scholarly article | Q13442814 |
P2093 | author name string | Kovács E | |
Boros I | |||
Farkas B | |||
Maresca B | |||
Horváth I | |||
Korányi L | |||
Balogh G | |||
Glatz A | |||
Török Z | |||
Jaszlits L | |||
Jednákovits A | |||
Vígh L | |||
Ferdinándy P | |||
Literáti PN | |||
P2860 | cites work | Role of the chaperonin cofactor Hsp10 in protein folding and sorting in yeast mitochondria | Q27938263 |
The heat-shock proteins | Q29617227 | ||
The heat-shock response | Q29619473 | ||
Requirement for hsp70 in the mitochondrial matrix for translocation and folding of precursor proteins | Q29620285 | ||
Spontaneous high expression of heat-shock proteins in mouse embryonal carcinoma cells and ectoderm from day 8 mouse embryo. | Q33933322 | ||
Pharmacological modulation of heat shock factor 1 by antiinflammatory drugs results in protection against stress-induced cellular damage | Q34036459 | ||
Expression of inducible stress protein 70 in rat heart myogenic cells confers protection against simulated ischemia-induced injury | Q34126736 | ||
Overexpression of the rat inducible 70-kD heat stress protein in a transgenic mouse increases the resistance of the heart to ischemic injury | Q34206249 | ||
Transgenic mice expressing the human heat shock protein 70 have improved post-ischemic myocardial recovery | Q34211550 | ||
Arachidonate is a potent modulator of human heat shock gene transcription | Q35104489 | ||
Evidence for a lipochaperonin: association of active protein-folding GroESL oligomers with lipids can stabilize membranes under heat shock conditions | Q36033850 | ||
Stress proteins and myocardial protection | Q36100886 | ||
The primary signal in the biological perception of temperature: Pd-catalyzed hydrogenation of membrane lipids stimulated the expression of the desA gene in Synechocystis PCC6803. | Q36571948 | ||
Membrane lipid perturbation modifies the set point of the temperature of heat shock response in yeast | Q37622138 | ||
Heat (shock) and the skin | Q37923851 | ||
Heat shock-induced myocardial protection against ischemic injury: a role for Hsp70? | Q40425584 | ||
Heat shock proteins and molecular chaperones: implications for adaptive responses in the skin | Q40500635 | ||
The role of heat shock proteins in the heart | Q40531193 | ||
Heat shock proteins and protection against myocardial ischemia | Q40531249 | ||
Molecular chaperones in protein folding: the art of avoiding sticky situations | Q40621904 | ||
Heat shock proteins and the kidney. | Q40678443 | ||
The heat shock and ethanol stress responses of yeast exhibit extensive similarity and functional overlap | Q40961419 | ||
Differential cytoprotection against heat stress or hypoxia following expression of specific stress protein genes in myogenic cells | Q41315610 | ||
Heat-shock protein induction in rat hearts. A direct correlation between the amount of heat-shock protein induced and the degree of myocardial protection | Q46262643 | ||
A new puffing pattern induced by temperature shock and DNP in drosophila | Q55918906 | ||
Protein folding in mitochondria requires complex formation with hsp60 and ATP hydrolysis | Q57073746 | ||
Folding of nascent polypeptide chains in a high molecular mass assembly with molecular chaperones | Q59060241 | ||
KATP channel modulation in working rat hearts with coronary occlusion: effects of cromakalim, cicletanine, and glibenclamide | Q70987512 | ||
Differential expression of heat shock protein 70 in well healing and chronic human wound tissue | Q71780662 | ||
Platelet-derived growth factor levels in wounds of diabetic rats | Q72020422 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1150-1154 | |
P577 | publication date | 1997-10-01 | |
P1433 | published in | Nature Medicine | Q1633234 |
P1476 | title | Bimoclomol: a nontoxic, hydroxylamine derivative with stress protein-inducing activity and cytoprotective effects | |
P478 | volume | 3 |
Q43701056 | A non-toxic heat shock protein 70 inducer, geranylgeranylacetone, suppresses apoptosis of cultured rat hepatocytes caused by hydrogen peroxide and ethanol |
Q37764922 | A survey and analysis of the role of molecular chaperone proteins and imidazole-containing dipeptide-based compounds as molecular escorts into the skin during stress, injury, water structuring and other types of cutaneous pathophysiology |
Q64060839 | Aberrant Phase Transitions: Side Effects and Novel Therapeutic Strategies in Human Disease |
Q28307965 | Activation of the heat shock response in a primary cellular model of motoneuron neurodegeneration-evidence for neuroprotective and neurotoxic effects |
Q42705248 | Administration of Hsp70 in vivo inhibits motor and sensory neuron degeneration. |
Q40490135 | Aging intervention, prevention, and therapy through hormesis |
Q92051377 | An endogenous peptide marker differentiates SOD1 stability and facilitates pharmacodynamic monitoring in SOD1 amyotrophic lateral sclerosis |
Q43205728 | Anti-ageing strategies: prevention or therapy? Showing ageing from within |
Q35007857 | Arrest of spermatogenesis in mice expressing an active heat shock transcription factor 1. |
Q43140234 | Bicyclol: a novel antihepatitis drug with hepatic heat shock protein 27/70-inducing activity and cytoprotective effects in mice |
Q53675317 | Bimoclomol elevates heat shock protein 70 and cytoprotects rat neonatal cardiomyocytes. |
Q73739599 | Bimoclomol, a heat shock protein co-inducer, acts by the prolonged activation of heat shock factor-1 |
Q35938537 | Biomarkers of cardiac disease |
Q35042117 | Biphasic effect of bimoclomol on calcium handling in mammalian ventricular myocardium |
Q36824283 | Cell stress induced HSP are targets of regulatory T cells: a role for HSP inducing compounds as anti-inflammatory immuno-modulators? |
Q38687050 | Changes in the plasma membrane in metabolic disease: impact of the membrane environment on G protein-coupled receptor structure and function |
Q39167151 | Chaperone Proteins in the Central Nervous System and Peripheral Nervous System after Nerve Injury |
Q41536919 | Chaperone co-inducer BGP-15 inhibits histone deacetylases and enhances the heat shock response through increased chromatin accessibility |
Q47596318 | Chaperone overload is a possible contributor to 'civilization diseases'. |
Q36777158 | Chaperones and proteases: cellular fold-controlling factors of proteins in neurodegenerative diseases and aging. |
Q35606907 | Chemical warfare agents: their past and continuing threat and evolving therapies. Part II of II. |
Q28285156 | Co-induction of the heat shock response ameliorates disease progression in a mouse model of human spinal and bulbar muscular atrophy: implications for therapy |
Q37981224 | Current and prospective disease-modifying therapies for amyotrophic lateral sclerosis |
Q35044717 | Cyclosporine A regulate oxidative stress-induced apoptosis in cardiomyocytes: mechanisms via ROS generation, iNOS and Hsp70 |
Q35096762 | Dealing with misfolded proteins: examining the neuroprotective role of molecular chaperones in neurodegeneration. |
Q40993382 | Delivery of a constitutively active form of the heat shock factor using a virus vector protects neuronal cells from thermal or ischaemic stress but not from apoptosis |
Q36293649 | Diabetic peripheral neuropathy: should a chaperone accompany our therapeutic approach? |
Q27333755 | Dihydropyridine Derivatives Modulate Heat Shock Responses and have a Neuroprotective Effect in a Transgenic Mouse Model of Alzheimer's Disease |
Q57364266 | Does the membrane's physical state control the expression of heat shock and other genes? |
Q48251431 | Effect of bimoclomol (N-[2-hydroxy-3-(1-piperidinyl) propoxy]-3 pyridine-carboximidoyl-chloride) on iminodipropionitrile-induced central effects |
Q74480170 | Enantioselective plasma protein binding of bimoclomol |
Q33725368 | Genetic modification of the Salmonella membrane physical state alters the pattern of heat shock response |
Q36446531 | HSP72 protects against obesity-induced insulin resistance |
Q48182249 | Heat Shock Proteins and Autophagy Pathways in Neuroprotection: from Molecular Bases to Pharmacological Interventions |
Q35560213 | Heat shock and UV-B-induced DNA damage and mutagenesis in skin |
Q33800745 | Heat shock factors and the control of the stress response |
Q43779606 | Heat shock protein 70 (Hsp70) protects postimplantation murine embryos from the embryolethal effects of hyperthermia |
Q39958439 | Heat shock protein 70 or heat shock protein 27 overexpressed in human endothelial cells during posthypoxic reoxygenation can protect from delayed apoptosis |
Q34866890 | Heat shock protein coinducers with no effect on protein denaturation specifically modulate the membrane lipid phase. |
Q33609597 | Heat shock protein expression during gametogenesis and embryogenesis |
Q34539778 | Heat shock protein-based therapy as a potential candidate for treating the sphingolipidoses. |
Q34388079 | Heat shock proteins and cardiovascular pathophysiology. |
Q34693063 | Heat shock proteins and the skin |
Q36896750 | Heat shock proteins are important mediators of skeletal muscle insulin sensitivity |
Q35545091 | Heat shock proteins as emerging therapeutic targets |
Q37411519 | Heat shock proteins in diabetes and wound healing |
Q47914826 | Heat shock proteins in inflammation and asthma: Dr Jekyll or Mr Hyde? |
Q34421860 | Heat shock proteins in the photobiology of human skin |
Q34911441 | Heat shock proteins modulate keloid formation |
Q46578441 | Heat shock proteins: new keys to the development of cytoprotective therapies |
Q36217181 | Heat shock response modulators as therapeutic tools for diseases of protein conformation |
Q27026884 | Heat shock transcription factor 1 as a therapeutic target in neurodegenerative diseases |
Q28364376 | Heat stress contributes to the enhancement of cardiac mitochondrial complex activity |
Q90049912 | Heat-Shock Proteins in Neuroinflammation |
Q28296634 | Hold me tight: Role of the heat shock protein family of chaperones in cardiac disease |
Q34170760 | Hsp70 and its molecular role in nervous system diseases |
Q33838876 | Hsp70 expression and induction as a readout for detection of immune modulatory components in food |
Q35808829 | Hyperfluidization-coupled membrane microdomain reorganization is linked to activation of the heat shock response in a murine melanoma cell line |
Q40427154 | Hyperthermic preconditioning of presynaptic calcium regulation in Drosophila |
Q24799234 | Hypothesis to explain poor outcomes in the ALLHAT and V-HeFT trials: decreased expression of heat shock proteins |
Q89479110 | Immune tolerance therapies for autoimmune diseases based on heat shock protein T-cell epitopes |
Q38210860 | Impaired proteostasis: role in the pathogenesis of diabetes mellitus |
Q73917954 | In vivo and in vitro acute cardiovascular effects of bimoclomol |
Q40424755 | Induced hsp70 is in small, cytoplasmic complexes in a cell culture model of renal ischemia: a comparative study with heat shock |
Q36336632 | Inducers and co-inducers of molecular chaperones |
Q40298208 | Induction of the 72-kilodalton heat shock protein and protection from ultraviolet B-induced cell death in human keratinocytes by repetitive exposure to heat shock or 15-deoxy-delta(12,14)-prostaglandin J2. |
Q34059530 | Inhibiting heat-shock protein 90 reverses sensory hypoalgesia in diabetic mice |
Q36845355 | Inhibitors of the heat shock response: biology and pharmacology |
Q73212370 | Ischemic "cross" tolerance in hypoxic ischemia of immature rat brain |
Q38107681 | Key role of lipids in heat stress management. |
Q30530764 | Lysosomal rerouting of Hsp70 trafficking as a potential immune activating tool for targeting melanoma |
Q27004531 | Lysosomal storage diseases and the heat shock response: convergences and therapeutic opportunities |
Q36893368 | Membrane regulation of the stress response from prokaryotic models to mammalian cells |
Q28741590 | Membrane-lipid therapy in operation: the HSP co-inducer BGP-15 activates stress signal transduction pathways by remodeling plasma membrane rafts |
Q37081783 | Membranes: a meeting point for lipids, proteins and therapies |
Q34505905 | Meta-analysis of heat- and chemically upregulated chaperone genes in plant and human cells. |
Q33526350 | Modulation of heat shock transcription factor 1 as a therapeutic target for small molecule intervention in neurodegenerative disease |
Q37853789 | Molecular chaperones and associated cellular clearance mechanisms against toxic protein conformers in Parkinson's disease |
Q35688796 | Molecular chaperones in Parkinson's disease--present and future |
Q80400955 | Molecular chaperones: the modular evolution of cellular networks |
Q33346818 | Molecular imaging-assisted optimization of hsp70 expression during laser-induced thermal preconditioning for wound repair enhancement |
Q34198919 | Molecular targets for pharmacological cytoprotection |
Q36434323 | Multiple thermometers in mammalian cells: why do cells from homeothermic organisms need to measure temperature? |
Q47807793 | Nitric oxide-heat shock protein axis in menopausal hot flushes: neglected metabolic issues of chronic inflammatory diseases associated with deranged heat shock response. |
Q28203731 | Nontoxic heat shock protein coinducer BRX-220 protects against acute pancreatitis in rats |
Q42047773 | Oral administration of geranylgeranylacetone plus local somatothermal stimulation: a simple, effective, safe and operable preconditioning combination for conferring tolerance against ischemia-reperfusion injury in rat livers |
Q47195096 | Oral bimoclomol elevates heat shock protein 70 and reduces myocardial infarct size in rats |
Q28301208 | Paeoniflorin, a novel heat shock protein-inducing compound |
Q43263762 | Pharmacologically activated migration of aortic endothelial cells is mediated through p38 SAPK. |
Q34778634 | Principles and practice of hormetic treatment of aging and age-related diseases |
Q33621868 | Protein Homeostasis in Amyotrophic Lateral Sclerosis: Therapeutic Opportunities? |
Q38078868 | Protein quality control system in neurodegeneration: a healing company hard to beat but failure is fatal |
Q38001437 | Restenosis and therapy |
Q28473241 | Riluzole increases the amount of latent HSF1 for an amplified heat shock response and cytoprotection |
Q45993961 | Role of ATP-dependent calcium regulation in modulation of Drosophila synaptic thermotolerance. |
Q33888036 | Role of heat shock proteins in gastric mucosal protection |
Q45867307 | Sensitization of tumor cells to fas killing through overexpression of heat-shock transcription factor 1. |
Q35801881 | Small molecule activators of the heat shock response and neuroprotection from stroke |
Q36791174 | Stress-induced rearrangements of cellular networks: Consequences for protection and drug design |
Q77318502 | Stress-inducible responses and heat shock proteins: new pharmacologic targets for cytoprotection |
Q27008867 | Structure and dynamics of molecular networks: a novel paradigm of drug discovery: a comprehensive review |
Q38635851 | Targeted Molecular Therapies for SBMA. |
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Q36010550 | The HSP co-inducer BGP-15 can prevent the metabolic side effects of the atypical antipsychotics. |
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Q60311176 | The heat shock protein amplifier arimoclomol improves refolding, maturation and lysosomal activity of glucocerebrosidase |
Q38992661 | The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosa. |
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Q43592881 | Whole body hyperthermia selectively induces heat shock protein 72 in neurons of the rat spinal cord |
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