Splitting hairs – discovery of a new DNA repair and transcription factor for the human disease trichothiodystrophy
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference16 articles.
1. Identification of TFB5, a new component of general transcription and DNA repair factor IIH;Ranish;Nat. Genet.,2004
2. A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A;Giglia-Mari;Nat. Genet.,2004
3. Nucleotide excision repair syndromes: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy;Bootsma,1998
4. Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes;Itin;J. Am. Acad. Dermatol.,2001
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1. XPC is an RNA polymerase II cofactor recruiting ATAC to promoters by interacting with E2F1;Nature Communications;2018-07-04
2. The intricate network between the p34 and p44 subunits is central to the activity of the transcription/DNA repair factor TFIIH;Nucleic Acids Research;2017-08-25
3. TFIIH Subunit Alterations Causing Xeroderma Pigmentosum and Trichothiodystrophy Specifically Disturb Several Steps during Transcription;The American Journal of Human Genetics;2015-02
4. Targeting the Nucleotide Excision Repair Pathway for Therapeutic Applications;DNA Repair in Cancer Therapy;2012
5. Ocular Manifestations of Trichothiodystrophy;Ophthalmology;2011-12
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