ライフサイエンスコーパス: cytoskeletal protein

1 mechanisms regulating the function of these cytoskeletal proteins.

2 spatial regulation of cell wall synthesis by cytoskeletal proteins.

3 proximal to the C terminus were enriched in cytoskeletal proteins.

4 such as RELN and associate with a number of cytoskeletal proteins.

5 switch for the interactions between Jak3 and cytoskeletal proteins.

6 ng step during interactions between Jak3 and cytoskeletal proteins.

7 nced matrix deposition, and dysregulation of cytoskeletal proteins.

8 biquitous tubulin and actin superfamilies of cytoskeletal proteins.

9 Bactofilins are fibre-forming bacterial cytoskeletal proteins.

10 ent enzymes, SNAREs, Rab GTPases, cargo, and cytoskeletal proteins.

11 nce of TNTs through its interaction with the cytoskeletal proteins.

12 ions, and nonequilibrium forces generated by cytoskeletal proteins.

13 c using a variety of different signaling and cytoskeletal proteins.

14 uter plexiform layer and that interacts with cytoskeletal proteins.

15 Rng3 chaperone and the presence of nonmyosin cytoskeletal proteins.

16 chment protein receptor (SNARE) proteins and cytoskeletal proteins.

17 al changes, and upregulate the expression of cytoskeletal proteins.

18 membrane to the basal lamina and underlying cytoskeletal proteins.

19 ulated process under the control of specific cytoskeletal proteins.

20 widespread functional homologs of eukaryotic cytoskeletal proteins.

21 ter regulation by intracellular signaling or cytoskeletal proteins.

22 Cytoskeletal protein 4.1 also showed dynamic phosphoryla

23 ) that control the structure and function of cytoskeletal protein 4.1R.

24 Dystrophin is a large, submembrane cytoskeletal protein, absence of which causes Duchenne m

25 ng pathways, mechanical stresses also direct cytoskeletal protein accumulation [5-7].

26 The cytoskeletal protein actin plays a critical role in main

27 eins FAK, paxillin, and vinculin but not the cytoskeletal protein actin remain behind after shear-ind

28 chaperonin-containing TCP-1 (CCT) folds the cytoskeletal protein actin.

29 gets for SpyA, prominent among which are the cytoskeletal proteins actin and vimentin.

30 in bacteria: the identification of numerous cytoskeletal proteins, actin homologues fulfilling spind

31 ein kinase C (PKC)-mediated loss of the host cytoskeletal protein adducin and weakening of the cellul

32 Calpha, but not PKCzeta, phosphorylating the cytoskeletal protein adducin of both Ser-726 and Thr-445

33 IP6K3 physiologically binds to the cytoskeletal proteins adducin and spectrin, whose mutual

34 cument mutations in ACTN1, which encodes the cytoskeletal protein alpha-actinin 1, in 10 of 239 conse

35 The cytoskeletal protein alpha-actinin is shared between the

36 n receptor-beta-catenin complex binds to the cytoskeletal protein alpha-catenin, which is essential f

37 e we apply CRISPR-Cas9 gene editing to tag a cytoskeletal protein (alpha-tubulin) and demonstrate a r

38 ins (E-cadherin, N-cadherin, and Integrins), cytoskeletal proteins (alpha-Smooth Muscle Actin, Viment

39 Here, we demonstrate that the submembranous cytoskeletal proteins alphaII and betaII spectrin are po

40 ny deafness mutations that disable hair-cell cytoskeletal proteins also disrupt bundles.

41 encode sarcomeric (contractile apparatus) or cytoskeletal proteins, although, in the case of left ven

42 We found two cytoskeletal proteins among six proteins tightly associa

43 main protein PDLIM2 (Mystique/SLIM), a known cytoskeletal protein and promoter of nuclear nuclear fac

44 morphology, and motility; genes that encode cytoskeletal proteins and cytokines; and genes that cont

45 PPTT further enhanced the remodeling of cytoskeletal proteins and decreased migration.

46 lack of NFL protein alters the expression of cytoskeletal proteins and disrupts other NF subunits, ca

47 In the myocyte, increases in the cytoskeletal proteins and improvements in the Ca(2)(+) h

48 tudied toxins: it directs the binding of two cytoskeletal proteins and inhibits FtsZ and MreB simulta

49 s often caused by mutations in sarcomere and cytoskeletal proteins and is also associated with metabo

50 r nmMLCK in hyperoxia-induced recruitment of cytoskeletal proteins and NADPH oxidase components to CE

51 h, accompanying significant rearrangement of cytoskeletal proteins and plasma membranes.

52 at were biotinylated, including membrane and cytoskeletal proteins and proteins involved in lipid met

53 sperm, where they function as intracellular cytoskeletal proteins and secreted hormones.

54 at ERK activation induces phosphorylation of cytoskeletal proteins and the adhesion molecule ICAM-4,

55 d, the majority of the observed changes were cytoskeletal proteins and their regulators.

56 roteins, including calcium-binding proteins, cytoskeletal proteins, and a nucleoprotein.

57 of SMalphaA and other smooth muscle-specific cytoskeletal proteins, and an increase in myofibroblast

58 unctions of specific cell adhesion proteins, cytoskeletal proteins, and crystallins in lens opacities

59 action contains important membrane proteins, cytoskeletal proteins, and cytosolic proteins that are s

60 several membrane or secreted proteins, many cytoskeletal proteins, and many nerve function proteins.

61 es including those encoding myofibrillar and cytoskeletal proteins, and proteins that regulate calciu

62 ity and stability of aquaporin-0, connexins, cytoskeletal proteins, and the mechanical properties of

63 receptors, immunoreceptors, motor proteins, cytoskeletal proteins, and their associated molecules.

64 ally alter key protein domains-especially in cytoskeletal proteins-and can harbor disease-causing mut

65 Cytoskeletal proteins anillin and septin have been found

66 Cytoskeletal proteins ankyrin-G (AnkG) and betaIV-spectr

67 how this is caused by proteolysis of the AIS cytoskeletal proteins ankyrinG and betaIV spectrin by th

68 The activity-regulated cytoskeletal protein Arc (also known as Arg3.1) is requi

69 Mutations in sarcomeric and cytoskeletal proteins are a major cause of hereditary ca

70 croRNAs) that control upstream regulators of cytoskeletal proteins are also increased in 24p3(-/-) ne

71 These cytoskeletal proteins are dynamic, but the driving force

72 Multi-protein complexes organized by cytoskeletal proteins are essential for cell wall biogen

73 and talin-1, another FERM domain-containing cytoskeletal protein, are required for integrin activati

74 ally regulated protease substrates comprised cytoskeletal proteins as well as intermediate filaments.

75 n addition, decreased vinculin (P < 0.05), a cytoskeletal protein associated with adherens junctions

76 atterned substrates, and imaged adhesion and cytoskeletal proteins at the ventral surface of growth c

77 Inhibition of MMP-9 increased the levels of cytoskeletal protein beta-dystroglycan and neural nitric

78 enerative disease caused by mutations in the cytoskeletal protein beta-III-spectrin.

79 The mammalian cytoskeletal proteins beta- and gamma-actin are highly h

80 te attachment, including modification of the cytoskeletal proteins beta-spectrin and PIEZO1.

81 We show that a cytoskeletal protein betaIII spectrin plays a key role f

82 proteins that are highly represented: actin/cytoskeletal protein binding, RNA binding, RNA splicing/

83 that HA-CD44 interaction induces ankyrin (a cytoskeletal protein) binding to MDR1 resulting in the e

84 robably by blocking the dephosphorylation of cytoskeletal proteins by calcineurin.

85 osttranslational folding of actins and other cytoskeletal proteins by the Tcp1-containing ring comple

86 Mass spectrometric studies identified cytoskeletal proteins (caldesmon-1 and vimentin), endopl

87 e identified a biomarker panel composed of 4 cytoskeletal proteins capable of differentiating CHD-pre

88 ted, including calpain-mediated breakdown of cytoskeletal proteins, cdk5 activation, tau hyperphospho

89 The discovery of cytoskeletal protein changes in maternal serum not only

90 v)1.5, without significant alteration of the cytoskeletal protein complex.

91 multiscale process in which nanometer-scale cytoskeletal protein complexes, individual cells, and gr

92 Importantly, the cytoskeletal protein composition of the TM cells was als

93 A small number of scaffolding and cytoskeletal proteins comprising the cytomatrix of the a

94 However, it is unclear how and what cytoskeletal proteins control maturation-associated alte

95 The septins are cytoskeletal proteins controlling behaviors such as cell

96 Further, the cytoskeletal protein cortactin, which is important for e

97 ht chain kinase (nmMLCK), a multi-functional cytoskeletal protein critical to vascular homeostasis, i

98 However, changes in a cytoskeletal protein, dematin, by zinc depletion were id

99 ell morphology has different requirements on cytoskeletal proteins dependent on the topographical env

100 lated cardiomyopathy that is associated with cytoskeletal protein disarray, contractile dysfunction,

101 y generated neurons, these cells express the cytoskeletal protein Doublecortin (DCX), yet they are ge

102 defined the short timescale dynamics of key cytoskeletal proteins during cytokinesis and under mecha

103 yonic splicing patterns of many synaptic and cytoskeletal proteins during differentiation of neuronal

104 The small G protein Rac regulates cytoskeletal protein dynamics in neuronal growth cones a

105 d muscle deterioration caused by lack of the cytoskeletal protein dystrophin.

106 muscle-wasting disease caused by lack of the cytoskeletal protein dystrophin.

107 mdx mouse, a deletion mutant that lacks the cytoskeletal protein, dystrophin.

108 ases, by the complete absence of the 427 kDa cytoskeletal protein, dystrophin.

109 nic disorder caused by the loss of the large cytoskeletal protein, dystrophin.

110 rentially expressed include genes coding for cytoskeletal proteins, enzymes, growth and transcription

111 ly expressed genes included those coding for cytoskeletal proteins, enzymes, transport proteins, extr

112 arious spatial patterns adopted by bacterial cytoskeletal proteins, especially the orientation and le

113 Talin, a cytoskeletal protein essential in mediating integrin act

114 Dystrophin-Dp71 being a key membrane cytoskeletal protein, expressed mainly in Muller cells t

115 resulted in decreased smooth muscle-specific cytoskeletal protein expression levels and reduced contr

116 cluding abnormal mitochondrial distribution, cytoskeletal protein expression, and ion transporter pol

117 NHE-1 protein was co-localized with cytoskeletal protein ezrin in lamellipodia of microglia

118 y was to investigate whether the sublamellar cytoskeletal protein ezrin is causally involved in cold

119 The cytoskeletal proteins ezrin and moesin participate in pa

120 trol over the precise spatial arrangement of cytoskeletal protein filaments is key for mechanical for

121 ues demonstrate that the linkage between the cytoskeletal protein filamin A and the platelet receptor

122 cur through the interaction of ROR2 with the cytoskeletal protein filamin A.

123 sense mutations in the gene that encodes the cytoskeletal protein filamin B (FLNB), but a subset do n

124 The cytoskeletal protein filamin is a key connecting element

125 the AR is driven by calpain cleavage of the cytoskeletal protein filamin, a pathway that shows diffe

126 ween the CFTR N terminus and the multidomain cytoskeletal protein filamin.

127 Actin, a highly conserved cytoskeletal protein found in all eukaryotic cells, faci

128 lar contraction and a major component of the cytoskeletal protein fraction in TM and CM cells, was re

129 to exhibit compositional similarity with the cytoskeletal protein fraction isolated from TM tissue.

130 depolymerization filaments of the bacterial cytoskeletal protein FtsZ (filament temperature-sensitiv

131 Bacterial cytoskeletal protein FtsZ assembles in a head-to-tail ma

132 ia and chloroplasts require the ring-forming cytoskeletal protein FtsZ for division.

133 division typically requires assembly of the cytoskeletal protein FtsZ into a ring (Z-ring) at the na

134 Assembly of the cytoskeletal protein FtsZ into a ring-like structure is

135 The bacterial cytoskeletal protein FtsZ is a GTPase that is thought to

136 iotics; to this end, the essential bacterial cytoskeletal protein FtsZ is a promising target.

137 inhibit the GTPase activity of the bacterial cytoskeletal protein FtsZ with an IC(50) value of 6.7 +/

138 ssembly/disassembly process of the essential cytoskeletal protein FtsZ.

139 mid-chloroplast FtsZ (Z) ring comprising two cytoskeletal proteins, FtsZ1 and FtsZ2.

140 tol 4,5-bisphosphate-binding sequence in the cytoskeletal protein gelsolin.

141 factor (SRF), a regulator of actin and other cytoskeletal protein genes.

142 he largest gene family among the three major cytoskeletal protein groups.

143 d ZO-1/2/3 and between ZO-1/2/3 and numerous cytoskeletal proteins has been demonstrated in vitro, fl

144 Kindlin-2, a widely distributed cytoskeletal protein, has been implicated in integrin ac

145 Kindlin-2, a widely distributed cytoskeletal protein, has been implicated in integrin ac

146 Although several cytoskeletal proteins have been identified as substrates

147 e association between phosphorylation of the cytoskeletal proteins HMW1 and HMW2 and membrane protein

148 tified, previous evidence suggested that the cytoskeletal protein HMW2 forms parallel bundles oriente

149 focal adhesions and associates with numerous cytoskeletal proteins; however, its physiological roles

150 ast, IgD signaling induced activation of the cytoskeletal protein HS1, along with F-actin polymerizat

151 0) promoted the phosphorylation of band 3, a cytoskeletal protein important for the function of the R

152 dant of these host proteins were chaperones, cytoskeletal proteins, importins, proteins involved in u

153 FtsZ is the major cytoskeletal protein in bacteria and a tubulin homologue

154 FtsZ is a tubulin homolog and the major cytoskeletal protein in bacterial cell division.

155 The tubulin homolog FtsZ is the major cytoskeletal protein in bacterial cytokinesis.

156 de new clues to the functional roles of this cytoskeletal protein in the adult brain.

157 le proteolysis of other sarcomeric and actin cytoskeletal proteins in dystrophic skeletal muscle.

158 ockout mice to investigate the role of these cytoskeletal proteins in mechanosensitive (MS) channel g

159 However, the contribution of cytoskeletal proteins in PH is still not fully understoo

160 derstanding of vRNA assembly and the role of cytoskeletal proteins in that process.

161 We hypothesized that degradation of cytoskeletal proteins in the brain can lead to DAI, and

162 However, the role of host cytoskeletal proteins in the cytoplasmic assembly of IAV

163 Force-sensitive cytoskeletal proteins, including myosin II motors and ac

164 ate the expression of smooth muscle-specific cytoskeletal proteins, including SMalphaA, in smooth mus

165 0) and ubiquitinated proteins, trapped other cytoskeletal proteins, including spinophilin, and led to

166 n cortex senses and transmits forces and how cytoskeletal proteins interact in response to the forces

167 Loss of function of KIND1, a cytoskeletal protein involved in beta1-integrin function

168 catenin signaling, and RHOQ, which encodes a cytoskeletal protein involved in insulin-mediated signal

169 Previously we identified ankyrin G (AnkG), a cytoskeletal protein involved in vesicular transport, as

170 Bacterial cells possess multiple cytoskeletal proteins involved in a wide range of cellul

171 late the activities and localization of many cytoskeletal proteins involved in crucial biological pro

172 are conserved guanosine triphosphate-binding cytoskeletal proteins involved in membrane remodeling.

173 Aberrant phosphorylation of neuronal cytoskeletal proteins is a key pathological event in neu

174 n capable of binding to ezrin-radixin-moesin cytoskeletal proteins is essential for optimal in vivo I

175 Aberrant hyperphosphorylation of neuronal cytoskeletal proteins is one of the major pathological h

176 Dystrophin, a cytoskeletal protein, is closely associated with the mem

177 to reside exclusively in the cytoplasm, the cytoskeletal protein keratin 17 (K17) has been recently

178 The cytoskeletal protein Keratin 17 (KRT17;K17) is robustly

179 tastases frequently expressed the epithelial cytoskeletal protein, keratin 14 (K14).

180 in the KRT3 or KRT12 genes, which encode the cytoskeletal protein keratins K3 and K12, respectively.

181 r of membrane-associated proteins (including cytoskeletal proteins, kinases, GTP-binding proteins, an

182 A cytoskeletal protein, KRI-1, plays a key role in the gen

183 hat proteolytic processing of TRAP5b and the cytoskeletal protein L-plastin was altered in cells trea

184 We analyzed the role of a prominent cytoskeletal protein, LEK1, in the immunoregulation of D

185 We examined cytoskeletal protein levels in the cerebral cortex of NF

186 There were dramatic changes in cytoskeletal protein levels, with actin levels increased

187 spectrometry analyses showed that regulatory cytoskeletal proteins, like plastin-2 that bundles actin

188 ClpGM6 is a cytoskeletal protein located within the flagellum along

189 raction and phosphorylation experiments with cytoskeletal proteins, mass spectrometric identification

190 indicate that changes in expression of other cytoskeletal proteins may compensate for decreased NFs.

191 this study illustrates how cytoskeletal protein metabolism is central to trauma and

192 a number of growth regulatory molecules and cytoskeletal proteins, miR-31 is involved in establishin

193 function highlights the flexibility of core cytoskeletal protein motifs, such that one type of cytos

194 Together with the FtsZ cytoskeletal protein, motility participates in the cell

195 of Escherichia coli mutants in the essential cytoskeletal protein MreB for subtle changes in cell sha

196 The cytoskeletal protein MreB is an essential component of t

197 protein with structural similarities to the cytoskeletal protein MreB.

198 The cytoskeletal proteins MreB and FtsZ, which respectively

199 d to inhibit the polymerization of bacterial cytoskeletal proteins, MreB and FtsZ.

200 In cells with cytoskeletal protein mutations, supernumerary ChR1 patch

201 invaginations and channels, and to visualize cytoskeletal proteins nearby.

202 wn that bacteria have elaborate life cycles, cytoskeletal protein networks and complex signal transdu

203 Up-regulated stress and cytoskeletal proteins normalized, whereas reduced contra

204 transmembrane (TM) protein that binds to the cytoskeletal protein, obscurin, and stabilizes the netwo

205 Cytoskeletal proteins of the axon (betaIV spectrin, anky

206 Host cytoskeletal proteins of the ezrin-moesin-radixin (EMR)

207 t regulate the interactions between Jak3 and cytoskeletal proteins of the villin/gelsolin family.

208 insights into the distinct roles of the two cytoskeletal proteins on the recycling processes of SK2

209 kDa), encoded by the single OBSCN gene, are cytoskeletal proteins originally identified in striated

210 Mutation of the cytoskeletal protein ParA specifically disrupted carboxy

211 Bacterial cytoskeletal proteins participate in a variety of proces

212 Understanding how signaling pathways and cytoskeletal proteins pattern cell walls during this for

213 own that through decreased activation of the cytoskeletal protein paxillin, growth factor-induced isc

214 , we demonstrate that CTN-1/alpha-catulin, a cytoskeletal protein, physically interacts with DYB-1/al

215 me'), alpha and dense granules, membrane and cytoskeletal proteins, platelet-derived microparticles,

216 Cytoskeletal proteins play a pivotal role in cytokinesis

217 ro models have revealed beta-III spectrin, a cytoskeletal protein present throughout the soma and den

218 ys despite their compositional similarity in cytoskeletal protein profile.

219 Bringing droplets to life: A cytoskeletal protein (red dots, see scheme) is expressed

220 signaling axis and how its interaction with cytoskeletal proteins regulates migratory and invasive n

221 ell biology, including the identification of cytoskeletal proteins, regulatory pathways, and mechanis

222 Cell wall expansion is orchestrated by cytoskeletal proteins related to actin (MreB) and tubuli

223 yet abnormalities in the signaling roles of cytoskeletal proteins remain largely unexplored.

224 Although many membrane and cytoskeletal proteins remained at their normal levels, t

225 d adhesions have revealed that signaling and cytoskeletal proteins reside at characteristic vertical

226 horylation cascade that includes erythrocyte cytoskeletal proteins resulting in changes in the viscoe

227 rotransmitters and their receptors, adhesion/cytoskeletal proteins, scaffold proteins, membrane trans

228 ge macromolecular complexes that can include cytoskeletal proteins, scaffolding proteins, signaling m

229 The cytoskeletal protein Shroom3 is a potent inducer of epit

230 n or AC) and is known to be dependent on the cytoskeletal protein Shroom3.

231 s, and several have been shown to cleave the cytoskeletal protein spectrin in vitro.

232 IP6K3 interacts with the cytoskeletal proteins spectrin and adducin whose altered

233 Our data demonstrate that actin cytoskeletal proteins such as fascin can be explored as

234 lood cells are frequently deformed and their cytoskeletal proteins such as spectrin and ankyrin-R are

235 types and bind directly to F-actin and other cytoskeletal proteins, suggesting ZO-1 and -2 might regu

236 The ubiquitously expressed cytoskeletal protein talin (Tln) is a component of muscl

237 The membrane localization and activation of cytoskeletal protein talin are key steps to initiate the

238 hymal transition (EMT) and together with the cytoskeletal protein talin assemble into a signaling com

239 -generating enzyme PIPKIgamma couples with a cytoskeletal protein talin to control the acquisition of

240 recruit focal adhesion kinase (FAK) and the cytoskeletal protein talin to nascent adhesions.

241 Binding of the cytoskeletal protein talin to the beta3 integrin cytopla

242 The cytoskeletal protein talin, an actin- and beta-integrin

243 The large cytoskeletal protein talin1 is not only pivotal for inte

244 94 expression markedly reduced levels of the cytoskeletal protein talin2 and specifically inhibited l

245 llular localization in concert with talin, a cytoskeletal protein targeted to focal adhesions.

246 ute microdialysis measurements of the axonal cytoskeletal protein tau in the brain extracellular spac

247 ty with beta-actin, forms a complex with the cytoskeletal proteins Tes and Mena in the subacrosomal l

248 n the gene encoding dystrophin, a structural cytoskeletal protein that also targets other proteins to

249 Cofilin is a major cytoskeletal protein that binds to both monomeric actin

250 Talin is a cytoskeletal protein that binds to integrin beta cytopla

251 mediated phosphorylation of filamin, a major cytoskeletal protein that can adopt an autoinhibited con

252 order characterized by loss of dystrophin, a cytoskeletal protein that connects the actin cytoskeleto

253 tor of integrin activation is talin, a large cytoskeletal protein that exists in an autoinhibited sta

254 tor of bacterial cell division, is a dynamic cytoskeletal protein that forms helices that condense in

255 Dematin is a broadly expressed membrane cytoskeletal protein that has been well characterized in

256 Talin is a large cytoskeletal protein that is involved in coupling the in

257 Doublecortin (DCX) is a cytoskeletal protein that is primarily expressed by neur

258 One gene at 6p22 is CAP2, which encodes a cytoskeletal protein that regulates actin dynamics.

259 SSeCKS/Gravin/AKAP12 ("SSeCKS") encodes a cytoskeletal protein that regulates G(1) --> S progressi

260 pectraplakins are an ancient family of giant cytoskeletal proteins that are essential for a diverse s

261 nical unfolding, and it can bind and recruit cytoskeletal proteins that are involved in mechanotransd

262 the redistribution of chaperones to damaged cytoskeletal proteins that are known targets for acrolei

263 Septins are cytoskeletal proteins that assemble into nonpolar filame

264 he links that exist between PAR networks and cytoskeletal proteins that both regulate PAR protein loc

265 neurons, interacts with adducins, which are cytoskeletal proteins that cap actin filaments' fast-gro

266 ne phosphorylation of enzymes, adaptors, and cytoskeletal proteins that collectively propagate the si

267 alization of actin and the ERM proteins, key cytoskeletal proteins that connect the plasma membrane t

268 Neurofilaments are intermediate cytoskeletal proteins that contribute to neuron structur

269 Cytoskeletal proteins that directly interact with the C

270 Septins are a family of 14 cytoskeletal proteins that dynamically form hetero-oligo

271 Cells are made up of complex assemblies of cytoskeletal proteins that facilitate force transmission

272 involves interaction of viral proteins with cytoskeletal proteins that form the nanotube connections

273 rganelles that are enriched with adaptor and cytoskeletal proteins that regulate signal transduction.

274 Several cytoskeletal proteins that were abundant in wild-type co

275 l conservation often observed for eukaryotic cytoskeletal proteins, the bacterial counterparts can di

276 mized phenotypic clustering and identify new cytoskeletal proteins, their functional hierarchy and pa

277 filaments via promiscuous interactions with cytoskeletal proteins, thus inducing apoptosis.

278 ows pinpointing the contribution of distinct cytoskeletal proteins to nuclear mechanical state in phy

279 Eukaryotic and prokaryotic cells use cytoskeletal proteins to regulate and modify cell shape.

280 educes rapid redistribution of the important cytoskeletal proteins to the periphery and their associa

281 Here we show that the same mutations in the cytoskeletal protein tubulin that alter asymmetry in pla

282 t down-regulation of the intestinal-specific cytoskeletal protein villin in MSI colon cancer, with co

283 Chemerin also increased expression of the cytoskeletal protein vimentin, implicating hypothalamic

284 observed that MBP-1 interacts with the host cytoskeletal protein vimentin.

285 our data uncover a novel mechanism whereby a cytoskeletal protein, vimentin, acts as a break on diffe

286 IpaA binds directly to and activates the cytoskeletal protein vinculin after injection in the hos

287 The cytoskeletal protein vinculin is a major regulator of ce

288 thought to involve its interactions with the cytoskeletal protein vinculin.

289 he mesenchymal protein signature enriched in cytoskeletal proteins was found to be predictive of surv

290 c surfactant insoluble fraction enriched for cytoskeletal proteins was isolated from human and porcin

291 ber of a rapidly growing family of bacterial cytoskeletal proteins, was previously proposed to resemb

292 g live cells expressing fluorescently tagged cytoskeletal proteins, we observed that actin stress fib

293 /NFTs, none of these phosphorylated neuronal cytoskeletal proteins were found.

294 Unexpectedly, the cytoskeletal proteins were not detected at nicotinic syn

295 r mechanism of interactions between Jak3 and cytoskeletal proteins where tyrosine phosphorylation of

296 of one or more members of a large family of cytoskeletal proteins, whose expression is cell- and tis

297 e the cell, we achieved specific labeling of cytoskeletal proteins with green and red fluorophores.

298 encoded by the single OBSCN gene, are giant cytoskeletal proteins with structural and regulatory rol

299 he level of interaction between Cx43 and the cytoskeletal protein ZO-1 is exclusively decreased at th

300 ew insights into the dynamic movement of the cytoskeletal protein zyxin.