Area of research
Molecular Biology · Organic Chemistry
Research interest
Research interests include Glycosylation and Glycoproteins Research, Carbohydrate Chemistry and Synthesis, Galectins and Cancer Biology, and Helicobacter pylori-related gastroenterology studies.
The butyrate-producing Gram-positive human gut bacterium, Hoskinsella mucinilytica, selectively targets host mucin N-acetylhexosamines.
Glycosphingolipids in human abdominal leiomyosarcoma and liposarcoma.
Seal milk oligosaccharides rival human milk complexity and exhibit functional dynamics during lactation.
Extended nuclear glycosylation regulates RNA processing
Dual human milk oligosaccharide-fibre utilisation drives gut microbiome selection during weaning
The role of
<i>Akkermansia muciniphila</i>
sulfatases in colonic mucin utilisation
Ion mobility-tandem mass spectrometry of mucin-type O-glycans
Ion mobility-tandem mass spectrometry of mucin-type O-glycans.
A monoallelic UXS1 variant associated with short-limbed short stature.
Sialidases and fucosidases of Akkermansia muciniphila are crucial for growth on mucin and nutrient sharing with mucus-associated gut bacteria.
Increasing Complexity of the N-Glycome During Caenorhabditis Development
Reproducing extracellular matrix adverse remodelling of non-ST myocardial infarction in a large animal model
N-glycan antennal modifications are altered in Caenorhabditis elegans lacking the HEX-4 N-acetylgalactosamine-specific hexosaminidase.
Reproducing extracellular matrix adverse remodelling of non-ST myocardial infarction in a large animal model.
Quantification of chondroitin sulfate, hyaluronic acid and <i>N</i>-glycans in synovial fluid - A technical performance study.
Predicting glycan structure from tandem mass spectrometry via deep learning
Ion Mobility-Tandem Mass Spectrometry of Mucin-type O-Glycans
A Complex Connection Between the Diversity of Human Gastric Mucin O-Glycans, Helicobacter pylori Binding, Helicobacter Infection and Fucosylation
Metabolic reprogramming and membrane glycan remodeling as potential drivers of zebrafish heart regeneration.
Computational Modeling of <i>O</i>-Linked Glycan Biosynthesis in CHO Cells.
Sialidases and Fucosidases of <i>Akkermansia muciniphila</i> are crucial for growth on mucin and nutrient sharing with mucus-associated gut bacteria
A single sulfatase is required to access colonic mucin by a gut bacterium.
Elastin-like recombinamers-based hydrogel modulates post-ischemic remodeling in a non-transmural myocardial infarction in sheep.
A single bacterial sulfatase is required for metabolism of colonic mucin O-glycans and intestinal colonization by a symbiotic human gut bacterium
Interleukin-22-mediated host glycosylation prevents Clostridioides difficile infection by modulating the metabolic activity of the gut microbiota.
Butyrate producing colonic Clostridiales metabolise human milk oligosaccharides and cross feed on mucin via conserved pathways.
NIST Interlaboratory Study on Glycosylation Analysis of Monoclonal Antibodies: Comparison of Results from Diverse Analytical Methods.
Cathepsin g Degrades Both Glycosylated and Unglycosylated Regions of Lubricin, a Synovial Mucin
Sulfated and sialylated N-glycans in the echinoderm Holothuria atra reflect its marine habitat and phylogeny
Identification by mass spectrometry and immunoblotting of xenogeneic antigens in the N- and O-glycomes of porcine, bovine and equine heart tissues.