| Year |
Citation |
Score |
| 2018 |
Miyatake S, Schneeberger S, Koyama N, Yokochi K, Ohmura K, Shiina M, Mori H, Koshimizu E, Imagawa E, Uchiyama Y, Mitsuhashi S, Frith MC, Fujita A, Satoh M, Taguri M, ... ... Hennet T, et al. Biallelic COLGALT1 variants are associated with cerebral small vessel disease. Annals of Neurology. PMID 30412317 DOI: 10.1002/Ana.25367 |
0.342 |
|
| 2017 |
Whitehead MWJ, Khanzhin N, Borsig L, Hennet T. Custom Glycosylation of Cells and Proteins Using Cyclic Carbamate-Derivatized Oligosaccharides. Cell Chemical Biology. PMID 28943358 DOI: 10.1016/J.Chembiol.2017.08.012 |
0.33 |
|
| 2016 |
Hülsmeier AJ, Tobler M, Burda P, Hennet T. Glycosylation site occupancy in health, congenital disorder of glycosylation and fatty liver disease. Scientific Reports. 6: 33927. PMID 27725718 DOI: 10.1038/Srep33927 |
0.314 |
|
| 2016 |
Baumann S, Hennet T. Collagen Accumulation in Osteosarcoma Cells lacking GLT25D1 Collagen Galactosyltransferase. The Journal of Biological Chemistry. 291: 18514-24. PMID 27402836 DOI: 10.1074/Jbc.M116.723379 |
0.353 |
|
| 2016 |
van Karnebeek CD, Bonafé L, Wen XY, Tarailo-Graovac M, Balzano S, Royer-Bertrand B, Ashikov A, Garavelli L, Mammi I, Turolla L, Breen C, Donnai D, Cormier V, Heron D, Nishimura G, ... ... Hennet T, et al. NANS-mediated synthesis of sialic acid is required for brain and skeletal development. Nature Genetics. PMID 27213289 DOI: 10.1038/Ng.3578 |
0.335 |
|
| 2015 |
Hennet T, Cabalzar J. Congenital disorders of glycosylation: a concise chart of glycocalyx dysfunction. Trends in Biochemical Sciences. 40: 377-84. PMID 25840516 DOI: 10.1016/J.Tibs.2015.03.002 |
0.395 |
|
| 2014 |
Hülsmeier AJ, Hennet T. O-Linked glycosylation in Acanthamoeba polyphaga mimivirus. Glycobiology. 24: 703-14. PMID 24794008 DOI: 10.1093/Glycob/Cwu034 |
0.363 |
|
| 2014 |
Rutschmann C, Baumann S, Cabalzar J, Luther KB, Hennet T. Recombinant expression of hydroxylated human collagen in Escherichia coli. Applied Microbiology and Biotechnology. 98: 4445-55. PMID 24362857 DOI: 10.1007/S00253-013-5447-Z |
0.355 |
|
| 2012 |
Hennet T. Diseases of glycosylation beyond classical congenital disorders of glycosylation. Biochimica Et Biophysica Acta. 1820: 1306-17. PMID 22343051 DOI: 10.1016/J.Bbagen.2012.02.001 |
0.353 |
|
| 2012 |
Schnaar R, Paulson JC, Macauley MS, Nycholat C, Pfrengle F, Rademacher C, Mahan A, Dionne K, Suscovich T, Alter G, Katoh T, Kiwamoto T, Brummet M, Bochner B, Tiemeyer M, ... ... Hennet T, et al. Program and abstracts for the 2012 Joint Meeting of the Society for Glycobiology & American Society for Matrix Biology Glycobiology. 22: 1518-1650. DOI: 10.1093/Glycob/Cws127 |
0.526 |
|
| 2012 |
Kurakevich E, Hennet T, Rogler G, Borsig L. Mo1737 Role of Sialylation by St3gal4 Sialyltransferase in Mouse Models of Colitis Gastroenterology. 142: S-673. DOI: 10.1016/S0016-5085(12)62591-8 |
0.303 |
|
| 2011 |
Perrin-Tricaud C, Rutschmann C, Hennet T. Identification of domains and amino acids essential to the collagen galactosyltransferase activity of GLT25D1. Plos One. 6: e29390. PMID 22216269 DOI: 10.1371/Journal.Pone.0029390 |
0.33 |
|
| 2011 |
Luther KB, Hülsmeier AJ, Schegg B, Deuber SA, Raoult D, Hennet T. Mimivirus collagen is modified by bifunctional lysyl hydroxylase and glycosyltransferase enzyme. The Journal of Biological Chemistry. 286: 43701-9. PMID 22045808 DOI: 10.1074/Jbc.M111.309096 |
0.353 |
|
| 2011 |
Hülsmeier AJ, Welti M, Hennet T. Glycoprotein maturation and the UPR. Methods in Enzymology. 491: 163-82. PMID 21329800 DOI: 10.1016/B978-0-12-385928-0.00010-9 |
0.348 |
|
| 2011 |
Haeuptle MA, Welti M, Troxler H, Hülsmeier AJ, Imbach T, Hennet T. Improvement of dolichol-linked oligosaccharide biosynthesis by the squalene synthase inhibitor zaragozic acid. The Journal of Biological Chemistry. 286: 6085-91. PMID 21183681 DOI: 10.1074/Jbc.M110.165795 |
0.386 |
|
| 2011 |
Lecca MR, Maag C, Berger EG, Hennet T. Fibrotic response in fibroblasts from congenital disorders of glycosylation. Journal of Cellular and Molecular Medicine. 15: 1788-96. PMID 21029365 DOI: 10.1111/J.1582-4934.2010.01187.X |
0.579 |
|
| 2010 |
Hülsmeier AJ, Deplazes P, Naem S, Nonaka N, Hennet T, Köhler P. An Echinococcus multilocularis coproantigen is a surface glycoprotein with unique O-gycosylation. Glycobiology. 20: 127-35. PMID 19822708 DOI: 10.1093/Glycob/Cwp155 |
0.361 |
|
| 2010 |
Haeuptle MA, Hülsmeier AJ, Hennet T. HPLC and mass spectrometry analysis of dolichol-phosphates at the cell culture scale. Analytical Biochemistry. 396: 133-8. PMID 19761748 DOI: 10.1016/J.Ab.2009.09.020 |
0.306 |
|
| 2009 |
Haeuptle MA, Hennet T. Congenital disorders of glycosylation: an update on defects affecting the biosynthesis of dolichol-linked oligosaccharides. Human Mutation. 30: 1628-41. PMID 19862844 DOI: 10.1002/Humu.21126 |
0.42 |
|
| 2009 |
Titz A, Butschi A, Henrissat B, Fan YY, Hennet T, Razzazi-Fazeli E, Hengartner MO, Wilson IB, Künzler M, Aebi M. Molecular basis for galactosylation of core fucose residues in invertebrates: identification of caenorhabditis elegans N-glycan core alpha1,6-fucoside beta1,4-galactosyltransferase GALT-1 as a member of a novel glycosyltransferase family. The Journal of Biological Chemistry. 284: 36223-33. PMID 19858195 DOI: 10.1074/Jbc.M109.058354 |
0.426 |
|
| 2009 |
Jaeken J, Vleugels W, Régal L, Corchia C, Goemans N, Haeuptle MA, Foulquier F, Hennet T, Matthijs G, Dionisi-Vici C. RFT1-CDG: deafness as a novel feature of congenital disorders of glycosylation. Journal of Inherited Metabolic Disease. S335-8. PMID 19856127 DOI: 10.1007/S10545-009-1297-3 |
0.401 |
|
| 2009 |
Jaeken J, Hennet T, Matthijs G, Freeze HH. CDG nomenclature: time for a change! Biochimica Et Biophysica Acta. 1792: 825-6. PMID 19765534 DOI: 10.1016/J.Bbadis.2009.08.005 |
0.404 |
|
| 2009 |
Vleugels W, Haeuptle MA, Ng BG, Michalski JC, Battini R, Dionisi-Vici C, Ludman MD, Jaeken J, Foulquier F, Freeze HH, Matthijs G, Hennet T. RFT1 deficiency in three novel CDG patients. Human Mutation. 30: 1428-34. PMID 19701946 DOI: 10.1002/Humu.21085 |
0.384 |
|
| 2009 |
Paesold-Burda P, Maag C, Troxler H, Foulquier F, Kleinert P, Schnabel S, Baumgartner M, Hennet T. Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation. Human Molecular Genetics. 18: 4350-6. PMID 19690088 DOI: 10.1093/Hmg/Ddp389 |
0.446 |
|
| 2009 |
Vesela K, Honzik T, Hansikova H, Haeuptle MA, Semberova J, Stranak Z, Hennet T, Zeman J. A new case of ALG8 deficiency (CDG Ih). Journal of Inherited Metabolic Disease. PMID 19688606 DOI: 10.1007/S10545-009-1203-Z |
0.344 |
|
| 2009 |
Schegg B, Hülsmeier AJ, Rutschmann C, Maag C, Hennet T. Core glycosylation of collagen is initiated by two beta(1-O)galactosyltransferases. Molecular and Cellular Biology. 29: 943-52. PMID 19075007 DOI: 10.1128/Mcb.02085-07 |
0.445 |
|
| 2009 |
Hennet T. From glycosylation disorders back to glycosylation: what have we learned? Biochimica Et Biophysica Acta. 1792: 921-4. PMID 19007883 DOI: 10.1016/J.Bbadis.2008.10.006 |
0.324 |
|
| 2008 |
Biellmann F, Hülsmeier AJ, Zhou D, Cinelli P, Hennet T. The Lc3-synthase gene B3gnt5 is essential to pre-implantation development of the murine embryo. Bmc Developmental Biology. 8: 109. PMID 19014510 DOI: 10.1186/1471-213X-8-109 |
0.601 |
|
| 2008 |
Haeuptle MA, Pujol FM, Neupert C, Winchester B, Kastaniotis AJ, Aebi M, Hennet T. Human RFT1 deficiency leads to a disorder of N-linked glycosylation. American Journal of Human Genetics. 82: 600-6. PMID 18313027 DOI: 10.1016/J.Ajhg.2007.12.021 |
0.45 |
|
| 2008 |
Biellmann F, Henion TR, Bürki K, Hennet T. Impaired sexual behavior in male mice deficient for the beta1-3 N-acetylglucosaminyltransferase-I gene. Molecular Reproduction and Development. 75: 699-706. PMID 18008318 DOI: 10.1002/Mrd.20828 |
0.323 |
|
| 2007 |
Hülsmeier AJ, Paesold-Burda P, Hennet T. N-glycosylation site occupancy in serum glycoproteins using multiple reaction monitoring liquid chromatography-mass spectrometry. Molecular & Cellular Proteomics : McP. 6: 2132-8. PMID 17823199 DOI: 10.1074/Mcp.M700361-Mcp200 |
0.311 |
|
| 2005 |
Müller R, Hülsmeier AJ, Altmann F, Ten Hagen K, Tiemeyer M, Hennet T. Characterization of mucin-type core-1 beta1-3 galactosyltransferase homologous enzymes in Drosophila melanogaster. The Febs Journal. 272: 4295-305. PMID 16128800 DOI: 10.1111/J.1742-4658.2005.04838.X |
0.424 |
|
| 2005 |
Weinstein M, Schollen E, Matthijs G, Neupert C, Hennet T, Grubenmann CE, Frank CG, Aebi M, Clarke JT, Griffiths A, Seargeant L, Poplawski N. CDG-IL: an infant with a novel mutation in the ALG9 gene and additional phenotypic features. American Journal of Medical Genetics. Part A. 136: 194-7. PMID 15945070 DOI: 10.1002/Ajmg.A.30851 |
0.335 |
|
| 2005 |
Lecca MR, Wagner U, Patrignani A, Berger EG, Hennet T. Genome-wide analysis of the unfolded protein response in fibroblasts from congenital disorders of glycosylation type-I patients. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 19: 240-2. PMID 15545299 DOI: 10.1096/Fj.04-2397Fje |
0.61 |
|
| 2004 |
García-Silva MT, Matthijs G, Schollen E, Cabrera JC, Sanchez del Pozo J, Martí Herreros M, Simón R, Maties M, Martín Hernández E, Hennet T, Briones P. Congenital disorder of glycosylation (CDG) type Ie. A new patient. Journal of Inherited Metabolic Disease. 27: 591-600. PMID 15669674 DOI: 10.1023/B:Boli.0000042984.42433.D8 |
0.375 |
|
| 2004 |
Schollen E, Frank CG, Keldermans L, Reyntjens R, Grubenmann CE, Clayton PT, Winchester BG, Smeitink J, Wevers RA, Aebi M, Hennet T, Matthijs G. Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency) Journal of Medical Genetics. 41: 550-556. PMID 15235028 DOI: 10.1136/Jmg.2003.016923 |
0.304 |
|
| 2004 |
Frank CG, Grubenmann CE, Eyaid W, Berger EG, Aebi M, Hennet T. Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL. American Journal of Human Genetics. 75: 146-50. PMID 15148656 DOI: 10.1086/422367 |
0.626 |
|
| 2004 |
Grubenmann CE, Frank CG, Hülsmeier AJ, Schollen E, Matthijs G, Mayatepek E, Berger EG, Aebi M, Hennet T. Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik. Human Molecular Genetics. 13: 535-42. PMID 14709599 DOI: 10.1093/Hmg/Ddh050 |
0.63 |
|
| 2003 |
Griffitts JS, Huffman DL, Whitacre JL, Barrows BD, Marroquin LD, Müller R, Brown JR, Hennet T, Esko JD, Aroian RV. Resistance to a Bacterial Toxin Is Mediated by Removal of a Conserved Glycosylation Pathway Required for Toxin-Host Interactions Journal of Biological Chemistry. 278: 45594-45602. PMID 12944392 DOI: 10.1074/Jbc.M308142200 |
0.318 |
|
| 2003 |
Zhang Y, Iwasaki H, Wang H, Kudo T, Kalka TB, Hennet T, Kubota T, Cheng L, Inaba N, Gotoh M, Togayachi A, Guo J, Hisatomi H, Nakajima K, Nishihara S, et al. Cloning and characterization of a new human UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase, designated pp-GalNAc-T13, that is specifically expressed in neurons and synthesizes GalNAc alpha-serine/threonine antigen. The Journal of Biological Chemistry. 278: 573-84. PMID 12407114 DOI: 10.1074/Jbc.M203094200 |
0.572 |
|
| 2003 |
Schenk B, Imbach T, Frank CG, Grubenmann CE, Raymond GV, Hurvitz H, Raas-Rotschild A, Luder AS, Jaeken J, Berger EG, Matthijs G, Hennet T, Aebi M, Jaeken J. MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If Journal of Clinical Investigation. 111: 925-925. DOI: 10.1172/Jci13419C1 |
0.567 |
|
| 2002 |
Hennet T. The galactosyltransferase family. Cellular and Molecular Life Sciences : Cmls. 59: 1081-95. PMID 12222957 DOI: 10.1007/S00018-002-8489-4 |
0.365 |
|
| 2002 |
Grubenmann CE, Frank CG, Kjaergaard S, Berger EG, Aebi M, Hennet T. ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg. Human Molecular Genetics. 11: 2331-9. PMID 12217961 DOI: 10.1093/Hmg/11.19.2331 |
0.623 |
|
| 2002 |
Müller R, Altmann F, Zhou D, Hennet T. The Drosophila melanogaster brainiac protein is a glycolipid-specific beta 1,3N-acetylglucosaminyltransferase. The Journal of Biological Chemistry. 277: 32417-20. PMID 12130631 DOI: 10.1074/Jbc.C200381200 |
0.646 |
|
| 2002 |
Malissard M, Dinter A, Berger EG, Hennet T. Functional assignment of motifs conserved in beta 1,3-glycosyltransferases. European Journal of Biochemistry. 269: 233-9. PMID 11784317 DOI: 10.1046/J.0014-2956.2001.02644.X |
0.61 |
|
| 2002 |
Schenk B, Imbach T, Frank CG, Grubenmann CE, Raymond GV, Hurvitz H, Korn-Lubetzki I, Revel-Vik S, Raas-Rotschild A, Luder AS, Jaeken J, Berger EG, Matthijs G, Hennet T, Aebi M. MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If. The Journal of Clinical Investigation. 108: 1687-95. PMID 11733564 DOI: 10.1172/Jci13419 |
0.602 |
|
| 2001 |
Bai X, Zhou D, Brown JR, Crawford BE, Hennet T, Esko JD. Biosynthesis of the linkage region of glycosaminoglycans: cloning and activity of galactosyltransferase II, the sixth member of the beta 1,3-galactosyltransferase family (beta 3GalT6). The Journal of Biological Chemistry. 276: 48189-95. PMID 11551958 DOI: 10.1074/Jbc.M107339200 |
0.579 |
|
| 2001 |
Henion TR, Zhou D, Wolfer DP, Jungalwala FB, Hennet T. Cloning of a mouse beta 1,3 N-acetylglucosaminyltransferase GlcNAc(beta 1,3)Gal(beta 1,4)Glc-ceramide synthase gene encoding the key regulator of lacto-series glycolipid biosynthesis. The Journal of Biological Chemistry. 276: 30261-9. PMID 11384981 DOI: 10.1074/Jbc.M102979200 |
0.611 |
|
| 2001 |
Aebi M, Hennet T. Congenital disorders of glycosylation: genetic model systems lead the way. Trends in Cell Biology. 11: 136-41. PMID 11306275 DOI: 10.1016/S0962-8924(01)01925-0 |
0.394 |
|
| 2000 |
Imbach T, Grünewald S, Schenk B, Burda P, Schollen E, Wevers RA, Jaeken J, de Klerk JB, Berger EG, Matthijs G, Aebi M, Hennet T. Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic. Human Genetics. 106: 538-45. PMID 10914684 DOI: 10.1007/S004390000293 |
0.583 |
|
| 2000 |
Zhou D, Henion TR, Jungalwala FB, Berger EG, Hennet T. The beta 1,3-galactosyltransferase beta 3GalT-V is a stage-specific embryonic antigen-3 (SSEA-3) synthase. The Journal of Biological Chemistry. 275: 22631-4. PMID 10837462 DOI: 10.1074/Jbc.C000263200 |
0.697 |
|
| 2000 |
Imbach T, Schenk B, Schollen E, Burda P, Stutz A, Grunewald S, Bailie NM, King MD, Jaeken J, Matthijs G, Berger EG, Aebi M, Hennet T. Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie. The Journal of Clinical Investigation. 105: 233-9. PMID 10642602 DOI: 10.1172/Jci8691 |
0.637 |
|
| 2000 |
Zhou D, Malissard M, Berger EG, Hennet T. Secretion and purification of recombinant beta1-4 galactosyltransferase from insect cells using pFmel-protA, a novel transposition-based baculovirus transfer vector. Archives of Biochemistry and Biophysics. 374: 3-7. PMID 10640389 DOI: 10.1006/Abbi.1999.1622 |
0.684 |
|
| 2000 |
Hennet T, Ellies LG. The remodeling of glycoconjugates in mice. Biochimica Et Biophysica Acta. 1473: 123-36. PMID 10580133 DOI: 10.1016/S0304-4165(99)00173-7 |
0.367 |
|
| 2000 |
Gr�newald S, Imbach T, Huijben K, Rubio-Gozalbo ME, Verrips A, De Klerk JBC, Stroink H, De Rijk-Van Andel JF, Van Hove JLK, Wendel U, Matthijs G, Hennet T, Jaeken J, Wevers RA. Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesis Annals of Neurology. 47: 776-781. DOI: 10.1002/1531-8249(200006)47:6<776::Aid-Ana10>3.0.Co;2-5 |
0.33 |
|
| 1999 |
Aebi M, Helenius A, Schenk B, Barone R, Fiumara A, Berger EG, Hennet T, Imbach T, Stutz A, Bjursell C, Uller A, Wahlström JG, Briones P, Cardo E, Clayton P, et al. Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG. First International Workshop on CDGS. Glycoconjugate Journal. 16: 669-71. PMID 11003549 DOI: 10.1023/A:1017249723165 |
0.523 |
|
| 1999 |
Zhou D, Berger EG, Hennet T. Molecular cloning of a human UDP-galactose:GlcNAcbeta1,3GalNAc beta1, 3 galactosyltransferase gene encoding an O-linked core3-elongation enzyme. European Journal of Biochemistry. 263: 571-6. PMID 10406968 DOI: 10.1046/J.1432-1327.1999.00541.X |
0.707 |
|
| 1999 |
Imbach T, Burda P, Kuhnert P, Wevers RA, Aebi M, Berger EG, Hennet T. A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic. Proceedings of the National Academy of Sciences of the United States of America. 96: 6982-7. PMID 10359825 DOI: 10.1073/Pnas.96.12.6982 |
0.615 |
|
| 1999 |
Zhou D, Dinter A, Gutiérrez Gallego R, Kamerling JP, Vliegenthart JF, Berger EG, Hennet T. A beta-1,3-N-acetylglucosaminyltransferase with poly-N-acetyllactosamine synthase activity is structurally related to beta-1,3-galactosyltransferases. Proceedings of the National Academy of Sciences of the United States of America. 96: 406-11. PMID 9892646 DOI: 10.1073/Pnas.96.2.406 |
0.714 |
|
| 1998 |
Hennet T, Chui D, Paulson JC, Marth JD. Immune regulation by the ST6Gal sialytransferase Proceedings of the National Academy of Sciences of the United States of America. 95: 4504-4509. PMID 9539767 DOI: 10.1073/Pnas.95.8.4504 |
0.508 |
|
| 1998 |
Hennet T, Dinter A, Kuhnert P, Mattu TS, Rudd PM, Berger EG. Genomic cloning and expression of three murine UDP-galactose: beta-N-acetylglucosamine beta1,3-galactosyltransferase genes. The Journal of Biological Chemistry. 273: 58-65. PMID 9417047 DOI: 10.1074/Jbc.273.1.58 |
0.624 |
|
| 1995 |
Hennet T, Hagen FK, Tabak LA, Marth JD. Genetics T-cell-specific deletion of a polypeptide N-acetylgalactosaminyl-transferase gene by site-directed recombination Proceedings of the National Academy of Sciences of the United States of America. 92: 12070-12074. PMID 8618846 DOI: 10.1073/Pnas.92.26.12070 |
0.567 |
|
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