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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.

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.

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.

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.

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.

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.

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