Showing results (431-440 of 458) with videos related to

Sort By:
Pageof 46
Glycobiology|July 27, 2023
A photoaffinity glycan-labeling approach to investigate immunoglobulin glycan-binding partnersMiles D Holborough-Kerkvliet, Greta Mucignato, Sam J Moons, et al.
Annals of the Rheumatic Diseases|January 15, 2015
Extensive glycosylation of ACPA-IgG variable domains modulates binding to citrullinated antigens in rheumatoid arthritisYoann Rombouts, Annemiek Willemze, Joyce J B C van Beers, et al.
Blood Advances|August 19, 2020
Biological and structural characterization of murine TRALI antibody reveals increased Fc-mediated complement activationEveline A N Zeeuw van der Laan, Saskia van der Velden, Arthur E H Bentlage, et al.
Ebiomedicine|June 25, 2022
Immunoassay for quantification of antigen-specific IgG fucosylationTonći Šuštić, Julie Van Coillie, Mads Delbo Larsen, et al.
Communications Biology|April 9, 2024
Pancreatic cancer-associated fibroblasts modulate macrophage differentiation via sialic acid-Siglec interactionsKelly Boelaars, Ernesto Rodriguez, Zowi R Huinen, et al.
Communications Biology|January 12, 2022
Analysis of the glyco-code in pancreatic ductal adenocarcinoma identifies glycan-mediated immune regulatory circuitsErnesto Rodriguez, Kelly Boelaars, Kari Brown, et al.
Human Molecular Genetics|September 13, 2011
Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adultsJennifer E Huffman, Ana Knezevic, Veronique Vitart, et al.
Science Advances|February 9, 2022
Surface Ig variable domain glycosylation affects autoantigen binding and acts as threshold for human autoreactive B cell activationTheresa Kissel, Changrong Ge, Lise Hafkenscheid, et al.
Cell Reports|November 9, 2025
Patient-derived organoids to study glycosylation dynamics during gastric diseaseLiliana Santos-Ferreira, Álvaro M Martins, Henrique O Duarte, et al.
Brain : a Journal of Neurology|February 26, 2014
Diagnostic serum glycosylation profile in patients with intellectual disability as a result of MAN1B1 deficiencyMonique Van Scherpenzeel, Sharita Timal, Daisy Rymen, et al.
Pageof 46