ライフサイエンスコーパス: reaggregation

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1 After reaggregation, 600 islet equivalents of the purified bet

2 sive function of C-cadherin in standard cell reaggregation and additional assays, C-cadherin levels w

3 of the starting material, is stable against reaggregation and can achieve solutions containing exclu

4 n-5 (alpha3beta1 integrin ligand), A431 cell reaggregation and motility functions were markedly impai

5 lly, in vitro cultures and cell dissociation-reaggregation assays suggest that Myo10 may be critical

6 We have used short-term reaggregation assays to compare the adhesive properties

7 adhesion, promotes cell-sorting behaviors in reaggregation assays, and inhibits medial-lateral cell i

8 l adhesion activity in cell dissociation and reaggregation assays.

9 After transgene silencing and reaggregation culture, the specified cells generate hema

10 Thymic reaggregation cultures demonstrated that CD4(+) T cells

11 C, suggest that positive selection in thymus reaggregation cultures is an exclusive property of corti

12 In reaggregation cultures with CD81-transfected fibroblasts

13 selection of T cells were examined in thymus reaggregation cultures, a system in which dispersed popu

14 f nanomaterials typically focus on retarding reaggregation, for example via surface modification, as

15 y affects neutrophil aggregation and permits reaggregation in the presence of a heterologous stimulus

16 th-forming capability after dissociation and reaggregation in vitro to investigate the mechanism that

17 We found that after dissociation and reaggregation, incisor, but not molar, mesenchyme exhibi

18 onic exfoliation method from graphite, where reaggregation is prevented by the addition of common cat

19 tion remained available to pyrene even after reaggregation occurred, suggesting an irreversible effec

20 ed as twin and larger sets by separation and reaggregation of blastomeres of cleavage-stage embryos.

21 spreading on laminin-5, and had no effect on reaggregation of cells plated on collagen I (alpha2beta1

22 s fiber formation, and temperature-dependent reaggregation of FmetHb S suggests that IHP stabilizes p

23 e direct observation of a rapid and specific reaggregation of retinal cell types into two discrete ty

24 nction as a strong stabilizing agent against reaggregation of single-layer nanosheets for greatly imp

25 ation-dispersion, and aggregation-dispersion-reaggregation of the NPs, are observed during the penetr

26 tes homophilic adhesion, as evidenced by the reaggregation of the transfected cells and the specific

27 Disaggregation and reaggregation of Xnr-2-producing tissues also extends th

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