We observed that slow-growing tumors induced by a low dose of MCA (5 μg) expressed high levels of cell surface NKG2D ligand and showed a trend to develop earlier in NKG2D-sufficient than NKG2D-deficient mice ( 35 ).
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We observed that slow-growing tumors induced by a low dose of MCA (5 μg) expressed high levels of cell surface NKG2D ligand and showed a trend to develop earlier in NKG2D-sufficient than NKG2D-deficient mice ( 35 ).