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

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

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

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

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

10 y affect large T binding to a cellular DnaK, heat shock protein 70.

11 o associated with high levels of cytoplasmic heat shock protein 70.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

33 er, recent discoveries of mitochondrial-like heat shock protein 70 and/or chaperonin 60 (cpn60) genes

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

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

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

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

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

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

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

41 4 associates with high mobility group box 1, heat shock protein 70, and heat shock protein 90; negati

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

58 that reacted in immunoblots with recombinant heat shock protein 70 (DmaK from Escherichia coli) but n

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

60 ons in infected mice did not usually express heat shock protein 70 except focally in a few tumors.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

75 ovel and differs from the CBF that activates heat shock protein 70 gene expression.

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

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

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

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

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

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

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

83 erved a significant decrease in constitutive heat shock protein 70 (HSC 70) in RAW cells, but not in

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

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

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

87 gate the regulation of the expression of the heat shock protein-70 (HSP-70) gene.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

128 n (CR) either acutely or chronically, alters heat shock protein 70 (hsp70) gene expression in the gut

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

159 Heat shock protein 70 (Hsp70) molecular chaperones play

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

161 nicillamine (SNAP) induced the expression of heat shock protein 70 (HSP70) mRNA and protein, which wa

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

163 Preferential translation of Drosophila heat shock protein 70 (Hsp70) mRNA requires only the 5'-

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 of Saccharomyces cerevisiae showed that the heat shock protein 70 (Hsp70) products of these genes, p

171 is controlled by the Drosophila melanogaster heat shock protein 70 (hsp70) promoter and epitope tagge

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

190 1 and 3, and a 70-kDa band was identified as heat shock protein 70 (hsp70), both of which are known a

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

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

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

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

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

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

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

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

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

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

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

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

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

204 ression of SSA1, which encodes a cytoplasmic heat shock protein 70 (Hsp70).

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

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

207 se (ATPase) domain of Escherichia coli DnaK [heat shock protein 70 (Hsp70)] was determined at 2.8 ang

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

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

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

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

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

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

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

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

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

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

218 ucleus (mac) of Oxytricha nova (On) encoding heat-shock protein 70 (Hsp70) was cloned and sequenced.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

243 atory reported previously that overexpressed heat shock protein 70 kDa (HSP-70) inhibited the activat

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

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

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

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

248 The heat shock protein 70 kDa sequences (HSP70) are of great

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 histochemistry and in situ hybridization for heat shock protein 70 revealed that individual hepatocyt

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

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

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