ライフサイエンスコーパス: membrane-bound

1 ssed alone, Loop1 remained intracellular and membrane-bound.

2 hich only the higher-affinity module remains membrane-bound.

3 t-studied bacterial chemoreceptor arrays are membrane-bound.

4 to our knowledge) new procedures to assemble membrane-bound 1:1 SNARE acceptor complexes that produce

5 ganelle acidification in all eukaryotes, and membrane-bound a-subunit isoforms of the V-ATPase are im

6 using DHLMP2A mice, which lack secreted and membrane-bound Ab, yet harbor marginal zone and follicul

7 components of the respiratory burst oxidase, membrane-bound adhesion molecules, and receptors that fa

8 he risk factor molecules stabilizes a common membrane-bound alpha-helical intermediate that, in turn,

9 The aggregation of membrane-bound alpha-synuclein (alphaS) into oligomers a

10 more than 70% of patients, 8 were soluble or membrane bound and expressed in the skin.

11 ein that cycles between nucleotide-dependent membrane-bound and cytosolic states.

12 We analyzed radiotracer uptake (both membrane-bound and internalized fractions) and the produ

13 chemical inhibition of Porcupine reduced the membrane-bound and secreted fractions of Wnt3 and eventu

14 In addition, membrane-bound angiotensin-converting enzyme activity de

15 uolar inclusions (AVIs), from more globular, membrane-bound anthocyanoplasts.

16 ns, it is now clear that the presentation of membrane-bound antigen plays a crucial role in B cell ac

17 assemblies provides an opportunity to image membrane-bound AQP4 antibodies (AQP4-IgG) and evaluate c

18 LA2) activity with a preferential release of membrane-bound arachidonic acid, stimulating the lipoxyg

19 Membrane-bound arrays are single layered; cytoplasmic ar

20 s and in different biochemical states (i.e., membrane bound as in brain microsomes from wild-type mic

21 Here we show that in addition to the membrane-bound Asp-His-His and Asp-His-His-associated (D

22 in pfmdr1, which encodes a digestive vacuole membrane-bound ATP-binding cassette transporter known to

23 positive pathogen Staphylococcus aureus, the membrane-bound ATP-dependent metalloprotease FtsH plays

24 ors for self-antigens that are recognized by membrane bound BCRs.

25 separate localization of both enzymes, as a membrane-bound beta-glucosidase could specifically diges

26 via activation of the ubiquitously expressed membrane-bound beta-receptor glycoprotein 130 (gp130).

27 The diversion of the membrane-bound beta-site amyloid precursor protein-(APP)

28 rgistic interaction that supports a role for membrane-bound BGLC3 in xyloglucan metabolism.

29 onment, but has been difficult to observe in membrane-bound biological systems.

30 anding of their biological functions, intact membrane-bound bitopic protein-protein complexes pose tr

31 tors and their precursors against a panel of membrane-bound CA isoforms, including tumor-overexpresse

32 pro-apoptotic potential between soluble and membrane-bound CD40 agonists.

33 nreplicating adenovirus encoding a chimeric, membrane-bound CD40 ligand (ISF35).

34 RNA granules are non-membrane bound cellular compartments that contain RNA an

35 The full-length, membrane-bound CH120.6 Env is indeed stable and conforma

36 d that its secretion is dependent on CpaB, a membrane-bound chaperone.

37 latory properties by coexpressing CAR with a membrane-bound chimeric IL-15 (mbIL15).

38 hese results suggest that local structure of membrane-bound chiral filaments is generically sensitive

39 Our models for eukaryotic membrane-bound cholesterol sensors are soluble bacterial

40 nd in some cases appears to divide, within a membrane-bound compartment for the entire 6-day time cou

41 racellular pathogens that replicate within a membrane-bound compartment inside infected host cells kn

42 xit via extrusion generates a distinct, host-membrane-bound compartment of Chlamydia separate from th

43 ocytes contain a Balbiani body, a large, non-membrane-bound compartment packed with RNA, mitochondria

44 ess to the host cell cytosol from within its membrane-bound compartment to acquire nutrients.

45 s move proteins and lipids from one internal membrane-bound compartment to another within the secreto

46 ate intracellular pathogen that resides in a membrane-bound compartment, the inclusion.

47 strate that FABP4 secretion is mediated by a membrane-bounded compartment, independent of the convent

48 at promotes maintenance of Mtb within intact membrane-bound compartments for efficient elimination.

49 n-induced transmembrane proteins) located in membrane-bound compartments inside cells.

50 required to build, maintain, and define many membrane-bound compartments is encoded by several paralo

51 Nature encapsulates reactions within membrane-bound compartments, affording sequential and sp

52 ses represent identity markers for different membrane-bound compartments, and each Rab organizes a co

53 nts that mediate degradation of pathogens in membrane-bound compartments, in a process termed xenopha

54 In living cells, reactions take place in membrane-bound compartments, often in response to change

55 ty of bacterial pathogens that reside within membrane-bound compartments.

56 First, accelerated recycling of the membrane-bound complement regulator CD59 to the RPE cell

57 Deficiency in the membrane-bound complement regulators CD55 and CD59 exace

58 However, the stability of the circa 70 kDa membrane-bound complex in model membranes renders high-r

59 ement system, consisting of soluble and cell membrane-bound components of the innate immune system, h

60 l granules contain microbicidal factors, the membrane-bound components of the respiratory burst oxida

61 nventional lipid bilayer model to generate a membrane-bound configuration of Tim1 in silico.

62 hat the existing crystal structure be in the membrane-bound conformation for effective x-ray reflecti

63 ly determined protein crystal structure in a membrane-bound conformation.

64 One highly tumorigenic MI line harbored membrane-bound, constitutively active, truncated EGFR.

65 Chemical analysis of membrane-bound containers such as secretory vesicles, or

66 ch spine morphology also forms a barrier for membrane-bound diffusion has remained unclear.

67 This shape-dependent membrane-bound diffusion in mature spines may contribute

68 other biological confounders further reduce membrane-bound diffusion in these spines.

69 the connection between spine morphology and membrane-bound diffusion through a combination of photoc

70 by co-immunoprecipitation experiments, where membrane-bound dimers were successfully pulled down from

71 ve (Ki67(-) ) cells was inversely related to membrane-bound E-cadherin.

72 Some protein components of intracellular non-membrane-bound entities, such as RNA granules, are known

73 dates, with structures that mimic the native membrane-bound Env spike (gp160).

74 a stabilized, cleaved trimer (SOSIP) or by a membrane-bound Env trimer with a truncated cytoplasmic t

75 tive trimeric form of an efficiently cleaved membrane-bound Env, 4-2.J41, may be beneficial for immun

76 It encodes a membrane-bound envelope protein with fusogenic activity

77 mcr-1 encodes a membrane-bound enzyme catalysing phosphoethanolamine tra

78 MMP-25 (membrane-type 6-MMP) is a membrane-bound enzyme predominantly expressed in leukocy

79 egrin and metalloproteinase 17 (ADAM17) is a membrane-bound enzyme that mediates shedding of many mem

80 embrane recruitment versus activation of the membrane-bound enzyme.

81 iquinone oxidoreductase), one of the largest membrane-bound enzymes in mammalian cells, powers ATP sy

82 iquinone oxidoreductase), one of the largest membrane-bound enzymes in the cell, powers ATP synthesis

83 Ephrin receptors interact with membrane-bound ephrin ligands to regulate contact-mediat

84 ranslational evidence that the ectodomain of membrane-bound ephrin-B2 is shed from fibroblasts into t

85 dual cytoplasmic/membrane localization, and membrane-bound EsaE interacts with the T7SS secretion AT

86 such as an oncoprotein, LMP1, into host cell membrane-bound EVs.

87 rect interaction by association of NM2s with membrane-bound F-actin or peripheral membrane proteins.

88 r by coupling the reoxidation of ETFred to a membrane-bound FeS oxidoreductase functioning as an ETF:

89 NADPH oxidase 1 (NOX1), a membrane-bound flavin dehydrogenase that generates O2(),

90 ed between a translational start codon and a membrane-bound fluorescent protein lacking its start cod

91 gating the conformational dynamics of intact membrane-bound FoF1 during rotational catalysis has prov

92 affinity for narrow mitochondria, acts as a membrane-bound force sensor to recruit the fission machi

93 But in agreement with previous work, the membrane bound form of Cripto-1 potentiated signaling, r

94 IL-15, which was primarily presented in its membrane-bound form by follicular dendritic cells.

95 t-transcriptional expression switch from the membrane-bound form of the immunoglobulin heavy chain to

96 hat is natively unfolded and monomeric and a membrane-bound form that is composed of an alpha-helical

97 otubule destabilization, enhanced the plasma membrane-bound fraction of ARHGAP18.

98 Thylakoid membrane-bound FtsH proteases have a well-characterized

99 Presumably, the thylakoid membrane-bound FtsH5 and FtsH2 have dual functions in th

100 structural and topological investigations of membrane-bound full-length bitopic protein complexes und

101 Targeting the membrane bound GC receptor or the recently discovered in

102 ion of wound healing by interaction with the membrane bound GC receptor, followed by stimulation of b

103 nchoring to the membrane, induces release of membrane-bound glycolytic enzymes and in turn switches g

104 ing to the membrane, enhances the release of membrane-bound glycolytic enzymes to the cytosol, induce

105 Endomucin is a membrane-bound glycoprotein expressed luminally by endot

106 as c2G4 and c4G7 bound to the base region of membrane-bound GP.

107 rocytes were prelabeled by the expression of membrane-bound Green fluorescent protein, we found that

108 with the hypotheses that Nogo receptors are membrane-bound growth cone repellent factors required fo

109 INM targeting, we establish that Atlastins, membrane-bound GTPases of the ER, sustain the efficient

110 stants of GCAP1 and GCAP2 to the full-length membrane-bound guanylate cyclase type 1.

111 Guanylyl cyclase C (GUCY2C), a membrane-bound guanylyl cyclase expressed in intestinal

112 Synergy also requires recruitment to membrane-bound H-Ras, which greatly speeds the formation

113 quence, RBCs that display a cell surface Ag, membrane-bound hen egg lysozyme, strongly activate Ag-sp

114 y, we investigated the involvement of plasma membrane-bound heparan and chondroitin sulfate proteogly

115 the lumen of the endoplasmic reticulum, is a membrane-bound hetero-pentameric complex consisting of G

116 sfer of electrons to oxygen is mediated by a membrane-bound heterodimer, comprising gp91phox and p22p

117 of methyl group oxidation to CO2 as well as membrane-bound heterodisulfide reductase and cytochromes

118 ng BAFF or APRIL multitrimers, IL-12p70, and membrane-bound HIV-1 Env gp140 induced tier 1 and tier 2

119 Studying the shedding of cell membrane-bound hTNF by Adam17, a known Fhl2 interacting

120 ed for MHC class I-related chain A and B and membrane-bound IL-15 in IFN-DC-mediated NK cell activati

121 distinct modes: classical signaling via its membrane-bound IL-6 receptor (IL-6R), and trans-signalin

122 e cytokine IL-6 with similar affinity as the membrane-bound IL-6R.

123 It appears expression of plasma membrane bound immunoglobulin (Ig) molecules that effici

124 To characterize the expression of membrane-bound immunoglobulin G (IgG), a fluorophore-lab

125 accharomyces cerevisiae, inactivation of the membrane-bound IMQC protease Oma1 interferes with oxidat

126 en Anaplasma phagocytophilum develops within membrane-bound inclusions in the host cell cytoplasm.

127 toma overexpressed gene, and BMP and activin membrane-bound inhibitor (BAMBI).

128 is an essential adhesion protein that links membrane-bound integrin and cadherin receptors through t

129 Disruption of these membrane-bound interactions (or encounters) can result i

130 initiated a phase 1 dose-escalation study of membrane-bound interleukin 21 (mbIL21) expanded donor NK

131 mechanism points to a critical role for the membrane-bound intermediate in disease pathogenesis, mak

132 s occur in specialized organelles, requiring membrane-bound intracellular transporters to partition M

133 d to examine the effects of shock waves on a membrane-bound ion channel.

134 teolytically cleaved, resulting in a cleaved membrane-bound isoform (cCDCP1).

135 the fixed and well-defined structure of the membrane-bound K segments suggests that dehydrins have t

136 Recent studies found that membrane-bound K-Ras dimers are important for biological

137 Membrane-bound Klotho acts as a permissive coreceptor fo

138 ase (pvLAAD) belongs to a class of bacterial membrane-bound LAADs mainly express in genus Proteus, Pr

139 Paraoxonase-2 (PON-2) is a membrane-bound lactonase with unique anti-oxidative and

140 lternative inflammatory mechanism, including membrane-bound lymphotoxin-beta receptor (LTbetaR) and C

141 nisms capable of biomineralizing nano-sized, membrane-bound, magnetic iron-rich mineral particles cal

142 east partly due to decreased delivery of the membrane-bound matrix metalloproteinase MMP-14 to the pl

143 recognize senescent cells by the presence of membrane-bound MDA-vimentin, presumably as part of a sen

144 MFN2 encodes mitofusin 2, a membrane-bound mediator of mitochondrial membrane fusion

145 ular silicone oil droplets, singly dispersed membrane-bound melanin granules, glial tissue (1 case),

146 h a nonheme diiron catalytic site; pMMO is a membrane-bound metalloenzyme with a unique tricopper clu

147 on fluorescence microscopy, we show that the membrane-bound metalloproteinase MT1-MMP is enriched not

148 with the ability to image cultured cells and membrane-bound microbeads in twelve independently-focusi

149 d as secreted/soluble antibodies (sIg) or as membrane-bound (mIg) B cell receptors (BCRs) through alt

150 iruses replicate their RNA genomes in novel, membrane-bounded mini-organelles, but the organization o

151 pe 1 matrix metalloproteinase (MT1-MMP) is a membrane-bound MMP that is highly expressed in cells wit

152 FoF1 is a membrane-bound molecular motor that uses proton-motive f

153 phyllobilin hydroxylation is catalyzed by a membrane-bound, molecular oxygen-dependent, and ferredox

154 Many membrane-bound molecules in cells form small clusters.

155 -bound enzyme that mediates shedding of many membrane-bound molecules, thereby regulating multiple ce

156 ormation on the dynamic interactions between membrane-bound molecules.

157 PS II, a membrane-bound multi-subunit pigment protein complex, co

158 acromolecules (e.g., tubulin and actin) as a membrane-bound multimeric complex that favors p35 bindin

159 f many proteins copurifying with Cdk5/p35 in membrane-bound multimeric complexes.

160 measured the diffusion coefficient of single membrane-bound Myo1c molecules by force-relaxation exper

161 experiments, and the ability of ensembles of membrane-bound Myo1c molecules to develop and sustain fo

162 " agent, thrombalexin (TLN), combines a cell-membrane-bound (myristoyl tail) anti-thrombin (hirudin-l

163 ze differential expression pattern of tomato membrane bound NAC transcription factors (SlNACMTFs) dur

164 ze differential expression pattern of tomato membrane bound NAC transcription factors (SlNACMTFs) dur

165 teria that synthesise magnetosomes, magnetic membrane-bound nanoparticles that have a variety of diag

166 human CD34(+) cells contains proangiogenic, membrane-bound nanovesicles called exosomes (CD34Exo).

167 Extracellular vesicles (EVs) are membrane-bound nanovesicles delivered by different cellu

168 The non-membrane-bound nature of the centrosome dictates that pr

169 a phenomenon that gives rise to diverse non-membrane-bound nuclear, cytoplasmic and extracellular co

170 8 C>T variant in the locus that contains the membrane bound O-acyltransferase domain-containing 7 gen

171 to a small, plant-specific subfamily of the membrane bound O-acyltransferases (MBOAT) that acylate d

172 Pneumococcal serotype 33A has two membrane-bound O-acetyltransferase genes, wciG and wcjE

173 rate selectivity exhibited by members of the membrane-bound O-acyl transferase family.

174 Recently, the rs641738 membrane-bound O-acyltransferase domain-containing 7 (MB

175 hematopoietic lineages by targeting Porcn, a membrane-bound O-acyltransferase that is indispensable f

176 Porcupine (PORCN) is a membrane-bound O-acyltransferase that palmitoleates the

177 t the palmitoylation of Wnt3 by Porcupine, a membrane-bound O-acyltransferase, plays a significant ro

178 estigating the interactions of the polytopic membrane-bound oligosaccharyl transferases (OTases) with

179 Membrane-bound OPH was shown to interact with the outer

180 er signals, as well as whether bacteria were membrane bound or cytosolic.

181 dies indicated that HA cleavage is driven by membrane-bound or extracellular serine proteases in the

182 roteolytic activities of more than two dozen membrane-bound or serum proteins.

183 % of global CO2 fixation occurs inside a non-membrane-bound organelle called the pyrenoid, which is f

184 and triacylglycerol (TAG) are stored in the membrane-bound organelle lipid droplet (LD) in essential

185 nd five-way interactions among six different membrane-bound organelles (endoplasmic reticulum, Golgi,

186 ization of the eukaryotic cell into discrete membrane-bound organelles allows for the separation of i

187 components to and from the cell surface and membrane-bound organelles and for changes in cell shape,

188 ghly compartmentalized space containing both membrane-bound organelles and the recently identified no

189 Lysosomes are membrane-bound organelles found in every eukaryotic cell

190 Lysosomes are membrane-bound organelles mainly involved in catabolic p

191 processes can be encapsulated within either membrane-bound organelles or proteinaceous compartments

192 Membrane-bound organelles serve as platforms for the ass

193 actors function to organize, shape, and move membrane-bound organelles, yet they remain poorly define

194 ting at intracellular contact points between membrane-bound organelles.

195 hich segregates distinct nutrient pools into membrane-bound organelles.

196 isible biota coming to rely on intracellular membrane-bound organelles.

197 e existing crystal structures for FVIII, its membrane-bound organization has not been resolved.

198 Although some mucins are membrane bound, our data indicate that MUCL1 is secreted

199 min-specific T cells in rat insulin promoter-membrane-bound ovalbumin transgenic mice after sham or I

200 is able to deliver electrons to a variety of membrane-bound oxidative partners, including the drug-me

201 Dynamic interactions between full-length membrane-bound P450 and its redox partner cytochrome b5

202 Toxoplasma multiplies in a membrane-bound parasitophorous vacuole (PV) that interac

203 of malaria, Plasmodium, replicates inside a membrane-bound parasitophorous vacuole (PV), which shiel

204 These cells bud off membrane-bound particles into the lumen of the gland, lo

205 her withdraw from or extend toward the inner membrane-bound PBP1A through peptidoglycan gaps and henc

206 applied to characterize model membranes and membrane-bound peptides and proteins, giving unique info

207 One can also obtain direct information for membrane-bound peptides or proteins by measuring RDCs us

208 Ectopic expression of a membrane-bound peroxidase allowed us to map synaptic sit

209 creen in zebrafish and identified Cavin-2, a membrane-bound phosphatidylserine-binding protein and cr

210 LPIAT1 is a membrane-bound phospholipid-remodeling enzyme that trans

211 , two possibly involved in biogenesis of the membrane-bound photosynthetic apparatus and one for phos

212 e light harvesting phycobilisome complex and membrane-bound photosystems was observed.

213 ch greatly speeds the formation of a stable, membrane-bound PI3Kalpha complex, modestly slows its off

214 inhibits the specific kinase activity of the membrane-bound PI3Kalpha molecule, but this minor enzyme

215 reveal that the pore assembly proceeds via a membrane-bound prepore intermediate state, typically con

216 Membrane-bound proteases are essential for epidermal int

217 alphaKL is expressed as a membrane-bound protein (mKL) and recognized as the corec

218 ome c oxidase from Thermus thermophilus is a membrane-bound protein complex that couples electron tra

219 e prokaryotes by shuttling electrons between membrane-bound protein complexes acting as electron acce

220 to obtain valuable structural information on membrane-bound protein complexes.

221 Although the membrane-bound protein EIN2 is critical for ethylene sig

222 that activation of the p120 form of Nrf1, a membrane-bound protein in the endoplasmic reticulum (ER)

223 to understand how bryostatin interacts with membrane-bound protein kinase C, offering insights for t

224 , and those aspects of Gag assembly into the membrane-bound protein lattice that are determined by MA

225 id bilayers is extended by the presence of a membrane-bound protein, up to around 10 A above that pro

226 omains act in concert to condense Gag into a membrane-bounded protein lattice that recruits genomic R

227 ically from the confined microenvironment of membrane bound proteins in adhesion zones.

228 th, and efficient association of soluble and membrane bound proteins.

229 e approach to solubilizing and administering membrane-bound proteins for future vaccine development.

230 specific water-protein chemical exchange in membrane-bound proteins in solid-state MAS NMR.

231 rane suppresses synthesis of the secreted or membrane-bound proteins including a number of oncogenes,

232 Water-protein chemical exchange in membrane-bound proteins is an important parameter for un

233 Numerous membrane-bound proteins undergo regulated intramembrane

234 As Stresses are perceived and transmitted by membrane-bound proteins, functional characterization of

235 racting proteins of which one-half comprised membrane-bound proteins, localized to the plasma membran

236 t of protein structure-steric pressure among membrane-bound proteins.

237 on modulate the complete energy landscape of membrane-bound proteins.

238 polysaccharides components of extracellular membrane-bound proteoglycans, namely aggregation factors

239 ting antennae, accelerating proton uptake by membrane-bound proton transporters.

240 The membrane-bound psoriasis-associated atypical chemokine r

241 the strategy to measure drug engagement of a membrane bound receptor (CD40) that is critical to immun

242 receptors (GPCRs) are the largest family of membrane-bound receptors and constitute about 50% of all

243 ults from sensing environmental cues through membrane-bound receptors and related intracellular signa

244 CD59 is a membrane-bound regulatory protein that inhibits the asse

245 n chlamydial pathogens form an intracellular membrane-bound replicative niche termed the inclusion, w

246 ing this approach, we discovered that plasma membrane-bound respiratory syncytial virus G rapidly rec

247 doplasmic reticulum and Golgi apparatus from membrane-bound ribosomes were not translocated to the ro

248 emble the requirements of PAO, we considered membrane-bound Rieske-type oxygenases as potential candi

249 Stress granules are non-membrane bound RNA-protein (RNP) assemblies that form wh

250 P granules are non-membrane-bound RNA-protein compartments that are involve

251 data demonstrate a cellular pathway whereby membrane-bound scavenger receptor type B-1 (SR-B1) in pa

252 Fibroblast Activation Protein (FAP) is a membrane-bound serine protease whose expression is often

253 oding approximately 100 million secreted and membrane-bound single-chain antibodies and identify anti

254 K-Ras4B is a membrane-bound small GTPase with a prominent role in can

255 ical relevance, the structural nature of the membrane-bound state alphaS remains elusive, in part bec

256 the regulation of EHD2 oligomerization in a membrane-bound state is crucial to restrict caveolae dyn

257 r the biological properties of alphaS in its membrane-bound state.

258 be the inner workings of FoF1 in its natural membrane-bound state.

259 ture and peroxidase activity of cyt-c in its membrane-bound state.

260 tein Nervous Wreck (Nwk) in both soluble and membrane-bound states.

261 human pigment synthesis are mediated by the membrane-bound, steroid hormone receptors G protein-coup

262 ized, to our knowledge for the first time, a membrane-bound stilbenoid-specific prenyltransferase act

263 an diseases, implies the formation of double-membrane-bound structures called autophagosomes (AP), wh

264 Here we report that these membrane-bound structures derive from mitophagosomes.

265 -liquid phase separation and liquid-like non-membrane-bound structures in cells.

266 of the hairpin nature of NRG1 type III, two membrane-bound stubs with a type 1 and a type 2 orientat

267 located in the cytosolic subunit A or in the membrane-bound subunit B.

268 ere, we use NMR spectroscopy to identify the membrane-bound surface of the S4S5 linker, and we show t

269 -glucan and chitin, which are synthesized by membrane-bound synthases at the growing cell tip.

270 duces regulatory T cells that express latent membrane-bound TGF-beta (latency-associated peptide [LAP

271 Depletion of mdbA, which encodes a membrane-bound thiol-disulfide oxidoreductase, abrogates

272 (FVIIa), a trypsin-like serine protease, and membrane-bound tissue factor (TF) initiates blood coagul

273 Detection of membrane-bound TLN was confirmed by immunohistochemistry

274 shedding of TNF type I receptor (TNFR1), the membrane-bound TNFR1 C-terminal fragment is subsequently

275 The membrane-bound transcription factor ATF6alpha is activat

276 The membrane-bound transcription factor ATF6alpha plays a cy

277 esponse element-binding protein 3-like 1), a membrane-bound transcription factor that blocks cell div

278 Here we utilize amber codon suppression in a membrane-bound transporter protein to encode photocrossl

279 Its uptake into the cell is mediated by membrane-bound transporters and coupled to Na(+) transpo

280 Membrane-bound transporters are known to be relevant, bu

281 Membrane-bound transporters extrude acid from cancer cel

282 viously reported that, upon irradiation, the membrane-bound tyrosine kinase receptor TIE2 translocate

283 ellular Chlamydia trachomatis replicate in a membrane-bound vacuole called inclusion, which serves as

284 [ACSL1 and ACSL3-6] translocates into the Ct membrane-bound vacuole, termed inclusion, and remains as

285 ation assays, we found that HPV resides in a membrane-bound vesicle until mitosis is completed and th

286 Extracellular vesicles (EVs) are membrane-bound vesicles and cell-cell EV communication i

287 In nodule cells, bacteria are enclosed in membrane-bound vesicles called symbiosomes and different

288 cellular vesicles (EVs) are nanometer-sized, membrane-bound vesicles released by cells into the extra

289 Exosomes are nano-sized, membrane-bound vesicles released from cells that transpo

290 Microvesicles are membrane-bound vesicles released from the cell surface a

291 doplasmic reticulum and actively exported in membrane-bound vesicles that are formed by the cytosolic

292 Artificial membrane-bound vesicles, known as liposomes, are versati

293 pport for the transient existence of nuclear membrane-bound vesicles.

294 al positive-strand RNA viruses, replicate in membrane-bound viral replicase complexes in the cytoplas

295 viral factors affecting the formation of the membrane-bound viral replication complex is a major fron

296 ment, encoding a transmembrane protein and a membrane-bound VirB4/HerA homolog, respectively.

297 dle stress, and to control the expression of membrane bound virulence factors.

298 ation of biological processes into discrete, membrane-bound volumes, is essential for cellular life.

299 rt (88% +/- 1%) of the antagonist uptake was membrane-bound, whereas 74% +/- 3% of the total receptor

300 TEMENT In this study, we identify MT3-MMP, a membrane-bound zinc protease, to be necessary for the de