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unfolded protein response (273) 273
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endoplasmic-reticulum stress (186) 186
endoplasmic reticulum stress (139) 139
endoplasmic reticulum stress - drug effects (139) 139
cell biology (133) 133
cell line, tumor (129) 129
biochemistry & molecular biology (125) 125
protein-serine-threonine kinases - metabolism (123) 123
apoptosis - drug effects (120) 120
endoplasmic reticulum - metabolism (116) 116
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activation (114) 114
endoplasmic reticulum (114) 114
messenger-rna (110) 110
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proteins (103) 103
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protein folding (95) 95
transcription factor chop - metabolism (92) 92
endoribonucleases - metabolism (90) 90
endoplasmic reticulum - drug effects (86) 86
article (85) 85
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rna, messenger - metabolism (80) 80
oxidative stress (78) 78
cells, cultured (77) 77
gene expression (77) 77
expression (75) 75
heat-shock proteins - genetics (75) 75
cell line (74) 74
mice, inbred c57bl (73) 73
stress (73) 73
protein binding (71) 71
unfolded protein response - drug effects (70) 70
x-box binding protein 1 - genetics (70) 70
rats (67) 67
transcription factor chop - genetics (65) 65
xbp1 (65) 65
protein-serine-threonine kinases - genetics (61) 61
blotting, western (60) 60
reverse transcriptase polymerase chain reaction (60) 60
phosphorylation (59) 59
transcription factor (59) 59
membrane proteins - metabolism (58) 58
rna, messenger - genetics (58) 58
signal transduction - drug effects (58) 58
activating transcription factor 6 - metabolism (55) 55
cells (52) 52
eif-2 kinase - metabolism (52) 52
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kinases (51) 51
analysis (50) 50
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gene expression regulation (44) 44
endoribonucleases - genetics (43) 43
up-regulation (43) 43
endocrinology & metabolism (42) 42
health aspects (42) 42
research article (41) 41
dose-response relationship, drug (40) 40
autophagy (39) 39
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nuclear proteins - genetics (38) 38
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ire1 (37) 37
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time factors (37) 37
transcription factor xbp-1 (37) 37
endoplasmic-reticulum (36) 36
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homeostasis (36) 36
tunicamycin - pharmacology (36) 36
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American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 2016, Volume 311, Issue 4, pp. H871 - H880
We previously reported that endoplasmic reticulum (ER) stress is induced in the subfornical organ (SFO) and the hypothalamic paraventricular nucleus (PVN) of... 
Heart failure | Brain | Sympathetic activity | Hypothalamic paraventricular nucleus | Mitogen-activated protein kinase | Subfornical organ | Endoplasmic reticulum stress | heart failure | ACTIVATION | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | INDUCED PHOSPHORYLATION | MYOCARDIAL-INFARCTION | ER STRESS | subfornical organ | KINASE | RATS | sympathetic activity | KAPPA-B | brain | endoplasmic reticulum stress | hypothalamic paraventricular nucleus | mitogen-activated protein kinase | UNFOLDED PROTEIN RESPONSE | PERIPHERAL VASCULAR DISEASE | UP-REGULATION | Cholagogues and Choleretics - pharmacology | Tumor Necrosis Factor-alpha - genetics | Heart Failure - physiopathology | Male | NF-KappaB Inhibitor alpha - genetics | Peptidyl-Dipeptidase A - drug effects | Interleukin-1beta - genetics | Sympathetic Nervous System - physiopathology | RNA, Messenger - metabolism | Activating Transcription Factor 6 - genetics | Subfornical Organ - drug effects | Brain - metabolism | Heat-Shock Proteins - genetics | Inflammation - metabolism | Receptor, Angiotensin, Type 1 - genetics | Cyclooxygenase 2 - genetics | p38 Mitogen-Activated Protein Kinases - metabolism | Real-Time Polymerase Chain Reaction | Echocardiography | Signal Transduction | Rats | Cyclooxygenase 2 - drug effects | Heart Failure - metabolism | Rats, Sprague-Dawley | Blotting, Western | Brain - drug effects | Tumor Necrosis Factor-alpha - drug effects | Mitogen-Activated Protein Kinase 3 - metabolism | Endoplasmic Reticulum Stress | Paraventricular Hypothalamic Nucleus - metabolism | Infusions, Intraventricular | Mitogen-Activated Protein Kinases - drug effects | Mitogen-Activated Protein Kinase 1 - metabolism | Interleukin-1beta - drug effects | Sympathetic Nervous System - drug effects | Mitogen-Activated Protein Kinase 1 - drug effects | X-Box Binding Protein 1 - drug effects | Sympathetic Nervous System - metabolism | Transcription Factor RelA - genetics | Activating Transcription Factor 6 - drug effects | Mitogen-Activated Protein Kinase 3 - drug effects | Taurochenodeoxycholic Acid - pharmacology | Peptidyl-Dipeptidase A - genetics | Renin-Angiotensin System | Receptor, Angiotensin, Type 1 - drug effects | RNA, Messenger - drug effects | Subfornical Organ - metabolism | Heat-Shock Proteins - drug effects | Activating Transcription Factor 4 - genetics | Activating Transcription Factor 4 - drug effects | NF-KappaB Inhibitor alpha - drug effects | Paraventricular Hypothalamic Nucleus - drug effects | p38 Mitogen-Activated Protein Kinases - drug effects | Animals | Transcription Factor RelA - drug effects | X-Box Binding Protein 1 - genetics | Mitogen-Activated Protein Kinases - metabolism | Physiological aspects | Cellular signal transduction | Endoplasmic reticulum | Health aspects | Mitogen-activated protein kinases | Cardiovascular Neurohormonal Regulation
Journal Article
Nature Medicine, ISSN 1078-8956, 06/2016, Volume 22, Issue 6, pp. 624 - 631
Cetuximab is a monoclonal antibody that is effective in the treatment of metastatic colorectal cancer (mCRC). Cetuximab blocks epidermal growth factor receptor... 
MEDICINE, RESEARCH & EXPERIMENTAL | 1ST-LINE TREATMENT | PLUS IRINOTECAN | EFFICACY | BIOCHEMISTRY & MOLECULAR BIOLOGY | METASTATIC COLORECTAL-CANCER | CELL BIOLOGY | CALRETICULIN EXPOSURE | COLON-CANCER | BRAF MUTATION | POOLED ANALYSIS | ENDOPLASMIC-RETICULUM | KRAS | Leucovorin - administration & dosage | Proto-Oncogene Proteins p21(ras) - genetics | Colorectal Neoplasms - genetics | Dendritic Cells - immunology | Humans | Cell Death - immunology | X-Box Binding Protein 1 - drug effects | Endoplasmic Reticulum Stress - immunology | Antineoplastic Combined Chemotherapy Protocols - pharmacology | Fluorouracil - administration & dosage | Calreticulin - drug effects | Calreticulin - metabolism | Camptothecin - administration & dosage | Dendritic Cells - drug effects | Indoles - pharmacology | Pyrimidinones - pharmacology | Antineoplastic Agents - pharmacology | Cell Death - drug effects | Camptothecin - analogs & derivatives | Disease Models, Animal | Phagocytosis - drug effects | X-Box Binding Protein 1 - immunology | Endoplasmic Reticulum Stress - drug effects | Antibodies, Monoclonal - pharmacology | HCT116 Cells | Phagocytosis - immunology | Cetuximab - pharmacology | Sulfonamides - pharmacology | Unfolded Protein Response | HT29 Cells | Animals | Colorectal Neoplasms - immunology | Proto-Oncogene Proteins B-raf - genetics | X-Box Binding Protein 1 - metabolism | Cell Line, Tumor | Mice | Pyridones - pharmacology | Physiological aspects | Genetic aspects | Immune response | Research | Drug therapy | Colorectal cancer | Care and treatment | Usage | Chemotherapy | Epidermal growth factor | Cell death | Analysis | Endoplasmic reticulum | Cancer | Monoclonal antibodies | Apoptosis | Immune system
Journal Article
Journal of Immunology, ISSN 0022-1767, 04/2018, Volume 200, Issue 7, pp. 2291 - 2303
Binge/moderate alcohol suppresses TLR4-MyD88 proinflammatory cytokines; however, alcohol's effects on TLR-TRIF signaling, especially after in vivo exposure in... 
TOLL-LIKE RECEPTOR | IN-VIVO | FACTOR-KAPPA-B | ENDOPLASMIC-RETICULUM STRESS | PROINFLAMMATORY CYTOKINES | IMMUNOLOGY | PATTERN-RECOGNITION RECEPTORS | HUMAN MONOCYTES | RESPIRATORY SYNCYTIAL VIRUS | IFN-BETA INDUCTION | INNATE IMMUNITY | Inflammation - pathology | Interleukin-6 - antagonists & inhibitors | Binge Drinking - pathology | Ethanol - toxicity | Humans | Middle Aged | Receptors, Neuropeptide Y - metabolism | Male | Monocytes - immunology | X-Box Binding Protein 1 - drug effects | Toll-Like Receptor 3 - antagonists & inhibitors | Lipopolysaccharides - immunology | Chemokine CCL5 - antagonists & inhibitors | Young Adult | Myeloid Differentiation Factor 88 - antagonists & inhibitors | Adult | Female | Poly I-C - immunology | Toll-Like Receptor 4 - antagonists & inhibitors | Macrophages - immunology | Cell Line | Adaptor Proteins, Vesicular Transport - antagonists & inhibitors | Chemokine CXCL10 - antagonists & inhibitors | Interferon-beta - antagonists & inhibitors | HSP70 Heat-Shock Proteins - metabolism | Monocytes - drug effects | Animals | Signal Transduction - drug effects | Adolescent | Macrophages - drug effects | RAW 264.7 Cells | Mice | Tumor Necrosis Factor-alpha - antagonists & inhibitors | Phosphoprotein phosphatase | β-Interferon | RANTES | Alcohol | Macrophages | Lipopolysaccharides | Alcohols | Interleukin 6 | Proteins | Signal transduction | Drug tolerance | Rodents | Toll-like receptors | IP-10 protein | Inhibition | Enzyme-linked immunosorbent assay | Ethanol | Cytokines | Immunoregulation | Exposure | Inflammation | Poly (I:C) | TLR4 protein | TLR3 protein | Signaling | Monocytes | Interferon regulatory factor 3 | Tumor necrosis factor | Alcoholic beverages | MyD88 protein | Protein phosphatase | Stress proteins | Comparative analysis | Chemokines
Journal Article
European Journal of Immunology, ISSN 0014-2980, 05/2008, Volume 38, Issue 5, pp. 1194 - 1203
Type I IFN are strongly induced upon engagement of certain pattern recognition receptors by microbial products, and play key roles in regulating innate and... 
Protein misfolding | Interferons | HLA‐B27 | Unfolded protein response | HLA-B27 | TRANSCRIPTION FACTOR XBP-1 | TRANSGENIC RATS | NECROSIS-FACTOR-ALPHA | unfolded protein | INTERFERON-BETA | ANKYLOSING-SPONDYLITIS | IMMUNOLOGY | PLASMA-CELL DIFFERENTIATION | MESSENGER-RNA | protein misfolding | IMMUNE-RESPONSES | GENE-EXPRESSION | AUTOIMMUNE MYOSITIS | RNA, Small Interfering - genetics | Gene Expression - drug effects | Humans | Rats, Inbred F344 | Endoplasmic Reticulum - metabolism | Interferon Regulatory Factor-7 - genetics | X-Box Binding Protein 1 | Interferon-alpha - genetics | Endoplasmic Reticulum - drug effects | Interferon-beta - genetics | Receptor, Interferon alpha-beta - genetics | Fibroblasts - metabolism | DNA-Binding Proteins - physiology | Interferon-beta - chemistry | Cytokines - metabolism | HLA-B7 Antigen - genetics | Animals, Genetically Modified | Rats | Regulatory Factor X Transcription Factors | Protein Folding | Mice, Knockout | Macrophages - metabolism | Animals | Interferon-beta - metabolism | Signal Transduction - drug effects | Tunicamycin - pharmacology | Fibroblasts - drug effects | Lipopolysaccharides - pharmacology | Thapsigargin - pharmacology | Macrophages - drug effects | Signal Transduction - physiology | Fibroblasts - cytology | Mice | Nuclear Proteins - physiology | Transcription Factors | HLA-B27 Antigen - genetics
Journal Article
Nature Immunology, ISSN 1529-2908, 05/2010, Volume 11, Issue 5, pp. 411 - 418
Sensors of pathogens, such as Toll-like receptors (TLRs), detect microbes to activate transcriptional programs that orchestrate adaptive responses to specific... 
UNFOLDED PROTEIN RESPONSE | PATHWAY | ER STRESS | HOST-DEFENSE | ENDOPLASMIC-RETICULUM STRESS | FRANCISELLA-TULARENSIS INFECTION | IMMUNOLOGY | LIVE VACCINE STRAIN | INFLAMMATORY RESPONSE | NEGATIVE REGULATOR | SYSTEMS BIOLOGY | RNA, Small Interfering - genetics | Endoribonucleases - genetics | Tularemia - metabolism | Toll-Like Receptor 2 - genetics | Membrane Glycoproteins - metabolism | Lipopeptides - pharmacology | Transcriptional Activation - drug effects | NADPH Oxidases - metabolism | Tularemia - genetics | Protein Splicing - genetics | Transcriptional Activation - immunology | X-Box Binding Protein 1 | Protein Splicing - drug effects | NADPH Oxidases - genetics | Stress, Physiological - drug effects | TNF Receptor-Associated Factor 6 - genetics | Transcription Factor CHOP - biosynthesis | Transcription Factors - immunology | Cytokines - genetics | Protein-Serine-Threonine Kinases - metabolism | DNA-Binding Proteins - immunology | Endoribonucleases - metabolism | Macrophages - pathology | Stress, Physiological - genetics | Myeloid Differentiation Factor 88 - genetics | Toll-Like Receptor 4 - genetics | Signal Transduction - genetics | Toll-Like Receptor 4 - immunology | Toll-Like Receptor 2 - metabolism | Toll-Like Receptor 4 - metabolism | Mice, Knockout | Macrophages - metabolism | Signal Transduction - drug effects | Tunicamycin - pharmacology | Lipopolysaccharides - pharmacology | Toll-Like Receptor 2 - immunology | Mice | Stress, Physiological - immunology | Endoribonucleases - immunology | Transcription Factor CHOP - genetics | NADPH Oxidases - immunology | DNA-Binding Proteins - metabolism | Signal Transduction - immunology | Macrophages - virology | Mice, Mutant Strains | Tularemia - immunology | Membrane Glycoproteins - immunology | Macrophages - immunology | Cytokines - immunology | Cell Line | Francisella tularensis - immunology | Protein Splicing - immunology | Protein-Serine-Threonine Kinases - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Immunity, Innate | NADPH Oxidase 2 | Regulatory Factor X Transcription Factors | Mice, Inbred C3H | Membrane Glycoproteins - genetics | Transcription Factors - metabolism | Animals | TNF Receptor-Associated Factor 6 - metabolism | Macrophages - drug effects | Protein-Serine-Threonine Kinases - immunology | Francisella tularensis - pathogenicity | Myeloid Differentiation Factor 88 - metabolism | Cytokines - biosynthesis | Cell receptors | Transcription factors | Immune response | Physiological aspects | Genetic aspects | Research | Health aspects | Francisella tularensis
Journal Article
Biochemical Journal, ISSN 0264-6021, 09/2011, Volume 438, Issue 2, pp. 369 - 378
Obesity is associated with induction of the ER (endoplasmic reticulum)-stress response signalling and insulin resistance. PTP1B (protein tyrosine phosphatase... 
Obesity | Insulin resistance | Endoplasmic reticulum (ER) stress | Metabolic syndrome | Protein tyrosine phosphatase 1B (PTP1B) | OXIDATIVE STRESS | ER STRESS | BIOCHEMISTRY & MOLECULAR BIOLOGY | protein tyrosine phosphatase 1B (PTP1B) | endoplasmic reticulum (ER) stress | INSULIN SENSITIVITY | metabolic syndrome | SIGNAL-TRANSDUCTION | GLUCOSE-HOMEOSTASIS | LEPTIN ACTION | IN-VIVO | GENE-EXPRESSION | BINDING PROTEIN-1 | insulin resistance | HEPATIC STEATOSIS | obesity | Organ Specificity - drug effects | Class Ia Phosphatidylinositol 3-Kinase - metabolism | Liver - pathology | Liver - enzymology | Humans | Protein Transport - drug effects | RNA, Messenger - metabolism | X-Box Binding Protein 1 | Gene Knockdown Techniques | DNA-Binding Proteins - metabolism | Endoplasmic Reticulum - pathology | Organ Specificity - genetics | Cell Nucleus - metabolism | Liver - drug effects | Endoplasmic Reticulum - drug effects | Gene Deletion | Eukaryotic Initiation Factor-2 - metabolism | Protein Tyrosine Phosphatase, Non-Receptor Type 1 - genetics | Stress, Physiological - drug effects | Homeostasis - drug effects | Protein-Serine-Threonine Kinases - metabolism | Endoribonucleases - metabolism | RNA, Messenger - genetics | Protein Tyrosine Phosphatase, Non-Receptor Type 1 - deficiency | Regulatory Factor X Transcription Factors | Hep G2 Cells | Obesity - pathology | Transcription Factors - metabolism | Activating Transcription Factor 6 - metabolism | Protein Tyrosine Phosphatase, Non-Receptor Type 1 - metabolism | Animals | Signal Transduction - drug effects | Tunicamycin - pharmacology | Lipid Metabolism - drug effects | Glucose - metabolism | Thapsigargin - pharmacology | Mice | Obesity - enzymology | Cell Nucleus - drug effects | ER stress | PTP1B
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2012, Volume 7, Issue 6, p. e38202
The rearrangement of intracellular membranes has been long reported to be a common feature in diseased cells. In this study, we used dengue virus (DENV) to... 
FATTY-ACID SYNTHESIS | HEPATITIS-C VIRUS | LIPID DROPLET | STEROL REGULATORY ELEMENT | RNA REPLICATION | ER STRESS | INFECTED CELLS | BIOLOGY | BINDING-PROTEIN | MEMBRANE-ALTERATIONS | VIRAL REPLICATION | Unfolded Protein Response - drug effects | Dengue Virus - drug effects | Lovastatin - pharmacology | Humans | Endoplasmic Reticulum - metabolism | Dengue - virology | Regulatory Factor X Transcription Factors | X-Box Binding Protein 1 | Virion - drug effects | DNA-Binding Proteins - metabolism | Transcription Factors - metabolism | Up-Regulation - drug effects | Activating Transcription Factor 6 - metabolism | Lipids - chemistry | Animals | Signal Transduction - drug effects | Endoplasmic Reticulum - drug effects | Cell Line, Tumor | Dengue - metabolism | Absorption - drug effects | Protein Biosynthesis - drug effects | Mice | Dengue Virus - metabolism | Sterol Regulatory Element Binding Protein 2 - metabolism | Infection | Medical research | Viral proteins | Dengue viruses | Physiological aspects | Medicine, Experimental | Protein biosynthesis | Health aspects | Protein binding | Actinomycin | Transcription factors | Membranes | Transcription | Viral diseases | Homeostasis | Lovastatin | Viruses | Lipids | Biosynthesis | Infections | Regulatory sequences | Confocal | Kinases | Autophagy | Proteins | Signal transduction | Hepatitis | Sterols | Protein folding | Sterol regulatory element-binding protein | Inhibition | Trends | Expansion | Public health | Elongation | Enlargement | Vector-borne diseases | Dengue fever | Dengue | Reabsorption | Embryo fibroblasts | Metabolism | Gene expression | Cholesterol | Studies | Cycloheximide | Infectious diseases | Inhibitors | Microscopy | Protein synthesis | Translation elongation | West Nile virus | Intracellular | Mutation | Endoplasmic reticulum | Reductase
Journal Article
Trends in Endocrinology & Metabolism, ISSN 1043-2760, 2016, Volume 27, Issue 3, pp. 119 - 122
X-box binding protein 1 (XBP1) is a major, well-conserved component of the unfolded protein response (UPR) that is crucial for glucose homeostasis and lipid... 
Endocrinology & Metabolism | unfolded protein response | glucose | lipogenesis | metabolic diseases | X-box binding protein 1 | Metabolic diseases | Glucose | Lipogenesis | Unfolded protein response | HOMEOSTASIS | UNFOLDED PROTEIN RESPONSE | DISEASES | ER-STRESS | ENDOCRINOLOGY & METABOLISM | IRE1-ALPHA-XBP1 PATHWAY | MICE | Endoribonucleases - chemistry | Endoribonucleases - genetics | Drugs, Investigational - pharmacology | X-Box Binding Protein 1 - agonists | Humans | Drugs, Investigational - therapeutic use | Glucose Metabolism Disorders - drug therapy | X-Box Binding Protein 1 - antagonists & inhibitors | Endoribonucleases - antagonists & inhibitors | Glucose Metabolism Disorders - physiopathology | Molecular Targeted Therapy | Islets of Langerhans - metabolism | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Islets of Langerhans - physiopathology | Insulin Secretion | Protein-Serine-Threonine Kinases - metabolism | Hypoglycemic Agents - therapeutic use | Unfolded Protein Response - drug effects | Islets of Langerhans - physiology | Endoplasmic Reticulum Stress - drug effects | Endoribonucleases - metabolism | Protein-Serine-Threonine Kinases - genetics | Hypoglycemic Agents - pharmacology | Gene Expression Regulation - drug effects | Insulin - metabolism | Animals | Signal Transduction - drug effects | Models, Biological | X-Box Binding Protein 1 - metabolism | Lipid Metabolism - drug effects | Glucagon - metabolism | Protein-Serine-Threonine Kinases - chemistry | X-Box Binding Protein 1 - genetics | Glucose metabolism | Physiological aspects | Genetic aspects | Genetic transcription | Dextrose | Protein binding
Journal Article
Oncogene, ISSN 0950-9232, 06/2016, Volume 35, Issue 22, pp. 2842 - 2851
Journal Article
Experimental Hematology, ISSN 0301-472X, 2011, Volume 39, Issue 10, pp. 999 - 1006
Objective Resveratrol, trans-3, 4′, 5,-trihydroxystilbene, suppresses multiple myeloma (MM). The endoplasmic reticulum (ER) stress response component... 
Hematology, Oncology and Palliative Medicine | Advanced Basic Science | PATHOGENESIS | MEDICINE, RESEARCH & EXPERIMENTAL | ACTIVATION | UNFOLDED PROTEIN RESPONSE | MESSENGER-RNA | ER STRESS | IRE1 | FACTOR-KAPPA-B | PROLIFERATION | DIFFERENTIATION | HEMATOLOGY | TRANSCRIPTION FACTOR | Sirtuin 1 - metabolism | Transcription, Genetic - drug effects | Apoptosis - drug effects | DNA, Neoplasm - metabolism | Humans | Neoplasm Proteins - physiology | Endoplasmic Reticulum - metabolism | Neoplasm Proteins - antagonists & inhibitors | Cell Line, Tumor - drug effects | Stilbenes - pharmacology | X-Box Binding Protein 1 | Endoribonucleases - physiology | Chromatin Immunoprecipitation | Protein Processing, Post-Translational - drug effects | Endoplasmic Reticulum - drug effects | Protein Binding - drug effects | Gene Expression Regulation, Neoplastic - drug effects | Phosphorylation - drug effects | Cell Line, Tumor - metabolism | RNA Splicing - drug effects | Unfolded Protein Response - drug effects | DNA-Binding Proteins - physiology | Transcription Factors - physiology | DNA-Binding Proteins - antagonists & inhibitors | Signal Transduction | Protein-Serine-Threonine Kinases - physiology | Transcription Factors - antagonists & inhibitors | Regulatory Factor X Transcription Factors | Multiple Myeloma - pathology | Drug Screening Assays, Antitumor | Stress (Physiology) | Multiple myeloma | Resveratrol | Protein binding | Endoplasmic Reticulum Stress Response | XBP1 | IRE1α | Multiple Myeloma
Journal Article