| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0968-0004(99)01373-0 |
| P698 | PubMed publication ID | 10322418 |
| P2093 | author name string | J Buchner | |
| P2860 | cites work | In vivo function of Hsp90 is dependent on ATP binding and ATP hydrolysis | Q22008008 |
| Identification of a protein with homology to hsp90 that binds the type 1 tumor necrosis factor receptor | Q24315622 | ||
| The human cytosolic molecular chaperones hsp90, hsp70 (hsc70) and hdj-1 have distinct roles in recognition of a non-native protein and protein refolding | Q24562938 | ||
| Inhibition of heat shock protein HSP90-pp60v-src heteroprotein complex formation by benzoquinone ansamycins: essential role for stress proteins in oncogenic transformation | Q24564127 | ||
| A new member of the hsp90 family of molecular chaperones interacts with the retinoblastoma protein during mitosis and after heat shock | Q24648784 | ||
| Crystal structure of an Hsp90-geldanamycin complex: targeting of a protein chaperone by an antitumor agent | Q27736012 | ||
| A molecular clamp in the crystal structure of the N-terminal domain of the yeast Hsp90 chaperone | Q27739168 | ||
| Identification and structural characterization of the ATP/ADP-binding site in the Hsp90 molecular chaperone | Q27740876 | ||
| hsp82 is an essential protein that is required in higher concentrations for growth of cells at higher temperatures | Q27930675 | ||
| Cdc37 is a molecular chaperone with specific functions in signal transduction | Q27936846 | ||
| Two chaperone sites in Hsp90 differing in substrate specificity and ATP dependence | Q27937497 | ||
| In vivo functions of the Saccharomyces cerevisiae Hsp90 chaperone | Q27937958 | ||
| Repression of heat shock transcription factor HSF1 activation by HSP90 (HSP90 complex) that forms a stress-sensitive complex with HSF1 | Q28118304 | ||
| The amino-terminal domain of heat shock protein 90 (hsp90) that binds geldanamycin is an ATP/ADP switch domain that regulates hsp90 conformation | Q28248831 | ||
| Antibiotic radicicol binds to the N-terminal domain of Hsp90 and shares important biologic activities with geldanamycin | Q28277057 | ||
| Hsp90 as a capacitor for morphological evolution | Q28290854 | ||
| Steroid receptor interactions with heat shock protein and immunophilin chaperones | Q29619628 | ||
| Hsp90 chaperones protein folding in vitro. | Q30351360 | ||
| Hepadnavirus assembly and reverse transcription require a multi-component chaperone complex which is incorporated into nucleocapsids | Q33885913 | ||
| ATP binding and hydrolysis are essential to the function of the Hsp90 molecular chaperone in vivo | Q33889333 | ||
| Transient interaction of Hsp90 with early unfolding intermediates of citrate synthase. Implications for heat shock in vivo | Q34307813 | ||
| The charged region of Hsp90 modulates the function of the N-terminal domain | Q34988119 | ||
| Two eukaryote-specific regions of Hsp82 are dispensable for its viability and signal transduction functions in yeast | Q35938409 | ||
| Ancient heat shock gene is dispensable | Q36207033 | ||
| Heat shock protein-peptide complexes, reconstituted in vitro, elicit peptide-specific cytotoxic T lymphocyte response and tumor immunity | Q36380745 | ||
| Heat-shock protein hsp90 governs the activity of pp60v-src kinase | Q36449591 | ||
| Progesterone receptor structure and function altered by geldanamycin, an hsp90-binding agent | Q36556311 | ||
| Pharmacologic shifting of a balance between protein refolding and degradation mediated by Hsp90 | Q37044062 | ||
| Mutant conformation of p53 translated in vitro or in vivo requires functional HSP90. | Q37402942 | ||
| Regulation of protein function through expression of chimaeric proteins | Q40535460 | ||
| Assisting spontaneity: the role of Hsp90 and small Hsps as molecular chaperones | Q40624749 | ||
| A role for Hsp90 in cell cycle control: Wee1 tyrosine kinase activity requires interaction with Hsp90. | Q40794316 | ||
| Dynamic activation of endothelial nitric oxide synthase by Hsp90. | Q41044129 | ||
| ATP-binding properties of human Hsp90. | Q41098714 | ||
| Chaperones get in touch: the Hip-Hop connection | Q41379488 | ||
| Reduced levels of hsp90 compromise steroid receptor action in vivo | Q45391521 | ||
| Mutations in Hsp83 and cdc37 impair signaling by the sevenless receptor tyrosine kinase in Drosophila. | Q45975761 | ||
| Hsp90 is obligatory for the heme-regulated eIF-2alpha kinase to acquire and maintain an activable conformation. | Q52524930 | ||
| Assessment of the ATP binding properties of Hsp90. | Q54590056 | ||
| Interaction of Endoplasmic Reticulum Chaperone GRP94 with Peptide Substrates Is Adenine Nucleotide-independent | Q63313318 | ||
| Chaperone function of Hsp90-associated proteins | Q71824848 | ||
| Molecular chaperone machines: chaperone activities of the cyclophilin Cyp-40 and the steroid aporeceptor-associated protein p23 | Q71824853 | ||
| Trypanosoma cruzi heat-shock protein 90 can functionally complement yeast | Q71965424 | ||
| Interaction between casein kinase II and the 90-kDa stress protein, HSP90 | Q72344048 | ||
| In vitro evidence that hsp90 contains two independent chaperone sites | Q73981312 | ||
| Monomer arrangement in HSP90 dimer as determined by decoration with N and C-terminal region specific antibodies | Q77789674 | ||
| Studies with Purified Chaperones Advance the Understanding of the Mechanism of Glucocorticoid Receptor-hsp90 Heterocomplex Assembly | Q81065585 | ||
| P433 | issue | 4 | |
| P1104 | number of pages | 6 | |
| P304 | page(s) | 136-141 | |
| P577 | publication date | 1999-04-01 | |
| P1433 | published in | Trends in Biochemical Sciences | Q1565711 |
| P1476 | title | Hsp90 & Co. - a holding for folding | |
| P478 | volume | 24 |
| Q44624987 | A Novel Binding Protein for a Member of CyP40-type Cyclophilins: N.crassa CyPBP37, a Growth and Thiamine Regulated Protein Homolog to Yeast Thi4p |
| Q34105936 | A Nucleotide-dependent molecular switch controls ATP binding at the C-terminal domain of Hsp90. N-terminal nucleotide binding unmasks a C-terminal binding pocket |
| Q40040751 | A critical role for HSP90 in cancer cell invasion involves interaction with the extracellular domain of HER-2. |
| Q44230449 | A dynamic structural model for estrogen receptor-alpha activation by ligands, emphasizing the role of interactions between distant A and E domains |
| Q73977972 | A glucosinolate mutant of Arabidopsis is thermosensitive and defective in cytosolic Hsp90 expression after heat stress |
| Q33830135 | A model for the cytoplasmic trafficking of signalling proteins involving the hsp90-binding immunophilins and p50cdc37. |
| Q35837624 | A molecular physiological review of vegetative desiccation tolerance in the resurrection plant Xerophyta viscosa (Baker) |
| Q34611485 | A novel method for detecting intramolecular coevolution: adding a further dimension to selective constraints analyses. |
| Q30856266 | A role for the Hsp40 Ydj1 in repression of basal steroid receptor activity in yeast |
| Q40301279 | A role for the Hsp90 molecular chaperone family in antigen presentation to T lymphocytes via major histocompatibility complex class II molecules |
| Q34433468 | A small heat shock protein is essential for thermotolerance and intracellular survival of Leishmania donovani |
| Q43577973 | A small molecule designed to bind to the adenine nucleotide pocket of Hsp90 causes Her2 degradation and the growth arrest and differentiation of breast cancer cells |
| Q24541564 | A subset of chaperones and folding enzymes form multiprotein complexes in endoplasmic reticulum to bind nascent proteins |
| Q28769077 | A transmembrane guanylyl cyclase (DAF-11) and Hsp90 (DAF-21) regulate a common set of chemosensory behaviors in caenorhabditis elegans |
| Q24543917 | A unique molecular chaperone Cosmc required for activity of the mammalian core 1 beta 3-galactosyltransferase |
| Q22011182 | ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF |
| Q40364751 | Adaptor heat shock protein complex formation regulates trafficking of the asialoglycoprotein receptor |
| Q84924077 | Agonistic encounters and cellular angst: social interactions induce heat shock proteins in juvenile salmonid fish |
| Q24295270 | Aha1 binds to the middle domain of Hsp90, contributes to client protein activation, and stimulates the ATPase activity of the molecular chaperone |
| Q40483613 | Aha1 competes with Hop, p50 and p23 for binding to the molecular chaperone Hsp90 and contributes to kinase and hormone receptor activation |
| Q91613178 | Alcohol Modulates the Biogenesis and Composition of Microglia-Derived Exosomes |
| Q50515667 | Alpha-complemented beta-galactosidase. An in vivo model substrate for the molecular chaperone heat-shock protein 90 in yeast. |
| Q33969470 | Alpha-crystallin-type heat shock proteins: socializing minichaperones in the context of a multichaperone network. |
| Q46253811 | Analysis of HspB1 (Hsp27) Oligomerization and Phosphorylation Patterns and Its Interaction with Specific Client Polypeptides |
| Q33225270 | Analysis of hypoxia-inducible factor-1alpha accumulation and cell cycle in geldanamycin-treated human cervical carcinoma cells by laser scanning cytometry |
| Q38503421 | Analysis of sexually dimorphic expression of genes at early gonadogenesis of pejerrey Odontesthes bonariensis using a heterologous microarray |
| Q41623374 | Apo-Hsp90 coexists in two open conformational states in solution. |
| Q43289861 | Apoptosis caused by Hsp90 inhibitor geldanamycin in Leishmania donovani during promastigote-to-amastigote transformation stage |
| Q40424897 | Aryl hydrocarbon (Ah) receptor levels are selectively modulated by hsp90-associated immunophilin homolog XAP2. |
| Q40592252 | Aryl hydrocarbon nuclear translocator (ARNT) promotes oxygen-independent stabilization of hypoxia-inducible factor-1alpha by modulating an Hsp90-dependent regulatory pathway |
| Q34460136 | BAG-1 family of cochaperones in the modulation of nuclear receptor action. |
| Q38203487 | Barcoding heat shock proteins to human diseases: looking beyond the heat shock response |
| Q28216259 | Binding of ATP to heat shock protein 90: evidence for an ATP-binding site in the C-terminal domain |
| Q51431702 | Bipartite Role of Heat Shock Protein 90 (Hsp90) Keeps CRAF Kinase Poised for Activation. |
| Q43572431 | Both the N- and C-terminal chaperone sites of Hsp90 participate in protein refolding |
| Q42743031 | Both the charged linker region and ATPase domain of Hsp90 are essential for Rad51-dependent DNA repair |
| Q28596567 | C-terminal domain of SMYD3 serves as a unique HSP90-regulated motif in oncogenesis |
| Q28271643 | C-terminal phosphorylation of Hsp70 and Hsp90 regulates alternate binding to co-chaperones CHIP and HOP to determine cellular protein folding/degradation balances |
| Q35097617 | CHIP: a quality-control E3 ligase collaborating with molecular chaperones |
| Q28581892 | CK2 binds, phosphorylates, and regulates its pivotal substrate Cdc37, an Hsp90-cochaperone |
| Q40763457 | CK2 controls multiple protein kinases by phosphorylating a kinase-targeting molecular chaperone, Cdc37. |
| Q44752936 | Calcineurin and heat-shock proteins modulation in clenbuterol-induced hypertrophied rat skeletal muscles |
| Q82685782 | Changes in the expression of heat-shock protein genes depending on different heat resistance of plants |
| Q38304970 | Chaperone network composition in Solanum lycopersicum explored by transcriptome profiling and microarray meta-analysis |
| Q27011776 | Chaperoning steroidal physiology: lessons from mouse genetic models of Hsp90 and its cochaperones |
| Q43028887 | Characterization of a novel complex from halophilic archaebacteria, which displays chaperone-like activities in vitro |
| Q44315461 | Characterization of a plant homolog of hop, a cochaperone of hsp90. |
| Q37308803 | Characterization of orchardgrass p23, a flowering plant Hsp90 cohort protein. |
| Q30679866 | Characterization of the cDNA encoding the 90 kDa heat-shock protein in the Lepidoptera Bombyx mori and Spodoptera frugiperda |
| Q34099877 | Characterizing heat shock protein 90 gene of Apolygus lucorum (Meyer-Dür) and its expression in response to different temperature and pesticide stresses |
| Q27938204 | Cns1 is an activator of the Ssa1 ATPase activity |
| Q24307587 | Cofactor Tpr2 combines two TPR domains and a J domain to regulate the Hsp70/Hsp90 chaperone system |
| Q92343830 | Comparative Proteomics and Physiological Analyses Reveal Important Maize Filling-Kernel Drought-Responsive Genes and Metabolic Pathways |
| Q33358679 | Comparison of good- and bad-quality cork: application of high-throughput sequencing of phellogenic tissue |
| Q27930200 | Contribution of N- and C-terminal domains to the function of Hsp90 in Saccharomyces cerevisiae |
| Q43664670 | Coordinated ATP hydrolysis by the Hsp90 dimer |
| Q27938998 | Cpr6 and Cpr7, two closely related Hsp90-associated immunophilins from Saccharomyces cerevisiae, differ in their functional properties |
| Q30993657 | DNA methylation, methyltransferases, and cancer |
| Q38297991 | DNA relaxation and cleavage assays to study topoisomerase I inhibitors |
| Q35096762 | Dealing with misfolded proteins: examining the neuroprotective role of molecular chaperones in neurodegeneration. |
| Q40906095 | Degradation of heterotrimeric Galpha(o) subunits via the proteosome pathway is induced by the hsp90-specific compound geldanamycin |
| Q31108274 | Development of a purine-scaffold novel class of Hsp90 binders that inhibit the proliferation of cancer cells and induce the degradation of Her2 tyrosine kinase |
| Q33281757 | Differential cerebral cortex transcriptomes of baboon neonates consuming moderate and high docosahexaenoic acid formulas |
| Q33938836 | Differential proteomic analysis of grapevine leaves by iTRAQ reveals responses to heat stress and subsequent recovery |
| Q28484844 | Differentially expressed genes in Hirudo medicinalis ganglia after acetyl-L-carnitine treatment |
| Q35816373 | Dimerization and N-terminal domain proximity underlie the function of the molecular chaperone heat shock protein 90 |
| Q44532388 | Dissection of the contribution of individual domains to the ATPase mechanism of Hsp90. |
| Q73270311 | DjlA is a third DnaK co-chaperone of Escherichia coli, and DjlA-mediated induction of colanic acid capsule requires DjlA-DnaK interaction |
| Q34088024 | Drug-induced ubiquitylation and degradation of ErbB receptor tyrosine kinases: implications for cancer therapy |
| Q28254233 | Drugging the cancer kinome: progress and challenges in developing personalized molecular cancer therapeutics |
| Q37489908 | Effect of geldanamycin on androgen receptor function and stability |
| Q40468950 | Effects of 17-allylamino-17-demethoxygeldanamycin (17-AAG) on pediatric acute lymphoblastic leukemia (ALL) with respect to Bcr-Abl status and imatinib mesylate sensitivity. |
| Q44106949 | Effects of glycyrrhizin on glucocorticoid signaling pathway in hepatocytes |
| Q34212832 | Efficient Hsp90-independent in vitro activation by Hsc70 and Hsp40 of duck hepatitis B virus reverse transcriptase, an assumed Hsp90 client protein. |
| Q34009537 | Efficient detection of proteins retro-translocated from the ER to the cytosol by in vivo biotinylation. |
| Q34093483 | Endoplasmic reticulum chaperone gp96 is required for innate immunity but not cell viability |
| Q36673389 | Endoplasmic reticulum chaperones are involved in the morphogenesis of rotavirus infectious particles |
| Q35188962 | Engineering an antibiotic to fight cancer: optimization of the novobiocin scaffold to produce anti-proliferative agents |
| Q28208008 | ErbB2 degradation mediated by the co-chaperone protein CHIP |
| Q44249797 | Essential role of the unusual DNA-binding motif of BAG-1 for inhibition of the glucocorticoid receptor |
| Q37490567 | Expression of a unique drug-resistant Hsp90 ortholog by the nematode Caenorhabditis elegans |
| Q33736465 | Expression of heat shock proteins and heat shock protein messenger ribonucleic acid in human prostate carcinoma in vitro and in tumors in vivo. |
| Q33948624 | Expression pattern of heat shock protein 90 gene of humphead snapper Lutjanus sanguineus during pathogenic Vibrio harveyi stress |
| Q28477776 | Extracellular heat shock protein (Hsp)70 and Hsp90α assist in matrix metalloproteinase-2 activation and breast cancer cell migration and invasion |
| Q34980355 | FLT3 in human hematologic malignancies |
| Q38270187 | Folding and stability of the ligand-binding domain of the glucocorticoid receptor |
| Q34400939 | From the cradle to the grave: molecular chaperones that may choose between folding and degradation |
| Q24291221 | Functional analysis of the Hsp90-associated human peptidyl prolyl cis/trans isomerases FKBP51, FKBP52 and Cyp40 |
| Q34545636 | Functional genomic approaches to understanding molecular chaperones and stress responses |
| Q31583023 | Functional interaction of human Cdc37 with the androgen receptor but not with the glucocorticoid receptor |
| Q44616327 | G Protein-coupled Receptor Kinase Interaction with Hsp90 Mediates Kinase Maturation |
| Q30715432 | GERp95 belongs to a family of signal-transducing proteins and requires Hsp90 activity for stability and Golgi localization |
| Q35929315 | Geldanamycin, an inhibitor of Hsp90 increases cytochrome P450 2E1 mediated toxicity in HepG2 cells through sustained activation of the p38MAPK pathway |
| Q33915513 | Gene expression profiling of human colon cancer cells following inhibition of signal transduction by 17-allylamino-17-demethoxygeldanamycin, an inhibitor of the hsp90 molecular chaperone. |
| Q52128467 | Genes upregulated in lead-resistant glioma cells reveal possible targets for lead-induced developmental neurotoxicity. |
| Q42878029 | Genetic engineering for heat tolerance in plants |
| Q42440163 | Genomic and transcriptional alterations in mouse fetus liver after transplacental exposure to cigarette smoke |
| Q37596071 | Global transcriptome analysis of the heat shock response of Shewanella oneidensis |
| Q55514211 | Glutathione modulates the expression of heat shock proteins via the transcription factors BZIP10 and MYB21 in Arabidopsis. |
| Q42480755 | HEAT SHOCK PROTEIN 90C is a bona fide Hsp90 that interacts with plastidic HSP70B in Chlamydomonas reinhardtii |
| Q42883440 | HSF-1, HIF-1 and HSP90 expression on recombinant Pichia pastoris under fed-batch fermentation. |
| Q43852434 | HSP70 overexpression increases resistance of V79 cells to cytotoxicity of airborne pollutants, but does not protect the mitotic spindle against damage caused by airborne toxins. |
| Q92922007 | HSP90 Interacts with the Fibronectin N-terminal Domains and Increases Matrix Formation |
| Q29617504 | HSP90 and the chaperoning of cancer |
| Q30373788 | Heat Shock Protein 90α Is a Potential Serological Biomarker of Acute Rejection after Renal Transplantation. |
| Q48331448 | Heat shock and developmental expression of hsp83 in the filarial nematode Brugia pahangi |
| Q39624638 | Heat shock protein 90 facilitates formation of the HBV capsid via interacting with the HBV core protein dimers. |
| Q38357729 | Heat shock protein 90 function is essential for Plasmodium falciparum growth in human erythrocytes. |
| Q39230727 | Heat shock protein 90 homeostasis controls stage differentiation in Leishmania donovani |
| Q22254677 | Heat shock protein 90 mediates protein-protein interactions between human aminoacyl-tRNA synthetases |
| Q26776302 | Heat shock protein 90 targeting therapy: state of the art and future perspective |
| Q35038788 | Heat shock protein and proteasome targeting agents |
| Q28272905 | Heat shock proteins and heat shock factor 1 in carcinogenesis and tumor development: an update |
| Q35545091 | Heat shock proteins as emerging therapeutic targets |
| Q33899708 | Heat shock proteins in cancer: diagnostic, prognostic, predictive, and treatment implications |
| Q34382527 | Histone deacetylase inhibitors: the epigenetic therapeutics that repress hypoxia-inducible factors |
| Q36780484 | Hormetic modulation of aging and longevity by mild heat stress |
| Q33950214 | Host cell factor requirement for hepatitis C virus enzyme maturation |
| Q52575458 | Hsc70/Hsp40 chaperone system mediates the Hsp90-dependent refolding of firefly luciferase. |
| Q34012698 | Hsp104 interacts with Hsp90 cochaperones in respiring yeast |
| Q34545594 | Hsp70 chaperone machines. |
| Q24533332 | Hsp70 regulates the interaction between the peroxisome targeting signal type 1 (PTS1)-receptor Pex5p and PTS1 |
| Q24596488 | Hsp70-RAP46 interaction in downregulation of DNA binding by glucocorticoid receptor |
| Q29618584 | Hsp90 as a capacitor of phenotypic variation |
| Q36635195 | Hsp90 as a target for drug development |
| Q36581399 | Hsp90 at the crossroads of genetics and epigenetics |
| Q35640147 | Hsp90 can accommodate the simultaneous binding of the FKBP52 and HOP proteins |
| Q38310098 | Hsp90 chaperone activity requires the full-length protein and interaction among its multiple domains |
| Q42316572 | Hsp90 dependence of a kinase is determined by its conformational landscape |
| Q27934627 | Hsp90 enables Ctf13p/Skp1p to nucleate the budding yeast kinetochore |
| Q42169358 | Hsp90 inhibition accelerates cell lysis. Anti-Hsp90 ribozyme reveals a complex mechanism of Hsp90 inhibitors involving both superoxide- and Hsp90-dependent events |
| Q38895392 | Hsp90 inhibitors radicicol and geldanamycin have opposing effects on Leishmania Aha1-dependent proliferation. |
| Q30846862 | Hsp90 is a core centrosomal component and is required at different stages of the centrosome cycle in Drosophila and vertebrates |
| Q38482173 | Hsp90 is essential for the synthesis and subsequent membrane association, but not the maintenance, of the Src-kinase p56(lck). |
| Q28204780 | Hsp90 phosphorylation is linked to its chaperoning function. Assembly of the reovirus cell attachment protein |
| Q36041929 | Hsp90 regulates O-linked β-N-acetylglucosamine transferase: a novel mechanism of modulation of protein O-linked β-N-acetylglucosamine modification in endothelial cells |
| Q34407370 | Hsp90 regulates activation of interferon regulatory factor 3 and TBK-1 stabilization in Sendai virus-infected cells |
| Q30838920 | Hsp90 regulation of fibroblast activation in pulmonary fibrosis |
| Q39304863 | Hsp90 rescues PTK6 from proteasomal degradation in breast cancer cells. |
| Q34138017 | Hsp90-binding immunophilins in plants: the protein movers |
| Q34473659 | Hsp90: a chaperone for protein folding and gene regulation |
| Q34319594 | Hsp90: chaperoning signal transduction |
| Q42477330 | HtpG is essential for the thermal stress management in cyanobacteria |
| Q34533865 | Human calmodulin methyltransferase: expression, activity on calmodulin, and Hsp90 dependence |
| Q40920382 | Hypoxia-induced activation of HIF-1: role of HIF-1alpha-Hsp90 interaction |
| Q40704635 | Identification of Hsp90 as a stimulatory host factor involved in influenza virus RNA synthesis |
| Q33422336 | Identification of differentially expressed genes in the growth plate of broiler chickens with thiram-induced tibial dyschondroplasia |
| Q90453929 | Identification of genes associated with stress tolerance in moth bean [Vigna aconitifolia (Jacq.) Marechal], a stress hardy crop |
| Q54039489 | IgA antibodies to the 27-kDa heat-shock protein in the genital tracts of women with gynecologic cancers. |
| Q54355782 | Immunohistochemical analysis of expressions of RB1, CDK4, HSP90, cPLA2G4A, and CHMP2B is helpful in distinction between myxofibrosarcoma and myxoid liposarcoma. |
| Q36690857 | Immunohistochemical detection of Hsp90 and Ki-67 in pterygium |
| Q24672548 | Impact of protein kinase PKR in cell biology: from antiviral to antiproliferative action |
| Q33812161 | In vitro reconstitution of a functional duck hepatitis B virus reverse transcriptase: posttranslational activation by Hsp90. |
| Q34327359 | In vitro reconstitution of functional hepadnavirus reverse transcriptase with cellular chaperone proteins |
| Q40585096 | Inhibition of GR-mediated transcription by p23 requires interaction with Hsp90. |
| Q28212970 | Inhibition of MDM2 by hsp90 contributes to mutant p53 stabilization |
| Q73176009 | Insight into the secondary structure of non-native proteins bound to a molecular chaperone alpha-crystallin. An isotope-edited infrared spectroscopic study |
| Q73272057 | Interactions of Hsp90 with histones and related peptides |
| Q42802682 | Intracellular localization of the 90 kDA heat shock protein (HSP90α) determined by expression of a EGFP—HSP90α‐fusion protein in unstressed and heat stressed 3T3 cells |
| Q58459479 | Investigating Coral Reef Degradation at Alina's Reef in the Florida Keys: Cellular Physiology of White Grunt (Haemulon plumieri) as a Biological Indicator |
| Q38760723 | Involvement of cell surface 90 kDa heat shock protein (HSP90) in pattern recognition by human monocyte-derived macrophages |
| Q34338431 | Involvement of tumor necrosis factor receptor-associated protein 1 (TRAP1) in apoptosis induced by beta-hydroxyisovalerylshikonin |
| Q77319142 | Isolation and quantification of the heat shock protein 90 alpha and beta isoforms from rat liver |
| Q43569162 | LY294002-geldanamycin heterodimers as selective inhibitors of the PI3K and PI3K-related family |
| Q35725137 | Leishmania donovani P23 protects parasites against HSP90 inhibitor-mediated growth arrest |
| Q30823415 | Ligand discrimination by TPR domains. Relevance and selectivity of EEVD-recognition in Hsp70 x Hop x Hsp90 complexes |
| Q78203578 | Localization of calponin binding sites in the structure of 90 kDa heat shock protein (Hsp90) |
| Q43687948 | Localization of the chaperone domain of FKBP52. |
| Q34267286 | Loss of HDAC6, a novel CHIP substrate, alleviates abnormal tau accumulation |
| Q51040073 | Low temperature or GroEL/ES overproduction permits growth of Escherichia coli cells lacking trigger factor and DnaK. |
| Q39974251 | MafG controls the hypoxic response of cells by accumulating HIF-1alpha in the nuclei |
| Q34124519 | Maturation of steroid receptors: an example of functional cooperation among molecular chaperones and their associated proteins |
| Q40736227 | Mechanism of constitutive activation of FLT3 with internal tandem duplication in the juxtamembrane domain |
| Q28272747 | Mechanisms of disease: the role of heat-shock protein 90 in genitourinary malignancy |
| Q42670673 | MnHSP90 cDNA characterization and its expression during the ovary development in oriental river prawn, Macrobrachium nipponense. |
| Q36638210 | Molecular Characteristic, Protein Distribution and Potential Regulation of HSP90AA1 in the Anadromous Fish Coilia nasus |
| Q34038270 | Molecular chaperones are nanomachines that catalytically unfold misfolded and alternatively folded proteins |
| Q36343046 | Molecular chaperones throughout the life cycle of the androgen receptor |
| Q34165962 | Molecular chaperones--cellular machines for protein folding |
| Q51263802 | Molecular chaperones: providing a safe place to weather a midlife protein-folding crisis. |
| Q42647966 | Molecular characterization and expression analysis of a heat shock protein 90 gene from disk abalone (Haliotis discus). |
| Q34470862 | Molecular characterization and expression of a heat shock protein gene (HSP90) from the carmine spider mite, Tetranychus cinnabarinus (Boisduval). |
| Q42634322 | Molecular cloning and expression analysis of a heat shock protein (Hsp90) gene from black tiger shrimp (Penaeus monodon). |
| Q38760108 | Molecular interactions of polo-like kinase 1 in human cancers. |
| Q41932080 | Molecular mechanisms of anti-aging hormetic effects of mild heat stress on human cells. |
| Q73135768 | Mutations in the Plk gene lead to instability of Plk protein in human tumour cell lines |
| Q41828115 | Neurite outgrowth mediated by the heat shock protein Hsp90α: a novel target for the antipsychotic drug aripiprazole |
| Q39074963 | No stress--Hsp90 and signal transduction in Leishmania |
| Q34994676 | Nonrandom tripeptide sequence distributions at protein carboxyl termini |
| Q37320252 | Novobiocin and additional inhibitors of the Hsp90 C-terminal nucleotide-binding pocket |
| Q40556496 | Nuclear translocation of papillomavirus minor capsid protein L2 requires Hsc70. |
| Q33734537 | NudC-like protein 2 regulates the LIS1/dynein pathway by stabilizing LIS1 with Hsp90. |
| Q44126025 | Overexpression of the wheat FK506-binding protein 73 (FKBP73) and the heat-induced wheat FKBP77 in transgenic wheat reveals different functions of the two isoforms |
| Q44242668 | Pasticcino2 is a protein tyrosine phosphatase-like involved in cell proliferation and differentiation in Arabidopsis. |
| Q37288545 | Pathology-dependent effects linked to small heat shock proteins expression: an update |
| Q39510533 | Pharmacological inhibition of HSP90 activity negatively modulates myogenic differentiation and cell survival in C2C12 cells |
| Q34380573 | Phosphoproteomic analysis reveals site-specific changes in GFAP and NDRG2 phosphorylation in frontotemporal lobar degeneration |
| Q28214608 | Phosphorylation and hsp90 binding mediate heat shock stabilization of p53 |
| Q24294328 | Phosphorylation of HSF1 by MAPK-activated protein kinase 2 on serine 121, inhibits transcriptional activity and promotes HSP90 binding |
| Q44094456 | Phosphorylation-dependent interaction of the asialoglycoprotein receptor with molecular chaperones |
| Q33923929 | Polypeptide release by Hsp90 involves ATP hydrolysis and is enhanced by the co-chaperone p23. |
| Q37532027 | Posttranslational modulation on the biological activities of molecular chaperones |
| Q33834707 | Production and purification of human Hsp90β in Escherichia coli |
| Q38509921 | Profiling neuroendocrine gene expression changes following fadrozole-induced estrogen decline in the female goldfish |
| Q39384090 | Protein SUMOylation and plant abiotic stress signaling: in silico case study of rice RLKs, heat-shock and Ca(2+)-binding proteins |
| Q34293903 | Protein translocation across membranes |
| Q36974914 | Protein transport across the parasitophorous vacuole of Plasmodium falciparum: into the great wide open |
| Q37383489 | Protein transport in organelles: The composition, function and regulation of the Tic complex in chloroplast protein import. |
| Q43156161 | Quality control of a cytoplasmic protein complex: chaperone motors and the ubiquitin-proteasome system govern the fate of orphan fatty acid synthase subunit Fas2 of yeast |
| Q28578339 | Rab-alphaGDI activity is regulated by a Hsp90 chaperone complex |
| Q28209725 | Radicicol represses the transcriptional function of the estrogen receptor by suppressing the stabilization of the receptor by heat shock protein 90 |
| Q41808075 | Rapid decrease of CD16 (FcγRIII) expression on heat-shocked neutrophils and their recognition by macrophages |
| Q34141716 | Recognition between flexible protein molecules: induced and assisted folding |
| Q44217992 | Redox control of Hsp70-Co-chaperone interaction revealed by expression of a thioredoxin-like Arabidopsis protein |
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| Q33713035 | Regulation of survivin function by Hsp90 |
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| Q39645245 | Requirement of Hsp90 for centrosomal function reflects its regulation of Polo kinase stability |
| Q33701406 | Retraction: Hsp90 interaction with INrf2(Keap1) mediates stress-induced Nrf2 activation |
| Q40734779 | Role of p50/CDC37 in hepadnavirus assembly and replication |
| Q39521915 | Role of the heat shock protein 90 in immune response stimulation by bacterial DNA and synthetic oligonucleotides |
| Q60017544 | Roles of heat shock factor 1 beyond the heat shock response |
| Q33336944 | SHEPHERD is the Arabidopsis GRP94 responsible for the formation of functional CLAVATA proteins |
| Q33906867 | Solid-phase parallel synthesis of a tetrahydroindazolone library containing three unique core skeletons. |
| Q43559891 | Specific association of a set of molecular chaperones including HSP90 and Cdc37 with MOK, a member of the mitogen-activated protein kinase superfamily |
| Q27931140 | Sti1 Is a Novel Activator of the Ssa Proteins |
| Q33334155 | Stress genes and proteins in the archaea |
| Q73408466 | Structural/functional assignment of unknown bacteriophage T4 proteins by iterative database searches |
| Q27652939 | Structure and Functional Studies of the CS Domain of the Essential H/ACA Ribonucleoparticle Assembly Protein SHQ1 |
| Q27622332 | Structure of TPR domain-peptide complexes: critical elements in the assembly of the Hsp70-Hsp90 multichaperone machine |
| Q34116190 | Structure, function, and mechanism of the Hsp90 molecular chaperone |
| Q31053524 | Study of therapy resistance in cancer cells with functional proteome analysis |
| Q36843657 | Substrate protein folds while it is bound to the ATP-independent chaperone Spy |
| Q35375097 | Synthesis and evaluation of poly(styrene-co-maleic acid) micellar nanocarriers for the delivery of tanespimycin |
| Q79236261 | Synthesis of novel fluorescent probes for the molecular chaperone Hsp90 |
| Q34662543 | T antigens of simian virus 40: molecular chaperones for viral replication and tumorigenesis |
| Q34330916 | Targeting telomeres and telomerase |
| Q39767891 | Targeting the insulin-like growth factor pathway in rhabdomyosarcomas: rationale and future perspectives. |
| Q43166064 | The 26S proteasome function and Hsp90 activity involved in the regulation of HsfA2 expression in response to oxidative stress. |
| Q42645780 | The ATPase cycle of the mitochondrial Hsp90 analog Trap1. |
| Q51042630 | The HSP90 chaperone machinery. |
| Q24535594 | The Hsp90 chaperone complex is both a facilitator and a repressor of the dsRNA-dependent kinase PKR |
| Q34159497 | The Hsp90 co-chaperones Cdc37 and Sti1 interact physically and genetically |
| Q28361507 | The Hsp90 family of proteins in Arabidopsis thaliana |
| Q36845743 | The Hsp90-Sti1 interaction is critical for Leishmania donovani proliferation in both life cycle stages |
| Q39992486 | The Leber congenital amaurosis protein AIPL1 functions as part of a chaperone heterocomplex |
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| Q43180721 | The balance of Polo-like kinase 1 in tumorigenesis |
| Q50493069 | The chlorate-resistant and photomorphogenesis-defective mutant cr88 encodes a chloroplast-targeted HSP90. |
| Q34861540 | The co-chaperone SGT of Leishmania donovani is essential for the parasite's viability |
| Q24652993 | The cochaperone Bag-1L enhances androgen receptor action via interaction with the NH2-terminal region of the receptor |
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| Q48086976 | The heat shock protein 90 of Eimeria tenella is essential for invasion of host cell and schizont growth |
| Q34966136 | The heat shock response and cytoprotection of the intestinal epithelium |
| Q24550978 | The hsp90 chaperone complex regulates intracellular localization of the dioxin receptor |
| Q40025733 | The interaction between Sgt1p and Skp1p is regulated by HSP90 chaperones and is required for proper CBF3 assembly |
| Q34814876 | The involvement of mammalian and plant FK506-binding proteins (FKBPs) in development |
| Q38212658 | The many functions of the endoplasmic reticulum chaperones and folding enzymes |
| Q73422790 | The molecular chaperone Cdc37 is required for Ste11 function and pheromone-induced cell cycle arrest |
| Q44295200 | The oligomeric state, complex formation, and chaperoning activity of hsp70 and hsp80 of Neurospora crassa |
| Q33967931 | The peptide near the C terminus regulates receptor CAR nuclear translocation induced by xenochemicals in mouse liver |
| Q33723746 | The role of HSP90 in evolution |
| Q34688320 | The role of chaperones in polyglutamine disease |
| Q38033199 | The role of heat shock protein 90 in modulating ischemia-reperfusion injury in the kidney. |
| Q34280951 | The role of heat shock proteins and their receptors in the activation of the immune system |
| Q33371122 | The stress responsive and morphologically regulated hsp90 gene from Paracoccidioides brasiliensis is essential to cell viability |
| Q33637496 | The synthesis and evaluation of flavone and isoflavone chimeras of novobiocin and derrubone |
| Q38268859 | The virus-induced HSPs regulate the apoptosis of operatus APCs that result in autoimmunity, not in homeostasis |
| Q36501370 | Therapy through chaperones: sense or antisense? Cystic fibrosis as a model disease |
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| Q39538968 | Transcriptional analysis of major heat shock genes of Helicobacter pylori |
| Q92404538 | Transcriptomic analysis reveals recovery strategies in strawberry roots after using a soil amendment in continuous cropping soil |
| Q53691564 | Transcriptomic study to understand thermal adaptation in a high temperature-tolerant strain of Pyropia haitanensis. |
| Q52678882 | Troglitazone induces differentiation in Trypanosoma brucei. |
| Q39987469 | Tubocapsenolide A, a novel withanolide, inhibits proliferation and induces apoptosis in MDA-MB-231 cells by thiol oxidation of heat shock proteins. |
| Q36370830 | Two distinct pathways mediated by PA28 and hsp90 in major histocompatibility complex class I antigen processing |
| Q28586476 | Unc45 activates Hsp90-dependent folding of the myosin motor domain |
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| Q34348757 | Unfolding the role of chaperones and chaperonins in human disease |
| Q44504087 | Use of modular substrates demonstrates mechanistic diversity and reveals differences in chaperone requirement of ERAD. |
| Q33955890 | Vegetative incompatibility in filamentous fungi: a roundabout way of understanding the phenomenon. |
| Q24317168 | XAP2 inhibits glucocorticoid receptor activity in mammalian cells |
| Q40774867 | c-Src and HSP72 interact in ATP-depleted renal epithelial cells. |
| Q48082512 | cDNA cloning, heat shock regulation and developmental expression of the hsp83 gene in the Mediterranean fruit fly Ceratitis capitata. |
| Q52599768 | p23 and HSP20/alpha-crystallin proteins define a conserved sequence domain present in other eukaryotic protein families. |
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