ライフサイエンスコーパス: secretion by

1 indicated that the enhancement of stimulated secretion by 0.1 ng/ml IL-1beta was mediated by the NF-k

2 Asn-168, Asn-538, and Asn-745 reduced rhDAO secretion by 13, 71, and 32%, respectively.

3 r reduction also decreases SP-stimulated TNF secretion by 30% (P < 0.05), suggesting an interaction b

4 50% (P < 0.001), and ST2 siRNA decreases TNF secretion by 30% (P < 0.05), when stimulated by SP and I

5 oss in people with obesity decreased insulin secretion by 35% even though insulin sensitivity did not

6 nondiabetic individuals, with lower insulin secretion (by 4% per copy, P = 4.1 x 10(-6)).

7 L) in combination also greatly stimulate TNF secretion (by 4,500-fold).

8 receptor antagonists and siRNA inhibits TNF secretion by 50% (P < 0.001) when stimulated by SP and I

9 tibody for IL-33 receptor, ST2, inhibits TNF secretion by 50% (P < 0.001), and ST2 siRNA decreases TN

10 ecreased very-low-density lipoprotein (VLDL) secretion by 50%.

11 n by 2.6-fold and 4.3-fold respectively, and secretion by 60% (from 1208.1 +/- 186 to 1934.4 +/- 135

12 ATPase activity reduced only N249Q/R345W F3 secretion (by 62%), demonstrating this variant's unique

13 7 +/- 1.7% and RANKL by 73 +/- 2.4%, and OPN secretion by 74 +/- 10%.

14 kHz and 27.1 mT significantly increased SEAP secretion by ~ 82% relative to control cells, with lesse

15 8/538/745 triple substitutions reduced rhDAO secretion by 85 and 94%.

16 mycin treatment selectively reduced R345W F3 secretion by 87% (vs. WT F3).

17 africanum L6 lineages, that restores ESAT-6 secretion by a PhoPR-independent mechanism.

18 ue to interruption in a balance between CCL2 secretion by a variety of cells and its uptake by consti

19 have now been shown to contribute to protein secretion by A. baumannii and other pathogenic species o

20 Syk mediates elevated IL-1beta secretion by activating ERK1/2, and both Syk and ERK1/2

21 Additionally, stimulation of IL1beta secretion by activation of c-Met induced tumor-associate

22 essin (AVP)-stimulated cAMP levels and Cl(-) secretion by ADPKD cells than inhibition of PDE1, and in

23 ed HDL (rHDL) attenuated IFN-gamma and IL-17 secretion by Ag-specific T cells upon stimulation of dra

24 egulatory molecule controlling mucus granule secretion by airway epithelial cells as well as directed

25 Active H(+) and HCO(3) (-) secretion by airway epithelial cells produce an ASL that

26 e ELISA revealed detectable amounts of SEl-K secretion by all isolates, with the highest secretion le

27 e that pancreatic Hhip gene inhibits insulin secretion by altering islet integrity and promoting Nox2

28 yltransferase and the stimulation of protein secretion by altering the activity of signal peptidase I

29 In addition, EhMIF enhanced TNF-alpha secretion by amplifying TNF-alpha production by lipopoly

30 c concentrations of insulin inhibit glucagon secretion by an indirect (paracrine) mechanism mediated

31 4 hours decreased glucose-stimulated insulin secretion by approximately 30% without affecting ATP syn

32 exposure, there is a decrease in angiogenin secretion by ARPE-19 cells, which was abrogated with a b

33 endent release of ATP triggering bicarbonate secretion by astrocytes via activation of metabotropic P

34 nd SLC26A4 (pendrin) and a persistent proton secretion by ATP12A.

35 in negatively regulating pancreatic insulin secretion by augmenting COX-2-dependent PGE2 production.

36 (+) CD4(+) T helper cells to induce antibody secretion by autologous naive B cells, higher frequencie

37 The data show that IL-10 secretion by B cells and CD1d expression on IL-10 secret

38 ATX secretion by B cells from control, but not Enpp2 knockou

39 ring B-cell activation, such as CXCL9/CXCL10 secretion by B cells.

40 and cellular senescence in promoting insulin secretion by beta cells and in regulating normal functio

41 though glucose is known to stimulate insulin secretion by beta cells, whether it directly engages nut

42 s of this hormone directly stimulate insulin secretion by beta cells.

43 ndoplasmic reticulum stress enhanced exosome secretion by beta-cells; induced exosomal release of the

44 gnaling in NHC cells; quercetin also reduced secretion by bile duct units isolated from rats.

45 ITPR3 is required for bicarbonate secretion by bile ducts, and its expression is reduced i

46 udies reveal that PITPNC1 promotes malignant secretion by binding Golgi-resident PI4P and localizing

47 Inhibition of Wnt secretion by blocking an essential post-translational mo

48 rculating and tonsil Tfh cells increased IgG secretion by blood Ag-induced, but not by BM, PCs.

49 stimulated NLRP3-dependent interleukin-1beta secretion by bone marrow-derived macrophages by activati

50 a potent stimulus for interleukin (IL)-1beta secretion by bone marrow-derived macrophages.

51 ets, since Ex-4 treatment stimulated insulin secretion by both juvenile and adult human beta cells.

52 We found that QUC inhibits IL-1beta secretion by both the NLRP3 and AIM2 inflammasome in a d

53 dicates that the negative regulation of BDNF secretion by C5L2 correlates with C5aR activation and it

54 e plasma membrane and the stimulation of its secretion by Ca(2+) and protein kinase C.

55 contrast, in IL-1beta-deficient mice, IL-12 secretion by CD11b(+) DCs prevails and supports antitumo

56 thermore, hyperlipidemic serum enhanced IL-6 secretion by CD1b+ DCs and increased IL-17A production b

57 mma and tumor necrosis factor-alpha cytokine secretion by CD4(+) T cells and antibody production pred

58 mportantly, CHQ-treated MoLC promoted IL-17A secretion by CD4(+) T cells and elevated RORC mRNA level

59 n DCs to express IL-12 and promote IFN-gamma secretion by CD4(+) T cells.

60 l proliferation (p=0.015, n=9), and IFNgamma secretion by CD4+ effector T cells (p=0.026, n=10).

61 ut instead they specifically stimulate IL-10 secretion by CD4+ T cells and efficiently mediate PSA-af

62 alpha (TNF-alpha), and interleukin 2 (IL-2) secretion by CD8(+) T cells.

63 hese acids at high titers requires efficient secretion by cell factories.

64 Exosome secretion by cells is a complex, poorly understood proce

65 Induction of IL-1beta secretion by CFT073 and tcpC-deficient CFT073 required t

66 T expression, and subsequent lower melatonin secretion by cholangiocytes, was associated with increas

67 rrini tetraspanin blocked EV uptake and IL-6 secretion by cholangiocytes.

68 njury, monocyte influx, and IL-6 and IL-beta secretion by circulating immune cells.

69 However, although effects on CCL2 secretion by co-overexpression of miR-92a/-193b and miR-

70 We demonstrated an increased secretion by cocultured cells of cytokines and chemokine

71 ages, and increased proinflammatory cytokine secretion by colon tissue and macrophages.

72 tially regulate human beta-defensin-1 and -2 secretion by colonic epithelial cells.

73 of disruption by antibiotic treatment since secretions by commensal bacteria modulate primary to sec

74 accompanied by the combination of lower IL-2 secretion by conventional CD4(+) T cells, increased IL-2

75 role in mediating glucose-stimulated insulin secretion by coupling metabolic signals to beta-cell mem

76 n cyclin-dependent kinase 4 levels and IL-12 secretion by DC.

77 leased by Vdelta2(+) cells upregulates IL-12 secretion by DCs in a positive feedback loop.

78 ound that mHtt in astrocytes impairs exosome secretion by decreasing alphaB-crystallin, a protein tha

79 een proposed that glucose regulates glucagon secretion by decreasing the conductance of either outwar

80 lodextrin also blocked ATP release and IL-33 secretion by decreasing the level of VDAC-1 expression i

81 tly induces inflammatory cytokine (TNFalpha) secretion by dendritic cells, and TNFalpha secretion is

82 n response sensor IRE1alpha supports protein secretion by deploying a kinase-endoribonuclease module

83 tion in keratinocytes, which increases IL-17 secretion by DETCs.

84 We aim to increase insulin secretion by developing strategies that work through mec

85 nflammasome activation and interleukin-1beta secretion by dietary fats.

86 s a hub molecule during collagen folding and secretion by directing other molecules to reach their ta

87 however, their effects on secondary exosome secretion by distal organs have not been explored.

88 (Th) 1 differentiation and interferon-gamma secretion by donor T cells, which is critical for inhibi

89 hanisms underlying the inhibition of insulin secretion by dopamine, which is synthesized in pancreati

90 re, TGF-beta1/ATM-initiated paracrine factor secretion by dysfunctional renal epithelium promotes int

91 ROS-dependent CypA secretion by ECs is an important signaling mechanism thr

92 escued the Golgi structure and reduced Abeta secretion by elevating alpha-cleavage of the amyloid pre

93 P gene expression was measured by RT-PCR and secretion by ELISA, luminex, or zymography.

94 succinimidyl ester dye dilution and cytokine secretion by ELISpot.

95 onset depends on the restoration of insulin secretion by endogenous beta-cells.

96 von Willebrand factor (vWF) secretion by endothelial cells (ECs) is essential for he

97 Conversely, blocking their secretion by endothelial cells using genetic, pharmacolo

98 strate that nGO-PEG indeed provokes cytokine secretion by enhancing integrin beta8-related signalling

99 (HR) expression were detected by qPCR and HA secretion by enzymatic immunoassay.

100 Proton secretion by epididymal clear cells is achieved via the

101 SP-A also decreased TNF-alpha and CXCL10 secretion by ex vivo-cultured human aMvarphis and M-CSF-

102 The reduction in postprandial insulin secretion by Ex-9 was greater in the H-GB group than in

103 suggest that oxytocin can modulate prolactin secretion by exciting TIDA neurons, and that this may se

104 secretory vesicles, which mediate regulated secretion by exocytosis.

105 he Golgi apparatus, thereby triggering their secretion by extracellular microvesicles.

106 e augmentation of glucose-stimulated insulin secretion by FA and 8-Br-cAMP in G-protein-coupled recep

107 Regulation of glucagon secretion by factors secreted by neighbouring beta- and

108 We demonstrated that the decrease in insulin secretion by fenofibrate and Wy14643 is accompanied by r

109 pithelial cell invasion is stimulated by the secretion by fibroblast of diffusible signaling molecule

110 OX-2 inhibitor celecoxib abrogates prolactin secretion by fibroblasts and reduces tumor initiation.

111 9 activity through the induction of IL-1beta secretion by fibroblasts.

112 encodes the proton pump responsible for acid secretion by gastric parietal cells.

113 Here, we show that mucus secretion by goblet cells is altered in the colon of TMF

114 IL-33-treated mice, IL-33 then induces IL-13 secretion by group 2 innate lymphoid cells and enteroid

115 In conclusion, angiogenin secretion by HCCs favors tumor development by inducing H

116 pletely abrogated TLR2-induced interleukin 8 secretion by HEK-293 cells in response to cSSSI pathogen

117 is pivotal for inflammasome-induced IL-1beta secretion by hematopoietic macrophages, microglial secre

118 ins and has significant implications in VLDL secretion by hepatocytes.

119 elevated C-C motif chemokine ligand 2 (CCL2) secretion by hepatocytes.

120 for up to 23% of the suppression of glucagon secretion by high glucose.

121 in a striking 10-fold increase in IFN-gamma secretion by HIV-1-specific CD4 T cells that is not obse

122 mor necrosis factor (TNF)-alpha and IL-1beta secretion by HL-60D cells.

123 xpression and regulation may affect glucagon secretion by human alpha-cells in response to SGLT2 inhi

124 ansion of human gammadelta T cells and IL-17 secretion by human CD4 T cells.

125 d R5-tropic) upregulates BAFF expression and secretion by human monocytes.

126 eron and stimulated proinflammatory cytokine secretion by human peripheral blood cells.

127 ly reduces lambda-light-chain production and secretion by human plasma cells regardless of sequence d

128 y constitute a target for modulating exosome secretion by human T cells.

129 risk allele showed greater induction of IL-6 secretion by hydrogen peroxide or benzo[a]pyrene diolepo

130 a direct and robust mediator of anion/fluid secretion by IECs in the human intestine.

131 evels of interleukin 10 and interferon gamma secretion by IEL, compared with injection of anti-CD3 on

132 While IgM and IgA secretion by IghPax5/+ plasma cells was normal, IgG secr

133 lates proliferation, differentiation, and Ab secretion by IgM+ B cells.

134 , and proliferation, differentiation, and Ab secretion by IgM+ B lymphocytes.

135 IL-4 secretion by ILC2s contributes to the allergic response

136 and TGF-beta1 significantly reduce cytokine secretion by ILC2s.

137 TNF is not required for IL-17A secretion by ILCs in vitro but synergizes with IL-17A to

138 this study, we assessed rhythms of cytokine secretion by immune cells and tested their response to s

139 nd related signaling to glucagon and insulin secretion by immunoassay.

140 es NGSIS, but not glucose-stimulated insulin secretion, by increasing mitochondrial proton leak.

141 h causes the repression of hydrolytic enzyme secretion by industrially relevant filamentous fungi.

142 ungus suppresses interleukin-1beta and IL-18 secretion by inhibiting both canonical and non-canonical

143 in WAT decreases leptin mRNA expression and secretion by inhibiting cAMP response element binding (C

144 e Element Binding Protein (ChREBP) and GLP-1 secretion by inhibiting glycolysis.

145 conductance regulator (CFTR)-mediated fluid secretion by inhibiting MRP4-mediated cAMP efflux.

146 expression or supplementation decreased IL-8 secretion by inhibiting Smad 3 phosphorylation.

147 till debated autocrine regulation of insulin secretion by insulin/insulin-like growth factor (IGF) 2-

148 t that microbiota dysregulation promotes LIF secretion by intestinal epithelial cells (IECs) in a mou

149 Moreover, glucagon secretion by islets from 31 donors at low glucose (1 mmo

150 ulted in enhanced proliferation and cytokine secretion by keyhole limpet hemocyanin-experienced CD4(+

151 daptors MyD88 and TRIF and required IFNgamma secretion by lamina propria lymphocytes.

152 omponents promotes p40 protein synthesis and secretion by LGG and enhances LGG-stimulated protective

153 Tomosyn causes an attenuation of insulin secretion by limiting the formation of the SNARE complex

154 endarterectomies and an analysis of protein secretion by lipid-loaded human vascular smooth muscle c

155 d A3 adenosine receptors, increases cytokine secretion by LPS activated monocytes.

156 aggregates induced NLRP3-dependent IL-1beta secretion by LPS-primed macrophages.

157 The NGF secretion by LTA-stimulated pulp fibroblasts, which is n

158 itically implicated in the modulation of NGF secretion by LTA-stimulated pulp fibroblasts.

159 silencing C5L2 significantly increases BDNF secretion by LTA-stimulated pulp fibroblasts.

160 ytes, and type I IFN blockade decreased IL-6 secretion by lupus keratinocytes.

161 found that a lack of IL-10, particularly its secretion by M s, compromised the recovery of SI epithel

162 Interleukin 1beta (IL-1beta) secretion by macrophage requires the effector caspases 1

163 ockade were associated with reduced cytokine secretion by macrophages in response to LPS and CLP, ult

164 ly impairs tumor necrosis factor (TNF)-alpha secretion by macrophages induced by Saccharomyces cerevi

165 IL-1alpha secretion by macrophages infected with ExoU-producing P.

166 DPSC/I-DPSC-mediated inhibition of TNF-alpha secretion by macrophages was abolished by pretreatment w

167 rgely reflecting increased type I interferon secretion by malignant cells and direct stimulation of i

168 ve signaling loop HK-1 promoted TNF and IL-6 secretion by MC degranulation and protein synthesis, the

169 gingivalis can dampen eATP-induced IL-1beta secretion by means of its fimbriae in a purinergic P2X7

170 primary effector pathway that modulates K(+) secretion, by metering sodium delivery to the collecting

171 thermore, we show that BM components require secretion by migrating macrophages (hemocytes) during th

172 Moreover, paracrine Hedgehog secretion by MM cells upregulated stromal CYP26 and furt

173 Rather, PDIA6 affected insulin secretion by modulating one of the activities of IRE1.

174 hese findings suggest that constitutive CCL2 secretion by monocytes and other cell types is counterac

175 otect mice from sepsis, and prevent IL-1beta secretion by monocytes from patients with CAPS.

176 serotype 2 (DENV-2) elevates mature IL-1beta secretion by monocytes independent of DENV replication b

177 ular DNA to trigger proinflammatory cytokine secretion by monocytes, in a STING- and inflammasome-dep

178 bsets on modulating proinflammatory cytokine secretion by monocytes.

179 oarthritisis associated with increased RANKL secretion by MSCs.

180 cytotoxicity, and cytokine and/or chemokine secretion by multiplex ELISA.

181 ESAT-6 stimulated significantly higher IL-6 secretion by murine bone marrow derived macrophages (BMD

182 We tested 17 proteins important for DNA secretion by N. gonorrhoeae for protein interactions.

183 their proinflammatory cytokine and ferritin secretion by negatively regulating Erk1/2 and p38 activa

184 hibitors PP2 and dasatinib reduced chemokine secretion by neutrophils and bone marrow-derived macroph

185 eted mice, we examined LPS-induced chemokine secretion by neutrophils and macrophages in wild type an

186 s, ATP-induced P2X7R activation and IL-1beta secretion by neutrophils likely has a significant, wide

187 sulin granule fractions and by inhibition of secretion by nimodipine and diazoxide.

188 ments demonstrated that regDC curb IFN-gamma secretion by NK cells through a dominant suppressive mec

189 Reduction of exosome secretion by nSMase2 loss of function improves pathology

190 o play roles in skeletal tissues through its secretion by osteoblasts, chondrocytes, and mesenchymal

191 during eATP-induced IL-1beta processing and secretion by P. gingivalis-infected macrophages.

192 Inhibition of CXCL5 secretion by P2X4 antagonists was lost in the absence of

193 reefold increase in the basal rate of proANP secretion by Pam (Myh6-cKO/cKO) myocytes was a major con

194 proteins and COPI vesicle formation, proANP secretion by Pam (Myh6-cKO/cKO) myocytes was unaffected.

195 lays an important role in regulating protein secretion by pancreatic acinar cells, as does Rab3D.

196 transporter 2 (SGLT2) inhibitors in glucagon secretion by pancreatic alpha-cells reported controversi

197 he first time that Pg LPS stimulates insulin secretion by pancreatic beta cell line MIN cells.

198 A variety of signals finely tune insulin secretion by pancreatic beta cells to prevent both hyper

199 Insulin secretion by pancreatic beta-cells in response to glucos

200 ritical regulator of glucose-induced insulin secretion by pancreatic beta-cells.

201 Insulin secretion by pancreatic islet beta cells is critical for

202 inhibition preserved glucose-induced insulin secretion by pancreatic microislets and viability of pri

203 Gastric acid secretion by parietal cells requires trafficking and exo

204 775L, 369L, or 241H increased interleukin 6 secretion by PBMCs in response to cSSSI pathogens.

205 ring RNA in DSCCs enabled increased IFNgamma secretion by PBMCs, whereas transfection of pCMV6-XL4/hP

206 leukin 1beta and tumor necrosis factor alpha secretion by PBMCs.

207 rization of the in vitro dynamics of insulin secretion by perifused fragments of 10 human insulinomas

208 a, immune cell composition, ex vivo cytokine secretion by peritoneal cells or bone marrow derived mac

209 expression significantly suppressed collagen secretion by phLF.

210 at thrombus formation is associated with PDI secretion by platelets, that inhibition of PDI blocked p

211 inimal change disease, we observed localized secretion by podocytes of hyposialylated Angptl4, a pro-

212 r mechanisms responsible for excess cortisol secretion by primary adrenal lesions and adrenocorticotr

213 inhibited LPS-stimulated TNF-alpha and IL-6 secretion by primary human monocytes.

214 f SOCE was associated with impaired chloride secretion by primary murine sweat glands.

215 (rhIL-15) synergistically enhanced cytokine secretion by proliferating HIVGag-specific CD8 T cells.

216 ed that Barr1 enhanced SU-stimulated insulin secretion by promoting SU-mediated activation of Epac2.

217 ons can dynamically control the capacity for secretion by promptly changing the number of plasma memb

218 on, decreased antiinflammatory growth factor secretion by proximal epithelial cells, and a subsequent

219 tifying C5L2 as a negative regulator of BDNF secretion by pulp fibroblasts under carious teeth.

220 Exosome secretion by purified platelets in vitro did not increas

221 Regulation of Nischarin-mediated exosome secretion by Rab14 seems to play an important role in co

222 enriched in astrocytes and mediates exosome secretion, by reducing the association of Sp1 with the e

223 mostly decrease the elasticity of bronchial secretions by reducing disulfide bonds in proteins.

224 ipin 5 (PLIN5) in beta-cells aids PP insulin secretion by regulating intracellular lipid metabolism.

225 Additionally, mTORC1 promoted TAG secretion by regulating phosphocholine cytidylyltransfer

226 s the selective decrease in amyloidogenic LC secretion by remodeling the endoplasmic reticulum proteo

227 In addition, reduced IFNgamma secretion by RSV-induced T cells in older vaccinees corr

228 y, and induction of proinflammatory cytokine secretion by S. Paratyphi A but not by S. Typhimurium, s

229 ucture of MTM and PKM and their simultaneous secretion by S. venezuelae bring about the possibility t

230 We investigated fluid secretion by sealed pancreatic ducts and the function of

231 ormal airways compensate for MCT-driven H(+) secretion by secreting HCO3(-), a process which is dysfu

232 y in pancreatic beta-cells decreases insulin secretion by selectively degrading insulin granules.

233 effects related to inhibition of creatinine secretion by selonsertib confounded eGFR differences at

234 ferase, Rac1 or Cdc42 depletion reduced IL-6 secretion by senescent cells.

235 pose tissue-derived factors regulate insulin secretion by silencing a pair of inhibitory neurons that

236 n of tumor necrosis factor-alpha (TNF-alpha) secretion by single monocytes in septic shock patients,

237 Moreover, oral anti-CD3 promotes XCL1 secretion by small intestine lamina propria gammadelta T

238 ts but not healthy donors show enhanced MMP1 secretion by smooth muscle cells and tumor cell invasion

239 nal part of the fusion complex that promotes secretion by SNARE interactions as well as concerted lip

240 activation, pyroptosis and interleukin-1beta secretion by soluble and crystalline Nlrp3 stimuli.

241 ion in human beta-cells and supports insulin secretion by stabilizing STX1A.

242 ion in human beta cells and supports insulin secretion by stabilizing Stx1a.

243 ides, human IAPP induces macrophage IL-1beta secretion by stimulating both the synthesis and processi

244 Ubiquitination then down-regulated zinc secretion by stimulating degradation of ZnT2.

245 ate resistance to RAF inhibitors through HGF secretion" by Straussman and colleagues, published in Na

246 between MM and stromal cells increased IL-8 secretion by stromal cells through cell-cell adhesion an

247 -ATPase, abolished dopamine-induced salivary secretion by suppressing fluid transport in type III aci

248 g radiosensitive cells, and altered cytokine secretion by surviving radioresistant cells.

249 tiation by altering proinflammatory cytokine secretion by T and B cells.

250 antigens that induce interferon gamma (IFN-) secretion by T cells from immune women could advance vac

251 and natural killer T cells, with lower IL-10 secretion by T cells.

252 protection is largely dependent on IFN-gamma secretion by T cells.

253 Ig secretion by terminally differentiated B cells is an imp

254 The myosin domain of Mcs1 enhances polar secretion by tethering vesicles at the site of exocytosi

255 a-interferon and tumor necrosis factor alpha secretion by Th1 cells, and 3) increased monocyte-mediat

256 CBP30 also inhibited IL-17A secretion by Th17 cells from healthy donors and patients

257 nce of ASCs 1) enhanced interleukin (IL)-17A secretion by Th17 cells, 2) inhibited gamma-interferon a

258 iferation of naive CD4(+) T cells and IL-17A secretion by Th17 cells.

259 l alloproliferation, inhibition of IFN-gamma secretion by the allostimulated T cells, and, conversely

260 nse of beta-ICs, thereby increasing net acid secretion by the CCD.

261 llenged mice revealed induction of IFN-gamma secretion by the CD4 and CD8 T cells compared with non-i

262 Fluid secretion by the ciliary body plays a critical and irrep

263 the role of this integrin in controlling the secretion by the epidermis of factors that modulate the

264 zation and that it relies on a novel CTD for secretion by the F. johnsoniae T9SS.

265 gA expression levels influence interleukin 8 secretion by the host gastric epithelial cells.

266 of rapamycin's inhibitory effect on IL-1beta secretion by the IL-1 receptor antagonist anakinra in ph

267 ction and the net balance of reabsorption or secretion by the kidney and intestine.

268 reticulum (ER) to the Golgi determines their secretion by the liver and is mediated by a specialized

269 l for caspase-1 autoproteolysis and IL-1beta secretion by the NLRC4, NLRP3 and AIM2 inflammasomes.

270 humans and pigs lacking CFTR, unchecked H(+) secretion by the nongastric H(+)/K(+) adenosine triphosp

271 ile GLP-1 is well known to stimulate insulin secretion by the pancreatic beta-cells, direct evidence

272 ence of native AVR3a is cleaved off prior to secretion by the pathogen and the N terminus of the matu

273 prolonged preservation of endogenous insulin secretion by the remaining beta cells in patients with n

274 absorption in Henle's loop and for potassium secretion by the stria vascularis in the inner ear.

275 d swine tracheas triggers CFTR-dependent ASL secretion by the submucosal glands.

276 Proteins involved in secretion by the T9SS include GldK, GldL, GldM, GldN, Sp

277 ramatically affect stimulated rates of fluid secretion by the tissue.

278 D-induced vascular endothelial growth factor secretion by the tumour cells.

279 be used for qualitative analysis of protein secretion by the yeast Komagataella phaffii.

280 r and mucosal epithelial cells into external secretions by the polymeric Ig receptor (pIgR).

281 ssion and matrix metalloproteinase-9 (MMP-9) secretion by these cells.

282 an amplitude of T2D islet clocks and insulin secretion by these islets.

283 Palmitate inhibited IGFBP-3 secretion by THP-1 macrophages and enhanced IL-8 express

284 l polarization resulted from decreased IL-12 secretion by Treg-DC, which may be post-transcriptionall

285 of Treg function and suggest that chemokine secretion by Tregs is a fundamental aspect of their ther

286 nhibits vascular endothelial growth factor A secretion by tumor cells, inducing cancer cell apoptosis

287 Our findings indicate that EN2 secretion by tumors may be a means of preventing viral-m

288 boosted the number of EC cells and their 5HT secretion by up to 430 and 390%, respectively.

289 ors and downstream signaling to induce their secretion by up-regulating the organic anion transporter

290 agon-like peptide 1 (GLP-1)-mediated insulin secretion by upregulating interleukin-6 (IL-6).

291 liferation, autophagy, apoptosis and insulin secretion by using mice with conditional (betaraKO) and

292 he electrical dynamics that underlie insulin secretion by utilizing a microwell-based aggregation met

293 Increased tau secretion by VAMP8 was also observed in murine hippocamp

294 Quantification of in vitro SEl-K secretion by various S. aureus isolates using this novel

295 can be released from cells: first, classical secretion by virtue of the N-terminal signal peptide; se

296 well as mineral imbalance stimulate exosome secretion by VSMCs, most likely by the activation of sph

297 nic transcription factor GLI2 modulating IgM secretion by WM malignant cells.

298 ntless (Wls), a gene required for Wnt ligand secretion by Wnt-producing cells, specifically in the ha

299 110delta diminished mycobacteria-induced TNF secretion by WT but not RP105(-/-) macrophages.

300 mate for glutathione synthesis and glutamate secretion by xc(-) antiporter system.