ライフサイエンスコーパス: lentoid

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1 me course nor extent of dye transfer between lentoids.

2 rmation of the lens-like structures known as lentoids.

3 The lentoids, a unique morphologic structure that is an indi

4 Lentoid bodies expressed and accumulated lens-specific m

5 The formation of lentoid bodies was most efficient in the presence of FGF

6 re allowed to differentiate in vitro to form lentoid bodies.

7 -like cells and differentiated 3-dimensional lentoid bodies.

8 Prox-1 and beta-crystallin-positive ectopic lentoid bodies.

9 FGF2 and Wnt-3a, yielding approximately 1000 lentoid bodies/30-mm well.

10 differentiate into gamma-crystallin-positive lentoids by high-dosage bFGF treatment.

11 -TPA-sensitive isoform) were detected in the lentoid cell.

12 ation of PKC gamma to the plasma membrane of lentoid cells and significantly reduced the transfer of

13 me, present in lens fibers, was activated in lentoid cells by TPA, a known activator of PKC.

14 of differentiated, fiber-like cells (termed lentoid cells) express Cx49 and connexin46 (Cx46), but n

15 minimal amounts of PKC alpha were present in lentoid cells.

16 cifer Yellow dye between epithelial, but not lentoid, cells.

17 In contrast to the epithelial connexins, the lentoid connexins Cx49 and Cx46 were unaffected by even

18 (PKC) isoenzymes in the chicken lens and in lentoid-containing cultures and to study the effects of

19 d S118 were constitutively phosphorylated in lentoid-containing cultures, and that treatment with TPA

20 Analysis of lentoid cultures by immunofluorescence revealed that PKC

21 In spite of lentoid dye transfer being refractory to beta-TPA, signi

22 ays in culture, cell morphology changed, and lentoid formation was evident.

23 Lentoids, multicellular structures with characteristics

24 ired lentoids was monitored by observing the lentoid-to-lentoid transfer of fluorescent dyes, either

25 ds was monitored by observing the lentoid-to-lentoid transfer of fluorescent dyes, either calcein or

26 Dye transfer between lentoids was inhibited upon the addition to the medium o

27 p junction formation between cells of paired lentoids was monitored by observing the lentoid-to-lento

28 c chicken lens epithelial cells that develop lentoids were used for differentiation-related studies,

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