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1 ities of intracellular hormone receptors and heat shock transcription factor.
2 s, one of which is regulated by the sigma 32 heat-shock transcription factor.
3 nducible transcription factor 1 (HIF-1), and heat shock transcription factors.
4 iptional response is mediated by a family of heat-shock transcription factors.
7 rotein folding and pro-survival machinery by heat shock transcription factor 1 (HSF1) ameliorates bio
8 wo key molecular components in the response, heat shock transcription factor 1 (HSF1) and extracellul
14 that male mice expressing an active form of heat shock transcription factor 1 (HSF1) in the testis a
15 ave implicated heat shock proteins (HSP) and heat shock transcription factor 1 (HSF1) in tumor progre
20 ther stresses, the inactive monomer of human heat shock transcription factor 1 (HSF1) is converted to
25 k proteins (HSPs), such as through activated heat shock transcription factor 1 (HSF1) via Hsp90 inhib
26 ructure is remarkably specific and activates heat shock transcription factor 1 (HSF1) with kinetics s
27 nes and components of protein homeostasis by heat shock transcription factor 1 (HSF1), the master str
31 inhibit the activity of NF-kappa B, activate heat shock transcription factor 1 and suppress cytokine
38 gulated at the level of mRNA translation via heat-shock transcription factor 1 (HSF1)-induced HuR act
42 ves an immediate and transient activation of heat-shock transcription factor-1 (HSF1) which results i
47 similar to the DNA-binding domain of a yeast heat shock transcription factor and a domain within ribo
48 istal domains encoded a binding site for the heat shock transcription factor and a putative binding s
49 dition, Ssa1 forms a regulatory complex with heat shock transcription factor and TATA-binding protein
50 the influence of mutations in the sigma(32) heat-shock transcription factor and the DnaK-DnaJ-GrpE a
51 nteraction between a chaperone protein and a heat shock transcription factor, and fine-tuned by phosp
54 ing Drosophila cultured cells the Drosophila heat shock transcription factor (dHSF) is localized in t
55 mportin-alpha3-binding NLS in the Drosophila heat-shock transcription factor (dHSF), and each Importi
56 ing studies have uncovered new functions for heat shock transcription factors (e.g., maintenance of i
57 refractory period for Hsp70 induction, HSF (heat-shock transcription factor) exhibited specific DNA-
58 y reveals a new function for a member of the heat-shock transcription factor family in stem cell deve
59 haracterized a 91 amino acid fragment of the heat shock transcription factor from the yeast Kluyverom
62 al heat-stress response genes, including two heat shock transcription factor genes, HsfA2 and HsfB1.
64 e deprivation-induced HSP70 gene expression, heat shock transcription factor-heat shock element bindi
72 In C. elegans, genetic studies suggest that heat-shock transcription factor HSF-1 is required for II
73 nts essential for induction and required the heat-shock transcription factor HSF-1, RNA polymerase II
77 A chaperone/Hsp functioning as repressor of heat shock transcription factor (HSF) could make activat
78 itro DNA-binding assays demonstrate that the heat shock transcription factor (HSF) from the yeast Sac
83 rate that the high-affinity binding site for heat shock transcription factor (HSF) is occupied indepe
92 promoter region next to the binding motif of heat shock transcription factor (HSF), -764G, was signif
93 e have identified direct target genes of the heat shock transcription factor (HSF), including genes e
94 in response to heat shock is mediated by the heat shock transcription factor (HSF), which in yeast ha
95 cerevisiae possesses a single gene encoding heat shock transcription factor (HSF), which is required
99 protein Hsp90 chaperone complex require the heat shock transcription factor (HSF); Saccharomyces cer
100 e that the insulin signaling pathway and the heat shock transcription factor (HSF-1) influence the am
102 eport here that the evolutionarily conserved heat-shock transcription factor (HSF) strongly influence
103 -bridged, circular oligonucleotide decoy for heat-shock transcription factor (HSF)-1, based on the se
105 an cells: a positive control mediated by the heat shock transcription factor HSF1 and a negative cont
107 pressed, with constitutive activation of the heat shock transcription factor HSF1 implicated in tumor
110 lian cells, this response is mediated by the heat shock transcription factor Hsf1, which is monomeric
114 esponse involves two regulatory systems: the heat shock transcription factor (Hsf1) and the Msn2 and
117 th live visualization of the dynamics of the heat shock transcription factor (HSF1), we show that exc
121 ss RNA-seq and ChIP-seq to discover that the heat shock transcription factor, Hsf1, binds distinct mo
123 lopmental and tissue-specific control of the heat shock transcription factors (HSFs) and their intera
128 tion of hydrophobic repeats, two families of heat shock transcription factors (HSFs) exist in plants.
131 gulator DRE-binding protein 2A (DREB2A), two heat shock transcription factors (HSFs), and several zin
132 of-function mutants of 15 Arabidopsis A-type heat-shock transcription factors (HSFs), and identified
133 hydrogen peroxide or menadione activates the heat shock transcription factor in mouse cells but does
138 modifier (SUMO) conjugation/deconjugation to heat shock transcription factors regulates DNA binding o
139 ng was noted in RIE-S cells, suggesting that heat-shock transcription factor regulation may explain t
140 teins was increased by overproduction of the heat-shock transcription factor sigma 32, or by addition
141 ns that are protease substrates in vivo: the heat shock transcription factor sigma32, the SOS mutagen
144 tion factor, dFOXO, that works alongside the heat shock transcription factor to activate transcriptio
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