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Current Pharmaceutical Design, ISSN 1381-6128, 2010, Volume 16, Issue 16, pp. 1813 - 1825
Journal Article
Journal Article
Journal of Inorganic Biochemistry, ISSN 0162-0134, 12/2015, Volume 153, pp. 49 - 59
Heart tissue becomes zinc-depleted and the capacity to mobilize labile zinc is diminished, indicating zinc dyshomeostasis during ischemia/reperfusion (I/R).... 
Hypoxia | Reoxygenation | Proteolysis | Caspase-3 | Zinc | Apoptosis | ACTIVATION | RAT | MITOCHONDRIAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | REPERFUSION INJURY | CARDIOMYOPATHY | CARDIAC-CELLS | DEATH | INTRACELLULAR ZINC | CHEMISTRY, INORGANIC & NUCLEAR | ACUTE MYOCARDIAL-INFARCTION | Receptor, Epidermal Growth Factor - genetics | Caspase Inhibitors - pharmacology | Phosphorylation | Receptor, ErbB-2 - genetics | Protein Multimerization | Caspase 3 - metabolism | Receptor, ErbB-2 - metabolism | RNA, Messenger - metabolism | Cell Hypoxia | Receptor, Epidermal Growth Factor - metabolism | Zinc Compounds - pharmacology | Amino Acid Chloromethyl Ketones - pharmacology | Receptor, ErbB-2 - antagonists & inhibitors | Proteasome Inhibitors - pharmacology | Benzothiazoles - pharmacology | Chlorides - pharmacology | Down-Regulation | RNA, Messenger - genetics | Rats | Tyrphostins - pharmacology | Cardiotonic Agents - pharmacology | Leupeptins - pharmacology | Myocytes, Cardiac - pathology | Animals | Myocytes, Cardiac - drug effects | Receptor, Epidermal Growth Factor - antagonists & inhibitors | Protein Kinase Inhibitors - pharmacology | Pyridines - pharmacology | Thiones - pharmacology | Quinazolines - pharmacology | Organometallic Compounds - pharmacology | Proteins | Membrane lipids | Inositol | RNA | Antifungal agents | Permeability | Antibacterial agents | Phosphotransferases | Tyrosine | Cell death
Journal Article
International Journal of Pharmaceutics, ISSN 0378-5173, 02/2015, Volume 479, Issue 1, pp. 88 - 95
Zinc oxide (ZnO) appears as a promising preservative for pharmaceutical or cosmetic formulations. The other ingredients of the formulations may have specific... 
Zinc oxide | Excipients | Challenge tests | Topical formulations | Interactions | Preservative | OUTER-MEMBRANE | SUSPENSIONS | EFFICACY | PARTICLES | COMPLEX-FORMATION | BACTERICIDAL ACTIVITY | ANTIBACTERIAL ACTIVITY | BUTYLATED HYDROXYTOLUENE | PSEUDOMONAS-AERUGINOSA | PHARMACOLOGY & PHARMACY | ZNO | Titanium - pharmacology | Antioxidants - chemistry | Magnesium Sulfate - pharmacology | Sodium Chloride - pharmacology | Anti-Infective Agents - pharmacology | Escherichia coli - drug effects | Pseudomonas aeruginosa - growth & development | Titanium - chemistry | Butylated Hydroxytoluene - chemistry | Candida albicans - growth & development | Preservatives, Pharmaceutical - pharmacology | Preservatives, Pharmaceutical - chemistry | Candida albicans - drug effects | Excipients - chemistry | Zinc Oxide - chemistry | Anti-Infective Agents - chemistry | Edetic Acid - pharmacology | Ascorbic Acid - chemistry | Escherichia coli - growth & development | Sodium Chloride - chemistry | Ascorbic Acid - analogs & derivatives | Chelating Agents - chemistry | Aspergillus - growth & development | Zinc Oxide - pharmacology | Antioxidants - pharmacology | Chelating Agents - pharmacology | Pseudomonas aeruginosa - drug effects | Aspergillus - drug effects | Magnesium Sulfate - chemistry | Edetic Acid - chemistry | Ascorbic Acid - pharmacology | Butylated Hydroxytoluene - pharmacology | Excipients - pharmacology | Staphylococcus aureus - drug effects | Staphylococcus aureus - growth & development | Administration, Topical | Life Sciences | Engineering Sciences | Chemical and Process Engineering | Pharmaceutical sciences
Journal Article
International Journal of Cancer, ISSN 0020-7136, 03/2004, Volume 109, Issue 1, pp. 1 - 8
Heme oxygenase‐1 (HO‐1), an inducible enzyme that catalyzes oxidative degradation of heme to form biliverdin, carbon monoxide and free iron, may protect tumor... 
heme oxygenase‐1 | zinc protoporphyrin | macromolecular therapeutics | tumor targeting/EPR effect | D‐amino acid oxidase | Macromolecular therapeutics | D-amino acid oxidase | Tumor targeting/EPR effect | Heme oxygenase-1 | Zinc protoporphyrin | HUMAN BRAIN-TUMORS | CANCER-CHEMOTHERAPY | INDUCED APOPTOSIS | NITRIC-OXIDE SYNTHASE | heme oxygenase-1 | MACROMOLECULAR DRUGS | MESSENGER-RNA | ONCOLOGY | GENE-EXPRESSION | SOLID TUMOR | HYDROGEN-PEROXIDE PRODUCTION | TARGETED DELIVERY | Oxidants - pharmacology | Body Weight | Reactive Oxygen Species - metabolism | Oxidative Stress | Coloring Agents - pharmacology | Annexin A5 - pharmacology | Humans | Male | Metalloporphyrins - pharmacology | Oxygen - metabolism | Dose-Response Relationship, Drug | Antineoplastic Agents - pharmacology | Heme Oxygenase (Decyclizing) - antagonists & inhibitors | Polyethylene Glycols - pharmacology | Oxidation-Reduction | Hydrogen Peroxide - pharmacology | Etoposide - pharmacology | Tetrazolium Salts - pharmacology | Cisplatin - pharmacology | Hydrogen Peroxide - metabolism | Mitomycin - pharmacology | Neoplasms - drug therapy | Proline - chemistry | Drug Synergism | Animals | Cell Line, Tumor | Mice | Thiazoles - pharmacology | Antineoplastic Agents, Phytogenic - pharmacology | Camptothecin - pharmacology | Doxorubicin - pharmacology | Apoptosis
Journal Article
Journal Article
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 2013, Volume 304, Issue 6, pp. C508 - C518
Younce CW, Burmeister MA, Ayala JE. Exendin-4 attenuates high glucose-induced cardiomyocyte apoptosis via inhibition of endoplasmic reticulum stress and... 
Heart | Glucagon-like peptide-1 | Hyperglycemia | CARDIAC-FUNCTION | PEPTIDE-1 RECEPTOR | OXIDATIVE STRESS | PHYSIOLOGY | GLP-1 | CONTRACTILE DYSFUNCTION | ER STRESS | glucagon-like peptide-1 | DIABETIC CARDIOMYOPATHY | heart | CELL BIOLOGY | hyperglycemia | ENDOTHELIAL-CELLS | ZINC-FINGER PROTEIN | Receptors, Glucagon - antagonists & inhibitors | Diabetic Cardiomyopathies - metabolism | Apoptosis - drug effects | Peptide Fragments - pharmacology | Exenatide | RNA, Messenger - biosynthesis | Isoquinolines - pharmacology | Sarcoplasmic Reticulum Calcium-Transporting ATPases - antagonists & inhibitors | Phosphorylation - drug effects | Transcription Factor CHOP - biosynthesis | Calcium-Binding Proteins - metabolism | Receptors, Glucagon - agonists | Sarcoplasmic Reticulum Calcium-Transporting ATPases - metabolism | Endoplasmic Reticulum Stress - drug effects | Colforsin - pharmacology | Heat-Shock Proteins - metabolism | Cells, Cultured | Hydrogen Peroxide - pharmacology | Rats | Receptors, Glucagon - metabolism | Sulfonamides - pharmacology | Unfolded Protein Response | Hypoglycemic Agents - pharmacology | Peptides - pharmacology | Hyperglycemia - metabolism | Membrane Proteins | Animals | Glucagon-Like Peptide-1 Receptor | Myocytes, Cardiac - physiology | Tunicamycin - pharmacology | Glucose - metabolism | Thapsigargin - pharmacology | Protein Kinase Inhibitors - pharmacology | Venoms - pharmacology | Enzyme Activation | Oxidative Stress - drug effects | Sarcoplasmic Reticulum Calcium-Transporting ATPases - genetics | Transcription Factor CHOP - metabolism | HSP70 Heat-Shock Proteins | Care and treatment | Heart cells | Physiological aspects | Stress (Physiology) | Dosage and administration | Health aspects | Endoplasmic reticulum | Apoptosis
Journal Article
11.