ライフサイエンスコーパス: secretion of

1 and gut microbial components that alter the secretion of 5HT.

2 e CNS axon regeneration in vivo, in part via secretion of a cocktail of growth factors.

3 h the activation of innate immunity, through secretion of a cytokinome that elicits recruitment and p

4 munication is mediated by the production and secretion of a hexapeptide (AimP) during lytic cycle.

5 model successfully predicts the increase in secretion of a monoclonal antibody after silencing a hig

6 elta-proteobacterium Myxococcus xanthus, the secretion of a novel biosurfactant polysaccharide (BPS)

7 um stimulation results in rapid cleavage and secretion of a POLGARF C-terminal fragment.

8 the inhibition of mutated EGFR promotes the secretion of a potent vasoconstrictor, endothelin-1 (EDN

9 cells to inflammatory M1 phenotype with the secretion of a proinflammatory chemokine CXCL10 due to a

10 r, our results demonstrate that the exosomal secretion of a psychosis-altered and glial-enriched miRN

11 Each ESX system mediates the secretion of a specific set of Esx, PE, and PPE proteins

12 ption may lead to defects in trafficking and secretion of a subset of proteins required for parasite

13 eased APP processing, resulting in increased secretion of Abeta peptides and an increased Abeta38 to

14 We directly demonstrate the secretion of acetylcholine (ACh) from BC upon stimulatio

15 ar autoactivation and constitutive low-grade secretion of activated FXII.

16 Secretion of activin A is known to be higher in tissues

17 Bacterial DNA and CpG DNA induce the secretion of ADAM10-bearing exosomes from human cells as

18 early (within 5-10 s following stimulation) secretion of ADP specifically dependent on SERCA3 stored

19 Hepatocytes were functional, based on secretion of albumin and apolipoprotein B and cytochrome

20 cient in deconstructing plant biomass by the secretion of an arsenal of plant cell wall-degrading enz

21 derlying mechanisms are unclear, but involve secretion of an unidentified mitogenic factor.

22 production of proinflammatory cytokines and secretion of anti-inflammatory cytokines that limit immu

23 increased TLR3 gene expression and increased secretion of anti-viral and pro-inflammatory cytokines (

24 paired spiral artery remodeling and abnormal secretion of antiangiogenic factors are thought to be im

25 gest that starvation-specific unconventional secretion of antioxidants and Acb1-like activities maint

26 nsporter to the cell membrane and diminished secretion of apoE.

27 om the intestine and liver via synthesis and secretion of apolipoprotein B (apoB)-containing lipoprot

28 can serve as a stand-alone signal to trigger secretion of autoreactive and class-switched IgG in vivo

29 itide 3-kinase (PI3K), have highly penetrant secretion of autoreactive IgM antibodies.

30 genesis is type 4b secretion system-mediated secretion of bacterial effectors into host cells that su

31 re essential for nuclear positioning and for secretion of basement membrane components via retrograde

32 ment epithelial (RPE) cells showed increased secretion of bFGF and conditioned medium from these cell

33 Active secretion of bile salts into the canalicular lumen drive

34 novel cancer-suppressing mechanism, via the secretion of bioactive factors by mammary cells, that is

35 The Ii-fur molecule directed secretion of both Ags in African green monkey cells and

36 5, Na(+) channels to control Ca(2+)-mediated secretion of both mucin 2 (MUC2) and MUC5AC from HT29-18

37 tor (G-CSF)-induced HSC mobilization via the secretion of calcitonin gene-related peptide (CGRP).

38 Although inappropriate tumoral secretion of calcitriol is typically associated with lym

39 PCE also induced the secretion of calprotectin (myeloid-related protein 8/14

40 (2020) show that the secretion of cancer-linked forms of mutant calreticulin

41 ed protein glycosylation, leading to reduced secretion of cancer-promoting growth factors, such as ch

42 VC treatment reduced activation and cytokine secretion of CD8(+) T cells via a CCR5-independent pathw

43 Pollen tube tip growth depends on balancing secretion of cell wall material with endocytic recycling

44 conditions increased apical and basolateral secretion of cGMP relative to the level under static con

45 Airway secretions of children infected with RSV, have significa

46 The size of the lumen is dependent on apical secretion of chloride ions, most notably by the CFTR cha

47 The secretion of chorionic gonadotropin by TSC-derived ST re

48 the mechanisms for post-Golgi transport and secretion of chylomicrons have not been identified.

49 How different ESX systems achieve specific secretion of cognate substrates remains elusive.

50 at these proteolytic maturations occur after secretion of collagen VI tetramers and during microfibri

51 Despite the secretion of compensatory IgM into the gut lumen, sIgAd

52 shape pathogen-specific immunity by inducing secretion of costimulatory cytokines during T-cell activ

53 injury, the neuroendocrine system increases secretion of counterregulatory hormones that promote rap

54 , IL-1beta, Ec-LPS, or Pg-LPS, increased the secretion of CSF-1 (P < 0.05) and Ec-LPS stimulation inc

55 Inflammatory stimuli increased the secretion of CSF-1 and IL-34 with comparable levels meas

56 ation of the model resulted in the polarized secretion of CXCL10, IL-8 and CCL-20 by IEC and could ef

57 etion of IL-1beta was undetectable, inhibits secretion of CXCL8 (P = 0.004).

58 elial cell height and apical and basolateral secretion of cyclic GMP (cGMP) under baseline, unstimula

59 HLA suppresses lipopolysaccharide-stimulated secretion of cytokines and expression of pro-inflammator

60 itical role in fibroblast activation through secretion of cytokines and growth factors.

61 the proinflammatory response, leading to the secretion of cytokines that help to orchestrate the immu

62 MC effector responses intact, including the secretion of cytokines via constitutive exocytosis.

63 phils and macrophages, the bacterial-induced secretion of cytokines was Fap2 independent.

64 was important for phosphorylation of p38 and secretion of cytokines.

65 We identify Lyn as a critical component for secretion of Dengue and Zika infectious particles and th

66 sponses, such as target cell killing and the secretion of different cytokines, that collectively cont

67 exity, however, obfuscates its impact on the secretion of different proteins.

68 otes many of the hallmarks of cancer via the secretion of diffusible factors that can affect cancer c

69 ncreas, exocrine and endocrine cells control secretion of digestive enzymes and production of hormone

70 us aureus in multiple tissue settings by the secretion of diverse cytokines.

71 influence Golgi/ER morphology and affect the secretion of diverse proteins across many tissues.

72 Secretion of ECM protein fibronectin (FN) by BM stromal

73 ion system (T3SS), which engages in one-step secretion of effectors(4), despite possessing a Sec sign

74 n in Hep3B cells also caused a defect in the secretion of endogenous EPO under conditions mimicking h

75 nt tau expressing primary neurons, while the secretion of endogenous wild-type tau was not affected.

76 at SURF4 overexpression results in increased secretion of EPO, suggesting a new strategy for more eff

77 R cargo receptor that mediates the efficient secretion of EPO.

78 an inducible gene circuit for the on-demand secretion of erythropoietin.

79 res ESX-5 for virulence, it tightly controls secretion of ESX-5 substrates to avoid elimination by ho

80 PE35/PPE68_1 determines the system-specific secretion of EsxB_1/EsxA_1.

81 The secretion of EVs from MRSA under antibiotic stressed con

82 ermeabilization and inflammation through the secretion of exosomal damage-associated molecular patter

83 itor, abrogated this process and cut off the secretion of exosomal PD-L1 by blocking the transcriptio

84 Mechanistically, secretion of exosomes by these spheres was essential for

85 es demonstrated that Nischarin regulated the secretion of exosomes from breast cancer cells.

86 ow inflammation alters cargo specificity and secretion of exosomes is unknown.

87 on of only one allele of Nischarin increased secretion of exosomes, and Rab14 activity modulated exos

88 ere, we present a method for stimulating the secretion of exosomes.

89 Their activation leads to robust secretion of exosomes.

90 Host cell contact triggers secretion of ExsE and sequestration of ExsD by ExsC to c

91 cells (HSCs), which promotes production and secretion of extracellular matrix (ECM) proteins and hep

92 ipid metabolism, unfolded protein responses, secretion of extracellular matrix proteins, and cell pro

93 broblasts to control their proliferation and secretion of extracellular matrix proteins.

94 oteomes, demonstrating that ECs polarize the secretion of extracellular vesicle cargoes to the apical

95 ophagy and exosome biogenesis leading to the secretion of extracellular vesicles (EVs) in vivo and ex

96 ion in Slac2-b-mutant KCs as well as reduced secretion of extracellular vesicles containing extracell

97 ng and pearled membrane structures and drive secretion of extracellular vesicles.

98 autocrine growth and significantly decreases secretion of FGF2-containing exosomes, resulting in less

99 pore, the key intermediate in unconventional secretion of FGF2.

100 location intermediates during unconventional secretion of FGF2.

101 Both infection groups had higher levels of secretion of gamma interferon (IFN-gamma), tumor necrosi

102 Secretion of glucagon from the pancreatic alpha-cells is

103 actors, which ultimately drive the pulsatile secretion of gonadotropin-releasing hormone.

104 orrect localization of GRAs into the PVM and secretion of GRA effectors into the host cytoplasm.

105 oid cells that promote tumorigenesis through secretion of growth- and survival-promoting cytokines th

106 ose and palmitate to produce Acetyl-CoA, and secretion of heparan sulfate proteoglycan (component of

107 ic acid polymers (NAPs) inhibit assembly and secretion of hepatitis B virus (HBV) subviral particles.

108 tric surgery results in increased intestinal secretion of hormones GLP-1 and anorexigenic PYY, which

109 g in microbial growth, phagocytic attack and secretion of host antimicrobial factors.

110 Our data support the concept that secretion of host peptides results in an environmentally

111 gingivalis in dual-species biofilms via the secretion of hydrogen peroxide (H(2)O(2)).

112 s pathway is conserved and implicated in the secretion of hydrolytic enzymes and toxins for a range o

113 mor-infiltrating CD8(+) T cells and elevated secretion of IFN-gamma, Cxcl9, and Cxcl10 in tumor micro

114 tentially exploited to prevent inappropriate secretion of IFN-I in autoimmune diseases or promote IFN

115 :C significantly enhanced the expression and secretion of IFNgamma, IDO, and HLA-G.

116 doses of WS-CM abolished agonist-stimulated secretion of IFNgamma, TNF and IL-2 proteins.

117 play an important role in allergies through secretion of IgE.

118 ally, nonfailing hMSCs exhibited >25x higher secretion of IGF (insulin-like growth factor)-1 compared

119 to the M2 phenotype, thereby increasing the secretion of IGF-1 and CCL20, which promoted tumor progr

120 In many cases, secretion of IL-1 cytokines appears to be closely couple

121 ws, whereas only clinical cows had increased secretion of IL-10, IL-12, and IL-18 upon stimulation of

122 egs provide cytoprotection for CEnCs through secretion of IL-10, indicating potentially novel therape

123 A higher secretion of IL-13 and IL-5 was detected in presence of

124 cyte integrin alpha3beta1 in controlling the secretion of IL-1alpha, a paracrine factor that regulate

125 inhibits (P < 0.0001) NT-stimulated (10 nM) secretion of IL-1beta (at 1 ng/mL) and CXCL8 (at 100 ng/

126 the NLRP3-caspase-1-mediated processing and secretion of IL-1beta and IL-18 and induces the inflamma

127 masomes, enabling processing, and facilitate secretion of IL-1beta and IL-18, as well as other signal

128 tivity did not attenuate CD11c expression or secretion of IL-1beta and MCP-1.

129 ex II formation, driving pyroptosis, and the secretion of IL-1beta in response to LPS alone.

130 Secretion of IL-1beta is a good surrogate of the differe

131 /mL) of embryonic microglia (HMC3), in which secretion of IL-1beta was undetectable, inhibits secreti

132 a(-/-) bone marrow-derived DCs show enhanced secretion of IL-1beta, whereas production of IL-10 and I

133 nd pro-IL-1beta, resulting in TLR4-dependent secretion of IL-1beta.

134 lp to CD11c(+) T-bet(+) B cells via the dual secretion of IL-21 and IFN-gamma in a CD40/CD40L-depende

135 rly step in the processing, mobilization and secretion of IL-33 by the airway epithelium.

136 y or reducing protein expression blocked the secretion of IL-33.

137 he endothelium, and we identify the distinct secretion of IL-6 as the paracrine cause of PI3Kalpha(H1

138 matory cell infiltration, iron overload, and secretion of IL-6 in lavage fluid.

139 ls of CD83, CD86, HLA-DR and CD54, increased secretion of IL12 and IL10 and higher tumour-antigen (TA

140 nzyme to the cellular surface and stimulated secretion of IL1beta.

141 ells from HDM +/- DEP exposed ST2(-/-) mice, secretion of IL5, IL13, IL6 and IL17A was abrogated by a

142 bility of CTB 100,000 g EVs to increase dESF secretion of IL8.

143 The mechanisms underlying the secretion of immunomodulatory RNA and DNA by pathogens s

144 recruitment of tolerogenic immune cells, and secretion of immunosuppressive cytokines.

145 e-up of human EEC subtypes and the regulated secretion of individual hormones.

146 In response to secretion of inflammatory cytokines (e.g., IL1B) from im

147 of NFkappaB, followed by the expression and secretion of inflammatory cytokines (IL [interleukin] 1B

148 r potential for virulence and did not induce secretion of inflammatory cytokines by epithelial cells.

149 profloxacin resistance and ability to induce secretion of inflammatory cytokines by HT-29 intestinal

150 Failing hMSCs exhibited increased secretion of inflammatory cytokines IL (interleukin)-1be

151 the cleavage of cysteine protease caspase-1, secretion of inflammatory cytokines, and induction of in

152 which promoted glycogen accumulation and the secretion of inflammatory cytokines, including interleuk

153 SMase in monocytes/macrophages inhibited the secretion of inflammatory mediators IL-1beta and MCP-1.

154 Astrocyte secretion of Inhibin A and downregulation of oligodendro

155 ues based on chemotactic cues and modulating secretion of instructive regenerative molecules in respo

156 Moreover, the secretion of insulin and C-peptide decreased.

157 lucose levels and reciprocally regulates the secretion of insulin and glucagon.

158 cretory granules (SGs) mediate the regulated secretion of insulin, which is essential for glucose hom

159 s in beta-cells, including the synthesis and secretion of insulin.

160 nd expand APCs in the tumor and induce local secretion of interferon beta (IFNbeta), which is a pro-i

161 lls increased numbers of intracellular 11G5, secretion of interleukin (IL) 6 and IL8, and markers of

162 Activation of inflammasomes induces the secretion of interleukin (IL)-1beta and IL-18 and drives

163 entration induces proteolytic processing and secretion of interleukin (IL)-33, a critical cytokine in

164 rATG exposure further resulted in hampered secretion of interleukin (IL)-7, IL-15, and IL-6, cytoki

165 ype characterized by elevated production and secretion of interleukin (IL)6.

166 ion of the NLRP3 inflammasome and consequent secretion of interleukin 1beta (IL-1beta).

167 ducing activation of the NLRP3 inflammasome, secretion of interleukin-1beta and interleukin-18, and p

168 ice destabilized Nfkappab1 mRNAs and reduced secretion of interleukin-2 (IL2) and interferon-gamma (I

169 roinflammatory response characterized by the secretion of interleukin-8 (IL-8; also called CXCL8) and

170 Increased secretion of interleukin-8 and higher expression levels

171 with IPF-RC during differentiation increases secretion of IPF biomarkers and RNA sequencing (RNA-seq)

172 velopment of a complex hard tissue, from the secretion of its organic macromolecular template to the

173 -expressing keratinocytes displayed abnormal secretion of key mediators of innate immunity.

174 s treated with drugs that block synthesis or secretion of lactate mimic the pgk1- / - phenotype, wher

175 hanisms to escape neutrophils, including the secretion of leucocidins (e.g. ionomycin).

176 l than controls, suggesting impaired hepatic secretion of lipid.

177 tioning is critically dependent on pulsatile secretion of luteinising hormone (LH).

178 inhibited lysosomal exocytosis, whereby the secretion of lysosomal-associated membrane protein 1 (LA

179 In vitro secretion of M-CSF by LPS-stimulated peripheral monocyte

180 nisms, partly by reducing the expression and secretion of macrophage colony-stimulating factor CSF1 b

181 The production and secretion of matrix proteins upon stimulation of fibrobl

182 tributes to age-related diseases through the secretion of matrix-degrading and inflammatory molecules

183 of exocyst, Endosidin2, reversibly augmented secretion of mature WPBs containing HMW forms of VWF.

184 nt dysregulation, Th2 skewing, and increased secretion of MCP-1.

185 These findings show that the secretion of metabolites belonging to the kynurenine pat

186 Our data indicate that secretion of miRNAs in EVs from the airway epithelium, i

187 required for PRR- and live bacterial-induced secretion of multiple cytokines.

188 vation in acetogens and accurately predicted secretion of multiple fermentation products.

189 non-traditional mechanisms such as increased secretion of myokines.

190 plays an important role in the synthesis and secretion of nectar sugar.

191 T, and allowed the selective translation and secretion of nerve growth factor (NGF) by PDAC cells to

192 141716A up-regulated KLF4 and STAT6, reduced secretion of Netrin-1, and increased migration toward th

193 Regulated secretion of neuropeptides and peptide hormones by secre

194 TGN is a key compartment for the sorting and secretion of newly synthesized proteins.

195 cidual stromal cell (dESF) transcription and secretion of NF-kappaB targets, including IL8, as measur

196 d insulin ((pro)insulin) content and insulin secretion of NIT-1 cells, autophagy inhibition using baf

197 tes development and aging in response to the secretion of numerous insulin peptides.

198 C. difficile infection is dependent on the secretion of one or more AB-type toxins: toxin A (TcdA),

199 The secretion of organic solutes by the proximal tubules is

200 cells have adapted to reduce expression and secretion of other expensive host cell proteins.

201 Vaginal secretions of p.o.-immunized animals neutralize Chlamydi

202 y, SLE LL37-specific T-cells promoted B-cell secretion of pathogenic anti-LL37 antibodies in vitro.

203 tion of effector T-cell function and ensuing secretion of pathogenic cytokines (eg, IL-17, interferon

204 d DCs and monocytes from blood and bronchial secretions of patients with varying COVID-19 severity an

205 The secretion of peptides and proteins is essential for surv

206 , while stage three was characterised by the secretion of phytotoxins, including colletotrichin and c

207 hormone (GnRH) leads to a marked decrease in secretion of pituitary gonadotropins LH and FSH and impa

208 er iron deprivation that is dependent on the secretion of plant-derived coumarins.

209 l tubular epithelial cells, resulting in the secretion of pro-fibrotic cytokines, thereby promoting i

210 ndent activation of NF-kappaB and consequent secretion of pro-inflammatory chemokine, CXCL1.

211 creased intestinal permeability and enhanced secretion of pro-inflammatory cytokines compared to NC c

212 ited effect on the viability of HBMEC or the secretion of pro-inflammatory cytokines or chemokines, e

213 Higher secretion of pro-inflammatory cytokines was seen in colo

214 ability of the viral protein to suppress the secretion of pro-inflammatory cytokines.

215 xposure of Kupffer cells to gp96 induced the secretion of pro-inflammatory cytokines.

216 ular senescence that is characterized by the secretion of pro-inflammatory molecules that promote the

217 with low fibrogenic features; and increased secretion of pro-tumor cytokines and CXCR2 ligands, util

218 lammasome assembly drives the maturation and secretion of proinflammatory cytokines and induces pyrop

219 Besides, inhibition of p38 suppressed the secretion of proinflammatory cytokines and promoted auto

220 ell lines or primary CML cells, resulting in secretion of proinflammatory cytokines and specifically

221 Increased secretion of proinflammatory cytokines by macrophages in

222 evelopment of inflammation by activating the secretion of proinflammatory cytokines, IL-1beta and IL-

223 ading to irreversible cell cycle arrest, and secretion of proinflammatory cytokines.

224 F-kappaB pathways that eventually led to the secretion of proinflammatory cytokines.

225 acrophage functions, regulatory T cells, and secretion of proresolving mediators.

226 COX2 is critical for the secretion of prostaglandin E2 and was strongly induced b

227 chinery, which enables the glucose-dependent secretion of protective immunomodulatory factor interleu

228 tate in solution and (ii) the production and secretion of redox-active, P. aeruginosa-produced phenaz

229 such threats by increasing the synthesis and secretion of renin.

230 ith Helicobacter pylori stimulates increased secretion of Rspo by myofibroblasts, leading to an incre

231 motes endoplasmic-reticulum localization and secretion of S100b-a protein that lacks a signal peptide

232 ssion of proteins involved in biogenesis and secretion of sEV, and triggered co-localization of multi

233 te transporter G2 (ABCG2) is involved in the secretion of several compounds in milk.

234 e show that Rab13 additionally regulates the secretion of sEVs corresponding to both traditional exos

235 s with loss or inhibition of PRKD1 increased secretion of sEVs; loss of PRKD1 reduced phosphorylation

236 ed mechanisms responsible for biogenesis and secretion of SGs, but how SGs mature remains poorly unde

237 Secretion of siderophores and organic acids as biochemic

238 coincide with cell wall synthesis, while the secretion of SlpA from the cell is relatively delocalize

239 We conclude that this delocalized secretion of SlpA leads to a pool of precursor in the ce

240 Overall, AM secretion of SOCS3 within EVs serves as a brake on airwa

241 Intercellular communication through the secretion of soluble factors plays a vital role in a wid

242 ty, a notion that was confirmed by increased secretion of soluble TNFR2.

243 we have shown that low oxygen increased the secretion of STC-1 but it required co-stimulation with t

244 th a cell wall-editing enzyme to mediate the secretion of substrate proteins from the periplasm to th

245 Selective secretion of succinate is facilitated by its transient p

246 manipulate stem cell homeostasis by inducing secretion of TGF-beta while protecting infected HPCs fro

247 ke, costimulatory molecule upregulation, and secretion of Th1 (IL-12)- and Th17 (IL-23, IL-1beta, and

248 ver, microbe-activated monocytes induced the secretion of Th17 and monocyte-recruiting chemokines CCL

249 ver, microbe-activated monocytes induced the secretion of Th17 and monocyte-recruiting chemokines che

250 and that this effect is counteracted by the secretion of the bacterial effector CT622/TaiP (transloc

251 In this study, we show that, in addition to secretion of the Breg immunosuppressive cytokines IL-10,

252 mechanism dependent on plant iron import and secretion of the coumarin fraxetin.

253 ues in vivo was then confirmed by monitoring secretion of the effector ExoU.

254 Importantly, we show that secretion of the engineered enzyme can aid the interming

255 Secretion of the enzyme requires a Type II secretion sys

256 system, also resulted in redirection and co-secretion of the Esx pair via ESX-5.

257 r, indicating that this pair could stimulate secretion of the EsxB_1/EsxA_1 pair.

258 Maximal secretion of the gonadotropin Luteinizing Hormone is sup

259 Secretion of the ligand prolactin by adjacent lung strom

260 ellular accumulation of amyloid precipitate, secretion of the major curli subunit, CsgA, is tightly r

261 variant resulted in impaired processing and secretion of the mature peptide.

262 ttach to substrates and the biosynthesis and secretion of the mucilage compounds of the Arabidopsis s

263 Proper secretion of the PE-PPE proteins requires the presence o

264 olumella cells provide a feedback signal via secretion of the peptide CLAVATA3/ESR-RELATED40 (CLE40),

265 lved in pollen tube attraction, and promotes secretion of the pollen tube chemoattractant LURE1.2.

266 i severely damages white button mushrooms by secretion of the pore-forming toxin tolaasin, the main v

267 atory function of hypoxic CAFs by decreasing secretion of the pro-angiogenic factor VEGFA and consequ

268 ound superior to ceftriaxone in reducing the secretion of the pro-inflammatory cytokine IL-8 by endoc

269 n vitro, and attenuates chemotherapy-induced secretion of the pro-inflammatory cytokines TNFalpha, IL

270 Because secretion of the profibrotic connective tissue growth fa

271 ls within 6 days, significantly decrease the secretion of the proinflammatory cytokine IL-6, and, via

272 In turn, Fap2-dependent invasion induced the secretion of the proinflammatory cytokines IL-8 and CXCL

273 n the presence of farnesol, there is reduced secretion of the Th1-inducing cytokine, IL-12, and incre

274 Macrophage production and secretion of these homeostatic factors are controlled by

275 Secretion of these proteins also occurs from activated c

276 induced CD62P expression; HMGB1 release; and secretions of thromboxane A(2), CXCL7, and IL-33 by mous

277 ed expression of costimulatory molecules and secretion of TNF and IL-1beta.

278 effect, as represented by a decrease in the secretion of TNFalpha, IL6 and IL12/IL23 (IL12p40) proin

279 otein that is essential for the assembly and secretion of triglyceride (TG)-rich, apoB-containing lip

280 anistically we found that TFEB regulates the secretion of truncated mutant tau lacking MTBR and this

281 tion still increases the ER stress-dependent secretion of TTR in non-native conformations under these

282 ed with CD200-coated particles decreased the secretion of tumor necrosis factor-alpha (TNF-alpha).

283 loid precursor protein in neurons and in the secretion of tumor necrosis factor-alpha from microglial

284 isms of chaperone-mediated stabilization and secretion of two distinct families of T6SS membrane prot

285 C3s) maintain intestinal homeostasis through secretion of type 3 cytokines such as interleukin (IL)-1

286 brosis) with nM concentrations of C9 reduced secretion of type I collagen.

287 ral nucleic acids induces the expression and secretion of type I IFNs (IFN-Is), important mediators o

288 by transcriptionally repressing STAT1/2 and secretion of Type I Interferons (IFNs).

289 rons.IMPORTANCE Viral infection triggers the secretion of type I interferons, which in turn induce th

290 ptidase to facilitate secretion, whereas the secretion of Typhoid toxin in Salmonella enterica serova

291 ly sculpt their microenvironment through the secretion of various cytokines, chemokines, and other fa

292 to nuclear factor-kB (NF-kB) activation and secretion of various cytokines.

293 eMSCs displayed robust and stable secretion of vascular endothelial growth factor (VEGF),

294 or cells via EMT cell-induced production and secretion of VEGF-C.

295 can be potentially achieved by detecting the secretion of volatile sulfur compounds (VSCs) in oral ca

296 GCs) are potent anti-inflammatory drugs, the secretion of which is mediated and controlled by the hyp

297 lly, loss of p53 in cancer cells induced the secretion of WNT ligands that stimulate tumour-associate

298 The secretion of Wnt ligands, the turnover of Wnt receptors,

299 r porcupine, both of which are essential for secretion of Wnts, caused misrotated sensory cells and s

300 old insulin SGs, revealing that preferential secretion of younger granules occurs in glucose-stimulat