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

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

7 idzin partially inhibited GIP, GLP-1 and PYY secretion by 45%, suggesting another glucose sensor migh

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

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

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

17 ification process requires (i) apical proton secretion by a vacuolar H(+)-ATPase, (ii) actin cytoskel

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

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

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

21 ytotoxic activity, and intratumoral cytokine secretion by adoptively transferred cells.

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

26 levels may affect glucose-stimulated insulin secretion by altering surface expression of K(ATP) chann

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

28 Additionally, stimulation of aldosterone secretion by AngII, but not by a high-K(+) diet, was imp

29 yperinsulinemic-euglycemic clamp and insulin secretion by applying mathematical modeling during the h

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

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

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

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

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

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

36 rotein-coupled receptor), stimulates insulin secretion by beta cells in the pancreas.

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

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

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

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

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

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

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

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

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

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

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

48 The interface is the site of active secretion by both players.

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

50 that downregulation of motility and type III secretion by c-di-GMP during infection plays a key role

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

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

53 Cytokine secretion by cancer cells contributes to cancer-induced

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

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

56 We found that IL-17 secretion by CD4(+) T cells following CFA immunization r

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

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

59 unction of NK cells and to lead to IFN-gamma secretion by CD8(+) T cells through interaction with its

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

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

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

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

64 of exocytosis, and the modulation of insulin secretion by circulating hormones and locally released n

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

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

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

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

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

70 um channel Kir6.2 play a key role in insulin secretion by coupling metabolic signals to beta-cell mem

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

72 ls exhibiting a 2.5-fold increase in albumin secretion by day 20 in culture differentiation, and sign

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

74 s TNF, IL-12, and IL-6, while inducing IL-10 secretion by DCs.

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

76 that SR/ER calcium depletion triggered MANF secretion by decreasing its retention.

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

78 .2 expression interfered with immunoglobulin secretion by delaying the kinetics of immunoglobulin ass

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

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

81 atostatin mediate glucose-stimulated insulin secretion by differential receptor signaling that is dep

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

83 iglyceride synthesis and subsequent VLDL/LDL secretion by directly and noncompetitively inhibiting he

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

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

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

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

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

89 the induction of yolk uptake and lipoprotein secretion by EECs to ensure embryo nutrition.

90 ve largely relied on measurement of cytokine secretion by effector T cells.

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

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

93 succinimidyl ester dye dilution and cytokine secretion by ELISpot.

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

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

96 on Willebrand factor (VWF) for its regulated secretion by endothelial cells.

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

98 we studied whether glucose modulates apelin secretion by enterocytes and the effects of apelin on in

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

100 Secretions by epithelial cells of the fallopian tube reg

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 o detect the protein and to characterize its secretion by F. johnsoniae.

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

108 ting the enhancement of postprandial insulin secretion by factors including the intestinal hormones g

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

110 ys a major role in the regulation of insulin secretion by fatty acids.

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

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

113 ociated with a significant increase in IL-22 secretion by gammadelta T cells and innate lymphoid cell

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

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

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

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

118 Mutations did not alter VWF secretion by HEK293T cells, multimeric structure, or sta

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

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

121 regulation of C3 gene expression and protein secretion by HepG2 cells.

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

123 0 blockade leads to restoration of IFN-gamma secretion by HIV-1-specific CD4 T cells in all categorie

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

125 17 induces CCR4-dependent CGRP synthesis and secretion by human airway epithelial cells.

126 for the real-time monitoring of nitric oxide secretion by human endothelial vein cells grown on the e

127 LDL) increase C3 gene expression and protein secretion by human macrophages.

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

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

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

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

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

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

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

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

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

137 Stimulation of endogenous PGE2 secretion by IL-1beta was associated with amelioration o

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

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

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

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

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

143 one secreted by adipocytes, inhibits insulin secretion by increasing KATP channel conductance in beta

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

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

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

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

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

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

150 Secretin stimulates ductal secretion by interacting with secretin receptor (SR) act

151 , rigorous demonstration of acid phosphatase secretion by intracellular Francisella has not been show

152 IL-21 enhanced Ig secretion by isolated SLO PC but not bone marrow PC.

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

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

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

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

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

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

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

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

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

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

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

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

165 h strongly reduced the LPS-induced IL-12p40 secretion by macrophages, whereas the production of TNF-

166 regulation, and promote ion reabsorption or secretion by many epithelia.

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

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

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

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

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

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

173 platelets increased TG- and TT-induced IL-10 secretion by monocytes (p < 0.05).

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

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

176 bsets on modulating proinflammatory cytokine secretion by monocytes.

177 oarthritisis associated with increased RANKL secretion by MSCs.

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

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

180 induce strong proliferation of and IFN-gamma secretion by naive human T cells.

181 ent advances in the regulation of pancreatic secretion by neural and hormonal mechanisms are discusse

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

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

184 CEACAM1 controls matrix metalloproteinase-9 secretion by neutrophils in postischemic inflammation at

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

186 re required for ASC/Nlrp3-dependent IL-1beta secretion by neutrophils.

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 In addition, doxorubicin enhanced VEGF secretion by normoxic tumor cells and stimulated tumor a

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

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

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

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

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

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

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

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

198 ted protein, plays a pivotal role in insulin secretion by pancreatic beta-cells.

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

200 Insulin secretion by pancreatic islet beta cells is critical for

201 Gastric acid secretion by parietal cells requires trafficking and exo

202 775L, 369L, or 241H increased interleukin 6 secretion by PBMCs in response to cSSSI pathogens.

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

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

205 trogens to promote the TLR-mediated cytokine secretion by pDCs through hematopoietic expression of es

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

207 expression significantly suppressed collagen secretion by phLF.

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

209 MMP-8 secretion by PMNs in response to fMLP or serum-opsonized

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

211 hesis that glycine regulates hepatic VLDL-TG secretion by potentiating NMDA receptor-mediated transmi

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

213 ng, the Rho GTPase Cdc42, controls IFN-gamma secretion by primary human CD4+ T lymphocytes.

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

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

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

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

218 Exosome secretion by purified platelets in vitro did not increas

219 esented on a cell surface, decreases insulin secretion by rat islets and MIN-6 cells, most likely by

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

221 Autophagy controls IL-1beta secretion by regulating inflammasome activation and by t

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

223 Additionally, mTORC1 promoted TAG secretion by regulating phosphocholine cytidylyltransfer

224 nism for controlling intestinal motility and secretion by regulating the excitability of musculomotor

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

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

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

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

229 ent advances in the regulation of pancreatic secretion by secretagogues, modulatory proteins and neur

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

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

232 Finally, chaperones serve as regulators of secretion by sequestering effectors and some structural

233 Addition of recombinant Munc18-1 blocked secretion by sequestering monomeric syntaxin, an effect

234 f proIL-1beta and for unconventional protein secretion by skin-derived keratinocytes.

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

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

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

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

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

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

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

242 ric G(z) protein, Galpha(z), impairs insulin secretion by suppressing production of cAMP.

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

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

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

246 Cytokine secretion by T lymphocytes plays a central role in mount

247 epend on Cdc42, is not required for cytokine secretion by T lymphocytes, whereas microtubule polymeri

248 enhancements to apoB-100 cellular uptake and secretion by T(1)AM were observed; however, multidose T(

249 nterestingly, miR142-3p also suppresses IL-6 secretion by targeting the 3' UTR of IL-6.

250 Ig secretion by terminally differentiated B cells is an imp

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

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

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

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

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

256 Cortisol secretion by the adrenals in patients with macronodular

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

258 e IL-12 stimulation, and subsequent IFNgamma secretion by the CAR(+) T cells.

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

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

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

262 Ammonia secretion by the collecting duct (CD) is critical for ac

263 Ammonium secretion by the collecting duct epithelia accounts for

264 y different mechanisms that target these for secretion by the dynamic T6SS organelle.

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

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

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

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

269 n response to treatment and interferon gamma secretion by the infused TILs in response to autologous

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

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

272 ogical cues and adjust glucose synthesis and secretion by the liver.

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

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

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

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

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

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

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

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

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

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

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

284 GldN, SprE, SprF, and SprT are involved in secretion by this system.

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

286 production, and hence for IL-6 and TNF-alpha secretion by TLR agonists that signal via MyD88.

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

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

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

290 Closure of K(ATP) channels controls glucagon secretion by two mechanisms, a direct stimulation of alp

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

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

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

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.