๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Xeroderma pigmentosum, Cockayne's syndrome, helicases, and DNA repair: What's the relationship?

โœ Scribed by Errol C. Friedberg


Book ID
119064224
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
325 KB
Volume
71
Category
Article
ISSN
0092-8674

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Phenotypic heterogeneity in the XPB DNA
โœ Kyu-Seon Oh; Sikandar G. Khan; N.G.J. Jaspers; Anja Raams; Takahiro Ueda; Alan L ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 417 KB

Defects in the xeroderma pigmentosum type B (XPB) gene (ERCC3), a DNA helicase involved in nucleotide excision repair (NER) and an essential subunit of the basal transcription factor, TFIIH, have been described in only three families. We report three new XPB families: one has two sisters with relati

Sensitivity of excision repair in normal
โœ James E. Cleaver ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 902 KB

Inhibition of the gap-filling, polymerizing step of excision repair by 1-0-D-arabinofuranosylcytosine (ara-C) after irradiation with ultraviolet light in human diploid fibroblasts resulted in the formation of persistent DNA strand breaks in G,, G,, and plateau phase cells, but not in S phase cells.