FANCD2 and DNA Damage

Investigators have dedicated considerable effort to understanding the molecular basis underlying Fanconi Anemia (FA), a rare human genetic disease featuring an extremely high incidence of cancer and many congenital defects. Among those studies, FA group D2 protein (FANCD2) has emerged as the focal p...

Descripción completa

Detalles Bibliográficos
Autores principales: Nepal, Manoj, Che, Raymond, Ma, Chi, Zhang, Jun, Fei, Peiwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578191/
https://www.ncbi.nlm.nih.gov/pubmed/28825622
http://dx.doi.org/10.3390/ijms18081804

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578191/
https://www.ncbi.nlm.nih.gov/pubmed/28825622
http://dx.doi.org/10.3390/ijms18081804

Ejemplares similares