ライフサイエンスコーパス: efflux

1 elate directly with an impact on Pgp-derived efflux.

2 amyloid precursor protein to facilitate iron efflux.

3 rescence specifically in HSCs because of dye efflux.

4 mulation, induced by the inhibition of auxin efflux.

5 hanced mitochondrial Na(+) uptake and Ca(2+) efflux.

6 Gbetagamma interacts with DAT to promote DA efflux.

7 enerate sufficient Fe(II) to suppress Cr(VI) efflux.

8 oward select xenobiotics by triggering their efflux.

9 d protection is the result of enhanced water efflux.

10 s exist for controlling lysosomal amino acid efflux.

11 hanistic insights into antibacterial peptide efflux.

12 facilitate efflux of the plant hormone auxin efflux.

13 te, which may facilitate efficient multidrug efflux.

14 orption and promoting macrophage cholesterol efflux.

15 m measurements of the intrinsic rate of acid efflux.

16 potassium (K(+)) channels and resultant K(+) efflux.

17 MCs in the lesions, and impaired cholesterol efflux.

18 howed increased channel activity and Mal(2-) efflux.

19 gger the exchange mode, leading to substrate efflux.

20 t with APOE's role in regulating cholesterol efflux.

21 is Xpr1 deficiency significantly affected Pi efflux.

22 oss of TSPO resulted in impaired cholesterol efflux.

23 and nutrient retention, but no effect on CO2 efflux.

24 drug delivery agents to evade P-gp-dependent efflux.

25 s greater than the diffusive sea-air methane efflux (17.3 +/- 4.8 mumol m(-2)d(-1)).

26 (FADS1), cellular cholesterol uptake (LDLR), efflux (ABCA1 and ABCG1), and inflammation (DHCR24).

27 was a low-affinity nitrate transporter with efflux activity.

28 cells was accompanied by an increase in its efflux activity.

29 strate this technology, targeting antifungal efflux and biofilm adhesion factors.

30 sequent edema can hinder cerebrospinal fluid efflux and can lead to locally increased pressures in th

31 ncreasing OsALMT4 expression affected malate efflux and compartmentation within the tissues, which in

32 ty, we estimated that most of the litter CO2 efflux and decay occurring in the dry season was due to

33 al MC1-R displayed a phenotype with impaired efflux and enhanced uptake of cholesterol.

34 d in regulating compound activation, uptake, efflux and importantly, target processes.

35 everal signaling events, including cytosolic efflux and influx of select ions, have been suggested.

36 SLC30A10 and SLC39A14 are manganese efflux and influx transporters, respectively.

37 tion of PKC reduces AMPH-stimulated dopamine efflux and locomotor activity.

38 inflammasome activation, which involved K(+) efflux and M1 protein internalization by clathrin-mediat

39 ting plant and fungal productivity, soil CO2 efflux and nutrient retention.

40 ses transcription of genes that promote zinc efflux and storage.

41 llular cholesterol mobilization, cholesterol efflux, and bile acid synthesis.

42 te macrophage M2 polarization or cholesterol efflux, and thereby MafB mediates their beneficial effec

43 The cholesterol efflux/apoA-1 ratio was inversely associated with T2DM d

44 ticipants who were in the higher cholesterol efflux/apoA-I presented significantly higher disposition

45 subjects who were in the higher cholesterol efflux/apoA-I quartile compared to subjects in the lowes

46 tes was analysed by quartiles of cholesterol efflux/apoA-I, incidence of T2DM was reduced by 54% in s

47 ion of the purinergic receptor P2X7 and K(+) efflux, apoptosis-associated speck-like protein with a C

48 ted cholesterol endocytosis, and cholesterol efflux are all essential to NCEH-1-mediated neuroprotect

49 nducible factor (HIF) that increases lactate efflux as a result of enhanced glycolysis, but it also e

50 very after photobleaching and a novel sterol efflux assay.

51 econstituted MscL in a liposomal fluorescent efflux assay.

52 ences using macroscopic rubidium ((86)Rb(+)) efflux assays and patch-clamp electrophysiology.

53 -) diminishes the inward tail current (Cl(-) efflux) at a membrane potential of -100 mV due to the lo

54 adation, calcium mobilization, and potassium efflux but not caspase-11.

55 uxin are regulated by facilitated uptake and efflux, but detailed molecular understanding of the carr

56 ession, and increased macrophage cholesterol efflux by inducing ATP-binding cassette subfamily A memb

57 nown crystal structures and show that Ca(2+) efflux by LMCA1 is rate-limited by phosphoenzyme formati

58 In neuronal cultures lithium attenuates iron efflux by lowering tau protein that traffics amyloid pre

59 nvasive infection, we demonstrated that iron efflux by PmtA is critical for bacterial survival during

60 However, amphetamine-induced efflux by SERT-DeltaN32 or SERT-DeltaN42 (but not by SER

61 ts as a lever to support amphetamine-induced efflux by SERT.

62 tatin (20 mg/day) did not change cholesterol efflux capacity (average percentage change -1.5%, 95% CI

63 ood samples were drawn to assess cholesterol efflux capacity (CEC) and changes in gene expression in

64 ggest that CD4(+)CD161(+) T cells with rapid efflux capacity contribute to the maintenance of viral-s

65 In conclusion, HDL cholesterol efflux capacity is not a prognostic cardiovascular risk

66 we investigated whether the HDL cholesterol efflux capacity is predictive for cardiovascular risk.

67 Both TMDs increased cholesterol efflux capacity relative to baseline (P=0.018 and P=0.01

68 In JUPITER, cholesterol efflux capacity was associated with incident CVD in indi

69 On-statin cholesterol efflux capacity was inversely associated with incident C

70 Cholesterol efflux capacity was moderately correlated with HDL chole

71 ression analyses, we found no association of efflux capacity with the combined primary end point (haz

72 erol levels, apolipoprotein A-I, cholesterol efflux capacity, and HDL particle number were assessed a

73 indices of HDL quality, such as cholesterol efflux capacity, and HDL quantity, such as HDL particle

74 to be largely determined by its cholesterol efflux capacity, which was shown to inversely correlate

75 isation, requires simultaneous modulation of efflux carrier level and polarity; and (3) multiple patt

76 The protein abundance of the auxin efflux carrier PIN2 is reduced at hypoxic conditions, a

77 ity; and (3) multiple patterns of influx and efflux carriers for maintaining an auxin pattern do not

78 We demonstrate that (1) when efflux carriers maintain polarity but change levels, mai

79 nvolve PIN-FORMED (PIN)-type plasma membrane efflux carriers that generate subcellular auxin gradient

80 unced polar distribution of PIN-FORMED auxin efflux carriers within the plasma membrane.

81 e polarly distributed PIN-FORMED (PIN) auxin efflux carriers.

82 ion requires coordination between influx and efflux carriers.

83 are present, S degrees is absent and slow H2 efflux causes growth inhibition.

84 Drug-effluxing CD4(+) T cells were characterized as CD161(+)C

85 Multidrug-effluxing CD4(+)CD161(+) T cells also resisted chemother

86 Multidrug-effluxing CD4(+)CD161(+) T cells were enriched within th

87 a subset of memory CD4(+) T cells capable of effluxing cellular toxins, including rhodamine (Rho), th

88 er sequences of mRNAs encoding ion uptake or efflux channels.

89 nt activity (-35%) and a reduced capacity to efflux cholesterol (-60%) compared to NC-HDL (p < 0.05).

90 nd reveals mechanistic divergence within the efflux class of ABC transporters.

91 sing element that drives the assembly of the efflux complex ahead of the transcription activation of

92 living Escherichia coli cells the tripartite efflux complex CusCBA of the resistance-nodulation-divis

93 stance has been reported, the most expressed efflux complex is MtrCDE.

94 Multicomponent efflux complexes constitute a primary mechanism for Gram

95 In contrast to other efflux conduits, the open complex only displays a slight

96 AT blocked the ability of mSIRK to induce DA efflux, consistent with a direct interaction of Gbetagam

97 Gaseous N2O and N2 effluxes, dissolved N2O flux, and traditionally measured

98 evealed that M2 polarization and cholesterol efflux do not necessarily represent inter-dependent even

99 to affect SLC30A9's highly conserved cation efflux domain, putatively disrupting its transmembrane h

100 In brief, ALMT4 likely mediates Mal(2-) efflux during ABA-induced stomatal closure and its activ

101 ntrolled by the balance between Ca entry and efflux during systole.

102 the balance between Ca(2+) entry and Ca(2+) efflux during systole.

103 al neurons, not astrocytes; mediates HCO3(-) efflux) enhances intracellular pH (pHi ) recovery (decre

104 We evaluated the effect on soil CO2 efflux (FCO2 ) of sudden changes in photosynthetic rates

105 y', in the presynaptic cytosol revealed acid efflux following nerve activity to be greater than that

106 ing and root trenching and measured soil CO2 efflux for over 1 yr in longleaf pine (Pinus palustris),

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

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

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

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

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

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

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

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

115 es a pronounced, delayed enhancement of K(+) efflux, generating an optimal intracellular environment

116 Cholesterol efflux genes (APOE and ABCA1) were identified as risk fa

117 UPEC upregulates the expression of Cu efflux genes during clinical UTI in patients as an adapt

118 involved in mitochondrial calcium influx and efflux have recently been identified.

119 TSPO expression was reduced and cholesterol efflux impaired.

120 demonstrate the essential nature of mCa(2+) efflux in cellular function and suggest that augmenting

121 ne leads to the critical enhancement of K(+) efflux in damaged neurons.

122 oA-I]-binding protein)-regulated cholesterol efflux in endothelial cells controls zebra fish embryoni

123 Radiotracer uptake and efflux in hNIS-transduced HCT116-C19 cells and the hNIS-

124 Both fluoxetine and thioridazine inhibited efflux in P. mirabilis, and molecular modelling predicte

125 permeabilization to propidium iodide and ATP efflux in response to C4.

126 inflammasome sensor NLRP3 and for potassium efflux in T. gondii-induced IL-1beta production.

127 both JJ-3-42 and lorcaserin reduced dopamine efflux in the infralimbic cortex, while only JJ-3-42 dec

128 longation and demonstrate the role of myosin efflux in the second phase.

129 n variants on SLC22A1-mediated acylcarnitine efflux in vitro, explaining their association with serum

130 the contribution of exosomes to active drug efflux increased with drug concentration and exceeded th

131 sk factors for AMD, although how cholesterol efflux influences accumulation of this lipid in sub-RPE

132 pase-1 inhibition, NLRP3 knockdown, and K(+) efflux inhibition and were not observed with other non-a

133 , which could potentially be targeted by new efflux inhibitors.

134 This myosin efflux is a novel feature of cytokinesis and its duratio

135 study evaluated whether baseline cholesterol efflux is associated with future development of type 2 d

136 ncement of evoked dopamine release and basal efflux is dependent on sigma receptor activation.

137 us expression system indicate that this acid efflux is mediated by conventional plasmamembrane acid t

138 AMPH-stimulated dopamine efflux is modulated by protein kinase C (PKC) activation

139 This efflux is necessary to ensure Fe(III) solubility and mob

140 Antibiotic efflux is one of the most critical mechanisms leading to

141 By an unknown mechanism, amino acid efflux is stimulated in plants by overexpression of a me

142 The last event increases chloride efflux, leading to compensatory chloride influx via NCC

143 function and suggest that augmenting mCa(2+) efflux may be a viable therapeutic strategy in disease.

144 clude metallopeptidases, multidrug-resistant efflux (MDR) pumps, TonB-dependent receptors and many pr

145 r endocytosis or exocytosis revealed an acid efflux mechanism reliant upon synaptic vesicle exocytosi

146 ve been resolved, shedding some light on the efflux mechanism underlying this intriguing system.

147 ment and should improve our understanding of efflux mechanisms based on MRP1.

148 ized that the same activity might drive acid efflux mechanisms to maintain pHcyto homeostasis.

149 ite previously implicated in AMPH-stimulated efflux mechanisms.

150 iotics that are currently ineffective due to efflux mechanisms.

151 The accelerated drug efflux mediated by ATP-binding cassette (ABC) transporte

152 both NLRP3 depletion and inhibition of K(+) efflux mitigated abacavir-induced mitochondrial reactive

153 In conclusion, HDL-cholesterol efflux normalised to apoA-I was inversely associated wit

154 Uptake and efflux of (18)F-IRS were performed with four NSCLC cell

155 c22a1, we uncovered a role of SLC22A1 in the efflux of acylcarnitines from the liver to the circulati

156 ciated with transmembrane proteins mediating efflux of administered drugs, thereby keeping their intr

157 adaptor protein and TolC exit duct to drive efflux of antibiotics and enterotoxin STII out of the ba

158 Pannexin-1 (Panx1) channels mediate the efflux of ATP and AMP from cancer cells in response to i

159 ABCC6 facilitates the cellular efflux of ATP, which is rapidly converted into pyrophosp

160 and inhibited DHPR and SERCA, inducing a net efflux of Ca(2+) from loaded microsomes, whereas BPA exh

161 SR-B1 also facilitates the efflux of cholesterol from peripheral tissues, including

162 wn, in vitro, to participate in the cellular efflux of desmosterol and amyloid-beta peptide (Abeta).

163 ss pathways by enhancing translocon-mediated efflux of ER calcium.

164 nonequilibrium factors, including influx and efflux of lipid molecules.

165 l vacuoles, specifically of K(+) and Mal(2-) Efflux of Mal(2-) from the vacuole is required for stoma

166 ition of mTOR strongly reduced the lysosomal efflux of most essential amino acids, converting the lys

167 (MRP1) expression, and greater MRP1-mediated efflux of NO2-OA-glutathione conjugates.

168 (eUnaG) to detect transporter-coupled influx/efflux of organic compounds.

169 s and are likely to contribute to the future efflux of PCBs from the lake to the air.

170 Our model considers the cellular uptake and efflux of PFOA via both passive diffusion and transport

171 ins (NBDs) to power the energetically uphill efflux of substrates by a dedicated transmembrane domain

172 ing in the inner membrane resulting in rapid efflux of succinate/fumarate and other dicarboxylates ca

173 ially facilitate phloem loading by enhancing efflux of symplasmic Suc for subsequent active uptake in

174 SbMATE mediates efflux of the anionic form of the organic acid, citrate,

175 major impact on the simultaneously measured efflux of the charged d-[(14) C]aspartate.

176 f the cell of PIN proteins, which facilitate efflux of the plant hormone auxin efflux.

177 Efflux of uncharged osmolytes (myo-inositol and taurine)

178 at an adequate rate is H(+)-coupled lactate efflux on monocarboxylate transporters (MCTs).

179 djacent to orthologs of the mmpS5-mmpL5 drug efflux operon.

180 lance equations to track C influxes into and effluxes out of individual pools in earth system models

181 ell death involves interplay between ATP/AMP efflux pathways and different cell-autonomous ectonucleo

182 ycline repressors (TetRs) modulate multidrug efflux pathways in several pathogenic bacteria.

183 selection, with most belonging to antibiotic efflux pathways.

184 e genes, arsP that encodes the ArsP MAs(III) efflux permease, and arsH encoding the ArsH MAs(III) oxi

185 The drug efflux process has been proposed to entail a synchronize

186 uding rhodamine (Rho), through the multidrug efflux protein MDR1 (also known as P-glycoprotein and AB

187 strain expressing the tetracycline-specific efflux pump (TetA) compared to the isogenic control.

188 ction proteins, VEGF-dependent permeability, efflux pump activity and receptor-mediated transcytosis

189 nesis identified the importance of the AcrAB efflux pump and lipopolysaccharide O-antigen synthesis f

190 us is recognised for its ability to modulate efflux pump and porin expression via two encoded transcr

191 Understanding the mechanism of efflux pump assembly and its dynamics could facilitate d

192 ucleotide polymorphisms (SNPs) as well as an efflux pump cmeB mutation that conferred modest resistan

193 and cadmium-dependent regulator of CadA, an efflux pump conferring cadmium resistance.

194 AcrA, a critical component of the AcrAB-TolC efflux pump in Escherichia coli.

195 of the Escherichia coli AcrAB-TolC multidrug efflux pump in resting and drug transport states, reveal

196 when the pools were co-administered with an efflux pump inhibitor.

197 Small molecule adjuvants that act as efflux pump inhibitors (EPIs) have the potential to rein

198 ant efflux pump of Staphylococcus aureus, an efflux pump inhibitors (EPIs) library was used for ligan

199 ine biofilms, highlighting the potential for efflux pump inhibitors (EPIs) to control catheter blocka

200 We previously reported that the Tet38 efflux pump is involved in internalization of Staphyloco

201 ancer types, the functional activity of this efflux pump is more difficult to elucidate, especially a

202 e report that AcrAB-TolC, the main multidrug efflux pump of Escherichia coli, exhibits a strong parti

203 Focusing on NorA, the most important efflux pump of Staphylococcus aureus, an efflux pump inh

204 CadC appears as the first metal efflux pump regulator repurposed during infection to fin

205 (formerly YdfM) serves as the primary Mn(II) efflux pump with MneS (formerly YeaB) playing a secondar

206 code a copper binding chaperone and a copper efflux pump, but in some the chaperone encoding gene has

207 Ferroportin (FPN), the iron efflux pump, is decreased, and transferrin receptor (TFR

208 P-glycoprotein, an ATP-driven efflux pump, regulates permeability of the blood-brain b

209 s of the Campylobacter jejuni CmeB multidrug efflux pump.

210 n MexA and OprM in the context of the entire efflux pump.

211 In Gram-negative bacteria, efflux pumps are able to prevent effective cellular conc

212 Tripartite efflux pumps are one of the major contributors to resist

213 pid, ceramide 1-phosphate (C1P), to modulate efflux pumps at the BBB.

214 ell lines with activated P-glycoprotein drug efflux pumps compared to drug-sensitive parent cells, de

215 Bacterial efflux pumps confer multidrug resistance by transporting

216 e assessed the transport activity of several efflux pumps in isolated rat brain capillaries.

217 Metal efflux pumps maintain ion homeostasis in the cell.

218 on independently within the trimer.Multidrug efflux pumps significantly contribute for bacteria resis

219 ng pharmacokinetic variability, induction of efflux pumps that transport the drug out of cells, and s

220 ight the importance of performing studies of efflux pumps under near-physiological conditions, in a l

221 were characterized as ABC efflux pumps, RND efflux pumps, and tetracycline MFS efflux pumps.

222 ing multidrug-resistance mechanisms, such as efflux pumps, are under development and hold promise for

223 st of the AR genes were characterized as ABC efflux pumps, RND efflux pumps, and tetracycline MFS eff

224 ng cation diffusion facilitator (CDF) family efflux pumps.

225 s diverse targets ranging from small RNAs to efflux pumps.

226 s, diverse secretion systems, and antibiotic efflux pumps.

227 umps, RND efflux pumps, and tetracycline MFS efflux pumps.

228 ll permeability, and induction/activation of efflux pumps.

229 sistance is represented by the inhibition of efflux pumps.

230 annotated as urea carboxylases and multidrug efflux pumps.

231 apparently not susceptible to the action of efflux pumps.

232 As-hyperaccumulator Pteris vittata arsenite efflux (PvACR3), on As tolerance, accumulation, transloc

233 proach is limited by local retention of cell-effluxed radiotracer.

234 Retinal efflux rate constant k2 was significantly decreased by 2

235 ion was observed between temocillin MICs and efflux rate of N-phenyl-1-naphthylamine (MexAB-OprM fluo

236 entrations increased growing-season soil CO2 efflux rates by increasing annual aboveground net primar

237 imental fire significantly elevated soil CO2 efflux rates in the next growing season.

238 improved Caco-2 permeability, reduced Caco-2 efflux, reduced hERG PC activity, and increased selectiv

239 agalactiae (PDB 3KKC) is the bona fide zinc efflux regulator SczA, and binds two zinc ions per proto

240 e the outer membrane, improved inhibition of efflux relative to 1, and potentiation of the activity o

241 otein(s) participating in the basolateral Pi efflux remains unknown.

242 losteric inhibition of DNA binding by the Zn efflux repressor CzrA (chromosomal zinc-regulated repres

243 sly shown that efficient PIN1-mediated auxin efflux requires activation through phosphorylation at th

244 und net primary production: aNPP) and soil C efflux (soil respiration: Rs).

245 The Bcr/CflA efflux system has previously been identified as importan

246 Mutations in the MexAB-OprM efflux system, naturally occurring in cystic fibrosis (C

247 Escherichia coli CusCFBA is a complex efflux system, responsible for transferring Cu(I) and Ag

248 trongly with the biofilm-associated Bcr/CflA efflux system.

249 ht the delicate balance of Mn(II) uptake and efflux systems controlled by MntR.

250 be broadly relevant to other multicomponent efflux systems.

251 CD4(+)CD161(+)Rho-effluxing T cells proliferated vigorously in response to

252 otent at inhibiting AMPH-stimulated dopamine efflux than [(3)H]dopamine uptake through the dopamine t

253 nnels and activates H(+) -ATPase proton pump efflux that dissociates periplasmic AGP-Ca(2+) resulting

254 e muscarinic M5R, results in DAT-mediated DA efflux through a Gbetagamma-dependent mechanism.

255 Polychaetes indirectly enhance methane efflux through bioturbation, while bivalves have a direc

256 ding/activating peptide, mSIRK, increases DA efflux through DAT in heterologous cells and primary dop

257 t TSPO specific ligands promoted cholesterol efflux to acceptor (apo)lipoprotein and human serum, whi

258 s identified to support a role of macrophage efflux to draining lymph nodes following treatment with

259 ages following TNF inhibition, positing that efflux to draining lymph nodes was involved.

260 of CUA-1 to basolateral membranes for copper efflux to peripheral tissues.

261 As(V) reduction in roots, decreased As(III) efflux to the external medium and markedly increased As

262 Adding N2O and N2 effluxes to catchment nitrogen output not only reduced t

263 c strategies to inhibit ABCB1/ABCG2-mediated efflux transport at the BBB have been successfully devel

264 ffective treatments using drugs that undergo efflux transport at the BBB.

265 tes the blood-brain barrier (BBB) because of efflux transport by P-glycoprotein (ABCB1) and breast ca

266 duced inhibition of the multidrug-resistance efflux transporter ABCB1, which is frequently expressed

267 an Arabidopsis (Arabidopsis thaliana) boron efflux transporter displayed boron deficiency phenotypes

268 ere we utilized FrvA, a high-affinity Fe(2+) efflux transporter from Listeria monocytogenes, as an in

269 Our findings demonstrate that the efflux transporter of the siderophore SA contributes to

270 increases the expression and activity of the efflux transporter P-glycoprotein (P-gp) encoded by ABCB

271 oupled conformational cycle of the mouse ABC efflux transporter P-glycoprotein (Pgp; also known as AB

272 ux transporters-Arabidopsis PM-located auxin efflux transporter PIN-formed 1 (PIN1) and Arabidopsis P

273 ed 1 (PIN1) and Arabidopsis PM-located auxin efflux transporter PIN-formed 3 (PIN3)-to the PM, thereb

274 Finally, both Arabidopsis thaliana auxin efflux transporter pin1 and influx transporter lax2 muta

275 ABCC6 is an efflux transporter primarily expressed in liver facilita

276 SLC30A10, a cell-surface-localized manganese efflux transporter, cause a heritable manganese metaboli

277 lls stably expressing specific uptake and/or efflux transporters revealed that OATP1B1, OATP1B3, and

278 lthough doxorubicin is a known substrate for efflux transporters such as P-glycoprotein (P-gp; MDR1,

279 s/regulators, soluble chaperones, and influx/efflux transporters that control the Cu(+) levels in P.

280 s, restrictive barrier formation, influx and efflux transporters with relevance to understanding peri

281 ellular drug concentrations mediated by drug efflux transporters, and permeability barriers associate

282 affect transport activity of two other major efflux transporters, multidrug resistance protein 2 and

283 expression alters the trafficking of 2 auxin efflux transporters-Arabidopsis PM-located auxin efflux

284 mbly allows the bacterial cell for efficient efflux upon cellular demand while still maintaining peri

285 es a cell death program initiating potassium efflux upstream of NLRP3.

286 greater influence during the wet season when efflux was high than during the dry season when efflux w

287 s across the Mediterranean Basin, litter CO2 efflux was largely explained by litter moisture driving

288 lux was high than during the dry season when efflux was low.

289 This efflux was proposed to rely on the N terminus, which was

290 Cholesterol efflux was quantified by incubation of cholesterol-loade

291 In vitro, radiotracer incorporation and efflux was similar with no effect on cell viability, fun

292 Increased MDCK efflux was utilized to identify compounds such as 33 wit

293 Given the role of AcrAB-TolC in multi-drug efflux we suggest that CsrA is a potential drug target.

294 antibiotic target alteration and antibiotic efflux were the dominant resistance mechanism categories

295 r techniques used to measure day respiratory efflux were valid and whether day respiration responded

296 oncentration and exceeded the p-glycoprotein efflux when the latter was saturated.

297 C1-R agonists similarly promoted cholesterol efflux, which is a counterregulatory mechanism against f

298 evel carbon exchange and soil carbon dioxide efflux with local meteorology data.

299 ecreases methamphetamine-stimulated dopamine efflux without affecting basal dopamine neurotransmissio

300 istency with C. albicans nomenclature) could efflux xenobiotics such as berberine, rhodamine 123, and