Basal transcription defect discriminates between xeroderma pigmentosum and trichothiodystrophy in XPD patients

Molecular Cell

Volumn 11, Issue 6, 2003, Pages 1635-1646

  Dubaele, Sandy ^a   De Santis, Luca Proietti ^a   Bienstock, Rachelle J ^b   Keriel, Anne ^a   Stefanini, Miria ^c   Van Houten, Bennett ^b   Egly, Jean Marc ^a  

^a INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^b NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES   (United States)

^c CNR   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; CELL NUCLEUS RECEPTOR; HELICASE; PROTEIN; PROTEIN SUBUNIT; PROTEIN TFIIHS; UNCLASSIFIED DRUG;

ARTICLE; CLINICAL FEATURE; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DISEASE SEVERITY; ENZYME ACTIVITY; GENE MUTATION; GENETIC ENGINEERING; GENOTYPE; HUMAN; HUMAN CELL; IN VITRO STUDY; INTRACELLULAR SPACE; PHENOTYPE; PROTEIN INTERACTION; TRANSACTIVATION; TRANSCRIPTION INITIATION; TRICHOTHIODYSTROPHY; XERODERMA PIGMENTOSUM;

EID: 0038094503     PISSN: 10972765     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1097-2765(03)00182-5     Document Type: Article

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