GLUT10—Lacking in Arterial Tortuosity Syndrome—Is Localized to the Endoplasmic Reticulum of Human Fibroblasts

GLUT10 belongs to a family of transporters that catalyze the uptake of sugars/polyols by facilitated diffusion. Loss-of-function mutations in the SLC2A10 gene encoding GLUT10 are responsible for arterial tortuosity syndrome (ATS). Since subcellular distribution of the transporter is dubious, we aime...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Int J Mol Sci
Hauptverfasser: Gamberucci, Alessandra, Marcolongo, Paola, Németh, Csilla E., Zoppi, Nicoletta, Szarka, András, Chiarelli, Nicola, Hegedűs, Tamás, Ritelli, Marco, Carini, Giulia, Willaert, Andy, Callewaert, Bert L., Coucke, Paul J., Benedetti, Angiolo, Margittai, Éva, Fulceri, Rosella, Bánhegyi, Gábor, Colombi, Marina
Format: Artigo
Sprache:Inglês
Veröffentlicht: MDPI 2017
Schlagworte:
Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5578206/
https://ncbi.nlm.nih.gov/pubmed/28829359
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms18081820
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge