Genetic variation in the NEIL2 DNA glycosylase gene is associated with oxidative DNA damage in BRCA2 mutation carriers

In this report, we have tried to gain molecular insight into a single nucleotide polymorphism (SNP) in the NEIL2 gene previously identified as “cancer risk modifier” for BRCA2 mutation carriers. To that end, we studied the role of this SNP (rs804271) on NEIL2 transcriptional regulation, oxidative DN...

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Detalles Bibliográficos
Autores principales: Benítez-Buelga, Carlos, Baquero, Juan Miguel, Vaclova, Tereza, Fernández, Victoria, Martín, Paloma, Inglada-Perez, Lucia, Urioste, Miguel, Osorio, Ana, Benítez, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5777719/
https://www.ncbi.nlm.nih.gov/pubmed/29383107
http://dx.doi.org/10.18632/oncotarget.22638

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5777719/
https://www.ncbi.nlm.nih.gov/pubmed/29383107
http://dx.doi.org/10.18632/oncotarget.22638

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