Disruption of TTDA Results in Complete Nucleotide Excision Repair Deficiency and Embryonic Lethality

PLoS Genetics

Volumn 9, Issue 4, 2013, Pages

  Theil, Arjan F ^a   Nonnekens, Julie ^a,b   Steurer, Barbara ^a   Mari, Pierre Olivier ^a,b   de Wit, Jan ^a   Lemaitre, Charlène ^a   Marteijn, Jurgen A ^a   Raams, Anja ^a   Maas, Alex ^a   Vermeij, Marcel ^a   Essers, Jeroen ^a   Hoeijmakers, Jan H J ^a   Giglia Mari, Giuseppina ^a,b   Vermeulen, Wim ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b UNIVERSITÉ PAUL SABATIER   (France)

Author keywords

[No Author keywords available]

Indexed keywords

OXIDIZING AGENT; TRANSCRIPTION FACTOR IIH; TRANSCRIPTION FACTOR IIH TTDA; UNCLASSIFIED DRUG; TRANSCRIPTION FACTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL VIABILITY; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; EMBRYO; EMBRYO DEATH; EXCISION REPAIR; FEMALE; GENE DISRUPTION; GENE INACTIVATION; GENE MUTATION; HUMAN; HUMAN CELL; MALE; MOUSE; NONHUMAN; NUCLEOTIDE EXCISION REPAIR DEFICIENCY; PHENOTYPE; PROTEIN FUNCTION; SENSITIVITY ANALYSIS; TRICHOTHIODYSTROPHY; TTDA GENE; ANIMAL; COCKAYNE SYNDROME; GENETIC TRANSCRIPTION; GENETICS; MUTATION;

MUS;

ANIMALS; COCKAYNE SYNDROME; DNA REPAIR; HUMANS; MUTATION; TRANSCRIPTION FACTOR TFIIH; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC; TRICHOTHIODYSTROPHY SYNDROMES;

EID: 84876823728     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1003431     Document Type: Article

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