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1 surround a single HSPC attached to a single mesenchymal stromal cell.
2 by Mcl-1 or by interactions with bone marrow mesenchymal stromal cells.
3 h the recipient's respiratory epithelium and mesenchymal stromal cells.
4 y in promoting osteogenic differentiation of mesenchymal stromal cells.
5 duces collagen deposition in the bone marrow mesenchymal stromal cells.
6 ose-derived stromal cells and marrow-derived mesenchymal stromal cells.
7 d defects in skull, articular cartilage, and mesenchymal stromal cells.
8 expressed in cells and tissues arising from mesenchymal stromal cells.
9 ng cord blood that was expanded ex vivo with mesenchymal stromal cells.
10 panded ex vivo in cocultures with allogeneic mesenchymal stromal cells.
11 l progenitor colony cells were surrounded by mesenchymal stromal cells.
12 through donor-derived mononuclear cells and mesenchymal stromal cells.
13 es, and an immunophenotype characteristic of mesenchymal stromal cells.
14 further improve the therapeutic potential of mesenchymal stromal cells.
15 sing the patient's own immune or bone marrow mesenchymal stromal cells.
16 A, which expressed surface markers common to mesenchymal stromal cells.
17 Endomyocardial injections of iron-labeled mesenchymal stromal cells admixed with tissue dye were p
18 sibility of using autologous adipose-derived mesenchymal stromal cells (AdMSCs) for the treatment of
20 agen VII expressed by intradermally injected mesenchymal stromal cells also exhibited a similar half-
22 erse relationship between a subpopulation of mesenchymal stromal cells and cancer cells in the bone m
23 ation inhibits the regenerative potential of mesenchymal stromal cells and derived extracellular vesi
25 after injury were restored by treatment with mesenchymal stromal cells and derived vesicles but not w
26 gineered by inducing chondrogenesis of human mesenchymal stromal cells and devitalized by the impleme
27 The niche is perivascular, created partly by mesenchymal stromal cells and endothelial cells and ofte
28 ramedullary bone and bone marrow using human mesenchymal stromal cells and endothelial colony-forming
29 rm repopulating of hematopoietic stem cells, mesenchymal stromal cells and endothelial progenitors.
30 ions reverted after treatment with wild-type mesenchymal stromal cells and extracellular vesicles but
33 The CD40/CD40L-assisted crosstalk between mesenchymal stromal cells and mast cells populating the
34 ne marrow myofibroblasts derive from Gli1(+) mesenchymal stromal cells and that a Gli inhibitor targe
35 t nonmalignant peripheral blood lymphocytes, mesenchymal stromal cells, and CD34-positive hematopoiet
36 signalling, adhesion to primary bone-marrow mesenchymal stromal cells, and proliferation of primary
37 plantation of cord-blood cells expanded with mesenchymal stromal cells appeared to be safe and effect
39 nvestigate the paracrine mechanisms by which mesenchymal stromal cells are protective in hypoxic pulm
40 re the safety, tolerability, and efficacy of mesenchymal stromal cell-based therapy in pilot clinical
41 In vitro studies have shown that bone marrow mesenchymal stromal cells (BM-MSC) protect AML blasts fr
44 ve this challenge, human bone marrow-derived mesenchymal stromal cells (BM-MSCs) were used to efficie
47 stem cells (iHepSCs) and bone marrow derived mesenchymal stromal cells (BMSCs) were used to CBTs for
49 -inducible factor 1alpha was knocked down in mesenchymal stromal cells by lentiviral transfer of shor
50 ave shown convincingly in rodent models that mesenchymal stromal cells can prolong solid organ graft
51 te+/-SE, 0.01+/-0.002; P<0.001), multipotent mesenchymal stromal cell colony maximum (estimate+/-SE,
52 mate+/-SE, 0.01+/-0.002; P=0.002) in BM, and mesenchymal stromal cell colony maximum in PB (estimate+
55 n in BM stromal elements, including CD146(+) mesenchymal stromal cells, correlates with the degree of
60 lving lipid mediators contribute to improved mesenchymal stromal cell efficacy when exposed to carbon
61 in situ differentiation of human BM-derived mesenchymal stromal cells, enables the robust engraftmen
62 in vivo selection of cytokines that improve mesenchymal stromal cell engraftment into the heart both
63 he batch transduction of bone marrow-derived mesenchymal stromal cells ex vivo, followed by intramyoc
65 separation efficacy of >98% in pre-purified mesenchymal stromal cells, extracted from human dental p
68 ng lipid mediators, and their importance for mesenchymal stromal cells function using gene silencing.
69 modulatory efficacy of regulatory T cells or mesenchymal stromal cells has been demonstrated in vitro
77 acts directly on Leptin-Receptor-expressing mesenchymal stromal cells in adult bone marrow to influe
78 s significantly augmented in macrophages and mesenchymal stromal cells in inflamed human pulp tissues
79 and osteogenic activity, a critical role for mesenchymal stromal cells in osteogenesis, and temporal
80 g regulates adipogenesis and osteogenesis by mesenchymal stromal cells in the bone marrow in response
81 ation toward CXCL12 and reducing adhesion to mesenchymal stromal cells in vitro We also found that HI
82 of mesenchymal stem cells (MSCs, also called mesenchymal stromal cells) in endogenous repair and cell
83 ing Dab2-deficient embryonic fibroblasts and mesenchymal stromal cells indicated that Dab2 promoted a
85 planting ceramic scaffolds coated with human mesenchymal stromal cells into immune-deficient mice, we
86 brain injured mice receiving human amniotic mesenchymal stromal cells intravenously or intracerebrov
91 about the potentially unfavorable effects of mesenchymal stromal cell (MSC) activation on the heart.
93 stretch have been investigated for inducing mesenchymal stromal cell (MSC) differentiation towards t
95 But the mechanisms underlying OA-mediated mesenchymal stromal cell (MSC) osteogenic differentiatio
96 to isolate a quiescent and undifferentiated mesenchymal stromal cell (MSC) population from the bone
101 ll apoptosis, and could overcome bone marrow mesenchymal stromal cell (MSC)-induced chemoresistance.
102 ion (DR) in both ex vivo bone marrow-derived mesenchymal stromal cells (MSC) and in vitro 3T3-L1 prea
106 contributions to primary myelofibrosis from mesenchymal stromal cells (MSC) have been suggested by m
107 premetastatic niche by examining the role of mesenchymal stromal cells (MSC) in cancer cell homing.
108 ure of leukemia cells to bone marrow-derived mesenchymal stromal cells (MSC) promotes accumulation of
109 posure of cultured mouse bone marrow-derived mesenchymal stromal cells (MSC) to hypoxia or an adenovi
111 (CAF) have been suggested to originate from mesenchymal stromal cells (MSC), but their relationship
112 ytic leukemic (CLL) cells and marrow-derived mesenchymal stromal cells (MSCs) activates both cell typ
117 vironments that modulate fate commitments of mesenchymal stromal cells (MSCs) are composed of chemica
128 ing in two murine models of BMF that Gli1(+) mesenchymal stromal cells (MSCs) are recruited from the
131 ed with long-term passaged (P10) aging human mesenchymal stromal cells (MSCs) could be used for bone
132 y demonstrated that coculture of islets with mesenchymal stromal cells (MSCs) enhanced islet insulin
133 ) cells in the presence of bone marrow-human mesenchymal stromal cells (MSCs) enhanced the production
134 in preparation for a first-in-human trial of mesenchymal stromal cells (MSCs) for septic shock, we ap
135 n a rapid expansion in clinical trials using mesenchymal stromal cells (MSCs) from a variety of tissu
136 d the adipogenic potential of marrow-derived mesenchymal stromal cells (MSCs) from mice with decrease
137 the BM extracellular fluid were elevated and mesenchymal stromal cells (MSCs) had a reduced capacity
139 f the identity and physiological function of mesenchymal stromal cells (MSCs) have been hampered by a
144 and safety of osteoarthritis treatment with mesenchymal stromal cells (MSCs) in humans and to obtain
145 strate expression exclusively in multipotent mesenchymal stromal cells (MSCs) in the bone marrow of t
146 eviously identified a resident population of mesenchymal stromal cells (MSCs) in the terminal airways
149 steering the chondrogenic differentiation of mesenchymal stromal cells (MSCs) into either permanent c
150 val, growth, and myogenic differentiation of mesenchymal stromal cells (MSCs) isolated from adipose o
151 one marrow (BMT) as well as ex vivo-expanded mesenchymal stromal cells (MSCs) leads to striking clini
152 the hypothesis that the favorable effects of mesenchymal stromal cells (MSCs) on infarct repair are m
153 ated when the CLL cells were cocultured with mesenchymal stromal cells (MSCs) or hyaluronic acid or w
161 local administration of bone marrow-derived mesenchymal stromal cells (MSCs) to these patients from
162 eutically relevant quantities of multipotent mesenchymal stromal cells (MSCs) via in vitro culture is
163 luid (SF) in the knee serve as reservoirs of mesenchymal stromal cells (MSCs) with potential therapeu
164 CSF) secreted from human bone marrow-derived mesenchymal stromal cells (MSCs), all of which also cont
165 one marrow (BM) affects local cells, such as mesenchymal stromal cells (MSCs), leading to osteolysis
166 emia (CLL) cells interact in the marrow with mesenchymal stromal cells (MSCs), which can enhance CLL-
174 deprivation and treated with human amniotic mesenchymal stromal cells or conditioned medium showed c
175 lled cortical impact received human amniotic mesenchymal stromal cells or phosphate-buffered saline i
176 deprivation were treated with human amniotic mesenchymal stromal cells or with their secretome (condi
177 ndent phenotypic changes of nonhematopoietic/mesenchymal stromal cells play a key role in TD humoral
180 originate from BM, or of healthy BM-derived mesenchymal stromal cells, protected hemophilia A mice f
183 arrow (BM) fibrosis thought to be induced by mesenchymal stromal cells stimulated by overproduced gro
184 rved between the amount of FSTL1 produced by mesenchymal stromal cells, stromal ST2 cells, and monocy
185 eview the available data on culture-expanded mesenchymal stromal cells tested in renal transplantatio
187 ous assessment of the safety and efficacy of mesenchymal stromal cell therapies to allow the translat
188 have produced promising results for HSCT and mesenchymal stromal cell therapy as alternatives to syst
190 poietic stem cell transplantation (HSCT) and mesenchymal stromal cell therapy have been proposed for
192 skin, and suggest an approach for improving mesenchymal stromal cell therapy in scleroderma and othe
193 preconditioning with carbon monoxide allowed mesenchymal stromal cells to be administered later after
195 dicating that the exposure of human amniotic mesenchymal stromal cells to the injured tissue is not n
201 y contrast, donor BM-derived mononuclear and mesenchymal stromal cells were more abundant and express
202 roinflammatory cytokines in BM-derived human mesenchymal stromal cells, which are part of the hematop
203 We hypothesized that preconditioning of mesenchymal stromal cells with carbon monoxide ex vivo w
205 , and activation of EphA3(+)/CD90(+)/Sca1(+) mesenchymal/stromal cells with an EphA3 agonist leads to
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