ライフサイエンスコーパス: membrane-associated

1 xperiments suggest that AmpR is likely to be membrane associated.

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

3 es within the KCNH subfamily of channels are membrane-associated.

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

5 t microvesicle formation by interfering with membrane-associated acid sphingomyelinase).

6 taining actin-binding domains, is a novel ER membrane-associated actin-binding protein.

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

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

9 LPS caused a TLR4-dependent activation of membrane-associated adaptor protein focal adhesion kinas

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

11 ructure of human FALDH, the first model of a membrane-associated aldehyde dehydrogenase.

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

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

14 In conclusion, a potential membrane-associated AmpR dimer regulates ampC expression

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

16 min (B12)-dependent enzymes that are usually membrane associated and oxygen sensitive, hindering deta

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

18 uted HDLs, finding that E2 and E2 oleate are membrane-associated and highly mobile.

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 terize PopB, the major translocator, in both membrane-associated and PcrH-bound forms.

22 Analysis of membrane-associated and raft microdomain proteins reinfo

23 onstructural protein 1 (NS1) is a conserved, membrane-associated and secreted glycoprotein with repli

24 ses, we determined, among multiple important membrane-associated and soluble cargos, the critical con

25 e products of both genes are predicted to be membrane associated, and the norE product is a member of

26 total of 282 proteins, including cytosolic, membrane-associated, and transmembrane proteins.

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

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

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

30 It is known that content of plasma membrane-associated ASGP-R is decreased after ethanol ex

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

32 autophagosomes and specifically acts only on membrane-associated Atg8 proteins, we elucidated its str

33 Torsins are membrane-associated ATPases whose activity is dependent

34 XIN BINDING PROTEIN 1 (ABP1) is an essential membrane-associated auxin receptor, but recent findings

35 gly, our study also revealed that the plasma membrane-associated BAK1 ectodomain was sufficient to in

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

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

38 , membrane binding and enzymatic activity of membrane-associated bee venom PLA2, covering a pressure

39 chemical analyses demonstrated CagA-mediated membrane-associated binding with phosphorylated SHP2.

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

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

42 catenin and displayed a reduced affinity for membrane-associated cadherins.

43 ent but Rim21-dependent manner by the plasma membrane-associated casein kinase 1 (CK1).

44 displayed a decreased ability to upregulate membrane-associated caspase-8 activity and increased nec

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

46 Production of membrane-associated cell surface receptors and their lig

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

48 t the basal state depends on the quantity of membrane-associated clathrin and is correlated to a sign

49 0 (ADAM10), resulting in the generation of a membrane-associated cleavage fragment in both THP-1 mono

50 ith cargo and thus contribute to stabilizing membrane-associated coatomer.

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

52 The resulting AKT2 fusion kinase is membrane-associated, constitutively phosphorylated, and

53 ate NMR (SSNMR) studies of FP structure in a membrane-associated construct (FP-Hairpin), which likely

54 The structure comprises an outer membrane-associated core complex connected by a central

55 nanosystem is developed for co-delivery of a membrane-associated cytokine (tumor-necrosis-factor-rela

56 etween the movement of so-called "naked" and membrane-associated cytoplasmic alphaherpesvirus capsids

57 interacts with and phosphorylates the plasma-membrane-associated cytoplasmic kinase BIK1, an importan

58 ostructure and dynamics of plasma membranes, membrane-associated cytoskeletal structures and extracel

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

60 mixture, we demonstrate that the artificial membrane-associated cytoskeleton, on the one hand, suppr

61 Whereas outer mitochondrial membrane-associated degradation is typically associated

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

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

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

65 release, maximal rate of uptake (Vmax), and membrane-associated dopamine transporter (DAT) levels we

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

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

68 ts involvement in previously uncharacterized membrane-associated drought sensing or signaling mechani

69 more, we discovered that silencing the inner membrane-associated dynamin optic atrophy 1 (OPA1) in fi

70 The membrane-associated E3 ubiquitin ligase ZNRF2 is release

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

72 The conserved membrane-associated effector protein PspA has four alpha

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

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

75 ltra-high-resolution imaging of specifically membrane-associated, endogenous syndapin I at membranes

76 Here we report that Clec16a is a membrane-associated endosomal protein that interacts wit

77 t the full O-linked glycosylation profile of membrane-associated Env is similar to that of soluble gp

78 gnized by the antibody in the context of the membrane-associated envelope oligomer.

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

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

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

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

83 reviously, we showed that Twinkle is tightly membrane-associated even in the absence of mtDNA, which

84 nderstand the spatiotemporal organization of membrane-associated events (signaling, fusion, fission,

85 Membrane-associated events during peroxisomal protein im

86 ted vesicle fusion, elucidated by the plasma membrane-associated exocyst subunits, indicates the pres

87 cortex signified that signals emanating from membrane-associated ezrin may locally act to modulate co

88 least partly through phosphorylation of the membrane-associated F-BAR protein Syp1, which colocalize

89 compounds induced a marked increase of some membrane associated fatty acids, particularly unsaturate

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

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

92 on of nonstructural (NS) proteins into viral membrane-associated foci, with this representing an earl

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

94 a soluble cytoplasmic form (UCH-L1(C)) and a membrane-associated form (UCH-L1(M)).

95 s of cells stably expressing either a plasma membrane-associated form of monomeric enhanced green flu

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

97 ulated equilibrium between water-soluble and membrane-associated forms.

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

99 ween membrane order and an energy-dependent, membrane-associated function in prokaryotes.

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

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

102 mDia1 deficiency led to a downregulation of membrane-associated genes and a specific upregulation of

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

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

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

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

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

108 , such as the transferrin receptor (TfR1), a membrane-associated glycoprotein critical for iron uptak

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

110 These findings support assembly of membrane-associated gp41 trimers through interleaving of

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

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

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

114 We determined previously that membrane-associated guanylate kinase (MAGUK) protein dis

115 ignaling complexes at excitatory synapses by membrane-associated guanylate kinase (MAGUK) proteins re

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

117 MAP1A has been reported to bind to the membrane-associated guanylate kinase (MAGUK) scaffolding

118 ponent caspase recruitment domain-containing membrane-associated guanylate kinase 1 (CARMA1) and/or t

119 GPR30 forms a plasma membrane complex with a membrane-associated guanylate kinase and AKAP5, which co

120 n that caspase recruitment domain-containing membrane-associated guanylate kinase protein (CARMA)3 is

121 /calmodulin-dependent serine protein kinase; membrane-associated guanylate kinase protein (MAGI)-1, M

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

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

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

125 The postsynaptic density (PSD)-95 family of membrane-associated guanylate kinases (MAGUKs) are major

126 GPR30 interacted with membrane-associated guanylate kinases, including SAP97 a

127 aspase activation and recruitment domain and membrane-associated guanylate-like kinase domain-contain

128 e PDZ domain-containing proteins include the membrane-associated guanylate-like kinases [postsynaptic

129 In this study, the interhelical geometry of membrane-associated HAfp is probed by solid-state NMR.

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

131 hat cardiomyocyte-specific overexpression of membrane-associated human stem cell factor (hSCF) enhanc

132 Membrane-associated Hyd-2 is an unusual heterotetrameric

133 Particulate membrane-associated hydrocarbon monooxygenases (pHMOs) a

134 that CtsE is a soluble protein while CtsP is membrane associated in C. jejuni.

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

136 mutation, with one MHR mutant arrested as a membrane-associated intermediate that is stable upon hig

137 While structures of membrane-associated intermediates would provide tremendo

138 nt and other MHR mutants arrested as labile, membrane-associated intermediates.

139 ever, the endoplasmic reticulum- and nuclear membrane-associated inverted formin-2 (INF2), a potent a

140 As this interaction is thought to be membrane-associated, involving a myriad of membrane-anch

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

142 The plasma-membrane-associated kinase BIK1, which is a direct subst

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

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

145 ll times and thereby prevented activation by membrane-associated kinases.

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

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

148 nges resulted in the rapid detachment of the membrane-associated lipid II synthase MurG and the phosp

149 imentin filaments target CARMIL2 to critical membrane-associated locations, where CARMIL2 regulates C

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

151 NFkappaB is activated, which up-regulates membrane-associated (ma) IL-15, caspase-1 and IL-1beta.

152 rides, liberating maltotetraose, whereas the membrane-associated maltogenic amylase EUR_01860 breaks

153 contain ordered arrays of what is likely the membrane-associated matrix protein, contain multiple cor

154 uctures with membranes as well as details of membrane-associated mechanisms of toxicity.

155 nce receptors are proteolytically cleaved by membrane-associated metalloproteases of the ADAM family,

156 Ank2-XL, and the MAP1B homolog Futsch form a membrane-associated microtubule-organizing complex that

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

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

159 ginae infection yielded increased expression membrane-associated mucins and evoked a robust proinflam

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

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

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

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

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

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

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

167 rations on flotation gradients and show that membrane-associated nucleoids accumulate at the top of t

168 simple model in which the formation of large membrane-associated nucleoprotein complexes physically o

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

170 al modification shown to play a role in many membrane-associated or extracellular processes such as v

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

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

173 stent with that, SodA, DoxX, and SseA form a membrane-associated oxidoreductase complex (MRC) that ph

174 We show that two membrane-associated, oxygen-dependent [NiFe] hydrogenase

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

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

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

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

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

180 rst time that a site-specific environment of membrane associated peptide can be probed by the submono

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

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

183 This approach identified the membrane-associated peroxidase GPx8 as a bona fide cellu

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

185 Here, we show the first study on membrane-associated pHLIP using solid-state NMR spectros

186 iochemistry and pharmacological targeting of membrane-associated phosphoinositides.

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

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

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

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

191 re, we demonstrate that enzymatically active membrane-associated PR3 on apoptotic cells triggered sec

192 Many cell-membrane-associated processes require transient spatiote

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

194 g a broader range of mTORC1 functions in the membrane-associated processes.

195 organization and have implications for many membrane-associated processes.

196 suggesting that a hitherto uncharacterized, membrane-associated protease accounts for TorsinA proces

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

198 rans-Golgi lumina were spanned by asymmetric membrane-associated protein arrays that had approximatel

199 Increased expression of the membrane-associated protein At14a-like1 (AFL1) led to in

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

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

202 verse range of known and novel cytosolic and membrane-associated protein complexes.

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

204 Dysferlin is a membrane-associated protein implicated in membrane resea

205 Dysferlin is a membrane-associated protein implicated in muscular dystr

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

207 The IM30 (inner membrane-associated protein of 30 kDa), also known as th

208 We conclude that FAM65B is a plasma membrane-associated protein of hair cell stereocilia tha

209 tein annexin A5 (ANXA5) is the most abundant membrane-associated protein of ~P23 mouse vestibular hai

210 Receptor-cargo docking occurs at the membrane-associated protein Pex14.

211 FTS_1680-encoded protein was identified as a membrane-associated protein required for full cytopathog

212 enuating Notch signaling by inducing Numb, a membrane-associated protein that inhibits Notch signalin

213 DAP12 is a cell membrane-associated protein that is expressed in myeloid

214 c envelopment, in a protein complex with the membrane-associated protein UL20 (UL20mp).

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

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

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

218 mon mitochondrial lipids, and abundant inner-membrane associated proteins concentrated in the bottom-

219 OMP component BamA along with several outer membrane associated proteins.

220 rvival in Opn1sw(-/-)Lrat(-) (/-) mice, cone membrane-associated proteins (e.g. Galphat2, GRK1 and GC

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

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

223 ly required for thorough characterization of membrane-associated proteins and were facilitated by the

224 Removal of membrane-associated proteins by proteases decreases the

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

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

227 The mistrafficking of cone membrane-associated proteins including cone opsins (M- a

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

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

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

231 plicates trans-synaptic interactions between membrane-associated proteins such as neurexins and neuro

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

233 es during maturation of cysteine-containing, membrane-associated proteins while ignoring the same cys

234 nstrated that the membrane alone, or through membrane-associated proteins, can effect dynamic changes

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

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

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

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

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

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

241 s of membrane lipids and integral as well as membrane-associated proteins.

242 the activity of many ion channels and other membrane-associated proteins.

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

244 e composition, shape and the organization of membrane-associated proteins.

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

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

247 alpha7-subunits is controlled by endogenous membrane-associated prototoxins in the Ly6 family.

248 ynaptic membrane, and depletes the number of membrane-associated PSD-95-like vertical filaments and t

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

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

251 ted from the environment to the reduction of membrane-associated quinones.

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

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

254 The membrane-associated receptors (mERs) underlying the acut

255 Significance statement: The membrane-associated receptors underlying the acute effec

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

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

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

259 polymerase (RdRp), which is mediated by two membrane-associated regions.

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

261 The coupling of membrane-associated replication complexes with virus int

262 The membrane-associated retinaldehyde reductase and retinol

263 a mediating their localization to substrate, membrane-associated RhoA.

264 idated vRNA, indicating that the presence of membrane-associated ribonucleic protein complexes in the

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

266 The ubiquitination is mediated by the membrane-associated RING-CH1 (MARCH1) ubiquitin ligase a

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

268 nd transduce auxin signal to activate plasma membrane-associated ROPs [Rho-like guanosine triphosphat

269 ion in the TGN by coexpression of the plasma membrane-associated scaffold PSD-95, which allows for tr

270 ongs to a newly identified secreted and cell membrane-associated SCUBE family, which is evolutionaril

271 The pathway involves the dendritic-membrane-associated Shh signal transducer Smoothened (Sm

272 derived chitin elicitors, phosphorylation of membrane-associated signaling complexes, activation of m

273 a secondary proteolytic cleavage within the membrane-associated SIRPalpha fragment by gamma-secretas

274 Slit in culture and the phenotype rescue by membrane-associated Slit2 activities.

275 interactions that govern the assembly of the membrane-associated Spir.FMN complex.

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

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

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

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

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

281 nd phase separation in several cytosolic and membrane-associated systems.

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

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

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

285 ARP), which is a docking receptor for latent membrane-associated TGF-beta (mLTGF-beta).

286 lation of THP-1 cells with ligands of plasma membrane associated TLRs 2 and 4, endosomal TLRs 7 and 8

287 found a variety of oligomerization states of membrane-associated transporters, revealing molecular as

288 However, selective monitoring of membrane-associated Trx activity has proved challenging

289 rin tetramers or higher order oligomers form membrane-associated two-dimensional networks in associat

290 Furthermore, the basement membrane-associated type IV collagens regulate ISC self-

291 The plasma membrane-associated tyrosine phosphatase PTPRO is freque

292 d oxidation and one-carbon metabolism to the membrane-associated ubiquinone pool.

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

294 Phototropins are plasma-membrane-associated UV-A/blue-light activated kinases th

295 uctural model where MAGUKs, corresponding to membrane-associated vertical filaments, are the essentia

296 Density gradients revealed the presence of membrane-associated virions in the sera, with a differen

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

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

299 Further analysis of membranes associated with isolated postsynaptic densitie

300 ; RSPO2 interacts with LGR5 to stabilize the membrane-associated zinc and ring finger 3 (ZNRF3).