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Lecca, M R; Maag, C; Berger, E G; Hennet, T (2011). Fibrotic response in fibroblasts from congenital disorders of glycosylation. Journal of Cellular and Molecular Medicine, 15(8):1788-1796.

Schaub, B E; Berger, E G; Rohrer, J (2008). Dissection of a novel molecular determinant mediating Golgi to trans-Golgi network transition. Cellular and Molecular Life Sciences, 65(22):3677-3687.

Lecca, M R; Wagner, U; Patrignani, A; Berger, E G; Hennet, T (2005). Genome-wide analysis of the unfolded protein response in fibroblasts from congenital disorders of glycosylation type-I patients. FASEB Journal, 19(2):240-242.

Grubenmann, C E; Frank, C G; Hülsmeier, A J; Schollen, E; Matthijs, G; Mayatepek, E; Berger, E G; Aebi, M; Hennet, Thierry (2004). Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik. Human Molecular Genetics, 13(5):535-542.

Berger, E G (2002). Ectopic localizations of Golgi glycosyltransferases. Glycobiology, 12(2):29R-36R.

Borsig, L; Imbach, T; Hochli, M; Berger, E G (1999). 1,3Fucosyltransferase VI is expressed in HepG2 cells and codistributed with 1,4galactosyltransferase I in the Golgi apparatus and monensin-induced swollen vesicles. Glycobiology, 9(11):1273-1280.

Berger, E G; Greber, U F; Mosbach, K (1986). Galactosyltransferase-dependent sialylation of complex and endo-N-acetylglucosaminidase H-treated core N-glycans in vitro. FEBS Letters, 203(1):64-68.

This list was generated on Fri Apr 19 06:28:17 2019 CEST.