ライフサイエンスコーパス: heat-shock protein

1 ants, detoxicants, and molecular chaperones (heat shock proteins).

2 s an endothelial-cell-specifically expressed heat shock protein.

3 e and cyclic AMP signaling and a cytoplasmic heat-shock protein.

4 oplasmic aggregates, which contained Hspa1B (heat shock protein 1B hsp70) and ubiquitinated proteins,

5 /-) heart, however, basal phosphorylation of heat shock protein 20 (Hsp20) is significantly decreased

6 K2 is a prominent kinase that phosphorylates heat shock protein 27 (Hsp27), an intensively investigat

7 ins, myeloid leukemia sequence 1 (Mcl-1) and heat shock protein 27 (HSP27), to block the two proteoly

8 horylation of one of these sites, S82 of the heat shock protein 27 kDa (HSP27), was especially abunda

9 annexin II/p36, stratifin/14-3-3 sigma, and heat shock protein 27, bind to the N-terminal domain of

10 ed by a transient increase of phosphorylated heat shock protein 27, p38 mitogen-activated protein kin

11 We saw a dramatic reduction in binding to heat shock proteins 27 and 40 following combined correct

12 We show that overexpression of yeast Heat shock protein 31 (Hsp31), a DJ-1 homolog with robus

13 DNAJC14, a heat shock protein 40 (Hsp40) cochaperone, assists with

14 Here, we demonstrate that cellular heat shock protein 40 (Hsp40/DnaJB1) facilitates the nuc

15 miR-155-3p promotes Th17 by inhibiting two heat shock protein 40 genes, Dnaja2 and Dnajb1.

16 target genes highlighted transcripts of two heat shock protein 40 genes, Dnaja2 and Dnajb1.

17 untranslated protein response, and Sec63, a heat shock protein-40 chaperone required for protein fol

18 Heat shock protein 47 (HSP47) is an endoplasmic reticulu

19 Among those, SERPINH1 encoding heat shock protein 47 (HSP47), a chaperone exclusive for

20 Two proteins, heat shock protein 47 (Hsp47/SERPINH1) and 65-kDa FK506-

21 s with ABMR expressed fascin1, vimentin, and heat shock protein 47 strongly, whereas those from norma

22 l transition (EndMT), fascin1, vimentin, and heat shock protein 47, for ABMR in 53 renal transplant b

23 n and extracellular matrix proteins, such as heat shock protein-47 (markers of collagen synthesis), m

24 Heat-shock protein 5 (HSPA5) is a marker for poor progno

25 Heat shock protein 60 (Hsp60) is a chaperone localizing

26 is showed that this antigenic fraction was a heat shock protein 60 (HSP60) of Strongyloides sp. The s

27 The levels of serum S. japonicum heat shock protein 60 (SjHSP60)-specific IgG and its sub

28 ion induced autoantibodies against dsDNA and heat shock protein 60 as well as antibody accumulation i

29 esponse (mtUPR) as measured by expression of heat shock protein 60, Clp protease, and Lon peptidase 1

30 P. aeruginosa GroEL, a homolog of heat shock protein 60, was identified as one of the fact

31 N)-gamma, CXCL9, Perforin 1, Granzyme B, and heat shock protein 60.

32 d protein response (reduced concentration of heat shock proteins 60 and 70).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

82 The positive metabolic actions of heat shock protein 72 (HSP72), which include increased o

83 null (dko) mice with BGP-15, a coinducer of heat shock protein 72, ameliorated the dystrophic pathol

84 hermia (MNFH) on the cell death rate and the heat shock proteins 72 (HSP72) induction behavior in ret

85 ity of the auxin co-receptor TIR1, involving HEAT SHOCK PROTEIN 90 (HSP90) [9].

86 was dependent on the chaperoning function of heat shock protein 90 (HSP90) and co-accompanied by the

87 This interaction was stabilized by heat shock protein 90 (HSP90) and followed by proteasoma

88 The chaperones heat shock protein 90 (HSP90) and heat shock cognate pro

89 lysosomal membrane, where it interacts with heat shock protein 90 (HSP90) and stabilizes binding of

90 with molecular targeted agents that inhibit heat shock protein 90 (Hsp90) and/or mammalian target of

91 tibodies targeting citrullinated isoforms of heat shock protein 90 (HSP90) are associated with rheuma

92 We found that the heat shock protein 90 (Hsp90) chaperone system of the ye

93 tein kinases are the most prominent group of heat shock protein 90 (Hsp90) clients and are recruited

94 of CK2 and EGFR also caused deactivation of heat shock protein 90 (Hsp90) co-chaperone Cdc37, which

95 Heat shock protein 90 (hsp90) drives heme insertion into

96 The heat shock protein 90 (Hsp90) family of molecular chaper

97 Nitration of the pro-survival chaperone heat shock protein 90 (Hsp90) in position 33 and 56 indu

98 We found that inhibitors of heat shock protein 90 (HSP90) induced apoptosis in BL ce

99 Heat shock protein 90 (Hsp90) inhibition by modulation o

100 Heat shock protein 90 (HSP90) inhibition is an attractiv

101 Here, we demonstrate that heat shock protein 90 (HSP90) inhibition using a purine-

102 We reasoned that newer heat shock protein 90 (HSP90) inhibitors could overcome

103 hat the combination of glutaminase (GLS) and heat shock protein 90 (Hsp90) inhibitors selectively tri

104 Heat shock protein 90 (HSP90) is a molecular chaperone t

105 Heat shock protein 90 (Hsp90) is an essential eukaryotic

106 The molecular chaperone heat shock protein 90 (Hsp90) is overexpressed during he

107 Acetylation of heat shock protein 90 (Hsp90) regulates downstream hormo

108 NMNAT2 complexes with heat shock protein 90 (HSP90) to refold aggregated prote

109 (SF3B2 and ataxin-2) of a chaperone protein, heat shock protein 90 (Hsp90) when co-administered with

110 Na(+) and/or K(+) flux and the activation of heat shock protein 90 (HSP90), a protein required for th

111 nt phenethyl isothiocyanate (PEITC) inhibits heat shock protein 90 (Hsp90), the main negative regulat

112 The chaperone HEAT SHOCK PROTEIN 90 (HSP90), which maintains phenotypi

113 ivity of these inhibitors was tested against heat shock protein 90 (HSP90), which possesses a similar

114 C-1-interacting proteins that are well-known heat shock protein 90 (Hsp90)-associated co-chaperones:

115 by association with the molecular chaperone heat shock protein 90 (Hsp90).

116 lic androgen receptor (AR) chaperone protein heat shock protein 90 (HSP90).

117 ed by rapid HDAC6-dependent deacetylation of heat shock protein 90 (HSP90).

118 protein 39 (WISp39) as a binding partner for heat shock protein 90 (Hsp90).

119 sing specific inhibitors revealed a role for heat shock protein 90 and glycogen synthase kinase 3 but

120 those, we chose to focus on an inhibitor of heat shock protein 90 beta (HSP90beta).

121 is the endoplasmic reticulum resident of the heat shock protein 90 kDa (Hsp90) family of molecular ch

122 itro; and enhanced the binding of acetylated heat shock protein 90 to lymphocyte-specific protein tyr

123 oximately 30%, but addition of siRNA(Hsp90) (heat shock protein 90) had little effect.

124 protein inhibitor of NOS1 (PIN), calmodulin, heat shock protein 90, and NOS interacting protein.

125 dehydrogenase, alpha-enolase, filamin-A, and heat shock protein 90, were identified in samples of api

126 inase induces its complexing with 14-3-3 and heat shock protein 90, which is facilitated by the longe

127 f RanBP9 to physically interact with tau and heat shock protein 90/heat shock cognate 70 (Hsp90/Hsc70

128 o address this need, we explored the role of heat-shock protein 90 (Hsp90) in opioid-induced MOR sign

129 Inhibition of the chaperone heat-shock protein 90 (HSP90) induces apoptosis, and it

130 We present here that heat-shock protein 90 (Hsp90) inhibitor 17-(allylamino)-

131 ylamino]-17-demethoxygeldanamycin (17AAG), a heat-shock protein 90 (Hsp90) inhibitor, prevents UVR-in

132 The molecular chaperone heat-shock protein 90 (Hsp90) is an essential component

133 homeostasis, molecular chaperones, including heat-shock protein 90 (Hsp90), represent attractive drug

134 nts specifically reacted with the sumoylated heat-shock protein 90 beta isoform-alpha (HSP90-SUMO1, w

135 directly interacts with PIH1D1, a subunit of heat-shock protein 90 cochaperone R2TP complex, which is

136 that the interactions of AID with eEF1A and heat-shock protein 90 kD (HSP90) are inversely correlate

137 Both intracellular and extracellular heat shock protein-90 (Hsp90) family proteins (alpha and

138 ugh interference of cyclophilin-D binding to heat shock protein-90 (Hsp90) in mitochondria, rendering

139 Heat shock protein-90 (Hsp90) is an essential molecular

140 onverted to kallikrein because of release of heat shock protein-90 (Hsp90).

141 ing breast cancer cells, MDA-MB-231, secrete heat shock protein-90alpha (Hsp90alpha) and use it to su

142 The molecular chaperone heat shock protein A2 (HSPA2), a member of the 70 kDa he

143 genes were those related to stress, such as heat shock proteins, abscisic acid (ABA) catabolism and

144 d of prestretch and finally treated with the heat shock protein alpha-B crystallin.

145 We have shown previously that the small heat shock protein alphaB-crystallin (alphaB) is exporte

146 The small heat shock protein alphaB-crystallin (CRYAB) has been im

147 Genetic mutations in the human small heat shock protein alphaB-crystallin have been implicate

148 The heat shock protein also seems to regulate the cross-talk

149 The heat shock protein and cell wall component Ssa1 was also

150 egulatory use of an evolutionarily conserved heat shock protein and present a distinctive mechanism f

151 to activate transcription of both the small heat shock protein and the large heat shock protein gene

152 of HSF1, where it binds to the promoters of heat shock proteins and an array of nonheat shock-regula

153 ly the genes associated with photosynthesis, heat shock proteins and antioxidants impinge on the comp

154 Genes coding for heat shock proteins and pilins were also induced in Delt

155 component systems (TCSs), the repressors of heat shock proteins and regulators involved in sugar tra

156 biotic-stress conditions, mainly by inducing heat shock proteins and supporting a conserved mechanism

157 shock proteins include ATP-independent small heat shock proteins and the larger ATP-dependent protein

158 PS also stimulated LRP1 shedding, as did the heat-shock protein and LRP1 ligand, calreticulin.

159 ral capsids, virus-like particles, ferritin, heat-shock proteins and chaperonins.

160 f cytosolic (e.g. glutathione peroxidase and heat shock proteins) and mitochondrial adaptive or stres

161 FTL578 (ornithine cyclodeaminase), FTL663 (heat shock protein), and FTL1228 (iron-sulfur activator

162 uch as Hikeshi, involved in the transport of heat-shock proteins, and NTF2, involved in the transport

163 notion that mitochondrial adaptations (e.g. heat shock proteins, antioxidant enzymes and sirtuin-1/P

164 thetic apparatus, the ROS-scavenging system, Heat Shock Proteins, aquaporins, expansins, and desiccat

165 Small heat shock proteins are known to stabilize several intra

166 ave demonstrated that the levels of HSF1 and heat shock proteins are significantly reduced in affecte

167 Heat shock proteins are synthesized constitutively in in

168 Small heat shock proteins are ubiquitous molecular chaperones

169 Although the antioxidant and heat-shock proteins are included in this category, one e

170 This fit well with the identification of heat-shock proteins as a class of antigens that showed o

171 terotetramer stage coinciding with increased heat shock protein association.

172 e encoding ascorbate peroxidase (AtApx2) and heat shock proteins [AtHsp18.1-CI, AtHsp22.0-ER, AtHsp25

173 Here, we demonstrate that heat shock protein beta-1 (HSPB1) is a negative regulato

174 3-3:serotonin N-acetyltransferase and 14-3-3:heat shock protein beta-6 complexes revealed similaritie

175 re commonly observed in experiments on small heat-shock proteins, but their connection to the biologi

176 rradiated whole tumor cells or tumor-derived heat shock proteins can generate tumor-specific immune r

177 f-antigens, such as apolipoprotein B-100 and heat shock proteins, can contribute to vascular inflamma

178 en interaction and heterodimer and homodimer heat shock protein complexes.

179 ns of co-opted cellular translation factors, heat shock proteins, DEAD-box helicases, lipid transfer

180 However, metazoans lack the key heat-shock protein disaggregase HSP100 of non-metazoan H

181 , resulting in a fusion of the genes for the heat shock protein, DNAJ (Hsp40) homolog, subfamily B, m

182 xpress a family of molecular chaperones, the heat shock proteins, during times of oxidative stress to

183 nitial phase of the heat-shock response, and heat-shock protein dynamics in the long-term heat-shock

184 ith the chaperone activity of a barley small heat shock protein essential for defense and stress resp

185 on chromosome 19 that fuses part of the DnaJ heat shock protein family (Hsp40) member B1 gene (DNAJB1

186 MIR21 was shown to target the DnaJ heat shock protein family (Hsp40) member B5 (DNAJB5).

187 n patient biopsy specimens and detected DnaJ heat shock protein family (Hsp40) member B9 (DNAJB9) as

188 cription factor of the so far unstudied DnaJ heat shock protein family (Hsp40) member C22 (Dnajc22).

189 bility that the S1R is a member of the small heat shock protein family is discussed.

190 d in hetero-oligomer formation between human heat-shock protein family B (small) member 1 (HSPB1) and

191 ave determined crystal structures of a small heat shock protein from Salmonella typhimurium in a dime

192 Further sequencing of the mycobacterial heat shock protein gene (hsp65) provided species-level t

193 Stress-induced expression of heat shock protein genes occurs in a background of prote

194 g which the transcript levels of some of the heat shock protein genes significantly reduced in respon

195 h the small heat shock protein and the large heat shock protein genes.

196 Heat shock protein gp96, also known as grp94, is an esse

197 nal downregulation of several members of the heat shock protein group as a specific effect of CPX tre

198 is the first report highlighting the role of heat shock protein Hps90Ec in the production of two seco

199 s (ERs), crucially, via its interaction with heat shock proteins (HSC70/HSP70).

200 eranylacetone (GGA), a drug that upregulates heat shock protein (HSP) 70 and HSP90.

201 Liver heat shock protein (HSP) 70 levels (at 72 hours) and mac

202 nd expressed marker proteins CD63, CD81, and heat shock protein (HSP) 70.

203 n is injured, there is a massive increase of heat shock protein (Hsp) 90alpha inside the wound bed.

204 Levels of heat shock protein (HSP) and interleukin 15 were measure

205 with fluorescence microscopy to investigate Heat Shock Protein (HSP) gene conformation and 3D nuclea

206 ve neuronal expression of HSP-16.48, a small heat shock protein (HSP) homolog of human alpha-crystall

207 Because the heat shock protein (Hsp) Hsp10-Hsp60 chaperone complex m

208 d Abs against the Mycobacterium tuberculosis heat shock protein (HSP)65 protect against the induction

209 Overexpression of Ssa2, a cytosolic heat shock protein (Hsp)70, was sufficient to partially

210 -cell non-Hodgkin lymphomas (B-NHLs) express heat shock protein (HSP)H1/105 in function of their aggr

211 Cytosolic and organelle-based heat-shock protein (HSP) chaperones ensure proper foldin

212 Our findings reveal that heat-shock protein (HSP) gene expression is suppressed d

213 Here we show that a heat shock protein, HSP105, is a previously unidentified

214 y, both CSEPs interact with the barley small heat shock proteins, Hsp16.9 and Hsp17.5, in a yeast two

215 factors DnaJ1, DnaJ2, and GrpE and the small heat shock protein Hsp20.

216 Mutations in the small heat shock protein Hsp27, encoded by the HSPB1 gene, hav

217 ry structure and dynamics of the human small heat-shock protein Hsp27 are linked to its molecular cha

218 508del, is initiated by binding of the small heat shock protein, Hsp27.

219 The Saccharomyces cerevisiae heat shock protein Hsp31 is a stress-inducible homodimer

220 Previously, we have reported that heat shock proteins, HSP40 and HSP70 reciprocally regula

221 ein in the sterol-regulated induction of the heat shock protein, HSP42 and HSP102, mRNAs.

222 hat ULBP2 was constitutively associated with heat shock protein HSP60.

223 ron tomography, we probed the effects of the heat shock protein Hsp70 chaperone system on the structu

224 The 70 kDa heat shock protein Hsp70 has several essential functions

225 models have revealed critical roles for the heat shock protein Hsp70 in cancer initiation and progre

226 Furthermore, mRNA for the major heat shock protein Hsp70 is transcribed at robust levels

227 clams was associated with overexpression of heat shock proteins HSP70, HSP90 and HSP60 and activatio

228 The 70 kDa heat shock protein (Hsp70) chaperone system is ubiquitou

229 The 70-kDa heat shock protein (Hsp70) family of chaperones bind cog

230 k protein A2 (HSPA2), a member of the 70 kDa heat shock protein (HSP70) family, plays an important ro

231 ecies of the Meliaceae family described as a heat shock protein Hsp90 inhibitor, on LPS-induced respo

232 no acid-changing mutations at 6 sites in the heat-shock protein Hsp90 in Saccharomyces cerevisiae und

233 The 90-kDa heat shock protein (Hsp90) chaperone system affects the

234 The 90-kDa heat shock protein (Hsp90) is a highly flexible dimer ab

235 The 90-kDa heat shock protein (Hsp90) is a widely conserved and ubi

236 The 90-kDa heat-shock protein (Hsp90) assists in the proper folding

237 Here we show that the small heat shock protein HspB1 (hsp25/27) is phosphorylated in

238 Small heat shock protein HSPB7 is highly expressed in the hear

239 e81) displayed improved binding to the small heat shock protein (HspB8) in ischemic skeletal muscle c

240 DP-43 clearance we over-expressed a range of heat shock proteins (HSPs) and identified DNAJB2a (encod

241 s and lipid metabolism and distinct forms of heat shock proteins (HSPs) and proteins with chaperon fu

242 Heat shock proteins (HSPs) are constitutively expressed

243 Heat shock proteins (HSPs) are induced by cellular stres

244 to previous beliefs that expression level of Heat Shock Proteins (HSPs) can be used as a measurement

245 induce autophagy and potentially protective heat shock proteins (HSPs) such as Hsp70 and Hsp27.

246 nism developed to increase the expression of heat shock proteins (HSPs) via a heat shock factor (HSF)

247 Whether MRP-1 is chaperoned by heat shock proteins (HSPs) was investigated by immunopre

248 A number of Heat Shock Proteins (HSPs), in the extracellular environ

249 s, controls the expression of cytoprotective heat shock proteins (HSPs), molecular chaperones/cochape

250 Induction of heat-shock proteins (HSPs), such as through activated he

251 The E. coli heat shock protein HtpG (Hsp90Ec) is the bacterial homol

252 ected and critical role for a specific small heat shock protein in directly modulating actin thin fil

253 rescued with therapeutic application of the heat shock protein in vivo.

254 ogical role for FOXO-dependent expression of heat shock proteins in vivo.

255 These results indicate that heat shock proteins, in particular Hsp90, stimulate APOB

256 Insect heat shock proteins include ATP-independent small heat s

257 sublethal exposure leads to the synthesis of heat shock proteins, including HSP70, which are able to

258 Cultured YAMC cell proliferation and heat shock protein induction were analzyed after butryat

259 p16.9 and Hsp17.5, confirming the CSEP-small heat shock protein interaction.

260 ormation of aggregates associated with small heat-shock proteins is observed.

261 Heat shock protein levels are often elevated in both car

262 g diapause, when ATP concentrations are low, heat shock proteins may sequester rather than fold prote

263 rt with cochaperones and accessory proteins, heat shock proteins mediate essential activities such as

264 o multiple cellular perturbations, including heat shock, protein misfolding, integrin engagement, and

265 HSF) oligomerization, as well as the role of heat-shock protein mRNA, and constructed an expanded mat

266 f the nucleotide binding domain (NBD) of the heat shock protein of 70 kDa (Hsp70) chaperone DnaK upon

267 In addition, the major heat shock proteins of the intracellular bacterium Chlam

268 Heat-shock protein of 90 kDa (Hsp90) is an essential mol

269 te of the insect, but the common function of heat shock proteins, often working in networks, is to ma

270 Owing to the dynamic nature of small heat shock protein oligomers, elucidating the structural

271 ammatory cytokines, NF-kappaB signaling, and heat shock protein pathway RNA transcripts.

272 Highly conserved molecular chaperone Hsp70 heat shock proteins play a key role in maintaining prote

273 at Rv3780 promoted robust degradation of the heat shock protein repressor, HspR.

274 is a well-characterized member of the small heat shock protein (sHsp) family that reduces mutant htt

275 Clustered class-I small heat-shock protein (sHSP) chaperone genes, SlHSP17.6, Sl

276 Small heat shock proteins (sHsps) are a family of ATP-independ

277 Small heat shock proteins (sHsps) are a ubiquitous family of m

278 Small heat shock proteins (sHSPs) are essential 'holdase' chap

279 Small heat shock proteins (sHsps) are virtually ubiquitous mol

280 The ubiquitous small heat shock proteins (sHSPs) are well documented to act i

281 onditions promoting protein unfolding, small heat shock proteins (sHsps) prevent the irreversible agg

282 Molecular chaperones, such as the small heat shock proteins (sHsps), maintain normal cellular fu

283 ilies Hsp70, Hsp104, Hsp90, Hsp60, and small heat-shock proteins (sHsps) apparently act as unfolding

284 Small heat-shock proteins (sHSPs) are a conserved group of mol

285 Small heat-shock proteins (sHsps) prevent aggregation of therm

286 ivo, molecular chaperones, such as the small heat-shock proteins (sHsps), normally act to prevent pro

287 Immune responses primed by endogenous heat shock proteins, specifically gp96, can be varied, a

288 passive molecular chaperones, such as small heat-shock proteins, suppress thermodynamic instabilitie

289 AlphaB-crystallin (alphaBC) is a small heat shock protein that is constitutively expressed by p

290 the expression of alphaB-crystallin, a small heat shock protein that is enriched in astrocytes and me

291 Bacteria encode heat shock proteins that aid in survival during stressfu

292 Astrocytic exosomes carry heat shock proteins that can reduce the cellular toxicit

293 uction with increased expression of specific heat shock proteins that was variable across tissues.

294 us proteins and small molecules ranging from heat shock proteins to small lipids, neurotransmitters,

295 Induction of neuroprotective heat-shock proteins via pharmacological Hsp90 inhibitors

296 lation of mitochondrial matrix proteases and heat shock proteins was initially described.

297 A number of heat shock proteins were also elevated.

298 transporters, cytochrome P450, ubiquitin and heat shock proteins were found associated with adaptatio

299 ected transcription factors, chaperones, and heat shock proteins) were highly expressed in Namikonga.

300 synthase, annexins, galectin, cathepsins and heat shock proteins), whereas the anti-inflammatory prot