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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...

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Dettagli Bibliografici
Pubblicato in:Int J Mol Sci
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2017
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Accesso online: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
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