Author

Göran Larson

Sahlgrenska University HospitalORCID 0000-0002-2616-0366Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:proteomics· 1 Organism:zebrafish· 1

Frequent Co-Authors

Adelbert De ClercqiD· 1 shared Andy WillaertiD· 1 shared B. V. Venkataram PrasadiD· 1 shared B. Vijayalakshmi AyyariD· 1 shared Carmen V. ApostoliD· 1 shared Charlotte Gistelinck· 1 shared Delfien SyxiD· 1 shared Fransiska MalfaitiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Adelbert De ClercqORCID

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2 papers

Recent·Most cited

Functional Diversity in GII.4 Norovirus Entry: HBGA Binding and Capsid Clustering Dynamics

B. Vijayalakshmi Ayyar, Carmen V. Apostol, Janam J. Dave, Soni Kaundal, Joseph A. Kendra, Frederick H. Neill, Khalil Ettayebi, Sarah Maher, Ramakrishnan Anish, Gabriel Ignacio Parra, Göran Larson, Robert L. Atmar, Sue E. Crawford, B. V. Venkataram Prasad, Mary Kolb Estes

The paper compares GII.4 norovirus variants to determine if clustering and entry mechanisms are conserved, finding clustering enhances entry and is mediated by specific residues and lipid rafts.

Proceedings of the National Academy of Sciences · Oct 1, 2025Peer-reviewedMicrobiology

b3galt6 knock-out zebrafish recapitulate β3GalT6-deficiency disorders in human and reveal a trisaccharide proteoglycan linkage region

Sarah Delbaere, Adelbert De Clercq, Shuji Mizumoto, Fredrik Noborn, Jan Willem Bek, Lien Alluyn, Charlotte Gistelinck, Delfien Syx, Phil Salmon, Paul J. Coucke, Göran Larson, Shuhei Yamada, Andy Willaert, Fransiska Malfait

This study shows that b3galt6 knock-out zebrafish exhibit human β3GalT6-deficiency disorders, revealing a novel proteoglycan linkage region mechanism.

Frontiers in Cell and Developmental Biology · Dec 10, 2020Peer-reviewedGenetics