ライフサイエンスコーパス: energy-dependent

1 ure medium and the export process is largely energy dependent.

2 Onset of myocardial relaxation is highly energy dependent.

3 This redistribution was energy dependent.

4 ultures and this latter effect appears to be energy-dependent.

5 This recovery is energy-dependent.

6 rexate was also concentrative, specific, and energy-dependent.

7 alogs and anion transport inhibitors, and 5) energy-dependent.

8 concentration-dependent, time-dependent, and energy-dependent.

9 delivers N-end rule substrates to ClpAP, an energy-dependent AAA+ protease, for degradation.

10 lytic specificity by tethering substrates to energy-dependent AAA+ proteases.

11 ionally measured in transmission through the energy-dependent absorption of X-rays or by observing X-

12 However, its accumulation depends on the energy-dependent acidification of vacuoles.

13 n, which bind to the TTT complex to regulate energy-dependent activation of mTORC1.

14 TonB system of proteins is required for the energy-dependent active transport of iron-bound substrat

15 Even though ATP powers virtually all energy-dependent activities, most cellular ATP is utiliz

16 immobilized but not soluble ICAM-1 triggers energy-dependent affinity maturation of LFA-1 to an adhe

17 The energy-dependent aggregation of ssDNA might represent a

18 tion studies that support its function as an energy-dependent aminophospholipid translocase.

19 Glycerol chemotaxis was energy dependent and coincident with an increase in memb

20 Nuclear translocation of beta-catenin is energy dependent and is inhibited by nonhydrolyzable GTP

21 The uptake of lipids is energy dependent and is likely via the clathrin-mediated

22 This process is energy dependent and is mediated through integrin cytopl

23 Viral entry was energy dependent and showed concentration-dependent inhi

24 ated system, which is temperature-, pH-, and energy-dependent and appears to be under the regulation

25 fect dendritic morphology, which is a highly energy-dependent and excitatory neurotransmitter-mediate

26 S subunit from the nucleus is known to be an energy-dependent and factor-mediated process, but very l

27 Uptake was energy-dependent and inhibited by ouabain and hypothermi

28 Internalization of MtDef4 in N. crassa is energy-dependent and involves endocytosis.

29 The latter recovery is energy-dependent and is blocked not only by actin-filame

30 ke of mercury(II), Hg(II), is believed to be energy-dependent and is enhanced by cysteine in diverse

31 not mix spontaneously, the fusion process is energy-dependent and mediated by viral envelope glycopro

32 titutively cycle to and from the Golgi in an energy-dependent and N-ethylmaleimide-sensitive manner.

33 Furthermore, the motility is energy-dependent and requires an intact actin cytoskelet

34 Protein import was also energy-dependent and saturable.

35 ation and signal processing step involves an energy-dependent and Sec-dependent pathway in S. marcesc

36 ted system that is temperature-, Na(+)-, and energy-dependent and seems to be under the regulation of

37 p75 is GTP-, Ran-, importin-alpha/beta-, and energy-dependent and that the protein competes with the

38 -inactivated MGMT in HT-29 cell extracts was energy-dependent and was markedly stimulated by ATP and

39 chromatin cells was temperature-, time-, and energy-dependent and was stimulated by cell depolarizati

40 Virus entry into C10 cells was energy dependent, and intracellular enveloped virions we

41 Transcytosis was energy dependent, and it was blocked by serotype-specifi

42 an active process, which is temperature and energy dependent, and may be regulated by phosphorylatio

43 We demonstrate that PMO cellular uptake is energy dependent, and that ATP from GF metabolism contri

44 tric charge (the gauge coupling constant) is energy dependent, and there is a previous claim that cha

45 blished unambiguously by refinement of X-ray energy-dependent anomalous scattering factors.

46 Photon energy dependent ARPES results suggest that the electron

47 of some thiols but not others; (2) uptake is energy dependent as evidenced by inhibition by a protono

48 of porphyrins into isolated mitochondria is energy-dependent, as expected for the movement of anions

49 e by a conserved pathway of HP68-containing, energy-dependent assembly intermediates that have specif

50 duce realistic radiographic patterns with an energy-dependent attenuation equivalent to that of tissu

51 ls for aerotaxis (taxis to oxygen) and other energy-dependent behavioral responses in Escherichia col

52 L-Carnitine uptake was also energy-dependent, being significantly (P < 0.01) inhibit

53 into Escherichia coli and shown to confer an energy-dependent bile acid uptake activity.

54 e (ABC) transporters, which are required for energy-dependent biliary secretion of bile acids (ABCB11

55 demonstrated by heterokaryon experiments and energy-dependent blockade of nuclear import and leptomyc

56 f [3H]-riboflavin is sodium, temperature and energy dependent but pH independent.

57 el substrates, we show that INM targeting is energy-dependent but distinct from import of soluble car

58 ndent phospholipase A(2) is activated during energy-dependent Ca(2+) accumulation under conditions wh

59 cytoplasmic ATP/ADP ratio decreases, causing energy-dependent Ca2+ buffering mechanisms to fail.

60 -expressing cells have a higher capacity for energy-dependent Ca2+ uptake and a greater resistance to

61 by reversal of the uniporter responsible for energy-dependent Ca2+ uptake.

62 agment, thus preventing apoptosis that is an energy-dependent cell death pathway.

63 -mediated apoptosis allowed expression of an energy-dependent cell death program that included the tr

64 Unlike in energy-dependent cells like myocytes, LPL is normally re

65 Autophagy is a highly regulated, energy dependent cellular process where proteins, organe

66 performing Pdr12-specific functions such as energy-dependent cellular extrusion of fluorescein and b

67 ility to monitor intracellular pH by imaging energy-dependent changes in cytosolic and mitochondrial

68 density of states and/or providing type- and energy-dependent charge carrier scattering.

69 experimentally reveal two distinct, incident energy-dependent charge separation mechanisms that resul

70 ied by partitioned quasiparticles, each with energy-dependent charge, being a superposition of an ele

71 In diatoms, the process of energy-dependent chlorophyll fluorescence quenching (qE)

72 tion on the roles of DNA-binding factors and energy-dependent chromatin remodeling machines in facili

73 Activator-induced, energy-dependent chromatin remodeling promoted efficient

74 Advanced methods for analysis of the energy-dependent CID cross section, considering both com

75 el the spacing of the eigenenergies with the energy dependent classical oscillation frequency decreas

76 he incomplete protein for degradation by the energy-dependent ClpXP protease.

77 The energy-dependent collision-induced dissociation cross se

78 Energy-dependent complexes, such as the 19S cap of the e

79 relies on sliding clamps that are loaded by energy-dependent complexes.

80 ated with nonphotochemical quenching and the energy-dependent component of nonphotochemical quenching

81 Given the complementarity of the energy-dependent component of NPQ (qE) and PGRL1-mediate

82 that members of this family were capable of energy-dependent concentration of the ammonium ion, NH(4

83 licates the beta cytoplasmic domain in a key energy-dependent conformational change in LFA-1 that is

84 onBDelta7 deletion did not prevent necessary energy-dependent conformational changes that occur in th

85 e and an additional component that resembles energy-dependent CQ efflux.

86 otype is complex with a component of reduced energy-dependent CQ uptake and an additional component t

87 In addition, an electron energy-dependent curve provided an overall picture on ho

88 ned the effect of the loss of ClpXP, a major energy-dependent cytoplasmic protease that degrades trun

89 both electron and hole-bands as well as the energy dependent density of states near the Fermi level.

90 Following the energy-dependent dissociation of the tripartite complex,

91 g magnetospheric disturbances shows a strong energy-dependent drift that leads to the formation of th

92 rane P-glycoprotein (P-gp), which acts as an energy dependent drug efflux pump.

93 CL 329,753, was dependent, in part, upon an energy-dependent drug efflux mechanism.

94 P-Glycoprotein (Pgp), an energy-dependent drug efflux pump responsible for multid

95 esistance is due to the presence of a novel, energy-dependent drug efflux pump similar to P-glycoprot

96 lytopic membrane protein and functions as an energy-dependent drug efflux pump.

97 lls, the resistant cells exhibited increased energy-dependent drug efflux.

98 treating HF and possibly diseases involving energy-dependent dysfunction in other organs with tempor

99 tional transporter protein that serves as an energy-dependent efflux mechanism for endogenously gener

100 refore examined whether E. coli possessed an energy-dependent efflux mechanism for these compounds.

101 g as a transmembrane transporter involved in energy-dependent efflux of anticancer/antiviral nucleoti

102 determined that AceI was able to mediate the energy-dependent efflux of chlorhexidine.

103 of the established transporters catalyze the energy-dependent efflux of phospholipids from cells.

104 e original protein and demonstrated restored energy-dependent efflux of tetracycline.

105 Reduced accumulation and energy-dependent efflux of topotecan was demonstrated by

106 n of most resistance systems is based on the energy-dependent efflux of toxic ions.

107 roup of metal resistance systems function by energy-dependent efflux of toxic ions.

108 The P-glycoprotein is an energy-dependent efflux pump capable of decreasing the i

109 complex in Neisseria gonorrhoeae encodes an energy-dependent efflux pump composed of the MtrC-MtrD-M

110 complex in Neisseria gonorrhoeae encodes an energy-dependent efflux pump system that is responsible

111 resistance to cancer cells by functioning as energy-dependent efflux pumps.

112 ts indicate that ABCG2 is a component of the energy-dependent efflux system for certain folates and a

113 ducibly by keratinocytes, is modulated by an energy-dependent efflux system termed mtr.

114 nistered to examine the effect of inhibiting energy-dependent electrolyte transport on tissue oxygena

115 By comparing beam energy-dependent electron beam-induced currents with Mon

116 oaded asolectin liposomes for studies of the energy-dependent electron transfer reactions within the

117 lower probability of manifesting excitation energy-dependent emission spectra, which in turn is prob

118 cal designs can deliver siRNA into cells via energy-dependent endocytosis, while only autonomously fo

119 Excitation energy-dependent energy transfer from the ligand to Eu3+

120 anism that likely involves the generation of energy-dependent engulfment signals.

121 Energy-dependent exciton quenching, or q(E), protects th

122 e are still far smaller than those formed in energy-dependent experiments ( approximately 21 nm(2)).

123 bility, mass spectrometry, and complementary energy-dependent experiments.

124 -glycoprotein (P-gp)] capable of binding and energy-dependent extrusion of structurally diverse organ

125 GT overexpression attenuated early, energy-dependent facets of cell death, blocking oxygen r

126 e of the autofluorescent protein, APC, in an energy-dependent fashion that required both ATP and GTP.

127 alphaIIbbeta3 bound PAC1 specifically in an energy-dependent fashion, and they underwent fibrinogen-

128 necessary to maintain a stable contact in an energy-dependent fashion, even after the IS was formed s

129 s routed to the nucleolus very rapidly in an energy-dependent fashion, whereas membrane translocation

130 d with the new model were shown to be highly energy dependent for most combinations of source-target

131 die through a more subtle, noninflammatory, energy-dependent form of cell death called apoptosis.

132 ors and subsequent calcium signaling and via energy-dependent glutamate transport.

133 nse of CR-39 to ions is studied based on the energy dependent growth rate of the track diameter to un

134 leotidase complex such as PAN to mediate the energy-dependent hydrolysis of folded-substrate proteins

135 ated mechanism, distinct from a carrier- and energy-dependent import mechanism and involves a direct

136 ntracellular zinc stores takes priority over energy-dependent import, and our results link the bioche

137 Therefore, verapamil produces an energy-dependent increase in the permeability of resista

138 tions by using both gate-modulated and laser-energy dependent inelastic scattering spectroscopy.

139 ivermectin was concentrative, specific, and energy-dependent (inhibition by NaCN).

140 The only known energy-dependent interaction occurs between the periplas

141 interaction between the cells, and show that energy-dependent interaction strength is optimal for the

142 hat reported the astounding observation that energy-dependent intracellular proteolysis was far more

143 ug-induced decrease in membrane viscosity is energy dependent: it did not happen in KCN-treated cells

144 e and xylem parenchyma cells are involved in energy-dependent K loading into the xylem and in control

145 s exhibits limited mobility but undergoes an energy-dependent local expansion immediately after DNA d

146 Energy-dependent machines with highly diverse quaternary

147 y, we predict the shape of the momentum- and energy-dependent magnetic resonance spectrum for the ide

148 rane vesicles accumulated taurocholate in an energy-dependent manner, apparently consuming delta pH w

149 eraction between TTT and Pontin/Reptin in an energy-dependent manner, thereby promoting mTORC1 activi

150 tween membrane and intracellular pools in an energy-dependent manner.

151 trinsic gastric myoelectrical activity in an energy-dependent manner.

152 MHC:peptide complexes in a temperature- and energy-dependent manner.

153 sport substances across cell membranes in an energy-dependent manner.

154 tles between the nucleus and cytoplasm in an energy-dependent manner.

155 ins that facilitate nutrient transport in an energy-dependent manner.

156 Cellular internalization occurred via an energy dependent mechanism.

157 jugates are internalized in HeLa cells by an energy-dependent mechanism and that the predominant path

158 These experimental results point to an energy-dependent mechanism driving fast motion of chroma

159 An energy-dependent mechanism of ERK2 export can also be di

160 Contraction is an energy-dependent mechanism that relies on the production

161 me degrades polyubiquitinated proteins by an energy-dependent mechanism.

162 n enter phagosomes also via a second unknown energy-dependent mechanism.

163 We propose that these energy-dependent mechanisms precisely synchronize membra

164 intain ion gradients by using sophisticated, energy-dependent membrane enzymes (membrane pumps) that

165 C) transporters are a diverse superfamily of energy-dependent membrane translocases.

166 roduces a link between membrane order and an energy-dependent, membrane-associated function in prokar

167 Apoptosis is an evolutionarily conserved, energy-dependent mode of cell death requiring the initia

168 Images of these energy-dependent modulations are Fourier analyzed to yie

169 The observed energy-dependent momentum structure and twisted dispersi

170 cation by lipoproteins, but not by SMase, is energy-dependent, N-ethylmaleimide-sensitive, and blocke

171 tion by Na+ at elevated pH, was deficient in energy-dependent Na+ extrusion.

172 system was also found to be temperature- and energy-dependent; Na(+)-independent, slightly higher at

173 inear susceptibility anomaly and a resonant, energy-dependent nematicity in the tunnelling density of

174 s transported in the polymerized state by an energy-dependent nocodazole/cold-sensitive transport mec

175 s a major photoprotection mechanism known as energy dependent nonphotochemical quenching.

176 A major component of NPQ is qE (energy-dependent nonphotochemical quenching), which allo

177 n increase in xanthophyll cycle activity and energy-dependent nonphotochemical quenching.

178 hZip2 activity was not energy-dependent, nor did it require K(+) or Na(+) gradi

179 important for mediating the assembly of the energy-dependent nucleolar silencing complex (eNoSC), wh

180 ndent process, suggesting the involvement of energy-dependent nucleosome remodeling factors.

181 Often these regulatory proteases are either energy-dependent or intramembrane-cleaving.

182 Previously we have described a stepwise, energy-dependent pathway for human immunodeficiency viru

183 This is the first report of a protein- and energy-dependent pathway for the inwardly directed trans

184 . graminearum autonomously using a partially energy-dependent pathway.

185 n is shown to occur via adsorption-mediated, energy-dependent pathways, resulting in accumulation of

186 bsequently are internalized by the cells via energy-dependent pathways.

187 and proliferation is regulated in part by an energy-dependent polyamine uptake system.

188 action at low fungicidal concentrations was energy-dependent, primarily actin-mediated, and disrupte

189 rgy independent, and transcellular, which is energy dependent-primarily focusing on the intestine.

190 ether maintenance of biofilm stability is an energy-dependent process and whether transcription and/o

191 Because ethidium bromide efflux is an energy-dependent process any disturbance in cellular ene

192 Apoptosis is an energy-dependent process characterized morphologically b

193 ion, alpha5beta1 integrin is activated in an energy-dependent process from the nonbinding ground stat

194 The nuclear import of PABP1 is an energy-dependent process since PABP1 fails to enter the

195 roposed to form a pilus-like structure in an energy-dependent process that requires the ATPase, EpsE.

196 ical nuclear localization signal (NLS) is an energy-dependent process that requires the heterodimer i

197 s, in particular cysteine, and that it is an energy-dependent process through heavy metal transporter

198 hypophosphorylated Cln2 in the nucleus is an energy-dependent process, but may not involve the RAN GT

199 lation in hepatoma cells is a reversible and energy-dependent process.

200 solateral Na+ extrusion via Na+,K+-ATPase an energy-dependent process.

201 are taken up from cell culture medium in an energy-dependent process.

202 ut instead enters the nucleus by means of an energy-dependent process.

203 adhesion requires divalent cations and is an energy-dependent process.

204 was inhibited at 4 degrees C, suggesting an energy-dependent process.

205 lationally imported into the organelle in an energy-dependent process.

206 RE-regulated gene transcription and altering energy dependent processes essential to neuronal cell su

207 ntial of the cytoplasmic membrane to support energy-dependent processes at the outer membrane of the

208 ATP-depleted conditions in yeast shows that energy-dependent processes strongly contribute to the pr

209 e intracellular levels of ATP and affect all energy-dependent processes within the cell.

210 is rather than oxidative phosphorylation for energy-dependent processes.

211 Immune responses are highly energy-dependent processes.

212 nvestigated the mechanism by which ClpAP, an energy-dependent protease from Escherichia coli, control

213 The 26 S proteasome is an energy-dependent protease that degrades proteins modifie

214 oteins related to the regulatory portions of energy-dependent proteases act as energy-dependent seque

215 Machines of protein destruction-including energy-dependent proteases and disassembly chaperones of

216 Both the Lon and ClpAP energy-dependent proteases contribute to HemA turnover i

217 protein folding and prevent aggregation, and energy-dependent proteases eliminate irreversibly damage

218 Energy-dependent proteases ensure the timely removal of

219 In archaea, two different types of energy-dependent proteases have been characterized: 20S

220 The energy-dependent proteases originally defined in Escheri

221 Bacteria use energy-dependent proteases to control protein destructio

222 st intracellular proteolysis is initiated by energy-dependent proteases, including Lon, ClpXP, and Hf

223 Energy-dependent proteases, such as ClpXP, are responsib

224 ger RNA), which signals their degradation by energy-dependent proteases.

225 s-induced increase in total and myofibrillar energy-dependent protein breakdown rates and blunted the

226 dependent proteases are responsible for most energy-dependent protein degradation across all species.

227 Energy-dependent protein degradation machines, such as t

228 Since BSEP is an energy-dependent protein responsible for the efflux of b

229 on of dexamethasone in normal rats increased energy-dependent proteolysis and ubiquitin mRNA levels.

230 Energy-dependent proteolysis was determined in incubated

231 -terminal coiled-coil, also facilitated this energy-dependent proteolysis.

232 HemA turnover in vivo, suggesting a role for energy-dependent proteolysis.

233 Proteasomes are the major energy-dependent proteolytic machines in the eukaryotic

234 Proteasomes are energy-dependent proteolytic machines.

235 and ultimately the function of this central energy-dependent proteolytic system.

236 earance of FIC1 in membrane preparations and energy-dependent PS translocation in cells.

237 The corrected data indicate that the energy-dependent (qE) and photoinhibitory (qI) component

238 cement in NPQ(max) was due to an increase in energy-dependent quenching (qE) relative to D3, combined

239 (VDE) are known to influence the dynamics of energy-dependent quenching (qE), the component of nonpho

240 two high NPQ QTLs, HQE1 (high qE 1, for high energy-dependent quenching 1) and HQE2, on chromosomes 1

241 Energy-dependent quenching of excess absorbed light ener

242 ophyll charge separation in the mechanism of energy-dependent quenching of excitations in photosynthe

243 Energy-dependent quenching of excitons in photosystem II

244 ation of photosynthetic light-harvesting via energy-dependent quenching.

245 ndent electron transport and photoprotective energy-dependent quenching.

246 Energy-dependent rate constants were measured as a funct

247 papillomavirus-like particles and virions in energy-dependent reactions.

248 o occur from the cytoplasmic membrane to the energy-dependent receptor in the outer membrane.

249 Transferrin iron utilization is an energy-dependent, receptor-mediated event in which two i

250 response surface was defined by a generator energy-dependent region and a generator current-limited

251 The transport processes through FepA are energy-dependent, relying on the periplasmic protein Ton

252 te DNA repair, modifications of histones and energy-dependent remodeling of chromatin are required, b

253 microbial hydrophobic agents (HAs) is due to energy-dependent removal of HAs from the bacterial cell

254 Eta-mediated transcription termination is energy-dependent, requires upstream DNA sequences, and d

255 s a function of magnetic field, we track the energy-dependent resonance position.

256 Here we report evidence for an energy-dependent rotation at this interface.

257 These results provide evidence for an energy-dependent rotation of the c ring relative to subu

258 to translocate across cell monolayers in an energy-dependent, saturable manner.

259 n excellent agreement with theory.Studies on energy-dependent scattering of ultracold atoms were prev

260 ysis activity, displayed the same reversible energy-dependent sedimentation characteristics as Vps33p

261 ortions of energy-dependent proteases act as energy-dependent sequestration proteins.

262 extracted with submolecular resolution from energy-dependent soft X-ray reflectivity data.

263 ngly small set of proteins and represents an energy-dependent steady state between formation and disa

264 These studies thus identify a novel energy-dependent step early in the CFTR maturation pathw

265 iments performed at 4 degrees C indicated an energy-dependent step in this process.

266 Furthermore, we reveal distinct energy-dependent steps in adaptor localization: a step t

267 is study is positioned between the two known energy-dependent steps: Deltapsi-driven presequence tran

268 closes its transmembrane channel, exhibited energy-dependent structural changes during iron and toxi

269 The energy-dependent study of the v ion provided an unambigu

270 tical image reconstruction that corrects for energy-dependent system blurring.

271 ighted roles for hormone homeostasis and the energy-dependent Target of Rapamycin (TOR) kinase in mer

272 ansmission characteristics that are strongly energy dependent, this heat dissipation is asymmetric--t

273 e function of all Clp ATPases is based on an energy-dependent threading of substrates through the nar

274 We found that Stx is capable of energy-dependent transport across the ER lumen, as has r

275 ungal peptide histatin 5, it did not require energy-dependent transport across the membrane.

276 Energy-dependent transport of glucose into cells mediate

277 of receptors, we propose a mechanism for the energy-dependent transport of siderophores.

278 o genes, hba2+/bfr1+ and pmd1+, which encode energy-dependent transport proteins involved in multidru

279 nticancer drugs is expression of one or more energy-dependent transporters that detect and eject anti

280 ompounds arises in part from the activity of energy-dependent transporters.

281 in (R2*, reciprocal to blood relaxation) and energy-dependent tubular function were assessed using bl

282 th of the orbitals relevant for transport is energy-dependent, unlike what is normally assumed in var

283 nstituted in E. coli phospholipids, exhibits energy-dependent uphill and energy-independent downhill

284 Energy-dependent uphill transport but not energy-indepen

285 aluated in terms of cell membrane integrity, energy-dependent uptake of acetylated low-density lipopr

286 The energy-dependent uptake of trace nutrients by Gram-negat

287 Thus, in fungi as in bacteria, subsequent energy-dependent utilization of methylammonium precludes

288 different, perhaps due to the involvement of energy-dependent vesicular cholesterol transport in the

289 Circulatory shock induces the loss of energy-dependent volume control mechanisms.

290 lear import of labeled plasmid was time- and energy-dependent, was inhibited by the lectin wheat germ

291 he directional type of motion appeared to be energy dependent, whereas the vibrational movement conti

292 ts on cardiac function: 1) optimized cardiac energy-dependent workload with improved cardiac index an

293 canning transmission electron microscopy and energy-dependent X-ray photoelectron spectroscopy, and p

294 sed during mild zinc deficiency, whereas the energy-dependent zinc importers are upregulated during s