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Journal Article
FEBS Letters, ISSN 0014-5793, 01/2014, Volume 588, Issue 1, pp. 175 - 183
Development of hepatocellular carcinoma (HCC) is accompanied by a continuous increase in reactive oxygen species (ROS) levels. To investigate the primary... 
Liver cancer | NF-κB | Mitochondria | Hepatocytes | TNF-α | Hepatocellular carcinoma (HCC) | Reactive oxygen species (ROS) | carbonyl cyanide m-chlorophenyl hydrazine | dichlorofluorescein diacetate | hepatitis B virus | tetramethylrhodamine ethyl ester | H2DCF-DA | TMRE | N-acetylcysteine | tumor necrosis factor-alpha | NAC | CCCP | ROS | reactive oxygen species | hepatitis C virus | HCV | HBV | CYTOKINES | TNF-alpha | BIOCHEMISTRY & MOLECULAR BIOLOGY | ISCHEMIA | DAMAGE | CELL BIOLOGY | OVEREXPRESSION | TUMOR-NECROSIS-FACTOR | HEPATOCELLULAR-CARCINOMA | NF-kappa B | BIOPHYSICS | RESPIRATION | FACTOR-INDUCED APOPTOSIS | RECEPTORS | TRANSCRIPTION FACTOR | Electron Transport Complex III - genetics | Electron Transport Complex III - metabolism | Reactive Oxygen Species - metabolism | Uncoupling Agents - pharmacology | Gene Expression - drug effects | Humans | NADH Dehydrogenase - genetics | NF-kappa B - metabolism | Hepatocytes - metabolism | Membrane Potential, Mitochondrial - drug effects | Antimycin A - pharmacology | RNA Interference | Carcinoma, Hepatocellular - genetics | Polymerase Chain Reaction | Rotenone - pharmacology | Liver Neoplasms - pathology | Hepatocytes - drug effects | ATPases Associated with Diverse Cellular Activities | RNA-Directed DNA Polymerase | Liver Neoplasms - genetics | Cells, Cultured | Mitochondria - metabolism | Mitochondria - drug effects | NADH Dehydrogenase - metabolism | Blotting, Western | Cell Movement - drug effects | Tumor Necrosis Factor-alpha - pharmacology | Animals | NF-kappa B - genetics | Carcinoma, Hepatocellular - pathology | Liver Neoplasms - metabolism | Cell Line, Tumor | Mice | Mitochondria - physiology | Carcinoma, Hepatocellular - metabolism
Journal Article
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 09/2011, Volume 301, Issue 3, pp. C695 - C704
Wang Y, Zang QS, Liu Z, Wu Q, Maass D, Dulan G, Shaul PW, Melito L, Frantz DE, Kilgore JA, Williams NS, Terada LS, Nwariaku FE. Regulation of VEGF-induced... 
Antioxidants | Mitochondria | Reactive oxygen species | Oxidant signaling | Endothelial cells | NADPH OXIDASE | endothelial cells | SUPEROXIDE | ACTIVATION | PHYSIOLOGY | OXIDATIVE DAMAGE | antioxidants | mitochondria | TERMINAL KINASE | CELL BIOLOGY | oxidant signaling | reactive oxygen species | IN-VIVO | TARGETED ANTIOXIDANTS | GROWTH-FACTOR | DYSFUNCTION | STRESS | DNA Polymerase gamma | RNA, Small Interfering - genetics | Reactive Oxygen Species - metabolism | Human Umbilical Vein Endothelial Cells - metabolism | Endothelium, Vascular - injuries | Humans | Cytoplasm - metabolism | Endothelium, Vascular - drug effects | Male | Extracellular Signal-Regulated MAP Kinases - metabolism | Cell Movement - physiology | DNA-Directed DNA Polymerase - genetics | Electron Transport Complex IV - metabolism | Endothelium, Vascular - physiology | Human Umbilical Vein Endothelial Cells - cytology | Superoxides - metabolism | p38 Mitogen-Activated Protein Kinases - metabolism | Phosphorylation - drug effects | Proto-Oncogene Proteins c-akt - metabolism | Vascular Endothelial Growth Factor A - pharmacology | Carotid Artery Injuries - pathology | von Willebrand Factor - metabolism | Cell Line | Human Umbilical Vein Endothelial Cells - drug effects | Transduction, Genetic | Catalase - genetics | Mice, Inbred C57BL | Cells, Cultured | Mitochondria - metabolism | Mitochondria - drug effects | Regeneration - physiology | p21-Activated Kinases - metabolism | Hydrogen Peroxide - metabolism | Catalase - metabolism | Cell Movement - drug effects | Regeneration - drug effects | Animals | Cyclooxygenase 2 - metabolism | Endothelium, Vascular - pathology | Cell Proliferation - drug effects | Mice | DNA-Directed DNA Polymerase - metabolism | Cytoplasm - drug effects | Hydrogen Peroxide - antagonists & inhibitors | rac1 GTP-Binding Protein - metabolism | Vitamin E - pharmacology | rac1 GTP-Binding Protein - genetics | Care and treatment | Atherosclerosis | Physiological aspects | Diagnosis | Research | Vascular endothelial growth factor | Cell migration | Vascular Biology
Journal Article
Cancer Science, ISSN 1347-9032, 06/2019, Volume 110, Issue 6, pp. 1974 - 1986
We previously found that circulating β2‐glycoprotein I inhibits human endothelial cell migration, proliferation, and angiogenesis by diverse mechanisms. In the... 
site‐directed mutagenesis | protein structure analysis | recombinant β2‐glycoprotein I polypeptide domain | anti‐melanoma cell migration | melanoma growth | site-directed mutagenesis | anti-melanoma cell migration | glycoprotein I polypeptide domain | recombinant β | Index Medicus | Original
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 12/2017, Volume 21, Issue 12, pp. 3254 - 3263
Mediator complex subunit 19 (Med19), a RNA polymerase II‐embedded coactivator, is reported to be involved in bladder cancer (BCa) progression, but its... 
Med19 | migration | proliferation | bladder cancer | Wnt/β‐catenin pathway | Wnt/β-catenin pathway | MEDICINE, RESEARCH & EXPERIMENTAL | COMPLEX | METASTASIS | TRANSCRIPTION | Wnt/beta-catenin pathway | RISK | SACCHAROMYCES-CEREVISIAE | CELL BIOLOGY | GROWTH | WNT | EXPRESSION | CARCINOMA | TUMORIGENESIS | Cyclin D1 - metabolism | RNA, Small Interfering - genetics | Cell Proliferation | Cadherins - metabolism | Mediator Complex - antagonists & inhibitors | Mediator Complex - metabolism | Humans | Gene Expression Regulation, Neoplastic | Glycogen Synthase Kinase 3 beta - genetics | Male | Wnt2 Protein - genetics | Matrix Metalloproteinase 9 - metabolism | Neoplasm Grading | Urinary Bladder Neoplasms - genetics | Matrix Metalloproteinase 9 - genetics | Urinary Bladder Neoplasms - pathology | Female | Cadherins - genetics | Wnt Signaling Pathway | Wnt2 Protein - antagonists & inhibitors | Mediator Complex - genetics | Glycogen Synthase Kinase 3 beta - metabolism | Urinary Bladder Neoplasms - surgery | beta Catenin - metabolism | beta Catenin - genetics | Wnt2 Protein - metabolism | Xenograft Model Antitumor Assays | Animals | Cyclin D1 - genetics | Mice, Nude | beta Catenin - antagonists & inhibitors | Urinary Bladder Neoplasms - therapy | Cell Line, Tumor | Mice | Mice, Inbred BALB C | Neoplasm Staging | Cell Movement | RNA, Small Interfering - metabolism | Cell proliferation | Leukocyte migration | Wnt protein | Bladder | Paraffin | Tissues | Ribonucleic acid--RNA | Bladder cancer | E-cadherin | DNA-directed RNA polymerase | Gelatinase B | Polymerase | Signaling | Signal transduction | Cell growth | Urinary bladder | Catenin | Cell migration | RNA polymerase II | Cancer | Tumors | Wnt | Original | β‐catenin pathway
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2014, Volume 9, Issue 3, p. e92059
Focal adhesion kinase (FAK) plays an important role in signal transduction pathways initiated at sites of integrin-mediated cell adhesion to the extracellular... 
CALCIUM OSCILLATIONS | TYROSINE PHOSPHORYLATION | CELL MOTILITY | MULTIDISCIPLINARY SCIENCES | IN-VIVO | BINDING-SITE | C-TERMINAL DOMAIN | KINASE INHIBITOR | P130CAS LOCALIZATION | ASTROCYTOMA-CELLS | FOCAL ADHESIONS | Paxillin - metabolism | Focal Adhesion Kinase 1 - genetics | Paxillin - genetics | Embryo, Mammalian | Humans | Crk-Associated Substrate Protein - metabolism | Recombinant Fusion Proteins | Protein Binding - drug effects | src-Family Kinases - metabolism | Phosphorylation - drug effects | Binding Sites | Focal Adhesion Kinase 1 - metabolism | Fibroblasts - metabolism | Cell Line | Mutagenesis, Site-Directed | Signal Transduction | Gene Expression Regulation | Cell Adhesion - drug effects | Crk-Associated Substrate Protein - genetics | Cell Movement - drug effects | Focal Adhesions - drug effects | Animals | Fibroblasts - drug effects | Focal Adhesions - metabolism | Fibroblasts - cytology | Mice | Protein Kinase Inhibitors - pharmacology | src-Family Kinases - genetics | Focal Adhesion Kinase 1 - antagonists & inhibitors | Cellular signal transduction | Metastasis | Integrins | Phosphorylation | Motility | Catalytic activity | Kinases | Metastases | Cell adhesion & migration | Signal transduction | Pathways | Cell adhesion | Cell cycle | Extracellular matrix | Catalysis | Inhibition | Localization | Adhesion | Signaling | Inhibitors | Mutagenesis | Signal processing | Transduction | Focal adhesion kinase | Paxillin | Cell migration | Cancer | Life Sciences
Journal Article