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Lancet (London, England)|October 16, 2022
Severe COVID-19 outcomes after full vaccination of primary schedule and initial boosters: pooled analysis of national prospective cohort studies of 30 million individuals in England, Northern Ireland, Scotland, and WalesUtkarsh Agrawal, Stuart Bedston, Colin McCowan, et al.
Cytogenetic and Genome Research|October 22, 2008
A 4,103 marker integrated physical and comparative map of the horse genomeT Raudsepp, A Gustafson-Seabury, K Durkin, et al.
BMJ Open|January 20, 2021
Protocol for the development of the Wales Multimorbidity e-Cohort (WMC): data sources and methods to construct a population-based research platform to investigate multimorbidityJane Lyons, Ashley Akbari, Utkarsh Agrawal, et al.
Heredity|November 2, 2022
Genetics of randomly bred cats support the cradle of cat domestication being in the Near EastSara M Nilson, Barbara Gandolfi, Robert A Grahn, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 25, 2020
Prevalence of Food Sensitization and Food Allergy in Children Across EuropeSarah A Lyons, Michael Clausen, André C Knulst, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 12, 2014
Comparative analysis of the domestic cat genome reveals genetic signatures underlying feline biology and domesticationMichael J Montague, Gang Li, Barbara Gandolfi, et al.
The Journal of Experimental Medicine|August 23, 2022
Monocyte-derived macrophages aggravate pulmonary vasculitis via cGAS/STING/IFN-mediated nucleic acid sensingNina Kessler, Susanne F Viehmann, Calvin Krollmann, et al.
Nature Communications|December 18, 2015
Ternary structure reveals mechanism of a membrane diacylglycerol kinaseDianfan Li, Phillip J Stansfeld, Mark S P Sansom, et al.
Antimicrobial Agents and Chemotherapy|September 30, 2024
Spectinamide MBX-4888A exhibits favorable lesion and tissue distribution and promotes treatment shortening in advanced murine models of tuberculosisAllison A Bauman, Jansy P Sarathy, Firat Kaya, et al.
American Journal of Human Genetics|May 11, 2020
Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant CiliopathyBenjamin Cogné, Xenia Latypova, Lokuliyanage Dona Samudita Senaratne, et al.
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