ライフサイエンスコーパス: membrane-bound

1 ntain sub-cellular compartments that are not membrane bound.

2 ARE assembly, even if none of the SNAREs are membrane bound.

3 increased in vitro specific accumulation of membrane-bound (89)Zr-labeled pertuzumab.

4 ary spastic paraplegia protein M1 Spastin, a membrane-bound AAA ATPase found on LDs, coordinates fatt

5 The mitochondrial membrane-bound AAA protein Bcs1 translocate substrates a

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

7 ession or mutations in the digestive vacuole membrane-bound ABC transporter PfMDR1 (P. falciparum mul

8 ssenger RNA levels were the highest of all 9 membrane-bound AC isoforms in mouse intestinal epithelia

9 imulations of the glycosylated, full-length, membrane-bound ACE2 receptor in both an apo and spike RB

10 s proteolytically cleaved, and acylated by a membrane-bound acyl transferase (MBOAT).

11 Membrane-bound adenylyl cyclase (AC) isoforms have disti

12 ciliary enrichment, most probes were weakly membrane bound and diffused through the connecting ciliu

13 eless, Rab29 only activates LRRK2 when it is membrane bound and GTP bound.

14 hieved in eukaryotic cells by utilizing both membrane-bound and membrane-less organelles.

15 gest that the relative mass densities across membrane-bound and membraneless compartments are robustl

16 The coordinated actions of membrane-bound and membraneless organelles ensure spatio

17 zation, as well as the emergence of distinct membrane-bound and membraneless organelles.

18 Glycans attached to lipids and membrane-bound and secreted proteins and peptides mediat

19 ntify experimental conditions that stabilize membrane-bound and shedding-resistant virus Env trimers

20 at CopL from the S. aureus clone USA300 is a membrane-bound and surface-exposed lipoprotein that bind

21 Four membrane-bound and three soluble HLA-G protein isoforms

22 These cytoplasmic viral factories are not membrane bound, and they serve to concentrate the viral

23 Most PSDs are membrane-bound, and classical radioisotope-based assays

24 for B cell responses to spatially restricted membrane-bound antigens, but not for soluble antigens, h

25 characterize antibody binding to soluble and membrane-bound antigens.

26 te (ATP) synthase in human mitochondria is a membrane bound assembly of 29 proteins of 18 kinds organ

27 g T7SS effectors EsxC, EsxA and EsxB, or the membrane-bound ATPase EssC, compared to the wild-type (W

28 autophagy receptors, which link cargo to the membrane-bound autophagosomal ubiquitin-like protein Atg

29 athogen Chlamydia trachomatis, grow within a membrane-bound bacterium-containing vacuole (BCV).

30 Mitochondrial membrane-bound Bax intensity significantly decreased in

31 ication of autoreactive B cells requires the membrane-bound BCR, as the soluble Ab may largely differ

32 d assay to investigate the autoreactivity of membrane-bound BCRs derived from different B cell develo

33 oy in vitro-generated Abs, which differ from membrane-bound BCRs.

34 Indeed, aPLs prefer membrane-bound beta(2)GPI to that in solution.

35 -xylosidase, beta-galactosidase, soluble and membrane-bound beta-glucosidases and two alpha-fucosidas

36 Exosomes are endocytic lipid-membrane bound bodies with the potential to be used as b

37 Cells possess non-membrane-bound bodies, many of which are now understood

38 Also, we removed together the enzyme's membrane bound c(8) ring and the delta-subunit from the

39 The resulting 120 kDa membrane-bound C-terminal fragment (CTF) of LDLR had red

40 ation in the TGN increases the levels of the membrane-bound C-terminal fragments of APP from both alp

41 compounds that displayed selectivity against membrane-bound CA IV.

42 (CA IX), and the cytosolic CA I, CA II, and membrane-bound CA IV.

43 accine target, a multifunctional enzyme or a membrane-bound cancer target.

44 This layer of membrane-bound, carbohydrate-rich molecules covers the l

45 the necessity of NL docking for transport of membrane-bound cargo in cells has not been tested.

46 argo enrichment into a constrained spherical membrane-bound carrier.

47 To date, the consequences of membrane-bound CD40L (mCD40L) on its immune-stimulatory

48 table associations with detergent-insoluble, membrane-bound cellular fractions.

49 Mitochondria is a double membrane-bound cellular organelle that generates energy

50 ts of the Bam and Sec machineries, including membrane-bound chaperones YfgM and PpiD.

51 e insulin signaling pathway, by a cytosolic, membrane-bound chimera between the AP20187-inducible F(V

52 uctures of human membrane-bound CHMP1B-only, membrane-bound CHMP1B + IST1, and IST1-only filaments by

53 membranes, we determined structures of human membrane-bound CHMP1B-only, membrane-bound CHMP1B + IST1

54 ous reports, we found Kv2.1 is trafficked to membrane-bound clusters observed both in vivo and in vit

55 Betaglycan (BG) is a membrane-bound co-receptor of the TGF-beta family that s

56 Phagocytes engulf pathogens into a membrane bound compartment called a phagosome, but what

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

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

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

60 s, chaperones and metabolic enzymes from non-membrane bound compartments.

61 th parallel actin bundles on which different membrane-bound compartments and mitochondria appear to t

62 tracellular vesicles (EVs), which are mobile membrane-bound compartments that participate in intercel

63 ochemical interactions between CAs and other membrane-bound compartments, for example aquaporins, are

64 CD55) is an efficient membrane bound complement regulator that inhibits both c

65 hese results suggest that soluble domains of membrane-bound complement inhibitors are potential candi

66 direct interaction of sphingolipid with the membrane-bound components of the SPT-regulatory apparatu

67 ted solid-state NMR experiments to probe the membrane-bound conformation and topology of the protein.

68 d crystalized conformation to a more native, membrane-bound conformation in silico.

69 pLGIC from its crystalized conformation to a membrane-bound conformation.

70 f oligomeric intermediates, sampling various membrane-bound conformational states of the protein, and

71 simulations capture the influence of various membrane-bound conformational states on the lipid and ch

72 reveal that alpha-syn adopts a multitude of membrane-bound conformations, which were not recapitulat

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

74 nding of the IgG1 format to cells expressing membrane-bound CoV-2 spike protein.

75 results in enhanced epithelial production of membrane-bound CSF1, a cytokine that promotes resident m

76 okine, CX3CL1 (fractalkine), is cleaved from membrane-bound CX3CL1 by proteases including CTSS.

77 n to replicate and package them in isolated, membrane-bound, cytoplasmic complexes, whereas the bacte

78 We found that the membrane-bound cytosolic peptides of FtsN and FtsQ co-mi

79 The resulting model of the membrane-bound Dfg5*GPI-CWP complex is validated by mole

80 trong resistance to both soluble DNase I and membrane-bound DNase on cells.

81 fter cleavage furrow closure, septins form a membrane-bound double ring that controls the organizatio

82 rface-contact interactions between different membrane-bounded droplets to transfer and co-locate disc

83 ve size and what are the dynamic features of membrane-bound Dvl complexes during Wnt pathway activati

84 to an increase in the total concentration of membrane-bound Dvl2 from 0.12/mum(2) to 0.54/mum(2) Wnt3

85 We found that membrane-bound Dvl2 is predominantly monomer in the abse

86 embrane-associated RING-CH (MARCH) family of membrane-bound E3 ubiquitin ligases regulates the levels

87 atic reactions, either by soluble enzymes or membrane-bound ectoenzymes, and uptake or clearance are

88 lectrons from the carbonyl of acetate to the membrane-bound electron transport chain that generates i

89 any oxidoreductases, including components of membrane-bound electron-transfer chains in living organi

90 However, both membrane-bound Env proteins on the surface of intact vir

91 ccinate dehydrogenase (SDH), a mitochondrial membrane-bound enzyme complex that is involved in both t

92 n of HA by myeloid cells was mediated by the membrane-bound enzyme hyaluronidase 2 (Hyal2).

93 , known as the "Na(+) pump," is a ubiquitous membrane-bound enzyme responsible for generating and mai

94 The Na(+)/K(+)-ATPase (NKA) is a ubiquitous membrane-bound enzyme responsible for generating and mai

95 to encode an important but poorly understood membrane-bound enzyme termed formate hydrogenlyase-2 (FH

96 cylglycerol kinase epsilon (DGKepsilon) is a membrane-bound enzyme that catalyzes the ATP-dependent p

97 glycosphingolipid formation is catalyzed by membrane-bound enzymes along the secretory pathway, degr

98 However, our knowledge regarding these membrane-bound enzymes has been greatly impeded by the l

99 Phospholipid synthesis is catalyzed by membrane-bound enzymes, which themselves require pre-exi

100 ed whether the loss or overexpression of the membrane-bound ephrin-B1 in astrocytes during postnatal

101 d proteins and microvesicles, and expressing membrane-bound factors.

102 Membrane-bound FasL, expressed by CD4(+) T cells, activa

103 croglia, likely due to reduced expression of membrane-bound Fcgamma receptors.

104 e basal body, and transitions to a canonical membrane-bound flagellum at the 'flagellar pore'.

105 enchymal stromal cells engineered to express membrane-bound FLT3L and stem cell factor (SCF) together

106 hough function depends on the proteins being membrane bound, for experimental reasons, most of the st

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

108 Although the function of its predominant membrane-bound form is well established, the source and

109 es was associated with the expression of the membrane-bound form of the CD40L by CD4(+) T cells in ly

110 In the active, membrane-bound form, the AI helices are displaced and en

111 ne of proteins to sort them into soluble and membrane-bound fractions.

112 pontaneous orientation of the SNARE motif of membrane-bound, full-length syntaxin1A with respect to t

113 A characterization of membrane-bound Gaussia luciferase (mbGluc) revealed that

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

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

116 ltransferase B (EmbB) belongs to a family of membrane-bound glycosyltransferases that build the lipid

117 ellular function that is further enhanced by membrane-bound GPBP-3 in mammalians, whereas GPBP-2 reta

118 ere found to be the natural ligands for cell membrane-bound guanylyl cyclase receptors that mediate t

119 he mIg is a symmetric complex of 2 identical membrane-bound heavy chains (mHC) and 2 identical light

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

121 The membrane-bound histidine sensor kinase, CpxA, is a bacte

122 nt structural data from an ancient relative, membrane-bound hydrogenase, cryo-EM on mammalian complex

123 ABHD12 is a membrane-bound hydrolytic enzyme that acts on the lysoph

124 Our results identify C3H as the only non-membrane bound hydroxylase in the lignin pathway and rev

125 arse-grained model that demonstrates similar membrane-bound I-BAR domain aggregation behavior as our

126 tional membrane-mediated interaction between membrane-bound I-BAR domains.

127 B cell antigen receptor (BCR) comprising the membrane-bound Ig (mIg) molecule and the Igalpha/Igbeta

128 ell line termed 'NKF' through overexpressing membrane bound IL-21 that is capable of inducing robust

129 Mechanistic studies revealed that membrane-bound IL-21 leads to an activation of a STAT3/c

130 s also provide mechanistic insights into how membrane-bound IL-21 regulates NK cell expansion.

131 tion of ADAM proteases, IL-6 in complex with membrane-bound IL-6R and gp130 activates classic signali

132 assic signaling by genetic conversion of all membrane-bound IL-6R into sIL-6R proteins phenocopying h

133 pattern and specifically bind and activate a membrane-bound immune receptor of tomato, the Cuscuta Re

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

135 atomically detailed structural ensemble of a membrane-bound intrinsically disordered protein.

136 Proton transfer through membrane-bound ion channels is mediated by both water an

137 th cases, a "respiratory shield" composed of membrane-bound iron-rich respiratory complexes may prote

138 ide myeloid cell activation via a trimerized membrane-bound isoleucine zipper (TMZ) CD40L.

139 haracterize the orientational preferences of membrane-bound K-Ras4B in 1.45-ms aggregate time of atom

140 the specific activity (turnover rate) of the membrane-bound kinase molecule.

141 tochastic fluctuations in the copy number of membrane-bound kinases and phosphatases.

142 le measurements and measured a 2D k (on) for membrane-bound kinesin-1 motors binding to the microtubu

143 oxide (H(2)O(2)) and increased expression of membrane-bound leukocyte adhesion molecule CD11b, leadin

144 Trans-interaction between EphB4 and its membrane-bound ligand ephrin B2 (EFNB2) mediates bi-dire

145 mpiling an extensive database of soluble and membrane-bound ligand-receptor interactions, we develope

146 Membrane-bound ligands for stimulation and co-stimulatio

147 aematopoietic growth factors, chemokines and membrane-bound ligands.

148 The formation of p62 non-membrane-bound liquid compartments is critical for its f

149 The membrane-bound, long form of MGAT4D, termed MGAT4D-L, in

150 gnetotactic bacteria (MTB), which synthesize membrane-bounded magnetic nanocrystals called magnetosom

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

152 the ability of nTDMS to characterize complex membrane-bound metalloenzymes.

153 Meprin beta is a membrane-bound metalloprotease involved in extracellular

154 These non-membrane-bound microcompartments exclude ribosomes and c

155 tosolic cycling of MinE and recombination of membrane-bound MinE, and that these differ in their in v

156 ids in the N-terminal domain of RsbR and the membrane-bound mini-protein Prli42 is essential for List

157 Membrane-bound mitochondrial trifunctional protein (TFP)

158 s modulate hematopoiesis through soluble and membrane bound molecules.

159 Membrane-bound mucins belong to a heterogeneous family o

160 eted protein named SmEnhancin, which digests membrane-bound mucins on the mosquito gut epithelia, the

161 conserved domains indicated that the studied membrane-bound mucins share common biological properties

162 Bacillus subtilis PdaC (BsPdaC) is a membrane-bound, multidomain peptidoglycan N-deacetylase

163 Notably, the optimized MORF3 mice, with a membrane-bound multivalent immunoreporter, confer Cre-de

164 se ADAM10 and lysosomal degradation generate membrane-bound N-terminal fragments (NTFs), which we ide

165 Na(+) /H(+) exchangers (NHEs) are ancient membrane-bound nanomachines that work to regulate intrac

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

167 xidation and lipophilic quinone reduction by membrane-bound NDH-2 followed the Michaelis-Menten model

168 nhibitors, were tested, they did not inhibit membrane-bound NDH-2.

169 assay for distinguishing between soluble and membrane-bound NE proteins.

170 a prototypical ternary system modeled after membrane-bound nephrin, the adaptor Nck1, and the actin

171 Membrane-bound NG2 is found to colocalize with pericellu

172 rvous system, but the mechanism by which the membrane-bound Nogo-A is presented intercellularly is no

173 aling is activated upon interactions between membrane-bound Notch receptors (Notch 1-4) and ligands (

174 transcriptional activation occurring in non-membrane bound nuclear compartments.

175 The size of the membrane-bound nucleus scales with cell size in a wide r

176 phospholipase domain containing 3), MBOAT7 (membrane bound O-acyltransferase domain containing 7), T

177 tic variant rs641738 near two genes encoding membrane bound O-acyltransferase domain-containing 7 (MB

178 As members of the membrane-bound O-acyltransferase (MBOAT) enzyme family,

179 ture of dimeric human DGAT1, a member of the membrane-bound O-acyltransferase (MBOAT) family, by cryo

180 lti-transmembrane enzyme that belongs to the membrane-bound O-acyltransferase (MBOAT) family.

181 DGAT1 belongs to the membrane-bound O-acyltransferase (MBOAT) superfamily, me

182 t the first structural model of a eukaryotic membrane-bound O-acyltransferase (MBOAT), ghrelin O-acyl

183 ing 3, transmembrane 6 superfamily member 2, membrane-bound O-acyltransferase domain containing 7, gl

184 ansmembrane 6 superfamily member 2 (TM6SF2), membrane-bound O-acyltransferase domain-containing (MBOA

185 as a key regulator of size and morphology of membrane-bound oligomers.

186 Membrane-bound oligosaccharides form the interfacial bou

187 Membrane-bound oligosaccharides with specific chemistrie

188 Proteoglycans can be cell membrane-bound or are part of the extracellular matrix.

189 lular components into organelles that can be membrane-bound or membraneless.

190 , including Chlamydia, establish a parasitic membrane-bound organelle inside the host cell that is es

191 The Golgi apparatus is a membrane-bound organelle that serves as the center for t

192 een the endoplasmic reticulum (ER) and other membrane-bound organelles allow for efficient transfer o

193 d bacterial infection, is executed by double-membrane-bound organelles called autophagosomes.

194 In eukaryotic cells, various membrane-bound organelles compartmentalize diverse cellu

195 swelling of cells converts the ER and other membrane-bound organelles into micrometer-scale large in

196 olling the self-organisation and dynamics of membrane-bound organelles such as the Golgi apparatus, r

197 Ribonucleoprotein (RNP) granules are non-membrane-bound organelles that have critical roles in th

198 ithin nuclear speckles (specific type of non-membrane-bound organelles).

199 and transport of membraneless condensates on membrane-bound organelles.

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

201 evelopment, the parasite replicates within a membrane-bound parasitophorous vacuole.

202 Extracellular vesicles (EVs) are small, membrane-bound particles released by all cells that have

203 TLRs, a family of membrane-bound pattern recognition receptors found on in

204 -timescale molecular dynamics simulations of membrane-bound PH-TH modules and observed that they dime

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

206 Membrane-bound plasmin is used by immune cells to degrad

207 AlgC-like membrane-bound PMMs appear to comprise yet another envir

208 te (Cu(B)) and one ~2 nanometers away in the membrane-bound PmoC subunit (Cu(C)).

209 cervate micro-droplets are reconfigured into membrane-bounded polyoxometalate coacervate vesicles (PC

210 -induced myokine released on cleavage of the membrane-bound precursor protein fibronectin type III do

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

212 nd CDKN2A/B, as well as gain of PTK6 and the membrane-bound progesterone receptor, PAQR8.

213 eral parasite surface proteins are shed by a membrane-bound protease called SUB2.

214 ease, a form of NCL with a deficiency in the membrane-bound protein CLN6.

215 microscopy (cryo-EM) structure of this large membrane-bound protein complex, we report an atomistic m

216 DSG3 is membrane-bound protein in HNSCC cells of invaded lymph n

217 captured based on antibody recognition of a membrane-bound protein marker that confers beta-lactam a

218 S (Regulator of Chromosome Segregation) is a membrane-bound protein that interacts with both DNA and

219 enomics approach, we have identified a small membrane-bound protein that we have called MspA.

220 otein family important for the regulation of membrane-bound protein trafficking.

221 e down-regulation of Ezrin, an actin-binding membrane-bound protein, which we found was critically in

222 A large fraction of soluble and membrane-bound proteins exists as non-covalent dimers, t

223 The function of membrane-bound proteins often depends on their interacti

224 G protein-coupled receptors (GPCRs) are membrane-bound proteins that depend on their lipid envir

225 Membrane-bound proteins, particularly ion channels and G

226 fluctuation signal for luminal, but not for membrane-bound, proteins.

227 Ligases and membrane-bound pyrophosphatases make pyrophosphate neede

228 Mon1-Ccz1 is an effector of Rab5, (ii) that membrane-bound Rab5 is the key factor to directly promot

229 Recent investigations implicate membrane-bound RAS dimers, oligomers, and nanoclusters a

230 acting on all three complement pathways as a membrane-bound receptor of C3b/C4b, C3/C5 convertase dec

231 ts of BMPs are mediated through binding with membrane bound receptors like BMPR-IB and initiating dow

232 chondrial NADH:ubiquinone oxidoreductase), a membrane-bound redox-driven proton pump, is one of the l

233 ction partners together within separated non-membrane-bound regions.

234 Finally, we demonstrate that fusion to the membrane-bound replication complex components permits ef

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

236 Our results reveal how a membrane-bound retrotranslocase cooperates with the Cdc4

237 and UFMylated RPL26 is highly enriched on ER membrane-bound ribosomes and polysomes.

238 t control global proteome composition via ER membrane-bound ribosomes.

239 Stress granules (SGs) are non-membrane-bound RNA-protein granules that assemble throug

240 The highly conserved membrane-bound rubredoxin-like protein RubA has previous

241 peptides and are exported through the inner-membrane-bound Sec machinery to the periplasm, followed

242 by altering its architecture and stabilizing membrane-bound Sec18 protomers.

243 s how actin and myosin organize around large membrane-bound secretory vesicles and generate the force

244 A), periplasmic nitrate reductase (napA) and membrane-bound selenate reductase (srdA) respectively.

245 he Gram-negative bacterium Escherichia coli, membrane-bound sensor CusS and its response regulator Cu

246 smembrane (TM) signaling is a key process of membrane-bound sensor kinases.

247 HH-producing cells signal at short range via membrane-bound SHH, only to receiving cells with primary

248 lls, where they reside in the cytoplasm as a membrane-bound signaling structure that we have named th

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

250 S. aureus produce membrane-bound, spherical, nano-sized, MVs packaged with

251 nformational dynamics of the soluble and the membrane-bound ST2 (sST2 and ST2).

252 Plasma levels of soluble membrane-bound ST2 (ST2) are elevated in human and murin

253 our data provide structural details of a key membrane bound state of FAK that is primed for efficient

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

255 ormational and topological properties of the membrane-bound state of alphaS, despite increasing its p

256 Defining the membrane-bound state of KRAS is fundamental to understan

257 ng I-soluble quencher in solution and in the membrane-bound state.

258 oop region, Syt1 adopts a dynamic, partially membrane-bound state.

259 luorescence quenching in solution and in the membrane-bound state.

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

261 egions of the cell and can condense into non-membrane-bound structures such as stress granules.

262 Extracellular vesicles (EV) are nanoscale membrane-bound structures that contain biological conten

263 t eliminated DNA is incorporated into double membrane-bound structures, similar to micronuclei, durin

264 ss zones revealed clusters of virions within membrane-bound structures, which we term membranous carr

265 intramembranous hydrolysis of more than 100 membrane-bound substrates.

266 unctions as a melanosome-associated protein, membrane-bound surface receptor, soluble ligand, or adhe

267 After the conversion of the resulting membrane-bound systems to full-membrane representations,

268 embranes recruit and activate talin, and the membrane-bound talin then activates vinculin.

269 ere, heterologous expression of both SOR and membrane-bound thiosulphate-quinone oxidoreductase (TQO)

270 In mHTT-expressing cell lines, membrane-bound TIM23-imported proteins have lower intram

271 Membrane-bound TIMP-1 is the PMN receptor for pro- and a

272 pro-Mmp-9 are required for their binding to membrane-bound Timp-1 on murine PMNs.

273 y anchoring MMP-8 and MMP-9 to PMN surfaces, membrane-bound TIMP-1 plays a counterintuitive role in p

274 Myrf is a membrane-bound transcription factor that plays a key rol

275 egulatory element-binding proteins (SREBPs), membrane-bound transcription factors whose proteolytic a

276 Here, I review recent insights into RIP of membrane-bound transcription factors, focusing on CREB3L

277 2P) is involved in proteolytic activation of membrane-bound transcription factors.

278 soluble chimeric gp140 SOSIP (ch.SOSIP) and membrane-bound trimers with intact transmembrane domain

279 pre-CD4-triggered state of both soluble and membrane-bound trimers.

280 ctivity is alleviated by coproduction of the membrane-bound TsaI immunity protein, which is encoded a

281 ity of A-subunit protein, which is shed from membrane bound TSHR, expressed at low levels in the thyr

282 E), which is responsible for the cleavage of membrane-bound tumor necrosis factor-alpha (TNF-alpha) a

283 releasing peripheral V(1) subcomplexes from membrane-bound V(o) subcomplexes.

284 f the bacteria are initially taken up into a membrane bound vacuole, the Salmonella-containing vacuol

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

286 s and autophagosomes in that they are single-membrane bound vacuoles formed by projection, ruffling,

287 . australis and Rickettsia-containing double-membrane-bound vacuoles in the BMMs of B6 mice.

288 zed with PLD1-hemagglutinin on intracellular membrane-bound vesicles and with PLD2-hemagglutinin at t

289 Tethered neutrophils enter in membrane-bound vesicles before penetrating into the mega

290 EVs are small membrane-bound vesicles capable of delivering biomolecul

291 Exosomes, small membrane-bound vesicles that carry a complex cargo (DNA,

292 o two tiers and contains an ordered array of membrane-bound vesicles with sub-wavelength diameters of

293 to mimic organelle functions using lamellar membrane-bound vesicles.

294 mune functions) to or from the PM via small, membrane-bound vesicles.

295 morphogen gradients produces a diversity of membrane-bounded vesicles that are spontaneously segrega

296 trand RNA [(+)RNA] viruses assemble numerous membrane-bound viral replicase complexes (VRCs) with the

297 plication, which occurs at poorly understood membrane-bound viral RNA replication complexes.

298 edicted in ten classes (Q10 = 68% +/- 1) and membrane-bound were distinguished from water-soluble pro

299 oving that Brachypodium also has soluble and membrane-bound xyloglucan glucosidases.

300 Membrane-bound Ypt7 activates HOPS to catalyze 4-SNARE c