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heat shock
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plant, cell & environment
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Bibliographies
[1]
Heat-priming improved heat tolerance of photosynthesis, enhanced terpenoid and benzenoid emission and phenolics accumulation in Achillea millefolium.
[2]
Hsp90 chaperonins possess ATPase activity and bind heat shock transcription factors and peptidyl prolyl isomerases.
[3]
triploidy determination in rainbow trout (oncorhynchus mykiss) based on erythrocytes dimensions
[4]
flp/frt recombination from yeast: application of a two gene cassette scheme as an inducible system in plants
[5]
synechococcus sp. strain pcc 7002 transcriptome: acclimation to temperature, salinity, oxidative stress and mixotrophic growth conditions
[6]
the inactivation of rnase g reduces the stenotrophomonas maltophilia susceptibility to quinolones by triggering the heat shock response.
[7]
ir-hsp: improved recognition of heat shock proteins, their families and sub-types based on g-spaced di-peptide features and support vector machine
[8]
global sumo proteome responses guide gene regulation, mrna biogenesis, and plant stress responses
[9]
nuclear phenotype changes after heat shock in panstrongylus megistus (burmeister)
[10]
pelleted bone marrow derived mesenchymal stem cells are better protected from the deleterious effects of arthroscopic heat shock
[11]
Effects of heat shock and nitrogen shock pre-treatments on ripening heterogeneity of Hass avocados stored in controlled atmosphere
[12]
Taurine Reduces Heat Stress by Regulating the Expression of Heat Shock Proteins in Broilers Exposed to Chronic Heat
[13]
Heat Shock Protein 60: Identification of an Undetected Allergen from .
[14]
Network analysis of oyster transcriptome revealed a cascade of cellular responses during recovery after heat shock.
[15]
HEAT SHOCK TRANSCRIPTION FACTOR A1b regulates heat tolerance in wheat and Arabidopsis through OPR3 and jasmonate signaling pathway.
[16]
Responses of olive plants exposed to different irrigation treatments in combination with heat shock: physiological and molecular mechanisms during exposure and recovery.
[17]
Genome-wide identification and analysis of biotic and abiotic stress regulation of small heat shock protein (HSP20) family genes in bread wheat.
[18]
Mechanism of HrcA function in heat shock regulation in Mycobacterium tuberculosis
[19]
The Heat Shock Response in Yeast Maintains Protein Homeostasis by Chaperoning and Replenishing Proteins.
[20]
Serum Heat Shock Protein Levels and the Relationship of Heat Shock Proteins with Various Parameters in Chronic Obstructive Pulmonary Disease Patients.
[21]
Ubiquitin and Heat Shock Factor-Type Transcriptional Factors Are Involved in 2-Dodecenoic Acid-Mediated Inhibition of Hyphal Growth.
[22]
Novel single nucleotide polymorphisms in the heat shock protein 70.1 gene in South African Nguni crossbred cattle.
[23]
Effects of purple sweet potato anthocyanins on development and intracellular redox status of bovine preimplantation embryos exposed to heat shock.
[24]
Heat shock protein 70 (HmHsp70) from Hypsizygus marmoreus confers thermotolerance to tobacco.
[25]
Heat Shock Protein 27 is overexpressed in the skin of bitumen exposed workers. Early observations.
[26]
Genome-wide Scanning and Characterization of Sorghum bicolor L. Heat Shock Transcription Factors.
[27]
The Host Heat Shock Protein MRJ/DNAJB6 Modulates Virus Infection.
[28]
Identification of watermelon heat shock protein members and tissue-specific gene expression analysis under combined drought and heat stresses.
[29]
Heat Shock Proteins in Cancer Immunotherapy.
[30]
Heat Shock Proteins: Agents of Cancer Development and Therapeutic Targets in Anti-Cancer Therapy.
[31]
Increased temperature-related adeno-associated virus vectors transduction of ovarian cancer cells - essential signatures of AAV receptor and heat shock proteins.
[32]
Expression of heat shock proteins in adult honey bee ( L.) workers under hot-arid subtropical ecosystems.
[33]
Naked mole-rats reduce the expression of ATP-dependent but not ATP-independent heat shock proteins in acute hypoxia.
[34]
Evaluation of immuno-modulating effect of recombinant heat shock protein 40 of in mice.
[35]
Heat shock-induced chaperoning by Hsp70 is enabled in-cell.
[36]
Involvement of heat shock protein 40 in the wing dimorphism of the house cricket Acheta domesticus
[37]
Long-term exposure to a 40-GHz electromagnetic field does not affect genotoxicity or heat shock protein expression in HCE-T or SRA01/04 cells
[38]
Muscadine grape skin extract inhibits prostate cancer cells by inducing cell-cycle arrest, and decreasing migration through heat shock protein 40
[39]
The heat shock protein 40 LeDnaJ regulates stress resistance and indole-3-acetic acid biosynthesis in Lentinula edodes
[40]
Upregulation of miR-370 and miR-543 is associated with reduced expression of heat shock protein 40 in spinocerebellar ataxia type 3
[41]
Immunization with plasmid DNA expressing Heat Shock Protein 40 confers prophylactic protection against chronic Toxoplasma gondii infection in Kunming mice
[42]
Farnesylated heat shock protein 40 is a component of membrane-bound RISC in Arabidopsis
[43]
Two J domains ensure high cochaperone activity of DnaJ, Escherichia coli heat shock protein 40
[44]
Molecular cloning, expression and functional characterization of the 40-kDa heat shock protein, DnaJ, from Bacillus halodurans
[45]
Effects of heat stress on serum cortisol, alkaline phosphatase activity and heat shock protein 40 and 90β mRNA expression in rainbow trout Oncorhynchus mykiss
[46]
Dnajb8, a member of the heat shock protein 40 family has a role in the tumor initiation and resistance to docetaxel but is dispensable for stress response
[47]
Human Heat shock protein 40 (Hsp40/DnaJB1) promotes influenza A virus replication by assisting nuclear import of viral ribonucleoproteins
[48]
Co-expression of heat shock protein (HSP) 40 and HSP70 in Pinctada martensii response to thermal, low salinity and bacterial challenges
[49]
miR-155-3p drives the development of autoimmune demyelination by regulation of heat shock protein 40
[50]
Expression of human DNAJ (Heat shock protein-40) B3 in humanized UDP-glucuronosyltransferase 1 mice
[51]
The J-domain of heat shock protein 40 can enhance the transduction efficiency of arginine-rich cell-penetrating peptides
[52]
Phosphorylation of heat shock protein 40 (Hsp40/DnaJB1) by mitogen-activated protein kinase-activated protein kinase 5 (MK5/PRAK)
[53]
Heat shock protein 40-Gok1 isolation from Toxoplasma gondii RH strain
[54]
Structural insights into the chaperone activity of the 40-kDa heat shock protein DnaJ: Binding and remodeling of a native substrate
[55]
Heat shock proteins 27, 40, and 70 as combinational and dual therapeutic cancer targets
[56]
An Exported Heat Shock Protein 40 Associates with Pathogenesis-Related Knobs in Plasmodium falciparum Infected Erythrocytes
[57]
Heat Shock Proteins and Autophagy Pathways in Neuroprotection: from Molecular Bases to Pharmacological Interventions
[58]
Prophylactic Antitumor Effect of Mixed Heat Shock Proteins/Peptides in Mouse Sarcoma
[59]
Evaluation of intracellular anion superoxide level, heat shock protein A2 and protamine positive spermatozoa percentages in teratoasthenozoospermia
[60]
Erratum: Discovery and Optimization of 4,5-Diarylisoxazoles as Potent Dual Inhibitors of Pyruvate Dehydrogenase Kinase and Heat Shock Protein 90 (Journal of Medicinal Chemistry (2014) 57:23 (9832-9843) DOI: 10.1021/jm5010144)
[61]
Expression patterns of heat shock protein genes in Rita rita from natural riverine habitat as biomarker response against environmental pollution.
[62]
Hsp90 chaperonins possess ATPase activity and bind heat shock transcription factors and peptidyl prolyl isomerases.
[63]
Hsp90 chaperonins possess ATPase activity and bind heat shock transcription factors and peptidyl prolyl isomerases
[64]
genome-wide identification, phylogenetic and expression analysis of the heat shock transcription factor family in bread wheat (triticum aestivum l.)
[65]
heat shock protein expression during gametogenesis and embryogenesis
[66]
matrine directly activates extracellular heat shock protein 90, resulting in axonal growth and functional recovery in spinal cord injured-mice
[67]
effects of theobroma cacao on heat shock protein 90 and asymmetric dimethylarginine of endothelial cells under the influence of plasma of pre-eclamptic patients
[68]
immunity to heat shock proteins and arthritic disorders
[69]
dual functions in response to heat stress and spermatogenesis: characterization of expression profile of small heat shock proteins 9 and 10 in goat testis
[70]
heat shock proteins 60 and 70 specific proinflammatory and cytotoxic response of cd4+cd28null cells in chronic kidney disease
[71]
effect of heat shock treatment and aloe vera coating to chilling injury symptom in tomato (lycopersicon asculantum mill.)
[72]
the effect of an eight-week aerobic exercise program with green tea supplementation on heat shock protein (hsp72) and bmi of obese women with type 2 diabetes
[73]
heat shock and other apoptosis-related proteins as therapeutic targets in prostate cancer
[74]
heat shock protein 90 (hsp90) as a molecular target for the development of novel drugs against the dermatophyte trichophyton rubrum
[75]
sumo-dependent synergism involving heat shock transcription factors with functions linked to seed longevity and desiccation tolerance
[76]
physical exercise enhanced heat shock protein 60 expression and attenuated inflammation in the adipose tissue of human diabetic obese
[77]
the inactivation of rnase g reduces the stenotrophomonas maltophilia susceptibility to quinolones by triggering the heat shock response.
[78]
ir-hsp: improved recognition of heat shock proteins, their families and sub-types based on g-spaced di-peptide features and support vector machine
[79]
the j-domain of heat shock protein 40 can enhance the transduction efficiency of arginine-rich cell-penetrating peptides
[80]
nuclear phenotype changes after heat shock in panstrongylus megistus (burmeister)
[81]
skeletal muscle heat shock protein 70: diverse functions and therapeutic potential for wasting disorders
[82]
administration of recombinant heat shock protein 70 delays peripheral muscle denervation in the sod1g93a mouse model of amyotrophic lateral sclerosis
[83]
commentary frontiers in immunologythe tricky balancing act of using heat shock proteins for cross-presentation
[84]
influence of sex on cytokines, heat shock protein and oxidative stress markers in response to an acute total body resistance exercise protocol
[85]
characterization of the novel mutant a78t-herg from a long qt syndrome type 2 patient: instability of the mutant protein and stabilization by heat shock factor 1
[86]
heat shock protein 27 phosphorylation state is associated with cancer progression
[87]
the synergistic effects of heat shock protein 70 and ginsenoside rg1 against tert-butyl hydroperoxide damage model in vitro
[88]
heat shock response associated with hepatocarcinogenesis in a murine model of hereditary tyrosinemia type i
[89]
discovery and development of natural heat shock protein 90 inhibitors in cancer treatment
[90]
stimulation of the fibrillar collagen and heat shock proteins by nicotinamide or its derivatives in non-irradiated or uva radiated fibroblasts, and direct anti-oxidant activity of nicotinamide derivatives
[91]
review article: heat shock protein 70 (hsp70) peptide activated natural killer (nk) cells for the treatment of patients with non-small cell lung cancer (nsclc) after radiochemotherapy (rctx) – from preclinical studies to a clinical phase ii trial
[92]
heat shock response and homeostatic plasticity
[93]
pelleted bone marrow derived mesenchymal stem cells are better protected from the deleterious effects of arthroscopic heat shock
[94]
pilot study of intratumoral injection of recombinant heat shock protein 70 in the treatment of malignant brain tumors in children
[95]
tandem duplication events in the expansion of the small heat shock protein gene family in solanum lycopersicum (cv. heinz 1706)
[96]
antibody to heat shock protein 70 (hsp70) inhibits human t-cell lymphoptropic virus type i (htlv-i) production by transformed rabbit t-cell lines
[97]
heat shock protein 90 and calcineurin pathway inhibitors enhance the efficacy of triazoles against scedosporium prolificans via induction of apoptosis
[98]
heat shock protein 90 is involved in the regulation of hmga2-driven growth and epithelial-to-mesenchymal transition of colorectal cancer cells