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1 ck expression of NKG2D ligands recognized by CIK cells.
3 of patient-derived cytokine-induced killer (CIK) cells against autologous bone sarcoma and STS, incl
6 These cells, termed cytokine-induced killer (CIK) cells, are composed primarily of T cells, and the p
7 CSCs, supporting the clinical development of CIK cells as a novel class of immunotherapy for use in s
9 umors (5), whereas all 10 mice that received CIK cells at week 8 developed lymphomas; however, these
10 To test the in vivo activity of the expanded CIK cells, CML was engrafted into severe combined immuno
12 Further in vivo analyses established that CIK cells could infiltrate tumors and that tumor growth
14 lls expanded from 21 patients, we found that CIK cells efficiently killed allogeneic and autologous s
20 lls, demonstrating a slower division rate of CIK cells, higher susceptibility to apoptosis, persisten
22 enefits of adjuvant cytokine-induced killer (CIK) cell immunotherapy for hepatocellular carcinoma (HC
23 showed that adoptive transfer of allogeneic CIK cells in a murine model caused minimal graft-versus-
24 icking and survival of luciferase-expressing CIK cells in an allogeneic bone marrow transplant model.
25 entional T cells that induced GVHD; however, CIK cells infiltrated GVHD target tissues much less and
36 or cell population [cytokine-induced killer (CIK) cells] with an oncolytic viral therapy to achieve d
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