ライフサイエンスコーパス: cell border

1 reserving microtubule trajectory to the cell-cell border.

2 precursor B cells clustered at the T cell-B cell border.

3 d by specific molecule(s) at the endothelial cell border.

4 gration of leukocytes across the endothelial cell border.

5 f connexin hemichannels directly to the cell-cell border.

6 the leukocyte with PECAM at the endothelial cell border.

7 diac gap junction protein, localized to cell-cell borders.

8 tly contact E-cadherin at dorso-ventral cell-cell borders.

9 in de novo endogenous Cx43 delivery to cell-cell borders.

10 InvEE tumours, where it accumulated at cell-cell borders.

11 in this process as it occurs at endothelial cell borders.

12 here key ciliary proteins distribute to cell-cell borders.

13 ichannels must be correctly targeted to cell-cell borders.

14 th retraction of keratin filaments from cell-cell borders.

15 ng, pronounced caveolar "towers" at the cell-cell borders.

16 Bazooka/PAR-3 protein at the reciprocal D-V cell borders.

17 and plaque components were recruited to cell-cell borders.

18 titutively recycles evenly along endothelial cell borders.

19 cells but is recruited by Vangl2 to anterior cell borders.

20 and is sufficient to direct plakophilin 2 to cell borders.

21 th abundant clear cytoplasm and well-defined cell borders.

22 s to merge puncta into a single row and seal cell borders.

23 ell migration and do not localize PECAM-1 to cell borders.

24 adient that "guides" neutrophils to the cell-cell border, (2) service as a "passive ligand" for neutr

25 are located predominantly along the T cell-B cell border and near bridging channels.

26 an enrichment of nonmuscle myosin II at A-P cell borders and Bazooka/PAR-3 protein at the reciprocal

27 tologically by cadherin localization to cell-cell borders and colocalization with the actin cytoskele

28 t fascin and beta-catenin colocalize at cell-cell borders and dynamic cell leading edges of epithelia

29 calized to adherens junctions at endothelial cell borders and forms a complex with alpha-, beta-, gam

30 eolin-1 and E-cadherin closely associated at cell borders and in internalized structures upon stimula

31 Dsg3 and other desmosomal proteins from cell-cell borders and prevents alterations in desmosome ultra

32 esulted in the accumulation of E-cadherin at cell borders and the formation of tightly adherent cells

33 ons, including cytoplasm, cytoskeleton, cell-cell border, and nucleus.

34 xin colocalize in the nucleus and at lateral cell borders, and show that axin2 is limited to the nucl

35 dens 1 (ZO-1), translocation of ZO-1 to cell-cell borders, and the formation of typical ZO-1 honeycom

36 omposite fluorescent tissue images, in which cell borders are not visible.

37 cement of vinculin staining was found at the cell borders as well as the cell interior.

38 of cell/cell contact, such as filopodia and cell borders, before the appearance of E-cadherin, sugge

39 (ZO) proteins, localize not only at the cell-cell borders but are also present in the nuclei.

40 ACF7 and the cytoskeleton reorganize at cell-cell borders but with different kinetics from adherens j

41 s in COS cells, the recruitment of DP-NTP to cell borders by the chimera required co-expression of pl

42 In addition to cell-cell borders, cadherins were unexpectedly observed to co

43 aining the sections with DNA dye (DAPI), and cell borders can be visualized with a dye-coupled antibo

44 t of functionally dedicated cell types: grid cells, border cells, head direction cells, and speed cel

45 hese highly specialized neurons include grid cells, border cells, head-direction cells, and irregular

46 Grid cells, border cells, head-directions cells, and conjunct

47 phologically distinct types of SCs, homogene cells, border cells, hyaline cells, ganglion cells, and

48 nhibits Rac1 activity and trafficking to the cell border during barrier recovery.

49 out embryogenesis, most notably in epidermal cells bordering each segment.

50 hat PMCA2 is rapidly delivered to the apical cell border from where it diffuses to the entire stereoc

51 to collagen fibrils over a large part of the cell border, have a flattened/spread (two-dimensional) a

52 calization of Ag-specific B cells to the B-T cell border; however, these cells do not proliferate or

53 an do FO cells, and are localized at the T/B cell border in spleen.

54 with the disappearance of ZO-2 staining from cell borders in 6-hour LPS-treated cells.

55 ibuted from the intercalated disk to lateral cell borders in failing tissue.

56 associated with basolateral, but not apical, cell borders in injured cells.

57 ing the recruitment of excess desmoplakin to cell borders in transiently transfected COS cells.

58 prephloem pathway, comprising at least seven cell border interfaces between mesophyll and sieve eleme

59 ed but was jagged, not linear along the cell-cell border like that observed for the full-length desmo

60 rthermore, mutation of E470 and E472 reduces cell border localization of occludin.

61 nolayer PECAM-1-regulated calcium signaling, cell border localization, nor the PECAM-1 cytoplasmic do

62 Adhesive forces at endothelial cell-cell borders maintain vascular integrity.

63 a membrane and is internalized at the apical cell border maintaining an estimated half-life of reside

64 expression shifted to placental trophoblast cells bordering maternal blood spaces and fetal placenta

65 -cadherin, as opposed to N-cadherin, to cell-cell borders more closely parallels that of connexin 56

66 evels of c-jun expression within a subset of cells bordering necrotic/apoptotic regions of the liver

67 heral regions of macrophages and in the cell-cell border of 293 epithelial cells.

68 ulin gene superfamily that localizes to cell-cell borders of confluent endothelial cells and has been

69 The presence of connexin 43 at the cell-cell borders of corneal fibroblasts is consistent with a

70 that claudin-18 is concentrated at the cell-cell borders of epithelial cells.

71 Fmi is first enriched at equatorial cell borders of R3/R4, positively interacting with Fz/Ds

72 tegrin was uniquely localized along the cell-cell borders of the differentiating fiber cells, similar

73 Expression is localized to cell-cell borders of the ICM and is detected at the very firs

74 nins, co-localized with cadherin at the cell-cell borders of the myofibroblasts.

75 Occludin, ZO-1, and ZO-2 were found at the cell borders of the superficial layer, whereas claudin-1

76 one N-terminal truncation mutant targeted to cell borders; other mutants showed variable cytoplasmic

77 Leukocyte migration across endothelial cell borders (paracellular) and through endothelial cell

78 transmigration occurring exclusively at the cell borders (paracellularly).

79 l actomyosin network detaches from AJs at AP cell borders, reducing coordination of actomyosin contra

80 xpressed in the developing cortical plate in cells bordering Reelin-expressing Cajal-Retzius cells an

81 mutant protein forms gap junction plaques at cell borders similar to wild-type (WT) Cx47 in transfect

82 d to give prominent punctate labeling at the cell borders, specifically in the corresponding transfec

83 to bind human BMEC by their tips near or at cell borders, suggesting a paracellular route of transmi

84 witching, and it sets up a longitudinal cell-cell border that is a site of apical polarization and lu

85 ne network just below the plasmalemma at the cell borders that is connected at intervals to the junct

86 he cortical regions and lamellipodia at cell-cell borders that protruded under neighboring cells.

87 e choroid plexus, the olfactory bulb, and in cells bordering the cerebral ventricles.

88 , unlike cuboidal ependymal cells, ependymal cells bordering the CVOs possess long processes that pro

89 nown to involve changes in the morphology of cells bordering the damage, such as the formation of lar

90 ealed a unique role for Isl1 in diencephalic cells bordering the internal capsule for the normal deve

91 rate that fragmented DNA was present only in cells bordering the OFZ.

92 After wounding of an epithelium, the cells bordering the wound form dynamic actin protrusions

93 wounded epithelia is primarily driven by the cells bordering the wound, which become motile after wou

94 by molecules concentrated at the endothelial cell border; these include platelet/endothelial cell adh

95 domain and enhanced its recruitment to cell-cell borders; this recruitment was not dependent on the

96 gmentation and occludin trafficking from the cell border to early and late endosomes, concomitant wit

97 king of MZ precursor B cells to the T cell-B cell border to provide costimulation of CD4 T cells.

98 n bands (DPABs) and migration of vinculin to cell borders under a uniform shear stress (10.5 dyne/cm2

99 it is normally targeted only to fusion-fated cell borders via mutual interaction between EFF-1-expres

100 typical punctate Cx43 immunofluorescence at cell borders was disrupted by 5 h.

101 F-actin staining around cell borders was more intense in both LPA- and S1P-treat

102 but concentrates at their distal ends and at cell borders when polarized.

103 At cell-cell borders where endogenous DP was undetectable by imm

104 cells, polycystin-1 localized to the lateral cell borders with N-terminal antibodies but not with a C