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 let binding blocked agonist-induced 22Na ion efflux from AChR-rich vesicles.

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

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

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

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

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

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

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

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

16 4RK augmented strongly CFTR-mediated iodide efflux from BHK cells expressing G551D-CFTR.

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

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

19 We characterized the efflux from brain of radioactively labeled viral coat HI

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

21 (3,4,5)P(3) is capable of stimulating Ca(2+) efflux from Ca(2+)-loaded plasma membrane vesicles prepa

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

41 K+ efflux from cells was quantified from increasing extrace

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

43 eruloplasmin in determining the rate of iron efflux from cells with mobilizable iron stores.

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

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

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

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

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

49 lity to promote cholesterol and phospholipid 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 f ABC1 reduces apolipoprotein-mediated lipid efflux from cultured cells, and increasing expression of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

82 Ca2+ efflux from hepatocyte populations was measured by using

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 Peptide efflux from isolated mitochondria was ATP dependent and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

113 Ciprofloxacin efflux from loaded cells occurred more rapidly than with

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

139 1 have a major role in promoting cholesterol efflux from macrophages to apolipoprotein A-1 and HDL an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

166 2-APB inhibited Ca(2+) efflux from mitochondria.

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

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

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

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

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

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

173 The rate of proton efflux from muscle fibres of Becker muscular dystrophy p

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

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

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

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

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

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

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

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

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

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

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

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

186 ABCA1 facilitates free cholesterol efflux from peripheral tissues.

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

188 ary cells or VPAC(1) receptor-dependent cAMP efflux from pinealocytes but strongly inhibited GHRH-sti

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

190 Studies of CaM efflux from preloaded nuclei in permeablized cells revea

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

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

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

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

195 processes, one of them being increased drug efflux from resistant cells which leads to a decreased i

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

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

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

199 blockers on copper and peroxide-induced K(+) efflux from seedling roots.

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

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

202 ode was used to monitor directly doxorubicin efflux from single preloaded cancer cells.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

228 of the cell, indicative of detection of Zn2+ efflux from the cell.

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

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

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

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

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

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

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

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

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

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

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

240 In plant cells, Ca(2+) efflux from the cytoplasm is mediated by H(+)/Ca(2+)-ant

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

242 riplasmic protein, which together coordinate efflux from the cytoplasmic membrane across the outer me

243 We examined the effect of hypoxia on Ca(2+) efflux from the cytosol in single Fura-2-loaded pulmonar

244 Calcium (Ca(2)+) efflux from the cytosol modulates Ca(2+) concentrations

245 conjugation by sulfotransferases followed by efflux from the enterocytes.

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

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

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

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

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

251 The slow accumulation of TPP+ and its slow efflux from the lens under conditions known to depolariz

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

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

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

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

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

257 ed induction of cholesterol and phospholipid efflux from the murine macrophage RAW264 cell line to li

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

259 talyzed prodrug conversion (k(1)(app)), 5-FU efflux from the observable tumor volume (k(2)(app)), and

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

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

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

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

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

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

266 Determining the amount of glutamate efflux from the synaptic cleft and the distance it diffu

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

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

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

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

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

272 SCP-2 differentially modulated sterol efflux from the two cytoplasmic pools.

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

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

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

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

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

278 8F]FBWAY ([18F]4b) showed an early rapid net efflux from the whole brain, clearing with a biological

279 Measurements of Na+ efflux from the wild-type strain, the nonpolar mrpA muta

280 ause of the higher thapsigargin-sensitive Ca efflux from the WT membranes.

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 igate the mechanism of ABC-1-dependent lipid efflux from these cells, apo A-1 was preincubated in the

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

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

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

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

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

292 5 mumol/L) significantly reduced cholesterol efflux from THP-1 and peripheral blood mononuclear cells

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

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.