overlapping end sequences

29 September 2017

1 reference

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In vivo reversion to normal of inherited mutations in humans

29 September 2017

1 reference

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Functional cloning of drug resistance genes from retroviral cDNA libraries

29 September 2017

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Arabidopsis mutants sensitive to gamma radiation include the homologue of the human repair gene ERCC1.

29 September 2017

1 reference

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The role of proteoglycans in aging, degeneration and repair of the intervertebral disc

29 September 2017

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When reverse genetics meets physiology: the use of site-specific recombinases in mice

29 September 2017

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Restoration of T cell-specific V(D)J recombination in DNA-PKcs(-/-) mice by ionizing radiation: The effects on survival, development, and tumorigenesis.

29 September 2017

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Correction of liver dysfunction in DNA repair-deficient mice with an ERCC1 transgene.

29 September 2017

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Back mutation can produce phenotype reversion in Bloom syndrome somatic cells

29 September 2017

1 reference

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Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Role of ERCC1 in removal of long non-homologous tails during targeted homologous recombination

29 September 2017

1 reference

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Defining the roles of nucleotide excision repair and recombination in the repair of DNA interstrand cross-links in mammalian cells

29 September 2017

1 reference

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Role of the nucleotide excision repair gene ERCC1 in formation of recombination-dependent rearrangements in mammalian cells

29 September 2017

1 reference

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Repair of an interstrand DNA cross-link initiated by ERCC1-XPF repair/recombination nuclease.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.

29 September 2017

1 reference

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The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect

29 September 2017

1 reference

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Sister chromatid exchanges are mediated by homologous recombination in vertebrate cells

29 September 2017

1 reference

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Nucleotide excision repair: from E. coli to man.

29 September 2017

1 reference

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Molecular mechanism of nucleotide excision repair.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Characterization of molecular defects in xeroderma pigmentosum group F in relation to its clinically mild symptoms

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Two pathways for removal of nonhomologous DNA ends during double-strand break repair in Saccharomyces cerevisiae

29 September 2017

1 reference

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A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

The Drosophila meiotic recombination gene mei-9 encodes a homologue of the yeast excision repair protein Rad1.

29 September 2017

1 reference

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

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

29 September 2017

1 reference

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Cataracts, microcephaly, kyphosis, and limited joint movement in two siblings: A new syndrome

29 September 2017

1 reference

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Autosomal recessive cerebro-oculo-facio-skeletal (COFS) syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Xeroderma pigmentosum groups C and F: additional assignments and a review of the subjects in Japan

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 830 published cases

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Different types of recombination events are controlled by the RAD1 and RAD52 genes of Saccharomyces cerevisiae

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Clinical and photobiological characteristics of xeroderma pigmentosum complementation group F: a review of cases from Japan

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Late onset of skin cancers in 2 xeroderma pigmentosum group F siblings and a review of 30 Japanese xeroderma pigmentosum patients in groups D, E and F.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Xeroderma pigmentosum--Cockayne syndrome complex: a further case

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

A case of xeroderma pigmentosum complementation group F with neurological abnormalities

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Xeroderma pigmentosum complementation group F: more assignments and repair characteristics

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Defective DNA cross-link removal in Chinese hamster cell mutants hypersensitive to bifunctional alkylating agents.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Clinical symptoms and DNA repair characteristics of xeroderma pigmentosum patients from Germany.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

A sixth complementation group in xeroderma pigmentosum

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

NER factors are recruited to active promoters and facilitate chromatin modification for transcription in the absence of exogenous genotoxic attack.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Topical thymidine dinucleotide application protects against UVB-induced skin cancer in mice with DNA repair gene (Ercc1)-deficient skin

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

XPF nuclease-dependent telomere loss and increased DNA damage in mice overexpressing TRF2 result in premature aging and cancer.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Reinvestigation of the classification of five cell strains of xeroderma pigmentosum group E with reclassification of three of them.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Role of reciprocal exchange, one-ended invasion crossover and single-strand annealing on inverted and direct repeat recombination in yeast: different requirements for the RAD1, RAD10, and RAD52 genes

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3139823

Analysis of DNA repair pathways of Schizosaccharomyces pombe by means of swi-rad double mutants

27 November 2018

1 reference

12 December 2020

Xeroderma pigmentosum and related disorders: examining the linkage between defective DNA repair and cancer

1 reference

12 December 2020

Metabolic Profiling of Accelerated Aging ERCC1d/−Mice

1 reference

12 December 2020

Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum

1 reference

12 December 2020

Repair of damage by ultraviolet radiation in xeroderma pigmentosum cell strains of complementation groups E and F

1 reference

12 December 2020

A case of xeroderma pigmentosum group F with late onset of clinical symptoms

1 reference

12 December 2020

Mice with DNA repair gene Ercc1 deficiency in a neural crest lineage are a model for late-onset Hirschsprung disease

1 reference

12 December 2020

Characterization of premature liver polyploidy in DNA repair (Ercc1)-deficient mice

1 reference

12 December 2020

Xeroderma pigmentosum complementation group F in a non-Japanese patient

1 reference

12 December 2020

Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4

1 reference

12 December 2020

Telomere shortening in peripheral blood cells was related with aging but not with white blood cell count

1 reference

12 December 2020

The repair and recombination enzyme ERCC1 is not required for immunoglobulin class switching

1 reference

12 December 2020

10.1016/J.DNAREP.2011.04.026

Identifiers

DOI

1 reference

1 reference

1 reference

PubMed publication ID

21612988

1 reference