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NKG2D triggers cytotoxicity in mouse NK cells lacking DAP12 or Syk family kinases
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Selective associations with signaling proteins determine stimulatory versus costimulatory activity of NKG2D
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Tumour-derived soluble MIC ligands impair expression of NKG2D and T-cell activation
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Cutting edge: Murine UL16-binding protein-like transcript 1: A newly described transcript encoding a high-affinity ligand for marine NKG2D
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Ectopic expression of retinoic acid early inducible-1 gene (RAE-1) permits natural killer cell-mediated rejection of a MHC class I-bearing tumor in vivo
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
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IFNγ and lymphocytes prevent primary tumour development and shape tumour immunogenicity
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ULBPs, novel MHC class I-related molecules bind to CMV glycoprotein UL16 and stimulate NK cytotoxicity through the NKG2D receptor
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Perforin-mediated cytotoxicity is critical for surveillance of spontaneous lymphoma
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Retinoic acid early inducible genes define a ligand family for the activating NKG2D receptor in mice
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