Fetal bovine serum impacts the observed N‐glycosylation defects in TMEM165 KO HEK cells
Sign Up to like & getrecommendations! Published in 2019 at "Journal of Inherited Metabolic Disease"
DOI: 10.1002/jimd.12161
Abstract: TMEM165 is involved in a rare genetic human disease named TMEM165‐CDG (congenital disorders of glycosylation). It is Golgi localized, highly conserved through evolution and belongs to the uncharacterized protein family 0016 (UPF0016). The use of… read more here.
Keywords: fetal bovine; glycosylation defects; glycosylation; hek cells ... See more keywords
N-Glycosylation Defects in Humans Lower Low-Density Lipoprotein Cholesterol Through Increased Low-Density Lipoprotein Receptor Expression
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DOI: 10.1161/circulationaha.118.036484
Abstract: Background: The importance of protein glycosylation in regulating lipid metabolism is becoming increasingly apparent. We set out to further investigate this by studying patients with type I congeni... read more here.
Keywords: low density; density lipoprotein; glycosylation defects;