(Q28268603)

xeroderma pigmentosum group G

inferred from title

1 reference

A O'Donovan

0 references

R D Wood

series ordinal

0 references

language of work or name

English

0 references

publication date

13 May 1993

0 references

published in

Nature

0 references

volume

363

0 references

issue

6425

0 references

page(s)

185-8

0 references

describes a project that uses

XP125LO LCL

0 references

cites work

A seventh complementation group in excision-deficient xeroderma pigmentosum

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Xeroderma pigmentosum complementation group G--report of two cases

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Transformation and immortalization of diploid xeroderma pigmentosum fibroblasts

1 reference

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

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

1 reference

7 January 2021

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

1 reference

7 January 2021