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1 newly diagnosed patients with chronic-phase chronic myeloid leukaemia.
2 ase is elevated in several cancers including chronic myeloid leukaemia.
3 eatment for patients in the chronic phase of chronic myeloid leukaemia.
4 atinib in previously untreated patients with chronic myeloid leukaemia.
5 BCR-ABL1 fusion gene is a driver oncogene in chronic myeloid leukaemia and 30-50% of cases of adult a
6 was demonstrated in acute myeloid leukaemia, chronic myeloid leukaemia and acute lymphoid leukaemia,
7 hosphatase activity of PP2A is suppressed in chronic myeloid leukaemia and other malignancies charact
8 To revise the current goals of therapy of chronic myeloid leukaemia and to incorporate the influen
10 tment options, side-effects, and outcomes of chronic myeloid leukaemia, and discusses the possibility
12 incorporate the influence of the underlying chronic myeloid leukaemia biology on directing therapeut
14 adult patients with acute myeloid leukaemia, chronic myeloid leukaemia, chronic myelomonocytic leukae
18 y diagnosed Philadelphia chromosome-positive chronic myeloid leukaemia (CML) in chronic phase after a
19 ntly activated and functionally required for chronic myeloid leukaemia (CML) in humans and in mouse m
26 has provided a curative treatment option for chronic myeloid leukaemia (CML) over the past 20-30 year
27 he ABL tyrosine kinase inhibitor imatinib in chronic myeloid leukaemia (CML) serves as a model for mo
32 b treatment of newly diagnosed chronic-phase chronic myeloid leukaemia compared with imatinib could n
35 rosine-kinase inhibitors, most patients with chronic myeloid leukaemia could enjoy a near normal life
38 inase inhibitors (TKIs) for the treatment of chronic myeloid leukaemia has changed patient outcome an
39 rs improve overall survival in patients with chronic myeloid leukaemia in chronic phase (CML-CP).
40 are available for treatment of patients with chronic myeloid leukaemia in chronic phase (CML-CP).
41 older with Philadelphia chromosome-positive chronic myeloid leukaemia in chronic phase and Eastern C
42 pen-label, randomised trial in patients with chronic myeloid leukaemia in chronic phase with suboptim
44 e recruited patients (aged >/=18 years) with chronic myeloid leukaemia in first chronic phase who had
49 reatment in the treatment of newly diagnosed chronic myeloid leukaemia suggest that this first-genera
50 Ponatinib has shown potent activity against chronic myeloid leukaemia that is resistant to available
51 six with myelodysplastic syndrome, five with chronic myeloid leukaemia (two with chronic-phase and th
52 hibitor imatinib is used in the treatment of chronic myeloid leukaemia, where it targets the intracel
53 ) therapy is feasible for some patients with chronic myeloid leukaemia with deep molecular responses;
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