ライフサイエンスコーパス: transport

1 e of WNK's cellular degradation on renal ion transport.

2 nce that vRNA-associated Rab11A have altered transport.

3 g metabolites that no longer inhibit OATP2B1 transport.

4 +):1ClO(4)(-)), which competes with I(-) for transport.

5 ic side of the membrane, is rate limiting to transport.

6 erone effects on substrate physical state or transport.

7 terconnected conducting channels for carrier transport.

8 kinesin-2 implicated in intracellular cargo transport.

9 species through the regulation of manganese transport.

10 le in MHV pathogenesis and retrograde axonal transport.

11 arborized system of tracks for intracellular transport.

12 countertransport occurring in active Ca(2+) transport.

13 ich this molecule influences dynein-mediated transport.

14 t roles in cell division and intraorganellar transport.

15 bud, thereby promoting efficient retrograde transport.

16 rgence but it is only implemented for photon transport.

17 iated facilitation of proton-coupled lactate transport.

18 omplex that also mediates SV40 ER-to-cytosol transport.

19 ctile activity is necessary for proper lymph transport.

20 nd plants, myosin/actin can drive long-range transport.

21 e design of CPPs for efficient transcellular transport.

22 el proteins, which are important in cellular transport.

23 transduction, contractile function, and ion transport.

24 a mechanism involving AQP3-mediated H(2)O(2) transport.

25 lateral roots (LRs), auxin levels and auxin transport.

26 band structure for efficient electron charge transport.

27 s because of their role in biological charge transport.

28 ion points, through which mature virions are transported.

29 e observation of large non-reciprocal charge transport(3) in a magnetic topological insulator, Cr-dop

30 uxiliary subunit, EMRE, essential for Ca(2+) transport(3-8).

31 and, at a second temperature, could grip and transport a cargo.

32 mbrane proteins and exhibit selective proton transport across lipid bilayers at a rate similar to tho

33 How cells adjust nutrient transport across their membranes is incompletely underst

34 minal domain (CTD) that modulates the Zn(2+) transport activity of HsZnT8; and two adjacent sites bur

35 Reductions of P-gp but not BCRP transport activity were blocked by a peroxisome prolifer

36 PfCRT3D7) lacks significant chloroquine (CQ) transport activity, but the introduction of the eight mu

37 ux-sensor where signaling is proportional to transport activity.

38 alone the molecular mechanism of the calcium transport activity.

39 b in their regulation of OAT1 expression and transport activity.

40 d SOS2, and these interactions modulate PUT3 transport activity.

41 Molecular transport after GUV permeabilization induced by multiple

42 inate their action to ensure smooth and fast transport along the flagellum without standing in each o

43 sediments during longshore drift and aeolian transport along the south-eastern Mediterranean coast le

44 in multiple cellular compartments and their transport among compartments.

45 ly reduced as a result of changes in hormone transport and a reduction in meristematic cell prolifera

46 lar grain boundaries which block the carrier transport and behave as the non-radiative recombination

47 es of intensive variables that control magma transport and dyke propagation through the crust are poo

48 ta-subunits that mediates respiratory oxygen transport and exchange by cooperatively binding oxygen w

49 ve analyses of cytotoxic granule maturation, transport and fusion in vitro with super-resolution imag

50 r elucidating molecular mechanisms of copper transport and homeostasis.

51 ary motor for microtubule minus-end-directed transport and is indispensable to eukaryotic cells.

52 ce of NUCB1 as an essential component of MMP transport and its overall impact on ECM remodeling.

53 highlighting the importance of both external transport and local emissions to PM(2.5) pollution in De

54 red by these ionic phenomena, the electronic transport and magnetic signature of the heterointerface

55 We propose that dynamic regulation of ion transport and metabolic plasticity are required to maint

56 xpression of genes involved in transmembrane transport and metabolism.

57 the-art numerical simulations of atmospheric transport and meteorological data to follow the trajecto

58 of glycerolipid, downregulation of ammonium transport and nitrate assimilation, restriction of prote

59 The combination of long-range exciton transport and slow annihilation highlights the unique at

60 acceptors exhibit balanced ambipolar charge transport and surprisingly long exciton diffusion length

61 C7A11A, a gene involved in cystine/glutamate transport and the biosynthesis of glutathione, an antiox

62 o withstand the forces associated with water transport and the physical weight of plant structures.

63 patial scale of organelles and intracellular transport and thereby affects biosynthesis.

64 ed(7), which suggests that additional energy transport and thermal effects could play an explicit rol

65 gulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Bindi

66 nation was the consequence of the long-range transport and wet deposition of fly ash from the combust

67 showed strong rheostatic effects on overall transport, and individual substitutions showed varied ef

68 s equipped with perfusion lines for chemical transport, and mirrors for laser beam guidance.

69 bited AQP3-facilitated H(2)O(2) and glycerol transport, and prevented liver injury in experimental an

70 ted Ca(2+) dynamics for mitochondrial axonal transport, and the therapeutic promise of TRPV4 antagoni

71 as an ideal platform for investigation of 2D transport anisotropy and chiral charge transport as a re

72 d cDC1, and this was not simply because they transport antigens to lymph nodes for processing by cDC2

73 mechanisms by which TBC1D23 regulates cargo transport are poorly understood.

74 We identify endosomal transport as a major functional cluster of TMEM16K in pr

75 of 2D transport anisotropy and chiral charge transport as a result of broken symmetry.

76 for mAb inhibition of AQP3-mediated H(2)O(2) transport as therapy for macrophage-dependent liver inju

77 In vitro transport assays confirmed that some of these compounds

78 b6 depleted cells, we found that anterograde transport at 32 degrees C, permissive conditions, throug

79 Mass transport at the PB thin film is shown not to be rate-li

80 n refractory arrest (at risk of intra-arrest transport) at that same time (unexposed), using a time-d

81 ons radial to the electrode disk, leading to transport away from the electrode.

82 This can only be attributed to the strong transport barriers across internal interfaces, as suppor

83 The ion transport behavior in these materials can be regulated t

84 A fundamental understanding of ion transport behavior in wood-based structures enhances the

85 s study hypothesized that the speciation and transport behaviors of phosphate ions are highly influen

86 ocesses that underpin osmolyte synthesis and transport, but the main computational approach for predi

87 Advances in anion transport by synthetic supramolecular systems are discus

88 l is contested and solutes are claimed to be transported by diffusion only.

89 biogenic CO(2) in biorefineries is captured, transported by pipeline, and injected into saline aquife

90 While, the estimated total mass of Hg transported by rivers is substantially less than the est

91 lar constructs to deliver outstanding charge-transport capabilities using metalloporphyrin-based supr

92 llular function requires molecular motors to transport cargoes to their correct intracellular locatio

93 8E, depending on their expression levels, to transport cGAMP and other 2'3'-cyclic dinucleotides.

94 d that impaired NADH oxidation upon electron transport chain (ETC) inhibition depletes asparagine, ac

95 interactions reduces mitochondrial electron transport chain activity.

96 ltured human cells with a defective electron transport chain decreased the extracellular lactate:pyru

97 ) is a vital lipid component of the electron transport chain that functions in cellular energy metabo

98 g wild-type genomes have functional electron transport chains and propagate more vigorously than mito

99 pothesis that impaired mitochondrial calcium transport contributes to the pathogenesis of Barth syndr

100 m of PfCRT (PfCRTDd2) enables the protein to transport CQ away from its site of antimalarial action.

101 brain, although its capacity for retrograde transport currently limits its use to unidirectional cir

102 Analyses of the transport cycle show that serine phosphorylation abolish

103 ition or rationality that underlies people's transport decision-making.

104 It is interesting to note that the transport-defective MNESmut was recruited to IBperi.

105 Ac) repeats, and previous studies have shown transport-dependent increases in E6 size consistent with

106 novel intercellular communication structures transporting different cargos with potential implication

107 Until now, the mechanism by which NIS transports different anion substrates with different sto

108 40 mV with a [Cl(-)](out) of 104 mm, but the transport direction did not reverse with a [Cl(-)](out)

109 s MlaFEDB, MlaC and MlaA-OmpF to monitor the transport direction of phospholipids.

110 three distinct temporal scaling laws for the transport distance of exhaled material including 1) tran

111 r in nuclei, positioning of nuclei to reduce transport distances to the cytoplasm were of less import

112 n and release involve movements of the bulky transport domain through the lipid bilayer.

113 fluid dynamics including flow, perivascular transport, drainage, and barriers.

114 (2-MAG), and membrane lipid biosynthesis and transport during nodule development.

115 esting that multiple lipid substrates may be transported each cycle.

116 f the endosomal sorting complex required for transport (ESCRT), a cellular machinery that coats the i

117 , the endosomal sorting complex required for transport (ESCRT)-III mediates abscission, the process t

118 The endosomal sorting complexes required for transport (ESCRTs) mediate diverse membrane remodeling e

119 -derived lymphoblastoid cells are capable of transporting exogenous spermine and its analogs into the

120 recent spectroscopic measurements(7-10), and transport experiments have shown changes in the Landau l

121 Anion transport experiments in POPC-based large unilamellar ve

122 Patients treated with intra-arrest transport (exposed) were matched with patients in refrac

123 , the urease operon, genes involved in metal transport (feoA, mntH, sirA), anaerobic metabolism genes

124 elt number-the dimensionless measure of heat transport-follows the classical power law of [Formula: s

125 ates that some mitochondria are retrogradely transported for degradation in the cell body, the precis

126 Furthermore, models of radionuclide transport from disposal boreholes must take into account

127 We find that proton transport from the central binding site to the lumen has

128 CHC22 functions in transport from the ERGIC, as demonstrated by an essentia

129 ompounds to the xylem, which indicated their transport from the roots to the upper parts of the plant

130 ol-3,5-bisphosphate synthesis and retrograde transport from the vacuole.

131 on, neuronal injury, autophagy and vesicular transport genes are observed in PD with and without deme

132 GNIFICANCE STATEMENT Disrupted mitochondrial transport has been linked to neurodegenerative disease.

133 ), the plasma membrane protein that actively transports I(-) (stoichiometry 2Na(+):1I(-)) in thyroid

134 The intraflagellar transport (IFT) machinery consists of the anterograde mo

135 The neonatal Fc receptor (FcRn) transports IgG across barriers, for example, the placent

136 The endosomal sorting complex required for transport-III (ESCRT-III) catalyzes membrane fission fro

137 psid variant capable of efficient retrograde transport in brain, was generated in mice using a direct

138 While the implication of cytoplasmic transport in d-Ser toxicity was unsurprising, disruption

139 Charge transport in DNA-based junctions has been reported using

140 SMGs and mucus strands disrupted mucociliary transport in EDA-KO pigs.

141 gion of the TGN devoted to specialized cargo transport in general rather than being specific for GLUT

142 SF) disrupts inactivation and K(+)-selective transport in hERG1, leading to arrhythmogenic phenotypes

143 of auxin distribution, measurement of auxin transport in protoplasts, and direct quantification of f

144 which suggests a potential role of vertical transport in structuring mesopelagic NCLDV communities.

145 ppreciated role for retrograde mitochondrial transport in the maintenance of a homeostatic distributi

146 terial cell wall constituents inhibit HCO(3) transport in the outer medullary collecting duct from th

147 recombination in the time domain and carrier transport in the spatial domain.

148 combination of techniques, including magneto-transport in the van der Pauw geometry, THz time-domain

149 trogen fixation in Ljsen1 plants reduce iron transport in yeast.

150 iven mechanism associated with photosynthate transport in yielding the observed patterns of soil CO(2

151 Recent work has established how miRNAs are transported in body fluids often within exosomes, which

152 more, we identify genes involved in cellular transport, including calcium transporters and cytoskelet

153 -type shoots induced a steeper GSA and auxin transport inhibitors counteracted the CEP receptor mutan

154 However, its mechanism of transport into plants is poorly understood.

155 n import genes; iron import can reflect iron transport into the cytosol or mitochondria.

156 Cryo-EM reveals that DNAs transported into E-S/E-K compartments are 'clamped' in a

157 Benthic microorganisms transported into the water column potentially influence

158 roxy)hexylthiophene] (P3HHT) that is able to transport ions and electrons/holes, as tested in electro

159 Transport is constant with coherent tunneling down to 10

160 The fidelity of quantum transport is defined as the transmission performance of

161 ; 2) a longer distance, ~1 m, where directed transport is driven by individual vortical puffs corresp

162 However, quantized disorder-resilient transport is observable in the edge currents of 2-dimens

163 ting enzyme of mitochondrial fatty acid (FA) transport, is repressed by hypoxia-inducible factors (HI

164 sco carboxylation, V(cmax) , and of electron transport, J(max) ) was reduced in warm-grown seedlings,

165 idual substitutions showed varied effects on transport kinetics (K(m) and V(max)) and substrate speci

166 omated and applied to characterize substrate transport kinetics and to test 294 top-marketed drugs fo

167 A hole-transporting large-bandgap polymer (poly[bis(4-phenyl)(2

168 In photosynthetic electron transport, large multiprotein complexes are connected by

169 olar cells, since these employ a p-type hole-transport layer (HTL) implemented using 1,2-ethanedithio

170 ectively facilitates hole extraction to hole transport layer and expels electrons toward cathode side

171 binding protein-related protein ORP1L, which transports LDL-derived cholesterol at membrane contacts

172 nal plug His-221 disrupts both signaling and transport, leading to dysregulation of both the Has and

173 Specifically, mass-transport limitations lead to large concentration gradie

174 k between physiological ROS signaling, AMPAR transport, localization, and excitatory transmission.

175 ng idea that m(6)A could also coordinate the transport, localization, and local translation of key mR

176 Four spirobisacridine (SBA) hole-transporting materials were synthesized and employed in

177 , X-ray computed tomography, grafting, auxin transport measurements and hormone quantification to dem

178 lter paper discs, air harvesters, and liquid transport media) and assessment of microbial bioload (gr

179 ic Ocean, the East Australian Current (EAC), transports microbial assemblages that maintain tropical

180 vels of expression of nuclear-encoded, TIM23-transported mitochondrial proteins ACO2, TUFM, IDH3A, CL

181 ical campaigns allowed developing a reactive transport model capable of reproducing the redox potenti

182 ion strategies, and enabling global chemical transport model development.

183 Earth Observing System (GEOS)-Chem chemical transport model, we find that global surface accumulatio

184 n models (DGVMs) coupled with an atmospheric transport model.

185 tration profiles using an unsteady diffusion transport model.

186 Geochemical reactive transport modelling, constrained by elemental budgets, i

187 re are relatively well studied, yet sediment transport models remain unable to account for the rapid

188 f particle dry deposition in global chemical transport models.

189 ital to build accurate equation of state and transport models.

190 y selective for the fluoride anion, which is transported more than 20 times faster than the chloride

191 lation in wild-type plants and a vacuolar Pi transport mutant, and then measuring the subsequent chan

192 This mode of forward transport necessitates a mechanism to prevent membrane m

193 thesis-driven resilience framework for urban transport NoNs, which we demonstrate on the London Rail

194 tracellular compartments to enable efficient transport of a virus between these compartments.

195 ditions assayed, thus supporting the use and transport of alternative collection media and specimen t

196 applied in relation to surface water, on the transport of antibiotics and ARGs in runoff and soil fol

197 We model chemotactic transport of bacteria within a leaf tissue in response t

198 ocess that combines the three steps of water transport of biocidal metal cations and soil solutes, de

199 , whereas the second module orchestrates the transport of both ions and proteins to the shell secreti

200 mantle, with important implications for the transport of carbon in aqueous fluids in the Earth's int

201 re implicated in the perception, storage and transport of chemosensory signaling molecules including

202 The intracellular transport of cholesterol from the PM to the ER is believ

203 angstrom diameter, mediate highly efficient transport of diverse types of anions, rather than cation

204 impact pathways mediating the metabolism and transport of glucose and pyruvate.

205 land cover change and soil erosion on river transport of Hg in a heavily ASGM-impacted watershed.

206 ic dynein is an AAA(+) motor that drives the transport of many intracellular cargoes towards the minu

207 logical pump that produces on-demand, robust transport of mechanical energy using a 1D magneto-mechan

208 cid is essential for engaging and initiating transport of multiple drugs and xenobiotics.

209 The transport of nascent HSV particles from neuron cell bodi

210 ecognition that dysregulated dynein-mediated transport of nephrin in R218Q knockin podocytes opens an

211 Regulated transport of nuclear proteins (e.g., transcription facto

212 inantly controlled by TPA diffusion, whereas transport of other active components was rendered noness

213 that PfCRT does not mediate the non-specific transport of other metabolites and/or ions.

214 porosity of the coating facilitated the mass transport of peptides through the PAN layer, thus enabli

215 ems as well as their effects on the fate and transport of pollutants in natural and engineered water

216 ew molecular system for vesicle-based axonal transport of proteins in male and female flies (Drosophi

217 Using two-color imaging we demonstrate co-transport of Rab11A and IAV vRNA in infected cells and p

218 Here, we used retrograde transneuronal transport of rabies virus to identify the cortical areas

219 odels remain unable to account for the rapid transport of sediment released from behind incinerated v

220 blish a new mechanistic link between reduced transport of synaptic cargos and impaired maintenance of

221 TFE3 were activated, as demonstrated by the transport of these proteins from the cytoplasm into the

222 Retrograde transport of this organelle has been implicated in turno

223 the precise impact of disrupting retrograde transport on the organelles and the axon was unknown.

224 rt distance of exhaled material including 1) transport over a short distance (<0.5 m) in a fraction o

225 Red blood cells (RBCs) transport oxygen to tissues and remove carbon dioxide.

226 hness is a key control on steepland sediment transport, particularly after wildfire when smoother sur

227 d sorts incoming virions into the retrograde transport pathway for trafficking to the nucleus.

228 o an intracellular compartment to initiate a transport pathway.

229 Clogging of fluid transport pathways in rocks from CO(2)-induced salt prec

230 to the testes with drugs that use endogenous transport pathways may lead to more effective treatments

231 Yet, little is known about the sources and transport pathways of Southern Hemisphere dust during th

232 ences exhibit unexpected and distinct charge transport pathways that enhance molecular conductance mo

233 reference pathways, including metabolic and transport pathways, transcriptional networks, hormone si

234 exhibit unusual surface states and anomalous transport phenomena.

235 e moved by distances 0, 2 or 3 in an optimal transport plan.

236 oupling plays essential roles in the quantum transport, polaritonic, and electrochemical properties o

237 al methods based on autoencoding and optimal transport principles for lineage tracing in settings whe

238 In each half cycle of the transport process, there is a state in which ions are st

239 Yet taste is complicated by the transport processes of stimuli through the papilla matri

240 Understanding and manipulating these transport processes on a molecular and supramolecular sc

241 f the regulatory pathways for multiple renal transport processes.

242 the influence of nanoconfinement on membrane transport properties and provide enhanced fundamental un

243 the possibility of strain engineering of the transport properties of BAs for application in electroni

244 By studying the generic spatial transport properties of such proteins, we investigate he

245 ng linkers result in dramatic changes in the transport properties of the metalloporphyrin-based wire.

246 However, their charge transport properties remain elusive, plagued by the issu

247 lating single crystals, leading to anomalous transport properties well above cryogenic temperatures.

248 s shown to exhibit not only exceptional bulk transport properties, with a sigma(o) among the highest

249 6 and CH1007 to ensure their superior charge-transport properties.

250 lymer batteries with good interfacial charge-transport properties.

251 to) conductivity and finally limits the hole-transporting property of the rear subcell.

252 The conserved transport protein particle (TRAPP) complexes regulate ke

253 tion, tunable pore size and excellent charge transport provides great opportunity to fabricate promis

254 Expanded air transport quality assurance protocols, including a requi

255 The underlying principle is that the acid transport rate is associated with the partition coeffici

256 ion of biotrickling filters that governs the transport rate of contaminants and oxygen from the gas p

257 uivalents, they could not appreciably affect transport rates of NBCe1 or other transporters carrying

258 ion for varied substrate specificity and ion transport ratio among CCCs.

259 disruption" results in a decrease in lactate transport, reduced glycolysis, and ultimately reduced ce

260 hanistic understanding of PLB-mediated SERCA transport regulation.

261 thesis that increased soil water storage and transport resulting from cultivation may enhance dissolu

262 results indicate that the beta-glucoside PTS transports salicin and its metabolism can differentially

263 These genes include, root-specific auxin transport, strigolactone and gibberellin biosynthesis, d

264 ive evidence of relationships between public transport strikes and either increased air pollution or

265 Thermoelectric transport studies further demonstrated that MoS(2) films

266 ng (3)H-leucine (the gold standard for LAT-1 transport studies) and JPH-203 (a specific LAT-1 inhibit

267 f mycolactone-inhibited Sec61 to effectively transport substrate proteins implies that signal peptide

268 ear of growth, overwintering biennial plants transport Suc through the phloem from photosynthetic sou

269 racellular vesicles (EVs) form an endogenous transport system for intercellular transfer of biologica

270 tions within beta-oxidation and the electron transport system serve as a barometer of substrate flux

271 ngstrom and establish a proteoliposome-based transport system that includes MlaFEDB, MlaC and MlaA-Om

272 uence suggesting an expansive short peptidic transport system within Devosia.

273 ClC-5 transport that provides three net negative charges appea

274 hence, diverse secretion systems evolved to transport the hydrophilic molecules to their sites of ac

275 acrophages take up HSV-1 via endocytosis and transport the virions into multivesicular bodies (MVBs).

276 oiodide-based thyroid cancer treatment, also transports the environmental pollutant perchlorate (stoi

277 hesis is completed at the inner membrane and transport them to the outer membrane.

278 highly modified landscapes, spatial nutrient transport theory suggests that such instabilities can be

279 cted to allow phase-coherent single-electron transport through a topological superconducting island v

280 -Labyrinth' framework which studies physical transport through disordered media allows us to formulat

281 e of host dynamics for guest entrance to and transport through the channels.

282 o, such basic questions as whether vesicular transport through the Golgi occurs in an anterograde (fr

283 features emerge mostly due to the different transport time scales at different regions of the flow n

284 Contrasting the space-time dynamics of transport times with reactive timescales of denitrificat

285 arrier (BBB) strongly impede hurdle for drug transport to brain.

286 y treatment with magnesium sulfate or during transport to facility.

287 rgency medical systems (EMS) with respect to transport to hospital during out-of-hospital cardiac arr

288 trary stimulus by explicitly linking hormone transport to local tissue deformation leading to the gen

289 corynomycolate (hTMCM) enables its efficient transport to the periplasm in Corynebacterium glutamicum

290 al trafficking pathways including retrograde transport to the trans-Golgi network (TGN), is involved

291 ely to have occurred in Mexico whence it was transported to Europe and ultimately improved into one o

292 here polaritons with opposite helicities are transported to opposite directions, is verified.

293 d plasma free fatty acids (FFAs), which were transported to the adipose tissue for storage and trigge

294 vious studies propose that microplastics are transported to the seafloor by vertical settling from su

295 Results show that gas is transported to the surface of the system via varying dom

296 y cofactor for dynein-mediated intracellular transport towards the minus-ends of microtubules.

297 The ordered macropores enhance ionic transport under high sulfur loading by forming sufficien

298 n-induced assembly to enable directional ion transport via forming vertically aligned nanosheets is r

299 Pepsin transport was observed by confocal laser scanning micros

300 ic materials with well-understood electronic transport within such structures will potentially lead t