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

Cell

Volumn 62, Issue 4, 1990, Pages 777-791

  Weeda, Geert ^a   van Ham, Reinier C A ^a   Vermeulen, Wim ^b   Bootsma, Dirk ^b   van der Eb, Alex J ^a   Hoeijmakers, Jan H J ^b  

^a LEIDEN UNIVERSITY   (Netherlands)

^b ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

RODENTIA;

HELICASE;

ARTICLE; COCKAYNE SYNDROME; CYTOCHEMISTRY; GENETIC ENGINEERING; HEREDITY; HUMAN; HUMAN CELL; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE; XERODERMA PIGMENTOSUM;

AMINO ACID SEQUENCE; BASE SEQUENCE; BLOTTING, NORTHERN; BLOTTING, SOUTHERN; CLONING, MOLECULAR; COCKAYNE SYNDROME; COMPARATIVE STUDY; DNA; DNA HELICASES; DNA REPAIR; DWARFISM; GENES, STRUCTURAL; HUMAN; MICROINJECTIONS; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; RESTRICTION MAPPING; RNA SPLICING; SUPPORT, NON-U.S. GOV'T; XERODERMA PIGMENTOSUM;

EID: 0025158110     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/0092-8674(90)90122-U     Document Type: Article

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