The role of WRNIP1 in genome maintenance

WRNIP1 interacts with WRN helicase, which is defective in the premature aging disease Werner syndrome. WRNIP1 belongs to the AAA+ ATPase family and is conserved from Escherichia coli to human. The protein contains an ubiquitin-binding zinc finger (UBZ) domain at the N terminus and an ATPase domain i...

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Detalles Bibliográficos
Autores principales: Yoshimura, Akari, Seki, Masayuki, Enomoto, Takemi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384577/
https://www.ncbi.nlm.nih.gov/pubmed/28118071
http://dx.doi.org/10.1080/15384101.2017.1282585

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384577/
https://www.ncbi.nlm.nih.gov/pubmed/28118071
http://dx.doi.org/10.1080/15384101.2017.1282585

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