Zobrazeno 1 - 2
of 2
pro vyhledávání: '"MESH: Trichothiodystrophy Syndromes"'
Autor:
Keronninn M. Lima-Bessa, Carlos Frederico Martins Menck, Alain Sarasin, Vanessa Chiganças, Anne Stary
Publikováno v:
Cancer Research
Cancer Research, American Association for Cancer Research, 2008, 68 (15), pp.6074-6083. ⟨10.1158/0008-5472.CAN-07-6695⟩
Cancer Research, American Association for Cancer Research, 2008, 68 (15), pp.6074-6083. ⟨10.1158/0008-5472.CAN-07-6695⟩
Most trichothiodystrophy (TTD) patients present mutations in the xeroderma pigmentosum D (XPD) gene, coding for a subunit of the transcription/repair factor IIH (TFIIH) complex involved in nucleotide excision repair (NER) and transcription. After UV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d9d51374082e9c2c1d44b68eaa28a68
https://doi.org/10.1158/0008-5472.can-07-6695
https://doi.org/10.1158/0008-5472.can-07-6695
Autor:
Mariana Fregoso, Mariana Herrera, Enrique Reynaud, Javier Aguilar-Fuentes, Jean-Marc Egly, Cathy Braun, Mario Zurita
Publikováno v:
PLoS Genetics
PLoS Genetics, Public Library of Science, 2008, 4 (11), pp.e1000253. ⟨10.1371/journal.pgen.1000253⟩
PLoS Genetics, Vol 4, Iss 11, p e1000253 (2008)
PLoS Genetics, 2008, 4 (11), pp.e1000253. ⟨10.1371/journal.pgen.1000253⟩
PLoS Genetics, Public Library of Science, 2008, 4 (11), pp.e1000253. ⟨10.1371/journal.pgen.1000253⟩
PLoS Genetics, Vol 4, Iss 11, p e1000253 (2008)
PLoS Genetics, 2008, 4 (11), pp.e1000253. ⟨10.1371/journal.pgen.1000253⟩
Mutations in certain subunits of the DNA repair/transcription factor complex TFIIH are linked to the human syndromes xeroderma pigmentosum (XP), Cockayne's syndrome (CS), and trichothiodystrophy (TTD). One of these subunits, p8/TTDA, interacts with p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43b22c0b3836986c54f2ed516b7d36b8
https://www.hal.inserm.fr/inserm-00350711
https://www.hal.inserm.fr/inserm-00350711
