ライフサイエンスコーパス: blastocoel

1 in the vectorial transport of water into the blastocoel.

2 th secreted glypicans and coreceptors in the blastocoel.

3 and the ingression of surface cells into the blastocoel.

4 t 2 h after PMCs began to migrate within the blastocoel.

5 ized cells covering the inner surface of the blastocoels.

6 rospective primary mesenchyme cells into the blastocoel, after which they migrate and then fuse to fo

7 stocoelar cells) are also present within the blastocoel and are migrating and fusing with one another

8 foxN2/3 morphant PMCs do not organize in the blastocoel and fail to join the PMC syncytium.

9 n C. elegans embryos involves formation of a blastocoel and the ingression of surface cells into the

10 ement of primary mesenchyme cells within the blastocoel and the shapes of the skeletal rods.

11 l cycle (32-cell stage) and ingress into the blastocoel at the 6th cycle (62-cell stage).

12 uce trophoblast stem cells, trophectoderm or blastocoel cavities, and therefore do not implant into t

13 It faces the blastocoel cavity and later gives rise to the extraembry

14 zation using endocytosis of ligands from the blastocoel cavity as a positioning cue.

15 pective head mesoderm cells to appear in the blastocoel cavity at the onset of gastrulation, stage 10

16 While a blastocoel cavity formed and epithelial cell polarity wa

17 rbed when this antibody is injected into the blastocoel cavity indicating that IMZ cell interaction w

18 e of 3.9 +/- 3.6 Pa, relative to the central blastocoel cavity of the embryo, was found to be consist

19 ssively restricted to the PE adjacent to the blastocoel cavity together with the transcription factor

20 t of epithelial polarity and appearance of a blastocoel cavity.

21 t of epithelial polarity and appearance of a blastocoel cavity.

22 marginal zone cells of the blastula into the blastocoel cavity.

23 cycle arrest in G2 phase, and eventually to blastocoel collapse, impaired NLS-mediated protein uptak

24 including the formation of an intercellular blastocoel, culminate in a morphological left-right asym

25 embryo volume and cell volume decrease, the blastocoel disappears, and 34.4% of the cell mass become

26 ary mesenchyme cells (PMCs) ingress into the blastocoel during an epithelial-to-mesenchymal transitio

27 vitation, as well as stimulating the rate of blastocoel expansion and increasing the number of trophe

28 P produced is used by the sodium pump during blastocoel expansion in the human and bovine blastocyst,

29 In Xenopus, the blastocoel-facing, basolateral surfaces where signaling

30 Never is the blastocoel filled by a mass of mesenchyme.

31 rive in part from cells at the centre of the blastocoel floor that express XHex, the Xenopus cognate

32 features of TE differentiation required for blastocoel formation include intercellular junction biog

33 is required to prevent oxidative stress when blastocoel formation is accompanied by increased oxidati

34 gesting that the PAR-3 protein has a role in blastocoel formation.

35 M and is detected at the very first signs of blastocoel formation.

36 itor W-7 exhibited a dose-dependent delay in blastocoel formation.

37 enuated the ionophore-induced stimulation of blastocoel formation.

38 ed Ca2+ signalling and a subsequent delay in blastocoel formation.

39 e apical or basal surfaces of cells prior to blastocoel formation; we demonstrate that this localizat

40 The blastocoel forms at the first cleavage division since fu

41 hesive interactions results in a loss of the blastocoel in early embryos and ripping of the ectoderma

42 Formation of the blastocoel in early Xenopus embryos was studied with a n

43 of this information on the oral side of the blastocoel in turn depends on Spdri expression in the or

44 Here, we report that the cleavage-stage blastocoel is traversed by hundreds of extremely long ce

45 Injection of hydrolytic sulfatase into the blastocoels of gastrula stage embryos resulted in severe

46 in PrE cells positioned in contact with the blastocoel, raising the possibility that these cells are

47 w been found to occur by invagination into a blastocoel, revealing an unanticipated embryological aff

48 In the blastocoel roof (BCR) of the Xenopus laevis embryo, epib

49 l tension promotes FN fibril assembly in the blastocoel roof (BCR), while reduced BCR tension inhibit

50 ir6.1 is localized to basal membranes on the blastocoel roof and cell-cell junctions.

51 o establish that radial intercalation in the blastocoel roof requires integrin-dependent contact of d

52 bronectin fibrils in vivo is correlated with blastocoel roof thickening and a loss of deep cell polar

53 ercalation movements, which are required for blastocoel roof thinning and epiboly.

54 Ectodermal cells from the blastocoel roof use alpha5beta1 integrins to assemble a

55 Head mesoderm migrates along the blastocoel roof, while trunk mesoderm undergoes converge

56 FN-dependent cellular rearrangements in the blastocoel roof.

57 the fibronectin matrix and thickening of the blastocoel roof.

58 essential for, mesoderm cell adhesion to the blastocoel roof.

59 ls and the cells of the substrate layer, the blastocoel roof.

60 Apoptotic cells accumulated in the blastocoel, suggesting that before the midblastula trans

61 zone adjacent to the interior margin of the blastocoel that is populated by cells derived from both

62 hogenesis, including PMC distribution in the blastocoel, the size of the skeleton and its branching p

63 Cells that ingress into the blastocoel undergo an apical flattening associated with

64 archenteron as well as in other areas of the blastocoel wall.

65 es as a polarized epithelium adjacent to the blastocoel, with a basement membrane separating it from