scholarly article | Q13442814 |
P2093 | author name string | Jason E Gestwicki | |
Victoria A Assimon | |||
Jennifer N Rauch | |||
Anne T Gillies | |||
P2860 | cites work | Molecular cloning, expression and localization of human 105 kDa heat shock protein, hsp105 | Q22001493 |
An evolutionarily conserved family of Hsp70/Hsc70 molecular chaperone regulators | Q22008599 | ||
Identification of CHIP, a novel tetratricopeptide repeat-containing protein that interacts with heat shock proteins and negatively regulates chaperone functions | Q22010047 | ||
The co-chaperone CHIP regulates protein triage decisions mediated by heat-shock proteins | Q24290709 | ||
Characterization of a brain-enriched chaperone, MRJ, that inhibits Huntingtin aggregation and toxicity independently | Q24292471 | ||
Chaperoned ubiquitylation--crystal structures of the CHIP U box E3 ubiquitin ligase and a CHIP-Ubc13-Uev1a complex | Q24296990 | ||
The diversity of the DnaJ/Hsp40 family, the crucial partners for Hsp70 chaperones | Q24301591 | ||
BAG-1 modulates the chaperone activity of Hsp70/Hsc70. | Q24313113 | ||
The diverse members of the mammalian HSP70 machine show distinct chaperone-like activities | Q24336905 | ||
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy | Q24337914 | ||
Localization and function in endoplasmic reticulum stress tolerance of ERdj3, a new member of Hsp40 family protein | Q24520303 | ||
BAG-2 acts as an inhibitor of the chaperone-associated ubiquitin ligase CHIP. | Q24534836 | ||
ERdj3, a stress-inducible endoplasmic reticulum DnaJ homologue, serves as a cofactor for BiP's interactions with unfolded substrates | Q24558672 | ||
A protein that interacts with members of the nuclear hormone receptor family: identification and cDNA cloning | Q24564631 | ||
Not all J domains are created equal: implications for the specificity of Hsp40-Hsp70 interactions | Q24644464 | ||
Hsp70 chaperones: cellular functions and molecular mechanism | Q24644472 | ||
Guidelines for the nomenclature of the human heat shock proteins | Q24653946 | ||
Heat shock factor 1 is a powerful multifaceted modifier of carcinogenesis | Q24655006 | ||
Convergent solutions to binding at a protein-protein interface | Q27621452 | ||
Structure of TPR domain-peptide complexes: critical elements in the assembly of the Hsp70-Hsp90 multichaperone machine | Q27622332 | ||
Structure of a Bag/Hsc70 complex: convergent functional evolution of Hsp70 nucleotide exchange factors | Q27630011 | ||
Structural analysis of BAG1 cochaperone and its interactions with Hsc70 heat shock protein | Q27630862 | ||
The crystal structure of the yeast Hsp40 Ydj1 complexed with its peptide substrate | Q27642692 | ||
Insights into Hsp70 Chaperone Activity from a Crystal Structure of the Yeast Hsp110 Sse1 | Q27648730 | ||
Structure of the Hsp110:Hsc70 nucleotide exchange machine | Q27650814 | ||
DnaJA1 antagonizes constitutive Hsp70-mediated stabilization of tau. | Q36020569 | ||
Mechanism of clathrin basket dissociation: separate functions of protein domains of the DnaJ homologue auxilin | Q36256904 | ||
Structural basis for the cooperation of Hsp70 and Hsp110 chaperones in protein folding | Q27650844 | ||
Structural basis of nucleotide exchange and client binding by the Hsp70 cochaperone Bag2 | Q27652982 | ||
Novel adenosine-derived inhibitors of 70 kDa heat shock protein, discovered through structure-based design | Q27654001 | ||
Solution conformation of wild-type E. coli Hsp70 (DnaK) chaperone complexed with ADP and substrate | Q27655465 | ||
Molecular Mechanism of the Negative Regulation of Smad1/5 Protein by Carboxyl Terminus of Hsc70-interacting Protein (CHIP) | Q27667356 | ||
Adenosine-derived inhibitors of 78 kDa glucose regulated protein (Grp78) ATPase: insights into isoform selectivity | Q27667602 | ||
Structural analysis of substrate binding by the molecular chaperone DnaK | Q27732810 | ||
NMR solution structure of the 21 kDa chaperone protein DnaK substrate binding domain: a preview of chaperone-protein interaction | Q27758070 | ||
The function of the yeast molecular chaperone Sse1 is mechanistically distinct from the closely related hsp70 family | Q27931591 | ||
Molecular chaperones of the Hsp110 family act as nucleotide exchange factors of Hsp70s | Q27931808 | ||
Exchangeable chaperone modules contribute to specification of type I and type II Hsp40 cellular function | Q27934055 | ||
YDJ1p facilitates polypeptide translocation across different intracellular membranes by a conserved mechanism | Q27937736 | ||
Specific interaction of the 70-kDa heat shock cognate protein with the tetratricopeptide repeats | Q28138187 | ||
Target-oriented and diversity-oriented organic synthesis in drug discovery | Q28138837 | ||
Polyglutamine length-dependent interaction of Hsp40 and Hsp70 family chaperones with truncated N-terminal huntingtin: their role in suppression of aggregation and cellular toxicity | Q28143597 | ||
The ubiquitin-related BAG-1 provides a link between the molecular chaperones Hsc70/Hsp70 and the proteasome | Q28144546 | ||
HspBP1, an Hsp70 cochaperone, has two structural domains and is capable of altering the conformation of the Hsp70 ATPase domain | Q28185756 | ||
More than folding: localized functions of cytosolic chaperones | Q28209802 | ||
The ATP hydrolysis-dependent reaction cycle of the Escherichia coli Hsp70 system DnaK, DnaJ, and GrpE | Q28239456 | ||
hsp70 genes in the human genome: Conservation and differentiation patterns predict a wide array of overlapping and specialized functions | Q28265695 | ||
Hop as an adaptor in the heat shock protein 70 (Hsp70) and hsp90 chaperone machinery | Q28291792 | ||
Tetratrico peptide repeat interactions: to TPR or not to TPR? | Q28297064 | ||
CHIP-mediated stress recovery by sequential ubiquitination of substrates and Hsp70 | Q28303344 | ||
Regulation of Hsp70 function by HspBP1: structural analysis reveals an alternate mechanism for Hsp70 nucleotide exchange | Q28305976 | ||
Cloning and functional analysis of BAG-1: a novel Bcl-2-binding protein with anti-cell death activity | Q28306175 | ||
Its substrate specificity characterizes the DnaJ co-chaperone as a scanning factor for the DnaK chaperone. | Q28354756 | ||
BAG3 protein is overexpressed in human glioblastoma and is a potential target for therapy | Q28564542 | ||
Reaching for high-hanging fruit in drug discovery at protein-protein interfaces | Q29547258 | ||
TPR proteins: the versatile helix | Q29547585 | ||
Molecular chaperones in protein folding and proteostasis | Q29547715 | ||
An ATPase domain common to prokaryotic cell cycle proteins, sugar kinases, actin, and hsp70 heat shock proteins | Q29615894 | ||
The HSP70 chaperone machinery: J proteins as drivers of functional specificity | Q29616140 | ||
HSP90 and the chaperoning of cancer | Q29617504 | ||
Small-molecule inhibitors of protein-protein interactions: progressing towards the dream | Q29617758 | ||
Molecular chaperones and protein quality control | Q29617795 | ||
Folding of newly translated proteins in vivo: the role of molecular chaperones | Q29619368 | ||
Heat shock proteins and biological response to hyperthermia | Q36290524 | ||
BiP mutants that are unable to interact with endoplasmic reticulum DnaJ proteins provide insights into interdomain interactions in BiP. | Q36446097 | ||
Molecular chaperones in signal transduction. | Q36446467 | ||
Hsp70 molecular chaperones: emerging roles in human disease and identification of small molecule modulators | Q36536342 | ||
The heat shock protein 70 family: Highly homologous proteins with overlapping and distinct functions. | Q36838138 | ||
To be, or not to be--molecular chaperones in protein degradation | Q36848211 | ||
Chemical control over protein-protein interactions: beyond inhibitors | Q37017699 | ||
HSF1-mediated BAG3 expression attenuates apoptosis in 4-hydroxynonenal-treated colon cancer cells via stabilization of anti-apoptotic Bcl-2 proteins | Q37152837 | ||
From hatching to dispatching: the multiple cellular roles of the Hsp70 molecular chaperone machinery | Q37292909 | ||
HspBP1 levels are elevated in breast tumor tissue and inversely related to tumor aggressiveness. | Q37308819 | ||
Role of the J-domain in the cooperation of Hsp40 with Hsp70. | Q37380910 | ||
The cochaperone BAG2 sweeps paired helical filament- insoluble tau from the microtubule. | Q37401466 | ||
Multi-faceted role of HSP40 in cancer | Q37429975 | ||
Inhibition of the JNK signalling pathway enhances proteasome inhibitor-induced apoptosis of kidney cancer cells by suppression of BAG3 expression | Q37434495 | ||
The role of molecular chaperones in human misfolding diseases | Q37459598 | ||
Multiple, but concerted cellular activities of the human protein Hap46/BAG-1M and isoforms | Q37462230 | ||
Pharmacological targeting of the Hsp70 chaperone | Q37622461 | ||
Heat shock proteins as suppressors of accumulation of toxic prefibrillar intermediates and misfolded proteins in neurodegenerative diseases | Q37695315 | ||
Chaperone-assisted degradation: multiple paths to destruction | Q37714916 | ||
Molecular Chaperones as Rational Drug Targets for Parkinsons Disease Therapeutics | Q37799850 | ||
Hsp70s contain a specific sulfogalactolipid binding site. Differential aglycone influence on sulfogalactosyl ceramide binding by recombinant prokaryotic and eukaryotic hsp70 family members | Q37874431 | ||
Heat shock protein 40 (Hsp40) plays a key role in the virus life cycle | Q37897736 | ||
Human DNAJ in cancer and stem cells | Q37934104 | ||
Different combinations of the heat-shock cognate protein 70 (hsc70) C-terminal functional groups are utilized to interact with distinct tetratricopeptide repeat-containing proteins | Q38296271 | ||
The conserved G/F motif of the DnaJ chaperone is necessary for the activation of the substrate binding properties of the DnaK chaperone | Q38298937 | ||
Expression of a mutant HSP110 sensitizes colorectal cancer cells to chemotherapy and improves disease prognosis | Q38331603 | ||
Ordered assembly of heat shock proteins, Hsp26, Hsp70, Hsp90, and Hsp104, on expanded polyglutamine fragments revealed by chemical probes | Q39242319 | ||
Molecular chaperone-mediated tau protein metabolism counteracts the formation of granular tau oligomers in human brain | Q39420620 | ||
Characterization of stress sensitivity and chaperone activity of Hsp105 in mammalian cells | Q39545229 | ||
Bag1 directly routes immature BCR-ABL for proteasomal degradation | Q39673043 | ||
A novel, small molecule inhibitor of Hsc70/Hsp70 potentiates Hsp90 inhibitor induced apoptosis in HCT116 colon carcinoma cells. | Q39762997 | ||
A small molecule inhibitor of inducible heat shock protein 70. | Q39789249 | ||
Macrocycles that inhibit the binding between heat shock protein 90 and TPR-containing proteins | Q39894584 | ||
An apoptosis-inducing small molecule that binds to heat shock protein 70. | Q39946872 | ||
BAG-1 associates with Hsc70.Tau complex and regulates the proteasomal degradation of Tau protein. | Q40063710 | ||
The antiapoptotic protein BAG3 is expressed in thyroid carcinomas and modulates apoptosis mediated by tumor necrosis factor-related apoptosis-inducing ligand. | Q40197354 | ||
Regulation of signaling protein function and trafficking by the hsp90/hsp70-based chaperone machinery | Q29620335 | ||
Phenothiazine-mediated rescue of cognition in tau transgenic mice requires neuroprotection and reduced soluble tau burden | Q30497435 | ||
A repeating amino acid motif in CDC23 defines a family of proteins and a new relationship among genes required for mitosis and RNA synthesis | Q30667531 | ||
Ligand discrimination by TPR domains. Relevance and selectivity of EEVD-recognition in Hsp70 x Hop x Hsp90 complexes | Q30823415 | ||
Synthetic small interfering RNA targeting heat shock protein 105 induces apoptosis of various cancer cells both in vitro and in vivo | Q33249303 | ||
High-throughput screen for small molecules that modulate the ATPase activity of the molecular chaperone DnaK. | Q33300867 | ||
An AlphaScreen-based high-throughput screen to identify inhibitors of Hsp90-cochaperone interaction | Q33408481 | ||
Thioflavin S (NSC71948) interferes with Bcl-2-associated athanogene (BAG-1)-mediated protein-protein interactions. | Q33494790 | ||
Small molecule DnaK modulators targeting the beta-domain | Q33495332 | ||
Interaction of the Hsp70 molecular chaperone, DnaK, with its cochaperone DnaJ. | Q33574540 | ||
Mutations in the DnaK chaperone affecting interaction with the DnaJ cochaperone. | Q33575042 | ||
Binding of a small molecule at a protein-protein interface regulates the chaperone activity of hsp70-hsp40. | Q33580742 | ||
Facilitating Akt clearance via manipulation of Hsp70 activity and levels. | Q33593935 | ||
Structure of clathrin coat with bound Hsc70 and auxilin: mechanism of Hsc70-facilitated disassembly | Q33697076 | ||
Inhibition of hsp70 by methylene blue affects signaling protein function and ubiquitination and modulates polyglutamine protein degradation | Q33855062 | ||
Overexpression of yeast Hsp110 homolog Sse1p suppresses ydj1-151 thermosensitivity and restores Hsp90-dependent activity | Q33902982 | ||
Heat shock protein 70 (hsp70) as an emerging drug target. | Q33956906 | ||
Mutagenesis reveals the complex relationships between ATPase rate and the chaperone activities of Escherichia coli heat shock protein 70 (Hsp70/DnaK) | Q33967227 | ||
J domain co-chaperone specificity defines the role of BiP during protein translocation | Q33991043 | ||
High-throughput screening identifies a bisphenol inhibitor of SV40 large T antigen ATPase activity | Q34030971 | ||
Cellular strategies for controlling protein aggregation | Q34143451 | ||
Successive action of DnaK, DnaJ and GroEL along the pathway of chaperone-mediated protein folding | Q34242618 | ||
From the cradle to the grave: molecular chaperones that may choose between folding and degradation | Q34400939 | ||
Single-molecule analysis of a molecular disassemblase reveals the mechanism of Hsc70-driven clathrin uncoating | Q34665652 | ||
Chemical screens against a reconstituted multiprotein complex: myricetin blocks DnaJ regulation of DnaK through an allosteric mechanism | Q34673896 | ||
The TPR snap helix: a novel protein repeat motif from mitosis to transcription | Q34840242 | ||
Versatile TPR domains accommodate different modes of target protein recognition and function | Q35056237 | ||
BAG-1: a multifunctional regulator of cell growth and survival | Q35078440 | ||
Effects of heat shock, heat shock protein 40 (HDJ-2), and proteasome inhibition on protein aggregation in cellular models of Huntington's disease | Q35084195 | ||
Modulation of protein-protein interactions with small organic molecules | Q35151091 | ||
Antimyeloma Effects of the Heat Shock Protein 70 Molecular Chaperone Inhibitor MAL3-101 | Q35251058 | ||
Molecular chaperones and regulation of tau quality control: strategies for drug discovery in tauopathies. | Q35313148 | ||
Heat shock protein 70 kDa chaperone/DnaJ cochaperone complex employs an unusual dynamic interface. | Q35571420 | ||
GrpE, a nucleotide exchange factor for DnaK. | Q35675546 | ||
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy | Q35857041 | ||
Structure, function and evolution of DnaJ: conservation and adaptation of chaperone function | Q40425170 | ||
Differential interactions of p23 and the TPR-containing proteins Hop, Cyp40, FKBP52 and FKBP51 with Hsp90 mutants | Q40425233 | ||
Small molecule modulators of endogenous and co-chaperone-stimulated Hsp70 ATPase activity. | Q40479992 | ||
Chaperone suppression of cellular toxicity of huntingtin is independent of polyglutamine aggregation | Q40773928 | ||
Human BAG-1/RAP46 protein is generated as four isoforms by alternative translation initiation and overexpressed in cancer cells | Q41007148 | ||
Proof that hsp70 is required for assembly of the glucocorticoid receptor into a heterocomplex with hsp90. | Q41486760 | ||
Stepwise assembly of a glucocorticoid receptor.hsp90 heterocomplex resolves two sequential ATP-dependent events involving first hsp70 and then hsp90 in opening of the steroid binding pocket | Q42056801 | ||
Methylthioninium chloride (methylene blue) induces autophagy and attenuates tauopathy in vitro and in vivo. | Q42077623 | ||
Mechanistic studies of Sansalvamide A-amide: an allosteric modulator of Hsp90. | Q42532832 | ||
Chemical manipulation of hsp70 ATPase activity regulates tau stability. | Q42630080 | ||
The ATPase domain of hsp70 possesses a unique binding specificity for 3'-sulfogalactolipids | Q42635324 | ||
High-throughput screen for Escherichia coli heat shock protein 70 (Hsp70/DnaK): ATPase assay in low volume by exploiting energy transfer. | Q42668370 | ||
A soluble sulfogalactosyl ceramide mimic promotes Delta F508 CFTR escape from endoplasmic reticulum associated degradation | Q42688247 | ||
Isolation of a mouse cDNA encoding mSTI1, a stress-inducible protein containing the TPR motif | Q42798330 | ||
ATPases as drug targets: insights from heat shock proteins 70 and 90. | Q42978771 | ||
BAG1 modulates huntingtin toxicity, aggregation, degradation, and subcellular distribution | Q43284919 | ||
Identification of an inhibitor of hsc70-mediated protein translocation and ATP hydrolysis | Q43508426 | ||
The antibacterial peptide pyrrhocoricin inhibits the ATPase actions of DnaK and prevents chaperone-assisted protein folding | Q43547658 | ||
Identification of essential residues in the type II Hsp40 Sis1 that function in polypeptide binding | Q43937089 | ||
Physical interaction between heat shock proteins DnaK, DnaJ, and GrpE and the bacterial heat shock transcription factor sigma 32 | Q43977199 | ||
C-terminal sequences outside the tetratricopeptide repeat domain of FKBP51 and FKBP52 cause differential binding to Hsp90. | Q44336552 | ||
Progressive decrease in chaperone protein levels in a mouse model of Huntington's disease and induction of stress proteins as a therapeutic approach | Q44872348 | ||
BAG-1M is up-regulated in hippocampus of Alzheimer's disease patients and associates with tau and APP proteins | Q44965883 | ||
Small-molecule inhibitors of IL-2/IL-2R: lessons learned and applied | Q45194822 | ||
Peptides and aptamers targeting HSP70: a novel approach for anticancer chemotherapy | Q45719919 | ||
BAG3 gene silencing sensitizes leukemic cells to Bortezomib-induced apoptosis | Q46181614 | ||
Chemical modulators of heat shock protein 70 (Hsp70) by sequential, microwave-accelerated reactions on solid phase. | Q46865084 | ||
Molecular chaperones and the stress of oncogenesis | Q47785215 | ||
Anticancer drugs up-regulate HspBP1 and thereby antagonize the prosurvival function of Hsp70 in tumor cells | Q48077559 | ||
Targeted disruption of Hsp110/105 gene protects against ischemic stress | Q49034531 | ||
Multiple domains of the co-chaperone Hop are important for Hsp70 binding. | Q51039772 | ||
Interaction between heat shock proteins and antimicrobial peptides. | Q52584182 | ||
Hsp110 protects heat-denatured proteins and confers cellular thermoresistance. | Q54147754 | ||
Molecular basis for regulation of the heat shock transcription factor sigma32 by the DnaK and DnaJ chaperones. | Q54414189 | ||
Interaction of the immunosuppressant deoxyspergualin with a member of the Hsp70 family of heat shock proteins | Q67563339 | ||
Snap helix with knob and hole: essential repeats in S. pombe nuclear protein nuc2+ | Q68697897 | ||
Quantitation of the interaction of the immunosuppressant deoxyspergualin and analogs with Hsc70 and Hsp90 | Q72266605 | ||
Dynamics of heat shock protein 90-progesterone receptor binding and the disactivation loop model for steroid receptor complexes | Q72669705 | ||
Ubiquitin-dependent degradation of certain protein substrates in vitro requires the molecular chaperone Hsc70 | Q73182515 | ||
Multistep mechanism of substrate binding determines chaperone activity of Hsp70 | Q73943514 | ||
The conserved carboxyl terminus and zinc finger-like domain of the co-chaperone Ydj1 assist Hsp70 in protein folding | Q74263782 | ||
D-peptide ligands for the co-chaperone DnaJ | Q74516752 | ||
Selectivity of the molecular chaperone-specific immunosuppressive agent 15-deoxyspergualin: modulation of Hsc70 ATPase activity without compromising DnaJ chaperone interactions | Q74623151 | ||
The chaperoning activity of hsp110. Identification of functional domains by use of targeted deletions | Q77772392 | ||
Allosteric regulation of Hsp70 chaperones involves a conserved interdomain linker | Q79278307 | ||
Spectroscopic and thermodynamic measurements of nucleotide-induced changes in the human 70-kDa heat shock cognate protein | Q79807928 | ||
Bag3 gene expression is regulated by heat shock factor 1 | Q80735914 | ||
Exchange we can believe in | Q81746418 | ||
Hsp70: anti-apoptotic and tumorigenic protein | Q84904226 | ||
P433 | issue | 3 | |
P304 | page(s) | 404-417 | |
P577 | publication date | 2013-01-01 | |
P1433 | published in | Current Pharmaceutical Design | Q5195068 |
P1476 | title | Hsp70 protein complexes as drug targets | |
P478 | volume | 19 |
Q48673647 | A systems biology approach reveals new endoplasmic reticulum-associated targets for the correction of the ATP7B mutant causing Wilson disease. |
Q54425017 | Adapting to stress - chaperome networks in cancer. |
Q42552152 | Analogs of the Allosteric Heat Shock Protein 70 (Hsp70) Inhibitor, MKT-077, as Anti-Cancer Agents |
Q28771764 | Binding of human nucleotide exchange factors to heat shock protein 70 (Hsp70) generates functionally distinct complexes in vitro |
Q50354200 | Cancer cell responses to Hsp70 inhibitor JG-98: Comparison with Hsp90 inhibitors and finding synergistic drug combinations. |
Q90736459 | Cold Exposure-Induced Up-Regulation of Hsp70 Positively Regulates PEDV mRNA Synthesis and Protein Expression In Vitro |
Q44710284 | Conformation transitions of the polypeptide-binding pocket support an active substrate release from Hsp70s |
Q35855961 | Dancing through Life: Molecular Dynamics Simulations and Network-Centric Modeling of Allosteric Mechanisms in Hsp70 and Hsp110 Chaperone Proteins |
Q40130410 | Defining Hsp70 Subnetworks in Dengue Virus Replication Reveals Key Vulnerability in Flavivirus Infection |
Q34995711 | Development of a capillary electrophoresis platform for identifying inhibitors of protein-protein interactions |
Q28533820 | Drug resistance in natural isolates of Leishmania donovani s.l. promastigotes is dependent of Pgp170 expression |
Q37079732 | Dynamical Structures of Hsp70 and Hsp70-Hsp40 Complexes. |
Q38702487 | Endoplasmic reticulum stress-induced degradation of DNAJB12 stimulates BOK accumulation and primes cancer cells for apoptosis |
Q89313592 | Exploration of Benzothiazole Rhodacyanines as Allosteric Inhibitors of Protein-Protein Interactions with Heat Shock Protein 70 (Hsp70) |
Q46296500 | Formal Models of Biological Systems |
Q36279553 | Hallmarks of therapeutic management of the cystic fibrosis functional landscape. |
Q46381883 | Heat Shock Protein 70 (Hsp70) Suppresses RIP1-Dependent Apoptotic and Necroptotic Cascades. |
Q38222563 | Heat shock protein 70 - the next chaperone to target in the treatment of human acute myelogenous leukemia? |
Q38815318 | Heat shock proteins as potential targets for protective strategies in neurodegeneration |
Q38690048 | Heat-shock protein 90 (Hsp90) promotes opioid-induced anti-nociception by an ERK mitogen-activated protein kinase (MAPK) mechanism in mouse brain. |
Q50134093 | High Throughput Screen for Inhibitors of Protein-Protein Interactions in a Reconstituted Heat Shock Protein 70 (Hsp70) Complex. |
Q38263003 | Hsp70 in cancer: back to the future |
Q41142344 | Hsp70/J-protein machinery from Glossina morsitans morsitans, vector of African trypanosomiasis |
Q34052565 | Human heat shock protein-specific cytotoxic T lymphocytes display potent antitumour immunity in multiple myeloma |
Q90058197 | Individualized management of genetic diversity in Niemann-Pick C1 through modulation of the Hsp70 chaperone system |
Q90683648 | Inducible HSP70 antagonizes cisplatin‑induced cell apoptosis through inhibition of the MAPK signaling pathway in HGC‑27 cells |
Q38796931 | Inhibition of stress-inducible HSP70 impairs mitochondrial proteostasis and function |
Q90539342 | Kinetics of the conformational cycle of Hsp70 reveals the importance of the dynamic and heterogeneous nature of Hsp70 for its function |
Q41106834 | Non-canonical Interactions between Heat Shock Cognate Protein 70 (Hsc70) and Bcl2-associated Anthanogene (BAG) Co-Chaperones Are Important for Client Release |
Q90293459 | Novel insights into molecular chaperone regulation of ribonucleotide reductase |
Q38093796 | Opportunities and challenges for molecular chaperone modulation to treat protein-conformational brain diseases |
Q94686440 | Pharmacological inhibition of PRMT7 links arginine monomethylation to the cellular stress response |
Q42367708 | Protein Cross-Linking Capillary Electrophoresis for Protein-Protein Interaction Analysis |
Q57854068 | Protein folding in the cell, from atom to organism |
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Q47141268 | Relax, Cool Down and Scaffold: How to Restore Surface Expression of Folding-Deficient Mutant GPCRs and SLC6 Transporters |
Q48215542 | Sensitizing tumor cells to conventional drugs: HSP70 chaperone inhibitors, their selection and application in cancer models. |
Q90058716 | Structural and functional analysis of the Hsp70/Hsp40 chaperone system |
Q38806853 | Targeting Allosteric Control Mechanisms in Heat Shock Protein 70 (Hsp70). |
Q47421684 | Targeting Heat Shock Protein 70 to Ameliorate c-Jun Expression and Improve Demyelinating Neuropathy. |
Q38869328 | Targeting the Diabetic Chaperome to Improve Peripheral Neuropathy |
Q92069535 | The Alpha Isoform of Heat Shock Protein 90 and the Co-chaperones p23 and Cdc37 Promote Opioid Anti-nociception in the Brain |
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Q60053980 | The Hsp70 co-chaperone Ydj1/HDJ2 regulates ribonucleotide reductase activity |
Q91386196 | The genome of a subterrestrial nematode reveals adaptations to heat |
Q34059324 | The hop-like stress-induced protein 1 cochaperone is a novel cell-intrinsic restriction factor for mitochondrial tombusvirus replication. |
Q38922557 | Validation of the Hsp70-Bag3 protein-protein interaction as a potential therapeutic target in cancer |
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