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Hülsmeier, A J; Hennet, T (2014). O-Linked glycosylation in Acanthamoeba polyphaga mimivirus. Glycobiology, 24(8):703-714.

Perrin-Tricaud, C; Rutschmann, C; Hennet, T (2011). Identification of domains and amino acids essential to the collagen galactosyltransferase activity of GLT25D1. PLoS ONE, 6(12):e29390.

Haeuptle, M A; Welti, M; Troxler, H; Huelsmeier, A J; Imbach, T; Hennet, T (2011). Improvement of dolichol-linked oligosaccharide biosynthesis by the squalene synthase inhibitor Zaragozic acid. Journal of Biological Chemistry, 286(8):6085-6091.

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.

Hülsmeier, A J; Welti, M; Hennet, T (2011). Glycoprotein maturation and the UPR. In: Conn, P M. The unfolded protein response and cellular stress. Part C. Amsterdam, NL: Elsevier, 163-82.

Luther, K B; Hülsmeier, A J; Schegg, B; Deuber, S A; Raoult, D; Hennet, T (2011). Mimivirus collagen is modified by bifunctional lysyl hydroxylase and glycosyltransferase enzyme. Journal of Biological Chemistry, 286(51):43701-43709.

Fuhrer, A; Sprenger, N; Kurakevich, E; Borsig, L; Chassard, C; Hennet, T (2010). Milk sialyllactose influences colitis in mice through selective intestinal bacterial colonization. Journal of Experimental Medicine, 207(13):2843-2854.

Haeuptle, M A; Hülsmeier, A J; Hennet, T (2010). HPLC and mass spectrometry analysis of dolichol-phosphates at the cell culture scale. Analytical Biochemistry, 396(1):133-138.

Hülsmeier, A J; Deplazes, P; Naem, S; Nonaka, N; Hennet, T; Köhler, P (2010). An Echinococcus multilocularis coproantigen is a surface glycoprotein with unique O-gycosylation. Glycobiology, 20(1):127-135.

Titz, A; Butschi, A; Henrissat, B; Fan, Y Y; Hennet, T; Razzazi-Fazeli, E; Hengartner, M O; Wilson, I B H; Kuenzler, M; Aebi, M (2009). Molecular basis for galactosylation of core fucose residues in invertebrates: Identification of Caenorhabditis elegans N-glycan core {alpha}1,6-fucoside {beta}1,4-galactosyltransferase GALT-1 as a member of a novel glycosyltransferase family. Journal of Biological Chemistry, 284(52):36223-36233.

Hennet, T (2009). From glycosylation disorders back to glycosylation: what have we learned? Biochimica et Biophysica Acta, 1792(9):921-924.

Vesela, K; Honzik, T; Hansikova, H; Haeuptle, M A; Semberova, J; Stranak, Z; Hennet, T; Zeman, J (2009). A new case of ALG8 deficiency (CDG Ih). Journal of Inherited Metabolic Disease, 32(S1):259-264.

Jaeken, J; Hennet, T; Matthijs, G; Freeze, H H (2009). CDG nomenclature: time for a change! Biochimica et Biophysica Acta, 1792(9):825-826.

Haeuptle, M A; Hennet, T (2009). Congenital disorders of glycosylation: an update on defects affecting the biosynthesis of dolichol-linked oligosaccharides. Human Mutation, 30(12):1628-1641.

Schegg, B; Hülsmeier, A J; Rutschmann, C; Maag, C; Hennet, T (2009). Core glycosylation of collagen is initiated by two {beta}(1-O)galactosyltransferases. Molecular and Cellular Biology, 29(4):943-952.

Paesold-Burda, P; Maag, C; Troxler, H; Foulquier, F; Kleinert, P; Schnabel, S; Baumgartner, M; Hennet, T (2009). Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation. Human Molecular Genetics, 18(22):4350-4356.

Hennet, T (2009). Diseases of Glycosylation. In: Gabius, H J. The Sugar Code - Fundamentals of Glycosciences. Weinheim: Wiley-VCH, 365-383.

Hennet, T (2009). How does a medical doctor become a glycobiologist. Biochimica et Biophysica Acta, 1792(9):824.

Vleugels, W; Haeuptle, M A; Ng, B G; Michalski, J C; Battini, R; Dionisi-Vici, C; Ludman, M D; Jaeken, J; Foulquier, F; Freeze, H H; Matthijs, G; Hennet, T (2009). RFT1 deficiency in three novel CDG patients. Human Mutation, 30(10):1428-1434.

Jaeken, J; Vleugels, W; Régal, L; Corchia, C; Goemans, N; Haeuptle, M A; Foulquier, F; Hennet, T; Matthijs, G; Dionisi-Vici, C (2009). RFT1-CDG: Deafness as a novel feature of congenital disorders of glycosylation. Journal of Inherited Metabolic Disease, 32(S1):335-338.

Jaeken, J; Hennet, T; Freeze, H; Matthijs, G (2008). On the nomenclature of congenital disorders of glycosylation (CDG). Journal of Inherited Metabolic Disease, 31(6):669-672.

Biellmann, F; Hulsmeier, A; Zhou, D; Cinelli, P; Hennet, T (2008). The Lc3-synthase gene B3gnt5 is essential to pre-implantation development of the murine embryo. BMC Developmental Biology, 8:109.

Haeuptle, M A; Pujol, F M; Neupert, C; Winchester, B; Kastaniotis, A J; Aebi, M; Hennet, T (2008). Human RFT1 deficiency leads to a disorder of N-linked glycosylation. American Journal of Human Genetics, 82(3):600-606.

Biellmann, F; Henion, T R; Bürki, K; Hennet, T (2008). Impaired sexual behavior in male mice deficient for the beta1-3 N-acetylglucosaminyltransferase-I gene. Molecular Reproduction and Development, 75(5):699-706.

Hülsmeier, A J; Paesold-Burda, P; Hennet, T (2007). N-glycosylation site occupancy in serum glycoproteins using multiple reaction monitoring liquid chromatography-mass spectrometry. Molecular & Cellular Proteomics, 6(12):2132-2138.

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.

This list was generated on Mon Jun 17 08:26:15 2019 CEST.