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5 ts from transfection experiments using human myelocytic cell line (U937) demonstrated a direct relati
7 s not inhibit phagocytosis by macrophage and myelocytic cell lines in vitro and is attenuated in an e
9 locytic leukemia (APL) was noted among acute myelocytic leukemia (AML) cases at the Los Angeles Count
11 ients who were recently diagnosed with acute myelocytic leukemia (AML) were assigned randomly to stan
12 ) have been evaluated in patients with acute myelocytic leukemia (AML), both as potential priming age
15 ped progressive blast crisis (BC) of chronic myelocytic leukemia (CML) while receiving therapy with i
17 mportant roles in the progression of chronic myelocytic leukemia (CML), we performed allelotype analy
18 ions (DLI) in patients with relapsed chronic myelocytic leukemia after allogeneic bone marrow transpl
19 elocytic leukemia and in some cases of acute myelocytic leukemia and acute lymphocytic leukemia, the
20 blood cells derived from patients with acute myelocytic leukemia and chronic myelocytic leukemia, whi
21 er survival in groups of patients with acute myelocytic leukemia and epithelial ovarian cancer who ha
22 n successfully administered to patients with myelocytic leukemia and has produced therapeutic effects
27 toire in four patients with relapsed chronic myelocytic leukemia who achieved a complete remission af
28 a RA-dependent manner in the NB-4, acute pro-myelocytic leukemia, and the MCF-7, breast carcinoma, ce
29 s with acute myelocytic leukemia and chronic myelocytic leukemia, which express BCR-Abl, demonstrate
34 clin A1 overexpression was observed in acute myelocytic leukemias, especially those that were at the
37 E- and P-selectin ligands in leukocytes and myelocytic or monocytic leukemia cells are carried by tr
38 tients lacking gp91(phox) (X-CGD), the human myelocytic PLB-985 cell line, PLB-985 cells in which gp9
39 ansition from the promyelocytic stage to the myelocytic stage of neutrophil development, being indisp
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