Transcription-Associated Breaks in Xeroderma Pigmentosum Group D Cells from Patients with Combined Features of Xeroderma Pigmentosum and Cockayne Syndrome

Defects in the XPD gene can result in several clinical phenotypes, including xeroderma pigmentosum (XP), trichothiodystrophy, and, less frequently, the combined phenotype of XP and Cockayne syndrome (XP-D/CS). We previously showed that in cells from two XP-D/CS patients, breaks were introduced into...

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Detalhes bibliográficos
Main Authors: Theron, Therina, Fousteri, Maria I., Volker, Marcel, Harries, Lorna W., Botta, Elena, Stefanini, Miria, Fujimoto, Mitsuo, Andressoo, Jaan-Olle, Mitchell, Jay, Jaspers, Nicolaas G. J., McDaniel, Lisa D., Mullenders, Leon H., Lehmann, Alan R.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Microbiology 2005
Assuntos:
Chromosome Structure and Dynamics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1234319/
https://ncbi.nlm.nih.gov/pubmed/16135823
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.25.18.8368-8378.2005
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