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Number of items: 18.

Dohrn, M F; Othman, A; Hirshman, S K; Bode, H; Alecu, I; Fähndrich, E; Karges, W; Weis, J; Schulz, J B; Hornemann, T; Claeys, K G (2015). Elevation of plasma 1-deoxy-sphingolipids in type 2 diabetes mellitus: a susceptibility to neuropathy? European Journal of Neurology, 22(5):806-814.

Oczos, J; Sutter, I; Kloeckener-Gruissem, B; Berger, W; Riwanto, M; Rentsch, K; Hornemann, T; von Eckardstein, A; Grimm, C (2014). Lack of paraoxonase 1 alters phospholipid composition, but not morphology and function of the mouse retina. Investigative Ophthalmology & Visual Science [IOVS], 55(8):4714-4727.

Aflaki, E; Doddapattar, P; Radović, B; Povoden, S; Kolb, D; Vujić, N; Wegscheider, M; Koefeler, H; Hornemann, T; Graier, W F; Malli, R; Madeo, F; Kratky, D (2012). C16 ceramide is crucial for triacylglycerol-induced apoptosis in macrophages. Cell Death and Disease, 3:e280.

Hornemann, T (2012). CME-Labor 27/Auflösung. Hochsensitive Troponine. Praxis, 101(20):1338-1339.

Othman, A; Rütti, M F; Ernst, D; Saely, C H; Rein, P; Drexel, H; Porretta-Serapiglia, C; Lauria, G; Bianchi, R; von Eckardstein, Arnold; Hornemann, T (2012). Plasma deoxysphingolipids: a novel class of biomarkers for the metabolic syndrome? Diabetologia, 55(2):421-431.

Rotthier, A; Penno, A; Rautenstrauss, B; Auer-Grumbach, M; Stettner, G M; Asselbergh, B; Van Hoof, K; Sticht, H; Lévy, N; Timmerman, V; Hornemann, T; Janssens, K (2011). Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I. Human Mutation, 32(6):E2211-E2225.

Garofalo, K; Penno, A; Schmidt, B P; Lee, H J; Frosch, M P; von Eckardstein, Arnold; Brown, R H; Hornemann, T; Eichler, F S (2011). Oral L-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1. Journal of Clinical Investigation, 121(12):4735-4745.

Karuna, R; Park, R; Othman, A; Holleboom, A G; Motazacker, M M; Sutter, I; Kuivenhoven, J A; Rohrer, L; Matile, H; Hornemann, T; Stoffel, M; Rentsch, K M; von Eckardstein, Arnold (2011). Plasma levels of sphingosine-1-phosphate and apolipoprotein M in patients with monogenic disorders of HDL metabolism. Atherosclerosis, 219(2):855-863.

Penno, A; Reilly, M M; Houlden, H; Laurá, M; Rentsch, K; Niederkofler, V; Stoeckli, E T; Nicholson, G; Eichler, F; Brown, R H; von Eckardstein, Arnold; Hornemann, T (2010). Hereditary sensory neuropathy type 1 is caused by the accumulation of two neurotoxic sphingolipids. Journal of Biological Chemistry, 285(15):11178-11187.

Bertea, M; Rütti, M F; Othman, A; Marti-Jaun, J; Hersberger, M; von Eckardstein, Arnold; Hornemann, T (2010). Deoxysphingoid bases as plasma markers in Diabetes mellitus. Lipids in Health and Disease, 9:84.

Rotthier, A; Auer-Grumbach, M; Janssens, K; Baets, J; Penno, A; Almeida-Souza, L; Van Hoof, K; Jacobs, A; De Vriendt, E; Schlotter-Weigel, B; Löscher, W; Vondráček, P; Seemann, P; De Jonghe, P; Van Dijck, P; Jordanova, A; Hornemann, T; Timmerman, V (2010). Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type I. American Journal of Human Genetics, 87(4):513-522.

Hornemann, T; Penno, A; Richard, S; Nicholson, G; van Dijk, F S; Rotthier, A; Timmerman, V; von Eckardstein, A (2009). A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated. Neurogenetics, 10(2):135-143.

Rütti, M F; Richard, S; Penno, A; von Eckardstein, A; Hornemann, T (2009). An improved method to determine serine palmitoyltransferase activity. Journal of Lipid Research, 50(6):1237-1244.

Tamehiro, N; Mujawar, Z; Zhou, S; Zhuang, D Z; Hornemann, T; von Eckardstein, A; Fitzgerald, M L (2009). Cell polarity factor Par3 binds SPTLC1 and modulates monocyte serine palmitoyltransferase activity and chemotaxis. Journal of Biological Chemistry, 284(37):24881-24890.

Eichler, F S; Hornemann, T; McCampbell, A; Kuljis, D; Penno, A; Vardeh, D; Tamrazian, E; Garofalo, K; Lee, H J; Kini, L; Seligman, M; Frosch, M; Gable, K; von Eckardstein, A; Woolf, C J; Guan, G; Harmon, J M; Dunn, T M; Brown, R H (2009). Overexpression of the wild-type SPT1 subunit lowers Desoxysphingolipid levels and rescues the phenotype of HSAN1. Journal of Neuroscience, 29(46):14646-14651.

Hornemann, T; Penno, A; Rütti, M F; Ernst, D; Kivrak-Pfiffner, F; Rohrer, L; von Eckardstein, A (2009). The SPTLC3 subunit of serine palmitoyltransferase generates short chain sphingoid bases. Journal of Biological Chemistry, 284(39):26322-26330.

Rudiger, A; Fischler, M; Harpes, P; Gasser, S; Hornemann, T; von Eckardstein, A; Maggiorini, M (2008). In critically ill patients, B-type natriuretic peptide (BNP) and N-terminal pro-BNP levels correlate with C-reactive protein values and leukocyte counts. International Journal of Cardiology, 126(1):28-31.

Tamehiro, N; Zhou, S; Okuhira, K; Benita, Y; Brown, C E; Zhuang, D Z; Latz, E; Hornemann, T; von Eckardstein, A; Xavier, R J; Freeman, M W; Fitzgerald, M L (2008). SPTLC1 binds ABCA1 to negatively regulate trafficking and cholesterol efflux activity of the transporter. Biochemistry, 47(23):6138-6147.

This list was generated on Sat Jul 22 15:36:26 2017 CEST.