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1 are completely enveloped by other cells in a reaggregate.
2 nic ectoderm that has been disaggregated and reaggregated.
3 TH9bcl-2 amplicon to transduce mesencephalic reaggregates.
4 onstruction and segregation of cell-specific reaggregates.
5 response of retinal neurites by hypothalamic reaggregates.
6 e seen to be distorted and excluded from the reaggregates.
7 er, leading to failed tooth formation in the reaggregates.
8                   Dispersed AChRs could also reaggregate at the junction once neurotransmission was r
9 binant limb buds composed of dissociated and reaggregated cells derived from anterior (A) and posteri
10 ion (GJ) assembly system with experimentally reaggregated cells, we analyzed "formation plaques" (FPs
11                                           In reaggregate culture experiments, thymic mesenchyme was r
12 gic neuron was examined in three-dimensional reaggregate culture in which these neurons undergo norma
13                To test this model, we used a reaggregate culture system in which a labeled population
14                           We have utilized a reaggregate culture system to test this model.
15 creening several proteins through an ex vivo reaggregate culture system, we identify BMPER as a novel
16 o a late environment were conducted, using a reaggregate culture system.
17 o MHC-expressing thymic stroma in short-term reaggregate culture.
18 tudies on thymocyte differentiation by using reaggregate cultures (RC) of double positive T cell rece
19 ized the effects of glutathione depletion on reaggregate cultures derived from ventral mesencephalic
20  cell line transfected with I-Ek was used in reaggregate cultures to study the role of peptides in po
21 ere isolated and evaluated for maturation in reaggregate cultures with wild-type or MHC molecule-defi
22 nal ability to mediate positive selection in reaggregate cultures, do not express mRNA for the key st
23 cytes by cortical thymic epithelial cells in reaggregate cultures, rather than causing deletion of th
24  dissociated into a cell suspension and then reaggregated (drMM) in the presence of human recombinant
25 al organization and thymocyte development in reaggregate fetal thymic organ cultures.
26 must divide, aggregate, detach, migrate, and reaggregate in relation to each other, but factors that
27 ans individual endothelial cells migrate and reaggregate in the coelomic domain to form the major tes
28 d purified thymic epithelial cells (TEC) are reaggregated in tissue culture.
29 f CD4+ T cells required TCR signaling in the reaggregates, indicating that transient recognition of s
30               Application of FGF3 to incisor reaggregates inhibits beta-catenin signaling activity an
31 neonatal retinal neurons have the ability to reaggregate into histotypic structures when grown in sus
32 vivo gene transfer of bcl-2 to mesencephalic reaggregates is ineffective in increasing grafted DA neu
33 t matured into agonist-responsive T cells in reaggregates lacking the same ligand.
34          Employing a culture architecture of reaggregated neurons fosters extension of dense beds of
35                In the present study, we used reaggregates of dissociated cells from freshly excised h
36     In vitro, retinal axons are inhibited by reaggregates of isolated hypothalamic, but not dorsal di
37 liferation of CD4+ and CD8+ cells is seen in reaggregates of purified MHC class II+ thymic epithelial
38 ration of granule cells from cerebellar cell reaggregates on a laminin substrate.
39 sociated with trypsin plus Ca2+ were able to reaggregate only in the presence of Ca2+.
40 itiation of positive selection, we have used reaggregate organ cultures to follow the maturation of p
41                               These chimeric reaggregated ovaries, grafted beneath the renal capsule
42 lar development appeared generally normal in reaggregated ovaries.
43 c to the oocyte was addressed using chimeric reaggregated ovaries.
44 ring thymic selection, we have established a reaggregate system in which molecular recruitment of GFP
45                            Experiments using reaggregate thymic organ cultures revealed the presence
46                                        Using reaggregated thymic organ culture and bone marrow chimer
47                   They were then examined in reaggregated thymic organ cultures containing mixtures o
48 thymocytes and selecting epithelial cells in reaggregate thymus cultures.

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