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1 er than the conventional dose used without a hematopoietic growth factor.
2 and IL-3, which is a novel property of this hematopoietic growth factor.
3 oteins is involved in signal transduction of hematopoietic growth factors.
4 ss regulated by a family of lineage specific hematopoietic growth factors.
5 pears to be under the control of an array of hematopoietic growth factors.
6 to expand in liquid cultures in response to hematopoietic growth factors.
7 s myelotoxicity is prevented with the use of hematopoietic growth factors.
8 ere cultured 4 days in serum-free media with hematopoietic growth factors.
9 e, with no patient requiring transfusions or hematopoietic growth factors.
10 kinase, which is activated in blood cells by hematopoietic growth factors.
11 cells (HSC) can be significantly expanded by hematopoietic growth factors.
12 in methylcellulose medium supplemented with hematopoietic growth factors.
13 current evidence on the role of recombinant hematopoietic growth factors.
14 ns only), mycophenolate mofetil, and porcine hematopoietic growth factors.
15 esis was not due to redundancy between these hematopoietic growth factors.
16 whether survivin expression was regulated by hematopoietic growth factors.
17 kinase is stimulated by various stresses and hematopoietic growth factors.
18 human bone marrow cells to exogenously added hematopoietic growth factors.
19 ), the growth of Mo7e cells was dependent on hematopoietic growth factors.
20 gnal transduction events elicited by several hematopoietic growth factors.
21 es, in the presence of suitable cocktails of hematopoietic growth factors.
22 blood stem cells through synergy with other hematopoietic growth factors, 5) expanding progenitor ce
24 HIP(-/-) mice are hyperresponsive to certain hematopoietic growth factors, a phenotype very similar t
27 ll factor (SCF), a potent comitogen for many hematopoietic growth factors, also synergized with GM-CS
29 oral and geographic variations in the use of hematopoietic growth factors among patients receiving ch
30 The contribution of interleukin-3 (IL-3), a hematopoietic growth factor and immunoregulatory cytokin
31 nt of apheresis technology, the discovery of hematopoietic growth factors and small molecule CXCR4 an
32 the molecular cloning and expression of many hematopoietic growth factors and their receptors, as wel
33 ylcellulose cultures in the absence of added hematopoietic growth factors and, at higher frequency, i
34 cyclosporine, mycophenolate mofetil, porcine hematopoietic growth factors, and anti-alphaGal antibody
35 luding: intravenous immunoglobulins, myeloid hematopoietic growth factors, and granulocyte transfusio
36 , pharmacological immunosuppression, porcine hematopoietic growth factors, and immunoadsorption of an
37 gene products of the Wnt family function as hematopoietic growth factors, and that they may exhibit
39 s) mobilized with high-dose chemotherapy and hematopoietic growth factors are now widely used to supp
43 t attempts to ex vivo expand HSPCs have used hematopoietic growth factors but have not achieved clini
44 and differentiation in the absence of added hematopoietic growth factors but that stimulation with c
46 lood by a wide variety of stimuli, including hematopoietic growth factors, chemotherapy, and chemokin
47 otics, prokinetics, bile acids, statins, and hematopoietic growth factors could also contribute to am
48 It was also demonstrated that these various hematopoietic growth factors, cytokines, and chemokines
49 in response to a number of stimuli including hematopoietic growth factors, cytotoxic agents, and cert
50 403) into normal mouse bone marrow generates hematopoietic growth factor-dependent cell lines frozen
51 retinoic acid receptor was used to establish hematopoietic growth factor-dependent, lympho-myeloid pr
56 advanced cancer patients with Flt3 ligand, a hematopoietic growth factor, expanded DCs 20-fold in viv
57 O) is a recently characterized member of the hematopoietic growth factor family that serves as the pr
58 matopoietic progenitors, serum levels of the hematopoietic growth factor Flt3 ligand were dramaticall
59 ents that might influence infection outcome (hematopoietic growth factors, fluconazole, graft-versus-
60 atic allografts from donors treated with the hematopoietic growth factor fms-like tyrosine kinase 3 l
61 row cells expressing p230 required exogenous hematopoietic growth factors for optimal growth, whereas
62 nonanemic low/intermediate-1 IPSS (n = 123), hematopoietic growth factors for patients with anemic lo
66 ntly been completed evaluating the effect of hematopoietic growth factors (granulocyte-macrophage col
67 human myeloid differentiation induced by the hematopoietic growth factor, granulocyte-macrophage colo
68 egulation of this protein in response to the hematopoietic growth factors, granulocyte-macrophage col
77 (PHSCs) requires ex vivo culture in multiple hematopoietic growth factors (HGFs) to promote cell divi
79 ectin domain family member 11A [CLEC11A]), a hematopoietic growth factor important for development of
80 onate, which is regulated by an early acting hematopoietic growth factor important for the growth and
81 icle reviews the clinical use of old and new hematopoietic growth factors in acquired and inherited b
82 on the patterns and correlates of the use of hematopoietic growth factors in community-dwelling elder
84 trated by the heightened growth responses to hematopoietic growth factors in hematopoietic cells of m
89 ry patterns of proliferation in a mixture of hematopoietic growth factors in the presence of differen
90 cellulose cultures and treated with selected hematopoietic growth factors in the presence or absence
91 actice guidelines, and practice patterns for hematopoietic growth factors in the supportive care of c
92 (P = 0.57); however, more patients received hematopoietic growth factors in the valganciclovir group
93 C do not proliferate in response to multiple hematopoietic growth factors in vitro and do not radiopr
94 ind and directly regulate the bioactivity of hematopoietic growth factors including interleukin-7 (IL
95 here was an increase in the mRNA for several hematopoietic growth factors including macrophage colony
96 ere is now good evidence that treatment with hematopoietic growth factors, including granulocyte colo
97 ling induced by engineered Notch ligands and hematopoietic growth factors influences hematopoietic st
98 rum-free cultures containing fibronectin and hematopoietic growth factors inhibited myeloid different
100 ntibody (mAb), cobra venom factor (CVF), pig hematopoietic growth factors (interleukin-3 (pIL3) and s
101 ontaining medium in the presence of multiple hematopoietic growth factors (interleukin-6, stem cell f
102 ion of DNA plasmids encoding cytokine and/or hematopoietic growth factors, interleukin-2 (IL-2), IL-1
103 t production of certain stromal cell-derived hematopoietic growth factors is deficient as a consequen
108 ting a potential non-hematopoietic effect of hematopoietic growth factors on iron absorption by the g
109 h high-risk aggressive lymphoma by utilizing hematopoietic growth factors or autologous peripheral bl
111 nditions and multipotent cells, mobilized by hematopoietic growth factors or emerging during parasiti
112 ormed cells exhibited complete dependency on hematopoietic growth factors, particularly GM-CSF and IL
113 bstantial geographic variation in the use of hematopoietic growth factors, ranging from 10.6% in Seat
114 in 1 transgene by expressing the nonlymphoid hematopoietic growth factor receptor c-MPL (myeloprolife
117 important factors for regulating a critical hematopoietic growth factor receptor, the M-CSF receptor
118 ively activating point mutations reported in hematopoietic growth factor receptors in patients with a
119 timulating factor receptor and several other hematopoietic growth factor receptors induce the tyrosin
121 after ex vivo culture in the presence of the hematopoietic growth factors recombinant murine stem cel
127 cells isolated in vitro responded poorly to hematopoietic growth factors, resulting in an up to 11-f
128 In this report, involvement of Bcl-3 in hematopoietic growth factor-stimulated erythroid prolife
129 cyte-macrophage colony-stimulating factor, a hematopoietic growth factor, stimulates cells of the int
131 es the possibility that excess expression of hematopoietic growth factors such as IL-3 and GM-CSF may
132 nous IFN-gamma affects the responsiveness to hematopoietic growth factors such as SCF in vitro, our r
133 ogeneic feeder cell layer, or IL-2 and other hematopoietic growth factors such as the c-kit ligand (K
134 compounds affected SCF synergism with other hematopoietic growth factors, such as interleukin-3 or g
135 gressive postremission therapy or the use of hematopoietic growth factor support does not appear to i
141 Colony-stimulating factor-1 (CSF-1) is a hematopoietic growth factor that is released by osteobla
142 phage colony-stimulating factor (M-CSF) is a hematopoietic growth factor that is responsible for the
143 ocyte colony-stimulating factor (G-CSF) is a hematopoietic growth factor that is widely used to treat
148 Mpl ligands are a family of closely related hematopoietic growth factors that bind to the thrombopoi
149 actors including VEGF, bFGF, IL-8, PDGF, and hematopoietic growth factors that promote endothelial ce
150 ctor (SLF) acts synergistically with various hematopoietic growth factors that use the Jak-Stat pathw
152 rapy for depression and the selective use of hematopoietic growth factors to ameliorate hematologic a
153 stem cells and retrovirus transduction using hematopoietic growth factors to introduce a reporter gen
160 ogenitor cell mobilization is the ability of hematopoietic growth factors with distinct cellular targ
161 ulocyte colony-stimulating factor (G-CSF), a hematopoietic growth factor, with or without dexamethaso
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