ライフサイエンスコーパス: membrane transport

1 main binds several Rab effectors involved in membrane transport.

2 ing, lipid metabolism, iron homeostasis, and membrane transport.

3 cellular processes, ranging from mitosis to membrane transport.

4 n accordance with the prevailing paradigm in membrane transport.

5 master regulator of early to late endocytic membrane transport.

6 sed by different bacteria to manipulate host membrane transport.

7 ing that this region plays an active role in membrane transport.

8 C population was homogeneous with respect to membrane transport.

9 nd its relationship to the kinetics of trans-membrane transport.

10 that subvert signaling pathways controlling membrane transport.

11 has great promise as an approach to measure membrane transport.

12 ful model for investigating myosin-dependent membrane transport.

13 lamine was the result of high-affinity outer membrane transport.

14 trypanosome transcriptome is associated with membrane transport.

15 Golgi structure and facilitating anterograde membrane transport.

16 e cell cycle, innate immunity, and lipid and membrane transport.

17 inhibitors are acting on outer mitochondrial membrane transport.

18 al basis of the alternating access model for membrane transport.

19 covery of chemicals that inhibit prokaryotic membrane transport.

20 he structural reorganizations that accompany membrane transport.

21 never demonstrated, ball-and-chain theory of membrane transport.

22 dination of these cytoskeletal assemblies in membrane transport.

23 bilizing molecules that inhibit all types of membrane transport.

24 senger implicated in signal transduction and membrane transport.

25 eports related to carbohydrate digestion and membrane transport.

26 further supporting a function in regulating membrane transport.

27 ry protein governing early to late endocytic membrane transport.

28 quirements of ferric iron (Fe3+) binding and membrane transport.

29 This code helps controlling vectoriality of membrane transport.

30 direct actions of pH(i) upon Cl(-)-dependent membrane transport.

31 itions where [Na](i) is controlled mainly by membrane transport.

32 fatty acid synthesis, resulting in aberrant membrane transport.

33 1-coated vesicles for anterograde TGN-plasma membrane transport.

34 their origins in guard cell homeostasis and membrane transport.

35 nes in the intermembrane space to facilitate membrane transport.

36 aluate the impact of co-addition of drugs on membrane transport.

37 e and reducing ferric to ferrous Fe prior to membrane transport.

38 s is independent of COPII- and COPI-mediated membrane transport.

39 s SV40 endoplasmic reticulum (ER)-to-cytosol membrane transport, a decisive infection step where dest

40 te this crucial role, the molecular basis of membrane transport across the symbiosomal membrane remai

41 consistent with biological knowledge (e.g., membrane transport activity for pH and MY or Wnt signali

42 ter exchange also correlates with ATP-driven membrane transport activity in yeast (Saccharomyces cere

43 ate the effect of bilayer composition on the membrane transport activity of two members of the small

44 on, the associated increase in SNAT2 protein/membrane transport activity were strongly suppressed in

45 MCOLN1 is an ion channel that regulates membrane transport along the endolysosomal pathway.

46 of sphingolipids, and, as a consequence, in membrane transport along the recycling endosome pathway.

47 ulate the function of proteins that regulate membrane transport and alter the phospholipid content of

48 tained in the Golgi, in the midst of dynamic membrane transport and cargo export, is a fundamental un

49 However, since Bic was found to inhibit the membrane transport and consumption rates of testosterone

50 TPases are conserved motors in key microbial membrane transport and filament assembly machineries, in

51 age-related changes in red blood cell (RBC) membrane transport and homeostasis.

52 h its interactions with proteins involved in membrane transport and in regulation of stress responses

53 n complex (EMC) called EMC1 promotes SV40 ER membrane transport and infection.

54 lfide bonds, a reaction important for its ER membrane transport and infection.

55 gene and defective alleles severely disrupt membrane transport and inhibit ER vesicle budding.

56 luding tubulogenesis of the excretory canal, membrane transport and ion channel function, and human g

57 and MotAB-type systems for energizing outer-membrane transport and motility than does Escherichia co

58 rial, intranasal theophylline (an epithelial membrane transport and proton secretion activator) incre

59 In the soma, transcripts for membrane transport and respiration were up-regulated, wh

60 on-pair receptors, including applications as membrane transport and salt solubilization agents and se

61 chemistry are the key factors that determine membrane transport and separation capabilities.

62 gen detection systems operate to induce both membrane transport and signal transduction.

63 y determining its effect on the major apical membrane transport and signaling processes involved in i

64 hat has been implicated in several important membrane transport and signaling processes.

65 duction, tying SYP121 function to guard cell membrane transport and stomatal control.

66 s, such as nonselective and carrier-mediated membrane transport and symplastic dispersal, that may ef

67 MPTP in its requirement for selective plasma membrane transport and the expression of acute hypotherm

68 s found to be axial, rather than radial (via membrane transport), and most of the axial resistance is

69 okinetics), the tat peptide (to improve cell membrane transport), and the (111)In-labeled antiRIalpha

70 o selected genes, KDELR3, GM130 (involved in membrane transport), and the proto-oncogene JUN, indicat

71 were impaired along with stomatal behaviour, membrane transport, and expression of genes associated w

72 ion, remodeling of the extracellular matrix, membrane transport, and metabolism.

73 in functional categories: GTPase activation, membrane transport, and mRNA metabolism/alternative spli

74 and the coatomer COPI, a complex involved in membrane transport, and shifts endosomal morphology enti

75 Rab11A, which mediates trans-Golgi-to-plasma-membrane transport, and that increased HIV Gag was seque

76 esses such as protein folding, drug binding, membrane transport, and the conformational changes criti

77 ociated defense; transcriptional regulation; membrane transport; and growth at 72 degrees C.

78 ence that the HCMV-induced remodeling of the membrane transport apparatus involves much more than sim

79 forced into membranes to create sensors, yet membrane transport applications of short CNTs remain und

80 he latter are master regulators of vesicular membrane transport, as they control the activity of memb

81 In a vesicular membrane transport assay, ABCC5 also transported exogeno

82 results, likely due to differences in active membrane transport between the cell types, the Caco-2-ba

83 The small GTPase Rab2 is required for membrane transport between the endoplasmic reticulum (ER

84 ously established that GAPDH is required for membrane transport between the endoplasmic reticulum and

85 Als2cr4 may be involved in membrane transport between the photoreceptor inner and o

86 temperature-dependent and blocked by the eCB membrane transport blockers, VDM11 and UCM707, but did n

87 ransport could be detected, while the Gu-100 membranes transported both ions significantly.

88 ccurate, real-time spectroscopic analysis of membrane transport by other cells.

89 cally divergent viruses require biosynthetic membrane transport by the COPI coatomer complex for effi

90 transmembrane proteins by sorting them into membrane transport carriers.

91 es a variety of cellular processes including membrane transport, cell proliferation, and survival, an

92 popolysaccharide biosynthetic pathway, outer membrane transport channels, ubiquinone biosynthetic pat

93 evidence of the influence of temperature on membrane-transport channels.

94 ization of a non-enveloped virus generates a membrane transport-competent viral particle.

95 Our findings explain how the inner-membrane transport complex controls efficient unidirecti

96 Reorganization of membrane transport components may provide a mechanism wh

97 adaptations in major metabolic pathways and membrane transport concurrent with aztreonam resistance,

98 ic factors, but ultimately depends on active membrane transport connecting axons and dendrites with t

99 AA+ family proteins, energy conversion, cell membrane transport, DNA or RNA replication and antiviral

100 ted to neurons, synapses, genic intolerance, membrane transport, epilepsy, and mental disorders.

101 opose that PA levels are critical for apical membrane transport events required for rhabdomere biogen

102 These data suggest that alsin is involved in membrane transport events, potentially linking endocytic

103 uit specific downstream effectors to mediate membrane-transport events.

104 the external supply, indicating that plasma membrane transport exceeded the rate of glucose phosphor

105 Membrane transport experiments conducted in whole cells

106 Sequence alignments and membrane transport experiments using (19)F NMR, osmotic

107 ion (Tat) systems of thylakoid and bacterial membranes transport folded proteins using the proton gra

108 The kinetic rate constant for Ni(2+) membrane transport for +/b BBMV was within the range for

109 la avoids fusion with lysosomes and subverts membrane transport from the endoplasmic reticulum to cre

110 uenced 14 metabolic core functions including membrane transport from which type VI secretion systems

111 nal tubules demonstrated progressive loss of membrane transport function after reperfusion with incre

112 opulations with distinct kinetic patterns of membrane transport in bulk tumor cells (BTCs) and tumor-

113 ationships and supports a prominent role for membrane transport in determining chemosensitivity.

114 and provided insight into the regulation of membrane transport in eukaryotic cells.

115 logy (PH) domain in UNC-104 is essential for membrane transport in living C. elegans, that this PH do

116 Despite extensive studies, the mechanisms of membrane transport in living microbial cells remain inco

117 anching through a mechanism that may involve membrane transport in the growth cone.

118 To understand further the role of membrane transport in this process, we analyzed the phen

119 Arf6 is known to regulate endosome-to-plasma membrane transport, in part through activation of type I

120 SCD1 and SCD2 function in clathrin-mediated membrane transport, including plasma membrane endocytosi

121 r intracellular application of an anandamide membrane transport inhibitor (VDM11).

122 tion requires cargo delivery via fusion with membrane transport intermediates and recycling of fusion

123 the cis-Golgi apparatus and tubulo-vesicular membrane transport intermediates.

124 Endoplasmic reticulum (ER)-to-cytosol membrane transport is a decisive infection step for the

125 Membrane transport is generally thought to occur via an

126 Guard cell membrane transport is integral to controlling stomatal a

127 ortly after birth, suggesting Syt11-mediated membrane transport is required for survival.

128 as biocompatible nanoprobes for the study of membrane transport kinetics in living microbial cells.

129 he time resolution of current techniques for membrane transport kinetics measurements, the lifetimes

130 a factor of 12 due to the alleviation of the membrane transport limitation.

131 teins that, although expressed at the plasma membrane, transport little or no I(-) These residues are

132 and their integration with the intracellular membrane transport machinery are virtually unknown.

133 in complex, is an essential component of the membrane transport machinery required for tethering and

134 ifferentiation, apoptosis, oxidative stress, membrane transport, matrix homeostasis, and cell adhesio

135 cuses primarily on new insights into osmotic membrane transport mechanisms and on novel membranes and

136 However, the membrane transport mechanisms and the signaling events i

137 This study investigated membrane transport mechanisms influencing relative chang

138 as aeruginosa is renowned for its intriguing membrane transport mechanisms, such as the interplay of

139 ell understood, much less is known about TIA membrane transport mechanisms.

140 mesophyll cells is mediated by two distinct membrane transport mechanisms: proton gradient-driven an

141 sibility of using this kind of electrodriven membrane transport methods for nuclear waste treatment.

142 Cytoplasmic dynein plays important roles in membrane transport, mitosis, and other cellular processe

143 are discussed in the context of established membrane transport modeling and previous work on the eff

144 mbrane model that accounts for the different membrane transport modes, nonisothermal effects, especia

145 st cellular processes, including metabolism, membrane transport, motility, and cell cycle.

146 e Golgi with the 4-phosphatase or disrupting membrane-transporting motors induces a decline in PM PI(

147 here in the cell neither blocked anterograde membrane transport nor cell motile functions.

148 dinated destabilization-stabilization drives membrane transport of a non-enveloped virus.

149 Aquaporin-8 (AQP8) channels facilitate the membrane transport of ammonia.

150 embrane, and RNA, we identify key factors in membrane transport of biopolymers.

151 n the ER and thus influences the anterograde membrane transport of both ceramide and proteins from th

152 affinity probe (RX-055) irreversibly blocked membrane transport of both endocannabinoids, providing m

153 ential role for this gene in Golgi to plasma membrane transport of chylomicron secretory vesicles.

154 an reduced folate carrier (hRFC) facilitates membrane transport of folates and antifolates.

155 propose that CLN3 facilitates TGN-to-plasma membrane transport of microdomain-associated proteins.

156 binding cassette (ABC) transporters catalyze membrane transport of micronutrients in prokaryotes.

157 en metabolism, as well as disruptions in the membrane transport of mitochondrial specific energy subs

158 rolysis, ABC transporters catalyze the trans-membrane transport of molecules.

159 osome and is required for endosome-to-plasma membrane transport of multiple cargos.

160 ss cell membranes, little is known about the membrane transport of other endocannabinoids, such as 2-

161 o palmitoyl-CoA were used to demonstrate the membrane transport of palmitoylcarnitine and free L-carn

162 escribe the application of ICP-MS to measure membrane transport of Rb and K ions by the Na,K-ATPase i

163 n reduced folate carrier (hRFC) mediates the membrane transport of reduced folates and classical anti

164 During ER-to-cytosol membrane transport of the nonenveloped polyomavirus SV40

165 e tip diameter, indicating diffusion-limited membrane transport of the redox molecules.

166 nd at the same time reduces the influence of membrane transport on the observed conversion rates.

167 ay diagrams showing biomolecular events like membrane transport or phosphorylation.

168 tic processes where membrane fouling occurs, membrane transport parameters A and B may not be useful

169 lume in target area), K(1) and k(2) (kinetic membrane transport parameters), k(3) and k(4) (intracell

170 lization had minimal impact on the intrinsic membrane transport parameters.

171 proteins contributes to productive NA plasma membrane transport partly by mediating escape from tethe

172 gest the importance of a separate microsomal membrane transport pathway for glucose transport.

173 the effector protein DrrA stimulates a host membrane transport pathway that enables ER-derived vesic

174 Autophagy is an important membrane transport pathway that is conserved among eukar

175 Autophagy is a conserved membrane transport pathway used to destroy pathogenic mi

176 of gene expression revealed up-regulation of membrane transport pathways in the resistant cells, and

177 ication, while also having the vacuole avoid membrane transport pathways that target bacteria for des

178 disease, intercepts material from host cell membrane transport pathways to create a specialized vacu

179 athogen Legionella pneumophila subverts host membrane transport pathways to promote fusion of vesicle

180 cortical reorganization leads to changes in membrane transport physiology.

181 Membrane transport plays a leading role in a wide spectr

182 -soluble vitamins appears to require its own membrane transport process for absorption across the ent

183 duction and its coupling to energy-requiring membrane transport processes and mechanisms of force gen

184 A model that accounts for these membrane transport processes is proposed.

185 features of the hepatocyte and highlight how membrane transport processes play a key role in healthy

186 luence upon Em of changes in Cm or Vc and of membrane transport processes such as the Na+-K+-ATPase a

187 behaviors of macromolecules, but its role in membrane transport processes such as vesicle fusion rema

188 n has evolved multiple mechanisms to control membrane transport processes that center on the involvem

189 ionarily conserved host factors that control membrane transport processes, which results in the forma

190 -dependent manner and has been implicated in membrane transport processes.

191 However, the mechanisms that control these membrane-transport processes are poorly understood.

192 e that Ypt/Rabs can regulate two independent membrane-transport processes by recruiting process-speci

193 O tests that are commonly used for measuring membrane transport properties (water and salt permeabili

194 ighlight the influence of nanoconfinement on membrane transport properties and provide enhanced funda

195 The membrane transport properties as well as performance wit

196 this work, is hindered by the unsatisfactory membrane transport properties.

197 ithin the beta-barrel of the bacterial outer-membrane transport protein BtuB by site-directed mutagen

198 ly the Escherichia coli ferric citrate outer-membrane transport protein FecA has been characterized;

199 gene, termed samt-1, coding for a candidate membrane transport protein for the presumptive donor sub

200 the gene for MDR1 (multidrug resistance), a membrane transport protein for which human polymorphisms

201 low nanomolar to millimolar) for an integral membrane transport protein in both detergent-solubilised

202 Furthermore, we show that a cellular vesicle membrane transport protein named hVAP-33 (the human homo

203 utilizing arginine alpha-decarboxylase and a membrane transport protein necessary for delivering argi

204 SERCA is a membrane transport protein that has been extensively stu

205 r family (NPF) 6.3 is a dual-affinity plasma membrane transport protein that has both high- and low-a

206 e bacteria involves the coupling of an outer membrane transport protein to the transperiplasmic prote

207 how that overexpression of the mitochondrial membrane transport protein UCP2 in cancer cells is suffi

208 se as a model the lactose permease (LacY), a membrane transport protein with a known three-dimensiona

209 lipids around the crystal structure of this membrane transport protein, followed by atomistic simula

210 Escherichia coli (LacY) is a highly dynamic membrane transport protein, while the Cys154-->Gly mutan

211 e region of the SLC25A40 inner mitochondrial membrane transport protein.

212 Escherichia coli (LacY) is a highly dynamic membrane transport protein.

213 omain protein that represents a new class of membrane transport protein.

214 r membrane and one lacking the relevant SbmA membrane transport protein.

215 ntly modified; for example, membrane fusion, membrane transport, protein disaggregation, and protein

216 n of genes encoding ribosomal, virulence and membrane transport proteins after both treatment times.

217 Assigning function to orphan membrane transport proteins and prioritizing candidates

218 ing the amount and the localization of these membrane transport proteins appears as a way to drive th

219 e than 400 members, the solute carrier (SLC) membrane transport proteins are the largest family of tr

220 Membrane transport proteins are therefore of upmost impo

221 cells, and approximately 25% of prokaryotic membrane transport proteins belong to this superfamily.

222 rane signaling events in the bacterial outer-membrane transport proteins BtuB, FecA, and FhuA.

223 h programs, we suggest that related cases of membrane transport proteins containing similar motifs ar

224 Solute carrier (SLC) membrane transport proteins control essential physiologi

225 howcases the potential of expressing desired membrane transport proteins in cell factories to achieve

226 ily that bind and deliver ligand to integral membrane transport proteins in the ATP-binding cassette,

227 n Latinos, notably in SLC genes that include membrane transport proteins involved in the transport of

228 nd recognition of ligands by bacterial outer membrane transport proteins is mediated in part by inter

229 perfamily, the largest family of ion-coupled membrane transport proteins known at present.

230 Membrane transport proteins play a crucial role in the i

231 of the kidney require an overlapping set of membrane transport proteins regulated by the forkhead tr

232 tion to the method of MD, we use a number of membrane transport proteins studied in our laboratory as

233 aling require Ca(2)(+) influx through plasma membrane transport proteins that are regulated by reacti

234 Membrane transport proteins that catalyse arsenic uptake

235 Granular biofilms were enriched in outer membrane transport proteins to scavenge the extracellula

236 In addition, cytoskeleton and membrane transport proteins were considerably altered du

237 important residues in hydrophobic domains of membrane transport proteins, and several critical roles

238 (LacY), a paradigm for the largest family of membrane transport proteins, catalyzes the coupled trans

239 (LacY), a paradigm for the largest family of membrane transport proteins, catalyzes the coupled trans

240 cedures to isolate the effects on individual membrane transport proteins, crofelemer at 50 microM had

241 mber of the major facilitator superfamily of membrane transport proteins, which contain two domains o

242 ikoshii, is an archaeal homolog of mammalian membrane transport proteins-known as excitatory amino ac

243 ed repeats found within the subunits of many membrane transport proteins.

244 ities of enzymes, transcription factors, and membrane transport proteins.

245 sterol-specific and reversible inhibition of membrane transport proteins.

246 formate/nitrite transporter (FNT) family of membrane transport proteins.

247 m involving secondary active Na(+)-dependent membrane transport proteins.

248 anism for this large and important family of membrane transport proteins.

249 the proper physiological functioning of many membrane transport proteins.

250 to measure rates of conformational change in membrane transport proteins.

251 and to identify putative regulatory sites of membrane transport proteins.

252 nce reconstitution, topology and activity of membrane transport proteins.

253 a prerequisite to understand the function of membrane transport proteins.

254 and release require vesicular and/or plasma membrane transport proteins.

255 H through the combined actions of a range of membrane transport proteins.

256 Drug membrane transport rate was evaluated in vitro and compa

257 f this method with compounds exhibiting slow membrane transport rates.

258 e observed that it has increased rates of Mn membrane transport, reduced cytotoxicity, and increased

259 Silencing of the host genes encoding the membrane transport regulators Rab5 or Rab7 interfered wi

260 cognized as the premier plant cell model for membrane transport, signaling, and homeostasis.

261 Apparent affinity constants of Sc(3+) with membrane transport sites (KSc-Rcell app) were surprising

262 of the MCM complex (DNA replication), RCN1 (membrane transport), SMC2 (chromatin dynamics), EDD1 (ub

263 By considering villous membrane to capillary membrane transport, stationary oxygen diffusion can be n

264 ses, including proliferation, apoptosis, and membrane transport steps.

265 The finding that fluid flow can regulate membrane transport suggests that mechanosensitive ATP re

266 ognate proteins subserve functions including membrane transport, synaptic transmission, transcription

267 asomal degradation, a complex bi-directional membrane transport system and a unique posttranslational

268 Our imaging data suggest that a novel membrane transport system operates in the cytosol of P.

269 ted endocytosis is an evolutionarily ancient membrane transport system regulating cellular receptivit

270 othetical lipoproteins as well as a putative membrane transport system.

271 The complete set of membrane transport systems and outer membrane channels o

272 Sodium/calcium (Na(+)/Ca(2+)) exchangers are membrane transport systems that regulate Ca(2+)-homeosta

273 environmental assaults: RNAi mechanisms and membrane transport systems that use ABC proteins.

274 We show here that one of these inner membrane transport systems, VctPDGC, also promotes iron

275 achieve voltage-switchability in artificial membrane transport systems.

276 athways (such as carbohydrate metabolism and membrane transport), the two reactors differed in the nu

277 living cell; its value is tightly coupled to membrane transport, the dynamics of transmembrane protei

278 d Rab13 have been found to mediate polarized membrane transport, the function of Rab10 in mammalian c

279 However, prior to membrane transport, the hydrophobic SV40 recruits the ER

280 Before membrane transport, the multidomain Gag protein of Rous

281 nrelated protein families mediate nucleoside membrane transport: the concentrative and equilibrative

282 phore, and is proposed to play a key role in membrane transport; the phagophore presumably expands by

283 to the classic "size/lipophilicity" rule of membrane transport, those molecular umbrellas that were

284 5, which explains how this protein modulates membrane transport through both the endocytic and exocyt

285 al between the rate of influx and outflux of membrane transport through the Golgi.

286 ill drive PEM design efforts towards optimal membrane transport, thus enabling more efficient polymer

287 reater understanding of how bacteria control membrane transport to create a replicative niche within

288 Viruses coopt cellular membrane transport to invade cells, establish intracellu

289 hotoreceptors, elevated levels of PA disrupt membrane transport to the apical domain.

290 ture virions (MVs) are wrapped with cellular membranes, transported to the periphery, and exported as

291 reduced extracellularly through trans-plasma membrane transport (tPMET), thereby suggesting that tPME

292 d included disruption of factors involved in membrane transport, transcriptional regulation, and intr

293 ron transport, ATP synthesis/transformation, membrane transport, translation, protein assembly/foldin

294 operties and is relevant in the formation of membrane transport vesicles in eukaryotic cells.

295 f the chloroplast suggest a possible role of membrane transport via vesicle trafficking from the inne

296 PG analysis showed that ABCB1 (C3435T)T/T (membrane transport) was associated with IP-related diarr

297 tabolism pathway, amino acid metabolism, and membrane transport were the functional traits of the lev

298 Here, we compare and contrast canonical membrane transport with a novel type of Ca(2+)-H+ coupli

299 Surprisingly, inhibition of Golgi membrane transport with brefeldin A did not prevent plas

300 oscopic level is key to our understanding of membrane transport, yet challenging to achieve experimen