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- W2051219819 endingPage "7330" @default.
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- W2051219819 abstract "Abstract The aberrant glycosylation profiles of mucin glycoproteins on epithelial tumour cells represent attractive target structures for the development of immunotherapy against cancer. Mucin‐type glycopeptides have been successfully investigated as molecularly defined vaccine prototypes for triggering humoral immunity but are susceptible to rapid in vivo degradation. As a potential means to enhance the bioavailabilities of the antigenic structures, hydrolysis‐resistant carbohydrate analogues with fluorine substituents at positions C6, C2′ and C6′ were synthesised and incorporated into the tandem repeat sequence of the mucin MUC1. The resulting pseudo‐glycopeptides can be used to elucidate the effects of chemically modified antibody determinants on metabolic and immunological properties." @default.
- W2051219819 created "2016-06-24" @default.
- W2051219819 creator A5015011046 @default.
- W2051219819 creator A5048700901 @default.
- W2051219819 creator A5078843265 @default.
- W2051219819 date "2010-06-21" @default.
- W2051219819 modified "2023-10-18" @default.
- W2051219819 title "Fluorinated Glycosyl Amino Acids for Mucin-Like Glycopeptide Antigen Analogues" @default.
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- W2051219819 doi "https://doi.org/10.1002/chem.200903294" @default.
- W2051219819 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20461825" @default.
- W2051219819 hasPublicationYear "2010" @default.
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