A unified model for the molecular basis of Xeroderma pigmentosum-Cockayne Syndrome

Nucleotide Excision Repair (NER) is a pathway that removes lesions distorting the DNA helix. The molecular basis of the rare diseases Xeroderma pigmentosum (XP) and Cockayne Syndrome (CS) are explained based on the defects happening in 2 NER branches: Global-Genome Repair and Transcription-Coupled R...

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Detalles Bibliográficos
Autores principales: Moriel-Carretero, María, Herrera-Moyano, Emilia, Aguilera, Andrés
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Addendum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588225/
https://www.ncbi.nlm.nih.gov/pubmed/26460500
http://dx.doi.org/10.1080/21675511.2015.1079362

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588225/
https://www.ncbi.nlm.nih.gov/pubmed/26460500
http://dx.doi.org/10.1080/21675511.2015.1079362

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