ライフサイエンスコーパス: heat-shock protein 70

1 reas in association with the immune adjuvant heat shock protein 70.

2 mass spectrometry to be actin, vimentin, and heat shock protein 70.

3 led us to consider HDJ-2, a co-chaperone of heat shock protein 70.

4 ha-synuclein through increased expression of heat shock protein 70.

5 in control DCs, covalently bind to chaperone heat shock protein 70.

6 sponse in vitro as measured by expression of heat shock protein 70.

7 hesis that curcumin can induce expression of heat shock protein 70.

8 l activity of HSF-1 and the transcription of heat shock protein 70.

9 The peptide was also shown to bind to heat shock protein 70.

10 ill being immunosuppressive, did not bind to heat shock protein 70.

11 rmed for glypican 3, glutamine synthase, and heat shock protein 70.

12 ogenes escape were partially attributable to heat shock protein-70.

13 ive protein, fibrin degradation product, and heat shock protein-70.

14 esis and mass spectrometry demonstrated that heat shock protein 70-1A (Hsp70-1A) protein levels were

15 as purified from mouse testis that contained heat shock protein 70-2, a testis-specific chaperone, an

16 Heat shock proteins 70, 90, and the TCP-1 ring complex h

17 lude the co-chaperone ST13, which stabilizes heat-shock protein 70, a modifier of alpha-synuclein mis

18 PanKs belong to the acetate and sugar kinase/heat shock protein 70/actin (ASKHA) protein superfamily

19 ifies a regulatory locus in the sugar kinase/heat shock protein 70/actin superfamily and suggests rel

20 as a member of the "acetate and sugar kinase/heat shock protein 70/actin" (ASKHA) superfamily.

21 Additionally heat shock protein 70 acts as one component of a bimodal

22 CA1-3 subfields and expressed high levels of heat shock protein 70 after kainate administration.

23 The protective effects of CREB and heat-shock protein 70 against polyQ are additive, sugges

24 up-regulation of superoxide dismutase 1 and heat shock protein 70, all consistent with increased oxi

25 ls exclusively through Toll-like receptor 4, heat shock protein 70 also signals through Toll-like rec

26 ed for 12 to 24 h at 38 degrees C accumulate heat shock protein 70 and develop a thermotolerance that

27 broblast growth factor), protein chaperones (heat shock protein 70 and glucose regulated protein 78),

28 in degrading enzyme and chaperone molecules (heat shock protein 70 and heat shock cognate protein 70)

29 eads to the association of nascent apoB with heat shock protein 70 and to its predisposition to ubiqu

30 Mechanisms of action included increasing heat shock protein 70 and truncating temperature-induced

31 The interaction between the Heat Shock Proteins 70 and 40 is at the core of the ATPa

32 Binding of TFAM with chaperones (heat shock proteins 70 and 60, Hsp70 and Hsp60 respectiv

33 racts with alpha-, beta-, and gamma-tubulin, heat shock proteins 70 and 90 (HSP-70; HSP-90), and the

34 In particular, protein chaperones (heat shock proteins 70 and 90), which aid protein foldin

35 Here we present evidence that implicates heat shock proteins 70 and 90, chemokine receptor 4 and

36 observed for several abundant proteins (e.g. heat shock proteins 70 and 90, Rubisco large subunit, an

37 and organization; prominent members include heat shock proteins 70 and 90.

38 ecrosis factor-alpha, heat shock protein 40, heat shock protein 70, and heat shock protein 90 by enzy

39 4 associates with high mobility group box 1, heat shock protein 70, and heat shock protein 90; negati

40 wever, several other stress genes (catalase, heat shock protein 70, and p53) were unaltered.

41 e of NOS2 inducers, as well as expression of heat shock protein 70, and the heat shock response due t

42 NA binding activity, and increased levels of heat shock protein 70, and these responses were not alte

43 eactive protein, fibrin degradation product, heat shock protein-70, and suPAR were measured in 3278 p

44 th nuclear domain 10 [ND10] structures), and heat shock protein 70- and 60-kDa isoforms (Hsp70 and Hs

45 removed or hydrolyzed ATP; in addition, anti-heat-shock protein 70 antiserum abrogated the activity t

46 sed the expression of heat shock protein 90, heat shock protein 70, Bcl-2, Bcl-xL, and cyclooxygenase

47 difference in expression of mRNA levels for heat shock protein 70, bcl-2, caspase 3, caspase 9 and i

48 e circumstances, DJ-1 increased the level of heat shock protein 70 but did not change the glutathione

49 s of curcumin and analyzed for expression of heat shock protein 70 by Western blot.

50 proteins such as Mycobacterium tuberculosis heat shock protein 70, calreticulin, domain II of Pseudo

51 proteins such as Mycobacterium tuberculosis heat shock protein 70, calreticulin, or the sorting sign

52 f DNA encoding Bcl-x(L) with DNA encoding E7/heat shock protein 70, calreticulin/E7, or Sig/E7/LAMP-1

53 and upregulated C1q, heat shock protein 60, heat shock protein 70, CCR2, and CXCL16 transcripts in r

54 r-HSVtk), combined with a plasmid expressing heat shock protein 70 (CMV-hsp70), along with systemic g

55 Tg overexpression of heat shock protein 70 could not rescue the phenotype of

56 , urease B, ABC transporter binding protein, heat shock protein 70 (DnaK), and alkyl hydroperoxide re

57 istones and other proteins, including HSP70 (heat-shock protein 70), estrogen receptor alpha, and RNA

58 Ileum heat shock protein 70 expression increased (P<0.05), whi

59 tic diversity is an important determinant of heat shock protein 70 expression involving local, likely

60 on of the heat shock response (as assayed by heat shock protein 70 expression).

61 ation is dependent on ATM but independent of heat shock protein 70 expression.

62 Discrete increases in heat shock protein-70 expression in dentine coincided wi

63 n of a heat shock response was determined by heat shock protein-70 expression.

64 Members of the eukaryotic heat shock protein 70 family (Hsp70s) are regulated by p

65 xorubicin treatment through interaction with heat shock protein 70 family proteins, causing their dea

66 bulin binding protein (BiP), a member of the heat shock protein 70 family, and vascular cell adhesion

67 les first through complex formation with the heat shock protein 70 family, specifically heat shock co

68 mbers of the antiapoptotic protein chaperone heat shock protein 70 family.

69 mploys specific primers from a member of the heat shock protein 70 family.

70 iculum member of the highly conserved HSP70 (heat shock protein 70) family of molecular chaperones.

71 dominant negative PI3K mice, and deletion of heat shock protein 70 from banded caPI3K mice had no eff

72 n the 39.5 degrees C cells in the absence of heat shock protein-70 gene activation.

73 s the assertion that an overlapping ORF of a heat-shock protein-70 gene, which exhibits some similari

74 ted by the protease activated receptor 2 and heat shock protein 70, have been described.

75 nown inhibitors of the apoptosome, including heat shock protein 70, heat shock protein 90, or X-linke

76 r no overlap with ubiquitin, proteasome, and heat shock protein 70/heat shock cognate 70 immunoreacti

77 Conversely, heat shock protein 70/heat shock cognate 70 was acetylat

78 Prior studies demonstrate that the heat shock protein 70 homolog, Ssa1, significantly contr

79 perones from the constitutive/heat-inducible heat shock protein 70 (Hsc/p70) family have been shown t

80 tion for inducible (Hsp70i) and constitutive heat shock protein 70 (Hsc70) in chronically hypoxic and

81 Three markers, heat shock protein 70 (HSP-70), chemokine (C-X-C motif)

82 tonic media there was activation of TauT and heat shock protein-70 (HSP-70) reporter activity and inc

83 Recent data suggest that heat shock protein-70 (HSP-70), an intracellular protein

84 Heat-shock protein 70 (HSP 70) plays a role in myocardia

85 Xenon exposure enhanced the expression of heat-shock protein 70 (HSP-70) and heme oxygenase 1 (HO-

86 Chaperone genes HSP70 (heat-shock protein 70), HSP60 and HSP27 significantly in

87 sembly of the replicase complex required the heat shock protein 70 (Hsp70 = yeast Ssa1/2p) present in

88 analysis to measure changes in expression of heat shock protein 70 (HSP70 cytoplasmic), HSP60 (mitoch

89 a 121-nucleotide sequence from the C. parvum heat shock protein 70 (hsp70 mRNA from U71181 gene).

90 Heat shock protein 70 (HSP70) acts in concert with sever

91 mong the members of the chaperone family are heat shock protein 70 (Hsp70) and 90 (Hsp90).

92 Tid1 also is known as a cochaperone of heat shock protein 70 (HSP70) and binds to HSP70 through

93 necrosis factor alpha (TNF-alpha) as well as heat shock protein 70 (HSP70) and Caspase 11 were found

94 e critical to the protein-folding machinery: heat shock protein 70 (Hsp70) and cochaperone heat shock

95 Heat shock protein 70 (Hsp70) and Hsp90 are molecular ch

96 say and identified the Cns1p cochaperone for heat shock protein 70 (Hsp70) and Hsp90 chaperones as a

97 nresolved function, binds concomitantly with heat shock protein 70 (Hsp70) and Hsp90, participates wi

98 s of ACT1 with other proteins, such as CD40, heat shock protein 70 (HSP70) and HSP90, were not affect

99 stem, we uncovered a surprising role for the heat shock protein 70 (Hsp70) and its ability to bind th

100 Molecular chaperones, such as heat shock protein 70 (Hsp70) and its bacterial ortholog

101 Although both the heat shock protein 70 (HSP70) and the activating transcr

102 lex with the expanded polyglutamine protein, heat shock protein 70 (Hsp70) and the proteasome, which

103 Molecular chaperones such as heat shock protein 70 (Hsp70) are crucial for protein fo

104 We identified heat shock protein 70 (HSP70) as a protein interactor of

105 In addition, we have identified heat shock protein 70 (HSP70) as a rKOR-interacting prot

106 e Vpr activities in fission yeast identified heat shock protein 70 (Hsp70) as a suppressor of Vpr-ind

107 r apoptosis susceptibility protein (CAS) and heat shock protein 70 (Hsp70) as mediators of PHAPI acti

108 In this article, we identify the cellular heat shock protein 70 (Hsp70) as the co-opted host facto

109 de the Trichinella spiralis virulence factor heat shock protein 70 (Hsp70) as well as endogenous Hsp7

110 in vivo, we have generated mice deficient in heat shock protein 70 (hsp70) by replacing the hsp70.1 o

111 re J domain that regulates the activities of heat shock protein 70 (Hsp70) by serving as cochaperone

112 We find that the heat shock protein 70 (Hsp70) chaperone pair Ssa1/Ssa2 a

113 Heat shock protein 70 (HSP70) chaperones play a central

114 rate that, although endogenous expression of heat shock protein 70 (HSP70) did not change during trop

115 lementary to unique sequences present on the heat shock protein 70 (HSP70) DNA/RNA target.

116 The extracellular presence of endotoxin-free heat shock protein 70 (HSP70) enhances the rate and capa

117 Extracellular heat shock protein 70 (Hsp70) exerts profound effects bo

118 Prior thermal stress is associated with heat shock protein 70 (HSP70) expression and protection

119 Inhibitors of heat-induced heat shock protein 70 (HSP70) expression have the potent

120 ment promoted hypertonicity-induced AQP1 and heat shock protein 70 (HSP70) expression in both N100 an

121 Molecular chaperones of the heat shock protein 70 (Hsp70) family counteract protein

122 unctions of the most abundant variant of the heat shock protein 70 (Hsp70) family in the brain, heat

123 The ER heat shock protein 70 (Hsp70) family member BiP is an AT

124 J domain through which it interacts with the heat shock protein 70 (Hsp70) family of chaperone protei

125 The versatile functions of the heat shock protein 70 (Hsp70) family of molecular chaper

126 aperones, such as those that are part of the heat shock protein 70 (Hsp70) family of proteins that bi

127 The highly conserved nature of the heat shock protein 70 (Hsp70) family, in conjunction wit

128 Heat shock protein 70 (HSP70) gene transfection has been

129 Heat shock protein 70 (Hsp70) has gained a lot of attent

130 Anti-heat shock protein 70 (HSP70) IgG was isolated from plas

131 ed using standard histochemical staining and heat shock protein 70 (HSP70) immunohistochemical staini

132 xamined the expression of the widely studied heat shock protein 70 (hsp70) in an in vitro-generated g

133 Heat shock protein 70 (Hsp70) in complex with bcl2 assoc

134 he potential role of the molecular chaperone heat shock protein 70 (HSP70) in prion replication in vi

135 olded proteins reveals an unexpected role of heat shock protein 70 (Hsp70) in promoting aggresome for

136 inner ear tissue released exosomes carrying heat shock protein 70 (HSP70) in response to heat stress

137 Increased expression of heat shock protein 70 (HSP70) in the brain has been exte

138 ated with an up-regulation of cytoprotective heat shock protein 70 (HSP70) in the ischemic brain hemi

139 d cleavage by interaction with the chaperone heat shock protein 70 (Hsp70) in the nucleus.

140 The role of heat shock protein 70 (Hsp70) in virus replication has b

141 Heat shock protein 70 (Hsp70) induction and specific cli

142 ty and depression levels are associated with Heat Shock Protein 70 (HSP70) induction in the colon of

143 ith the pharmacochaperone noribogaine or the heat shock protein 70 (HSP70) inhibitor pifithrin-mu suc

144 The discovery and development of heat shock protein 70 (Hsp70) inhibitors is currently a

145 We recently showed that the induction of heat shock protein 70 (HSP70) inhibits ototoxic drug-ind

146 Stress-inducible heat shock protein 70 (hsp70) interacts with superoxide

147 Heat shock protein 70 (Hsp70) is a highly conserved and

148 Heat shock protein 70 (hsp70) is a potent adjuvant that

149 The highly conserved heat shock protein 70 (Hsp70) is a ubiquitous molecular

150 Heat shock protein 70 (Hsp70) is an important emerging c

151 Heat shock protein 70 (Hsp70) is an important molecular

152 Upregulation of heat shock protein 70 (HSP70) is beneficial in cardiopro

153 Heat shock protein 70 (Hsp70) is incorporated within the

154 Heat shock protein 70 (Hsp70) is well documented to poss

155 CRP), fibrin degradation products (FDP), and heat shock protein 70 (HSP70) levels-would be a powerful

156 and slightly lagging behind the increase in heat shock protein 70 (HSP70) levels.

157 uired for nuclear speckle association of the heat shock protein 70 (Hsp70) locus.

158 lutinin-tagged TRIM5alpha suggested that the heat shock protein 70 (Hsp70) may serve as a TRIM5alpha-

159 ING IMMUNOGLOBULIN PROTEIN (BIP), encoding a heat shock protein 70 (HSP70) molecular chaperone, reduc

160 gies to afford a series of modulators of the heat shock protein 70 (Hsp70) molecular chaperone.

161 Heat shock protein 70 (Hsp70) molecular chaperones play

162 -terminal nucleotide-binding domain (NBD) of heat shock protein 70 (Hsp70) molecular chaperones reduc

163 ase mRNA during virus infection and in human heat shock protein 70 (hsp70) mRNA for selective transla

164 ransproter (SMIT), aldose reductase (AR) and heat shock protein 70 (HSP70) mRNA were significantly de

165 as a model Ag to Mycobacterium tuberculosis heat shock protein 70 (HSP70) on the potency of Ag-speci

166 ect of linkage to Mycobacterium tuberculosis heat shock protein 70 (HSP70) on the potency of antigen-

167 Heat shock protein 70 (Hsp70) plays a central role in pr

168 The molecular chaperone heat shock protein 70 (Hsp70) plays a vital role in cell

169 Molecular chaperone Heat Shock Protein 70 (Hsp70) plays an important protect

170 Heat shock protein 70 (HSP70) protects the gastric mucos

171 and that pkr disruption profoundly inhibits heat shock protein 70 (HSP70) synthesis and blocks the d

172 ion (IR); however, hyperthermia also induces heat shock protein 70 (HSP70) synthesis and HSP70 expres

173 urface plasmon resonance (SPR) biosensor and heat shock protein 70 (Hsp70) that recognizes and traps

174 across the substrate binding domain (SBD) of heat shock protein 70 (Hsp70) to pinpoint mechanical uni

175 tress response, as determined by the lack of heat shock protein 70 (Hsp70) upregulation after several

176 afety and efficacy of the vaccine candidate, heat shock protein 70 (HSP70) was inserted into the rVSV

177 characterized at 50-1000 mg/L, and levels of heat shock protein 70 (hsp70) were characterized at subl

178 y of SPIONs by coating them with recombinant heat shock protein 70 (Hsp70) which is known to chaperon

179 The interaction of human heat shock protein 70 (HSP70) with human apurinic/apyrim

180 a42 neurotoxicity through engineering of the Heat shock protein 70 (Hsp70), a chaperone that has demo

181 aptors that provide substrate specificity to heat shock protein 70 (Hsp70), a molecular chaperone.

182 th gold nanoparticles to sensitively analyze heat shock protein 70 (HSP70), a potential biomarker tha

183 blot analysis showed elevated expression of heat shock protein 70 (HSP70), a putative cardioprotecti

184 We also found that heat shock protein 70 (Hsp70), although not required for

185 The tombusvirus replicase complex contains heat shock protein 70 (Hsp70), an abundant cytosolic cha

186 ified up-regulation of the inducible form of heat shock protein 70 (Hsp70), and further explored the

187 d a robust increase in the folding chaperone heat shock protein 70 (Hsp70), and NAC mitigated this ef

188 onstrate that heat shock protein 90 (Hsp90), heat shock protein 70 (Hsp70), and several cochaperones

189 1 and 3, and a 70-kDa band was identified as heat shock protein 70 (hsp70), both of which are known a

190 ds on the TPR1 domain known to interact with heat shock protein 70 (Hsp70), but not on the TPR2 domai

191 ds on the TPR1 domain known to interact with heat shock protein 70 (Hsp70), but not on the TPR2 domai

192 antibodies (intrabodies) and the chaperone, heat shock protein 70 (Hsp70), have each shown potential

193 Dimeric yeast Mge1, the cochaperone of heat shock protein 70 (Hsp70), is essential for exchangi

194 n and metalloprotease domain 22 (Adam22) and heat shock protein 70 (Hsp70), respectively.

195 ession of molecular chaperones, specifically heat shock protein 70 (Hsp70), suppresses phenotypes rel

196 Here, we reported that heat shock protein 70 (Hsp70), which is thought to prote

197 tions, which is consistent with conventional heat shock protein 70 (HSP70)-client interaction mechani

198 In the current study, we have generated heat shock protein 70 (Hsp70)-secreting murine ovarian c

199 ation after pre-fusion the HyT degrader with heat shock protein 70 (HSP70).

200 relies on a multiprotein complex formed with heat shock protein 70 (Hsp70).

201 this fusion enzyme is the ability to recruit heat shock protein 70 (Hsp70).

202 lowing a blood meal prompts the synthesis of heat shock protein 70 (Hsp70).

203 forms of nitric oxide synthase activity, and heat shock protein 70 (Hsp70).

204 ically, resulted in a robust upregulation of heat shock protein 70 (HSP70).

205 ate with ATP-dependent chaperones, including heat shock protein 70 (Hsp70).

206 ccumulation of complexes containing GC-A and heat shock protein 70 (hsp70).

207 e factors (NEFs) for the molecular chaperone heat shock protein 70 (Hsp70).

208 ochondrial membrane 34 (TOMM34) orchestrates heat shock protein 70 (HSP70)/HSP90-mediated transport o

209 The heat shock protein 70 (Hsp70):c-terminus of Hsp70-intera

210 llular stress response protein and chaperone heat shock protein-70 (Hsp70).

211 Heat shock proteins 70 (hsp70) derived from tissues and

212 enous heat-inducible transcripts--intronless heat-shock protein 70 (HSP70) and intron-containing HSP8

213 ads to time and dose dependent activation of heat-shock protein 70 (Hsp70) as well as Hsp32 in EC.

214 The intracellular chaperone heat-shock protein 70 (Hsp70) can be secreted from cells

215 The ATP-dependent protein chaperone heat-shock protein 70 (Hsp70) displays broad anti-aggreg

216 Heat-shock protein 70 (hsp70) is a stress-responsive gen

217 function and tumor-associated expression of heat-shock protein 70 (HSP70) is consistent with HSP70 f

218 As reported previously, overexpression of heat-shock protein 70 (Hsp70) rescues polyglutamine-depe

219 contributing factor in tauopathies, and the heat-shock protein 70 (Hsp70) seems to play an important

220 ultiple DAMPs, including calreticulin (CRT), heat-shock protein 70 (HSP70), and HSP90 on their plasma

221 es heat-shock cognate 71-kDa protein (HSC70)/heat-shock protein 70 (HSP70), HSP90, and J-domain co-ch

222 The heat-shock protein 70 (Hsp70)-based import motor, associ

223 ng-pad insertion lines containing 1360 and a heat-shock protein 70 (hsp70)-driven white reporter to e

224 some-mediated pathway in a manner similar to heat-shock protein 70 (Hsp70).

225 d to unfractionated tumor lysate or purified heat-shock protein 70 (HSP70).

226 Heat shock protein 70s (Hsp70s) are encoded by a multige

227 The heat shock protein 70s (HSP70s) are molecular chaperones

228 Elevated levels of the inducible heat-shock protein 70 (Hsp72) have been implicated in ma

229 Overexpression of the inducible heat shock protein 70, Hsp72, has broadly cytoprotective

230 tern (DAMP) response including elevations in heat-shock protein 70, IL-1, IL-18, and TNFalpha indicat

231 ive protein, fibrin degradation product, and heat shock protein-70 improved risk reclassification.

232 However, the involvement of heat shock protein 70 in adaptation to chronic hypoxemia

233 eurotrophic factor and the protein chaperone heat-shock protein-70 in the striatum and cortex, which

234 n-ubiquitinated exosomal proteins, including heat shock protein 70, in comparison with exosomes isola

235 kin-10 levels decreased after P, H, and P/H; heat shock protein 70 increased after P; and interleukin

236 lial and inducible NO synthase isoforms, and heat shock protein 70), increased expression of the hypo

237 The mechanism of heat shock protein 70 induction depends on activation of

238 ein 90, glutathione S-transferase (GST), and heat shock protein 70 interacted with maspin with the hi

239 and ubiquitin ligase, the C-terminal Hsp70 (heat shock protein 70)-interacting protein (CHIP) links

240 iated ubiquitin (Ub) E3 ligase C terminus of heat shock protein 70-interacting protein (CHIP), increa

241 amma-amino-n-butyric acid transporter 1, and heat shock protein 70) is also decreased in the medulla

242 D), aconitase, glutathione peroxidase (GPx), heat shock protein 70, isoprostane, and reactive oxygen

243 tion of different posttranslational forms of heat shock protein 70 kD.

244 The constitutively expressed heat shock protein 70 kDa (Hsc70) is a major chaperone p

245 Heat Shock Protein 70 kDa (Hsp70) family molecular chape

246 The heat shock protein 70 kDa (Hsp70)/DnaJ/nucleotide exchan

247 Bag1 is a regulator of heat shock protein 70 kDa (Hsp70/Hsc70) family proteins

248 Overexpression of heat shock protein 70 kDa alters the susceptibility of t

249 Hsp70s (heat shock protein 70 kDa) are central to protein foldin

250 Hsp70 (heat shock protein 70 kDa) chaperones are key to cellula

251 osteroviruses encode a homolog of the HSP70 (heat shock protein, 70 kDa) family of cellular proteins.

252 Cellular protein homeostasis depends on heat shock proteins 70 kDa (Hsp70s), a class of ubiquito

253 ripts--namely, for Fc gamma receptor IIA and heat-shock protein (70 kDa)--that were significantly ass

254 several other cancer cell types, depend upon heat-shock protein 70 kDA (HSP70) for survival.

255 erize signal propagation in Escherichia coli heat-shock protein 70-kDa.

256 Furthermore, plasma heat shock protein 70 levels were negatively correlated

257 n 70, which did not affect non-ubiquitinated heat shock protein 70 levels.

258 -5 DNA binding activity and up-regulation of heat shock protein 70 levels.

259 sults indicate the possible involvement of a heat-shock protein 70-linked peptide chaperone in a cros

260 ar factor-kappaB for their ability to induce heat shock protein 70 may be a valid screening method to

261 itic RNAs, including Cdg7_FLc_0990, involved heat-shock protein 70-mediated nuclear importing mechani

262 efore tested and showed that upregulation of heat shock protein 70 mitigates CAG-repeat RNA toxicity.

263 disturbances in liver function, induction of heat shock protein 70, modulation of trace elements, alt

264 factor 1 (HSF1) and induction of target gene heat shock protein 70 (molecular weight, 70 kDa) confirm

265 gamma-amino-n-butyric acid transporter 1 and heat shock protein 70 mRNA in osmotically stressed MDCK

266 Heat shock protein-70 mRNA expression was not detectable

267 Mitochondrial heat shock protein 70 (mtHsp70) functions in unfolding,

268 ased neuronal staining for the mitochondrial heat shock protein 70 (mtHSP70) stress marker.

269 process is facilitated by the mitochondrial heat shock protein 70 (mtHsp70), a chaperone contributin

270 otif and the chaperone protein mitochondrial heat shock protein 70 (mtHsp70).

271 Here we provide evidence that when purified heat shock protein 70 or chaperone-rich cell lysate (CRC

272 Heat shock protein 70-peptide complexes (Hsp70.PC-F) wer

273 In previous studies, we have shown that heat shock protein 70-peptide complexes (HSP70.PCs) deri

274 Mortalin/GRP75, the mitochondrial heat shock protein 70, plays a role in cell protection f

275 hypoxia-inducible factors 1alpha and 2alpha, heat shock protein 70, presence of nitrotyrosine residue

276 protein, lactate dehydrogenase activity, and heat shock protein 70; promoted the activation of NF-kap

277 hat expression of a heterologous gene with a heat shock protein 70 promoter could be elevated to 500-

278 by a marked attenuation in induction of the heat shock protein 70 promoter driven-luciferase reporte

279 ied by transiently transfecting cells with a heat shock protein 70 promoter-luciferase reporter plasm

280 d to the CBF which was shown to activate the heat shock protein 70 promoter.

281 gene under the control of a human inducible heat shock protein 70 promotional sequence.

282 ve protein, fibrin degradation products, and heat shock protein-70 representing these 3 pathways was

283 ing commercially available recombinant human heat shock protein 70 (rhHsp70), recent studies have sho

284 pendent of phosphoinositide 3-kinase-Akt and heat-shock protein 70; signalling mediators often defect

285 and show that heat shock protein 90, but not heat shock protein 70, stabilizes bluetongue virus prote

286 nd the phosphate binding motifs of the actin/heat shock protein 70/sugar kinase superfamily, a human

287 xtracts induced glutathione transferases and heat shock protein 70, suggesting that the toxicity also

288 ro and a more efficient cooperation with the heat shock protein 70 system in client folding.

289 Curcumin induced expression of heat shock protein 70, the major inducible heat shock pr

290 Curcumin-mediated expression of heat shock protein 70 was reduced substantially in fibro

291 factor-1 in curcumin-mediated expression of heat shock protein 70 was tested in embryonic fibroblast

292 and placental levels of 4-hydroxynonenal and heat shock protein 70 were increased while placental hea

293 cofilin, tubulin, heat shock protein 90, and heat shock protein 70 were substantial components.

294 r-associated molecular patterns (EN-RAGE and heat shock protein 70) were substantially higher in pati

295 ppocampal pyramidal neurons or expression of heat shock protein 70, whereas wild-type mice lost 68-79

296 exosomes with higher levels of ubiquitinated heat shock protein 70, which did not affect non-ubiquiti

297 likely in response to the endogenous ligand heat shock protein 70, which was found to be elevated in

298 t of either glucose-related 78 kd protein or heat shock protein 70 with >/= 14 mg/m(2) and decreased

299 in the key proteins in aldose reductase and heat-shock protein-70 within living cancer cells.

300 This method is based on the Xenopus heat shock protein 70 (Xhsp70 [3]) promoter driving the