ライフサイエンスコーパス: pumping

1 bacteria) by regulating pharyngeal activity (pumping).

2 asing up to 200 K under non-resonant optical pumping.

3 water started to infiltrate due to municipal pumping.

4 mphangiogenesis, and dysfunctional lymphatic pumping.

5 hed the energy investment in reclaimed water pumping.

6 s) generated by circularly polarized optical pumping.

7 the laser technique of spin-exchange optical pumping.

8 ar microcavities with optical and electrical pumping.

9 hickness, suggesting the suppression of spin pumping.

10 describing the molecular mechanism of proton pumping.

11 s system and muscle in generating pharyngeal pumping.

12 tonic neurotransmitter release may regulate pumping.

13 accommodate vortex ring formation for volume pumping.

14 s, which are responsible for contraction and pumping.

15 a capillary without the need of any external pumping.

16 ir optical properties associated with proton pumping.

17 , and found three neural circuits that alter pumping.

18 m, respectively, that did not disrupt proton pumping.

19 ate stabilization-change mechanism of proton pumping.

20 donor risk index, waitlist time, and kidney pumping.

21 factor of 2 larger photoemission during spin pumping.

22 ng for each phase and gain assisted enhanced pumping.

23 rotation by blocking ATPase-dependent proton pumping.

24 tals realized with direct-current electrical pumping.

25 by modulating a commitment to bursts of fast pumping.

26 nation of a high-yield spin-exchange optical pumping (129)Xe polarizer, custom-built radiofrequency c

27 Radiolabeling was performed by pumping (89)Zr-oxalate and DFO-Bz-trastuzumab into the m

28 The power of each lens is controlled by pumping a liquid in and out of the lens chamber using se

29 By pumping a microcavity with a spatially structured light

30 Proton pumping A-type cytochrome c oxidase (CcO) terminates the

31 In our simulations the faster SR Ca pumping accelerates action potential-induced Ca transien

32 In addition, the pumping accuracy is almost unchanged up to 7.4 GHz, prob

33 he process to thermodynamically drive proton pumping across its membrane domain.

34 n many biochemical processes, such as proton pumping across membranes and enzyme catalysis.

35 the damping, via d-d hybridisation and spin-pumping across the interface, and the mediation of the m

36 es the free energy of the reaction to proton pumping across the membrane.

37 Low cytosolic pH required increased proton pumping across the thylakoid membrane and elevated adeno

38 activities and supported NADH-linked proton pumping activities in the host membranes almost as effic

39 ultaneously measured the light-driven proton-pumping activities of each bio-pixel.

40 protein that synthesizes ATP through proton-pumping activity across the membrane.

41 The proton-pumping activity contributes to the proton electrochemic

42 iteria of light-dependent electrogenic Na(+) pumping activity in vitro, namely, light-induced passive

43 ndosomes resulting from inhibition of proton pumping activity of vacuolar-type H(+)-ATPase (v-ATPase)

44 While proton-pumping activity was disrupted in many of the spectrally

45 drolase activity, which is coupled to proton-pumping activity.

46 C-terminal domain enabled ATPase and proton-pumping activity.

47 ping at half the pacing frequency or stopped pumping altogether, possibly due to UNC-68 leakiness and

48 ssessing the energy used on postsynaptic ion pumping and action potentials, we show that, instead, th

49 uring cell expansion that coordinates proton pumping and cellulose synthesis.

50 ic vessel density, impairs collecting vessel pumping and decreases transport of macromolecules.

51 ion by means of circularly polarized optical pumping and determined a valley lifetime of 40 nanosecon

52 Such a mechanism may require less H(+)-pumping and energy for upregulating pH compared with the

53 erarchical micro- and nanochannels for water pumping and escaping, solar steam generation device base

54 tion of "direct feeding at the breast (DBF), pumping and feeding breast milk (BM), and formula (FF) i

55 The recent epidemic of pumping and feeding in the United States and the use of

56 onally recommended, but associations between pumping and HM-feeding durations are unknown.

57 transmembrane potential generated by proton pumping and is capable of restoring microbicidal functio

58 an be reached by a dynamical balance between pumping and losses, so the intrinsically nonequilibrium

59 We examined pharyngeal pumping and observed that clozapine-induced inhibition o

60 ide-band spectral detection, and (c) focused pumping and over-the-cone detection.

61 We develop a general technique for optical pumping and preparation of the molecule into a pure init

62 hese results highlight the potential of spin pumping and spin transfer torque for device applications

63 e develop and test a mechanistic model, the "pumping and streamline segregation" or PASS model, for n

64 6 is increased, which slows down both proton pumping and the chemical catalysis.

65 ugh the D-channel, which impairs both proton pumping and the chemical reaction.

66 oncollinear geometry, (b) low coherence-time pumping and ultra-wide-band spectral detection, and (c)

67 a histamine-gated chloride channel abolishes pumping, and optogenetic stimulation of pharyngeal muscl

68 cific reactant preparation by infrared laser pumping, and ultrahigh vacuum surface analysis technique

69 ream fish assemblages related to groundwater pumping, and we predict similar transformations worldwid

70 tribution that allows for preferential fluid pumping around the drop rim.

71 On the other hand, pumping at 400 nm excites the molecule into the quintet

72 Pumping at 530 nm leads to ultrafast nonradiative relaxa

73 flat and smooth spectra can be generated by pumping at any resonances in the optical C-band.

74 The pharynx either locked in pumping at half the pacing frequency or stopped pumping

75 g-range calcium transport is based on active pumping at multiple cells along boring filaments, orches

76 Here, we report a study of spin pumping at the TI-ferromagnet interface, investigating s

77 de C. elegans, whose food uptake consists of pumping bacteria from the environment into the gut, prov

78 ously unreported spatiotemporal variation in pumping behavior in urease-based pumps and uncover the m

79 e pumping frequency and types of reasons for pumping between 1.5 and 4.5 mo postpartum are associated

80 , we find that the frequency and duration of pumping bursts increase and the duration of long pauses

81 Removal of food initially suppressed pumping but after 2 h this was accompanied by intermitte

82 es of lymphatic muscle and the regulation of pumping by lymphatic preload, afterload, spontaneous con

83 transitions to demonstrate strong population pumping by resonant excitation of the bound exciton tran

84 8% NaCl under seven extraction cycles of air pumping by syringe.

85 )-ATPase SERCA promotes muscle relaxation by pumping calcium ions from the cytoplasm into the sarcopl

86 well known that sufficiently strong optical pumping can drive exciton-polaritons to quantum degenera

87 Optical pumping can facilitate charge, spin, and valley Hall eff

88 rent, unlike spin currents generated by spin-pumping, can be directly detected without the need of an

89 cted to waste to avoid exceeding the maximum pumping capacity of the MS system.

90 ents suffer progressive decay in the heart's pumping capacity to the point of heart failure.

91 rkedly decreased collecting lymphatic vessel pumping capacity, decreased lymphatic vessel density, de

92 sections, paper, and plant material on a low pumping capacity, single-quadrupole mass spectrometer.

93 y lymphatics and decreased collecting vessel pumping capacity.

94 mospheric accumulation of carbon dioxide by 'pumping' carbon to the deep sea.

95 rid and semiarid soils: atmospheric pressure pumping, carbonate dissolution, and percolation of soil

96 Artificial mixing caused by this continuous pumping changed the lake from a meromictic to holomictic

97 the previously unknown structure of the ion-pumping channel in the C-type Coxs and provides insight

98 Proton-pumping complex I of the mitochondrial respiratory chain

99 ildup of excitons under on- and off-resonant pumping conditions allows us to distinguish between the

100 however, cause many drawbacks such as a high pumping cost and a need for periodic replacement due to

101 overy of the first (to our knowledge) sodium-pumping Cox (Scox), a cbb3 cytochrome from the extremely

102 hey play a central role in Cu homeostasis by pumping Cu ions across cell membranes with energy derive

103 one part per million (ppm) reveals that the pumping current deviates from the ideal value by only ab

104 level in silicon up to 7.4 GHz, at which the pumping current exceeds 1 nA.

105 molar levels of sulfide inhibited the proton-pumping cytochrome bo oxidase that is regarded as the pr

106 behaviors modulated during sleep-pharyngeal pumping, defecation, locomotion, head movement, and avoi

107 ffers from the well-established mechanism of pumping dsDNA into a preformed protein capsid exemplifie

108 D-channel is kinetically favored over proton pumping due to the loss of a kinetic gate in the N139 re

109 of submarine groundwater discharge is tidal pumping, due to the large tidal oscillations, whereas at

110 l proton transport events that enable proton pumping during first steps of oxidation of the fully red

111 erve and are recruited into action for extra pumping during the long-lasting cardiac action potential

112 dic droplet device and test its integrity by pumping dye through the channels.

113 mbined effects of continuous labeling (label pumping), dynamic reversible binding, and water detectio

114 Hyperpolarization via optical pumping/dynamic nuclear polarization should function at

115 However, in a dynamic regime where the pumping effect is significant, these band-gaps become as

116 e Boltzmann transport theory with the charge pumping effect reveals the topological-in-origin nonline

117 effect can be interpreted as a bulk quantum pumping effect.

118 annel is imperative to achieving high proton-pumping efficiency in the WT CcO.

119 sue patch to prevent dilation and to improve pumping efficiency of the infarcted heart offers a promi

120 o spatial sample frequencies at twice of the pumping electric field wave.

121 Additionally, we find that significant pumping energy is required to overcome frictional pressu

122 ated based on the measured pressure drop and pumping energy model.

123 ance due to water flux decline and increased pumping energy requirements from spacer blockage highlig

124 a flow electrode effects the electrical and pumping energy requirements of a FCDI system.

125 Coxs studied to date are redox-driven proton-pumping enzymes belonging to one of three subfamilies: A

126 Pumping flow rates from 5.3 to 40 microL min(-1) under d

127 Groundwater pumping for agriculture is a major driver causing declin

128 rther demonstrate the existence of adiabatic pumping for each phase and gain assisted enhanced pumpin

129 njection analysis (microFIA) through passive pumping for performing tear glucose analyses in a simple

130 resis loop and ferromagnetic reso-nance with pumping frequencies from 12- 40 GHz.

131 d the effect of shear rates by varying fluid pumping frequencies using 4 set-points and the effect of

132 We examined whether and how the pumping frequency and types of reasons for pumping betwe

133 The linear dispersion of the pumping frequency vs: the resonance field has been obser

134 Nonelective pumping reasons and higher pumping frequency were associated with shorter HM-feedin

135 ld-sweep linewidths decrease with increasing pumping frequency, and the frequency-sweep linewidths st

136 nsity, decreased collecting lymphatic vessel pumping frequency, decreased lymphatic trafficking of im

137 Here we show that spin pumping, frequently used in nanoscale spintronic devices

138 -funnel solar cells, non-contact chromophore pumping from a proximal LED, and markedly reduced gain t

139 that impair, and sometimes decouple, proton pumping from the chemical catalysis.

140 fish assemblages associated with groundwater pumping from the United States High Plains Aquifer.

141 scularity, reduced fibrosis, and recovery of pumping function compared with controls.

142 unts of ATP in order to support the constant pumping function in the context of changing energy deman

143 hitecture, which change force production and pumping function in the diseased heart or stem cell-deri

144 proves that the dual light-driven H(+)/Na(+) pumping function of IAR is intrinsic to the single rhodo

145 As the pumping function of its heart is acutely dispensable for

146 Besides its canonical proton-pumping function, V-ATPase's membrane sector, Vo, has be

147 oxygen species, in addition to its distinct pumping function.

148 se conditions affect the light-driven proton pumping functional exertion as well.

149 a nanolocker with the potential of molecular pumping has also been designed with the cooperation of t

150 heat at high temperatures, but liquid-metal pumping has been limited by the corrosion of metal infra

151 hes by small-stream fishes where groundwater pumping has increased depth to groundwater.

152 The mechanisms controlling the pumping have not, however, been completely elucidated.

153 w that both the speed and direction of fluid pumping (i) depend on the enzyme activity and coverage,

154 y retains the unique properties of redox-MHD pumping (i.e., programmable fluid speeds and flow patter

155 er biochemical data, suggest that the proton pumping in complex I is activated by a unique combinatio

156 ep that could thermodynamically drive proton pumping in complex I.

157 Groundwater pumping in Dhaka has caused large-scale drawdown that ex

158 e and decreased V-ATPase activity and proton pumping in isolated vacuolar vesicles.

159 c catalysis can be harnessed for "on demand" pumping in nano- and microfluidic devices powered by an

160 Due to pumping in the anomalous dispersion region with two Zero

161 We scored pumping in the presence of food and over an extended tim

162 make use of the physical mechanism of proton pumping in the so-called Complex I within mitochondria m

163 torsional excitation is a form of parametric pumping in the system, which results in the breakage of

164 ydrolyze ATP in the V1 domain coupled to ion pumping in VO.

165 we show that this picture breaks for optical pumping-instead, the added complexity of a realistic mat

166 Our approach to liquid-metal pumping is enabled by the use of ceramics for the mechan

167 We show pumping is fine-tuned by context-specific neural mechani

168 lts elucidate the mechanisms by which proton pumping is impaired, thus revealing key kinetic gating f

169 Pumping is nationally recommended, but associations betw

170 These results indicate that trap-mediated SE pumping is promising for achieving the practical operati

171 odel of vesicle acidification, revealed that pumping is stochastically interrupted by long-lived (~10

172 e key physical mechanism governing the fluid pumping is the conversion of electrical energy into hydr

173 eme a to the BNC, but that the former (i.e., pumping) is kinetically favored whereas the latter (i.e.

174 ersion, improving allocation, and more often pumping less-than-ideal, yet potentially transplantable

175 mpartment without increasing permanently the pumping losses.

176 In particular, the proton-pumping machinery of these Coxs has not yet been elucida

177 lays a central role in activating the proton pumping machinery.

178 ht illumination, and miniaturized 3D printed pumping manifolds that were integrated to enable time-re

179 This pattern suggests that tidal pumping may sustain dissimilatory nitrate reduction in i

180 nit may be combined with quantitative proton-pumping measurements for mechanistic studies.

181 ith a wirelessly controlled Archimedes screw pumping mechanism are engineered.

182 To better understand the proton-pumping mechanism of the wild-type (WT) CcO, much attent

183 hic disaggregase, Hsp104(N), with an altered pumping mechanism.

184 confirming the existence of a proton (H(+)) pumping mechanism.

185 These devices work by different pumping mechanisms, have various flow capacities, are in

186 Rhodopsins are light-driven ion-pumping membrane proteins found in many organisms and ar

187 This pumping motion likely drives directional substrate trans

188 ngle X-ray scattering revealed a peristaltic pumping motion upon ATP hydrolysis, which drives directi

189 x-ray scattering has revealed a peristaltic pumping motion upon ATP hydrolysis.

190 Mitochondrial proton-pumping NADH:ubiquinone oxidoreductase (respiratory comp

191 Mitochondrial complex I (proton-pumping NADH:ubiquinone oxidoreductase) is an essential

192 We show that asymmetric optical pumping of a symmetric resonator enables a dramatic chir

193 ose through passive dehydration or by active pumping of anions through SLAC, a phospho-activated memb

194 global estimates of the eddy-driven vertical pumping of biophysical and chemical tracers.

195 With selective pumping of chlorophyll f at 740 nm, we observe a final a

196 ian) quantum system, which requires constant pumping of energy and continuously decays, releasing coh

197 t transistor to realize efficient electrical pumping of exciton-polaritons at room temperature with h

198 that the surge is caused by a self-generated pumping of fluid through the packing.

199 the way towards efficient energy conversion, pumping of fluids at nanoscale, and drug delivery.

200 We report efficient pumping of fluids through nanofluidic funnels when a sym

201 lated with wavelength, enabling non-resonant pumping of high-quality micro-lasers and solar-pumped la

202 Our work demonstrates optical pumping of interlayer electric polarization, which may p

203 propose an additional mechanism where active pumping of ions and water at the cell poles and the divi

204 rrent is attributed to enhanced electrogenic pumping of Na(+) that accumulated in the diffusion-restr

205 ard continuous wave operation and electrical pumping of solid-state organic lasers are reviewed, and

206 We studied how light inhibits pumping of the Caenorhabditis elegans pharynx, a myogeni

207 IN brain drug delivery by FUS-induced active pumping of the drug and demonstrated that FUS-enhanced I

208 Optical pumping of the nanocavity induces a localized, phase-loc

209 and numerical results indicate that gradual pumping of the network combined with multiple spectral a

210 s, feeding occurs via rhythmic contractions (pumping) of the pharynx, a neuromuscular feeding organ.

211 s that can contribute to the coordination of pumping on a network basis.

212 TRH signaling have no defects in pharyngeal pumping or isthmus peristalsis rates, but their growth d

213 the switch between these states but not the pumping or leakage rates.

214 e whether FUS enhances IN delivery by active pumping or passive diffusion.

215 acial stress resulted from electrochemically pumping oxygen into or out of PCO films, leading to meas

216 Cytochrome bo3 is a respiratory proton-pumping oxygen reductase that is a member of the heme-co

217 level the activity of the prototypic proton-pumping P-type ATPase Arabidopsis thaliana isoform 2 (AH

218 The charge-pumping phenomenon is generic and gives a deeper underst

219 cellular pathway plausible, it renders water pumping physiologically negligible because the passive f

220 pared with CEF pathways involving non-proton-pumping plastoquinone reductases.

221 d 2 orders of magnitude reduction in optical pumping power for a room-temperature maser by coupling a

222 fit from the lower resistance values and low pumping power required, obtaining high net power densiti

223 ume of the maser cavity yet the peak optical pumping power was 1.4 kW.

224 ification, the detector can harvest wireless pumping power with its end-rings and amplify Magnetic Re

225 z) soliton mode locking is achieved with low pumping powers (parametric oscillation threshold powers

226 panding donor pool and changes in biopsy and pumping practices.

227 We also observed an increase in the pumping pressure required to force water through the spa

228 The non reciprocity of the pumping process makes the system a good optical diode.

229 sight on the structural mechanism of the ion pumping process.

230 coupled to the quinone site and involved in pumping protons from the matrix into the intermembrane s

231 idopsis (Arabidopsis thaliana) type I proton-pumping pyrophosphatase (AVP1) in phloem loading was ana

232 We conclude that the Proton-Pumping Pyrophosphatase AVP1 localized at the plasma mem

233 Proton-pumping pyrophosphatases (H(+)-PPases) are shown to part

234 ed LCRs and examined LCR regulation by SR Ca pumping rate (Pup) that provides a major contribution to

235 d with cutaneous lymphatic collecting vessel pumping rate (r = -0.9812, P < 0.0005) and initial lymph

236 draulic connection to disconnection when the pumping rate exceeds the maximum seepage flux of the str

237 es, including developmental rate, pharyngeal pumping rate, brood size, body movement, activation of t

238 alized cutaneous lymphatic collecting vessel pumping rate, lymphatic vessel density, lymphatic leakin

239 of QD emission intensity at constant optical pumping rate.

240 ation of SWCNT polaritons, exciton-polariton pumping rates approximately 10(4) times higher than in c

241 ulatory domain of AHA2 reduced the intrinsic pumping rates but increased the dwell time in the active

242 Nonelective pumping reasons and higher pumping frequency were associ

243 We classified pumping reasons as nonelective [e.g., because of a diffi

244 In this development, spin pumping represents a convenient way to electrically dete

245 se of HPMS provides a way to eliminate turbo pumping requirements, leading to significant reduction i

246 rmal contractions, demonstrating that normal pumping requires nervous system function.

247 t clozapine-induced inhibition of pharyngeal pumping requires sms-1, a finding that may explain the r

248 The results for below-gap optical pumping reveal energy-gain and -loss Floquet replica val

249 Finally, a new clade of likely proton-pumping rhodopsin with non-canonical amino acids in the

250 Proton-pumping rhodopsins (PPRs) are photoactive retinal-bindin

251 Our work points to a new spin-valley pumping scheme in nanoscale devices, provides a fundamen

252 used as buffer gas in spin-exchange optical pumping (SEOP), was replaced by molecular hydrogen witho

253 xt of superconducting qubits, we implement a pumping sequence to reduce the number of unpaired electr

254 s from ice sheets, glaciers, and groundwater pumping, slowing the rate of sea level rise by 0.71 +/-

255 a continuous-wave diode laser as an optical pumping source.

256 nel (EDIF) at approximately 4 Torr, a single pumping stage was sufficient to handle the gas load.

257 s but increased the dwell time in the active pumping state.

258 ocene aquifers and is also abstracted by the pumping station.

259 The proton-pumping stoichiometry of complex I (i.e. the number of p

260 e a simple method for determining the proton-pumping stoichiometry of complex I in inverted membrane

261 By virtue of this proton-pumping stoichiometry, we hypothesize that NADPH dehydro

262 for the delivery of electrons to the proton pumping subunit.

263 ction, tonic muscle stimulation causes rapid pumping, suggesting tonic neurotransmitter release may r

264 uscle health, including increased pharyngeal pumping, swimming movement, and reduced percentage of se

265 The gradient pumping system consisted of two nanoflow pumps controlle

266 cibility (RSD < 0.17%) demonstrated that the pumping system could successfully generate ultrahigh pre

267 al applications through the integration of a pumping system for buffer exchange and a pulsed laser sy

268 Finally, we describe the caveolae pumping system, a promising active transport alternative

269 veloped and integrated with a small nanoflow pumping system.

270 s that involve flexible microfluidic probes, pumping systems, microscale inorganic LEDs, wireless-con

271 By optically pumping the metamaterial we experimentally show that clo

272 Using wavelength-selective optical pumping, the laser restricts the volume from which OPNMR

273 e regime is thereby achieved with an optical pumping threshold as low as 27 nanowatts at 130 kelvin,

274 ervation of multimode lasing with an optical pumping threshold density of 3.0 kW cm(-2).

275 Second, light inhibits pumping through the RIP-I1-MC neuron polysynaptic circui

276 s well as for maintaining their high rate of pumping through two distinct mechanisms.

277 f imaging-based feedback and pressure driven pumping to accurately control the size of microdroplets

278 opological insulator requires high-frequency pumping to obtain well-separated Floquet bands, a follow

279 n in respiration rate, likely due to reduced pumping to prevent clogging, whereas sustained high sedi

280 oton system realized in a specific regime of pumping to the exciton state and depletion of the reserv

281 s generated using the spin Hall effect, spin pumping torques generated by magnetisation dynamics in m

282 ve alternative oxidase (AOX) is a non-proton-pumping ubiquinol oxidase that catalyzes the reduction o

283 rising dedicated electronics, shielding, and pumping unit controlled by custom firmware to enable mea

284 the hydrophilic arm to four putative proton-pumping units.

285 ow proton transfer to the BNC, but no proton pumping until a proton has reached E286.

286 The membrane sector (Vo) of the proton pumping vacuolar ATPase (V-ATPase, V1Vo-ATPase) from Sac

287 intercalated cells (ICs) express the proton pumping vacuolar H(+)-ATPase (V-ATPase) and are extensiv

288 Here, we demonstrate robust SE pumping via a single-trap level in silicon up to 7.4 GHz

289 First, light inhibits pumping via the I2 neuron monosynaptic circuit.

290 Pumping was unaffected by laser ablation of connectivity

291 In this structural variant, proton pumping was uncoupled from internal electron transfer an

292 sodium glucose cotransporter SGLT1 in either pumping water or passively channeling water contrast wit

293 ween nonlinear effects that require external/pumping waves (cross-phase modulation and parametric pro

294 ate the mechanism of the redox-driven proton pumping, we investigated the kinetics of electron and pr

295 elucidate its molecular mechanism for Na(+) pumping, we perform here extensive classical and quantum

296 s, allowing the lymphatic vessels to provide pumping when needed but remain open when flow can be dri

297 could be used without increasing energy for pumping when using oxidized active material.

298 wing intraband, on-plasmon-resonance optical pumping, which enables modulation of the full-visible sp

299 cations including in characterising acoustic pumping within microfluidic channels.

300 The extent of mixing was observed when pumping yellow and blue solutions into the inlets of a Y