ライフサイエンスコーパス: electrical resistance

1 ntestinal tissue resistance (transepithelial electrical resistance).

2 a corresponding decrease in transepithelial electrical resistance).

3 specific antigen dramatically increases the electrical resistance.

4 pidly develops a substantial transepithelial electrical resistance.

5 helium integrity by reducing transepithelial electrical resistance.

6 simultaneous measurement of transendothelial electrical resistance.

7 ator) to CEM as well as HGF-induced trans-EC electrical resistance.

8 BC binding but not their ability to decrease electrical resistance.

9 d on random walks, information diffusion and electrical resistance.

10 er integrity as measured by transendothelial electrical resistance.

11 ell adhesion as measured by transendothelial electrical resistance.

12 rmeability was monitored with measurement of electrical resistance.

13 ity changes were measured by transepithelial electrical resistance.

14 y attenuated the decrease in transepithelial electrical resistance.

15 ll permeability measured as transendothelial electrical resistance.

16 ght junctions as measured by transepithelial electrical resistance.

17 neously large transverse thermopower and low electrical resistance.

18 t mounts, and measurement of transepithelial electrical resistance.

19 ion in vitro as measured by transendothelial electrical resistance.

20 n and resulted in decreased transendothelial electrical resistance.

21 herin expression and reduced transepithelial electrical resistance.

22 s and reverses reductions in transepithelial electrical resistance.

23 r properties as measured by transendothelial electrical resistance (1,450 +/- 140 ohm cm2), and they

24 hours; P < .001) and reduced transepithelial electrical resistance (281.1 +/- 4.9 vs 370.6 +/- 5.7 Om

25 nt tightness as measured by transendothelial electrical resistance (~5,000 Omegaxcm(2)).

26 layers generated significant transepithelial electrical resistance (750 Omega cm2) and potential diff

27 agents decreased endothelial cell monolayer electrical resistance (a measure of endothelial cell sha

28 hrombin-induced decrease in transendothelial electrical resistance (a measure of increased transendot

29 resulted in an increase in transendothelial electrical resistance, a measure of monolayer integrity.

30 tter studies, the transendothelial monolayer electrical resistance, a measure of the loss of endothel

31 Transepithelial electrical resistance, a measure of tight junction perme

32 osphorylation (antimycin A), transepithelial electrical resistance, a measure of TJ integrity, droppe

33 Electrical resistance across cell monolayers positively

34 impedance sensing (ECIS) was used to measure electrical resistance across cultured rabbit corneal epi

35 tic effect on barrier properties, increasing electrical resistance across monolayers of either glomer

36 AT1002 reduced transepithelial electrical resistance across rat small intestine, ex viv

37 ponse was measured by the change in the BP's electrical resistance after antigens were introduced.

38 cted against the decrease in transepithelial electrical resistance after enteropathogenic E. coli inf

39 esulted in a decrease in the transepithelial electrical resistance, an increase in the efflux of mann

40 tro, as demonstrated through transepithelial electrical resistance analysis.

41 VEGF-C effects on trans-endothelial electrical resistance and albumin flux across GEnC monol

42 rier function as measured by transepithelial electrical resistance and also reduced paracellular flux

43 aldehyde-induced decrease in transepithelial electrical resistance and an increase in inulin permeabi

44 calcium-induced increase in transepithelial electrical resistance and barrier to inulin permeability

45 aracellular barriers vary among epithelia in electrical resistance and behave as if they are lined wi

46 new model and conceptual framework based on electrical resistance and capacitance variations of the

47 rs as indicated by increased transepithelial electrical resistance and cell height.

48 time points, 5-HT decreased transepithelial electrical resistance and disrupted tight junctions.

49 onitored by measurements of transendothelial electrical resistance and endothelial cell permeability

50 iffusion landscape that featured diminishing electrical resistance and entropy in the direction of ch

51 rface were assessed by using transepithelial electrical resistance and fluorescein isothiocyanate-dex

52 re asthma were assessed with transepithelial electrical resistance and fluorescent dextran passage.

53 Measurements of endothelial transmonolayer electrical resistance and immunofluorescent analysis of

54 by 3-NC-induced decrease in transepithelial electrical resistance and increase in mannitol flux over

55 ITC dextran leakage, decreased transcellular electrical resistance and increased angiogenic potential

56 on, as measured by decreased transepithelial electrical resistance and increased fluorescein isothioc

57 onal correlates in decreased transepithelial electrical resistance and increased fluorescein permeabi

58 TNF-alpha lowered transepithelial electrical resistance and increased fluorescent dextran

59 ty, as measured by a loss of transepithelial electrical resistance and increased flux of bovine serum

60 oincident with a decrease in transepithelial electrical resistance and increased flux of small but no

61 n of CB2R agonist increased transendothelial electrical resistance and increased the amount of tight

62 Furthermore, decreased transepithelial electrical resistance and increased translocation of ZO-

63 The study reveals that electrical resistance and interfacial bonding status are

64 hout a detectable change in transendothelial electrical resistance and inulin permeability.

65 aracellular permeability properties, such as electrical resistance and ion selectivity that would com

66 Permeability was assessed by measuring electrical resistance and mannitol fluxes and actin orga

67 on was characterized through transepithelial electrical resistance and mannitol tracer flux.

68 tion as indicated by lowered transepithelial electrical resistance and mislocalization of the tight j

69 ch as postdeformation temporal relaxation of electrical resistance and nonmonotonic changes in resist

70 erature, with the concurrent modification in electrical resistance and optical properties being capab

71 ammonia by monitoring in situ changes in the electrical resistance and optical spectra of films of po

72 ed functionally by measuring transepithelial electrical resistance and permeability.

73 in FAK expression also prolonged the drop in electrical resistance and prevented the recovery seen in

74 coli -associated decrease in transepithelial electrical resistance and redistribution of tight juncti

75 In contrast, UK14304 augmented electrical resistance and reduced macromolecular transpo

76 hagy significantly increased transepithelial electrical resistance and reduced the ratio of sodium/ch

77 restricting the decrease in transepithelial electrical resistance and the increase in epithelial per

78 Transepithelial electrical resistance and tight junction protein archite

79 sed to assay actin cytoskeletal changes, and electrical resistance and tracer experiments with Transw

80 s measured by assaying transendothelial cell electrical resistance and tracer flux.

81 um switch, a decrease in the transepithelial electrical resistance, and by the inability of these cel

82 ZO-1 and Occludin, decreased transepithelial electrical resistance, and increased fluorescein isothio

83 elial integrity, measured as transepithelial electrical resistance, and markers of the peroxidation p

84 o the cytosol, and a reduced transepithelial electrical resistance, and stimulated CRC cell prolifera

85 dens 1, the establishment of transepithelial electrical resistance, and the paracellular flux assay.

86 h decreased small intestinal transepithelial electrical resistance, and was followed by the productio

87 within minutes but decreased transepithelial electrical resistance at 6 to 22 h.

88 th opposite positive and negative changes in electrical resistance at the transformation temperature.

89 The expansion did not increase the electrical resistance but increased the absorption in th

90 : this caused no change in trans-endothelial electrical resistance, but increased the albumin passage

91 ity of glycocalyx, reduced trans-endothelial electrical resistance by 59%, and increased albumin flux

92 tly reduced the thrombin-induced decrease in electrical resistance by approximately 50 %.

93 how a 6-fold increase in the transepithelial electrical resistance by decreasing paracellular permeab

94 Ag2Te, are non-magnetic materials, but their electrical resistance can be made very sensitive to magn

95 Using this approach, the electrical resistance, carrier mobilities and bandgaps o

96 nctions and the decrease in transendothelial electrical resistance caused by both agents.

97 chemically reversible diagnostic pattern of electrical resistance changes upon exposure to different

98 CCL2-induced reductions in transendothelial electrical resistance, claudin-5 and occludin became int

99 High transendothelial electrical resistances, comparable to those reported in

100 of junctional proteins and transendothelial electrical resistance compared with normal human dermal

101 ity monitored by changes in transendothelial electrical resistance, cytoskeletal remodeling caused by

102 ic current, Ca2+ entry, and transendothelial electrical resistance decrease elicited by H2O2 were inh

103 , cationic current, and the transendothelial electrical resistance decrease.

104 hrombin-induced decrease in transendothelial electrical resistance (decrease in mock transfected cell

105 The transepithelial electrical resistance decrement was secondary to the zon

106 ic and non-magnetic (spacer) materials whose electrical resistance depends on the spin state of elect

107 Reasons for the electrical resistance displayed by the so-called B-wire

108 dexamethasone stimulation of transepithelial electrical resistance, disrupted the induced localizatio

109 ical calculation indicates that the trend of electrical resistance drop still holds under the present

110 L. interrogans did not alter transepithelial electrical resistance during cell translocation.

111 ed transient preservation of transepithelial electrical resistance during the early stage of hypoxia

112 gnificantly attenuates this transendothelial electrical resistance elevation.

113 o decreased trans-monolayer transendothelial electrical resistance for 3 hours (with maximal effect s

114 dent fashion for the loss of transepithelial electrical resistance, for increased monolayer permeabil

115 ture, and VEGF-C increased trans-endothelial electrical resistance in a dose-dependent manner with a

116 mping rate of atomic motion (the analogue of electrical resistance in a solid) in the confining parab

117 Real-time acquisition of transendothelial electrical resistance in an all-human, in vitro, 3-dimen

118 nical superconductivity, which requires zero electrical resistance in an applied magnetic field and d

119 The observation of vanishing electrical resistance in condensed matter has led to the

120 dextran flux, and decreased transepithelial electrical resistance in JAM-A(-/-) mice.

121 triggered a small decline in transepithelial electrical resistance in polarized cultures, this did no

122 infection caused a loss of transendothelial electrical resistance in primary mouse brain endothelial

123 s in short-circuit current and decreases the electrical resistance in rat jejunum mounted in an Ussin

124 netoresistance is the change in a material's electrical resistance in response to an applied magnetic

125 ap area and 60% decrease in transendothelial electrical resistance) in WT but not Trpc1(-/-) ECs.

126 both stretchable and transparent, but their electrical resistances increase steeply with strain <100

127 e stress-induced decrease in transepithelial electrical resistance, increase in inulin permeability,

128 The oxidative stress-induced decrease in electrical resistance, increase in inulin permeability,

129 n vitro including decreased transendothelial electrical resistance, increased actinomyosin stress fib

130 nnitol increases sixfold but transepithelial electrical resistance increases >40%.

131 d a fourfold increase in the transepithelial electrical resistance indicated the formation of functio

132 ure was an increase in the trans-endothelial electrical resistance, indicating the induction of barri

133 was accompanied by reduced transendothelial electrical resistance, indicating the paracellular route

134 to the composition of the solvent, and whose electrical resistance is sensitive to physical deformati

135 for epitaxial thin films extracted from the electrical resistance measured in very high magnetic fie

136 Remote electrical resistance measurement is evaluated here as a

137 compression, and match the result of in situ electrical resistance measurement under high pressure co

138 Electrical resistance measurements across human lung end

139 maintained, as assessed by transendothelial electrical resistance measurements at the end of the exp

140 ll substrate sensing and by transendothelial electrical resistance measurements in an in vitro human

141 on between these spectroscopic findings with electrical resistance measurements leads to a more compr

142 roscopy, X-ray diffraction, four-point probe electrical resistance measurements, IR spectroscopy, and

143 d by immunoblot analysis and transepithelial electrical resistance measurements, respectively.

144 ts integrity was assessed by transepithelial electrical resistance measurements.

145 nolayers was examined using transendothelial electrical resistance measurements.

146 bitor SK1-I decreased basal transendothelial electrical resistance more in WT ECs (48 and 72% reducti

147 nolayers achieved a maximal transendothelial electrical resistance of 130 Omega cm2, but lacked real

148 The electrical resistance of a conductor is intimately relat

149 aseous molecules such as NO(2) or NH(3), the electrical resistance of a semiconducting SWNT is found

150 surface traps which ultimately increase the electrical resistance of a solid.

151 llary method based on the measurement of the electrical resistance of a solution placed inside the ca

152 The electrical resistance of an array of these nanowires inc

153 keratinocyte monolayers had trans-epithelial electrical resistance of approximately 176 to 208 omega.

154 dependent reduction in the trans-epithelial electrical resistance of Caco-2 monolayers and an impres

155 The transepithelial electrical resistance of cecal explants from C57BL/6 and

156 ET increased the transendothelial electrical resistance of endothelial monolayers, a respo

157 ect of angiotensin-(1-7) on transendothelial electrical resistance of human pulmonary microvascular e

158 after Kammerlingh Onnes discovered that the electrical resistance of mercury falls to zero below a t

159 amine-stimulated changes in transendothelial electrical resistance of microvascular endothelial cells

160 We explore the contributions to the electrical resistance of monolayer and bilayer graphene,

161 The through-nanowire electrical resistance of PEDOT-DFA nanowires is measured

162 The electrical resistance of skin, a surrogate measure of th

163 iginated from the large surface area and low electrical resistance of the AFFs.

164 vary significantly with the transepithelial electrical resistance of the cells or when STb was appli

165 strong deviation from planarity, the similar electrical resistance of the different systems, planar a

166 pression resulted in increased transmembrane electrical resistance of the endothelial monolayer and p

167 based biosensor that measures the changes in electrical resistance of the enzyme-plated interdigitate

168 15-HETE on permeability and transepithelial electrical resistance of the IEB were measured using Cac

169 ent particles on the surface touched and the electrical resistance of the micro-channel dropped by se

170 The electrical resistance of the nanoparticle assemblies is

171 and significantly increased transendothelial electrical resistance of the nonbarrier human umbilical

172 otoresistor, and (iii) the variations in the electrical resistance of the photoresistor were correlat

173 pproximately approximately 40 degrees C, the electrical resistance of the protoplasmic tube increases

174 sor during the forced exhalation reduced the electrical resistance of the sensor, which was converted

175 e parasite compared with the transepithelial electrical resistance of their wild-type counterparts, s

176 g an array of virus-PEDOT nanowires with the electrical resistance of these nanowires for transductio

177 ed transendothelial potential difference and electrical resistance of this BBB model.

178 rating structure with good stability and low electrical resistance (only about 1Omega/ square).

179 age of current (measured as transendothelial electrical resistance or TEER).

180 no effect on the decrease in transepithelial electrical resistance or the redistribution of occludin.

181 baking, crustless cakes were baked using an electrical resistance oven (ERO).

182 157:H7-induced reductions in transepithelial electrical resistance (P < .01), decreased permeability

183 l cells were used to measure transepithelial electrical resistance, paracellular flux of fluorescein

184 ECs) by means of analysis of transepithelial electrical resistance, paracellular flux, mRNA expressio

185 ed barrier function as determined by reduced electrical resistance, paracellular permeability assays,

186 were assessed by measuring transendothelial electrical resistance, permeability of differently sized

187 trated by measurements of the transmonolayer electrical resistance, permeability of endothelial monol

188 toxin A-mediated decline in transepithelial electrical resistance preceded changes in cell morpholog

189 exhibit an unprecedentedly large and tunable electrical resistance range from 10(2) to 10(8) Omega co

190 d 4-HNE-induced decrease in transendothelial electrical resistance, reactive oxygen species generatio

191 1% O(2)) as well as enhanced transepithelial electrical resistance recovery after prolonged hypoxia i

192 PLVAP inhibition attenuated transendothelial electrical resistance reduction induced by VEGF in BRB m

193 Because the relative change of the electrical resistance represents the sensor's response,

194 te dehydrogenase leakage and transepithelial electrical resistance, respectively.

195 The dc electrical resistance response of the composites was fou

196 permeability that effected changes in the dc electrical resistance response of these compositionally

197 ly to relate the QCM frequency change and dc electrical resistance response to the analyte concentrat

198 vascular endothelial cells did not alter the electrical resistance response.

199 Thus, in the absence of any scattering, the electrical resistance should vanish altogether.

200 itself to be the best candidate for quantum electrical resistance standards due to its wide quantum

201 s.Memristors can switch between high and low electrical-resistance states, but the switching behaviou

202 Remarkably, electrical resistance studies show that epithelial barri

203 , an agent that also increases intercellular electrical resistance, suggesting H+ permeation via gap

204 Memristive devices are electrical resistance switches that can retain a state o

205 l resistance and voltage were measured by an electrical resistance system, and paracellular tracer fl

206 udin and form a barrier with a transcellular electrical resistance (TCER) greater than 100 ohm cm2 an

207 with an effective temperature coefficient of electrical resistance (TCR) of -1,730% K(-1), approximat

208 permeability coefficient and transepithelial electrical resistance (TEER) across the cell monolayer w

209 d irreversibly increased the transepithelial electrical resistance (TEER) after UV activation.

210 was monitored by measuring transendothelial electrical resistance (TEER) and albumin flux.

211 In vitro changes in transendothelial electrical resistance (TEER) and flux of fluorescent dex

212 The effect of HA and CS on transendothelial electrical resistance (TEER) and labeled albumin flux ac

213 estigated by measurement of transendothelial electrical resistance (TEER) and passage of labeled albu

214 ex (AJC) function, measuring transepithelial electrical resistance (TEER) and permeability to fluores

215 ls (C6) to obtain elevated trans-endothelial electrical resistance (TEER) and selective permeability

216 Transendothelial electrical resistance (TEER) and uptake of [35S]GSH from

217 PEI having the most dramatic transepithelial electrical resistance (TEER) decreases of (35.3+/-8.5%)

218 easuring transendothelial or transepithelial electrical resistance (TEER) is a widely used method to

219 elivery studies, relying on transendothelial electrical resistance (TEER) measurements without other

220 shown by permeability and trans-endothelial electrical resistance (TEER) studies.

221 Transepithelial electrical resistance (TEER) was measured in human Caco-

222 Trans-epithelial electrical resistance (TEER) was used to measure the bar

223 etinal barrier permeability (transepithelial electrical resistance (TEER)) was measured in cultured r

224 ment of transendothelial and transepithelial electrical resistance (TEER), an accepted quantification

225 Cytotoxicity, transepithelial electrical resistance (TEER), and permeability was measu

226 ght junctions giving a high transendothelial electrical resistance (TEER), and strongly polarised (ap

227 Trans-endothelial electrical resistance (TEER), IL-6 release and NO levels

228 rs but significantly reduces transepithelial electrical resistance (TEER), indicating an increase of

229 r silencing of PKD increased transepithelial electrical resistance (TEER), resulting in a tighter epi

230 st BBB models display a low transendothelial electrical resistance (TEER), which is a measure of the

231 35% reduction in intestinal transepithelial electrical resistance (TEER).

232 antagonists increased their transepithelial electrical resistance (TEER).

233 as well as by measuring the transendothelial electrical resistance (TEER).

234 er function (as assessed by transendothelial electrical resistance [TEER]), whereas overexpression of

235 it tight barrier properties (transepithelial electrical resistance, TEER, approximately 1 k(Omega)/cm

236 NFalpha consistently reduced transepithelial electrical resistance (TER) >80%.

237 d dose-dependent increases in transmonolayer electrical resistance (TER) across both human and bovine

238 were evaluated by measuring transepithelial electrical resistance (TER) after exposure of human epit

239 vivo assessed by decreases in transmonolayer electrical resistance (TER) and isolated perfused lung p

240 Basal transepithelial electrical resistance (TER) and mannitol fluxes were not

241 We measured changes in transendothelial electrical resistance (TER) and observed that APC produc

242 The transepithelial electrical resistance (TER) and paracellular flux of MDC

243 Transepithelial electrical resistance (TER) and real-time cellular analy

244 (hfRPE) was assessed by the transepithelial electrical resistance (TER) and the transepithelial diff

245 function was measured as the transepithelial electrical resistance (TER) and the transmonolayer diffu

246 ial EPEC-induced decrease in transepithelial electrical resistance (TER) but halted the progressive d

247 (HBEpCs) with LPA increased transepithelial electrical resistance (TER) by approximately 2.0-fold an

248 in 042 induces a decrease in transepithelial electrical resistance (TER) compared to uninfected contr

249 tight junctions and based on transepithelial electrical resistance (TER) contain "tight" and "leaky"

250 ch techniques, measurement of the translayer electrical resistance (TER) has been consistently used t

251 the establishment of maximum transepithelial electrical resistance (TER) in MDCK-gE cells; MDCK-gI an

252 rger Cpe30 peptide affected trans-epithelial electrical resistance (TER) in peptide-treated Caco-2BBe

253 in two days when assessed by transepithelial electrical resistance (TER) measurement across the cell

254 The transepithelial electrical resistance (TER) of cells decreased at the sa

255 d dose-dependently elevated transendothelial electrical resistance (TER) of EC monolayers (>50% incre

256 rrier properties measured as transepithelial electrical resistance (TER) or permeability and reduces

257 unction was monitored by the transepithelial electrical resistance (TER) or the permeation of small o

258 ty was assessed by measuring transepithelial electrical resistance (TER) or the transepithelial passa

259 Transepithelial electrical resistance (TER) was measured using a voltohm

260 ers (Costar, Cambridge, MA), transepithelial electrical resistance (TER) was measured using a voltohm

261 h a cell monolayer, whereas transendothelial electrical resistance (TER) was measured using the ECIS

262 EHEC-induced reduction in transepithelial electrical resistance (TER), a measure of barrier functi

263 Transendothelial electrical resistance (TER), a measure of barrier integr

264 and stimulates the monolayer transepithelial electrical resistance (TER), a reliable in vitro measure

265 Resultant changes in the transendothelial electrical resistance (TER), an indicator of integrity o

266 ithelial monolayer with high transepithelial electrical resistance (TER), and polarized secretion of

267 h a significant reduction in transepithelial electrical resistance (TER), indicating a global loss of

268 the EPEC-induced decrease in transepithelial electrical resistance (TER), mutation of both espG and o

269 estimated by measurement of transendothelial electrical resistance (TER), of PAE/Npn and PAE/KDR cell

270 and stimulates the monolayer transepithelial electrical resistance (TER), which is a reliable in vitr

271 adherens junctions) and the transepithelial electrical resistance (TER), which reflects tight juncti

272 sion of sodium fluorescein and transcellular electrical resistance (TER).

273 a time-dependent decrease in transepithelial electrical resistance (TER).

274 effects on human transendothelial monolayer electrical resistance (TER).

275 simultaneous measurement of transepithelial electrical resistance (TER).

276 ry artery EC as measured by transendothelial electrical resistance (TER).

277 investigated by analysis of transepithelial electrical resistance (TER).

278 y in the development of peak transepithelial electrical resistance (TER).

279 and Na(+) (derived from the transepithelial electrical resistance, TER) and the flux of NaCl and mPE

280 time-dependent decrease in transendothelial electrical resistance that correlated with increased per

281 xygen dramatically influences the nanotubes' electrical resistance, thermoelectric power, and local d

282 These states often dictate the junction electrical resistance through the well-known Fermi level

283 t of defined characteristics, including high-electrical-resistance tight junctions.

284 ng both transendothelial and transepithelial electrical resistance to monitor cell function in real-t

285 perturbed TJ gate function (transepithelial electrical resistance, tracer diffusion) in a dose-depen

286 derstanding magnetoresistance, the change in electrical resistance under an external magnetic field,

287 Mo3Se3 undergo reversible increases of their electrical resistance (up to 70%) upon exposure to vapor

288 chanism of a wire can be revealed by how its electrical resistance varies with length.

289 Notably, transepithelial electrical resistance was dramatically reduced, neutroph

290 ent were blocked and the induced increase of electrical resistance was markedly blunted.

291 ctroscopy measurements demonstrated that the electrical resistance was not altered by peptide incorpo

292 of cell adhesion and loss of transepithelial electrical resistance was prevented by incubation with C

293 The effect of NC-1059 on transepithelial electrical resistance was reversible.

294 Reductions in transepithelial electrical resistance were also dependent on functional

295 4-HNE-induced changes in transendothelial electrical resistance were calcium independent, as 4-HNE

296 on, bacterial adherence, and transepithelial electrical resistance were examined in response to apica

297 of HBMECs and a decrease in transendothelial electrical resistance were observed.

298 oth intraluminal zonulin and transepithelial electrical resistance were similar to those detected in

299 s by EPEC leads to a loss of transepithelial electrical resistance, which also requires the type III

300 Unfortunately, the weak variation of electrical resistance with temperature results in limite