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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Foilsithe in:Cell Mol Biol Lett
Main Authors: Miglionico, Rocchina, Armentano, Maria Francesca, Carmosino, Monica, Salvia, Antonella Maria, Cuviello, Flavia, Bisaccia, Faustino, Ostuni, Angela
Formáid: Artigo
Teanga:Inglês
Foilsithe: Versita 2014
Ábhair:
Short Communication
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6275862/
https://ncbi.nlm.nih.gov/pubmed/25169437
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2478/s11658-014-0208-2
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