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Biotechnology and Bioengineering, ISSN 0006-3592, 11/2017, Volume 114, Issue 11, pp. 2560 - 2570
Journal Article
Diabetes, ISSN 0012-1797, 04/2013, Volume 62, Issue 4, pp. 1227 - 1237
Journal Article
Biotechnology and Bioengineering, ISSN 0006-3592, 03/2019, Volume 116, Issue 3, pp. 569 - 580
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2011, Volume 6, Issue 9, pp. e24660 - e24660
Journal Article
European Journal of Immunology, ISSN 0014-2980, 02/2011, Volume 41, Issue 2, pp. 491 - 502
Plasma cells (PCs) secrete copious levels of immunoglobulins. To achieve this, their endoplasmic reticulum (ER) undergoes expansion in a process that requires... 
ER stress | Plasma cells | MTOR | Unfolded protein response | MAMMALIAN TARGET | SECRETORY APPARATUS | UNFOLDED PROTEIN | ER-STRESS | TRANSCRIPTION FACTOR XBP-1 | IMMUNOLOGY | TRANSLATIONAL CONTROL | B-CELLS | INDUCED GENE-EXPRESSION | TUBEROUS SCLEROSIS COMPLEX | MESSENGER-RNA | mTOR | TOR Serine-Threonine Kinases - metabolism | Phosphoprotein Phosphatases - metabolism | Protein Biosynthesis - physiology | Plasma Cells - drug effects | TOR Serine-Threonine Kinases - antagonists & inhibitors | Signal Transduction - immunology | Protein Folding - drug effects | Endoplasmic Reticulum - drug effects | Tumor Suppressor Proteins - genetics | Eukaryotic Initiation Factor-2 - metabolism | Plasma Cells - metabolism | Stress, Physiological - drug effects | Phosphorylation - drug effects | Cell Differentiation - physiology | Fumonisins - pharmacology | B-Lymphocytes - metabolism | Stress, Physiological - physiology | B-Lymphocyte Subsets - drug effects | B-Lymphocytes - cytology | Mice, Inbred C57BL | Endoplasmic Reticulum - physiology | Mice, Transgenic | Sirolimus - pharmacokinetics | B-Lymphocytes - drug effects | Animals | Apoptosis - immunology | Phosphoprotein Phosphatases - genetics | Activating Transcription Factor 4 - metabolism | B-Lymphocyte Subsets - metabolism | Signal Transduction - drug effects | Ribosomal Protein S6 - metabolism | Tunicamycin - pharmacology | Lipopolysaccharides - pharmacology | Antibody Formation | Thapsigargin - pharmacology | Protein Biosynthesis - drug effects | Mice | Plasma Cells - cytology | Proteins | Phosphorylation | Protein synthesis | Rodents | Endoplasmic reticulum | Immune system | Apoptosis | Index Medicus
Journal Article
Cell Structure and Function, ISSN 0386-7196, 01/2019, Volume 44, Issue 2, pp. 75 - 83
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2014, Volume 9, Issue 10, pp. e110942 - e110942
The unfolded protein response (UPR) is an endoplasmic reticulum (ER)-to-nucleus signaling cascade induced in response to ER stress. The UPR aims at restoring... 
B-CELLS | MESSENGER-RNA | REGULATED IRE1-DEPENDENT DECAY | ER STRESS | MULTIDISCIPLINARY SCIENCES | IN-VIVO | TRANSCRIPTION FACTOR XBP1 | INFECTION | ENDOPLASMIC-RETICULUM STRESS | PLASMA-CELLS | UNFOLDED-PROTEIN-RESPONSE | Fibroblasts - virology | Endoplasmic Reticulum - genetics | Unfolded Protein Response - genetics | Membrane Proteins - genetics | Virus Replication - genetics | Humans | Gene Expression Regulation | Protein-Serine-Threonine Kinases - genetics | Apoptosis - genetics | Muromegalovirus - pathogenicity | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Endoplasmic Reticulum Stress - genetics | Fibroblasts - pathology | Regulatory Factor X Transcription Factors | X-Box Binding Protein 1 | Protein-Serine-Threonine Kinases - biosynthesis | RNA, Messenger - biosynthesis | Membrane Proteins - biosynthesis | Animals | Mice | Muromegalovirus - genetics | Infection | RNA | Gene expression | Health aspects | Protein binding | Apoptosis | Transcription factors | Pathogenesis | Homeostasis | Infections | Genomes | Kinases | Macrophages | Nuclei | Delay | Clonal deletion | Protein folding | Cell cycle | Fibroblasts | Deletion | Stresses | Cytomegalovirus | Phenotypes | Immunoglobulins | Bacterial infections | Splicing | Metabolism | Stress | Virology | Signaling | Genetic engineering | Endoplasmic reticulum | Viral infections | Peritoneum | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2013, Volume 8, Issue 12, pp. e81065 - e81065
Background and Aims: C/EBP homologous protein (CHOP) plays pro-apoptotic roles in the integrated stress response. Recently, a tumor suppressive role for CHOP... 
INDUCED APOPTOSIS | ROLES | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | ENDOPLASMIC-RETICULUM STRESS | PROTEOLYSIS | ATF6 | CONTRIBUTES | TUMORS | PROGRESSION | HEPATOCARCINOGENESIS | Diethylnitrosamine - toxicity | Transcription Factor CHOP - genetics | Carcinoma, Hepatocellular - chemically induced | Humans | Liver Neoplasms - chemically induced | Inflammation - metabolism | Cell Nucleus - metabolism | Liver Neoplasms - pathology | Carcinoma, Hepatocellular - immunology | Macrophages - immunology | Unfolded Protein Response - drug effects | Liver Neoplasms - immunology | Transcription Factor CHOP - deficiency | Gene Knockout Techniques | Disease Progression | Carcinogenesis - drug effects | Animals | Active Transport, Cell Nucleus - drug effects | Carcinoma, Hepatocellular - pathology | Liver Neoplasms - metabolism | Macrophages - drug effects | Mice | Cell Nucleus - drug effects | Transcription Factor CHOP - metabolism | Carcinoma, Hepatocellular - metabolism | RNA | Lung cancer | Analysis | Physiological aspects | Hepatoma | Protein binding | Apoptosis | Crosstalk | Carbon tetrachloride | Parenchyma | Hepatocellular carcinoma | Homology | mRNA | CCAAT/enhancer-binding protein | Kinases | Macrophages | Machinery | Carcinogenesis | Recruitment | Liver cancer | Signal transduction | Carcinogens | Pathways | Diethylnitrosamine | Rodents | Immune system | Stresses | Metabolism | CCL4 protein | Stress | Nodules | Signaling | γ-Interferon | Human pathology | Endoplasmic reticulum | Tumors | Cancer | Index Medicus
Journal Article