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The FEBS Journal, ISSN 1742-464X, 02/2018, Volume 285, Issue 3, pp. 416 - 431
Bax and Bak are members of the Bcl‐2 family and core regulators of the intrinsic pathway of apoptosis. Upon apoptotic stimuli, they are activated and... 
DRP | mitochondria | 2 family | apoptosis | BAX | BCL | mitochondrial outer membrane permeabilization | BAK | BCL-2 family | DRP1 | OUTER-MEMBRANE | PROAPOPTOTIC BAX | BIOCHEMISTRY & MOLECULAR BIOLOGY | PORE FORMATION | BH3 DOMAINS | CELL-DEATH | PROSURVIVAL BCL-2 PROTEINS | CYTOCHROME-C | CONFORMATIONAL-CHANGES | BH3-ONLY PROTEINS | MEMBRANE PERMEABILIZATION | Mitochondrial Dynamics | Mitochondria - enzymology | bcl-2-Associated X Protein - chemistry | Proto-Oncogene Proteins c-bcl-2 - agonists | Humans | Protein Multimerization | bcl-2-Associated X Protein - agonists | bcl-2 Homologous Antagonist-Killer Protein - metabolism | Proto-Oncogene Proteins c-bcl-2 - metabolism | Mitochondrial Membranes - chemistry | Proto-Oncogene Proteins c-bcl-2 - chemistry | Mitochondrial Membranes - enzymology | Protein Interaction Domains and Motifs | Mitochondria - chemistry | Dimerization | Apoptosis Regulatory Proteins - chemistry | bcl-2-Associated X Protein - metabolism | Mitochondria - metabolism | Lipid Mobilization | Apoptosis Regulatory Proteins - metabolism | Mitochondrial Membranes - metabolism | Animals | Models, Biological | Apoptosis Regulatory Proteins - agonists | Protein Conformation | Lipid Bilayers - chemistry | Lipid Bilayers - metabolism | Porosity | bcl-2 Homologous Antagonist-Killer Protein - chemistry | Apoptosis | bcl-2 Homologous Antagonist-Killer Protein - agonists | Mitochondria | Regulators | Oligomerization | Bax protein | Bcl-2 protein | Spatial discrimination | Organelles
Journal Article
Journal Article
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 09/2016, Volume 60, Issue 9, pp. 5294 - 5301
The mechanism of colistin-induced neurotoxicity is still unknown. Our recent study (L.Zhang,Y.H.Zhao,W.J. Ding,G.Z. Jiang, Z.Y. Lu, L. Li, J. L. Wang, J.Li,... 
DEATH RECEPTOR | INHIBITION | MITOCHONDRIAL | PATHWAY | BAX | AMPK | MICROBIOLOGY | PHARMACOLOGY & PHARMACY | DRAM | PUMA | STRESS | MEMBER | AMP-Activated Protein Kinases - metabolism | Microtubule-Associated Proteins - genetics | TOR Serine-Threonine Kinases - metabolism | Tumor Suppressor Protein p53 - antagonists & inhibitors | Apoptosis - drug effects | Microtubule-Associated Proteins - metabolism | bcl-2-Associated X Protein - agonists | Caspase 3 - metabolism | Neurons - cytology | PC12 Cells | Autophagy - drug effects | Tumor Suppressor Protein p53 - genetics | TOR Serine-Threonine Kinases - antagonists & inhibitors | Toluene - analogs & derivatives | Colistin - pharmacology | TOR Serine-Threonine Kinases - genetics | Caspase 3 - genetics | Apoptosis Regulatory Proteins - genetics | Cell Differentiation | Membrane Proteins - metabolism | Neurons - metabolism | Microtubule-Associated Proteins - agonists | Neurons - drug effects | Toluene - pharmacology | bcl-2-Associated X Protein - genetics | Signal Transduction | Benzothiazoles - pharmacology | Membrane Proteins - genetics | Gene Expression Regulation | Tumor Suppressor Protein p53 - metabolism | bcl-2-Associated X Protein - metabolism | Rats | Membrane Proteins - agonists | Apoptosis Regulatory Proteins - metabolism | Animals | Apoptosis Regulatory Proteins - agonists | Anti-Bacterial Agents - pharmacology | AMP-Activated Protein Kinases - genetics | Index Medicus
Journal Article
Oncogene, ISSN 0950-9232, 09/2011, Volume 30, Issue 37, pp. 3918 - 3929
The BH3 mimetic ABT737 induces autophagy by competitively disrupting the inhibitory interaction between the BH3 domain of Beclin 1 and the anti-apoptotic... 
autophagy | ABT737 | Bcl-2 family protein | Beclin 1 | CELLS | COMPLEX | BIOCHEMISTRY & MOLECULAR BIOLOGY | IKK | INDUCTION | CELL BIOLOGY | ONCOLOGY | GENETICS & HEREDITY | BCL-2 FAMILY | BH3-ONLY PROTEINS | Phosphorylation | Nitriles - pharmacology | Ribosomal Protein S6 Kinases - metabolism | TOR Serine-Threonine Kinases - metabolism | Humans | Autophagy - drug effects | Biphenyl Compounds - pharmacology | I-kappa B Kinase - metabolism | Nitrophenols - pharmacology | Phosphotransferases (Phosphate Group Acceptor) - metabolism | Benzopyrans - pharmacology | Oncogene Protein v-akt - metabolism | Proto-Oncogene Proteins c-mdm2 - metabolism | Beclin-1 | Tumor Suppressor Protein p53 - metabolism | Glycogen Synthase Kinase 3 - metabolism | Sulfonamides - pharmacology | Membrane Proteins - agonists | Piperazines - pharmacology | Signal Transduction - drug effects | Apoptosis Regulatory Proteins - agonists | Cell Line, Tumor | Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors | Sirtuins - metabolism | Acetyl-CoA Carboxylase - metabolism | Autophagy (Cytology) | Cellular proteins | Care and treatment | Physiological aspects | Genetic aspects | Cellular signal transduction | Research | Cancer | Proteins | Signal transduction | Biomimetics | Cellular biology | Gene expression | Sirtuins | TOR protein | MDM2 protein | Bcl-2 protein | Glycogen synthase kinase 3 | AKT protein | Dephosphorylation | IKK protein | p53 protein | Allosteric properties | NF- Kappa B protein | Bcl-x protein | I Kappa B kinase | Lipid kinase | Phagocytosis | Ubiquitin-protein ligase
Journal Article
Toxicology Letters, ISSN 0378-4274, 09/2016, Volume 258, pp. 227 - 236
Application of cisplatin (DDP) for treating lung cancer is restricted due to its toxicity and lung cancer’s drug resistance. In this study, we examined the... 
AIFM2 | Lung cancer | Transcriptome | Cytotoxicity | Cisplatin | Jinfukang | Apoptosis | PATHWAYS | INDUCTION | MODEL | CHEMOTHERAPY | THERAPY | GENE | RESISTANCE | TOXICOLOGY | EXPRESSION | Lung Neoplasms - drug therapy | Apoptosis - drug effects | Humans | Lung Neoplasms - metabolism | Drugs, Chinese Herbal - pharmacology | Drug Resistance, Neoplasm | Neoplasm Proteins - antagonists & inhibitors | Gene Expression Profiling | Mitochondrial Proteins - genetics | Mitochondrial Proteins - agonists | Gene Regulatory Networks - drug effects | Neoplasm Proteins - metabolism | Antineoplastic Combined Chemotherapy Protocols - pharmacology | RNA Interference | Mitochondrial Proteins - metabolism | Apoptosis Regulatory Proteins - genetics | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | Neoplasm Proteins - genetics | A549 Cells | Mitochondrial Proteins - antagonists & inhibitors | Cisplatin - pharmacology | Apoptosis Regulatory Proteins - metabolism | Drug Synergism | Neoplasm Proteins - agonists | Apoptosis Regulatory Proteins - antagonists & inhibitors | Adenocarcinoma, Bronchiolo-Alveolar - metabolism | Apoptosis Regulatory Proteins - agonists | Cell Line, Tumor | RNA, Small Interfering | Antineoplastic Agents, Phytogenic - pharmacology | Adenocarcinoma, Bronchiolo-Alveolar - drug therapy | Analysis | Cancer cells | Marine sciences | Medicine, Chinese | Biomedical engineering | RNA sequencing | Respiratory agents | Drug resistance | Index Medicus | Herbal medicine | Stresses | Biotechnology | Lungs | Toxicity | Activation | Cancer
Journal Article
Toxicology Letters, ISSN 0378-4274, 09/2016, Volume 258, pp. 126 - 133
Sulindac has anti-neoplastic properties against colorectal cancers; however, its use as a chemopreventive agent has been limited due to toxicity and efficacy... 
Colon cancer | Sulindac | Vitamin C | ROS | p53 | SUPPRESSION | ASCORBIC-ACID | THERAPY | NONSTEROIDAL ANTIINFLAMMATORY DRUGS | PATHWAY | COLORECTAL-CANCER | PHARMACOLOGY | GROWTH | TOXICOLOGY | MUTATIONS | Colonic Neoplasms - diet therapy | Reactive Oxygen Species - metabolism | Tumor Suppressor Protein p53 - antagonists & inhibitors | Apoptosis - drug effects | Antioxidants - metabolism | Colonic Neoplasms - drug therapy | Humans | Oxidants - metabolism | Drug Resistance, Neoplasm | Colonic Neoplasms - metabolism | Reactive Oxygen Species - agonists | Tumor Suppressor Protein p53 - genetics | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Ascorbic Acid - metabolism | Osmolar Concentration | RNA Interference | Proto-Oncogene Proteins - agonists | Tumor Suppressor Protein p53 - agonists | Apoptosis Regulatory Proteins - genetics | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | Carcinoma - drug therapy | Proto-Oncogene Proteins - metabolism | Carcinoma - diet therapy | Food-Drug Interactions | HCT116 Cells | Tumor Suppressor Protein p53 - metabolism | Proto-Oncogene Proteins - genetics | Combined Modality Therapy | Apoptosis Regulatory Proteins - metabolism | Apoptosis Regulatory Proteins - agonists | Carcinoma - metabolism | Dietary Supplements | Sulindac - pharmacology | Medical colleges | Nonsteroidal anti-inflammatory drugs | Tumor proteins | Apoptosis | Index Medicus | Therapy | Effectiveness | Strategy | Colon | Combinatorial analysis | Cancer
Journal Article
Food and Chemical Toxicology, ISSN 0278-6915, 09/2013, Volume 59, pp. 657 - 669
Dioscin, a natural product obtained from medicinal plants shows lipid-lowering, anti-cancer and hepatoprotective effects. However, the effect of it on... 
Dioscin | Mitochondrial pathways | C6 glioma cells | DNA damage | ROS | Apoptosis | OXIDATIVE STRESS | PROTEIN | FOOD SCIENCE & TECHNOLOGY | MITOCHONDRIA | CANCER | CELL-DEATH | BCL-2 | GENE-THERAPY | GENERATION | TOXICOLOGY | CYTOCHROME-C RELEASE | Neoplasm Transplantation | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Male | Neoplasm Proteins - antagonists & inhibitors | Membrane Potential, Mitochondrial - drug effects | Neoplasm Proteins - metabolism | Reactive Oxygen Species - agonists | Glioblastoma - metabolism | Saponins - therapeutic use | Diosgenin - therapeutic use | Antineoplastic Agents, Phytogenic - therapeutic use | Diosgenin - analogs & derivatives | Permeability - drug effects | Diosgenin - pharmacology | Rats | Mitochondria - drug effects | Mitochondria - pathology | Rats, Sprague-Dawley | Apoptosis Regulatory Proteins - metabolism | Animals | Neoplasm Proteins - agonists | Tumor Burden - drug effects | Calcium Signaling - drug effects | Glioblastoma - pathology | Apoptosis Regulatory Proteins - antagonists & inhibitors | Survival Analysis | Apoptosis Regulatory Proteins - agonists | Cell Line, Tumor | Cell Proliferation - drug effects | DNA Damage | Antineoplastic Agents, Phytogenic - pharmacology | Glioblastoma - drug therapy | Saponins - pharmacology | Drug therapy | Gliomas | DNA | Index Medicus
Journal Article
Biology of Reproduction, ISSN 0006-3363, 2012, Volume 87, Issue 6, pp. 152 - 152
Mono-(2-ethylhexyl) phthalate (MEHP) is the active metabolite of the most commonly used plasticizer, di-(2-ethylhexyl) phthalate, and is considered to be a... 
Ovary | Oxidative stress | Toxicology | toxicology | REPRODUCTIVE-SYSTEM | GERM-CELL APOPTOSIS | KAPPA-B | HORMONAL-REGULATION | DI-(2-ETHYLHEXYL) PHTHALATE | RAT TESTIS | ovary | SUPEROXIDE-DISMUTASE EXPRESSION | REPRODUCTIVE BIOLOGY | LACTATIONAL EXPOSURE | DI(2-ETHYLHEXYL)PHTHALATE EXPOSURE | oxidative stress | MOLECULAR-MECHANISMS | Oxidoreductases - antagonists & inhibitors | Diethylhexyl Phthalate - antagonists & inhibitors | Reactive Oxygen Species - metabolism | RNA, Messenger - metabolism | Oxidoreductases - chemistry | Cell Cycle Proteins - antagonists & inhibitors | Ovarian Follicle - drug effects | Diethylhexyl Phthalate - toxicity | Infertility, Female - chemically induced | Diethylhexyl Phthalate - analogs & derivatives | Female | Free Radical Scavengers - therapeutic use | Acetylcysteine - therapeutic use | Ovarian Follicle - metabolism | Oxidoreductases - metabolism | Endocrine Disruptors - chemistry | Cell Cycle Proteins - metabolism | Cell Cycle Proteins - agonists | Plasticizers - toxicity | Random Allocation | Down-Regulation - drug effects | Mice, Inbred Strains | Infertility, Female - metabolism | Apoptosis Regulatory Proteins - metabolism | Endocrine Disruptors - toxicity | Up-Regulation - drug effects | Infertility, Female - pathology | Animals | Apoptosis Regulatory Proteins - antagonists & inhibitors | Apoptosis Regulatory Proteins - agonists | Infertility, Female - prevention & control | Mice | Oxidative Stress - drug effects | Ovarian Follicle - pathology | Index Medicus
Journal Article
Apoptosis, ISSN 1360-8185, 7/2013, Volume 18, Issue 7, pp. 777 - 785
Degeneration of intervertebral disc (IVD) is mainly a chronic process of excessive destruction of the extracellular matrix (ECM), and also is thought to be the... 
Biochemistry, general | Biomedicine | Cell death | Intervertebral disc | Cancer Research | Oncology | Degeneration | Cell Biology | Virology | REGIONAL-DISTRIBUTION | FAS LIGAND | INDUCED APOPTOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | HUMAN LUMBAR DISC | MEDIATED APOPTOSIS | END-PLATE | CELL BIOLOGY | IN-VITRO | NOTOCHORDAL CELLS | NUCLEUS PULPOSUS CELLS | GENE-EXPRESSION | RNA, Small Interfering - genetics | Transcription Factor CHOP - genetics | Caspase Inhibitors - pharmacology | Low Back Pain - prevention & control | Humans | Extracellular Matrix - metabolism | Stress, Mechanical | Intervertebral Disc Degeneration - metabolism | Intervertebral Disc Degeneration - therapy | Intervertebral Disc Degeneration - pathology | Extracellular Matrix - genetics | Caspases - metabolism | Apoptosis Regulatory Proteins - genetics | Cell Death - drug effects | Intervertebral Disc - pathology | Intervertebral Disc Degeneration - genetics | Signal Transduction | Caspases - genetics | Extracellular Matrix - drug effects | Gene Expression Regulation | Transcription Factor CHOP - antagonists & inhibitors | Intervertebral Disc - metabolism | Apoptosis Regulatory Proteins - metabolism | Animals | Apoptosis Regulatory Proteins - antagonists & inhibitors | Apoptosis Regulatory Proteins - agonists | Intervertebral Disc - drug effects | Transcription Factor CHOP - metabolism | Extracellular Matrix - pathology | RNA, Small Interfering - metabolism | Biochemistry | Health aspects | Backache | Analysis
Journal Article
Molecular and Cellular Endocrinology, ISSN 0303-7207, 05/2012, Volume 355, Issue 1, pp. 25 - 40
► Pterostilbene increases the intracellular neutral lipid accumulation thereby causing differentiation of MCF-7 cells. ► Pterostilbene causes the accumulation... 
MCF-7 cells | Autophagy | Pterostilbene | ROS | ACTIVATED RECEPTOR-GAMMA | PROTEIN-KINASE | PHOSPHOINOSITIDE 3-KINASE | STRUCTURAL DETERMINANTS | CELL BIOLOGY | CHOLESTEROL-METABOLISM | BREAST-CANCER CELLS | JNK ACTIVATION | ENDOCRINOLOGY & METABOLISM | BINDING-SITE | ENDOPLASMIC-RETICULUM | MAMMARY EPITHELIAL-CELLS | Reactive Oxygen Species - metabolism | Triglycerides - biosynthesis | Microtubule-Associated Proteins - genetics | Humans | Stilbenes - pharmacology | Receptors, Steroid - agonists | Autophagy - drug effects | Oxidoreductases Acting on CH-CH Group Donors - antagonists & inhibitors | Breast Neoplasms - metabolism | Liver X Receptors | Apoptosis Regulatory Proteins - genetics | Female | Oxidoreductases Acting on CH-CH Group Donors - genetics | CCAAT-Enhancer-Binding Proteins - genetics | Gene Expression Regulation, Neoplastic - drug effects | Microtubule-Associated Proteins - agonists | Beclin-1 | Biomarkers - metabolism | Membrane Proteins - genetics | Orphan Nuclear Receptors - agonists | Signal Transduction - genetics | Breast Neoplasms - drug therapy | Membrane Proteins - agonists | Orphan Nuclear Receptors - genetics | Breast Neoplasms - genetics | Receptors, Steroid - genetics | Signal Transduction - drug effects | Cell Differentiation - drug effects | Apoptosis Regulatory Proteins - agonists | Cell Line, Tumor | Dehydrocholesterols - metabolism | CCAAT-Enhancer-Binding Proteins - agonists | Dehydrocholesterols - antagonists & inhibitors | Cells | Proteins | Cellular | Inhibitors | Markers | Breast | Lipids | Differentiation | Cancer
Journal Article
Apoptosis, ISSN 1360-8185, 3/2015, Volume 20, Issue 3, pp. 399 - 409
The anthraquinone compound rhein is a natural agent in the traditional Chinese medicine rhubarb. Preclinical studies demonstrate that rhein has anticancer... 
Biochemistry, general | FOXO | Biomedicine | Bim | Cancer Research | Oncology | The unfolded protein response | Cell Biology | Virology | Cancer | Apoptosis | PATHWAYS | TARGET | LEUKEMIC-CELLS | ER STRESS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ENDOPLASMIC-RETICULUM STRESS | MEDIATED APOPTOSIS | LYSINATE SUPPRESSES | CELL BIOLOGY | INHIBITION | GROWTH | FOXO3A | Transcription Factor CHOP - genetics | Phosphorylation | Epithelial Cells - metabolism | Apoptosis - drug effects | Epithelial Cells - drug effects | Humans | Thapsigargin - antagonists & inhibitors | Gene Expression Regulation, Neoplastic | Mammary Glands, Human - metabolism | Proto-Oncogene Proteins c-akt - genetics | Heat-Shock Proteins - genetics | Caspases - metabolism | Bcl-2-Like Protein 11 | MCF-7 Cells | Forkhead Transcription Factors - metabolism | Proto-Oncogene Proteins - agonists | Apoptosis Regulatory Proteins - genetics | Eukaryotic Initiation Factor-2 - metabolism | Phenylbutyrates - pharmacology | Female | Membrane Proteins - metabolism | Epithelial Cells - cytology | Proto-Oncogene Proteins c-akt - metabolism | Mammary Glands, Human - drug effects | Proto-Oncogene Proteins - metabolism | Cell Line | Mammary Glands, Human - cytology | Signal Transduction | Caspases - genetics | Membrane Proteins - genetics | Heat-Shock Proteins - metabolism | Proto-Oncogene Proteins - genetics | Forkhead Transcription Factors - genetics | Membrane Proteins - agonists | Apoptosis Regulatory Proteins - metabolism | Hep G2 Cells | Eukaryotic Initiation Factor-2 - genetics | Apoptosis Regulatory Proteins - agonists | Thapsigargin - pharmacology | Anthraquinones - pharmacology | Antineoplastic Agents, Phytogenic - pharmacology | Forkhead Box Protein O3 | Transcription Factor CHOP - metabolism | Proteins | Glucose | Dextrose | Protein binding
Journal Article