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Volumn 46, Issue 9, 1998, Pages 679-680
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Mutations in XPD helicase prevent its interaction and regulation by p44, another subunit of TFIIH, resulting in xeroderma pigmentosum (XP) and trichothiodystrophy (TTD) phenotypes;Les mutations de l'helicase XPD empechent son interaction et sa regulation par le p44, autre sous-unite du TFIIH, conduisant aux phenotypes xeroderma pigmentosa (XP) et trichothiodystrophie
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Author keywords
DNA repair; Genetic diseases; Helicase; Transcription
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Indexed keywords
HELICASE;
CARBOXY TERMINAL SEQUENCE;
CATALYSIS;
CLINICAL FEATURE;
CONFERENCE PAPER;
ENZYME ACTIVITY;
EXCISION REPAIR;
GENE MUTATION;
GENETIC CODE;
GENETIC DISORDER;
GENETIC TRANSCRIPTION;
TRICHOTHIODYSTROPHY;
XERODERMA PIGMENTOSUM;
DNA HELICASES;
DNA REPAIR;
GENE EXPRESSION REGULATION;
HUMANS;
MUTATION;
TRANSCRIPTION FACTOR TFIIH;
TRANSCRIPTION FACTORS;
TRANSCRIPTION FACTORS, TFII;
XERODERMA PIGMENTOSUM;
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EID: 0032441345
PISSN: 03698114
EISSN: None
Source Type: Journal
DOI: None Document Type: Conference Paper |
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Times cited : (9)
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References (0)
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