ライフサイエンスコーパス: cytoskeletal protein

1 membrane to the basal lamina and underlying cytoskeletal proteins.

2 ulated process under the control of specific cytoskeletal proteins.

3 widespread functional homologs of eukaryotic cytoskeletal proteins.

4 ter regulation by intracellular signaling or cytoskeletal proteins.

5 mechanisms regulating the function of these cytoskeletal proteins.

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

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

8 switch for the interactions between Jak3 and cytoskeletal proteins.

9 ls suggested dysregulation of sarcomeric and cytoskeletal proteins.

10 ng step during interactions between Jak3 and cytoskeletal proteins.

11 nced matrix deposition, and dysregulation of cytoskeletal proteins.

12 biquitous tubulin and actin superfamilies of cytoskeletal proteins.

13 , cell signaling, and metabolism, as well as cytoskeletal proteins.

14 Bactofilins are fibre-forming bacterial cytoskeletal proteins.

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

16 ttachment complexes and on interactions with cytoskeletal proteins.

17 eptide sequence KRR to ezrin-radixin-moiesin cytoskeletal proteins.

18 gulating transcription factors, enzymes, and cytoskeletal proteins.

19 spatial regulation of cell wall synthesis by cytoskeletal proteins.

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

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

22 Cytoskeletal protein 4.1 also showed dynamic phosphoryla

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

24 were not associated with adverse impacts on cytoskeletal protein abundance in situ, the coexposure o

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

26 ated by supracellular networks formed by the cytoskeletal protein actin and the molecular motor nonmu

27 of MreB, a bacterial homologue of eukaryotic cytoskeletal protein actin F.

28 The cytoskeletal protein actin plays a critical role in main

29 The cytoskeletal protein actin polymerizes into filaments th

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

31 Synapses are enriched in the cytoskeletal protein actin, which determines the shape o

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

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

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

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

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

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

38 The cytoskeletal protein alpha-actinin is shared between the

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

40 ational folding of adjacent domains from the cytoskeletal protein alpha-spectrin using force profile

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

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

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

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

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

46 We found two cytoskeletal proteins among six proteins tightly associa

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

48 s are caused by altered expression levels of cytoskeletal proteins and contribute to muscle wasting a

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

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

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

52 Strikingly, cytoskeletal proteins and enzymes involved in energy met

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

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

55 All4981 interacts with known cytoskeletal proteins and is indispensable for Anabaena

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

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

58 Cytoskeletal proteins and post-translational modificatio

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

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

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

62 protein-protein interaction modules found in cytoskeletal proteins and transcriptional regulators.

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

64 f proteins regulating amino acid metabolism, cytoskeletal proteins, and cellular response to stress.

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

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

67 l as abnormal expression and localization of cytoskeletal proteins, and loss of intracellular nicotin

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

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

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

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

72 Cytoskeletal proteins anillin and septin have been found

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

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

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

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

77 These cytoskeletal proteins are dynamic, but the driving force

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

79 Metabolic, mitochondrial, sarcomeric, and cytoskeletal proteins are susceptible to 4HNE-adduction

80 rowth factor-beta (TGF-beta) pathway and the cytoskeletal proteins are upregulated in rapid aging DPS

81 Cytoskeletal proteins are well conserved between animal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

99 The septins are cytoskeletal proteins controlling behaviors such as cell

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

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

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

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

104 Sarcomeric (myosin) and cytoskeletal proteins (desmin, tubulin) also underwent 4

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

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

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

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

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

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

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

112 enesis proteins that are linked to a dynamic cytoskeletal protein, either the actin-like MreB or the

113 mplicated a role for gamma-adducin (ADD3), a cytoskeletal protein encoded by Add3.

114 otein (MAP) 2 has been perceived as a static cytoskeletal protein enriched in neuronal dendritic shaf

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

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

117 Carcinoma Amplified Sequence 3 (BCAS3) is a cytoskeletal protein essential for EC migration and spro

118 Talin, a cytoskeletal protein essential in mediating integrin act

119 Spectrins are cytoskeletal proteins essential for membrane biogenesis

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

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

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

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

124 age progression via temporal dynamics of the cytoskeletal protein, F-actin.

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

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

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

128 The cytoskeletal protein filamin is a key connecting element

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

130 eterooligomeric complex required for de novo cytoskeletal protein folding.

131 d during myogenic differentiation) and ANK1 (cytoskeletal protein) for diastolic function; TSPAN16 an

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

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

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

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

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

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

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

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

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

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

142 SPECC1L dosage and function and that SPECC1L cytoskeletal protein functions downstream of IRF6 in pal

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

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

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

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

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

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

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

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

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

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

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

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

159 The emerging role of cytoskeletal proteins in the cell nucleus has become a n

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

161 the AIS requires membrane, scaffolding, and cytoskeletal proteins, including Ankyrin-G and TRIM46.

162 he actin-binding domains (ABDs) of conserved cytoskeletal proteins, including beta-III-spectrin, alph

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

164 exists in a complex with a variety of actin cytoskeletal proteins, including paxillin and LPP.

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

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

167 In the cytoplasm, acetylation of a number of cytoskeletal proteins, including tubulin, cortactin, and

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

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

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

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

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

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

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

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

176 The actin family of cytoskeletal proteins is essential to the physiology of

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

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

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

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

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

182 s in Leishmania mexicana have identified the cytoskeletal protein KHARON as being important for both

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

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

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

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

187 ClpGM6 is a cytoskeletal protein located within the flagellum along

188 usly, we showed that a hierarchy of spectrin cytoskeletal proteins maintains nodal Na(+) channels (Li

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

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

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

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

195 The cytoskeletal protein MreB is an essential component of t

196 protein with structural similarities to the cytoskeletal protein MreB.

197 The cytoskeletal proteins MreB and FtsZ, which respectively

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

199 In cells with cytoskeletal protein mutations, supernumerary ChR1 patch

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

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

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

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

204 Cytoskeletal proteins of the axon (betaIV spectrin, anky

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

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

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

208 pecial focus on actin, here we summarize how cytoskeletal proteins operate in the nucleus and how the

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

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

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

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

213 Cytoskeletal proteins play a pivotal role in cytokinesis

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

215 ys despite their compositional similarity in cytoskeletal protein profile.

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

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

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

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

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

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

222 Outer dense fibre 2 (Odf2 or ODF2) is a cytoskeletal protein required for flagella (tail)-beatin

223 The F1-F3 FERM subdomains of cytoskeletal proteins resemble a cloverleaf, but in tali

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

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

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

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

228 The cytoskeletal protein Shroom3 is a potent inducer of epit

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

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

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

232 How then does a non-cytoskeletal protein, SpmX, define and constrain PG synt

233 ed function with other lissencephaly-encoded cytoskeletal proteins such as alpha-N-catenin (CTNNA2) a

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

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

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

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

238 poptotic molecule procaspase 12 and podocyte cytoskeletal protein talin 1.

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

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

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

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

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

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

245 94 expression markedly reduced levels of the cytoskeletal protein talin2 and specifically inhibited l

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

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

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

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

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 in-4 (ACTN4)-an important actin crosslinking cytoskeletal protein that provides structural support fo

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

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

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

260 Septins are cytoskeletal proteins that assemble into nonpolar filame

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

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

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

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

265 Neurofilaments are intermediate cytoskeletal proteins that contribute to neuron structur

266 Cytoskeletal proteins that directly interact with the C

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

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

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

270 Septins are conserved GTP-binding cytoskeletal proteins that polymerize into filaments by

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

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

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

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

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

276 force generators is likely prevented by the cytoskeletal protein titin that connects the thick filam

277 nteractions converge on ankyrin and spectrin cytoskeletal proteins to cluster nodal Na(+) channels du

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

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

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

281 rotective heat shock proteins, disruption of cytoskeletal proteins via histone deacetylases, and the

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

286 The cytoskeletal protein vinculin is a major regulator of ce

287 Although neutrophils express the cytoskeletal protein vinculin, they do not form mature f

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

289 avinculin, a larger isoform of the essential cytoskeletal protein vinculin.

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

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

292 mulatory hydrogels and DCs expressing mutant cytoskeletal proteins, we find that increasing stiffness

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

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

295 Argonaute 1-4, glycolytic enzymes, and cytoskeletal proteins were not detected in exosomes.

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

297 ave also identified endogenous peptides from cytoskeletal proteins, which can be reliably monitored i

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

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

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