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1 reserving microtubule trajectory to the cell-cell border.
2  the leukocyte with PECAM at the endothelial cell border.
3  precursor B cells clustered at the T cell-B cell border.
4 d by specific molecule(s) at the endothelial cell border.
5 gration of leukocytes across the endothelial cell border.
6 f connexin hemichannels directly to the cell-cell border.
7 ell migration and do not localize PECAM-1 to cell borders.
8 equisite for full-length Cx43 trafficking to cell borders.
9 diac gap junction protein, localized to cell-cell borders.
10 here key ciliary proteins distribute to cell-cell borders.
11 cells but is recruited by Vangl2 to anterior cell borders.
12 d(3+) triggers the appearance of ZO-2 at the cell borders.
13 tly contact E-cadherin at dorso-ventral cell-cell borders.
14  in de novo endogenous Cx43 delivery to cell-cell borders.
15  InvEE tumours, where it accumulated at cell-cell borders.
16  in this process as it occurs at endothelial cell borders.
17 ichannels must be correctly targeted to cell-cell borders.
18 th retraction of keratin filaments from cell-cell borders.
19 ng, pronounced caveolar "towers" at the cell-cell borders.
20  Bazooka/PAR-3 protein at the reciprocal D-V cell borders.
21 and plaque components were recruited to cell-cell borders.
22 titutively recycles evenly along endothelial cell borders.
23 and is sufficient to direct plakophilin 2 to cell borders.
24 th abundant clear cytoplasm and well-defined cell borders.
25 s to merge puncta into a single row and seal cell borders.
26 adient that "guides" neutrophils to the cell-cell border, (2) service as a "passive ligand" for neutr
27 are located predominantly along the T cell-B cell border and near bridging channels.
28  an enrichment of nonmuscle myosin II at A-P cell borders and Bazooka/PAR-3 protein at the reciprocal
29 tologically by cadherin localization to cell-cell borders and colocalization with the actin cytoskele
30 /14-3-3zeta and ZO-2/14-3-3sigma move to the cell borders and dissociate.
31 t fascin and beta-catenin colocalize at cell-cell borders and dynamic cell leading edges of epithelia
32 calized to adherens junctions at endothelial cell borders and forms a complex with alpha-, beta-, gam
33 eolin-1 and E-cadherin closely associated at cell borders and in internalized structures upon stimula
34 Dsg3 and other desmosomal proteins from cell-cell borders and prevents alterations in desmosome ultra
35 ages showed that the ID represented apposing cell borders and provided detailed insight into the comp
36 minished myosin-II localisation on neighbour cell borders and shortening of basally-extending microtu
37  adhesions show the progressive loss of cell-cell borders and the appearance of focal adhesions with
38 esulted in the accumulation of E-cadherin at cell borders and the formation of tightly adherent cells
39 ons, including cytoplasm, cytoskeleton, cell-cell border, and nucleus.
40 xin colocalize in the nucleus and at lateral cell borders, and show that axin2 is limited to the nucl
41 dens 1 (ZO-1), translocation of ZO-1 to cell-cell borders, and the formation of typical ZO-1 honeycom
42 ellular bridges, elongated cell shape, sharp cell borders, angular nuclei with homogenous chromatin (
43 ing to the characteristic undulations in the cell borders are elusive.
44 omposite fluorescent tissue images, in which cell borders are not visible.
45 cement of vinculin staining was found at the cell borders as well as the cell interior.
46  of cell/cell contact, such as filopodia and cell borders, before the appearance of E-cadherin, sugge
47 (ZO) proteins, localize not only at the cell-cell borders but are also present in the nuclei.
48 ACF7 and the cytoskeleton reorganize at cell-cell borders but with different kinetics from adherens j
49 s in COS cells, the recruitment of DP-NTP to cell borders by the chimera required co-expression of pl
50                          In addition to cell-cell borders, cadherins were unexpectedly observed to co
51 aining the sections with DNA dye (DAPI), and cell borders can be visualized with a dye-coupled antibo
52 -actin and cell adhesion molecules at border cell- border cell contacts.
53   E-cadherin and myosin colocalize at border cell-border cell contacts and cooperate to transmit dire
54  mechanism for the interaction between place cells, border cells, and grid cells.
55 t of functionally dedicated cell types: grid cells, border cells, head direction cells, and speed cel
56 hese highly specialized neurons include grid cells, border cells, head-direction cells, and irregular
57                                         Grid cells, border cells, head-directions cells, and conjunct
58 phologically distinct types of SCs, homogene cells, border cells, hyaline cells, ganglion cells, and
59 nhibits Rac1 activity and trafficking to the cell border during barrier recovery.
60 es of trajectories that do not interact with cell borders (e.g., cell membrane or nucleus).
61 out embryogenesis, most notably in epidermal cells bordering each segment.
62 of follicular helper T (T(FH)) cells and T-B cell border-enriched fibroblastic reticular cells, is de
63 hat PMCA2 is rapidly delivered to the apical cell border from where it diffuses to the entire stereoc
64 sequences of anomalous particle motions near cell borders from both theoretical and experimental pers
65 to collagen fibrils over a large part of the cell border, have a flattened/spread (two-dimensional) a
66 calization of Ag-specific B cells to the B-T cell border; however, these cells do not proliferate or
67 an do FO cells, and are localized at the T/B cell border in spleen.
68 with the disappearance of ZO-2 staining from cell borders in 6-hour LPS-treated cells.
69 that the appearance of extended lateral cell-cell borders in culture arises as a consequence of crowd
70 ibuted from the intercalated disk to lateral cell borders in failing tissue.
71 associated with basolateral, but not apical, cell borders in injured cells.
72 ing the recruitment of excess desmoplakin to cell borders in transiently transfected COS cells.
73 cyte pseudopod with PECAM at the endothelial cell border initiates transendothelial migration (TEM, d
74 ing, strengthening tissues: CXE in xylem and cells bordering intercellular canals and MXE in sclerenc
75 prephloem pathway, comprising at least seven cell border interfaces between mesophyll and sieve eleme
76 der shear stress, it redistributes along the cell borders into the flow direction.
77 ed but was jagged, not linear along the cell-cell border like that observed for the full-length desmo
78 rthermore, mutation of E470 and E472 reduces cell border localization of occludin.
79 nolayer PECAM-1-regulated calcium signaling, cell border localization, nor the PECAM-1 cytoplasmic do
80          Adhesive forces at endothelial cell-cell borders maintain vascular integrity.
81 a membrane and is internalized at the apical cell border maintaining an estimated half-life of reside
82  fide centrosomes and multiplexed these with cell border markers to identify individual cells within
83  expression shifted to placental trophoblast cells bordering maternal blood spaces and fetal placenta
84 -cadherin, as opposed to N-cadherin, to cell-cell borders more closely parallels that of connexin 56
85 evels of c-jun expression within a subset of cells bordering necrotic/apoptotic regions of the liver
86 heral regions of macrophages and in the cell-cell border of 293 epithelial cells.
87 ulin gene superfamily that localizes to cell-cell borders of confluent endothelial cells and has been
88      The presence of connexin 43 at the cell-cell borders of corneal fibroblasts is consistent with a
89  that claudin-18 is concentrated at the cell-cell borders of epithelial cells.
90          Fmi is first enriched at equatorial cell borders of R3/R4, positively interacting with Fz/Ds
91 tegrin was uniquely localized along the cell-cell borders of the differentiating fiber cells, similar
92              Expression is localized to cell-cell borders of the ICM and is detected at the very firs
93 nins, co-localized with cadherin at the cell-cell borders of the myofibroblasts.
94   Occludin, ZO-1, and ZO-2 were found at the cell borders of the superficial layer, whereas claudin-1
95 erentiation, formation of the reactive glial cell border, or graft axon outgrowth.
96 one N-terminal truncation mutant targeted to cell borders; other mutants showed variable cytoplasmic
97       Leukocyte migration across endothelial cell borders (paracellular) and through endothelial cell
98  transmigration occurring exclusively at the cell borders (paracellularly).
99 l actomyosin network detaches from AJs at AP cell borders, reducing coordination of actomyosin contra
100 xpressed in the developing cortical plate in cells bordering Reelin-expressing Cajal-Retzius cells an
101  that GDNF specifically recruits DSG2 to the cell borders, resulting in increased DSG2-mediated inter
102 mutant protein forms gap junction plaques at cell borders similar to wild-type (WT) Cx47 in transfect
103 d to give prominent punctate labeling at the cell borders, specifically in the corresponding transfec
104 iffness, we show that the presence of a cell-cell border substantially decreases the overall contract
105  to bind human BMEC by their tips near or at cell borders, suggesting a paracellular route of transmi
106 witching, and it sets up a longitudinal cell-cell border that is a site of apical polarization and lu
107 ne network just below the plasmalemma at the cell borders that is connected at intervals to the junct
108 he cortical regions and lamellipodia at cell-cell borders that protruded under neighboring cells.
109 e choroid plexus, the olfactory bulb, and in cells bordering the cerebral ventricles.
110 , unlike cuboidal ependymal cells, ependymal cells bordering the CVOs possess long processes that pro
111 nown to involve changes in the morphology of cells bordering the damage, such as the formation of lar
112 ealed a unique role for Isl1 in diencephalic cells bordering the internal capsule for the normal deve
113 rate that fragmented DNA was present only in cells bordering the OFZ.
114 cluding ambient barcodes and recovering real cells bordering the quality threshold.
115         After wounding of an epithelium, the cells bordering the wound form dynamic actin protrusions
116 wounded epithelia is primarily driven by the cells bordering the wound, which become motile after wou
117 by molecules concentrated at the endothelial cell border; these include platelet/endothelial cell adh
118  domain and enhanced its recruitment to cell-cell borders; this recruitment was not dependent on the
119 gmentation and occludin trafficking from the cell border to early and late endosomes, concomitant wit
120 king of MZ precursor B cells to the T cell-B cell border to provide costimulation of CD4 T cells.
121 n bands (DPABs) and migration of vinculin to cell borders under a uniform shear stress (10.5 dyne/cm2
122 it is normally targeted only to fusion-fated cell borders via mutual interaction between EFF-1-expres
123  typical punctate Cx43 immunofluorescence at cell borders was disrupted by 5 h.
124                      F-actin staining around cell borders was more intense in both LPA- and S1P-treat
125                      Upon collision with the cell border, waves may initiate the formation of protrus
126 but concentrates at their distal ends and at cell borders when polarized.
127                                      At cell-cell borders where endogenous DP was undetectable by imm
128                                   At the B-T cell border, where both responses originate, B cells als
129 cells, polycystin-1 localized to the lateral cell borders with N-terminal antibodies but not with a C

 
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