Dysregulation of gene expression in ABCC6 knockdown HepG2 cells

ABCC6 protein is an ATP-dependent transporter that is mainly found in the basolateral plasma membrane of hepatocytes. ABCC6 deficiency is the primary cause of several forms of ectopic mineralization syndrome. Mutations in the human ABCC6 gene cause pseudoxanthoma elasticum (PXE), an autosomal recess...

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Detalles Bibliográficos
Autores principales: Miglionico, Rocchina, Armentano, Maria Francesca, Carmosino, Monica, Salvia, Antonella Maria, Cuviello, Flavia, Bisaccia, Faustino, Ostuni, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Versita 2014
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275862/
https://www.ncbi.nlm.nih.gov/pubmed/25169437
http://dx.doi.org/10.2478/s11658-014-0208-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275862/
https://www.ncbi.nlm.nih.gov/pubmed/25169437
http://dx.doi.org/10.2478/s11658-014-0208-2

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