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?:authorAffiliation
  • [\'Immunotherapy Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.\', \'Immunotherapy Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea; Department of Biochemistry, School of Life Sciences, Chungbuk National University, Cheongju, Republic of Korea.\', \'Immunotherapy Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea; Department of Functional Genomics, University of Science and Technology, Daejeon, Republic of Korea.\', \'MRC Human Immunology Unit, Medical Research Council (MRC) Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine (WIMM), John Radcliffe Hospital, University of Oxford, Oxford, UK. Electronic address: hashem.koohy@rdm.ox.ac.uk.\', \'Immunotherapy Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea; Department of Functional Genomics, University of Science and Technology, Daejeon, Republic of Korea. Electronic address: haiyoung@kribb.re.kr.\', \'Immunotherapy Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea; Department of Functional Genomics, University of Science and Technology, Daejeon, Republic of Korea. Electronic address: ipchoi@kribb.re.kr.\']
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  • -1
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?:doi
  • S0008-8749(21)00173-810.1016/j.cellimm.2021.104454
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  • Cellular immunology
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  • 34773897
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  • 1.355
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is ?:relation_isRelatedTo_publication of
?:title
  • SARS-CoV-2 peptides bind to NKG2D and increase NK cell activity.
?:type
?:year
  • 2022

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