ライフサイエンスコーパス: cell interaction

1 rises from the head-tail symmetry of cell-to-cell interaction).

2 uence survival, cell morphology, and cell-to-cell interaction.

3 se to the oxidative burst that follows PC-GB cell interaction.

4 artmentalized and indicate ongoing local T/B cell interaction.

5 -12 and IFN-gamma cytokine levels and BMM -T cell interaction.

6 provide a higher fluid mixing and treatment-cell interaction.

7 can directly activate basophils via cell-to-cell interaction.

8 nutrients can affect growth but also a cell-cell interaction.

9 eable, allowing the possibility of PMP-tumor cell interaction.

10 ype that is suitable for the study of immune cell interactions.

11 pes, following tissue-specific rules of cell-cell interactions.

12 nism by which the Ihog proteins mediate cell-cell interactions.

13 t the effects of hypoxia on direct PMN-tumor cell interactions.

14 HSCs will be of value for research into cell-cell interactions.

15 lyses and is a promising tool to quantify NP-cell interactions.

16 , a protein that facilitates vascular-immune cell interactions.

17 minished exposure of Env that mediates virus-cell interactions.

18 s, highlighting the complexity of these cell-cell interactions.

19 es (ReCVs) to study enteric calicivirus host cell interactions.

20 nt membrane function that helps control cell-cell interactions.

21 of bacterial cell-to-cell and bacteria-host cell interactions.

22 tility phases are dominated by physical cell-cell interactions.

23 iological systems exhibiting typical cell to cell interactions.

24 ividual cells, synaptic spines and rare cell-cell interactions.

25 inoculum and parameters that describe virus-cell interactions.

26 scillations, which can influence microbubble-cell interactions.

27 l as increases migration, invasion, and cell-cell interactions.

28 , all of which may be involved in monocyte-T-cell interactions.

29 pact on understanding other enterovirus-host cell interactions.

30 er and the fetus, and is thus the epitome of cell interactions.

31 egulator of AJ mechanics and long-range cell-cell interactions.

32 titers, suggesting insulin-specific T- and B-cell interactions.

33 sue dissociation, losing information on cell-cell interactions.

34 rom stromal, lymphoid, or antigen presenting cell interactions.

35 nce of single cell analysis when studying NP-cell interactions.

36 properties are known to affect nanoparticle-cell interactions.

37 nvolving both homotypic and heterotypic cell-cell interactions.

38 ved as signaling molecules that mediate cell-cell interactions.

39 t role in redox signalling and pathogen-host cell interactions.

40 e theoretically calculated limit and cell-to-cell interactions.

41 sion, and impaired melanoma cell-endothelial cell interactions.

42 during the morphogenic process based on cell-cell interactions.

43 d regulates melanoma cell migration and cell-cell interactions.

44 pathways, chemokines, and tumor-endothelial cell interactions.

45 ng and therapeutic targeting of T(FH) cell-B cell interactions.

46 sociated PMN phenotypes and direct PMN-tumor cell interactions.

47 signaling, chemokines, and tumor-endothelial cell interactions.

48 een cell-extracellular matrix (ECM) and cell-cell interactions.

49 ve and specific labeling of cells after cell-cell interactions.

50 rocess and its application in modifying cell-cell interactions.

51 tabolism as crucial for cancer - endothelial cells interaction.

52 l signal transduction; 8) alters direct cell-cell interactions; 9) alters survival, proliferation, ce

53 and the identification of higher order cell-cell interactions across a wide range of cell types.

54 is dynamic and plays signaling roles in cell-cell interaction, adaptation to antibiotics, and sensati

55 of these human cellular models to study cell-cell interactions among progenitors, neurons, astrocytes

56 nregulation of p120-catenin compromises cell-cell interaction and communication, disrupts collective

57 aive B and cognate T follicular helper (Tfh) cell interaction and initiation of the GC reaction.

58 n effects of nanotopography on altering cell-cell interaction and osteogenic gene expression at the s

59 n of GPVI efficiently impairs platelet-tumor cell interaction and tumor metastasis.

60 nd (Dll) pathway, a master regulator of cell-cell interaction and vascular patterning.

61 ignaling, Polycomb repression, innate immune cell interactions and a cluster of zinc finger-encoding

62 ich repeat domain protein that mediates cell-cell interactions and affinity.

63 at colonize human host via extensive cell-to-cell interactions and biofilm formation.

64 consistent with a role for cognate CD4(+) T cell interactions and CD40 signalling in cDC1 licensing.

65 cific molecular components that mediate cell-cell interactions and describe metabolic interactions, s

66 ace molecules required for NKT and apoptotic cell interactions and developed suppressive immune funct

67 ating single-cell signatures to explore cell-cell interactions and differentiation state.

68 are essential for long-lasting cognate Tfh-B cell interactions and efficient selection of low-affinit

69 g, leading to increased melanoma-endothelial cell interactions and enhanced tumor dissemination.

70 we investigated in vitro macrophage-myogenic cell interactions and found that Dysf-deficient muscle i

71 oduction, or (3) through interruption of T-B-cell interactions and further studied the effects of ant

72 ding is important in understanding EV71-host cell interactions and has potential impact on understand

73 tion between these processes and competitive cell interactions and how this affects disease progressi

74 s) transporter contributes to bacterial-host cell interactions and in vivo virulence.

75 n, thereby compromising pericyte-endothelial cell interactions and inter-endothelial cell junctions.

76 lation and function of epidermal cell-immune cell interactions and into how components that are class

77 These glycoconjugates are involved in host-cell interactions and may be associated with the virulen

78 Bacteria-tumor cell interactions and metabolic crosstalk were extensive

79 By preserving cell-cell interactions and minimizing clonal selection, GBOs

80 Correct cell/cell interactions and motion dynamics are fundamental in

81 , including drug candidates that affect cell/cell interactions and motion dynamics.

82 plications in understanding heterotypic cell-cell interactions and novel drug screening in diseased h

83 We use this to monitor the history of cell interactions and occurrences of neighbour exchange

84 use SEGGA to analyze changes in cell shape, cell interactions and planar polarity during convergent

85 Some are likely involved in cell-cell interactions and potentially important for episymbi

86 This might influence directly cell-to-cell interactions and the community effects within the c

87 owing understanding of dynamic tumour-immune cell interactions and the mechanisms by which tumour cel

88 brain function that emerge from complex cell-cell interactions and to improve our mechanistic underst

89 ent 3D skin model to investigate epidermal-T cell interactions and to understand the pathophysiology

90 EphA2, a guidance molecule involved in cell-cell interactions and tumorigenesis.

91 in during BBB maturation that regulates cell-cell interactions and Wnt/beta-catenin activity.

92 ce, but also aberrant T-cell spreading, cell-cell interaction, and migration.

93 es relating to cell surface signalling, cell-cell interaction, and protein translation (p < 0.01).

94 n-vivo 'features' such as tumor penetration, cell interactions, and increased resistance to therapeut

95 proteins involved in energy metabolism, cell-cell interactions, and protein-protein signaling was con

96 f cell-autonomous metabolic regulation, cell-cell interactions, and systemic physiology.

97 standing the role of exosomal CYP2E1 in cell-cell interactions, and their effects on drug-induced tox

98 ne deletion affects T cell function, and B:T cell interactions are critical for in vivo immune respon

99 It is thought that these cell-cell interactions are critical for the formation of mixe

100 Transient cell-cell interactions are formed between T cells and both MF

101 Studies of HuNoV host cell interactions are limited by the lack of a simple, r

102 d with the loss of efficacy when direct cell-cell interactions are prevented suggest that the regulat

103 of inter-leukemic communication and cell-to-cell interactions are proposed to be important for optim

104 DC-NK cell interactions are thought to influence the developme

105 r transcriptome database for changes in cell-cell interactions as the characteristic of malignancy.

106 resulting system-level model captures virus-cell interactions as well as competing energetic mechani

107 elucidate multiscale cellular changes (cell-cell interactions as well as subcellular changes) that a

108 protective barrier around the cell, and cell-cell interaction, as well as surface adhesion.

109 was, in part, caused by uncoupling of Tfh-B cell interactions, as evidenced by reduced expression of

110 nsmission via neuronal-glial and glial-glial cell interactions, as well as the involvement of spinal

111 that are highlighting the importance of cell-cell interaction at the NMJ in spinal muscular atrophy (

112 to understand and quantify Bdellovibrio host cell interactions at a molecular level.

113 Microenvironment cues and cell-to-cell interactions balance stem cell quiescence with prol

114 putational method to infer potential cell-to-cell interactions based on transcriptome data of sorter-

115 ons for therapies that target B cells or B-T-cell interactions because the loss of humoral immunity l

116 nd ultrastructural evidence of enhanced cell-cell interactions between astrocytes and Agrp neurons (k

117 ion system (T6SS) mediates antagonistic cell-cell interactions between competing Gram-negative bacter

118 Improvement of cell-cell interactions between epithelium and mesenchyme is a

119 plying this pipeline of methodology to study cell interactions between other immune cell types to rev

120 ian constructs that recapitulate native cell-cell interactions between ovarian granulosa and theca ce

121 This mechanism relies on cell interactions between two functionally distinct cell

122 part of an emerging, exciting theme of cell-cell interactions both within and between species, and i

123 ly reveal a mechanism for Ihog-mediated cell-cell interactions but also suggest a direct Hh-mediated

124 stances that prevent the first step of virus-cell interaction by mimicking heparan sulfate proteoglyc

125 nt process shaping the success of T(fh)-GC B cell interactions by influencing costimulatory and cytok

126 attributed to a physical hindrance of SiO(2)-cell interactions by the SOM and enhanced SOM viscosity

127 r to synergize their respective strength and cell interaction capabilities.

128 w play a dominant role in NP margination and cell interaction, compared to Brownian motion, gravity,

129 dings suggest that airway smooth muscle/mast cell interactions contribute to asthma severity by trans

130 Colony fitness depends on cell interactions, cooperation, and the division of labo

131 Craniofacial development depends on cell-cell interactions, coordinated cellular movement and dif

132 acrophages as gatekeepers of the cancer-host cell interaction: depriving transplants from macrophages

133 can also be applied to study potential cell-cell interactions due to in vivo proximity in research f

134 mics of IAV and human epithelial respiratory cell interaction during early infection at the single-ce

135 izes the role of cell motion, guided by cell-cell interactions during differentiation, in forming bio

136 ptors (Eph) and their ephrin ligands control cell interactions during normal development, and reemerg

137 Further, we identify cell-cell interactions during the organization of the primiti

138 Here we explore FCSC and endothelial cell interactions during vascularized bone formation.

139 question as to when genes that regulate cell-cell interactions emerged during evolution.

140 Studies of immune cell interactions, epithelial cell barriers, neuronal co

141 ernal (cutaneous and gut microbiota and host cell interaction) exposures.

142 These findings provide a new aspect of virus-cell interaction for rendering efficient HBV replication

143 affected the outcome of Chlamydia-dendritic cell interactions for both the bacterium and the host ce

144 ions of the growing field of phage-mammalian cell interactions for phage therapy.

145 Automated profiling of cell-cell interactions from high-throughput time-lapse imagin

146 ight discoveries enabled by analyses of cell-cell interactions from transcriptomic data and review th

147 that a computational model of repulsive cell-cell interactions generates a mosaic with grain boundari

148 c seeding of cancer cells, endothelial-tumor cell interactions govern extravasation to the bone and p

149 luable for investigation of niche-supporting cell interactions, have the potential to lead to a thera

150 Furthermore, analyses of cell-to-cell interactions highlight different networks of macrop

151 that uterine decidual cells represent a cell-cell interaction hub with a large number of potential in

152 Unbiased analysis of cell-cell interactions identifies a shift from airway structu

153 ure in-depth studies of VF dynamics and host cell interactions.IMPORTANCE MRV has historically been u

154 have revealed a multitude of individual cell-cell interactions important for this self-organisation,

155 o develop new models to study niche-leukemic cell interaction in human myeloid malignancies; and fina

156 show the importance of an antibody/effector cell interaction in mediating humoral immunity.

157 vidence of a strong tumor-circulating immune cell interaction in responder patients but not in those

158 omplexity of cell fate specification by cell-cell interactions in a rapidly dividing embryo.

159 lar junctions, because the weakening of cell-cell interactions in an alpha-catenin knockdown monolaye

160 ate our understanding of the outputs of cell-cell interactions in cancer as well as across many biolo

161 erformance and algorithmic design choices of cell interactions in continuous and discrete space where

162 derstand the molecular aspects of virus-host cell interactions in detail.

163 ton intravital microscopy as a tool to study cell interactions in different areas of the immune syste

164 However, the outcome and dynamics of CAR T cell interactions in distinct anatomical sites are poorl

165 ll responses and follicular T helper (TFH)-B cell interactions in germinal centers.

166 ated the role of the NKG2D axis in T cell/NK cell interactions in hepatitis B.

167 Our findings suggest that cell-cell interactions in highly folded environment of mammal

168 G) has led to fundamental insights into cell-cell interactions in immunotherapy.

169 ge analysis workflow to analyze nanoparticle-cell interactions in metastatic tumors.

170 photon time-lapse images of T cell-dendritic cell interactions in mouse spleens.

171 new study identifies a role for neuron-skin cell interactions in preventing the bundling of dendriti

172 phenotypes, their functional states and cell-cell interactions in relation to lesion morphometry and

173 ltiple human liver cell types can mimic cell-cell interactions in specific types of DILI.

174 ibility and the strongest alteration of cell-cell interactions in SSc lesions.

175 Elucidating the component cell interactions in the osteogenic-vascular niche and t

176 sh it as a novel, important mediator of DC-T cell interactions in type-2 immunity.

177 unction intercellular communication and cell-cell interactions in vitro.

178 level of diversity in the outcomes of CAR T cell interactions in vivo, with important clinical impli

179 n, and indeed such a model fits the bare-tip/cell interaction, in agreement with earlier work.

180 increased strength of patients' tumor-immune cell interaction, including increased cytotoxic differen

181 ng suggests that faster dopamine-induced T-B-cell interactions increase total germinal centre output

182 ptor binding assays and analysis of antibody-cell interactions indicated that rabbit vaccine-induced

183 Cell-cell interactions influence all aspects of development,

184 al human pulmonary microvascular endothelial cell interactions, inhibited tube stability, and disrupt

185 monstrate how the transfer of molecular wood cell interactions into hemicellulose-based materials may

186 nti-CD20 therapies demonstrate that B- and T-cell interaction is a major driver of multiple sclerosis

187 r understanding of their biogenesis and host cell interaction is incomplete.

188 uptake selectivity, in which a nanoassembly-cell interaction is turned on, only in the concurrent pr

189 Understanding cell-cell interactions is critical in most, if not all, resea

190 ect examination of viral particles and virus-cell interactions is now possible via advanced microscop

191 ls are governed by a complex network of cell-cell interactions, knowing the specific immune cell comp

192 Epithelial and mast cell interactions, leading to the synthesis of 15-Oxo-ET

193 d IL-6 in myofibroblasts (MFs) - lung cancer cell interactions, lung cancer cells (Lewis and CTM-167

194 Accordingly, we propose that cell-cell interaction may be a factor responsible for the gra

195 into a single new living entity through cell-cell interactions, migration or cellular extensions betw

196 ith a prisoner's dilemma game-theoretic cell-cell interaction model to design chemotherapeutic strate

197 nce by a balance of cell-substratum and cell-cell interactions, modulated by cell phenotype-specific

198 at plays a pivotal role in a variety of cell-cell interactions, mostly studied during development.

199 To investigate the cell-cell interactions necessary for the formation of retinal

200 trates that CCL2 enables the prolonged MSC-T cell interactions needed for sufficient suppression of a

201 idation and Assessment of Regulatory Cell-to-cell Interaction Networks (SEARCHIN) to identify ligand-

202 c analysis of cellular compositions and cell-cell interaction networks showed that CM contractility a

203 to specific experimental conditions, when GO-cell interactions occur.

204 tion from pluripotency fails to recapitulate cell interactions occurring during organogenesis.

205 In a TH2-promoting environment, T-cell/B-cell interactions occurring in regional lymph nodes lead

206 consequences of healthy NK cell-HIV-infected cell interactions occurring in the HIV eclipse phase, wh

207 subsequent juxtaposition, and essential cell-cell interactions of endocardial and myocardial cells th

208 alterations in cellular function and cell-to-cell interactions of pulmonary resident cells and system

209 e distinct molecular mechanisms: direct cell-cell interaction on adjacent cells, stabilization of adj

210 ied, but the effects of macrophage-apoptotic cell interactions on macrophage behaviour are poorly und

211 niques, we investigate the influence of cell-cell interactions on spermatozoa swimming behavior in co

212 the differential impact of stochasticity in cell interactions on wild-type and mutant patterns, and

213 the basis for studying complex parasite-host cell interactions or drug effects with spatio-temporal r

214 , further spirometric loss, implicating cell-cell interactions or overlapping inflammatory pathways w

215 Cell-cell interactions orchestrate organismal development, ho

216 rotein 1) regulates cell proliferation, cell-cell interactions, organ size, and tumorigenesis.

217 e summarize the biochemical activities, host cell interaction partners, and physiological functions o

218 ive albumin, thus showing the most favorable cell interaction profiles (low uptake by J774A.1 macroph

219 Moreover, collective cell interactions, proliferation, cancer-associated fibr

220 Many recent studies have shown host cell interactions promote virulence factor expression, f

221 ated cells act as facilitators in tumor-host cell interactions promoting the establishment of distant

222 gh deregulation of the expression of cell-to-cell interaction proteins and protein secretion.

223 These findings indicate that OPC-endothelial cell interactions regulate neonatal white matter vascula

224 whether pilus length is critical for cell-to-cell interactions remain unknown.

225 macroscopic patterns resulting from cell-to-cell interactions remains largely qualitative.

226 dary lymphoid organs are pivotal for B and T cell interactions required for induction of humoral immu

227 poses challenges for understanding the cell-cell interactions required for organ homeostasis and how

228 Since defects can provide insight into cell-cell interactions responsible for pattern formation, her

229 erial interactions as well as bacterial-host cell interactions resulting in microbial growth, phagocy

230 cal adhesion kinases inhibitor (FAKi 14) and cell interactions show exponential changes of cellular a

231 n on cellular molecular composition and drug-cell interaction, showing the potential of SRS in drug d

232 progenitor migrations, timings, dynamic cell-cell interactions, signaling activities, and routes unde

233 tially a fundamental form of eukaryotic cell-cell interaction, since it also occurs in multicellular

234 Cell-cell interactions, soluble factors, and extracellular ma

235 that are involved in a diverse array of host cell interactions, some of which directly activate cell

236 elp facilitate several leukocyte-endothelial cell interactions, such as leukocyte rolling, adhesion,

237 Cell competition is a form of cell interaction that causes the elimination of less fit

238 ings identify emperipolesis as a new cell-in-cell interaction that enables neutrophils and potentiall

239 have developed a simple model for virus-host cell interaction that is driven by its adhesion to cell

240 We aimed to investigate the ILC3-B-cell interaction that probably takes place in human tons

241 cells and platelets contributes to the cell-cell interactions that are involved in the pathogenesis

242 acellular bacterium, inhibiting microbe-host cell interactions that facilitate invasion can disrupt i

243 Yet, little is known about the cell-cell interactions that imprint the tissue-specific ident

244 insights into SARS-CoV-2 S glycoprotein-host cell interactions that likely contribute to the transmis

245 cells ignores physiologically relevant cell-cell interactions that may be critical for circuit level

246 growth arrest is more likely related to the cell interactions that mediate size control in normal ti

247 iew we focus on epithelial and innate immune cell interactions that mediate wound healing and restora

248 The rapid T-B-cell interactions that occur during this process are rem

249 nd products and their receptors mediate cell-cell interactions that regulate several biological funct

250 nity to uncover transcriptional programs and cell interactions that regulate synovial joint developme

251 otif (TAZ) in hepatocytes to facilitate cell-cell interactions that stimulate liver inflammation and

252 For host-cell interaction, the human fungal pathogen Candida glab

253 MS-derived BWMs require two distinct cell-cell interactions, the first inhibitory and the second,

254 ulation and the frequency of platelet-immune cell interaction, thereby limiting hepatic immune cell t

255 Chlamydia-host cell interaction therefore constitutes a unique system t

256 proliferation, death, migration, and cell-to-cell interaction through contact inhibition.

257 ideal system with which to study plant cell-cell interactions, tip growth, cell migration, the modul

258 gth of the TIM-PS bond that allows the virus-cell interaction to resist external mechanical perturbat

259 t humans, we examined the adipocyte-leukemia cell interactions to determine if they are essential for

260 tanding of gene regulatory networks and cell-cell interactions to enable the reliable and robust engi

261 erference with PDGF-BB or PDGF receptor-beta cell interactions to implicate PDGF-BB as a primary effe

262 ls of details: from the biochemistry of cell-cell interactions to the ecological dynamics of populati

263 etion and attenuated leukocyte-smooth muscle cell interactions under high glucose or lipopolysacchari

264 of SLURP1 on neutrophil-vascular endothelial cell interactions using human umbilical vein endothelial

265 within the IVD, specifically, mast cell-IVD cell interactions using immunohistochemistry and 3D in-v

266 impact of HIV antigenemia on B cells and Tfh cell interactions warrants further exploration.

267 LMVEC or MLMVEC), and neutrophil-endothelial cell interaction was measured.

268 insight into the dynamics of place and grid cell interaction, we built a computational model with th

269 To study cancer cell-vascular cell interactions, we engineered a 2-layer hydrogel with

270 f diverse biochemical stimuli and juxtacrine cell interactions, we present evidence that a proinflamm

271 ology in CD19-hBtk mice was dependent on B-T cell interaction, whereas IL-10 production and IgM autoa

272 ex vivo, and enhances leukocyte-endothelial cell interaction, which is mediated via PGE receptor-4 (

273 n these communities engage in extensive cell-cell interactions, which are both beneficial and antagon

274 omplex homeostatic mechanisms and local cell-cell interactions, which can become dysregulated in obes

275 he neuroanatomical basis for tanycyte/neural cell interactions, which will be useful to further under

276 dly to C. albicans hyphae via direct cell-to-cell interaction, while the cariogenic pathogen Streptoc

277 cture through increased cell-matrix and cell-cell interactions, while compact dense microstructure in

278 thelial ICAM-1 and VCAM-1 was confirmed by T-cell interaction with EECM-BMEC-like cells.

279 ll shape recognition can also be achieved by cell interaction with imprints that can be made into pol

280 assessed the consequences of prostate cancer cell interaction with neural cells, which are rich in th

281 Tumor cell interaction with platelets produces chimeric extrac

282 NK cell interaction with soluble or surface-bound IL-15Ralp

283 egenerative factors) and membrane-based cell-cell interaction with the injured cells.

284 Tumor cell interaction with various cellular components of the

285 our molecular understanding of those social cell interactions with a relevant function in tumor init

286 YTHDF3 promotes cancer cell interactions with brain endothelial cells and astro

287 st IAV-specific T cell responses relies on T cell interactions with dendritic cells (DCs).

288 T cell development depends upon cell-cell interactions with epithelial cells in the thymus.

289 microscopy, we captured 2,330 hours of tumor cell interactions with functional microvessels and provi

290 fluence Th cell differentiation by biasing T cell interactions with IL-2-consuming DCs, but instead,

291 r morphology is sculpted by specific cell to cell interactions with neurons and each other.

292 that migratory DCs execute targeted cell-to-cell interactions with stationary MCs before leaving the

293 nced breast cancer patients, depend on tumor cell interactions with the mineralized bone extracellula

294 hat allows real-time study of host-malignant cell interactions within a multicellular tissue architec

295 PEL is a cationic polymer that promotes cell-cell interactions within the biofilm matrix through elec

296 icrobes, diet, host factors, drugs, and cell-cell interactions within the cancer itself likely involv

297 from a limited understanding of immune-islet cell interactions within the pancreas and relevant immun

298 hrough multi-faceted roles inhibiting cancer cell interactions within the peritoneal milieu.

299 ting that CXCR3 facilitates dendritic cell-T cell interactions within the tumor microenvironment.

300 Thus, the ability to record cell-cell interactions would facilitate mechanistic delineati