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European journal of immunology, ISSN 0014-2980, 05/2008, Volume 38, Issue 5, pp. 1194 - 1203
Journal Article
Journal Article
Nature immunology, ISSN 1529-2916, 03/2010, Volume 11, Issue 5, pp. 411 - 418
... through a group of receptors referred to as pathogenrecognition receptors, the best-studied of which are the Toll-like receptors (TLRs) (1). The cytoplasmic domains of TLRs... 
Life Sciences & Biomedicine | Immunology | Science & Technology | 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 | Index Medicus
Journal Article
Nature (London), ISSN 1476-4687, 01/2002, Volume 415, Issue 6867, pp. 92 - 96
The unfolded protein response (UPR), caused by stress, matches the folding capacity of endoplasmic reticulum (ER... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Transcription Factors - chemistry | Caenorhabditis elegans Proteins - chemistry | Caenorhabditis elegans Proteins - metabolism | Endoplasmic Reticulum - metabolism | Molecular Sequence Data | RNA, Messenger - metabolism | Stem Cells - metabolism | Caenorhabditis elegans Proteins - secretion | Endoplasmic Reticulum - secretion | X-Box Binding Protein 1 | DNA-Binding Proteins - metabolism | Transcription Factors - secretion | RNA Splicing | RNA, Helminth - metabolism | Base Sequence | Protein Denaturation | Fibroblasts | Nucleic Acid Conformation | RNA, Helminth - genetics | Protein-Serine-Threonine Kinases - metabolism | DNA-Binding Proteins - secretion | Cell Line | Caenorhabditis elegans - metabolism | Introns - genetics | Caenorhabditis elegans - genetics | RNA, Messenger - genetics | Protein-Serine-Threonine Kinases - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | DNA-Binding Proteins - chemistry | Regulatory Factor X Transcription Factors | Protein Folding | Membrane Proteins | Transcription Factors - metabolism | RNA, Helminth - chemistry | Animals | Caenorhabditis elegans - cytology | RNA, Messenger - chemistry | Mice | Caenorhabditis elegans Proteins - genetics | Physiological aspects | Genetic aspects | Messenger RNA | DNA binding proteins | Research | Endoplasmic reticulum | Proteins | Mutation | Ribonucleic acid--RNA | Ribonucleic acid | Genes | Worms | Index Medicus
Journal Article
Journal Article
Diabetologia, ISSN 0012-186X, 6/2010, Volume 53, Issue 6, pp. 1120 - 1130
...)–C/EBP homologous protein (CHOP) branch of the unfolded protein response, but defective X-box binding protein 1 (XBP1... 
Human Physiology | Secretion | Metabolic Diseases | Internal Medicine | Insulin | PDX-1 | Unfolded protein response | Medicine & Public Health | ER-stress | UPR | Beta cell | XBP-1 | Apoptosis | Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Rats, Wistar | Apoptosis - drug effects | Maf Transcription Factors - genetics | Cell Count | Homeodomain Proteins - metabolism | Endoplasmic Reticulum - metabolism | Male | X-Box Binding Protein 1 | DNA-Binding Proteins - metabolism | Insulin-Secreting Cells - metabolism | Transfection | RNA Interference | Endoplasmic Reticulum - drug effects | Trans-Activators - genetics | Indoles - pharmacology | Interleukin-8 - pharmacology | Insulin-Secreting Cells - cytology | Maf Transcription Factors - metabolism | Insulin - genetics | Insulin Secretion | Cell Survival - drug effects | Endoplasmic Reticulum - genetics | Cells, Cultured | Rats | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Regulatory Factor X Transcription Factors | Blotting, Western | Homeodomain Proteins - genetics | Transcription Factors - metabolism | Insulin - metabolism | Animals | Analysis of Variance | Insulin-Secreting Cells - drug effects | Fluorescent Antibody Technique | Trans-Activators - metabolism | RNA, Small Interfering | Apoptosis - physiology | Interferon-gamma - pharmacology | Animal experimentation | Medical colleges | Pancreatic beta cells | Anopheles | Messenger RNA | Viral proteins | Type 1 diabetes | Protein binding | RNA | Genes | Glucose | Dextrose | Proteins | Glucose metabolism | Adenoviruses | Index Medicus
Journal Article
Trends in endocrinology and metabolism, ISSN 1043-2760, 03/2016, 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... 
Endocrinology & Metabolism | unfolded protein response | glucose | lipogenesis | metabolic diseases | X-box binding protein 1 | Metabolic diseases | Glucose | Lipogenesis | Unfolded protein response | Life Sciences & Biomedicine | Science & Technology | 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 | Index Medicus
Journal Article
PloS one, ISSN 1932-6203, 04/2019, Volume 14, Issue 4, pp. e0212235 - e0212235
.... In vascular smooth muscle cell (VSMCs), multiple modulators of protein handling machinery regulate intimal hyperplasia... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Cell Proliferation | Humans | Myocytes, Smooth Muscle - pathology | Transglutaminases - genetics | Male | Carotid Arteries - cytology | GTP-Binding Proteins - genetics | Ubiquitination | Protein-Serine-Threonine Kinases - metabolism | Disease Models, Animal | Endoribonucleases - metabolism | Signal Transduction | Muscle, Smooth, Vascular - cytology | Unfolded Protein Response | Hyperplasia - etiology | Mice, Knockout | Hyperplasia - pathology | Muscle, Smooth, Vascular - pathology | Animals | X-Box Binding Protein 1 - metabolism | Transglutaminases - metabolism | Neointima - pathology | Carotid Arteries - surgery | Carotid Arteries - pathology | Mice | Protein Processing, Post-Translational | Ligation - adverse effects | X-Box Binding Protein 1 - genetics | Cell Movement | GTP-Binding Proteins - metabolism | Transglutaminases | Research | Vascular smooth muscle | Binding proteins | Hyperplasia | Oxidative stress | Animal models | Transcription factors | Platelet-derived growth factor | Disease | Veterans | Homeostasis | Smooth muscle | Catalytic activity | Carotid arteries | Modulators | Proteins | Vascular diseases | Ischemia | Protein folding | Rodents | Atherosclerosis | Post-translation | Activating transcription factor 1 | Extracellular matrix | Catalysis |