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1 modes of migration that are associated with terminal maturation.
2 ncluding GATA-1 to block differentiation and terminal maturation.
3 be down-regulated to allow cells to undergo terminal maturation.
4 cell cycle in chondrocytes and to defects in terminal maturation.
5 onsistent with a role of T-bet in regulating terminal maturation.
6 tients with STAT1 GOF mutations had impaired terminal maturation.
7 ine megakaryocytes, which also have impaired terminal maturation.
8 ATA-1 proliferation arrest and Epo-dependent terminal maturation.
9 iently than C/EBPalpha-ER and did not direct terminal maturation.
10 CML), Bcr-Abl(+) myeloblasts fail to undergo terminal maturation.
11 ferentiation as the cells eventually undergo terminal maturation.
12 ortant role in megakaryocyte endomitosis and terminal maturation.
13 to maintain erythroid cell viability during terminal maturation.
14 d in differentiating oligodendrocytes before terminal maturation.
15 id cells undergoing erythropoietin-dependent terminal maturation, although transcripts derived from t
17 revealed that although AAMphi had undergone terminal maturation and differentiation, they entered a
18 at GATA3 is a critical regulator for NK cell terminal maturation and egress out of the BM and that im
21 organs, Ag-driven B cell activation induces terminal maturation and Ig isotype class switch (class s
22 esults identify T-bet as a key factor in the terminal maturation and peripheral homeostasis of NK and
24 c cytokines because it is necessary both for terminal maturation and regulation of lineage-specific m
26 enic lineage probably influences chondrocyte terminal maturation and turnover of the cartilage matrix
27 o the erythroid lineage, vary further during terminal maturation, and are strongly associated with ch
28 ecreased efficiency, caused a delay in their terminal maturation, and did not invoke V(alpha)14iNKT c
29 a key role in CD4(+) T-cell priming, B-cell terminal maturation, and immunoglobulin (Ig) class-switc
31 that share many morphologic features during terminal maturation but have marked differences in cell
32 proplatelet formation and other features of terminal maturation, but continued to proliferate aberra
33 NKT) cells in the periphery due to a halt in terminal maturation, but despite this deficiency, T-bet(
36 hermore, mice lacking T-bet exhibited both a terminal maturation defect of iNKT cells and a predomina
37 n recovery and similar to beta(Delta/Delta), terminal maturation defects in both bone marrow and sple
38 perturb either axonal arborization or nerve terminal maturation, depending on the stage of deletion.
39 es Itk and Rlk provide important signals for terminal maturation, efficient cytokine production, and
40 ocytes arise from a common progenitor, their terminal maturation follows very different paths; erythr
41 ast cell line that undergoes GATA1-dependent terminal maturation, identifying 2616 GATA1-responsive g
44 demonstrate that 1) human DCs do not undergo terminal 'maturation' in response to TNF-alpha, 2) DC ph
45 r completely each of the changes that typify terminal maturation, including (a) secretion of relative
52 caspase-3-uncleavable GATA-1 mutant restores terminal maturation of beta-TM erythroblasts, which may
54 hage interactions play a central role in the terminal maturation of erythroblasts, including enucleat
55 tween erythroblasts and macrophages promotes terminal maturation of erythroid cells by suppressing ap
57 both normal regulation of proliferation and terminal maturation of megakaryocytes, and further, that
58 ar to those found in progenitor cells delays terminal maturation of MEL and G1ER cells, two cell mode
60 data suggest that Sall3 is required for the terminal maturation of neurons destined for the glomerul
64 regulated cyclin E activity causes defective terminal maturation of nucleated erythroblasts in vivo H
66 role in globin switching; and (3) during the terminal maturation of red cells, where it helps control
69 ulted in the successful Ly49 acquisition and terminal maturation of the NK cells; however, it could o
70 rrier is established through the coordinated terminal maturation of the retinal pigment epithelium (R
72 sentation, have been termed T cell-mediated "terminal maturation" of DC, Here we report that XS52 cel
73 hly expressed in the Mo lineage up to 80% at terminal maturation, present on 20% to 30% of maturing M
75 stration of polycistronic RNA processing, 3'-terminal maturation, RNA editing, turnover, and translat
77 shion, with the CD56(bright) stage preceding terminal maturation to the CD56(dim) stage, considered t
78 w that Nurr1 and Pitx3 cooperatively promote terminal maturation to the midbrain DA neuron phenotype
80 CD56bright NK cells, and this impairment in terminal maturation was also observed in Irf8-/-, but no
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