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Nature Communications|October 1, 2015
Structural basis of glycan specificity in neonate-specific bovine-human reassortant rotavirusLiya Hu, Sasirekha Ramani, Rita Czako, et al.
Science Immunology|January 16, 2026
Intestinal epithelial TLR5 signaling promotes barrier-supportive macrophagesMing-Ting Tsai, Ryann Callaghan, Charles Ng, et al.
The Pediatric Infectious Disease Journal|June 3, 2016
Rotavirus Serum IgA Immune Response in Children Receiving Rotarix Coadministered With bOPV or IPVSasirekha Ramani, Nora Mamani, Rodolfo Villena, et al.
Nature Communications|March 11, 2022
Atomic structure of the predominant GII.4 human norovirus capsid reveals novel stability and plasticityLiya Hu, Wilhelm Salmen, Rong Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2008
Integrins alpha1beta1 and alpha2beta1 are receptors for the rotavirus enterotoxinNeung-Seon Seo, Carl Q-Y Zeng, Joseph M Hyser, et al.
Biorxiv : the Preprint Server for Biology|September 30, 2024
CONFORMATIONAL FLEXIBILITY IS A CRITICAL FACTOR IN DESIGNING BROAD-SPECTRUM HUMAN NOROVIRUS PROTEASE INHIBITORSSon Pham, Boyang Zhao, Neetu Neetu, et al.
The Journal of Infectious Diseases|October 21, 2006
Antibody prevalence and titer to norovirus (genogroup II) correlate with secretor (FUT2) but not with ABO phenotype or Lewis (FUT3) genotypeMalin Modin Larsson, Gustaf E P Rydell, Ammi Grahn, et al.
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