Shwachman–Bodian–Diamond syndrome (SBDS) protein deficiency impairs translation re-initiation from C/EBPα and C/EBPβ mRNAs

Mutations in the Shwachman–Bodian–Diamond Syndrome (SBDS) gene cause Shwachman–Diamond Syndrome (SDS), a rare congenital disease characterized by bone marrow failure with neutropenia, exocrine pancreatic dysfunction and skeletal abnormalities. The SBDS protein is important for ribosome maturation an...

Descripción completa

Detalles Bibliográficos
Autores principales: In, Kyungmin, Zaini, Mohamad A., Müller, Christine, Warren, Alan J., von Lindern, Marieke, Calkhoven, Cornelis F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Gene regulation, Chromatin and Epigenetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872075/
https://www.ncbi.nlm.nih.gov/pubmed/26762974
http://dx.doi.org/10.1093/nar/gkw005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872075/
https://www.ncbi.nlm.nih.gov/pubmed/26762974
http://dx.doi.org/10.1093/nar/gkw005

Ejemplares similares