Résultats de la recherche

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TFIIH: when transcription met DNA repair
TFIIH subunit alterations causing xeroderma pigmentosum and trichothiodystrophy specifically disturb several steps during transcription
The phosphorylation of the androgen receptor by TFIIH directs the ubiquitin/proteasome process
Dynamic partnership between TFIIH, PGC-1alpha and SIRT1 is impaired in trichothiodystrophy
XPD mutations in trichothiodystrophy hamper collagen VI expression and reveal a role of TFIIH in transcription derepression
Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosum
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin

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