ライフサイエンスコーパス: heat-shock protein

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

2 obable trehalose-phosphate phosphatase 2 and heat shock protein.

3 in elevated expression of a large number of heat shock proteins.

4 the chemistry of probes for the biomarkers, heat shock protein 10 and lysophosphatidic acid.

5 Heat Shock Protein 101 (HSP101), the homolog of Caseinol

6 n particular class B J-domain proteins and a heat shock protein 110 (Hsp110)-type nucleotide exchange

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

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

9 orskolin (FSK) as well as the induction of p-heat shock protein 20 after 4 h of stimulation with ISO

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

11 n early dissemination is mediated by MK2 and heat shock protein 27 (Hsp27).

12 and expression of the downstream MK2 target, heat shock protein 27 (HSP27); and markers of epithelial

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

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

15 heavy chain-binding protein (BiP) homologue Heat-Shock Protein 4 (HSP-4), is selectively induced in

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

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

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

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

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

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

22 The human mitochondrial heat shock protein 60 (hsp60) is a tetradecameric chaper

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

24 ccupying the surface presented LAP receptor, heat shock protein 60 and ameliorates the Lm-induced int

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

26 n protein (LAP) with the host cell receptor (heat shock protein 60) disrupts the epithelial barrier,

27 this study, we found that the GroEL protein (heat shock protein 60) of Mycoplasma gallisepticum could

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

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

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

31 ssion of glial fibrillary acidic protein and heat shock protein 60.

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

33 ceraldehyde-3-phosate dehydrogenase (G3PDH), heat-shock protein 60 (HSP60), DNA-dependent RNA polymer

34 (30)); MSH2 (MutShomolog 2) and HSP60 (heat-shock protein 60)(24); ULBP4 (UL16-binding protein

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 Here, we identified Leishmania donovani heat shock protein 78 (LdHSP78), a putative caseinolytic

77 , we demonstrate that Mettl21c trimethylates heat shock protein 8 (Hspa8) at Lys-561 to enhance its s

78 treatment, and this effect was dependent on heat-shock protein 86 (HSP86) as HSP86-deficient Ret cel

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

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

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

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

83 on to the nucleus to identify a link between heat shock protein 90 (HSP90) and protein kinase A (PKA)

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

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

86 ach identified geldanamycin, an inhibitor of heat shock protein 90 (HSP90) as a candidate therapeutic

87 sGC (sGCbeta) is critical for function, and heat shock protein 90 (HSP90) associates with heme-free

88 Heat shock protein 90 (HSP90) binds to the N-terminal re

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

90 s, previously isolated from ICC samples, are heat shock protein 90 (HSP90) clients and undergo rapid

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

92 Cumulative evidence suggests that the heat shock protein 90 (Hsp90) co-chaperone UNC-45 myosin

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

94 Leveraging the unique surface expression of heat shock protein 90 (Hsp90) in breast cancer provides

95 rticipate in communicating with LGG and that heat shock protein 90 (HSP90) in these vesicles might me

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

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

98 Heat shock protein 90 (Hsp90) is a eukaryotic chaperone

99 Heat shock protein 90 (Hsp90) is a highly conserved mole

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

101 Heat shock protein 90 (Hsp90) is a molecular chaperone t

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

103 Heat shock protein 90 (Hsp90) is an evolutionarily conse

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

105 function of the dimeric molecular chaperone heat shock protein 90 (Hsp90), including transient, ATP-

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

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

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

109 er promoted T lymphocyte trafficking through heat shock protein 90 (Hsp90)-induced alpha4 integrin ac

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

111 1 from the TRIM23 complex that also contains heat shock protein 90 (Hsp90).

112 rough a proteomics screen, we identified the heat shock protein 90 B (hsp90B) chaperone as a direct M

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

114 Ganetespib, a highly potent heat shock protein 90 inhibitor, blocks multiple oncogen

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

116 d by the endoplasmic reticulum (ER)-resident heat shock protein 90 paralog, glucose regulated protein

117 ng cascade was mediated downstream by Hsp90 (heat shock protein 90), which in turn modulated mitochon

118 Our data identify and show that heat shock protein 90, but not heat shock protein 70, st

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

120 he impact of phosphosites in the L. donovani heat shock protein 90.

121 mplex that includes at least HYL1, AGO1, and HEAT SHOCK PROTEIN 90.

122 ctor receptor, cyclin-dependent kinases, and heat shock protein 90.

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

124 Heat shock proteins 90 (Hsp90) and 70 (Hsp70) are two fa

125 We discovered that levels of heat-shock protein 90 (HSP90) are increased in eEF2K-dep

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

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

128 ging human brain that may be reversible with heat-shock protein 90 (Hsp90) inhibitors.

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

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

131 r), GSK-690693 (AKT inhibitor), and KW-2478 (heat-shock protein 90 inhibitor) were substrates.

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

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

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

135 1 (HSF1) phosphorylation, which induced the heat shock protein 90alpha (HSP90alpha) expression, lead

136 Extracellular heat shock protein-90alpha (eHsp90alpha) plays an essent

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

138 protein 20), is the partner of mitochondrial heat shock protein A9 (HSPA9).

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

140 The small heat shock protein alphaA-crystallin is a molecular chap

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

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

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

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

145 Increasing expression of heat shock proteins also resolved neurofilament bundles,

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

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

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

149 tion of protein-coding genes (PCGs), such as heat shock proteins and cytoskeletal regulators, is crit

150 The major heat shock proteins and molecular chaperones Hsp70 and H

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

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

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

154 lines, even though the myeloma cells induced heat-shock proteins and increased protein degradation si

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

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

157 ve glycation, including translation factors, heat shock proteins, and histones.

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

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

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

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

162 terotetramer stage coinciding with increased heat shock protein association.

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

164 s of BAG3-interacting proteins, such as p62, heat shock protein B8, and alphaB-crystallin.

165 3-3:serotonin N-acetyltransferase and 14-3-3:heat shock protein beta-6 complexes revealed similaritie

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

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

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

169 Heat shock proteins/cognates 70 are chaperones essential

170 nt, including exhaustion of cardioprotective heat shock proteins, disruption of cytoskeletal proteins

171 When the J-domain of the heat shock protein DnaJB1 is fused to the catalytic (C)

172 eins known to underlie thermal stress (i.e., heat shock proteins) even at low temperatures that refle

173 is characterized by in-frame fusion of DnaJ heat shock protein family (Hsp40) member B1 (DNAJB1) wit

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

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

176 A human molecular chaperone protein, DnaJ heat shock protein family (Hsp40) member B6 (DNAJB6), ef

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

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

179 Mortalin [also known as heat shock protein family A (HSP70) member 9 (HSPA9) or

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

181 DNAJC7 encodes a member of the heat-shock protein family, HSP40, which, along with HSP7

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

183 vented the normal upregulation of a group of heat shock protein genes in response to elevated tempera

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

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

186 ated with differential upregulation of three heat-shock protein genes, allowed aphids to occupy highe

187 e responses during ciliate exposure, such as heat shock proteins, glutathione metabolism, and the rea

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

189 proteins, and the recruitment of a cellular heat shock protein, Hsc70, to nuclear domains.

190 UIMs function by interacting with the heat shock protein, Hsc70-4, whose reduction diminishes

191 The molecular chaperone heat shock protein (HSP) 101 is a protein disaggregase t

192 Heat shock protein (Hsp) 104 is a hexameric ATPases asso

193 Heat shock protein (Hsp) 70 modulators are being develop

194 We investigated a role for heat shock protein (hsp) 90 in Mb maturation in C2C12 sk

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

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

197 ntributing to PIC assembly and expression of Heat Shock Protein (HSP) genes.

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

199 conditions screened, combined inhibition of heat shock protein (Hsp)-90 and MEK was found to produce

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

201 d to the erythrocyte; among them is a single heat shock protein (Hsp)70-class protein chaperone, P. f

202 ly on nonhistone substrates such as tubulin, heat shock protein (HSP)90, Foxp3, and cortactin, to nam

203 Heat shock proteins (Hsp) are a class of stress-inducibl

204 e under conditions that induce expression of heat shock proteins (Hsp; thought to be immune adjuvants

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

206 The functional information on heat-shock proteins (Hsp) and heat-shock promoters from

207 DnaK, homologs of the respective eukaryotic heat shock proteins Hsp104 and Hsp70, are essential in t

208 dosage-sensitive proteins such as the small heat shock protein Hsp20, which exists in a dodecameric

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

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

211 es the interaction between p53 and the small heat shock proteins HSP27 (also known as HSPB1) and alph

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

213 The small heat-shock protein HSP27 is a redox-sensitive molecular

214 protective enzymes (NQO1, HO-1, AKR1C1), and heat shock proteins (HSP27 and HSP70), increased.

215 508del, is initiated by binding of the small heat shock protein, Hsp27.

216 rtial unfolding of its structure convert the heat shock protein Hsp33 into a highly active chaperone

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

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

219 The core chaperones, such as the heat shock proteins Hsp60, Hsp70, and Hsp90, are widely

220 ing to four major insect Hsp families (small heat-shock proteins, Hsp60, Hsp70, and Hsp90) in S. frug

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

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

223 The 70 kDa heat shock protein (HSP70) family of chaperones are the

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

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

226 ion: an expanded repertoire of 70 kilodalton heat-shock proteins (Hsp70) and avrRpt2 induced gene 1 (

227 is mellifera) and expression of a ubiquitous heat shock protein, HSP70, in their central nervous syst

228 We provide evidence that the heat shock protein HSP90 enhances wound responses at ET

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

230 Small-molecule inhibitors for the 90-kDa heat shock protein (HSP90) have been extensively exploit

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

232 tion is necessary for the phosphorylation of heat shock protein (HSP90) that binds to unliganded AR i

233 zed groups of client proteins for the 90-kDa heat shock protein (HSP90), a molecular chaperone that s

234 The molecular chaperone 90-kDa heat-shock protein (Hsp90) assists the late-stage foldin

235 STIP1 is a co-chaperone for the heat-shock protein, HSP90, and has been shown to have di

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

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

238 rexpressed in metastatic PCs, TRPM8, and the heat shock protein HSPB8, whose levels were significantl

239 pha), the transcription factor ATF4, and the heat shock protein HSPB8.

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

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

242 Heat shock proteins (HSPs) are a large group of chaperon

243 Heat shock proteins (Hsps) are highly conserved molecula

244 Induction of heat shock proteins (HSPs) confers protection against am

245 Induction of heat shock proteins (HSPs) in response to heat stress (H

246 ria synthesize a family of proteins known as heat shock proteins (HSPs) to facilitate adaptation and

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

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

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

250 Heat shock proteins (HSPs), through regulation of extrac

251 ating transcription factors (e.g., Atf4) and heat-shock proteins (Hsps).

252 w that in Mycobacterium smegmatis, the small heat shock protein HspX plays a critical role in the pol

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

254 ted athanogene 3 (BAG3) is a co-chaperone to heat shock proteins important in degrading misfolded pro

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

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

257 results in the selective induction of small heat shock proteins in adulthood, thereby protecting aga

258 expression and cell surface localization of heat shock proteins in murine breast (4T1) and prostate

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

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

261 plementary target-engagement method, HIPStA (Heat Shock Protein Inhibition Protein Stability Assay),

262 ncreased abundance of proteins classified as heat shock proteins, intracellular traffic, disease/defe

263 Heat shock protein levels are often elevated in both car

264 Heat shock proteins of 70 kDa (Hsp70s) are ubiquitous an

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

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

267 n significant reduction in the expression of heat-shock proteins, previously implicated in Tau proteo

268 the mammalian stage of Leishmania parasites, heat shock proteins show increased phosphorylation, indi

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

270 Small heat shock proteins (sHSPs) are a class of ATP-independe

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

272 Small heat shock proteins (sHsps) are a family of ubiquitous i

273 Small heat shock proteins (sHsps) are a ubiquitous and ancient

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

275 Small heat shock proteins (sHSPs) are an ubiquitous protein fa

276 Small heat shock proteins (sHsps) are conserved, ubiquitous me

277 Small heat shock proteins (sHSPs) are nature's 'first responde

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

279 Small heat shock proteins (sHsps) constitute a diverse chapero

280 Small heat shock proteins (sHSPs) delay protein aggregation in

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

282 inducing those of the ATP-independent small heat shock proteins (sHSPs).

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

284 Small heat-shock proteins (sHSPs) are molecular chaperones tha

285 Small heat-shock proteins (sHsps) are molecular chaperones tha

286 Small heat-shock proteins (sHSPs) are ubiquitously expressed m

287 Small heat-shock proteins (sHsps) compose the most widespread

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

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

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

291 EVs with neuroprotective molecules including heat shock proteins, synapsin 1, unique microRNAs, and g

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

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

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

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

296 ess response, measured via the production of heat shock proteins (the heat shock response (HSR)), was

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

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

299 A number of heat shock proteins were also elevated.

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