ライフサイエンスコーパス: electrical resistance

1 ntestinal tissue resistance (transepithelial electrical resistance).

2 ion in vitro as measured by transendothelial electrical resistance.

3 n and resulted in decreased transendothelial electrical resistance.

4 herin expression and reduced transepithelial electrical resistance.

5 s and reverses reductions in transepithelial electrical resistance.

6 specific antigen dramatically increases the electrical resistance.

7 pidly develops a substantial transepithelial electrical resistance.

8 helium integrity by reducing transepithelial electrical resistance.

9 simultaneous measurement of transendothelial electrical resistance.

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

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

12 er integrity as measured by transendothelial electrical resistance.

13 ell adhesion as measured by transendothelial electrical resistance.

14 rmeability was monitored with measurement of electrical resistance.

15 y attenuated the decrease in transepithelial electrical resistance.

16 ll permeability measured as transendothelial electrical resistance.

17 ght junctions as measured by transepithelial electrical resistance.

18 nutrient transporters and trans-endothelial electrical resistance.

19 by qRT-PCR, immunoblot, and transepithelial electrical resistance.

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

21 ity changes were measured by transepithelial electrical resistance.

22 neously large transverse thermopower and low electrical resistance.

23 t mounts, and measurement of transepithelial electrical resistance.

24 by XPS, water uptake, permselectivities, and electrical resistances.

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

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

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

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

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

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

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

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

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

34 sequently, the large (~80%) variation in the electrical resistance across the droplet is correlated t

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

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

37 A decrease of BLFO electrical resistance agrees strongly with the UPS data

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

39 tro, as demonstrated through transepithelial electrical resistance analysis.

40 ed physiologically relevant transendothelial electrical resistance and accurately predicted blood-to-

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 Chitosan strongly reduced transepithelial electrical resistance and facilitated transepithelial al

52 bstrate impedance sensing, trans-endothelial electrical resistance and FITC-dextran permeability assa

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

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

55 Measurements of endothelial transmonolayer electrical resistance and immunofluorescent analysis of

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

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

58 cell lines led to diminished transepithelial electrical resistance and increased dextran flux, sugges

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

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

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

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

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

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

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

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

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

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

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

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

71 ir-liquid interface to study transepithelial electrical resistance and paracellular flux of fluoresce

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

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

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

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

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

77 Transepithelial electrical resistance and tight junction protein archite

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

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

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

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

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

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

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

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

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

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

88 e creatine levels), qRT-PCR, transepithelial electrical resistance, barrier function, actin localizat

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

109 Further, the short-time fluctuations in the electrical resistance during an antibiotic susceptibilit

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

132 al reduction of bulk silica, due to its high electrical resistance, is of limited viability, namely,

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

134 Remote electrical resistance measurement is evaluated here as a

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

136 Electrical resistance measurements across human lung end

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

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

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

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

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

142 ts integrity was assessed by transepithelial electrical resistance measurements.

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

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

145 The electrical resistance of a conductor is intimately relat

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

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

148 The electrical resistance of an array of these nanowires inc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

163 15-HETE on permeability and transepithelial electrical resistance of the IEB were measured using Cac

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

165 We measure the electrical resistance of the microchannels, which increa

166 The electrical resistance of the nanoparticle assemblies is

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

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

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

170 The electrical resistance of the sensor varied linearly (R(2

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

172 stabilized on the SAuNPs, which changes the electrical resistance of the sensor.

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

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

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

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

177 re restored barrier properties, indicated by electrical resistance or 70-kDa RITC-dextran permeabilit

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

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

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

181 157:H7-induced reductions in transepithelial electrical resistance (P < .01), decreased permeability

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

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

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

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

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

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

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

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

190 1% O(2)) as well as enhanced transepithelial electrical resistance recovery after prolonged hypoxia i

191 levated barrier resistance (transendothelial electrical resistance), reduced paracellular permeabilit

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

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

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

198 The change in electrical resistance show a nearly linear correlation w

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

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

201 Remarkably, electrical resistance studies show that epithelial barri

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

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

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

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

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

207 ithelium with goblet cells, trans-epithelial electrical resistance (TEER) (>400 Ohms.cm(2)), and cyst

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 Transepithelial electrical resistance (TEER) and FITC-Dextran permeabili

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

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

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

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

216 BBB models demonstrate low transendothelial electrical resistance (TEER) and poor BBB phenotype.

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

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

219 ested with in vitro cellular transepithelial electrical resistance (TEER) in air-interface culture (A

220 atment increased intestinal trans-epithelial electrical resistance (TEER) in primary human colon tiss

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

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

223 onditions, permeability and transendothelial electrical resistance (TEER) of human or mouse lung micr

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

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

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

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

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

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

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

231 itatively by calculating the transepithelial electrical resistance (TEER), by fitting an equivalent c

232 DH) activity, cell necrosis, transepithelial electrical resistance (TEER), fluorescein isothiocyanate

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

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

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

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

237 ier function was assessed as transepithelial electrical resistance (TEER).

238 35% reduction in intestinal transepithelial electrical resistance (TEER).

239 rrier next to the well-known transepithelial electrical resistance (TEER).

240 antagonists increased their transepithelial electrical resistance (TEER).

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

242 e assessed barrier function (transepithelial electrical resistance [TEER] and permeability to 4-kDa f

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

265 upports to measure ion flux (transepithelial electrical resistance (TER)) and FITC-dextran (FD4) perm

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

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

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

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

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

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

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

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

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

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

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

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

278 simultaneous measurement of transepithelial electrical resistance (TER).

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

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

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

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

283 devices have considerable noise and drift in electrical resistance that erodes the precision and cons

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

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

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 or FOXP3-positive cells, and transepithelial electrical resistance was measured to determine epitheli

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

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

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

295 Reductions in transepithelial electrical resistance were also dependent on functional

296 4-HNE-induced changes in transendothelial electrical resistance were calcium independent, as 4-HNE

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

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

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

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