ライフサイエンスコーパス: membrane-associated

1 ted cells; 63% of these were predicted to be membrane associated.

2 that BB0345 was intracellular and partially membrane associated.

3 ating T cells at single-molecule levels when membrane-associated.

4 involvement of betaPFOs and, more generally, membrane-associated Abeta oligomers in AD.

5 Plasma membrane-associated abscisic acid (ABA) signal transduct

6 fted gene in the VP1 region that expresses a membrane-associated accessory protein that limits AAV pr

7 a-Syn PFF cell entry by maintaining a plasma membrane-associated actin network that controls membrane

8 Membrane-associated actin regulation factors, such as my

9 onsists of a fluid lipid bilayer coupled via membrane-associated actin-binding proteins to dynamic ac

10 he axon to show that the recently discovered membrane-associated actin-spectrin scaffold plays a prom

11 PatA is an essential membrane associated acyltransferase involved in the bios

12 ntermediate, suggesting a mechanism by which membrane-associated aggregation may be propagated.

13 the presence of the highly expressed plasma membrane-associated ALP, DNA-lipid-P is converted to lip

14 DPW3 encodes a novel membrane-associated alpha integrin-like protein conserve

15 Sucrase-isomaltase (SI) is an intestinal membrane-associated alpha-glucosidase that breaks down d

16 ment of A53T-SNCA mice with GZ667161 reduced membrane-associated alpha-synuclein in the CNS and ameli

17 Here, we reveal that the membrane-associated amyloid precursor protein (APP) is h

18 zation mechanisms, with the enzyme remaining membrane-associated and able to support sustained downst

19 we show that Bax retrotranslocation shuttles membrane-associated and membrane-integral Bax from isola

20 ternative clearance pathways including Golgi membrane-associated and nucleophagy-based LaminB1 degrad

21 ial study of neurolastin revealed that it is membrane-associated and partially co-localizes with endo

22 Analysis of membrane-associated and raft microdomain proteins reinfo

23 Nonstructural protein 1 (NS1) is a membrane-associated and secreted glycoprotein that funct

24 High-resolution analysis of membrane-associated and soluble ribosome footprints reve

25 UNC-119 protein provides a link between the membrane-associated Ankyrin (UNC-44) and the microtubule

26 For the first time, down-regulation of membrane-associated antigen following mAb treatment was

27 Upon stimulation with membrane-associated antigen, CD23 KO causes significant

28 naling reactions and enhances the ability of membrane-associated antigens to induce transcriptional r

29 Among them, the plasma membrane-associated Arabidopsis proteins OCTOPUS (OPS) a

30 d that LPS treatment augmented the levels of membrane-associated Arl8b, a lysosomal GTPase required f

31 ing processes in the presence and absence of membrane associated Atg17.

32 We present a 1-MDa, membrane-associated, Bam[(BC)(2)DEFGHI](2) complex from

33 ASL intracellular dynamics and show that the membrane-associated BASL is slowly replenished at the co

34 The conserved ER membrane-associated BAX inhibitor 1 (BI1) modulates ER s

35 Membrane-associated BBA57 lipoprotein was solubilized by

36 apid, multiplexed detection and screening of membrane-associated biological targets.

37 The outer membrane-associated BoMan26B initially acts on the polys

38 F-deficient mice and those that express only membrane-associated but not secreted TNF revealed that C

39 interaction of the channel with a peripheral membrane-associated Ca(2+)-binding protein, likely ANXA1

40 These data identify annexins as mediators of membrane-associated Ca2+ release during membrane repair

41 Annexins are a family of membrane-associated Ca2+-binding proteins implicated in

42 ng, in part through the activation of plasma membrane-associated calcium release-activated channels.

43 Unexpectedly, neither the presence of membrane-associated cargo nor accessory factors substant

44 brane fusion process by which the soluble or membrane-associated cargoes of a secretory vesicle are d

45 nactivating a small percentage of protective membrane associated catalase molecules on tumor cells.

46 and H(2)O(2.) (1)O(2) then inactivates some membrane-associated catalase molecules on at least a few

47 ow efficiency as local inactivation of a few membrane-associated catalase molecules.

48 other mouse models, the levels of the plasma membrane-associated caveolar coat proteins caveolin3 and

49 -like nanoparticles that present clusters of membrane-associated CD4 (CD4-VLPs) to permit high-avidit

50 components is fundamental for understanding membrane-associated cellular processes.

51 Indy (mIndy, Slc13a5) encoding for a plasma membrane-associated citrate transporter expressed highly

52 Together they form a periodic membrane-associated complex that anchors axonal and dend

53 lakin that tethers intermediate filaments to membrane-associated complexes.

54 43 had a half-life that was 50% shorter than membrane-associated Cx43.

55 ealing that IQCJ-SCHIP1 contributes to nodal membrane-associated cytoskeleton organization, likely th

56 Whereas outer mitochondrial membrane-associated degradation is typically associated

57 rein, we report a network that responds to a membrane-associated dimeric protein with the uncaging of

58 further demonstrate that in the presence of membrane-associated, disease-causing prion protein (Ctm)

59 e cell, with the CTC mediating attachment to membrane-associated division proteins.

60 CK proteins share catalytic (DOCK(DHR2)) and membrane-associated (DOCK(DHR1)) domains.

61 e globular domain and a predicted N-terminal membrane-associated domain.

62 increased levels of both total and synaptic membrane-associated dopamine transporters.

63 n drives the association of GRK2 with plasma membrane-associated DOR.

64 The membrane-associated E3 ubiquitin ligase ZNRF2 is release

65 t corresponding to ct694-ctl0063translocated membrane-associated effector A (TmeA).

66 vily regulated by secondary factors, such as membrane-associated EGF-CFC family proteins.

67 by results obtained for luminal and nuclear membrane-associated EGFP-tagged proteins.

68 rotein phosphatases that are predicted to be membrane-associated either integrally or peripherally.

69 adapted to interrogate interactions between membrane-associated Env and the matrix domain of Gag.

70 MT-4 cells express higher levels of plasma-membrane-associated Env than nonpermissive cells, and En

71 f SK1 to the plasma membrane and enhance the membrane-associated enzymatic activity of SK1, as well a

72 in lipid A biosynthesis is catalysed by the membrane-associated enzyme LpxH.

73 terized family of guidance molecules are the membrane-associated ephrins, which together with their c

74 at the InsP(3)R is regulated by a peripheral membrane-associated ER-luminal protein that strongly inh

75 romodulatory effects are likely mediated via membrane-associated estrogen receptors; however, the loc

76 Membrane-associated events during peroxisomal protein im

77 to the extracellular space, hereafter called membrane-associated extracellular RNAs (maxRNAs).

78 hermore, adipose triglyceride lipase, plasma membrane-associated fatty acid binding protein and AMPKg

79 utations in FDXR, encoding the mitochondrial membrane-associated flavoprotein ferrodoxin reductase re

80 uptake, glucose-induced currents, and plasma membrane-associated fluorescence after 1 hour.

81 Through the physical mechanism of membrane-associated folding, pHLIPs are triggered by the

82 t replicate the structural properties of the membrane-associated form of vCD200 that is naturally pro

83 a soluble form (largely in the nucleus) to a membrane-associated form where the enzyme becomes activa

84 litate the coherent treadmilling dynamics of membrane-associated FtsZ bundles in reconstituted system

85 ality of TMEM260 and that attenuation of the membrane-associated functions of this protein is a princ

86 rties suggest that CARMILs play a variety of membrane-associated functions related to actin assembly

87 ng factor Get3 and are then delivered to the membrane-associated Get1/2 complex for insertion into ER

88 ion of synaptic inhibition is initiated by a membrane-associated glucocorticoid receptor in BLA princ

89 ar glucocorticoid application, implicating a membrane-associated glucocorticoid receptor.

90 Plasma membrane-associated glutamate transporters play a key ro

91 ipid second messengers through hydrolysis of membrane-associated glycerophospholipids.

92 For the membrane-associated glycine-conjugated GC and GCDC (pKa

93 Mucin 1 protein (MUC1) is a membrane-associated glycoprotein overexpressed in the ma

94 sistance to Shiga toxin, which uses a plasma membrane-associated glycosphingolipid, globotriaosylcera

95 PimA belongs to a large family of membrane-associated glycosyltransferases for which the u

96 s a conformation that is open for binding to membrane-associated GTPase Arl6 and a large positively c

97 K-Ras is a membrane-associated GTPase that cycles between active an

98 To explore the role of the Discs large/membrane-associated guanylate kinase (Dlg/MAGUK) family

99 KEY POINTS: The membrane-associated guanylate kinase (MAGUK) family of s

100 The membrane-associated guanylate kinase (MAGUK) family of s

101 respectively) displayed impaired binding to membrane-associated guanylate kinase (MAGUK) proteins.

102 Here, we identify the PDZ domain-containing Membrane-associated Guanylate Kinase (MaGUK) PSD93 as a

103 PSD-95 is a member of the membrane-associated guanylate kinase class of proteins t

104 ke membrane protein (CLMP), occludin (OCLN), membrane-associated guanylate kinase inverted 1 (MAGI1),

105 WW domain-containing scaffold protein called membrane-associated guanylate kinase with inverted orien

106 resynaptic contact and recruitment of MAGUK (membrane-associated guanylate kinase) scaffolding protei

107 PSD-95, a membrane-associated guanylate kinase, is the major scaff

108 dentified novel disease-causing mutations in membrane-associated guanylate kinase, WW, and PDZ domain

109 ctivation of PTEN by TF, the association of "membrane-associated guanylate kinase-with inverted confi

110 Membrane-associated guanylate kinases (MAGUKs) are a fam

111 ansmission via disc-large (DLG) subfamily of membrane-associated guanylate kinases (MAGUKs).

112 Exosomes contain an array of membrane-associated, high-order oligomeric protein compl

113 Hrs localizes to the plasma membrane and the membrane-associated Hrs facilitates assembly of signalin

114 We show here that membrane-associated IL-15Ralpha-IL-15 complexes are tran

115 Thus, trans-endocytosis of membrane-associated IL-15Ralpha-IL-15 provides a mode of

116 the SCAR/WAVE complex have been found to be membrane associated in plants [3].

117 ed dendritic cells and macrophages expressed membrane-associated inducible Hsp70.

118 eract with differently composed membranes or membrane-associated interaction partners and thereby reg

119 While structures of membrane-associated intermediates would provide tremendo

120 Additional key players are the cell membrane-associated iron transporters, particularly ferr

121 Here, we show that MEMBRANE ASSOCIATED KINASE REGULATOR2 (MAKR2) controls t

122 Hh stimulates the binding of Smo to a plasma membrane-associated kinase Gilgamesh (Gish)/CK1gamma and

123 Here, we show that the membrane-associated kinase Gilgamesh (Gish)/CK1gamma mai

124 pin (phot1) is a blue light-activated plasma membrane-associated kinase that acts as the principal ph

125 ed, whereas AQP3 increased, levels of plasma membrane-associated lateral junctional proteins.

126 alters the conformational equilibrium of the membrane-associated lid domain of MGL to favour closed c

127 logical function of an Arabidopsis thylakoid membrane-associated lipase, PLASTID LIPASE1 (PLIP1).

128 -weight, covalently attached bacterial outer membrane-associated lipid that is required for activatio

129 and demonstrates early and broad changes in membrane associated lipids.

130 how herein that a previously uncharacterized membrane-associated M. tuberculosis protein encoded by R

131 a large unstructured loop, and finally, the membrane-associated MA-helix that continues into the las

132 ing motor TraB, which may be shared by other membrane-associated machineries involved in DNA binding

133 The RhoGTPases are characterized as membrane-associated molecular switches that cycle betwee

134 to interrogate the diffusion path-lengths of membrane associated molecules.

135 phipathic antimicrobial peptides, a class of membrane-associated molecules that specifically target a

136 observed to acquire APC-derived membrane and membrane-associated molecules through trogocytosis in di

137 osomes and microvilli, and the production of membrane-associated mucins and Toll-like receptors (TLRs

138 tochondria, CoQ lipids are built by an inner membrane-associated, multicomponent, biosynthetic pathwa

139 ERBB1/2/4 inhibitor neratinib caused plasma membrane-associated mutant K-RAS to localize in intracel

140 de polymorphisms in mmpL3, encoding an inner membrane-associated mycolic acid flippase in M. tubercul

141 und proteins, functional characterization of membrane-associated NAC transcription factors in tomato

142 ts production and scavenging rates, in which membrane-associated NADPH oxidases are known to play a c

143 performed an overexpression screen of known membrane-associated NE proteins.

144 ntal challenge in distinguishing luminal and membrane-associated NE proteins.

145 To our surprise, we found that membrane-associated neuropilin-1 is polysialylated at ap

146 entry by inhibiting Cdr2, which forms stable membrane-associated nodes at mid-cell.

147 We conclude that membrane-associated Nogo-A produced in oligodendrocytes

148 catalytic domain interacts directly with the membrane-associated NTD, which serves as both a membrane

149 s of CsgA, the major subunit of curli, and a membrane-associated nucleator protein, CsgB.

150 e, and it is accompanied by the formation of membrane-associated oligomers.

151 the cytosol limits inhibitory antibodies to membrane-associated or extracellular targets.

152 lsive guidance molecule member a (RGMa) is a membrane-associated or released guidance molecule that i

153 pilin-2, which is polysialylated when either membrane-associated or soluble.

154 ycine alpha-hydroxylating monooxygenase from membrane-associated PAL.

155 es was exposed, generating a shorter form of membrane-associated PAL.

156 e in these samples, indicative of a role for membrane-associated PANX1 in small arteries of hypertens

157 clinical research on Alzheimer's disease and membrane-associated pathologies in general.

158 translational modifications; therefore, many membrane-associated pathways might employ similar mechan

159 RNase E/enolase distribution changes from membrane-associated patterns under aerobic to diffuse pa

160 The data suggest that appropriate levels of membrane-associated PDPK1 are required for stabilization

161 To advance mechanistic understanding of membrane-associated peptide folding and insertion, we ha

162 o characterize the self-assembly behavior of membrane-associated peptides, very few of which have bee

163 n, spectrin, and associated molecules form a membrane-associated periodic skeleton (MPS) in neurons.

164 ctin, spectrin, and related molecules form a membrane-associated periodic skeleton (MPS) in neurons.

165 ate the behavior of the actin-spectrin-based Membrane-associated Periodic Skeleton (MPS), and effects

166 For a better understanding of this membrane-associated periodic skeleton (MPS), it is impor

167 hrough establishing the actin-spectrin-based membrane-associated periodic skeleton as well as enablin

168 Key membrane-associated Pexs (MbPex3, MbPex11, and MbPex14)

169 tion that may explain its widely pleiotropic membrane-associated phenotypes across organisms.

170 Herzog functions as a membrane-associated phosphatase and controls embryonic p

171 We found that the VAP-interacting membrane-associated phosphatidylinositol (PtdIns) transf

172 iochemistry and pharmacological targeting of membrane-associated phosphoinositides.

173 formatics analysis, those differences in the membrane-associated phosphoproteins composition were ass

174 Of the 1112 membrane-associated phosphoproteins identified, 64 and 2

175 Ras function by mediating interactions with membrane-associated PIP2 lipids; these insights that may

176 tion fractionation experiments revealed that membrane-associated platelet polyphosphate is condensed

177 ctivation profiles than natural, monovalent, membrane-associated pMHC.

178 A plasma membrane-associated polarity crescent defined by BREAKIN

179 Our findings identify membrane-associated polyphosphate in a nanoparticle stat

180 The apparent polymer size of membrane-associated polyphosphate largely exceeds that o

181 In contrast to soluble polyphosphate, membrane-associated polyphosphate nanoparticles potently

182 In this study, we show that the membrane-associated pore-forming protein Perforin-2 (P2)

183 Many cell-membrane-associated processes require transient spatiote

184 KIN is capable of simulating a wide array of membrane-associated processes, including adsorption, des

185 Transforming growth factor-beta membrane associated protein (TIMAP) is an endothelial ce

186 , we identified an accessory protein, 17 kDa membrane-associated protein (MAP17), that increased SGLT

187 one Sox2-replacing antibody antagonizes the membrane-associated protein Basp1, thereby de-repressing

188 MyoA is part of a membrane-associated protein complex called the glideosom

189 oteins FeoA and FeoC and a large cytoplasmic-membrane-associated protein FeoB, which has an N-termina

190 ithin the cell as part of the soluble and/or membrane-associated protein fraction.

191 te the applicability of TurboID in capturing membrane-associated protein interactomes using Lotus jap

192 PHB2 binds the autophagosomal membrane-associated protein LC3 through an LC3-interacti

193 IRE1alpha, an ER membrane-associated protein mediating unfolded protein r

194 Moreover, GacJ, a small membrane-associated protein, formed a complex with GacI

195 egulates cilia disassembly, ciliary entry of membrane-associated protein, Hedgehog signaling, and emb

196 We show that a gut-membrane-associated protein, named Mesh, plays an import

197 antibodies (against agrin, adipocyte plasma membrane-associated protein, Rho GDP-dissociation inhibi

198 that requires A-type lamin, an inner nuclear membrane-associated protein, to accelerated aging observ

199 MURC, a plasma membrane-associated protein, was found to be more abunda

200 tein light chain 3 (LC3), the autophagosomal membrane-associated protein.

201 g of the gl14 gene, which encodes a putative membrane-associated protein.

202 platelet activation (APMAP [adipocyte plasma membrane-associated protein], GPLD1 [phosphate inositol-

203 sidues, near the protein termini, and within membrane associated proteins.

204 In contrast, other membrane-associated proteins and non-CME endocytic prote

205 biosynthesis as well as other cell wall and membrane-associated proteins and ROS scavenging enzymes.

206 Accordingly, several receptors and other membrane-associated proteins are organized and functiona

207 Removal of membrane-associated proteins by proteases decreases the

208 etergents to isolate the PSD and release its membrane-associated proteins complicates studies of thes

209 Out of 1736 soluble proteins and 2187 membrane-associated proteins identified, 288 and 56, res

210 to 2 s, and similarly high turnover rates of membrane-associated proteins in CME.

211 ated lysosomal hydrolytic enzymes and plasma membrane-associated proteins in the supernatant of Tat-e

212 After SPB insertion, membrane-associated proteins including the conserved Ndc

213 ion, CEP-290 prevents inappropriate entry of membrane-associated proteins into cilia and keeps ARL-13

214 Such signals include membrane-associated proteins of the oligodendrocyte plas

215 09 differentially phosphorylated residues of membrane-associated proteins on activation of the intrac

216 Phase separation of membrane-associated proteins participates in various tra

217 ilayers and the membrane-proximal regions of membrane-associated proteins play important roles in reg

218 cted for immunoblotting against B. miyamotoi membrane-associated proteins separated by 2-dimensional

219 , and did not bind to any of the 5,300 human membrane-associated proteins tested.

220 nments, placing cPLA2delta into the class of membrane-associated proteins that contain a tandem pair

221 he targeted degradation of extracellular and membrane-associated proteins using conjugates that bind

222 r examine the interaction of PorB with outer membrane-associated proteins, including PorA and RmpM.

223 Several cytosolic and membrane-associated proteins, including the Rab family m

224 Three membrane-associated proteins, Kibra, Merlin, and Expande

225 ver, by mediating interactions with numerous membrane-associated proteins, they are key components in

226 age-gated calcium channels are extracellular membrane-associated proteins, which are post-translation

227 Extracellular and membrane-associated proteins-the products of 40% of all

228 cytosolic and nuclear proteins, but also in membrane-associated proteins.

229 omplex derived from the peripheral stalk and membrane-associated proteins.

230 rves as a prototype to model large, dynamic, membrane-associated proteins.

231 arge that in turn modulate interactions with membrane-associated proteins.

232 ted that EGRs target cytoskeleton and plasma membrane-associated proteins.

233 he membrane on the structure and dynamics of membrane-associated proteins.

234 s are responsible for ectodomain shedding of membrane-associated proteins.

235 density fractions at the buoyant density of membrane-associated proteins.

236 acterization of lateral interactions between membrane-associated proteins.

237 d BBS proteins, and reduced ciliary entry of membrane-associated proteins.

238 ot aggregate and did not bind to 5,300 human membrane-associated proteins.

239 ment for a large number of transmembrane and membrane-associated proteins.

240 n for a class of linkers of lipid-activated, membrane-associated proteins.

241 may necessitate extensive adaptation of the membrane-associated proteome.

242 s and conformationally activates the tightly membrane-associated pseudo-effector SepL and its chapero

243 In Arabidopsis, YDA is activated by the membrane-associated pseudokinase SHORT SUSPENSOR (SSP) t

244 ped virions but circulates in the blood in a membrane-associated, quasi-enveloped form (eHEV).

245 llowing an early burst of translocation, the membrane-associated RAF1-mVenus was undetectable by micr

246 Self-assembly of plasma membrane-associated Ras GTPases has major implications t

247 rexpression in NIH-3T3 fibroblasts increases membrane-associated Ras, induces the transformed phenoty

248 Inhibiting GPR30, a membrane-associated receptor, limited aldosterone's effe

249 Several cytoplasmic and membrane-associated redox-active protein genes were diff

250 s are corrinoid and Fe-S cluster-containing, membrane-associated reductive dehalogenases.

251 ctural modeling of SynDIG1 suggests that the membrane-associated region forms a three-helical bundle

252 The myristoylated and membrane-associated regulatory beta-subunits restrict nu

253 EN controls multicellular assembly through a membrane-associated regulatory protein complex composed

254 ch would facilitate virus replication within membrane-associated replication compartments.

255 ed by soluble AhlC to hide their hydrophobic membrane associated residues.

256 We found that the distribution of membrane-associated retromer is predominantly comprised

257 ay demonstrated specific interactions of the membrane-associated rhabdovirus MPs only with their cogn

258 pe anti-CD98 Ab, UM7F8, is due to Ab-induced membrane-associated ring CH (MARCH) E3 ubiquitin ligase-

259 The membrane-associated RING-CH (MARCH) family of membrane-b

260 ng the expression of MARCH8, a member of the membrane-associated RING-CH (MARCH) proteins.

261 unable to be ubiquitinated or mice that lack membrane-associated RING-CH 8 (MARCH8), the E3 ubiquitin

262 erol accelerates the ubiquitination of SM by membrane-associated ring-CH type finger 6 (MARCH6), a ke

263 The E3 ligase membrane-associated ring-CH-type finger 6 (MARCH6) is a

264 ecent work by Tada and colleagues identifies membrane-associated-RING-CH8 (MARCH8) as a potent anti-H

265 r, BASIC LEUCINE ZIPPER 17 (bZIP17), and the membrane-associated RNA splicing factor, INOSITOL REQUIR

266 f XP revealed plasma and trans Golgi network membrane-associated roles in virus assembly and/or relea

267 (H), V(H)-Fc ab8, bound with high avidity to membrane-associated S glycoprotein and to mutants found

268 Here, we show that the membrane-associated sensory input domain of PA1396 has f

269 ther mutagenesis screening revealed that the membrane-associated serine protease HtrA mediates select

270 I hypothesize that several membrane-associated serine proteinases (MASPs), in syner

271 rafficking pathway controls the abundance of membrane-associated soluble proteins, as shown for absci

272 GrlA transitions from an inactive, membrane-associated state and relocalizes to the cytopla

273 P2-binding protein cofilin from its inactive membrane-associated state into the cytoplasm where it me

274 ith a conserved phenylalanine residue in the membrane-associated stretch between transmembrane region

275 Intramembrane proteases (IPs) cleave membrane-associated substrates in nearly all organisms a

276 preventing the up-regulation of the granule membrane-associated subunit of the NADPH oxidase at the

277 demonstrate a novel mechanism in which cell membrane-associated syndecan-1 regulates the innate immu

278 ns-SNARE complexes ("SNAREpins") with target membrane-associated t-SNAREs, a zippering-like process r

279 alloproteinases (Timps), cleave secreted and membrane-associated targets to sculpt the extracellular

280 racterized as a specific mAb for VZV ORF9, a membrane-associated tegument protein that interacts with

281 eins from different orthopoxviruses bound to membrane-associated TNF and dampened inflammatory gene e

282 F-alpha gene and the activity of ADAM17, the membrane-associated TNF-alpha-converting enzyme.

283 s the myelin regulatory factor (MYRF), an ER membrane-associated transcription factor (TF) released b

284 ltiple factors act in the UPR, including the membrane-associated transcription factor, BASIC LEUCINE

285 The GLUT (SLC2) family of membrane-associated transporters are described as glucos

286 suicides, and depressed nonsuicides, plasma membrane-associated tubulin showed significant decreases

287 lated with the islets) and restored basement membrane-associated type VI collagen, which were associa

288 The plasma membrane-associated tyrosine phosphatase PTPRO is freque

289 cter lari, catalyze transfer of glycans from membrane-associated undecaprenol diphosphate-linked subs

290 wild-type at late stages of infection where membrane-associated uORF protein facilitates virus relea

291 The membrane-associated viral protein 6K(2) plays a key role

292 While it is known that the membrane-associated viral protein 6K2 plays a role in th

293 cussed and compared with previous studies of membrane-associated water phases and the impact of membr

294 M1 is peripherally membrane associated, whereas NP associates with viral RN

295 Thus, the increase in total plasma membrane associated with cell proliferation is likely to

296 lized lipid raft invaginations of the plasma membrane associated with cell signaling and membrane com

297 have been elusive due to complexities in the membrane associated with the hidden architecture of mult

298 sed with clinically significant retrocorneal membranes associated with DSAEK failure at the Bascom Pa

299 Further analysis of membranes associated with isolated postsynaptic densitie

300 ion and cellular stresses activate the inner membrane-associated zinc metallopeptidase OMA1 that clea