未登录
分享
收藏
分享
收藏
分享
收藏
分享
收藏
分享
收藏Golgi enzymes are enriched in perforated zones of Golgi cisternae but are depleted in COPI vesicles
Kweon, HS; Beznoussenko, GV; Micaroni, M; Polishchuk, RS; Trucco, A; Martella, O; Di Giandomenico, D; Marra, P; Fusella, A; Di Pentima, A; Berger, EG; Geerts, WJC; Koster, AJ; Burger, KNJ; Luini, A; Mironov, AA
分享
收藏
分享
收藏Deficiency of UDP-galactose:N-acetylglucosamine β-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId
Hansske, B; Thiel, C; Lübke, T; Hasilik, M; Höning, S; Peters, V; Heidemann, PH; Hoffmann, GF; Berger, EG; von Figura, K; Körner, C
分享
收藏
分享
收藏Small cargo proteins and large aggregates can traverse the Golgi by a common mechanism without leaving the lumen of cisternae
Mironov, AA; Beznoussenko, GV; Nicoziani, P; Martella, O; Trucco, A; Kweon, HS; Di Giandomenico, D; Polishchuk, RS; Fusella, A; Lupetti, P; Berger, EG; Geerts, WJC; Koster, AJ; Burger, KNJ; Luini, A
分享
收藏MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If
Schenk, B; Imbach, T; Frank, CG; Grubenmann, CE; Raymond, GV; Hurvitz, H; Raas-Rotschild, A; Luder, AS; Jaeken, J; Berger, EG; Matthijs, G; Hennet, T; Aebi, M
分享
收藏Immobilisation on polystyrene of diazirine derivatives of mono- and disaccharides:: Biological activities of modified surfaces
Chevolot, Y; Martins, J; Milosevic, N; Léonard, D; Zeng, S; Malissard, M; Berger, EG; Maier, P; Mathieu, HJ; Crout, DHG; Sigrist, H
分享
收藏
分享
收藏
分享
收藏
分享
收藏
分享
收藏Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic
Imbach, T; Grünewald, S; Schenk, B; Burda, P; Schollen, E; Wevers, RA; Jaeken, J; de Klerk, JBC; Berger, EG; Matthijs, G; Aebi, M; Hennet, T
分享
收藏
分享
收藏Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie
Imbach, T; Schenk, B; Schollen, E; Burda, P; Stutz, A; Grünewald, S; Bailie, NM; King, MD; Jaeken, J; Matthijs, G; Berger, EG; Aebi, M; Hennet, T
分享
收藏
分享
收藏