Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5 (Q28268603)

xeroderma pigmentosum group G

inferred from title

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A O'Donovan

1

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R D Wood

series ordinal

2

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language of work or name

English

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publication date

13 May 1993

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published in

Nature

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volume

363

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page(s)

185-8

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issue

6425

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describes a project that uses

XP125LO LCL

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cites work

A seventh complementation group in excision-deficient xeroderma pigmentosum

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7 January 2021

Studies on a new case of xeroderma pigmentosum (XP3BR) from complementation group G with cellular sensitivity to ionizing radiation.

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A mild form of xeroderma pigmentosum assigned to complementation group G and its repair heterogeneity

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Xeroderma pigmentosum complementation group G--report of two cases

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Transient correction of excision repair defects in fibroblasts of 9 xeroderma pigmentosum complementation groups by microinjection of crude human cell extracts

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Microinjection of partially purified protein factor restores DNA damage specifically in group A of xeroderma pigmentosum cells

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

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Complementation of the xeroderma pigmentosum DNA repair synthesis defect with Escherichia coli UvrABC proteins in a cell-free system

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Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening

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Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene

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7 January 2021

A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome

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Isolation of the functional human excision repair gene ERCC5 by intercosmid recombination

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7 January 2021

Isolation and partial characterization of virus-transformed cell lines representing the A, G and variant complementation groups of xeroderma pigmentosum

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Transformation and immortalization of diploid xeroderma pigmentosum fibroblasts

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7 January 2021

Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2

1 reference

7 January 2021

Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids

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Precise localization of the excision repair gene, ERCC5, to human chromosome 13q32.3-q33.1 by direct R-banding fluorescence in situ hybridization

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7 January 2021

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

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Xeroderma pigmentosum complementation group H is withdrawn and reassigned to group D

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7 January 2021

Clinical and biochemical studies in three patients with severe early infantile Cockayne syndrome

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Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation

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7 January 2021

SSL2, a suppressor of a stem-loop mutation in the HIS4 leader encodes the yeast homolog of human ERCC-3

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7 January 2021

A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3, a human excision repair gene.

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Repair capability and the cellular age response for killing and mutation induction after UV.

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7 January 2021