scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Hassan Y Naim | Q61100085 |
Abdullah Hoter | Q61100118 | ||
P2093 | author name string | Marwan E El-Sabban | |
P2860 | cites work | Comparative genomics and evolution of the HSP90 family of genes across all kingdoms of organisms | Q21266601 |
A direct interaction between EXT proteins and glycosyltransferases is defective in hereditary multiple exostoses | Q22010746 | ||
Grp78, Grp94, and Grp170 interact with alpha1-antitrypsin mutants that are retained in the endoplasmic reticulum | Q24300563 | ||
Sequence and regulation of a gene encoding a human 89-kilodalton heat shock protein | Q24304965 | ||
PINK1 protects against oxidative stress by phosphorylating mitochondrial chaperone TRAP1 | Q24312106 | ||
Identification of a protein with homology to hsp90 that binds the type 1 tumor necrosis factor receptor | Q24315622 | ||
Hsp90 cochaperone Aha1 downregulation rescues misfolding of CFTR in cystic fibrosis | Q24316177 | ||
Molecular chaperone TRAP1 regulates a metabolic switch between mitochondrial respiration and aerobic glycolysis | Q24337960 | ||
Innate immune recognition of viral infection | Q24498364 | ||
The hsp90 chaperone complex regulates intracellular localization of the dioxin receptor | Q24550978 | ||
The ATPase cycle of Hsp90 drives a molecular 'clamp' via transient dimerization of the N-terminal domains | Q24599484 | ||
Heat shock protein gp96 is a master chaperone for toll-like receptors and is important in the innate function of macrophages | Q24609722 | ||
Modulation of Akt kinase activity by binding to Hsp90 | Q24648565 | ||
A new member of the hsp90 family of molecular chaperones interacts with the retinoblastoma protein during mitosis and after heat shock | Q24648784 | ||
Guidelines for the nomenclature of the human heat shock proteins | Q24653946 | ||
Cytoprotective mitochondrial chaperone TRAP-1 as a novel molecular target in localized and metastatic prostate cancer | Q24654354 | ||
HLA-DR associates with specific stress proteins and is retained in the endoplasmic reticulum in invariant chain negative cells | Q24675139 | ||
Mechanisms of Hsp90 regulation | Q26741834 | ||
Extracellular HSPs: The Complicated Roles of Extracellular HSPs in Immunity | Q26747413 | ||
GRP94 is an Essential Regulator of Pancreatic β Cell Development, Mass and Function in Male Mice | Q47260586 | ||
Immunization with α-synuclein/Grp94 reshapes peripheral immunity and suppresses microgliosis in a chronic Parkinsonism model | Q47662675 | ||
Heat-shock protein 90: a novel autoantigen in human carotid atherosclerosis | Q47691117 | ||
A small-molecule screen reveals that HSP90β promotes the conversion of induced pluripotent stem cell-derived endoderm to a hepatic fate and regulates HNF4A turnover | Q48343445 | ||
Targeting HSP90 Ameliorates Nephropathy and Atherosclerosis Through Suppression of NF-κB and STAT Signaling Pathways in Diabetic Mice. | Q50580624 | ||
The HSP90 chaperone machinery. | Q51042630 | ||
Expression of heat shock genes during differentiation of mammalian osteoblasts and promyelocytic leukemia cells | Q52232519 | ||
Mutational analysis of Hsp90 alpha dimerization and subcellular localization: dimer disruption does not impede "in vivo' interaction with estrogen receptor. | Q52521481 | ||
Heat shock proteins 70 and 90 inhibit early stages of amyloid beta-(1-42) aggregation in vitro. | Q53381705 | ||
Heat shock protein 75 (TRAP1) antagonizes reactive oxygen species generation and protects cells from granzyme M-mediated apoptosis. | Q53551868 | ||
TRAP1 Regulation of Cancer Metabolism: Dual Role as Oncogene or Tumor Suppressor. | Q53698115 | ||
GRP94 (endoplasmin) co-purifies with and is phosphorylated by Golgi apparatus casein kinase. | Q53809608 | ||
Cellular HSP90 (HSP86) mRNA level and in vitro differentiation of mouse embryonal carcinoma (F9) cells. | Q54288392 | ||
Cell surface expression of the endoplasmic reticular heat shock protein gp96 is phylogenetically conserved | Q56902083 | ||
Hsp90 charged-linker truncation reverses the functional consequences of weakened hydrophobic contacts in the N domain | Q58360990 | ||
Structural Analysis of E. coli hsp90 reveals dramatic nucleotide-dependent conformational rearrangements | Q34575808 | ||
Roles of heat-shock proteins in innate and adaptive immunity | Q34576423 | ||
On the brotherhood of the mitochondrial chaperones mortalin and heat shock protein 60. | Q34703664 | ||
Exploiting the mitochondrial unfolded protein response for cancer therapy in mice and human cells | Q34755334 | ||
The Hsp90 chaperone machinery | Q34774579 | ||
Increased expression of Gp96 by HBx-induced NF-κB activation feedback enhances hepatitis B virus production | Q34775798 | ||
The charged region of Hsp90 modulates the function of the N-terminal domain | Q34988119 | ||
Mitochondria in cell death: novel targets for neuroprotection and cardioprotection | Q35134634 | ||
Endoplasmic reticulum heat shock protein gp96 maintains liver homeostasis and promotes hepatocellular carcinogenesis | Q35204677 | ||
Expression of heat-shock protein gp96 in gallbladder cancer and its prognostic clinical significance | Q35404849 | ||
A fragment of secreted Hsp90α carries properties that enable it to accelerate effectively both acute and diabetic wound healing in mice | Q35484843 | ||
Development of Radicicol Analogues | Q35551879 | ||
Post-translational modifications of Hsp90 and their contributions to chaperone regulation | Q35581165 | ||
Tumor rejection antigens of chemically induced sarcomas of inbred mice | Q35605797 | ||
The high-affinity HSP90-CHIP complex recognizes and selectively degrades phosphorylated tau client proteins | Q35629026 | ||
Hsp90 molecular chaperone inhibitors: are we there yet? | Q35655105 | ||
Secreted heat shock protein-90 (Hsp90) in wound healing and cancer | Q35696767 | ||
Charged linker sequence modulates eukaryotic heat shock protein 90 (Hsp90) chaperone activity | Q35779397 | ||
Conformational processing of oncogenic v-Src kinase by the molecular chaperone Hsp90. | Q35796269 | ||
The molecular chaperone gp96/GRP94 interacts with Toll-like receptors and integrins via its C-terminal hydrophobic domain | Q35838953 | ||
Two eukaryote-specific regions of Hsp82 are dispensable for its viability and signal transduction functions in yeast | Q35938409 | ||
Deletion of muscle GRP94 impairs both muscle and body growth by inhibiting local IGF production | Q36183694 | ||
Roles of heat shock protein gp96 in the ER quality control: redundant or unique function? | Q36305376 | ||
Membrane biogenesis during B cell differentiation: most endoplasmic reticulum proteins are expressed coordinately | Q36383421 | ||
Mitochondrial membrane permeability transition and cell death | Q36485017 | ||
Role of TRAP1 and estrogen receptor alpha in patients with ovarian cancer -a study of the OVCAD consortium | Q36498614 | ||
Shuttling of the chaperones Unc45b and Hsp90a between the A band and the Z line of the myofibril | Q36534622 | ||
Inhibitors of the HSP90 molecular chaperone: current status | Q36543819 | ||
A bipartite operator interacts with a heat shock element to mediate early meiotic induction of Saccharomyces cerevisiae HSP82. | Q36556247 | ||
Hsp90 as a target for drug development | Q36635195 | ||
Aberrantly upregulated TRAP1 is required for tumorigenesis of breast cancer | Q36689020 | ||
Molecular chaperones and protein kinase quality control. | Q36690540 | ||
Chaperone regulation of the heat shock protein response | Q36700315 | ||
Essential roles of grp94 in gut homeostasis via chaperoning canonical Wnt pathway | Q36799166 | ||
The 90-kDa heat shock protein, HSP90, binds and protects casein kinase II from self-aggregation and enhances its kinase activity. | Q34363897 | ||
Phylogenetic analysis of the 90 kD heat shock family of protein sequences and an examination of the relationship among animals, plants, and fungi species | Q34367390 | ||
p185erbB2 binds to GRP94 in vivo. Dissociation of the p185erbB2/GRP94 heterocomplex by benzoquinone ansamycins precedes depletion of p185erbB2. | Q34377527 | ||
Properties of the permeability transition pore in mitochondria devoid of Cyclophilin D. | Q34406704 | ||
A role for Hsp90 in retinoid receptor signal transduction | Q34454414 | ||
TRAP1 controls mitochondrial fusion/fission balance through Drp1 and Mff expression | Q34532535 | ||
Iron chelation study in a normal human hepatocyte cell line suggests that tumor necrosis factor receptor-associated protein 1 (TRAP1) regulates production of reactive oxygen species | Q34559849 | ||
The hsp90-binding antibiotic geldanamycin decreases Raf levels and epidermal growth factor signaling without disrupting formation of signaling complexes or reducing the specific enzymatic activity of Raf kinase | Q41127933 | ||
Resistance to paclitxel in breast carcinoma cells requires a quality control of mitochondrial antiapoptotic proteins by TRAP1. | Q41134535 | ||
Disruption of the Raf-1-Hsp90 Molecular Complex Results in Destabilization of Raf-1 and Loss of Raf-1-Ras Association | Q41282697 | ||
Conformation-defective herpes simplex virus 1 glycoprotein B activates the promoter of the grp94 gene that codes for the 94-kD stress protein in the endoplasmic reticulum. | Q41348511 | ||
Cell cycle regulation of the chicken hsp90 alpha expression | Q41569378 | ||
Role of molecular chaperones and TPR-domain proteins in the cytoplasmic transport of steroid receptors and their passage through the nuclear pore | Q41592060 | ||
Heat shock protein HSP90 and its association with the cytoskeleton: a morphological study | Q41604618 | ||
Targeting Heat Shock Proteins in Cancer: A Promising Therapeutic Approach | Q41660505 | ||
Several regions of human estrogen receptor are involved in the formation of receptor-heat shock protein 90 complexes | Q41714269 | ||
Identification of an HSP90 modulated multi-step process for ERBB2 degradation in breast cancer cells | Q41773399 | ||
Hsp90 chaperones PPARγ and regulates differentiation and survival of 3T3-L1 adipocytes. | Q41849041 | ||
Drosophila Trap1 protects against mitochondrial dysfunction in a PINK1/parkin model of Parkinson's disease. | Q41892915 | ||
Participation of the lipoprotein receptor LRP1 in hypoxia-HSP90alpha autocrine signaling to promote keratinocyte migration | Q42166748 | ||
The charged linker region is an important regulator of Hsp90 function | Q42575028 | ||
The ATPase cycle of the mitochondrial Hsp90 analog Trap1. | Q42645780 | ||
Structure of unliganded GRP94, the endoplasmic reticulum Hsp90. Basis for nucleotide-induced conformational change | Q42659468 | ||
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 | Q42802682 | ||
Cell cycle-dependent regulation of cellular ATP concentration, and depolymerization of the interphase microtubular network induced by elevated cellular ATP concentration in whole fibroblasts | Q42818151 | ||
The benzoquinone ansamycin 17-allylamino-17-demethoxygeldanamycin binds to HSP90 and shares important biologic activities with geldanamycin | Q42826312 | ||
Extracellular heat shock protein-90alpha: linking hypoxia to skin cell motility and wound healing | Q42929540 | ||
Control of pancreatic bile-salt-dependent-lipase secretion by the glucose-regulated protein of 94 kDa (Grp94). | Q42998256 | ||
GP96 is a GARP chaperone and controls regulatory T cell functions. | Q43135547 | ||
Detection of the ATPase activity of the molecular chaperones Hsp90 and Hsp72 using the TranscreenerTM ADP assay kit. | Q43165992 | ||
Cell surface expression of heat shock protein gp96 enhances cross-presentation of cellular antigens and the generation of tumor-specific T cell memory | Q43589172 | ||
Localization of the heat shock-induced proteins in Drosophila melanogaster tissue culture cells | Q43813270 | ||
Determinants of efficacy of immunotherapy with tumor-derived heat shock protein gp96 | Q44441511 | ||
Necrotic but not apoptotic cell death releases heat shock proteins, which deliver a partial maturation signal to dendritic cells and activate the NF-kappa B pathway | Q44539124 | ||
Impact of the tumor necrosis factor receptor-associated protein 1 (Trap1) on renal DNaseI shutdown and on progression of murine and human lupus nephritis | Q45794152 | ||
The specific interaction of the Rous sarcoma virus transforming protein, pp60src, with two cellular proteins | Q45801434 | ||
Purification of Drosophila hsp 83 and immunoelectron microscopic localization. | Q45805890 | ||
Hsp90 binds microtubules and is involved in the reorganization of the microtubular network in angiosperms. | Q45907925 | ||
Amyloid-β peptide-induced secretion of endoplasmic reticulum chaperone glycoprotein GRP94. | Q45908078 | ||
TRAP1, a novel mitochondrial chaperone responsible for multi-drug resistance and protection from apoptotis in human colorectal carcinoma cells | Q46122145 | ||
Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's disease | Q46280273 | ||
Quality control and fate determination of Hsp90 client proteins | Q26853052 | ||
GRP94: An HSP90-like protein specialized for protein folding and quality control in the endoplasmic reticulum | Q26860153 | ||
Orchestration of secretory protein folding by ER chaperones | Q27013551 | ||
Toll-Like Receptors and Viruses: Induction of Innate Antiviral Immune Responses | Q27487393 | ||
Structural and functional analysis of the middle segment of hsp90: implications for ATP hydrolysis and client protein and cochaperone interactions | Q27640863 | ||
Structure of the N-terminal domain of GRP94. Basis for ligand specificity and regulation | Q27642019 | ||
Different Poses for Ligand and Chaperone in Inhibitor-Bound Hsp90 and GRP94: Implications for Paralog-Specific Drug Design | Q27654646 | ||
Paralog-selective Hsp90 inhibitors define tumor-specific regulation of HER2 | Q27679845 | ||
Structural Asymmetry in the Closed State of Mitochondrial Hsp90 (TRAP1) Supports a Two-Step ATP Hydrolysis Mechanism | Q27681454 | ||
A molecular clamp in the crystal structure of the N-terminal domain of the yeast Hsp90 chaperone | Q27739168 | ||
Structural basis for inhibition of the Hsp90 molecular chaperone by the antitumor antibiotics radicicol and geldanamycin | Q27766755 | ||
Two chaperone sites in Hsp90 differing in substrate specificity and ATP dependence | Q27937497 | ||
Clients and Oncogenic Roles of Molecular Chaperone gp96/grp94 | Q28075479 | ||
Comparative analysis of the ATP-binding sites of Hsp90 by nucleotide affinity cleavage: a distinct nucleotide specificity of the C-terminal ATP-binding site | Q28205041 | ||
The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore | Q28241418 | ||
Cyclophilin D-dependent mitochondrial permeability transition regulates some necrotic but not apoptotic cell death | Q28242641 | ||
Selective targeting of the stress chaperome as a therapeutic strategy | Q28248791 | ||
The amino-terminal domain of heat shock protein 90 (hsp90) that binds geldanamycin is an ATP/ADP switch domain that regulates hsp90 conformation | Q28248831 | ||
The Hsp90 chaperone machinery: conformational dynamics and regulation by co-chaperones | Q28249196 | ||
Hsp90 isoforms: functions, expression and clinical importance | Q28255212 | ||
Heat shock proteins and heat shock factor 1 in carcinogenesis and tumor development: an update | Q28272905 | ||
Multiple molecular chaperones interact with apolipoprotein B during its maturation. The network of endoplasmic reticulum-resident chaperones (ERp72, GRP94, calreticulin, and BiP) interacts with apolipoprotein b regardless of its lipidation state | Q28278880 | ||
The HSP90 family of genes in the human genome: insights into their divergence and evolution | Q28280296 | ||
The 90-kDa molecular chaperone family: structure, function, and clinical applications. A comprehensive review | Q28283466 | ||
Hsp90 inhibitors: small molecules that transform the Hsp90 protein folding machinery into a catalyst for protein degradation | Q28289317 | ||
Voltage-dependent anion channels are dispensable for mitochondrial-dependent cell death | Q28297152 | ||
Multiple molecular chaperones complex with misfolded large oligomeric glycoproteins in the endoplasmic reticulum | Q28302040 | ||
Chaperone function of a Grp 94-related protein for folding and transport of the pancreatic bile salt-dependent lipase | Q28302440 | ||
Clinicopathologic significance of TRAP1 expression in colorectal cancer: a large scale study of human colorectal adenocarcinoma tissues | Q28468570 | ||
Several endoplasmic reticulum stress proteins, including ERp72, interact with thyroglobulin during its maturation | Q28579236 | ||
Participation of GRP94-related protein in secretion of pancreatic bile salt-dependent lipase and in its internalization by the intestinal epithelium | Q28583996 | ||
Regulation and function of the human HSP90AA1 gene | Q28646043 | ||
Mitochondrial membrane permeabilization in cell death | Q29547425 | ||
HSP90 and the chaperoning of cancer | Q29617504 | ||
A Remodeled Hsp90 Molecular Chaperone Ensemble with the Novel Cochaperone Aarsd1 Is Required for Muscle Differentiation | Q36811722 | ||
α7 helix region of αI domain is crucial for integrin binding to endoplasmic reticulum chaperone gp96: a potential therapeutic target for cancer metastasis | Q36947798 | ||
TRAP1 rescues PINK1 loss-of-function phenotypes | Q36950677 | ||
Hsp90 regulation of mitochondrial protein folding: from organelle integrity to cellular homeostasis | Q37056146 | ||
The chaperone activity of GRP94 toward insulin-like growth factor II is necessary for the stress response to serum deprivation | Q37127277 | ||
Novobiocin and additional inhibitors of the Hsp90 C-terminal nucleotide-binding pocket | Q37320252 | ||
Oxidative metabolism drives inflammation-induced platinum resistance in human ovarian cancer | Q37353982 | ||
Compartmentalized cancer drug discovery targeting mitochondrial Hsp90 chaperones | Q37396817 | ||
Two mammalian heat shock proteins, HSP90 and HSP100, are actin-binding proteins | Q37404795 | ||
GRP94 in ER quality control and stress responses | Q37707530 | ||
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association | Q37719873 | ||
Reactive oxygen species: stuck in the middle of neurodegeneration | Q37737502 | ||
Viral interaction with molecular chaperones: role in regulating viral infection | Q37749671 | ||
Intracellular protozoan parasites of humans: the role of molecular chaperones in development and pathogenesis | Q37800962 | ||
TRAP-1, the mitochondrial Hsp90. | Q37924023 | ||
Evolution and function of diverse Hsp90 homologs and cochaperone proteins | Q37947016 | ||
Broad action of Hsp90 as a host chaperone required for viral replication | Q37966479 | ||
Heat shock protein 90 from neglected protozoan parasites | Q37971264 | ||
Role of endoplasmic reticulum stress in metabolic disease and other disorders. | Q37976132 | ||
TRAP1 regulation of mitochondrial life or death decision in cancer cells and mitochondria-targeted TRAP1 inhibitors | Q37979012 | ||
The therapeutic target Hsp90 and cancer hallmarks | Q38037753 | ||
Hsp90: structure and function | Q38041439 | ||
Structure, function and regulation of the hsp90 machinery | Q38117496 | ||
Mitochondrial oxidative phosphorylation TRAP(1)ped in tumor cells | Q38204516 | ||
TRAP1 revisited: novel localizations and functions of a 'next-generation' biomarker (review). | Q38225819 | ||
Mutational analysis of hsp90 binding to the progesterone receptor. | Q38315811 | ||
Structures of the N-terminal and middle domains of E. coli Hsp90 and conformation changes upon ADP binding | Q38327853 | ||
Heat-induced chaperone activity of HSP90. | Q38361901 | ||
Transgenic Expression of the Mitochondrial Chaperone TNFR-associated Protein 1 (TRAP1) Accelerates Prostate Cancer Development | Q38740217 | ||
Unusual Suspects in the Twilight Zone Between the Hsp90 Interactome and Carcinogenesis | Q38750410 | ||
Impact of Posttranslational Modifications on the Anticancer Activity of Hsp90 Inhibitors. | Q38750414 | ||
The role of endoplasmic reticulum stress in neurodegenerative disease | Q38999268 | ||
The role of heat shock protein 90 in migration and proliferation of vascular smooth muscle cells in the development of atherosclerosis | Q39013502 | ||
Immune chaperone gp96 drives the contributions of macrophages to inflammatory colon tumorigenesis | Q39014670 | ||
Transforming growth factor alpha (TGFalpha)-stimulated secretion of HSP90alpha: using the receptor LRP-1/CD91 to promote human skin cell migration against a TGFbeta-rich environment during wound healing | Q39024877 | ||
Inhibition of HSP90 in Trypanosoma cruzi induces a stress response but no stage differentiation | Q39030722 | ||
Tumor-specific cell surface expression of the -KDEL containing endoplasmic reticular heat shock protein gp96 | Q60021885 | ||
The endoplasmic reticulum stress protein GRP94, in addition to BiP, associates with unassembled immunoglobulin chains | Q67907315 | ||
Characterization of the hydrophobic region of heat shock protein 90 | Q68040923 | ||
Endoplasmic reticulum contains a common, abundant calcium-binding glycoprotein, endoplasmin | Q68189236 | ||
The 90-kilodalton peptide of the heme-regulated eIF-2 alpha kinase has sequence similarity with the 90-kilodalton heat shock protein | Q68532171 | ||
Four intracisternal calcium-binding glycoproteins from rat liver microsomes with high affinity for calcium. No indication for calsequestrin-like proteins in inositol 1,4,5-trisphosphate-sensitive calcium sequestering rat liver vesicles | Q69752169 | ||
Selective release from cultured mammalian cells of heat-shock (stress) proteins that resemble glia-axon transfer proteins | Q69948836 | ||
Purification of the major mammalian heat shock proteins | Q70603283 | ||
The calmodulin-binding domain of the mouse 90-kDa heat shock protein | Q70695616 | ||
Protein C Nagoya, an elongated mutant of protein C, is retained within the endoplasmic reticulum and is associated with GRP78 and GRP94 | Q71099742 | ||
Interaction between casein kinase II and the 90-kDa stress protein, HSP90 | Q72344048 | ||
Association of Hsp47, Grp78, and Grp94 with procollagen supports the successive or coupled action of molecular chaperones | Q72631726 | ||
Novobiocin and related coumarins and depletion of heat shock protein 90-dependent signaling proteins | Q73402066 | ||
Virally induced lytic cell death elicits the release of immunogenic GRP94/gp96 | Q73694719 | ||
TAP-translocated peptides specifically bind proteins in the endoplasmic reticulum, including gp96, protein disulfide isomerase and calreticulin | Q73814928 | ||
In vitro evidence that hsp90 contains two independent chaperone sites | Q73981312 | ||
Calreticulin, PDI, Grp94 and BiP chaperone proteins are associated with retained COMP in pseudoachondroplasia chondrocytes | Q74257251 | ||
Import and processing of heart mitochondrial cyclophilin D | Q78003307 | ||
Molecular cloning, cellular expression and characterization of Arabian camel (Camelus dromedarius) endoplasmin | Q88920889 | ||
Calcium binding to a remote site can replace magnesium as cofactor for mitochondrial Hsp90 (TRAP1) ATPase activity | Q89507389 | ||
Molecular chaperone gp96 is a novel therapeutic target of multiple myeloma | Q39090150 | ||
Hsp90 inhibits α-synuclein aggregation by interacting with soluble oligomers. | Q39109956 | ||
The Chaperone TRAP1 As a Modulator of the Mitochondrial Adaptations in Cancer Cells. | Q39239549 | ||
Development of a Grp94 inhibitor | Q39340802 | ||
Release of the glucose-regulated protein 94 by baby hamster kidney cells | Q39364507 | ||
TRAP1 and the proteasome regulatory particle TBP7/Rpt3 interact in the endoplasmic reticulum and control cellular ubiquitination of specific mitochondrial proteins | Q39462054 | ||
Identification of heat-shock protein 90 beta in Japanese encephalitis virus-induced secretion proteins. | Q39495631 | ||
Molecular chaperones as a common set of proteins that regulate the invasion phenotype of head and neck cancer. | Q39530406 | ||
Mitochondrial chaperone Trap1 and the calcium binding protein Sorcin interact and protect cells against apoptosis induced by antiblastic agents. | Q39677773 | ||
(-)-Epigallocatechin-3-gallate is a novel Hsp90 inhibitor | Q39900860 | ||
Regulation of tumor cell mitochondrial homeostasis by an organelle-specific Hsp90 chaperone network. | Q40063505 | ||
Tumor necrosis factor-associated protein 1 (TRAP-1) protects cells from oxidative stress and apoptosis | Q40081584 | ||
HSP90 cross-links branched actin filaments induced by N-WASP and the Arp2/3 complex. | Q40126654 | ||
The peptide-binding activity of GRP94 is regulated by calcium. | Q40148862 | ||
Mitochondrial defects and neurodegeneration in mice overexpressing wild-type or G399S mutant HtrA2. | Q40278299 | ||
Geldanamycin induces Hsp70 and prevents alpha-synuclein aggregation and toxicity in vitro | Q40517262 | ||
Regulation of stability of cyclin-dependent kinase CDK11p110 and a caspase-processed form, CDK11p46, by Hsp90. | Q40519604 | ||
MZB1 is a GRP94 cochaperone that enables proper immunoglobulin heavy chain biosynthesis upon ER stress | Q40553936 | ||
Significant correlation between expression level of HSP gp96 and progression of hepatitis B virus induced diseases. | Q40569116 | ||
Hsp70 Reduces alpha-Synuclein Aggregation and Toxicity | Q40573441 | ||
Assisting spontaneity: the role of Hsp90 and small Hsps as molecular chaperones | Q40624749 | ||
TorsinA and heat shock proteins act as molecular chaperones: suppression of alpha-synuclein aggregation | Q40691639 | ||
Association of B lymphocyte antigen receptor polypeptides with multiple chaperone proteins | Q40777840 | ||
A role for Hsp90 in cell cycle control: Wee1 tyrosine kinase activity requires interaction with Hsp90. | Q40794316 | ||
Stoichiometry, abundance, and functional significance of the hsp90/hsp70-based multiprotein chaperone machinery in reticulocyte lysate. | Q40798891 | ||
Expression of stable hepatitis B viral polymerase associated with GRP94 in E. coli | Q40858417 | ||
Supervising the fold: functional principles of molecular chaperones | Q40949089 | ||
The assembly of progesterone receptor-hsp90 complexes using purified proteins | Q40992366 | ||
Interleukin-6 upregulates GP96 expression in breast cancer | Q41117591 | ||
The endoplasmic reticulum-resident stress protein gp96 binds peptides translocated by TAP. | Q41118696 | ||
Crystal structure of an Hsp90-nucleotide-p23/Sba1 closed chaperone complex | Q29617515 | ||
The heat-shock response | Q29619473 | ||
Hsp90 chaperones protein folding in vitro. | Q30351360 | ||
GRP94 is essential for mesoderm induction and muscle development because it regulates insulin-like growth factor secretion | Q30480141 | ||
The 90-kDa heat shock protein Hsp90 protects tubulin against thermal denaturation | Q30493832 | ||
Endocytosis and sorting of ErbB2 and the site of action of cancer therapeutics trastuzumab and geldanamycin | Q30839490 | ||
Identification of the peptide-binding site in the heat shock chaperone/tumor rejection antigen gp96 (Grp94). | Q30840326 | ||
Evidence for reversible, non-microtubule and non-microfilament-dependent nuclear translocation of hsp90 after heat shock in human fibroblasts | Q30996996 | ||
Developmentally induced changes of the proteome in the protozoan parasite Leishmania donovani | Q33188528 | ||
SHEPHERD is the Arabidopsis GRP94 responsible for the formation of functional CLAVATA proteins | Q33336944 | ||
Heat-shock protein gp96/grp94 is an essential chaperone for the platelet glycoprotein Ib-IX-V complex | Q33395341 | ||
Hsp90 and co-chaperones twist the functions of diverse client proteins | Q33607477 | ||
gp96, an endoplasmic reticulum master chaperone for integrins and Toll-like receptors, selectively regulates early T and B lymphopoiesis | Q33754609 | ||
The Role of DAF-21/Hsp90 in Mouth-Form Plasticity in Pristionchus pacificus | Q33757213 | ||
BiP (GRP78) and endoplasmin (GRP94) are induced following rotavirus infection and bind transiently to an endoplasmic reticulum-localized virion component | Q33786055 | ||
Drosophila glycoprotein 93 Is an ortholog of mammalian heat shock protein gp96 (grp94, HSP90b1, HSPC4) and retains disulfide bond-independent chaperone function for TLRs and integrins | Q33798177 | ||
In vitro reconstitution of a functional duck hepatitis B virus reverse transcriptase: posttranslational activation by Hsp90. | Q33812161 | ||
GHKL, an emergent ATPase/kinase superfamily | Q33818817 | ||
Endoplasmic reticulum chaperone gp96 is essential for infection with vesicular stomatitis virus | Q33859437 | ||
Hepadnavirus assembly and reverse transcription require a multi-component chaperone complex which is incorporated into nucleocapsids | Q33885913 | ||
The hsp90-related protein TRAP1 is a mitochondrial protein with distinct functional properties | Q33888203 | ||
ATP binding and hydrolysis are essential to the function of the Hsp90 molecular chaperone in vivo | Q33889333 | ||
Global targeting of subcellular heat shock protein-90 networks for therapy of glioblastoma | Q33907712 | ||
Heat shock protein 90 in neurodegenerative diseases | Q33961301 | ||
Endoplasmic reticulum chaperone gp96 is required for innate immunity but not cell viability | Q34093483 | ||
The mitochondrial chaperone protein TRAP1 mitigates α-Synuclein toxicity | Q34154475 | ||
Molecular chaperones--cellular machines for protein folding | Q34165962 | ||
Overexpression of tumor necrosis factor receptor-associated protein 1 (TRAP1), leads to mitochondrial aberrations in mouse fibroblast NIH/3T3 cells | Q34179900 | ||
Hsp90 structure and function studied by NMR spectroscopy. | Q34239529 | ||
Transient interaction of Hsp90 with early unfolding intermediates of citrate synthase. Implications for heat shock in vivo | Q34307813 | ||
HSP90 inhibitors: current development and potential in cancer therapy | Q34322146 | ||
In vitro reconstitution of functional hepadnavirus reverse transcriptase with cellular chaperone proteins | Q34327359 | ||
Involvement of tumor necrosis factor receptor-associated protein 1 (TRAP1) in apoptosis induced by beta-hydroxyisovalerylshikonin | Q34338431 | ||
Ligand-induced conformational shift in the N-terminal domain of GRP94, an Hsp90 chaperone | Q34338453 | ||
P275 | copyright license | Creative Commons Attribution | Q6905323 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | catalysis | Q82264 |
molecular biology | Q7202 | ||
molecular chaperones | Q422496 | ||
P304 | page(s) | 2560 | |
P577 | publication date | 2018-08-29 | |
P1433 | published in | International Journal of Molecular Sciences | Q3153277 |
P1476 | title | The HSP90 Family: Structure, Regulation, Function, and Implications in Health and Disease | |
P478 | volume | 19 |
Q93118409 | 17-Aminogeldanamycin selectively diminishes IRE1α-XBP1s pathway activity and cooperatively induces apoptosis with MEK1/2 and BRAFV600E inhibitors in melanoma cells of different genetic subtypes |
Q89820902 | 2-Methoxyestradiol and Its Combination with a Natural Compound, Ferulic Acid, Induces Melanoma Cell Death via Downregulation of Hsp60 and Hsp90 |
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