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2004, 2nd ed., ISBN 9780306478635, [ix], 194
Book
1997, Molecular biology intelligence unit (Unnumbered), ISBN 9780412117510, 240
Book
Experimental Cell Research, ISSN 0014-4827, 09/2019, Volume 382, Issue 2, pp. 111473 - 111473
ErbB3, which belongs to the epidermal growth factor receptor (EGFR) or ErbB family of receptor tyrosine kinases, is involved in progression of several human... 
Receptor internalization | Endosomal sorting | Phorbol 12-myristate 13-acetate (PMA) | Receptor recycling | ErbB3 | Protein kinase C (PKC) | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2013, Volume 8, Issue 1, pp. e54122 - e54122
Background: The self-renewal of human pluripotent stem (hPS) cells including embryonic stem and induced pluripotent stem cells have been reported to be... 
MAINTENANCE | EPSILON-PKC | MAINTAIN PLURIPOTENCY | WNT/BETA-CATENIN | MULTIDISCIPLINARY SCIENCES | SERUM-FREE MEDIUM | GROWTH-FACTOR | DIFFERENTIATION | INDUCTION | CULTURE | HUMAN EMBRYONIC STEM | Immunohistochemistry | Protein Kinase C - genetics | Cell Proliferation | Tetradecanoylphorbol Acetate - pharmacology | Humans | Alkaline Phosphatase - metabolism | Fibroblast Growth Factor 2 - pharmacology | Maleimides - pharmacology | Glycogen Synthase Kinase 3 beta | Phosphatidylinositol 3-Kinases - metabolism | Extracellular Signal-Regulated MAP Kinases - metabolism | RNA Interference | Protein Kinase C - metabolism | Indoles - pharmacology | Phosphorylation - drug effects | Chromones - pharmacology | Proto-Oncogene Proteins c-akt - metabolism | Cell Line | Pluripotent Stem Cells - cytology | Protein Kinase C-epsilon - genetics | Morpholines - pharmacology | Glycogen Synthase Kinase 3 - metabolism | Blotting, Western | Pluripotent Stem Cells - metabolism | Protein Kinase C-delta - metabolism | Activins - pharmacology | Signal Transduction - drug effects | Protein Kinase C-epsilon - metabolism | Carbazoles - pharmacology | Protein Kinase C-delta - genetics | Phosphatases | Synthesis | Glycogen | Analysis | Stem cells | Fibroblast growth factors | Mitogens | Protein kinases | Fibroblast growth factor | Cell culture | Alkaline phosphatase | Phosphorylation | Protein kinase C | Disease | Laboratories | AKT protein | Kinases | Phosphatase | Proteins | Cell cycle | Inhibition | Growth factors | Fibroblast growth factor 2 | RNA-mediated interference | Extracellular signal-regulated kinase | Glycogen synthase kinase 3 | MAP kinase | siRNA | Ribonucleic acid--RNA | Insulin | Embryos | 1-Phosphatidylinositol 3-kinase | Signaling | Molecular modelling | Inhibitors | Isoforms | Differentiation | Activin | Acetic acid | Phorbol 12-myristate 13-acetate | Pluripotency | Index Medicus | RNA | Ribonucleic acid
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2012, Volume 7, Issue 1, pp. e29622 - e29622
GNAQ mutations at codon 209 have been recently identified in approximately 50% of uveal melanomas (UM) and are reported to be oncogenic through activating the... 
MULTIPLE-MYELOMA | GLIOMA-CELLS | COLON-CANCER | PKC ISOFORMS | HETEROTRIMERIC G-PROTEINS | BETA INHIBITOR | INDUCED APOPTOSIS | BRAF MUTATIONS | BIOLOGY | LUNG-CANCER CELLS | MAPK PATHWAY | Apoptosis - drug effects | Humans | Melanoma - enzymology | Molecular Sequence Data | Extracellular Signal-Regulated MAP Kinases - metabolism | Cyclin D1 | Uveal Neoplasms - enzymology | Cyclin-Dependent Kinase Inhibitor p27 - metabolism | Mitogen-Activated Protein Kinase Kinases - metabolism | Isoenzymes - metabolism | Protein Kinase C - metabolism | Indoles - pharmacology | Bromodeoxyuridine - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Cell Survival - drug effects | Uveal Neoplasms - pathology | Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors | GTP-Binding Protein alpha Subunits - genetics | Protein Kinase C - antagonists & inhibitors | Melanoma - pathology | Enzyme Activation - drug effects | Mutation - genetics | Uveal Neoplasms - drug therapy | Cell Cycle Checkpoints - drug effects | Protein Kinase Inhibitors - therapeutic use | GTP-Binding Protein alpha Subunits, Gq-G11 | Melanoma - drug therapy | Cell Line, Tumor | Indoles - therapeutic use | Cell Proliferation - drug effects | Protein Kinase Inhibitors - pharmacology | Isoenzymes - antagonists & inhibitors | Drug Screening Assays, Antitumor | Codon | Angiogenesis inhibitors | Protein kinases | Melanoma | Apoptosis | Phosphorylation | Protein kinase C | Bcl-2 protein | Leukemia | Metastasis | Kinases | Accumulation | Medical schools | Skin cancer | Anticancer properties | Proteins | Signal transduction | Tumorigenesis | Inhibition | Extracellular signal-regulated kinase | MAP kinase | Survivin | Signaling | Inhibitors | Womens health | Pancreatic cancer | Isoforms | Cyclin-dependent kinase inhibitor p27 | Antitumor activity | Sensitivity enhancement | Mutation | Viability | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2014, Volume 9, Issue 2, pp. e88405 - e88405
NADPH oxidase5 (Nox5) is a novel Nox isoform which has recently been recognized as having important roles in the pathogenesis of coronary artery disease, acute... 
ESOPHAGEAL ADENOCARCINOMA CELLS | OXYGEN SPECIES PRODUCTION | OXIDATIVE STRESS | MULTIDISCIPLINARY SCIENCES | PKC-ALPHA | ENDOTHELIAL-CELLS | HEART-FAILURE | GENE-EXPRESSION | SMOOTH-MUSCLE-CELLS | EXPRESSION PROFILES | DEPENDENT ACTIVATION | Protein Kinase C - genetics | RNA, Small Interfering - genetics | Phosphorylation | Reactive Oxygen Species - metabolism | Protein Kinase C-alpha - metabolism | Humans | Protein Kinase C-alpha - genetics | NADPH Oxidases - metabolism | Cercopithecus aethiops | NADPH Oxidase 5 | Hyperglycemia - metabolism | Animals | Protein Isoforms - metabolism | RNA Interference | Protein Kinase C - metabolism | HEK293 Cells | Superoxides - metabolism | Hyperglycemia - enzymology | Membrane Proteins - metabolism | COS Cells | Protein Isoforms - genetics | Oxidases | Superoxide | Genetic engineering | Protein kinases | Heart attack | Myocardial infarction | Reactive oxygen species | Protein kinase C | Calcium | Pathogenesis | Smooth muscle | Cardiovascular disease | Biology | Activation | Kinases | NAD(P)H oxidase | Proteins | Signal transduction | Toxicology | Hyperglycemia | Atherosclerosis | Physiology | Inhibition | Heart diseases | Heart failure | Enzymes | Calcium (intracellular) | Complications | Diabetes mellitus | Fetuses | Coronary artery | Pharmacology | Forensic medicine | Gene expression | Coronary artery disease | Endothelial cells | Inhibitors | Nitric oxide | Isoforms | Infarction | Ventricle | Diabetes | Auditory defects | Cancer | Index Medicus
Journal Article
Journal Article
Journal Article
Science, ISSN 0036-8075, 4/2010, Volume 328, Issue 5976, pp. 372 - 376
Journal Article
Journal Article
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 11/2018, Volume 62, Issue 11
Antiretroviral therapy (ART) does not cure HIV-1 infection due to the persistence of proviruses in long-lived resting T cells. Strategies targeting these... 
Ingenols | HIV | HIV latency | HIV persistence | PKC agonist | PLASMA VIREMIA | RESERVOIR | ingenols | IMMUNODEFICIENCY-VIRUS-INFECTION | CD4(+) T-CELLS | MICROBIOLOGY | HIV-1-INFECTED PATIENTS | VALPROIC ACID | REACTIVATION | ACTIVE ANTIRETROVIRAL THERAPY | IN-VIVO | PHARMACOLOGY & PHARMACY | EX-VIVO
Journal Article