A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations-Reference-Cited by-同舟云学术

A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations

Published:1994-05 Issue:3 Volume:314 Page:233-248
ISSN:0921-8777
Container-title:Mutation Research/DNA Repair
language:en
Short-container-title:Mutation Research/DNA Repair

Author:

Itoh Toshiki,Ono Tomomichi,Yamaizumi Masaru

Publisher

Elsevier BV

Subject

Genetics,Toxicology,Molecular Biology

Reference36 articles.

1. Xeroderma pigmentosum neurologic abnormalities correlate with colony-forming ability after ultraviolet radiation;Andrews;Proc. Natl. Acad. Sci. USA,1978

2. The influence of caffeine on cell survival in excision-proficient and excision-deficient xeroderma pigmentosum and normal human cell strains following ultraviolet-light irradiation;Arlett;Mutation Res.,1975

3. Evidence for repair of cyclobutane pyrimidine diemrs with normal repair of other DNA photoproducts in a transcriptionally active gene transfected into Cockayne syndrome cells;Barrett;Mutation Res.,1991

4. Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening;Busch;Mutagenesis,1989

5. Xeroderma pigmentosum;Cleaver,1989

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