XPD Mutations Prevent TFIIH-Dependent Transactivation by Nuclear Receptors and Phosphorylation of RARα

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Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH

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Stimulation of RARα Activation Function AF-1 through Binding to the General Transcription Factor TFIIH and Phosphorylation by CDK7

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Substrate specificity of the cdk‐activating kinase (CAK) is altered upon association with TFIIH

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Purification and interaction properties of the human RNA polymerase B(II) general transcription factor BTF2.

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Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH

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TFIIH with Inactive XPD Helicase Functions in Transcription Initiation but Is Defective in DNA Repair

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Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH

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