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1  showed similar integrative, migrational and differentiative abilities to those of transplanted wild-
2 stem cells have equivalent proliferative and differentiative abilities.
3 , C1QB, GBP6, DUSP3, and GAS6 exhibited high differentiative ability for ATB from ORDs, LTBI or HC wh
4 ggesting that SOCE is necessary for the anti-differentiative action of muscarinic receptor-dependent
5  interaction serves to retain cells in a pre-differentiative, actively proliferative state despite th
6 the DDR1 sequences) and markedly reduced the differentiative activity of the receptor.
7  and yolk sac cells are compromised in their differentiative and growth potential.
8  this differentiation process to compare the differentiative and invasive potential of cytotrophoblas
9 ntrol of proliferation is distinguished from differentiative and maturational responses to ecdysteroi
10 y of ligands of erbB receptors, induces both differentiative and mitogenic effects on cultured human
11  exhibits functional dichotomy with both pro-differentiative and pro-proliferative target genes.
12 gest that BMP-2 and FGF-4 possess respective differentiative and proliferative activities, the combin
13 ratinocyte Growth Factor (KGF or FGF7) has a differentiative and proliferative effect on the epitheli
14  vitro without the concomitant loss of their differentiative and proliferative potential in vivo have
15 topoietic progenitor cells compromised their differentiative and proliferative potential, and enhance
16 cally inactive SHP-2 mutant suppressed their differentiative and proliferative responses to IL-3, dem
17  (ii) retinoid X receptors mediate prominent differentiative and weak proliferative effects; (iii) th
18 ess molecules relating to anti-inflammatory, differentiative, and metabolic processes, e.g., the anti
19 ng in the Ras pathway to transmit mitogenic, differentiative, and oncogenic signals to the downstream
20 ate that GSK3 inhibition acts to prime a pro-differentiative/apoptotic transcription program in the n
21 etween self-renewing symmetric divisions and differentiative asymmetric divisions is necessary for no
22        Thus, the different morphogenetic and differentiative behavior of neural crest subsets in vivo
23 om adults have exceptional proliferative and differentiative capability in vitro yet respond minimall
24 peritoneal mesothelial cells have a range of differentiative capacities and are the direct progenitor
25 hese adult bone marrow cells have tremendous differentiative capacity as they can also differentiate
26       Here, we examine the developmental and differentiative capacity of cerebral organoids.
27 In contrast, the increased proliferation and differentiative capacity of p27(Kip1)-deficient T cells
28 ich is typified by reduced proliferative and differentiative capacity, is not well explored.
29 dividuals, eg, self-renewal and multilineage differentiative capacity, might be perturbed due to the
30  for the proper positional specification and differentiative cell fate of enteric neurons.
31 tem cells (MSC) display great proliferative, differentiative, chemotactic, and immune-modulatory prop
32 the regulatory syntax predictive of the full differentiative complexity of the immune system.
33 tigens that, if circumvented by survival and differentiative cues, yields B cells with the autoimmune
34 s to respond to survival, proliferative, and differentiative cues.
35 lopoiesis directly by replacing cytokine and differentiative cues.
36 to be strictly dependent on signaling by the differentiative cytokines, IL-12 and IL-4, recent data i
37 tion, implicating EKLF sumoylation status in differentiative decisions emanating from the MEP.
38 tric, proliferative division, to asymmetric, differentiative division.
39 in-of-function transgenics, Neurog2 promoted differentiative divisions and extended the period of Tbr
40 rogenitor cells (NSCs) from proliferative to differentiative divisions to generate neurons.
41 cells from symmetric (growth) to asymmetric (differentiative) divisions.
42 ated by retinoic acid receptors, whereas its differentiative effect at high dose may be mediated by r
43 n studies revealed a pro-proliferative, anti-differentiative effect of PKD on keratinocyte maturation
44 e 1,25-(OH)2D3 has antiproliferative and pro-differentiative effects in both melanocytes and cutaneou
45         Thus, the anti-proliferative and pro-differentiative effects of Blimp1 in effector or exhaust
46 chimeric transcription factors can block the differentiative effects of growth factors.
47 ntrol of its p35 subunit, which requires the differentiative effects of IFN-gamma for expression.
48 proliferation and the pro-proliferative/anti-differentiative effects of PKD co-expression on keratino
49 costatin M (OM) exerts growth-inhibitory and differentiative effects on breast cancer cells.
50 phin best characterized for its survival and differentiative effects on neurons expressing the trk B
51            We conclude that progestins exert differentiative effects on tumors characterized by trans
52 ven when leukemic cells are resistant to its differentiative effects.
53 hts into the regulation of proliferative and differentiative events during central nervous system dev
54 n of PR and Stat5-mediated proliferative and differentiative events in the mammary gland.
55 , CD19, is likewise essential for key B cell differentiative events including the formation of B-1, g
56 environments that are likely to induce these differentiative events.
57 hown to function both as a proliferative and differentiative factor for megakaryocytes and as a survi
58 s on the role of activin as a target-derived differentiative factor in neural development that has ad
59 te strong responses to ubiquitous growth and differentiative factors.
60 a homogenous population with regard to their differentiative fate as SNS neurons, these results indic
61 and memory CD4 T cell subsets and follow the differentiative fate of effector cells in vivo.
62  cell-bound ligands profoundly influence the differentiative fate of lymphocytes during an immune res
63  single cells and analysis of the subsequent differentiative fate of these cells as an immune respons
64 work towards redefining the identity and the differentiative fate of these primitive cells.
65 sis and inflicts different proliferative and differentiative fates in the two daughters.
66 ML pathogenesis by inhibiting the normal pro-differentiative function of ATRA, paving the way for new
67            Thus, the signals which mediate a differentiative function of the IL7R in B lymphopoiesis
68  were normal in number, in proliferative and differentiative function, and in migration and homing to
69  by these regions and that proliferative and differentiative functions can be induced by different re
70 nitors, stimulating mitogenic, survival, and differentiative growth response pathways.
71  progesterone can be either proliferative or differentiative in different target cells.
72 e doubt on the hypothesis of hierarchical or differentiative loss of tumorigenicity.
73 5, a proliferative marker, and involucrin, a differentiative marker, respectively.
74  to expect that special developmental and/or differentiative mechanisms operate in response to inflam
75 cells (RGCs) to switch from proliferative to differentiative neuron-generating divisions, but the mol
76       Here we identify the white matter as a differentiative niche for glioblastomas with oligodendro
77 pe, suggesting the existence of an Ag-driven differentiative pathway from B-2 to B-1.
78 (SHH), but the precise role of Nurr1 in this differentiative pathway has not been established.
79  suggesting that these subsets constituted a differentiative pathway with progressive telomere shorte
80 -2 and B-1, further evidence of a B-2 to B-1 differentiative pathway.
81              Thus, the growth inhibitory and differentiative pathways activated by TGF-beta and activ
82 activation process and to further define the differentiative pathways and functional characteristics
83   These results are key to understanding how differentiative pathways are controlled and cellular phe
84  shaft and sheath cells in the post-mitotic (differentiative) phase.
85  we performed a comprehensive analysis of DC differentiative potential among lymphoid and B lymphoid
86                  Rat PDL DPCs also exhibited differentiative potential characteristic of stem cells.
87 vity, proliferative capacity, karyotype, and differentiative potential in routine culture and under c
88 ntraindividual consistency, enabling similar differentiative potential of individuals using single ha
89                       This approach uses the differentiative potential of MSCs induced by the tumor m
90       Whether memory B cells possess altered differentiative potentials and respond in a qualitativel
91                     To better understand the differentiative processes occurring within murine GCs, w
92  supporting somatic cells guides many of the differentiative processes of gametogenesis.
93 cated in a wide variety of proliferative and differentiative processes.
94 y and anchorage-dependent growth by inducing differentiative programs and cell cycle progression, (ii
95 uired for the execution of developmental and differentiative programs in a variety of cell and tissue
96 can be induced to initiate morphogenetic and differentiative programs that include progenitor cell se
97 ective target for a HOX protein and link the differentiative properties of a transcription factor and
98 es most colon cancer cell lines to undergo a differentiative response and reverse their malignant phe
99 tially regulated two-stage mechanism for the differentiative response of PC12 cells to NGF.
100 gulated kinase, an event associated with the differentiative response of these cells.
101 ases that activate mitogenic, motogenic, and differentiative responses in different tissues.
102 -dependent signaling pathway participates in differentiative responses of cells in the developing CNS
103 echanisms that relay information to initiate differentiative responses of neural precursor cells are
104  required for IL-4-induced proliferative and differentiative responses, both signaling proteins are d
105 the Ras-MAP kinase pathway that mediates the differentiative responses, the signal transduction pathw
106 bringing about Ag-specific proliferative and differentiative responses.
107 rrent work supports a dual proliferative and differentiative role for the LF receptor, but only a dif
108 tiative role for the LF receptor, but only a differentiative role for the SF1a receptor.
109 us, our results indicate that AQP3 has a pro-differentiative role in epidermal keratinocytes and that
110 n factor will be present when needed for its differentiative role.
111 functions as a pro-proliferative and/or anti-differentiative signal in keratinocytes and hypothesized
112 " this primary alcohol to PLD2 to form a pro-differentiative signal, such that the action of AQP3 to
113  to catenin, regulation of beta-catenin as a differentiative signaling molecule, and promotion of mic
114  that initially integrates proliferative and differentiative signals and subsequently maintains stabi
115 of partial receptor complexes that transduce differentiative signals during thymic development.
116 t cytokine receptors can provide the trophic/differentiative signals for subsequent CD8(+) thymocyte
117 ng-bone growth in chrondrocytes, it produces differentiative signals similar to those of FGFR1, to wh
118  receptors provide both survival and trophic/differentiative signals with varying degrees of redundan
119 onal, inflammatory, mitogenic, apoptotic and differentiative signals.
120 mal proliferative signals and contributes to differentiative signals.
121 nds upon a wide variety of proliferative and differentiative signals.
122 lasmic domain in mediating proliferative and differentiative signals; and (4) the regulation of proli
123  involvement of coreceptors in signaling and differentiative stage of the responding cell.
124                              Knowing at what differentiative stage(s) developing B cells undergo rece
125 candidate for a gene that might regulate the differentiative state of VSMCs.
126 ssion of satellite cells into the myogenin+, differentiative state.
127                   Cornification is the final differentiative step for epidermal keratinocytes and inv
128              The precise mechanisms of these differentiative steps remain elusive.
129 scues GZ exit, suggesting a model for future differentiative therapies.
130 as well as in both the proliferative and the differentiative zones of the brain and neural tube.

 
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