The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes

Human Molecular Genetics

Volumn 8, Issue 6, 1999, Pages 1125-1133

  Riou, Lydia ^a   Zeng, Lin ^a   Chevallier Lagente, Odile ^a   Stary, Anne ^a   Nikaido, Osamu ^b   Taïeb, Alain ^c   Weeda, Geert ^d   Mezzina, Mauro ^a   Sarasin, Alain ^a  

^a IFR 1221   (France)

^b KANAZAWA UNIVERSITY   (Japan)

^c HÔPITAL PELLEGRIN   (France)

^d ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CELL DNA; COMPLEMENTARY DNA; HELICASE;

ADULT; ALLELE; ARTICLE; CASE REPORT; COCKAYNE SYNDROME; CONTROLLED STUDY; DNA REPAIR; DNA SYNTHESIS; GENE MUTATION; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; MALE; MOLECULAR CLONING; NUCLEIC ACID BASE SUBSTITUTION; PHENOTYPE; PLASMID; PRIORITY JOURNAL; SCHOOL CHILD; SKIN FIBROBLAST; TRICHOTHIODYSTROPHY; ULTRAVIOLET IRRADIATION; XERODERMA PIGMENTOSUM;

CELL LINE, TRANSFORMED; CHILD; CHILD, PRESCHOOL; COCKAYNE SYNDROME; DNA; DNA HELICASES; DNA REPAIR; DNA, COMPLEMENTARY; DNA-BINDING PROTEINS; GENE EXPRESSION REGULATION; HAIR DISEASES; HUMANS; MALE; MIDDLE AGED; MUTATION; PYRIMIDINE DIMERS; RECOMBINANT FUSION PROTEINS; TRANSFECTION; ULTRAVIOLET RAYS; XERODERMA PIGMENTOSUM;

EID: 0033010376     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.6.1125     Document Type: Article

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