ライフサイエンスコーパス: efflux from

1 induced inflammation and reduces cholesterol efflux from 3T3-L1 adipocytes.

2 em here using the example of monitoring drug efflux from a monolayer of cancer cells with microvoltam

3 lated at the cellular level by inhibition of efflux from a plasma membrane (PM) carrier.

4 eleration phenomenon (e.g., increased tracer efflux from a vesicle caused by increased substrate conc

5 apoA-I-mediated cholesterol and phospholipid efflux from ABCA1-expressing cells without altering the

6 ed for their ability to inhibit mitoxantrone efflux from ABCG2-transfected HEK293 cells.

7 xygen-glucose deprivation-evoked L-glutamate efflux from adult rat cerebrocortical prisms.

8 Nicotine-stimulated (86)Rb(+) efflux from all brain regions was significantly less in

9 Nicotine-stimulated (86)Rb(+) efflux from all brain regions was significantly reduced

10 se G, both stimulates plasma membrane Ca(2+) efflux from and inhibits ATP-stimulated Ca(2+) influx in

11 I in the liver did not stimulate cholesterol efflux from any extrahepatic tissue.

12 These data suggest that iron efflux from astrocytes plays a role in remyelination by

13 However, cholesterol efflux from AT to plasma HDL was similar for both genoty

14 lationship between specific changes in auxin efflux from axillary buds and bud outgrowth after shoot

15 tyric acid (PCIB), effectively blocked auxin efflux from axillary buds of intact and decapitated plan

16 ence inhibits Hsmr-mediated ethidium bromide efflux from bacterial cells.

17 4RK augmented strongly CFTR-mediated iodide efflux from BHK cells expressing G551D-CFTR.

18 Increased HDL improved cholesterol efflux from bone marrow progenitors, suppressing their p

19 ds would exacerbate acid-induced net calcium efflux from bone.

20 o hypoxia in the brain and an impaired Abeta efflux from brain caused by reduced LRP levels.

21 n oligosaccharides, rapidly inhibits lactate efflux from breast carcinoma cells; down-regulation of e

22 common cause of MDR involves increased drug efflux from cancer cells mediated by members of the ATP-

23 onship allowed us to successfully predict Zn efflux from Cd data gathered from aquatic species belong

24 transporter uses energy of ATP hydrolysis to efflux from cells a variety of structurally dissimilar h

25 a network of genes that mediate cholesterol efflux from cells and its transport in plasma.

26 transporter G1 (ABCG1) promotes cholesterol efflux from cells and regulates intracellular cholestero

27 This increase was accompanied by K+ efflux from cells and was virtually absent when extracel

28 , higher PS exposure, and higher cholesterol efflux from cells by both ABCA1-dependent and ABCA1-inde

29 A-I loses its ability to promote cholesterol efflux from cells by the ATP-binding cassette transporte

30 In contrast, palytoxin-induced K(+) efflux from cells expressing either the native alpha3 an

31 and degradation, resulting in decreased iron efflux from cells into plasma.

32 ellular minocycline or doxycycline triggered efflux from cells loaded with these antibiotics.

33 Assays measuring the efflux from cells of [(3)H]chloramphenicol and [(3)H]tri

34 cellular zinc availability by promoting zinc efflux from cells or into intracellular vesicles, while

35 We showed that NO-mediated iron efflux from cells required glutathione (GSH) and that th

36 A1 (encoded by ABCA1) regulates cholesterol efflux from cells to apolipoproteins A-I and E (ApoA-I a

37 ABCA1) is a pivotal regulator of cholesterol efflux from cells to apolipoproteins, whereas sterol-res

38 er G1 in macrophages and apoE in cholesteryl efflux from cells to cholesterol ester-rich (CE-rich) HD

39 ester, stimulation of free cholesterol (FC) efflux from cells to HDL and phospholipid vesicles, and

40 ate that ABCG1 and ABCG4 promote cholesterol efflux from cells to HDL.

41 ed quantitatively with decreased cholesterol efflux from cells via the ATP-binding cassette transport

42 K+ efflux from cells was quantified from increasing extrace

43 eruloplasmin in determining the rate of iron efflux from cells with mobilizable iron stores and has p

44 n of hepcidin, a hormone that regulates iron efflux from cells.

45 c and serves a role in mediating cholesterol efflux from cells.

46 r that gives rise to passive and active drug efflux from cells.

47 the ability of apoA-I to promote cholesterol efflux from cells.

48 lity to promote cholesterol and phospholipid efflux from cells.

49 e G2 (ABCG2) transporter-mediated irinotecan efflux from cells.

50 reorganize lipids and to promote cholesterol efflux from cells.

51 nergy supplied by NADH oxidation, reflecting efflux from cells.

52 inib, a potent tyrosine kinase inhibitor, is effluxed from cells by the breast cancer resistance prot

53 Furthermore, we discovered that PIP2 is effluxed from cells to apoA1, where it is associated wit

54 e is known about how metals such as iron are effluxed from cells, a necessary step for transport from

55 lodextrin (CYCLO), a modifier of cholesterol efflux from cellular membrane and endo-lysosomal compart

56 sis by choline depletion reduces cholesterol efflux from cholesterol-enriched cells.

57 Basal cholesterol efflux from cholesterol-loaded macrophages to HDL was si

58 )/apoE(-/-) mice, and attenuated cholesterol efflux from cholesterol-loaded macrophages to plasma in

59 out a 45-min incubation period, and enhanced efflux from control tissue.

60 ineffective in eliciting catecholamine (CA) efflux from control, CIH or CH rats.

61 However, choline efflux from CP was not stimulated by a trans-applied H(+

62 deprivation has no effect on the rate of CQ efflux from CQR lines implying that mutant PfCRT does no

63 as an acceptor of ABCA1-mediated cholesterol efflux from cultured macrophages.

64 lix 10) abolished ABCA1-mediated cholesterol efflux from cultured RAW mouse macrophages treated with

65 ermal HA and a marked increase in neutrophil efflux from cutaneous blood vessels were observed in Has

66 +)/Ca(2+) exchanger (I(NCX))-mediated Ca(2+) efflux from cytosol, thereby reducing EADs.

67 DA uptake, the variant exhibits anomalous DA efflux from DA-loaded cells.

68 cellular glutathione content and glutathione efflux from DCs.

69 tem was used to continually monitor soil CO2 efflux from December 2010 through November 2011 in each

70 hese changes was a 66% increase in (86)Rb(+) efflux from diabetic choroid plexus compared with contro

71 osol, ER and mitochondria), Ca(2+) influx to/efflux from each compartment and Ca(2+) buffering.

72 creted AIBP positively regulates cholesterol efflux from endothelial cells and that effective cholest

73 nding protein (AIBP) accelerates cholesterol efflux from endothelial cells to HDL and thereby regulat

74 bility across the intestinal wall, or active efflux from enterocytes and extensive conjugation.

75 absorption, namely via ferroportin-dependent efflux from enterocytes, and thus offers potential as a

76 sink of 1.3 +/- 3.1 Tg C yr(-1), while CO(2) efflux from estuaries to the atmosphere, removed the maj

77 ethanol significantly inhibited cholesterol efflux from fibroblasts to HDL and to apolipoprotein A-I

78 roplets filled with only buffer, the rate of efflux from filled droplets to empty droplets was depend

79 efficient in mediating cellular cholesterol efflux from foam cell macrophages and to identify the ce

80 has enhanced ability to promote cholesterol efflux from foam cells in an ABCG1-dependent pathway due

81 is is likely to reduce the rate of glutamine efflux from glia and result in the observed decrease of

82 nt outward-rectifying K+ channels mediate K+ efflux from guard cells during stomatal closure and from

83 Our results demonstrate that iron efflux from hBMVEC Fpn requires the action of an exocyto

84 Ca2+ efflux from hepatocyte populations was measured by using

85 Our results show that glutathione efflux from hepatocytes results in high local concentrat

86 , expression of these genes, and cholesterol efflux from hepatocytes.

87 y, SAA, but not apoA-I, promoted cholesterol efflux from HepG2 cells in an SR-BI-dependent manner as

88 onstrate that TO-901317 restores cholesterol efflux from HIV-infected T lymphocytes and macrophages.

89 hat streptolysin O (SLO)-induced glutathione efflux from host cellular stores is a previously unappre

90 The kinetics of sterol efflux from human aortic smooth muscle cells equilibrate

91 cular mechanisms of ritonavir on cholesterol efflux from human macrophage-derived foam cells, which i

92 lipopolysaccharide impaired (3)H-cholesterol efflux from human macrophages to apolipoprotein A-I and

93 on and we demonstrate that increased lactate efflux from hypoxic cancer cells favors the growth of no

94 ding of integrin beta2 to promote macrophage efflux from inflammatory sites, and the release of solub

95 nergy supplied by NADH oxidation, reflecting efflux from intact cells.

96 istine and calcein, and decreases in calcein efflux from intact MRP1-expressing human tumour cells.

97 metazoan homologues may be involved in sugar efflux from intestinal, liver, epididymis and mammary ce

98 ctionally important in mediating cholesterol efflux from intracellular cholesterol pools.

99 led for a short period, suggesting defective efflux from intracellular stores but not from the plasma

100 inositol 1,4,5-triphosphate-stimulated Ca2+ efflux from intracellular stores.

101 n and degradation and thereby decreases iron efflux from iron exporting tissues into plasma.

102 Peptide efflux from isolated mitochondria was ATP dependent and

103 evels of ABC1 mRNA, protein, and cholesterol efflux from J774 mouse macrophages +/- exposure to a cAM

104 estimate the rates of entry into (K(1)) and efflux from (k(2)) the brain.

105 Overall, HDL-mediated sterol efflux from L-cell fibroblasts reflected that of the cyt

106 lied to observe the mechanism of sphingosine efflux from large and giant unilamellar vesicles; a grad

107 alization of ABCA1 and decreased cholesterol efflux from late endosomal cholesterol pools, providing

108 ase is characterized by impaired cholesterol efflux from late endosomes and lysosomes and secondary a

109 membrane protein is required for cholesterol efflux from late endosomes and lysosomes.

110 To assess cholesterol efflux from late endosomes, HEK293 cells were transientl

111 l understood, including the route of sucrose efflux from leaf mesophyll cells and transport across va

112 profiles revealed significantly higher drug efflux from leukemic SP cells than from non-SP cells.

113 ally, SCP-2 expression also inhibited sterol efflux from lipid droplets, an effect related to decreas

114 ons; (ii) lipoprotein-mediated sterol uptake/efflux from lipid rafts/caveolae and caveolae was rapid

115 e rate and lipoprotein specificity of sterol efflux from lipid rafts/caveolae or caveolae to lipoprot

116 onsequently, the rate of peptide-induced dye efflux from lipid vesicles.

117 d to as VAL-PVC/SiNW-FET) to detect the K(+)-efflux from live chromaffin cells.

118 Ciprofloxacin efflux from loaded cells occurred more rapidly than with

119 that gp120 alone can alter CD4(+) influx and efflux from lymph nodes in a fashion consistent with the

120 Stimulating calcium efflux from lysosomes with a TRPM1 agonist promoted calc

121 ystinosin, a symporter that mediates cystine efflux from lysosomes.

122 Further, MafB promotes cholesterol efflux from macrophage foam cells by directly up-regulat

123 ding cassette A1, which promotes cholesterol efflux from macrophage foam cells in the arterial wall.

124 acrophages and probably mediates cholesterol efflux from macrophage foam cells to the major HDL fract

125 its apolipoproteins can promote cholesterol efflux from macrophage foam cells via the ATP-binding ca

126 protein A-I facilitates cellular cholesterol efflux from macrophage foam cells within the intima of t

127 Cholesterol efflux from macrophage foam cells, a key step in reverse

128 h-density lipoprotein to promote cholesterol efflux from macrophage foam cells, direct experimental s

129 diovascular disease by promoting cholesterol efflux from macrophage foam cells.

130 with reduced ability to promote cholesterol efflux from macrophage foam cells.

131 17-sHDL exhibited more efficient cholesterol efflux from macrophages and enhanced atheroma-targeting

132 sporter ABCA1 is a key player in cholesterol efflux from macrophages and has been shown via human gen

133 ency of CETP (CETP-D) to promote cholesterol efflux from macrophages and have evaluated the role of A

134 myristoylated HIV Nef inhibited cholesterol efflux from macrophages and hepatocytes.

135 s ABCA1 and ABCG1, which promote cholesterol efflux from macrophages and suppress atherosclerosis in

136 LeTx exposure results in early K(+) efflux from macrophages associated with caspase-1 activa

137 I therapies and the promotion of cholesterol efflux from macrophages by the ABCA1 and ABCG1 transport

138 e had reduced ability to promote cholesterol efflux from macrophages ex vivo via ABCA1.

139 bility to promote ABCA1-mediated cholesterol efflux from macrophages ex vivo.

140 roperties and ability to promote cholesterol efflux from macrophages in vitro.

141 was an increase in HDL-mediated cholesterol efflux from macrophages in vitro.

142 Oral D-4F also promoted reverse cholesterol efflux from macrophages in vivo.

143 were to determine whether LeTx-induced K(+) efflux from macrophages is mediated by toxin effects on

144 METHODS AND We measured cholesterol efflux from macrophages of wild-type (WT) and SMS2 knock

145 stronger potential for promoting cholesterol efflux from macrophages than from wild-type mice (p < 0.

146 1 have a major role in promoting cholesterol efflux from macrophages to apolipoprotein A-1 and HDL an

147 ciency led to a markedly reduced cholesterol efflux from macrophages to apoM-deficient HDL compared t

148 e found that IL10 also increases cholesterol efflux from macrophages to protect against toxicity of f

149 ABCA1-mediated cholesterol and phospholipid efflux from macrophages when ABCA1 was induced by a cAMP

150 ound can induce APO-AI-dependent cholesterol efflux from macrophages with full efficacy.

151 e binding transporter A1 (ABCA1) cholesterol efflux from macrophages, a potentially pro-atherosclerot

152 , vascular tone in aortic rings, cholesterol efflux from macrophages, and expression of SMC phenotypi

153 ular energy status can influence cholesterol efflux from macrophages, and that miR-33 reduces cholest

154 Inhibited RCT was downstream of cholesterol efflux from macrophages, since macrophage efflux of a fl

155 lays a central role in promoting cholesterol efflux from macrophages, thereby reducing the risk of fo

156 ansgenes can result in increased cholesterol efflux from macrophages, unaccompanied by changes in pla

157 ritonavir significantly inhibits cholesterol efflux from macrophages, which may be mediated by mitoch

158 , have a major role in promoting cholesterol efflux from macrophages.

159 erms of their ability to promote cholesterol efflux from macrophages.

160 ve inhibition in ABCA1-dependent cholesterol efflux from macrophages.

161 TLR3/4 ligands strongly inhibit cholesterol efflux from macrophages.

162 ation of foam cells by enhancing cholesterol efflux from macrophages.

163 c endothelial cells, and reduced cholesterol efflux from macrophages.

164 ins by macrophages, and reducing cholesterol efflux from macrophages.

165 correlate with the magnitude of cholesterol efflux from macrophages; more understanding of the contr

166 Iron efflux from mammalian cells is supported by the synergis

167 rowth results from the decreasing fatty acid efflux from membranes with increasing phospholipid conte

168 Insulin secretion and cholesterol efflux from MIN6N8 beta-cells were determined after incu

169 endoplasmic reticulum arises through Ca(2+) efflux from mitochondria during brief openings of the mi

170 Thus, two pathways of peptide efflux from mitochondria exist that may allow communicat

171 ay be controlled by calcium accumulation and efflux from mitochondria in their immediate vicinity.

172 at polyunsaturated fatty acids induce Ca(2+) efflux from mitochondria, an action that may deplete [Ca

173 totic proteins BAK and BAX, and cytochrome c efflux from mitochondria.

174 2-APB inhibited Ca(2+) efflux from mitochondria.

175 Thus, although rHDL stimulated cholesterol efflux from most tissues and increased net cholesterol m

176 in the molecule to ABCA1-mediated FC and PL efflux from mouse J774 macrophages and human skin fibrob

177 igher level of isotopic and mass cholesterol efflux from mouse peritoneal macrophages labeled with [(

178 obucol inhibited ABCA1-dependent cholesterol efflux from mouse primary hepatocytes, and this effect w

179 n-dependent DA release and non-exocytotic DA efflux from mouse striatal slices and extracellular, int

180 cellular glycolysis during anoxia to lactate efflux from muscle during sustained, aerobic contraction

181 The rate of proton efflux from muscle fibres was significantly reduced in D

182 Moreover we found that that the (36)Cl efflux from NCBE-expressing oocytes, interpreted by othe

183 ate that vigabatrin induces spontaneous GABA efflux from neighboring cells via reversal of GABA trans

184 ransporter type A1), but reduces cholesterol efflux from neuronal cells leading to the accumulation o

185 int to a primary role of MtMATE67 in citrate efflux from nodule cells in response to an Fe signal.

186 have previously demonstrated that spermidine efflux from oocytes is a simple electrodiffusive process

187 he apical membrane inner monolayer, and drug efflux from P-gp into the apical chamber, as well as the

188 , ex vivo insulin secretion, and cholesterol efflux from pancreatic beta-cells.

189 nd SR-BI expression and impaired cholesterol efflux from partially differentiated adipocytes.

190 t (67%) and HDL3-dependent (30%) cholesterol efflux from pBCEC.

191 mass may have offset roughly half the carbon efflux from peat oxidation.

192 that may be responsible for net cholesterol efflux from peripheral cells as well as the rapid hepati

193 assette transporter A1 and facilitates lipid efflux from peripheral cells.

194 ABCA1 facilitates free cholesterol efflux from peripheral tissues.

195 still plays an important role in cholesterol efflux from peripheral tissues.

196 evidence that pendrin mediates apical iodide efflux from polarized mammalian cells loaded with iodide

197 Attenuated Pi efflux from PPIP5K KO cells was quantitatively phenocopi

198 Moreover, Pi efflux from PPIP5K KO cells was rescued by restoration o

199 a1-syntrophin expression reduced cholesterol efflux from primary skin fibroblasts by 50% while decrea

200 a-hypoglycaemia) in vitro enhanced glutamate efflux from rat cerebrocortical prisms.

201 ound that zinc gluconate inhibited potassium efflux from RBC exposed to total venom or purified porin

202 ical pathway for the regulation of potassium efflux from RBCs is the Gardos channel, a calcium-activa

203 was identical in a genotype showing citrate efflux from root apices (cv Carazinho) to one that lacke

204 es, and 15-25% higher glucose-derived carbon efflux from roots, suggesting that SWEET2 has a role in

205 gulators of NPD1 and of its polarized apical efflux from RPE cells.

206 in a microfluidic chamber, measuring protein efflux from single organisms in real time.

207 and temporally resolved measurement of Zn2+ efflux from single pancreatic beta-cells.

208 e present study, [3H]ryanodine binding, Ca2+ efflux from skeletal sarcoplasmic reticulum (SR) vesicle

209 ediate apoplastic phloem loading and sucrose efflux from source leaves in Arabidopsis and agricultura

210 No difference in cholesterol efflux from SR-BI+/+ apoE-/- or SR-BI-/- apoE-/- macroph

211 ompartment was approximately 35% higher than efflux from the abluminal side to the lumen.

212 de anions and suggest that hypoxia-evoked CA efflux from the adrenal medulla contributes, in part, to

213 (prebeta-1 HDL) and its role in cholesterol efflux from the artery wall, offer a means of assessing

214 Because hepcidin reduces iron efflux from the basolateral enterocyte, it is uncertain

215 absorption, perhaps by mediating cholesterol efflux from the basolateral surface of enterocytes, it r

216 rotein creates a situation where net protein efflux from the bead is thermodynamically favorable.

217 nt role of uptake compared to desorption and efflux from the biofilm.

218 ic subjects, which suggests that these cells efflux from the blood into the airways in patients with

219 ot only reduces influx but also mediates the efflux from the brain back to the blood compartment, wit

220 reased levels of Abeta in plasma, suggesting efflux from the brain into the vascular compartment.

221 ement of substances into and enhancing their efflux from the brain.

222 ssociated protein (MRP) responsible for drug efflux from the cancer cells (pump resistance) and (b) B

223 ntent of Ca(2+) release and therefore Ca(2+) efflux from the cell as a consequence of wave propagatio

224 Cu(+)-ATPases drive metal efflux from the cell cytoplasm.

225 R calcium release, resulting in reduced Ca2+ efflux from the cell leading to increased SR calcium con

226 r the proposed role of MCT4 in mediating the efflux from the cell of glycolytically derived lactic ac

227 r Ca(2+) transient activates a larger Ca(2+) efflux from the cell that balances the increased influx.

228 During alternation, the Ca(2+) efflux from the cell was also a steeper function of SR C

229 ally (69.3 +/- 6% at 8 Hz) to the total Ca2+ efflux from the cell.

230 n, apparently by competing for dexamethasone efflux from the cell.

231 pathway but rather due to inhibition of iron efflux from the cell.

232 ynthesis of cysteinyl leukotrienes and their efflux from the cell.

233 ) is dissipated by scavenging enzymes and by efflux from the cell.

234 ) , and both appear to be required for metal efflux from the cell.

235 sin leakage, oxidative stress, and potassium efflux from the cell.

236 ts suggest that HMA2 is responsible for Zn2+ efflux from the cells and therefore is required for main

237 composed of glucose-derived mannose and its efflux from the cells can account for most of the mannos

238 sette (ABC) transporters mediate cholesterol efflux from the cells to apolipoprotein A-I (apoA-I) and

239 sequela thereof, such as potassium or water efflux from the cells, inhibits growth.

240 c accumulation of the contrast agent and its efflux from the cells, most of these imaging methods ina

241 ing of Zn accumulation and an increase in Zn efflux from the cells.

242 aspase-1 via a mechanism involving potassium efflux from the cells.

243 y bed compared to arterial blood, indicating efflux from the CNS into the peripheral blood (p < 0.000

244 stent with viability depends not only on NH3 efflux from the cytoplasm but also on the conversion of

245 Transporter-mediated Ca(2+) efflux from the cytoplasm is an important component of p

246 sal Ca(2+) influx required to balance Ca(2+) efflux from the cytoplasm through ATP- and proton-couple

247 Ca(2+) efflux from the endoplasmic reticulum into the cytoplasm

248 conjugation by sulfotransferases followed by efflux from the enterocytes.

249 ling of the respective compartment by Ca(2+) efflux from the ER and/or the mitochondria.

250 calculated by subtracting the predicted H(+) efflux from the experimental net H(+) influx.

251 n channel (SLAC1) that, in turn, mediate ion efflux from the guard cells.

252 terest as a practical measure of cholesterol efflux from the human brain.

253 Leptin inhibited NE efflux from the hypothalamus in a dose-dependent manner.

254 in mice inhibits the accelerated macrophage efflux from the inflammatory site to the lymphatics, but

255 ted proteins use proton cotransport to drive efflux from the lysosome.

256 e hypothesize that by allowing dicarboxylate efflux from the matrix, PTP opening during reperfusion m

257 This study provides evidence that Ca(2+) efflux from the mitochondria in vascular endothelial cel

258 ere, we show that the time required for Smac efflux from the mitochondria of cells subjected to staur

259 physiologically that PINK1 regulates calcium efflux from the mitochondria via the mitochondrial Na(+)

260 tein raises cellular iron by inhibiting iron efflux from the monocytemacrophage cell line THP-1, and

261 mately 28 Tg of N are lost annually via N(2) efflux from the natural soil.

262 verage sea surface temperature driving a CO2 efflux from the ocean, but our data do not allow specifi

263 ent to drive an 18% annual increase in CO(2) efflux from the P-fertilized plots.

264 yte transendothelial migration or macrophage efflux from the peritoneal cavity but regulates macropha

265 y electrodes are used to measure cholesterol efflux from the plasma membrane surface of a single neur

266 of tropical peatland degradation, but CO(2) efflux from the recently-burnt, cleared swamp forest was

267 of Al(3+) in the rhizosphere induces citrate efflux from the root apex of the Al-tolerant maize (Zea

268 estigate the function of TSPO in cholesterol efflux from the RPE cells.

269 inding indicates that the plants capture CO2 efflux from the soil.

270 ume is possible when this is offset by a net efflux from the t-system to the cell and thence to the E

271 to the thylakoid membrane, and allows proton efflux from the thylakoid lumen by proton/potassium anti

272 imarily by altering the resistance of proton efflux from the thylakoid lumen, whereas modulation of p

273 Kcne2 deletion doubled the rate of free I(-) efflux from the thyroid following ClO(4)(-) injection, a

274 erstitial fluid pressure, which drives fluid efflux from the tumor core.

275 , AVT4, and AVT6, are involved in amino acid efflux from the vacuole and, as such, are the first to b

276 Q3: Does malate efflux from the vacuole set the pace of decarboxylation?

277 lux systems, while Fre7p plays no role in Fe-efflux from the vacuole.

278 Ca(2+) signal responsible for triggering ion efflux from the vacuole.

279 iation with vesicles and peptide-induced dye efflux from the vesicle lumen were examined experimental

280 In that transient state tp10 "catalyzes" dye efflux from the vesicle lumen.

281 (13)C-BV IXdelta and BV IXbeta products are effluxed from the cell by an as yet unidentified transpo

282 onic lipophilic compounds, many of which are effluxed from the cell by QacA via the proton motive for

283 If FC is not effluxed from the cell, it becomes esterified, CE drople

284 d from the brain endothelial cytosol and was effluxed from the endothelial cells.

285 4)] in, and PINFORMED7 (PIN7)-mediated auxin efflux from, the medial domain.

286 igh-density lipoprotein-specific cholesterol efflux from these cells.

287 ed that these proteins are required for iron efflux from these cells.

288 Rather, A2E prevents cholesterol efflux from these organelles, which in turn indirectly i

289 ine habitats, but the carbon dioxide (CO(2)) effluxes from these net heterotrophic systems contribute

290 from bulk endosomes, indicating that calcium efflux from this compartment is critical for this proces

291 5 mumol/L) significantly reduced cholesterol efflux from THP-1 and peripheral blood mononuclear cells

292 nascent HDL markedly stimulated cholesterol efflux from tissues into plasma.

293 afferent membrane potentials; the potassium efflux from type I hair cells results from the interdepe

294 e and has been shown to suppress cholesterol efflux from virus-infected macrophages by inducing Nef-d

295 We have examined the cholesterol efflux from wild-type (WT) and mutant forms of SR-BI exp

296 le (rHDL(apoA-I)) binding to and cholesterol efflux from wild-type (WT) and mutant forms of the HDL r

297 Cholesterol efflux from wild-type, ABCA1(-/-), SR-BI(-/-), and ABCG1

298 poE4-259 caused similar (20-25%) cholesterol efflux from WT SR-BI.

299 We have now measured (36)Cl(-) efflux from Xenopus oocytes expressing bi- or tripartite

300 tilbene-2,2' disulfonic acid-sensitive 36Cl- efflux from Xenopus oocytes.