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Dissection of TMEM165 function in Golgi glycosylation and its Mn(2+) sensitivity
Since 2012, the interest for TMEM165 increased due to its implication in a rare genetic human disease named TMEM165-CDG (Congenital Disorder(s) of Glycosylation). TMEM165 is a Golgi localized protein, highly conserved through evolution and belonging to the uncharacterized protein family 0016 (UPF001...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Biochimie |
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| Κύριοι συγγραφείς: | , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2019
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6857530/ https://ncbi.nlm.nih.gov/pubmed/31351090 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biochi.2019.07.016 |
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