ライフサイエンスコーパス: crosstalk

1 d deleterious tumor microenvironmental (TME) crosstalk.

2 teractions and characterizes their molecular crosstalk.

3 ging to describe breast cancer-LEC metabolic crosstalk.

4 es shift up to 220 nm minimizes fluorescence crosstalk.

5 nd IFNbeta controlling dendritic cell-T cell crosstalk.

6 ecular mechanisms that mediate this cellular crosstalk.

7 ignals with improved robustness to noise and crosstalk.

8 haviour is regulated through niche-dependent crosstalk.

9 tein expression can be coupled via E3 ligase crosstalk.

10 in OA, their individual roles, and potential crosstalk.

11 is regulated via integrin/TGF-beta signaling crosstalk.

12 faces, which, however, are marred by channel crosstalk.

13 s elusive how these epigenetic modifications crosstalk.

14 actuators to be multiplexed without spectral crosstalk.

15 miRNAs mediating cardiomyocyte to fibroblast crosstalk.

16 tial mediator of AGE-ECM-adipocyte metabolic crosstalk.

17 in regulating human ECM-adipocyte metabolic crosstalk.

18 lator of LD organization and inter-organelle crosstalk.

19 ein-coupled receptors controlling CDC42-RHOA crosstalk.

20 contacts that represent potential points of crosstalk.

21 ciples relating to receptor interactions and crosstalk.

22 emerging roles for astrocytes in immune cell crosstalk.

23 ocyte-macrophage-hepatic stellate cell (HSC) crosstalk.

24 , and provide mechanistic insight into their crosstalk.

25 moresistance via bidirectional tumor-stromal crosstalk.

26 , and mTORC1/2 signaling, suggesting pathway crosstalk.

27 ity and the mediator molecules enabling such crosstalk.

28 ong overlapping units and investigated their crosstalk.

29 g, potentially enabling metabolic and immune crosstalk.

30 uggests that these pathways have significant crosstalk.

31 sident macrophages in modulating SNS-adipose crosstalk.

32 , and discovery of missing context-dependent crosstalks.

33 ons, we provide evidence that stromal-immune crosstalk acts via a diverse array of immunoregulatory m

34 tudy provides a humanized model to study the crosstalk among HSPCs, leukemia, and their MSC niche, an

35 ing cycle and underscores the complexity and crosstalk among the motor's multiple AAA+ domains.

36 Understanding the molecular signaling crosstalk among the tumor cells, pDCs and immune cells w

37 The major issue is modeling the complex crosstalk among transcription factors (TFs) and their ta

38 Cellular crosstalk analysis revealed stagewise utilization of spe

39 Our data thus reveal extensive crosstalk and a global impact of the minor spliceosome o

40 nts, which include an increase in inter-loop crosstalk and a propensity for a neutral binding surface

41 The fractal topology minimises fluorescence crosstalk and allows quantitative decoding of quantized

42 Knockout of TRIM21 or PHLDA3 promotes crosstalk and cell proliferation.

43 n complex called the PANoptosome and enables crosstalk and co-regulation among these processes.

44 Understanding crosstalk and competition for E3 ligases will be key in

45 c analysis in Salmonella revealed regulatory crosstalk and hierarchical control of H-NS homologs.

46 g RNA circuitry can invert responses, reduce crosstalk and improve sensitivity without protein engine

47 Interorgan crosstalk and interdependent mechanisms include hemodyna

48 neurotransmitters appear to facilitate this crosstalk and positive-feedback loops between multiple t

49 ogical role of EVs in osteolineage cell-HSPC crosstalk and promotes the utility of EVs and their carg

50 ions, acting as key nodes for interorganelle crosstalk and signal transduction.

51 le secreted myokine, facilitates muscle-bone crosstalk and skeletal remodeling in part by its action

52 e functions of UBR5 in regulating the OC-TME crosstalk and suggests that UBR5 is a potential therapeu

53 ent sensing, metabolic adaptation, organelle crosstalk, and aging.

54 tion potential generation and inter-neuronal crosstalk, and modulate synaptic plasticity in neural ne

55 few years that mediate such adipocyte-neuron crosstalk are also reviewed.

56 er, the molecular mechanisms underlying this crosstalk are incompletely understood.

57 echanisms underlying ECM-adipocyte metabolic crosstalk are poorly defined.

58 c health and highlight adipocyte-endothelial crosstalk as a potential target for prevention of ectopi

59 haracterization of the blueprint of SC-niche crosstalk, as well as understanding how it becomes dysre

60 s related to ECM maturation at P7 and immune crosstalk at P30.

61 In conclusion, while functional crosstalk between 5-HT2A and mGlu2 was demonstrated, it

62 s pharmacology approaches to investigate the crosstalk between AD and psychosis.

63 Next, we review the extensive crosstalk between adipocytes and resident innate immune

64 We explore mechanisms of crosstalk between astrocytes and other cells in the CNS

65 Therefore, IL-10-mediated crosstalk between B cells, macrophages, and cDC1s in the

66 th the microenvironment, we investigated the crosstalk between BCR and WNT/beta-catenin signaling and

67 Here we examine the crosstalk between BMP-9 and LDL and how it influences th

68 icate newly discovered bridging vessels that crosstalk between brain and skull marrow, a finding of p

69 Understanding the functional crosstalk between BRCA1-BARD1 and its cofactors and anta

70 gulation of BR signaling, multiple points of crosstalk between BRs and other hormones or stress respo

71 a cytokinome that enables metastasis through crosstalk between cancer and immune microenvironment.

72 This crosstalk between cancer cells and neurons represents me

73 While ECM maturation and crosstalk between cardiac fibroblasts (CFs) and cardiomy

74 reased in C4KO hearts after TAC and mediated crosstalk between cardiomyocytes and fibroblasts to modu

75 Crosstalk between CD33 and TREM2 includes regulation of

76 We conclude that APC/C coordinates crosstalk between cell cycle and chromatin regulatory pr

77 ss the evidence that supports a role for the crosstalk between cell fate and tissue shape during earl

78 nd ECM remodelling, implicating a reciprocal crosstalk between cell mechanics and metabolism.

79 homeostasis and activation, and focus on the crosstalk between cell signaling and RNA-binding protein

80 , in progressively complex preparations, the crosstalk between cell types in development and disease.

81 The crosstalk between deregulated hepatocyte metabolism and

82 ology of each oxidase component, the complex crosstalk between different oxidase components and the c

83 host-microbiome interactions, including the crosstalk between distal and local sites, will translate

84 ole of this protein in the regulation of the crosstalk between diverse developmental and stress-respo

85 Absence of spectral crosstalk between Dr-Trks and blue-light-activatable LOV

86 k within this circuit, highlighting the deep crosstalk between E2F, SCF-Cyclin F, and APC/C in regula

87 t to the great arteries, relies on a complex crosstalk between endothelial (ECs) and smooth muscle (S

88 These data suggest that a crosstalk between endothelial cells and stem cells withi

89 r, the functional relevance of the molecular crosstalk between endothelial cells and stem cells withi

90 el negative feedback mechanism that controls crosstalk between energy homeostasis and the vitamin D p

91 Pial collateral remodeling is limited by the crosstalk between EphA4-Tie2 signaling in vascular endot

92 Crosstalk between epithelial and mesenchymal cells under

93 s provide insights into how lineage-specific crosstalk between epithelium and neighboring mesenchymal

94 A prominent pathway involves crosstalk between excitatory and inhibitory synapses whe

95 arby glycinergic synapses would permit rapid crosstalk between excitatory and inhibitory synapses.

96 lastoma multiforme (GBM); however, the exact crosstalk between GAMs and glioblastoma cells is not ful

97 Whether there is reciprocal crosstalk between glioblastoma and neurons remains poorl

98 sor in liver cancer and establish a critical crosstalk between hepatocyte metabolism and HSC senescen

99 Thus, PRMT5-mediated crosstalk between histone marks contributes to its funct

100 Here, our current understanding of receptor crosstalk between IL-4R and BCR is summarized along with

101 here that epigenetic mechanisms regulate the crosstalk between IL-6 and vascular endothelial growth f

102 ects of global IL10 deletion, and that local crosstalk between IL10-producing immune cells and adipoc

103 nt of the cilia proteome that is involved in crosstalk between immune and nonimmune cells in various

104 n ADPKD but rather plays a major role in the crosstalk between immune and tubular cells that shapes d

105 suggesting its potential role in mediating a crosstalk between inflammation and trophoblast different

106 Immune cell-derived exosomes can mediate crosstalk between innate and adaptive immunity and regul

107 nized, sensitized signaling clusters, direct crosstalk between integrin and growth-factor-signaling,

108 Molecular crosstalk between intra-tumor blood vessels and tumor ce

109 Spectral crosstalk between isotopes was more likely mediated by h

110 Here, the complex crosstalk between juvenile hormone (JH) and the two nutr

111 This crosstalk between kynurenine metabolism and the MAS may

112 y offers a key insight into the mechanism of crosstalk between linkage-specific ubiquitylation at DNA

113 id metabolic genes, indicating the potential crosstalk between lipid metabolism and immune response.

114 Crosstalk between liver and skeletal muscle is vital for

115 inst P. aeruginosa infection by facilitating crosstalk between macrophages and neutrophils via regula

116 This study provides evidence for a two-way crosstalk between macrophages and nociceptors in the per

117 roliferative cell components in the TME, the crosstalk between macrophages and Tregs contributes to p

118 ffecting intrinsic cancer cell signaling and crosstalk between malignant cells and the microenvironme

119 in gene expression are driven by distinctive crosstalk between mesenchymal and epithelial subsets of

120 ering of cell-free systems by exploiting the crosstalk between metabolic networks in cells, leading t

121 Substantial evidence implicates crosstalk between metabolic tissues and the immune syste

122 hydrolysis, and allows for the bidirectional crosstalk between mitochondria and lysosomes and the reg

123 ltogether, our study reveals the mechanistic crosstalk between mitochondrial translation, mitochondri

124 spectraplakin Short-stop (Shot) promotes the crosstalk between MTs and actin, which leads to the exte

125 itions could slow down tumour growth through crosstalk between muscle, adipose tissue and tumour.

126 Finally, crosstalk between Na(V)1.5 channels and mitochondria was

127 Crosstalk between neighboring cells underlies many biolo

128 essential role in brain homeostasis and the crosstalk between neural cells and the periphery.

129 se (AD) is arguably the clearest instance of crosstalk between neurodegenerative and cerebrovascular

130 Here, we propose that the crosstalk between neurotransmission and neuroinflammatio

131 A better understanding of the crosstalk between NRF2 and primary cilia/Hh signaling co

132 des new insight into the molecular nexus for crosstalk between oncogenic signaling and RTK traffickin

133 Under stress conditions crosstalk between organelles and cell to cell response i

134 cellular trafficking, facilitating signaling crosstalk between organelles.

135 chemical studies and screens to decipher the crosstalk between organotypic endothelial cells and pare

136 Finally, we show that the crosstalk between osteocalcin and IL-6 is conserved betw

137 anisms that regulate the highly orchestrated crosstalk between ovarian cancer cells and various cance

138 Experimental quantification of asymmetric crosstalk between pairs of strains parametrized the mode

139 s and different cell populations, as well as crosstalk between pathways, is aiding the discovery and

140 uring energetic stress and unveil a point of crosstalk between pro-survival and pro-death pathways.

141 r results have shown that there is extensive crosstalk between RAGE and TLRs.

142 nvolvement of these peptides in facilitating crosstalk between Sertoli and germ cells to support sper

143 Spermatogenesis is supported by intricate crosstalk between Sertoli cells and germ cells including

144 Crosstalk between signaling networks can help coordinate

145 re multiple protein components; however, the crosstalk between spatially separated granules remains u

146 The crosstalk between stress granules and inflammasomes and

147 that result in chronic inflammation initiate crosstalk between stressed resident cells and infiltrati

148 ings provide new insights into the signaling crosstalk between stroma and epithelium during tissue re

149 is for dissecting the cellular and molecular crosstalk between stroma, ECM and thymocytes, and offer

150 F2alpha-RAB27B pathway additionally mediates crosstalk between stromal and endothelial cells via VEGF

151 olecular approaches, we demonstrate that the crosstalk between Target of Rapamycin (TOR) and Fibrobla

152 endent mechanisms were needed to explain the crosstalk between TGFbeta and pro-inflammatory signallin

153 ance and cooperation, and there is extensive crosstalk between the 2 to maintain this balance, includ

154 gether, our data indicate that PTPN-mediated crosstalk between the ABA signaling and AsA biosynthesis

155 in signaling in weight cycling, indicating a crosstalk between the adipose tissue and liver.

156 complex molecular mechanisms controlling the crosstalk between the adipose tissue and the cardiovascu

157 TORC1 to Rheb on the lysosome and is another crosstalk between the amino acid and growth factor signa

158 gest that Pol-beta and Ku70 coordinate 2-way crosstalk between the BER and NHEJ pathways.

159 ndothelial cells (BMECs) leads to an altered crosstalk between the BMEC niche and HSPCs, which instru

160 tic targets aimed at preserving a fine-tuned crosstalk between the different cardiac cells in order t

161 Crosstalk between the different cell death pathways like

162 network provided a global overview into the crosstalk between the different signalling pathways invo

163 tic insight into the coordinated morphogenic crosstalk between the epithelium and vasculature, we int

164 y, these findings suggest that bidirectional crosstalk between the gut and the brain may influence di

165 ds bridging the GNRs give rise to electronic crosstalk between the individual 1D channels, leading to

166 Although the precise nature of the crosstalk between the liver and other organs has not yet

167 gdoms, of cell cycle regulation, through the crosstalk between the mechanistic target of rapamycin, m

168 Importantly, a crosstalk between the microtubule-binding domain and the

169 Also, we discuss the crosstalk between the nerve fibers and the cancer.

170 Crosstalk between the oncogenic RTK hepatocyte growth fa

171 Absence of spectral crosstalk between the opto-RTKs and green fluorescent pr

172 mphasis on wingless/int-1 protein signaling, crosstalk between the pathways, and controversial result

173 ere, we demonstrate the important reciprocal crosstalk between the PI3K/AKT signal and pentose phosph

174 ng were identified as potential mediators of crosstalk between the placenta and maternal brain and fe

175 lar cholesterol levels are regulated through crosstalk between the plasma membrane (PM), where most c

176 type neurons play a sex-specific role in the crosstalk between the somatotropic and gonadotropic axes

177 Here, we reveal a dynamic two-way crosstalk between the spindle and cortical motor complex

178 ne biosynthesis, demonstrating an unexpected crosstalk between the strigolactone and karrikin signall

179 we aim to show the role of chemistry in the crosstalk between the surface physicochemical properties

180 key mediators of heart regeneration, yet the crosstalk between them is unclear.

181 ese mechanisms operates and whether there is crosstalk between them.

182 Crosstalk between theoretical and empirical research has

183 The crosstalk between these 2 major liver-residing pathogens

184 an early vulnerability to PEs and suggesting crosstalk between these lysophosphatidylcholines, phosph

185 istolochic acid nephropathy further suggests crosstalk between these repressors.

186 We therefore explored potential crosstalk between these two functionally relevant pathwa

187 olism during exercise, as well as unexpected crosstalk between this innate immune sensor and autophag

188 To explore the biological significance of crosstalk between Toll-like receptors (TLRs) and B cell

189 karyotic gene expression relies on extensive crosstalk between transcription and RNA processing.

190 mmune infiltrates, their roles in regulating crosstalk between tumor cells and T cells, and finally t

191 The crosstalk between tumor cells and the adjacent normal ep

192 nto the mechanism of infiltrative nature via crosstalk between tumor cells and their microenvironment

193 d importance of functional heterogeneity and crosstalk between tumor cells is poorly understood.

194 K cascade is activated and fine-tuned by the crosstalk between two major insect hormones, 20-hydroxye

195 We discuss the emerging signaling crosstalk between UPR stress sensors and the DDR, as wel

196 nemes select self-renewal-promoting Wnts via crosstalk between Wnt receptors, activation of ionotropi

197 The model predicted new crosstalks between calcium/calmodulin-dependent pathways

198 on extracellular vesicle-mediated bilateral crosstalk, between glioblastoma cells and astrocytes, hi

199 emains challenging due to the high degree of crosstalk both within and between kingdoms, metabolite-f

200 teractions govern bidirectional cytoskeletal crosstalk by coordinating microtubule and actin dynamics

201 SerpinB2 influences tubule-macrophage crosstalk by supporting tubular CCL2 expression and regu

202 In mouse models, mast cell-ILC2 crosstalk can drive local inflammation.

203 under certain pathological conditions, this crosstalk can go beyond physiological control, resulting

204 -PanT) into proteoliposomes, and assayed for crosstalk during active transport.

205 ies have indicated oligodendroglial-vascular crosstalk during brain development, but the underlying m

206 ll types and dissected their transitions and crosstalk during fibrogenesis.

207 This work reports crucial cellular crosstalk during lung development involving Cyp26b1-expr

208 y illustrated dynamically changing cell type crosstalk during pathological cardiac hypertrophy but al

209 chronic HBV infection to study the pathogen-crosstalk during the different immune phases of schistos

210 e defined by proliferation state, signalling crosstalk, epigenetics and metabolism, and propose an up

211 This epigenetic crosstalk establishes an intragenomic conflict: silencin

212 Such a crosstalk-free duplex imaging capability of CFR enables

213 -photon methods suffer from higher levels of crosstalk from neuropil, resulting in a decreased signal

214 by ELOB/C transmitting long-range allosteric crosstalk from the substrate through CUL5 to the RBX2 fl

215 two tumor populations uncovers the paracrine crosstalk from tumor core that promotes malignancy and t

216 We also extensively survey TF-RBP crosstalk, highlighting how SUB1, a previously uncharact

217 , little is known of how the inter-organelle crosstalk impacts cancer cells owing to the lack of appr

218 involved in the OC-TME interactions, how the crosstalk impinges on OC aggression and chemoresistance

219 he landscape of dysregulated receptor-ligand crosstalk in cancer, including selective loss of functio

220 cells, supporting the importance of Wnt/Fgf crosstalk in early tracheal development.

221 ic AML infiltration and dissect the cellular crosstalk in human BM, we established humanized ex vivo

222 wledge, a novel mediator of myeloid cell-IEC crosstalk in maintaining epithelial barrier integrity, s

223 role for ILC2s and pathogenic ILC2-mast cell crosstalk in mastocytosis.

224 dase components and the consequences of this crosstalk in mediating cardiovascular disease processes,

225 mechanisms for microbiota-mediated gut-bone crosstalk in mice models of hyperparathyroidism that may

226 ts also describe a platform for RNA-mediated crosstalk in PH, providing an impetus for developing blo

227 netic pathways are involved in plant-microbe crosstalk in photosynthetic tissues compared to partiall

228 an interleukin-10 (IL-10)-dependent cellular crosstalk in the marginal zone (MZ) that promoted bacter

229 The resulting gene network exhibits reduced crosstalk in the sensing of the two different ROS.

230 indings highlight neural/stromal/immune-cell crosstalk in tissue repair, suggesting future therapeuti

231 Nevertheless, studying intercellular crosstalk in vivo remains a relevant challenge, due main

232 g networks, yielding insights into new-found crosstalks in beta-adrenergic cardiac hypertrophy.

233 red a vascular program induced by a cellular crosstalk initiated by CM, characterized by a reduction

234 that glucosinolate/phenylpropanoid metabolic crosstalk involves the transcriptional regulation of KFB

235 We further propose that crosstalk involving Notch and PP2A enables tuning and in

236 r data indicate that axonal-cancer metabolic crosstalk is a critical adaptation to support PDAC growt

237 biological processes, and disruption of this crosstalk is linked to diseases such as acute myeloid le

238 The mechanism of organ crosstalk is mediated by a feed-forward regulatory loop

239 This crosstalk is under the control of signals mediated by va

240 Organelle crosstalk is vital for cellular functions.

241 While the scope of this crosstalk is well-recognized, precise molecular links ar

242 insights into how this enteric neuro-immune crosstalk may occur.

243 onstrate that this alternative phytohormonal crosstalk mechanism integrates BR signaling into auxin-d

244 dy suggests that blockade of this reciprocal crosstalk mechanism may have a therapeutic benefit for c

245 Here, we reveal an alternative phytohormone crosstalk mechanism, revealing that BR signaling control

246 We also identify compensatory crosstalk mechanisms between Notch and Wnt signaling tha

247 ously unreported mode of platelet-neutrophil crosstalk, mechanosensitive NET production, and provide

248 synapses by local heterosynaptic plasticity crosstalk mediated by NMDAR-dependent MEK/ERK signaling.

249 ograms, potential pathologic ligand-receptor crosstalk, novel genes, and the improved injury response

250 iquitination in DNA methylation control, PTM crosstalk, nucleosome structure, and phase separation.

251 To investigate how the context-dependent crosstalk of different cell types enables physiological

252 This study aims at clarifying the crosstalk of hepatocytes (HC), hepatic stellate cells (H

253 uglycemic clamp, and postprandial interorgan crosstalk of lipid and glucose metabolism was evaluated,

254 HSC play a crucial role in the cellular crosstalk of rapid liver regeneration.

255 The responsivity of the hypothalamus and the crosstalk of the hypothalamus with reward-related brain

256 This crosstalk orchestrates Wnt signaling, ESC polarization,

257 veal an elaborate co-transcriptional histone crosstalk pathway involving the consecutive ubiquitylati

258 ived Notch signalling, and that this stromal crosstalk pathway underlies inflammation and pathology i

259 rrelate with alterations of microglia-neuron crosstalk pathways and have long-lasting effects, both a

260 fic data and identify main reactions and new crosstalks regulating context-specific response.

261 lling and its role in colon-bladder neuronal crosstalk remain elusive.

262 tors; however, the molecules mediating their crosstalk remain incompletely understood.

263 ut the basic molecular events mediating this crosstalk remain poorly understood.

264 stence of gonadal steroid-sensitive neuronal crosstalk remains undefined.

265 oviding further evidence for a bidirectional crosstalk.SIGNIFICANCE STATEMENT The interaction of the

266 pread beyond their captured regions and 24nt crosstalk siRNAs were linked with CHH methylation.

267 on, hardware versus object scatter, spectral crosstalk, spatial resolution, spatial registration accu

268 ns is underpinned by complex auxin-cytokinin crosstalk that is regulated, at least in part, by change

269 inpoint NAV1 as a key player in the actin-MT crosstalk that promotes MT persistence at the GC periphe

270 are two major issues, optical and electrical crosstalk, that need to be addressed when the pixel dime

271 teins, GAS2-like 1 (G2L1) regulates actin-MT crosstalk through its associations with plus-end microtu

272 that responds to a plant cytokinin, without crosstalk to extant pathways.

273 ntiviral cells, participate in innate immune crosstalk underlying mucosal antifungal immunity.

274 Cellular crosstalk was investigated in vitro.

275 Pronounced functional crosstalk was observed between the two receptors in 5-HT

276 cteria-tumor cell interactions and metabolic crosstalk were extensively studied by measuring the kine

277 blue spectral region ensures the absence of crosstalk with a number of orange/red fluorescent protei

278 ar dendritic cells required CXCL12-dependent crosstalk with B cells and dictated GC output by retaini

279 mucosal layer, which is accomplished through crosstalk with enterocytes and other immune cells.

280 ation of lysine 79 in histone H3 and explain crosstalk with histone H2B ubiquitination.

281 dead hepatocytes instigate the profibrogenic crosstalk with HSC and macrophages, including the reacti

282 ignalling interactions with cancer cells and crosstalk with infiltrating leukocytes.

283 lth, covering its role in tumorigenesis, its crosstalk with innate immunity responses and its potenti

284 stabilizing Lin28, but also participated in crosstalk with Lin28 mRNA through competition for miR-12

285 nic periventricular endothelial cells (PVEC) crosstalk with neural progenitor cells (NPC) promoting m

286 ia coli that exhibit concentration-dependent crosstalk with non-cognate ROS.

287 infarction (MI); however, how these factors crosstalk with other cell types mediating repair is not

288 ction, regulation by accessory proteins, and crosstalk with other GPCRs.

289 The extensive crosstalk with other pathways implicated in cardiomyocyt

290 This PTHrP-PPR signaling appears to crosstalk with other signaling pathways and regulates pr

291 Besides regulation of gene expression, its crosstalk with protein phosphorylation is vital for cell

292 eroid models and established uncharacterized crosstalk with RAB/RHO.

293 Through modulating immune responses and via crosstalk with surrounding renal cells, lymphatic vessel

294 issue-specific carcinogens and their complex crosstalk with the compromised DNA repair machinery of B

295 We discuss nerve fiber crosstalk with the main different components of the tumo

296 g cells within the mammalian brain and their crosstalk with the periphery in both health and disease.

297 Furthermore, mitochondria can engage in crosstalk with the tumor microenvironment, and signals f

298 O (Small Ubiquitin-related Modifier) pathway crosstalks with the ubiquitin-proteasome pathway to affe

299 r, AKI dramatically modified ligand-receptor crosstalk, with potential pathologic epithelial-to-strom

300 This function requires an intensive crosstalk within liver cellular structures, but also wit