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Hugo Osório

Researcher at University of Porto

Publications -  121
Citations -  3853

Hugo Osório is an academic researcher from University of Porto. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 25, co-authored 102 publications receiving 2843 citations. Previous affiliations of Hugo Osório include Intelligence and National Security Alliance & Spanish National Research Council.

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Identification of distinct nanoparticles and subsets of extracellular vesicles by asymmetric flow field-flow fractionation.

TL;DR: It is shown that AF4 can serve as an improved analytical tool for isolating extracellular vesicles and addressing the complexities of heterogeneous nanoparticle subpopulations, and three nanoparticle subsets demonstrated diverse organ biodistribution patterns, suggesting distinct biological functions.
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Alterations in glycosylation as biomarkers for cancer detection

TL;DR: The application of these glycosylation modifications as biomarkers for cancer detection in tumour tissues and serological assays is summarised.
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Reactivity of Human Salivary Proteins Families Toward Food Polyphenols

TL;DR: Results obtained when all the main families of salivary proteins are present in a competitive assay, like in the oral cavity, demonstrate that condensed tannins interact first with acidic PRPs and statherin and thereafter with histatins, glycosylated PRPs, and bPRPs.
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Fut2-null mice display an altered glycosylation profile and impaired BabA-mediated Helicobacter pylori adhesion to gastric mucosa

TL;DR: This study has used an animal model of nonsecretors, Fut2-null mice, to characterize the glycosylation profile and evaluate the effect of the observed glycan expression modifications in the process of H. pylori adhesion, and demonstrated expression of terminal difucosylated glycan structures.
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CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings

TL;DR: The findings indicate that CNS clinical involvement occurs in ATTR-V30M patients regardless of LT, and longer disease duration after LT can provide the necessary time for transthyretin amyloidosis to progress until it becomes clinically relevant.