European research network aimed at improving the diagnosis and treatment of congenital glycosylation defects.
Systematic search for novel Congenital Disorders of Glycosylation (CDG): the identification of new defects in ER and Golgi and a functional study of TPARL, a new gene with a possible role in pH and Ca2+ homeostasis.
Differential Effects of D-Galactose Supplementation on Golgi Glycosylation Defects in TMEM165 Deficiency
INHIBITION OF COG5, A GENE FROM THE C7Q22 OSTEOARTHRITIS SUSCEPTIBILITY LOCUS, INDUCES GLYCOSYLATION DEFECTS AND AFFECTS CHONDROGENESIS AND OSTEOGENESIS BY DISTURBING WNT SIGNALING
Exposure of Trypanosoma brucei to an N-acetylglucosamine-binding lectin induces VSG switching and glycosylation defects resulting in reduced infectivity