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1 GF signaling in trans from the surface of an adjacent cell.
2 ersing the spin, we move the spinner into an adjacent cell.
3 h that each cell interacted with exactly one adjacent cell.
4 ls controlling behavioral output relative to adjacent cells.
5 e amnioserosa are apparently asynchronous in adjacent cells.
6 to translocate toxic effector proteins into adjacent cells.
7 axons and failed to spread from axon tips to adjacent cells.
8 trongly guided by physical forces imposed by adjacent cells.
9 evolution and mediates communication between adjacent cells.
10 spread from the silencing initiation site to adjacent cells.
11 nautonomously regulated by the properties of adjacent cells.
12 on the surface, and wide connection with the adjacent cells.
13 mpact the expression of these genes in these adjacent cells.
14 herin that forms homodimeric bridges between adjacent cells.
15 sin, and intercellular adhesions interfacing adjacent cells.
16 transfer of ions and small molecules between adjacent cells.
17 with both the extracellular matrix (ECM) and adjacent cells.
18 through linked hemichannels from each of two adjacent cells.
19 w bacteria to exit from host cells to infect adjacent cells.
20 ane proteins that form gap junctions between adjacent cells.
21 intercellular pores linking the cytoplasm of adjacent cells.
22 raction between the contractile ring and the adjacent cells.
23 elium disrupts AJs but only when depleted in adjacent cells.
24 f the plasma membrane, which are engulfed by adjacent cells.
25 to the apoplasm, and subsequent import into adjacent cells.
26 ght asymmetries in the Dl or N activities of adjacent cells.
27 passage of ions and small molecules between adjacent cells.
28 enic requirements and negative regulation by adjacent cells.
29 es specifying the probabilities of moving to adjacent cells.
30 capacity to unload cholesterol directly onto adjacent cells.
31 align themselves with similar structures in adjacent cells.
32 sion follows reception of the Wnt8 ligand by adjacent cells.
33 l and are aligned with similar structures in adjacent cells.
34 rmed by the docking of two hemichannels from adjacent cells.
35 ve lost viability when the fungus moved into adjacent cells.
36 ular channels that connect the cytoplasms of adjacent cells.
37 forms due to a difference in Notch levels in adjacent cells.
38 gnate receptors expressed within the same or adjacent cells.
39 the proximodistal junctional region between adjacent cells.
40 may be involved in the communication between adjacent cells.
41 asm; however, mutant virus did not spread to adjacent cells.
42 innervation may influence gene expression in adjacent cells.
43 in from the cytoplasm to the cell surface of adjacent cells.
44 cell contractility, and forces generated by adjacent cells.
45 elopment by regulating communication between adjacent cells.
46 iate the gated transfer of molecules between adjacent cells.
47 ase on the originally triggered cells and on adjacent cells.
48 shape by linking the actin cytoskeletons of adjacent cells.
49 unctional hemichannels, one from each of the adjacent cells.
50 e TMV replication immediately after entry to adjacent cells.
51 ing ions and small molecules to move between adjacent cells.
52 ing appears necessary for synchronization of adjacent cells.
53 syndecan-2-mediated inside-out signaling to adjacent cells.
54 ion of proteins and their ability to move to adjacent cells.
55 ssion of nectin-1 in trans on the surface of adjacent cells.
56 m and propelled by actin-based motility into adjacent cells.
57 one cell may activate signaling processes in adjacent cells.
58 nt cells by interconnecting the cytoplasm of adjacent cells.
59 e Ca(2+) firing sites in the same cell or in adjacent cells.
60 with its transmembrane ligands expressed on adjacent cells.
61 specific sites of contact (plaques) between adjacent cells.
62 hrinA1, which is anchored to the membrane of adjacent cells.
63 tion and the coalescing of cell cytoplasm of adjacent cells.
64 le tethers that bind to surface receptors on adjacent cells.
65 erentiation and promote the lignification of adjacent cells.
66 f attachment of the myofilament apparatus to adjacent cells.
67 s and their complex interaction with MCTs in adjacent cells.
68 ell adhesion by linking the cytoskeletons of adjacent cells.
69 ons, here termed listeriopods, and spread to adjacent cells.
70 r protoplast and at the radial walls between adjacent cells.
71 walls and interconnect the cytoplasm between adjacent cells.
72 JAM and cell surface receptors expressed on adjacent cells.
73 provide for the direct communication between adjacent cells.
74 th those less fit being eliminated by fitter adjacent cells.
75 omeostasis, supporting communication between adjacent cells.
76 g the anticlinal pavement cell walls between adjacent cells.
77 all positively charged ions to cross between adjacent cells.
78 ch, enabling them to trans-activate Notch on adjacent cells.
79 n the extracellular matrix or the surface of adjacent cells.
80 cal microtubules and actin filaments between adjacent cells.
81 ation but also promote stem cell division in adjacent cells.
82 migrates and accumulates at lower levels in adjacent cells.
83 ent cell separation and hydraulic changes in adjacent cells.
84 evels of WUS protein in the rib meristem and adjacent cells.
85 lasma membrane protrusions that project into adjacent cells.
86 llular matrix, or tethered to the surface of adjacent cells.
87 correlation was found between the events in adjacent cells.
88 the rib meristem and lower nuclear levels in adjacent cells.
89 lation was found between the firing sites in adjacent cells.
90 preserving stable adherens junctions between adjacent cells.
91 the host cytosol and for bacterial spread to adjacent cells.
92 g channels that penetrate the septum between adjacent cells.
93 mediate intercellular communication between adjacent cells.
94 chemical cues in both stimulated tissues and adjacent cells.
95 both within the plasma membrane and between adjacent cells.
96 r by the adhesion protein surface-exposed in adjacent cells.
97 hanically couples the actin cytoskeletons of adjacent cells.
98 itude and diversity between HCV-infected and adjacent cells.
99 by interacting in the intercellular space of adjacent cells.
100 escaped and gained access to the cytosol of adjacent cells.
102 lar motors(1-3), extrinsic forces exerted by adjacent cells(4-7) and mechanical resistance forces due
103 e ability of HIV-1 to mediate fusion between adjacent cells, a process referred to as "fusion-from-wi
106 ons that allow exchange of molecules between adjacent cells also seem to have an important role.
107 of an electrical axo-axonal coupling between adjacent cells and a reciprocal inhibition between the m
108 junction channels span the membranes of two adjacent cells and allow the gated transit of molecules
109 lls direct the spindle orientations of their adjacent cells and are consistent with a mechanism of or
110 nd messengers, and small metabolites between adjacent cells and are formed by two unrelated protein f
112 ntracellular replication before spreading to adjacent cells and causing extensive cellular damage.
113 essential for mediating interactions between adjacent cells and coordinating cellular and organ respo
115 dium and these vesicles can communicate with adjacent cells and even cells of the immune system.
116 cribed in glioma cells can be transferred to adjacent cells and induces targeted inhibition of protei
117 two processes: cell-to-cell movement between adjacent cells and long-distance movement that allows th
118 components, and possibly other proteins, in adjacent cells and may therefore directly mediate these
119 R-1260b could act as a transfer messenger to adjacent cells and mediate the infiltrative growth of MF
120 an organizer that promotes stem cell fate in adjacent cells and patterns the surrounding stem cell ni
121 dherins function to promote adhesion between adjacent cells and play critical roles in such cellular
122 lasma membrane protrusions that project into adjacent cells and resolve into vacuoles from which the
123 Cellular response to physical cues from adjacent cells and the extracellular matrix leads to a d
124 interactions with other surface molecules on adjacent cells and through these interactions initiate s
125 sion of sessile epithelial cells attached to adjacent cells and to the basement membrane into dissoci
126 , and remodeling through direct contact with adjacent cells and via paracrine and endocrine factors t
127 tution by stem cells, paracrine effects from adjacent cells, and circulating anti-aging molecules may
128 y measuring gap sizes, angles formed between adjacent cells, and curvatures of cell surfaces at gaps.
129 ular expansion and coordination of growth of adjacent cells, and defects in karyokinesis and cytokine
130 ion, intracellular multiplication, spread to adjacent cells, and induction of brisk inflammatory resp
131 th the cell surface, can act on unstimulated adjacent cells, and is specifically inhibited by TIMP-3,
132 cells, replicate intracellularly, spread to adjacent cells, and provoke an intense inflammatory resp
133 ell-fate decisions--including cell death--in adjacent cells, and raise the possibility that they do s
134 ic organization, membrane apposition between adjacent cells, and structure and distribution of pili a
135 this localization is not coordinated between adjacent cells, and the crescents subsequently are lost
136 1 in PECs can also affect gene expression in adjacent cells, and this effect is abolished by the T164
137 chsous (Ds), which form heterodimers between adjacent cells; and the Golgi kinase Four-jointed (Fj),
138 move laterally, they are pushed sideways by adjacent cells; and when cells move forward, they are pu
139 hesions of cells to extracellular matrix and adjacent cells are mediated by integrins and VE-cadherin
140 polarized'), or when tight junctions between adjacent cells are opened, heregulin-alpha activates its
142 Fate maps show that polarizing region and adjacent cells are specified in parallel through a serie
143 ular matrix proteins and counterreceptors on adjacent cells, are implicated in synapse maturation and
145 m of an infected cell suddenly flows into an adjacent cell, as visualized through wild-type MV-expres
148 secreted Nkx3.1 protein can translocate into adjacent cells, bind to the regulatory sequence of Nkx3.
150 rmed membrane protrusions that extended into adjacent cells, but the protrusions rarely resolved into
151 olipases C (PLCs) also resulted in spread to adjacent cells, but these triple mutants became trapped
152 influence the effects of mineral coatings on adjacent cells, but to date it has not been practical to
154 ving epithelial cell to adapt to the loss of adjacent cells by dedifferentiating and proliferating.
155 s), which are proteinaceous channels, couple adjacent cells by permitting direct exchange of intracel
156 hannels (GJCs) that connect the cytoplasm of adjacent cells by the end-to-end docking of two Cx hemic
157 r matrix (ECM), or cell-surface molecules on adjacent cells can activate signaling pathways that comm
158 we discuss recent work that shows that tumor-adjacent cells can respond to genotoxic stress by activa
160 systematic map of the visual field, in which adjacent cell clusters represent adjacent points of visu
161 lls indicated the presence of Cx31.9 between adjacent cells, consistent with its localization to gap
162 res maintenance of adhesive contacts between adjacent cells, coordination of polarized cell protrusio
163 ructs causes induction of ectopic Endo 16 in adjacent cells, demonstrating further that Pmar1 control
165 The molecular mechanism to understand why adjacent cells develop into bile ducts or grow actively
168 lt in a checkerboard spatial pattern whereby adjacent cells express opposing levels of Notch and Delt
169 is of cortical peritubular capillaries, with adjacent cells expressing pericyte-like markers; we spec
176 erent ability of adherent cells to move into adjacent cell-free areas, thus providing information on
177 els that physically connect the cytoplasm of adjacent cells, gap junctions permit transport of a dive
178 which target the tumor-interacting and tumor-adjacent cells, have overcome some of these challenges,
179 diate fusion between the plasma membranes of adjacent cells, HIV-1 enters through an endocytic pathwa
180 rmation and movement of VRCs was repeated in adjacent cells in 3-4 h vs. 20 h from primary infected c
183 OA cartilage reflect the increased number of adjacent cells in clusters that are able to interact dir
184 scopy confirmed disorganized capillaries and adjacent cells in cortical peritubular spaces in mutant
185 ting the transfer of small molecules between adjacent cells in culture, indicating its potential role
187 induced a physical separation of the TJs of adjacent cells in immunofluorescence staining of the TJ
196 ected by three promoters and this results in adjacent cells in the same tissue containing different i
199 separated by a completed peptidoglycan wall, adjacent cells in these chains were often compartmentali
200 osely with the extracellular matrix and with adjacent cells including pericytes and smooth muscle cel
201 ceptors to ephrinB ligands on the surface of adjacent cells initiates signaling cascades that regulat
202 oordinating growth and communication between adjacent cells is a critical yet poorly understood aspec
203 tems indicate that localised signalling from adjacent cells is a general mechanism for defining the p
204 icles into axons and extracellular spread to adjacent cells is fundamentally important for identifyin
207 issemination of virus from infected cells to adjacent cells is promoted by the polymerization of acti
210 in the stele, the SHR protein moves into an adjacent cell layer, where it specifies endodermal cell
211 The vertebrate liver and heart arise from adjacent cell layers in the anterior lateral (AL) endode
212 h whether GLK proteins are able to influence adjacent cell layers, we used tissue-specific promoters
215 ells; and why junctional buttressing between adjacent cells may benefit renal epithelium in maximizin
216 y growing cells, the resistance to stress in adjacent cells mechanically isolates rapidly growing cel
217 the talks revealed how interactions between adjacent cells mediated by Notch regulate development an
218 response to laser pulsing, forming pores in adjacent cell membranes through which cargo is gently dr
219 metrically, instructing unequal responses in adjacent cell membranes to establish molecular asymmetry
222 echanism by which mechanical stresses signal adjacent cells not only within the epithelium, but other
223 as a diffusible signal for the induction in adjacent cells of genes encoding cellular protectants su
226 ted specifically at the interface of the two adjacent cells of the developing sporangium, the mother
227 idney, while the tip cells interact with the adjacent cells of the metanephric mesenchyme, inducing t
229 subsequent uptake of lysosomal hydrolases by adjacent cells, often referred to as "cross-correction."
230 suming that information is exchanged between adjacent cells only, under the guidance of gene expressi
231 thod as selected cells could differ from the adjacent cells or could belong to the same cell populati
234 pithelial cells in culture make contact with adjacent cells, PLAC-24 is specifically recruited to the
235 eractions between Eph kinases and ephrins on adjacent cells play a central role in neuronal patternin
236 ell by transfer from the polar septum to the adjacent cell pole where SpoIIE is protected from proteo
237 nd neuronal migration, inhibit the mixing of adjacent cell populations in the developing optic lobe.
238 essential for the docking of connexons from adjacent cells, preventing the formation of functional g
239 sing cells to GCV, and its overexpression in adjacent cells protects them from bystander cell death.
240 nal (R3) activates the Notch receptor in the adjacent cell (R4) via the ligand Delta, resulting in R3
241 Prior to activation, Itgalpha5 expressed on adjacent cells reciprocally and non-cell-autonomously in
242 e model based solely on interactions between adjacent cells reproduced 99% of the spatial structure a
243 F S/L gene lost adherence to the stratum and adjacent cells, resulting in an altered plaque morpholog
244 ction foci progressively expanded locally to adjacent cells, resulting in meningitis, choroiditis, en
246 ization at specific sites of contact between adjacent cells showed significant reduction in the high-
249 mechanisms: direct cell-cell interaction on adjacent cells, stabilization of adjacent cell surface r
250 between the hemopexin domain of MT1-MMP and adjacent cell surface molecules is responsible for outsi
251 eraction on adjacent cells, stabilization of adjacent cell surface receptors on the same cell, and in
257 se mixtures of tumour cells (TCs) and tumour-adjacent cells (TACs), and the intricate interconnection
258 osphorylation of EGFR on the cell surface of adjacent cells than equivalent levels of mature TGFalpha
259 idly from one cell and immediately invade an adjacent cell, thereby minimizing exposure to the extrac
260 hages within tissues transfer cholesterol to adjacent cells, thereby contributing to the ability to u
261 ddition to serving as a rigid anchor between adjacent cells, this study implicates desmosomal cadheri
263 tructure to epithelial tissues by connecting adjacent cells through homophilic E-cadherin interaction
265 ne protrusions that resolve into vacuoles in adjacent cells, through a poorly understood mechanism.
266 id residues from the gangliosides present on adjacent cells, thus creating cell to cell interactions.
267 ligands for HVEM when presented in trans by adjacent cells, thus forming a bidirectional signaling p
268 ith localized inhibition of outgrowth of the adjacent cell to form interdigitating lobes and indentat
269 veloped particle could potentially infect an adjacent cell to mediate the cell-to-cell spread that is
270 stem cell-inducing transcription factor into adjacent cells to activate a negative regulator, thereby
273 nnels that directly connect the cytoplasm of adjacent cells to allow for the intercellular transfer o
274 but also forces the lateral membrane of the adjacent cells to bend towards the initiating cells, the
275 n, particularly pheomelanin, photosensitizes adjacent cells to caspase-3 independent apoptosis, and t
277 lop into oogonia that enter meiosis, recruit adjacent cells to form follicle-like structures, and lat
278 bility in individual cells or couple between adjacent cells to form gap junctions and thereby provide
280 on molecules that interact with neurexins on adjacent cells to promote glutamatergic and GABAergic sy
282 binds to transmembrane receptors located on adjacent cells triggering a tyrosine kinase cascade.
284 e gradient into discrete transitions between adjacent cell types is the genetic toggle switch, compos
285 evelopment involves the formation of several adjacent cell types required for normal male fertility.
288 ected cGAS(+)STING(-) cells can migrate into adjacent cells via gap junctions to function in trans in
289 teroid-receptor positive cells but rather in adjacent cells via paracrine signaling involving several
290 scent proteins provides a way to distinguish adjacent cells, visualize cellular interactions and perf
291 lular movement of the VRCs and the spread to adjacent cells was blocked by inhibitors of filamentous
292 as accompanied by movement of the protein to adjacent cells, where it directly activated homeotic tar
294 tiated by trans binding between cadherins on adjacent cells, which is followed by the clustering of c
295 ponents initiate and reinforce senescence in adjacent cells, which is likely to create a positive fee
296 rs are delivered, but not in nonhaustoriated adjacent cells, which show high PR1::GUS expression leve
297 ression of cambial and phloem markers in the adjacent cells, which suggests that a local auxin-signal
298 ach capturing the transcriptomes of multiple adjacent cells, with scRNA-Seq generated from the same s
300 ong growth-derived maximal tensile stress in adjacent cells would mechanically isolate rapidly growin