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Miyatake, Satoko; Schneeberger, Sacha; Koyama, Norihisa; et al; Hennet, Thierry (2018). Biallelic COLGALT1 variants are associated with cerebral small vessel disease. Annals of Neurology, 84(6):843-853.

Whitehead, Marek W J; Khanzhin, Nikolay; Borsig, Lubor; Hennet, Thierry (2017). Custom Glycosylation of Cells and Proteins Using Cyclic Carbamate-Derivatized Oligosaccharides. Cell Chemical Biology, 24(11):1336-1346.e3.

Weiss, G Adrienne; Hennet, Thierry (2017). Mechanisms and consequences of intestinal dysbiosis. Cellular and Molecular Life Sciences, 74(16):2959-2977.

Rommel, Anna J; Hülsmeier, Andreas J; Jurt, Simon; Hennet, Thierry (2016). Giant mimivirus R707 encodes a glycogenin paralogue polymerizing glucose through α- and β-glycosidic linkages. Biochemical Journal, 473(20):3451-3462.

Hülsmeier, Andreas J; Tobler, Micha; Burda, Patricie; Hennet, Thierry (2016). Glycosylation site occupancy in health, congenital disorder of glycosylation and fatty liver disease. Scientific Reports, 6:33927.

Elison, Emma; Vigsnaes, Louise K; Rindom Krogsgaard, Laura; Rasmussen, Julie; Sørensen, Nikolaj; McConnell, Bruce; Hennet, Thierry; Sommer, Morten O A; Bytzer, Peter (2016). Oral supplementation of healthy adults with 2'-O-fucosyllactose and lacto-N-neotetraose is well tolerated and shifts the intestinal microbiota. The British Journal of Nutrition, 116(8):1356-1368.

Baumann, Stephan; Hennet, Thierry (2016). Collagen accumulation in osteosarcoma cells lacking GLT25D1 collagen galactosyltransferase. Journal of Biological Chemistry, 291(35):18514-18524.

van Karnebeek, Clara D M; Bonafé, Luisa; Wen, Xiao-Yan; Tarailo-Graovac, Maja; Balzano, Sara; Royer-Bertrand, Beryl; Ashikov, Angel; Garavelli, Livia; Mammi, Isabella; Turolla, Licia; Breen, Catherine; Donnai, Dian; Cormier, Valerie; Heron, Delphine; Nishimura, Gen; Uchikawa, Shinichi; Campos-Xavier, Belinda; Rossi, Antonio; Hennet, Thierry; Brand-Arzamendi, Koroboshka; Rozmus, Jacob; Harshman, Keith; Stevenson, Brian J; Girardi, Enrico; Superti-Furga, Giulio; Dewan, Tammie; Collingridge, Alissa; Halparin, Jessie; Ross, Colin J; Van Allen, Margot I; et al (2016). NANS-mediated synthesis of sialic acid is required for brain and skeletal development. Nature Genetics, 48(7):777-784.

Hennet, Thierry; Borsig, Lubor (2016). Breastfed at Tiffany's. Trends in Biochemical Sciences, 41(6):508-518.

Hennet, Thierry; Cabalzar, Jürg (2015). Congenital disorders of glycosylation: a concise chart of glycocalyx dysfunction. Trends in Biochemical Sciences, 40(7):377-384.

Huang, Yen-Lin; Chassard, Christophe; Hausmann, Martin; von Itzstein, Mark; Hennet, Thierry (2015). Sialic acid catabolism drives intestinal inflammation and microbial dysbiosis in mice. Nature Communications, 6:9141.

Hennet, Thierry; Weiss, Adrienne; Borsig, Lubor (2014). Decoding breast milk oligosaccharides. Swiss Medical Weekly, 144:w13927.

Shah, Nikunj; Hülsmeier, Andreas J; Hochhold, Nina; Neidhart, Michel; Gay, Steffen; Hennet, Thierry (2014). Exposure to Mimivirus collagen promotes arthritis. Journal of Virology, 88(2):838-845.

Rutschmann, Christoph; Baumann, Stephan; Cabalzar, Jürg; Luther, Kelvin B; Hennet, Thierry (2014). Recombinant expression of hydroxylated human collagen in Escherichia coli. Applied Microbiology and Biotechnology, 98(10):4445-4455.

Weiss, Gisela A; Chassard, Christophe; Hennet, Thierry (2014). Selective proliferation of intestinal Barnesiella under fucosyllactose supplementation in mice. The British Journal of Nutrition, 111(9):1602-1610.

Kurakevich, Ekaterina; Hennet, Thierry; Hausmann, Martin; Rogler, Gerhard; Borsig, Lubor (2013). Milk oligosaccharide sialyl(α2,3)lactose activates intestinal CD11c+ cells through TLR4. Proceedings of the National Academy of Sciences of the United States of America, 110(43):17444-17449.

Hennet, Thierry (2012). Diseases of glycosylation beyond classical congenital disorders of glycosylation. Biochimica Et Biophysica Acta, 1820(9):1306-1317.

Weiss, G Adrienne; Hennet, Thierry (2012). The role of milk sialyllactose in intestinal bacterial colonization. Advances in Nutrition, 3(3):483S-488S.

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.

This list was generated on Sun May 26 18:04:50 2019 CEST.