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Technologiepark Zwijnaarde 927, VIB
9052 Zwijnaarde - Wim.Nerinckx@UGent.be
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The inhibitor endosidin 4 targets SEC7 domain-type ARF GTPase exchange factors and interferes with subcellular trafficking in eukaryotes
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Tozasertib analogues as inhibitors of necroptotic cell death
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When PERK inhibitors turn out to be new potent RIPK1 inhibitors : critical issues on the specificity and use of GSK2606414 and GSK2656157
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A bacterial glycosidase enables mannose-6-phosphate modification and improved cellular uptake of yeast-produced recombinant human lysosomal enzymes
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Necrostatin-1 analogues: critical issues on the specificity, activity and in vivo use in experimental disease models
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Synthesis and evaluation of 2-deoxy-2-amino-β-cellobiosides as cellulase inhibitors
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An alternative approach for the synthesis of fluorogenic substrates of endo-beta-(1 -> 4)-xylanases and some applications
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Theory and computation show that Asp463 is the catalytic proton donor in human endoplasmic reticulum alpha-(1 -> 2)-mannosidase I
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Modulation of activity by Arg407: structure of a fungal alpha-1,2-mannosidase in complex with a substrate analogue
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The fate of beta-D-mannopyranose after its formation by endoplasmic reticulum alpha-(1 -> 2)-mannosidase I catalysis