ライフサイエンスコーパス: membrane transport

1 sed by different bacteria to manipulate host membrane transport.

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

3 C population was homogeneous with respect to membrane transport.

4 fatty acid synthesis, resulting in aberrant membrane transport.

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

6 that subvert signaling pathways controlling membrane transport.

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

8 ful model for investigating myosin-dependent membrane transport.

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

10 trypanosome transcriptome is associated with membrane transport.

11 Golgi structure and facilitating anterograde membrane transport.

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

13 inhibitors are acting on outer mitochondrial membrane transport.

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

15 he structural reorganizations that accompany membrane transport.

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

17 dination of these cytoskeletal assemblies in membrane transport.

18 bilizing molecules that inhibit all types of membrane transport.

19 senger implicated in signal transduction and membrane transport.

20 eports related to carbohydrate digestion and membrane transport.

21 further supporting a function in regulating membrane transport.

22 ry protein governing early to late endocytic membrane transport.

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

24 This code helps controlling vectoriality of membrane transport.

25 1-coated vesicles for anterograde TGN-plasma membrane transport.

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

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

28 y not clearly distinguished the two steps of membrane transport.

29 NSF) is an essential protein required during membrane transport.

30 5)P2-containing rafts provides a trigger for membrane transport.

31 GTPase Sec4p, a regulator of Golgi to plasma membrane transport.

32 their origins in guard cell homeostasis and membrane transport.

33 nes in the intermembrane space to facilitate membrane transport.

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

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

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

37 main binds several Rab effectors involved in membrane transport.

38 cellular processes, ranging from mitosis to membrane transport.

39 n accordance with the prevailing paradigm in membrane transport.

40 master regulator of early to late endocytic membrane transport.

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

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

47 adipocytes, one dependent upon intracellular membrane transport and another independent of the classi

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

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

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

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

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

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

54 activities: mitosis, nucleic acid synthesis, membrane transport and integrity, and phosphatase- and k

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

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

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

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

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

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

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

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

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

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

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

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

67 seful for future modeling studies of Bruch's membrane transport and to identify those moieties respon

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 n localization, chromosome partitioning, and membrane transport, and a group of metabolic enzymes wit

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

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

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

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

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

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

78 as transcription, DNA repair, ribosomal and membrane transport, and the proteasome.

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

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

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

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

83 ort complex (GTC), identified in an in vitro membrane transport assay, (b) the ldlCp complex, identif

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

85 conjugate with the relative rates of through-membrane transport being 7.7:4.1:1 for 5'-GMP, 5'-AMP, a

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

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

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

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

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

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

92 (PIP(3)), was added exogenously to SMG via a membrane-transporting carrier in the presence of PI 3-ki

93 transmembrane proteins by sorting them into membrane transport carriers.

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

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

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

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

98 Reorganization of membrane transport components may provide a mechanism wh

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

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

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

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

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

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

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

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

107 re measurements, partition coefficients, and membrane transport experiments.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 Guard cell membrane transport is integral to controlling stomatal a

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

128 RG2 wild-type cells suggest a possible cell membrane transport limitation for FHBG and FHPG.

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

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

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

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

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

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

135 This study investigated membrane transport mechanisms influencing relative chang

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

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

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

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

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

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

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

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

144 ure transcripts, including lipid, energy and membrane transport mRNAs, were tightly associated with a

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

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

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

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

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

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

151 However, membrane transport of DNA is an inefficient process, and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 fluence cell polarity, microtubule dynamics, membrane transport pathways and transcription factor act

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

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

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

175 cortical reorganization leads to changes in membrane transport physiology.

176 Membrane transport plays a leading role in a wide spectr

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

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

179 ting a role for these proteins in epithelial membrane transport processes in the nematode.

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

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

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

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

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

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

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

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

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

189 The membrane transport properties as well as performance wit

190 cs of lipids, protein-lipid interaction, and membrane transport properties.

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

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

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

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

195 To study this issue, lactose permease, a membrane transport protein from Escherichia coli, is tra

196 of signal transduction in which an integral membrane transport protein functions to link the extrace

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

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

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

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

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

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

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

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

205 e derivatives with respect to a well studied membrane transport protein, the lactose permease of Esch

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

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

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

209 ntrance loops are unlikely in this polytopic membrane transport protein.

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

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

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

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

214 Assigning function to orphan membrane transport proteins and prioritizing candidates

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

216 cation diffusion facilitator (CDF) family of membrane transport proteins are found in eukaryotes and

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

218 conducted bioinformatic analyses of integral membrane transport proteins belonging to dozens of famil

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

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

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

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

223 signed for describing the predicted cellular membrane transport proteins in organisms whose complete

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

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

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

227 Membrane transport proteins play a crucial role in the i

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

229 Amt proteins are the first hyperthermophilic membrane transport proteins shown to be active in a meso

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

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

232 Membrane transport proteins that catalyse arsenic uptake

233 Likewise, expression of several membrane transport proteins that interact directly with

234 Membrane transport proteins that transduce free energy s

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 e putative extracellular signaling proteins, membrane transport proteins, and novel secreted proteins

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

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

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

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

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

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

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

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

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

247 the proper physiological functioning of many membrane transport proteins.

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

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

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

251 nd phosphatases), whereas PlantsT focuses on membrane transport proteins.

252 g, and characterization of a large number 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 ed repeats found within the subunits of many membrane transport proteins.

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

258 ise to speculation about the mechanism(s) of membrane 'transport' proteins for fatty acids and choles

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

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

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

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

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

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

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

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

267 RP1) is a member of the ATP-binding cassette membrane transport superfamily and is responsible for mu

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

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

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

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

272 olar function and probably for the endocytic membrane transport system.

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

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

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

276 For each organism, the complete set of membrane transport systems was identified and classified

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

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

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

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

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

282 Before membrane transport, the multidomain Gag protein of Rous

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

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

285 5, which explains how this protein modulates membrane transport through both the endocytic and exocyt

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

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

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

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

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

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

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

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

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

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

296 for TC10 regulating actin polymerization on membrane transport vesicles.

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

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 ibly to membranes have a central function in membrane transport within the secretory pathway.