scholarly article | Q13442814 |
P2093 | author name string | Yahara I | |
Miyata Y | |||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 7042-7047 | |
P577 | publication date | 1992-04-01 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | The 90-kDa heat shock protein, HSP90, binds and protects casein kinase II from self-aggregation and enhances its kinase activity | |
P478 | volume | 267 |
Q31037344 | A gene located at 72A in Drosophila melanogaster encodes a novel zinc-finger protein that interacts with protein kinase CK2. |
Q34454414 | A role for Hsp90 in retinoid receptor signal transduction |
Q91627037 | A role for epigenetic adaption in evolution |
Q33957138 | A trans-activation domain in yeast heat shock transcription factor is essential for cell cycle progression during stress |
Q39971416 | Ability of CK2beta to selectively regulate cellular protein kinases. |
Q73107890 | Analysis of the native forms of the 90 kDa heat shock protein (hsp90) in plant cytosolic extracts |
Q24336102 | Apigenin inhibits proliferation and induces apoptosis in human multiple myeloma cells through targeting the trinity of CK2, Cdc37 and Hsp90 |
Q36298518 | Association of casein kinase 2 with nuclear chromatin in relation to androgenic regulation of rat prostate |
Q48253943 | Association of protein kinase CK2 with eukaryotic translation initiation factor eIF-2 and with grp94/endoplasmin |
Q52565856 | Brassica napus hsp90 can autophosphorylate and phosphorylate other protein substrates. |
Q24655034 | CDC37 is required for p60v-src activity in yeast |
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. |
Q35860589 | Casein Kinase 2 (CK2)-mediated Phosphorylation of Hsp90β as a Novel Mechanism of Rifampin-induced MDR1 Expression |
Q35640239 | Casein kinase 2 phosphorylation of Hsp90 threonine 22 modulates chaperone function and drug sensitivity |
Q40637227 | Casein kinase II in signal transduction and cell cycle regulation |
Q35111101 | Casein kinase II induced polymerization of soluble TDP-43 into filaments is inhibited by heat shock proteins |
Q34564806 | Cdc37 interacts with the glycine-rich loop of Hsp90 client kinases |
Q46922786 | Central NPY-Y5 sub-receptor partially functions as a mediator of NPY-induced hypothermia and affords thermotolerance in heat-exposed fasted chicks |
Q63640946 | Cloning of cDNAs for genes that are early-responsive to dehydration stress (ERDs) inArabidopsis thaliana L.: identification of three ERDs as HSP cognate genes |
Q27931200 | Cns1 is an essential protein associated with the hsp90 chaperone complex in Saccharomyces cerevisiae that can restore cyclophilin 40-dependent functions in cpr7Delta cells |
Q27489790 | Cochaperone Activity of Human Butyrate-Induced Transcript 1 Facilitates Hepatitis C Virus Replication through an Hsp90-Dependent Pathway |
Q39815562 | Dephosphorylation and inactivation of Akt/PKB is counteracted by protein kinase CK2 in HEK 293T cells |
Q84904193 | Detecting HSP90 phosphorylation |
Q47362584 | Detecting Posttranslational Modifications of Hsp90. |
Q41764723 | Distinct functions of the 90 kDa heat-shock protein (hsp90) in oestrogen and mineralocorticosteroid receptor activity: effects of hsp90 deletion mutants |
Q40021444 | Distinct roles of the molecular chaperone hsp90 in modulating dioxin receptor function via the basic helix-loop-helix and PAS domains |
Q37421566 | Drosophila protein kinase CK2 is rendered temperature-sensitive by mutations of highly conserved residues flanking the activation segment. |
Q46529513 | Evaluating CK2 activity with the antibody specific for the CK2-phosphorylated form of a kinase-targeting cochaperone Cdc37. |
Q24304321 | Expression and characterization of human FKBP52, an immunophilin that associates with the 90-kDa heat shock protein and is a component of steroid receptor complexes |
Q35133239 | Expression of recombinant human casein kinase II and recombinant heat shock protein 90 in Escherichia coli and characterization of their interactions |
Q36562473 | Functional interference between hypoxia and dioxin signal transduction pathways: competition for recruitment of the Arnt transcription factor |
Q33888219 | Geldanamycin as a potential anti-cancer agent: its molecular target and biochemical activity |
Q24548039 | Genetic analysis of viable Hsp90 alleles reveals a critical role in Drosophila spermatogenesis |
Q48041180 | Genomic organization of hsp90 gene family in Arabidopsis |
Q42041495 | H11 has dose-dependent and dual hypertrophic and proapoptotic functions in cardiac myocytes. |
Q42150510 | HSF1 stress response pathway regulates autophagy receptor SQSTM1/p62-associated proteostasis |
Q34333109 | Heat shock protein hsp90 regulates dioxin receptor function in vivo |
Q34911441 | Heat shock proteins modulate keloid formation |
Q48086826 | Heat-inducible rice hsp82 and hsp70 are not always co-regulated |
Q39978383 | Hsp70 associates with Rictor and is required for mTORC2 formation and activity |
Q92376493 | Hsp90 Chaperones Bluetongue Virus Proteins and Prevents Proteasomal Degradation |
Q33701406 | Hsp90 Interaction with INrf2(Keap1) Mediates Stress-induced Nrf2 Activation |
Q93014135 | Hsp90 inhibitors suppress P53 phosphorylation in LPS - induced endothelial inflammation |
Q36919284 | Hsp90 is required for pheromone signaling in yeast |
Q28284142 | Hsp90 phosphorylation, Wee1 and the cell cycle |
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 |
Q44885931 | Identification and characterization of proteins that interact with Drosophila melanogaster protein kinase CK2. |
Q34849635 | Identification of HSP90 as potential biomarker of biliary atresia using two-dimensional electrophoresis and mass spectrometry |
Q27940260 | Identification of SSF1, CNS1, and HCH1 as multicopy suppressors of a Saccharomyces cerevisiae Hsp90 loss-of-function mutation |
Q36660658 | Identification of a 60-kilodalton stress-related protein, p60, which interacts with hsp90 and hsp70 |
Q41415913 | Identification of transactivation and repression functions of the dioxin receptor and its basic helix-loop-helix/PAS partner factor Arnt: inducible versus constitutive modes of regulation |
Q27937090 | In vivo analysis of the Hsp90 cochaperone Sti1 (p60) |
Q27937958 | In vivo functions of the Saccharomyces cerevisiae Hsp90 chaperone |
Q24564127 | Inhibition of heat shock protein HSP90-pp60v-src heteroprotein complex formation by benzoquinone ansamycins: essential role for stress proteins in oncogenic transformation |
Q42159763 | Insulin regulation of mitogen-activated protein kinase kinase (MEK), mitogen-activated protein kinase and casein kinase in the cell nucleus: a possible role in the regulation of gene expression |
Q40555899 | Interaction of activated Cdc42-associated tyrosine kinase ACK2 with HSP90. |
Q36653910 | Interaction of glucocorticosteroid receptor and wild-type or mutated 90-kDa heat shock protein coexpressed in baculovirus-infected Sf9 cells |
Q42507191 | Interspecific transgenic analysis of basal versus heat-shock-induced expression of a Drosophila pseudoobscura hsp82-neo fusion gene in D. melanogaster |
Q36705300 | Isolation of Hsp90 mutants by screening for decreased steroid receptor function |
Q37308841 | Low concentration of GA activates a preconditioning response in HepG2 cells during oxidative stress-roles of Hsp90 and vimentin |
Q28481516 | Mapping the Hsp90 genetic interaction network in Candida albicans reveals environmental contingency and rewired circuitry |
Q34792400 | Maturation of the tyrosine kinase c-src as a kinase and as a substrate depends on the molecular chaperone Hsp90. |
Q42670673 | MnHSP90 cDNA characterization and its expression during the ovary development in oriental river prawn, Macrobrachium nipponense. |
Q27932967 | Mutational analysis of Hsp90 function: interactions with a steroid receptor and a protein kinase |
Q34380573 | Phosphoproteomic Analysis Reveals Site-Specific Changes in GFAP and NDRG2 Phosphorylation in Frontotemporal Lobar Degeneration |
Q24647502 | Phosphorylation of the immunosuppressant FK506-binding protein FKBP52 by casein kinase II: regulation of HSP90-binding activity of FKBP52 |
Q42118514 | Polymorphic glutathione S-transferase subunit 3 of rat liver exhibits different susceptibilities to carbon tetrachloride: differences in their interactions with heat-shock protein 90. |
Q35581165 | Post-translational modifications of Hsp90 and their contributions to chaperone regulation |
Q42606695 | Protein phosphatase 2C, encoded by ptc1+, is important in the heat shock response of Schizosaccharomyces pombe |
Q44878387 | Purification and Characterization of a Soluble Phosphatidylinositol 4-Kinase from Carrot Suspension Culture Cells |
Q42816826 | Purification and characterization of porcine testis 90-kDa heat shock protein (HSP90) as a substrate for various protein kinases |
Q54621052 | Reconstitution of Arabidopsis casein kinase II from recombinant subunits and phosphorylation of transcription factor GBF1. |
Q40519604 | Regulation of stability of cyclin-dependent kinase CDK11p110 and a caspase-processed form, CDK11p46, by Hsp90. |
Q39540221 | Role of HSP90 in salt stress tolerance via stabilization and regulation of calcineurin |
Q34275132 | Role of chaperones in nuclear translocation and transactivation of steroid receptors |
Q39510526 | Stimulation of CK2-dependent Grp94 phosphorylation by the nuclear localization signal peptide |
Q28359659 | Substrate-binding characteristics of proteins in the 90 kDa heat shock protein family |
Q33302931 | Systems analysis of chaperone networks in the malarial parasite Plasmodium falciparum |
Q52716432 | Targeting the Hsp90-Cdc37-client protein interaction to disrupt Hsp90 chaperone machinery. |
Q34336709 | Temperature-sensitive mutants of hsp82 of the budding yeast Saccharomyces cerevisiae |
Q24561774 | The 25-kDa FK506-binding protein is localized in the nucleus and associates with casein kinase II and nucleolin |
Q42106101 | The 90 kDa heat-shock protein (hsp90) modulates the binding of the oestrogen receptor to its cognate DNA. |
Q30493832 | The 90-kDa heat shock protein Hsp90 protects tubulin against thermal denaturation |
Q58692662 | The HSP90 Family: Structure, Regulation, Function, and Implications in Health and Disease |
Q42040986 | The Hsp90 chaperone complex A potential target for cancer therapy? |
Q40256118 | The Ydj1 molecular chaperone facilitates formation of active p60v-src in yeast |
Q24336430 | The carboxy-terminal region of mammalian HSP90 is required for its dimerization and function in vivo |
Q33886429 | The heat shock protein 83 (Hsp83) is required for Raf-mediated signalling in Drosophila |
Q24562938 | The human cytosolic molecular chaperones hsp90, hsp70 (hsc70) and hdj-1 have distinct roles in recognition of a non-native protein and protein refolding |
Q90327665 | The molecular chaperone Hsp90 maintains Golgi organization and vesicular trafficking by regulating microtubule stability |
Q38037753 | The therapeutic target Hsp90 and cancer hallmarks |
Q28307703 | Threonine 22 phosphorylation attenuates Hsp90 interaction with cochaperones and affects its chaperone activity |
Q72827469 | Translational regulation of the heat shock response |
Q35938409 | Two eukaryote-specific regions of Hsp82 are dispensable for its viability and signal transduction functions in yeast |
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