about
XT-II, the second isoform of human peptide-O-xylosyltransferase, displays enzymatic activityInfluenza Neuraminidase Inhibitors: Synthetic Approaches, Derivatives and Biological ActivityBiochemical correlation of activity of the α-dystroglycan-modifying glycosyltransferase POMGnT1 with mutations in muscle-eye-brain disease.Chemoenzymatic synthesis of sialooligosaccharides on arrays for studies of cell surface adhesionComparative characterisation of recombinant invertebrate and vertebrate peptide O-Xylosyltransferases.Enzymatic glycosylation of peptide arrays on gold surfacesA versatile gold surface approach for fabrication and interrogation of glycoarrays.SPOT synthesis of peptide arrays on self-assembled monolayers and their evaluation as enzyme substrates.Enzymatic glycosylations on arrays.MALDI-ToF MS analysis of glycosyltransferase activities on gold surface arrays.Discovery and characterization of a novel extremely acidic bacterial N-glycanase with combined advantages of PNGase F and A.Discrimination of in vitro and in vivo digestion products of meat proteins from pork, beef, chicken, and fish.More Than Just Oligomannose: An N-glycomic Comparison of Penicillium SpeciesDiscovery and Biochemical Characterization of the UDP-Xylose Biosynthesis Pathway in Sphaerobacter thermophilus.PNGases as valuable tools in glycoprotein analysis.Effects of microvirin monomers and oligomers on hepatitis C virus.Functional analysis of anomeric sugar kinases.Development of Dictyostelium discoideum is associated with alteration of fucosylated N-glycan structuresBiological and biochemical properties of two Xenopus laevis N-acetylgalactosaminyltransferases with contrasting roles in embryogenesis.Discrimination of epimeric glycans and glycopeptides using IM-MS and its potential for carbohydrate sequencing.Discovery and Biochemical Characterization of a Thermostable Glucose-1-phosphate Nucleotidyltransferase from Thermodesulfatator indicus.Editorial: Recent Achievements in Glycoenzyme Discovery.Engineering of an Episomal Plasmid Suitable for High-Throughput Expression in Pichia pastoris.Qualitative and Quantitative Analysis of Carbohydrate Modification on Glycoproteins from Seeds of Ginkgo biloba.Characterisation of a Bacterial Galactokinase with High Activity and Broad Substrate Tolerance for Chemoenzymatic Synthesis of 6-Aminogalactose-1-Phosphate and Analogues.The Shewanella woodyi galactokinase pool phosphorylates glucose at the 6-position.Discovery and biochemical characterization of a mannose phosphorylase catalyzing the synthesis of novel β-1,3-mannosides.Cloning, purification and biochemical characterization of two β-N-acetylhexosaminidases from the mucin-degrading gut bacterium Akkermansia muciniphila.One assay for all: exploring small molecule phosphorylation using amylose-polyiodide complexes.Green and efficient extraction of rutin from tartary buckwheat hull by using natural deep eutectic solvents.Quantification of sialic acids in red meat by UPLC-FLD using indoxylsialosides as internal standards.Chemoenzymatic synthesis of O-mannosylpeptides in solution and on solid phase.Comparison of anti-pathogenic activities of the human and bovine milk N-glycome: Fucosylation is a key factor.An integrated 3D-printed platform for the automated isolation of N-glycans.Applications of a highly α2,6-selective pseudosialidase.Determination of Sialic Acids in Liver and Milk Samples of Wild-type and CMAH Knock-out Mice.Rapid Sample Preparation Methodology for Plant N-Glycan Analysis Using Acid-Stable PNGase H+.The fucosidase-pool of Emticicia oligotrophica: Biochemical characterization and transfucosylation potential.2-Pyridylfuran: A New Fluorescent Tag for the Analysis of CarbohydratesSequential processing of mannose-containing glycans by two α-mannosidases from Solitalea canadensis
P50
Q24603487-B1744089-A373-4DA0-A303-370ADB0A35BAQ28079041-95F2255B-41ED-4ED3-B6EA-BF1E28683840Q30400284-7F875D87-4B04-4D32-BC76-7BB4C911A223Q31004823-5F24E2E8-F4C3-4BAD-B935-4B38C5EDC247Q33258672-94661D96-2CEB-4D4F-B5D1-7A13DC6FFADEQ33323195-6FC84B38-9BA9-425B-87B9-2B80228B21D4Q33344603-E3E3935E-0119-4B75-A7F0-27C6325E9BC1Q33372398-81B4A217-74BA-454D-8F55-F43BAE6D8940Q33667348-D4132848-2353-4738-AB26-0A1C16D211D7Q34068241-8F80CF2D-F9F2-455C-8212-7A7AEFE1CE73Q34507845-5C75447F-48AC-4A69-AC23-E21216060A69Q35727799-A1DF5D07-1C07-4FD0-8CFD-1DDE9C7E66F6Q35826749-CF1A755D-F287-480F-8250-02CF5A35AC95Q36175215-66F57BCD-1739-4439-8B23-CE8ABD43C868Q38224287-FE85238B-4838-499D-8A4A-CFC606BA3F1BQ38683495-7E817977-1F16-4E8D-BF45-7ED4C674D23CQ38879393-113A76CD-D1AE-4A14-84A0-D13BED2754A1Q39941358-AAD655C8-7F50-4EAF-BCDB-DDBF4CB963ACQ41758636-D24565FC-234F-4A04-B8E8-CB6DDC7B2DB5Q45174457-D7BA1431-9E40-4D1A-81D1-8D659AAE44A7Q46331269-83762A8C-F5D3-4013-8BC7-4C902B75B355Q47581593-29450534-5E66-43A5-9DBF-E667B07236A8Q47629394-8C6B010F-2765-448E-868B-17B67E29B681Q47963464-8BD86105-EBAC-429D-B5D5-46AA619659E5Q48200960-6ECACF5A-77AC-4F73-AB14-316CB4DF756BQ49713563-BEDB5C50-2ED5-4A9A-BE72-A24E25C31F00Q49954455-99B1C1AA-E727-4519-9A6B-19F8E407AD2EQ50167847-0B0A7A54-C451-41A7-97FD-341031EFE372Q50210710-CBA63DB8-5390-44EC-9F44-E761CD14D4A5Q50212735-032A4FB2-46E4-4776-8276-D90543131596Q50249140-ED972DCF-3877-474A-8E39-135C4397FA32Q50501683-77EEEB39-4DA6-4DDF-B258-6EB863206A98Q50972984-386A5B43-21C1-43B2-9B90-01432B430365Q51637314-AF581186-D8CD-48C6-A4FE-94FDE4819D5EQ52366969-8BAAAD61-1B73-43BD-9F1E-2253C73F645DQ52428419-E0601245-6C75-497A-BBDB-2037FD4AB000Q52838354-384733E4-4724-4D75-8FF7-0E92D8C9C970Q54249719-25664FA5-7CD5-4BFA-87ED-C36ACD1B8ECBQ57533255-BF1B2B63-22DE-4777-B705-03C865117C1CQ59243309-FA62882F-250B-4942-B7DC-F83930E1DB1B
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Josef Voglmeir
@ast
Josef Voglmeir
@en
Josef Voglmeir
@es
Josef Voglmeir
@nl
Josef Voglmeir
@sl
type
label
Josef Voglmeir
@ast
Josef Voglmeir
@en
Josef Voglmeir
@es
Josef Voglmeir
@nl
Josef Voglmeir
@sl
prefLabel
Josef Voglmeir
@ast
Josef Voglmeir
@en
Josef Voglmeir
@es
Josef Voglmeir
@nl
Josef Voglmeir
@sl
P106
P21
P31
P496
0000-0002-4096-4926