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International Journal of Oncology, ISSN 1019-6439, 1/2016, Volume 48, Issue 1, pp. 281 - 292
Theaflavin-3, 3′-digallate (TF3) is a black tea poly-phenol produced from polymerization and oxidization of the green tea ployphenols epicatechin gallate and... 
theaflavin-3 | Akt pathway | Notch-1 pathway | c-Myc | 3′-digallate | tumor angiogenesis | C-Myc | Tumor angiogenesis | 3'-digallate | A ktpathway | Theaflavin-3 | CANCER-CELLS | MAJOR COMPONENT | FOXO TRANSCRIPTION FACTORS | INHIBITS TUMOR-GROWTH | GREEN TEA | theaflavin-3, 3 '-digallate | IN-VITRO | BLACK TEA POLYPHENOL | ONCOLOGY | SIGNALING PATHWAY | HIF-1-ALPHA | Oncogene Protein v-akt - biosynthesis | Vascular Endothelial Growth Factor A - biosynthesis | Mitogen-Activated Protein Kinase Kinases - genetics | Humans | Ovarian Neoplasms - pathology | Catechin - administration & dosage | Vascular Endothelial Growth Factor A - genetics | Neovascularization, Pathologic - pathology | Ovarian Neoplasms - genetics | Proto-Oncogene Proteins c-myc - biosynthesis | Oncogene Protein v-akt - genetics | Female | Hypoxia-Inducible Factor 1, alpha Subunit - biosynthesis | Carcinoma - pathology | Ovarian Neoplasms - drug therapy | Carcinoma - drug therapy | Hypoxia-Inducible Factor 1, alpha Subunit - genetics | Mitogen-Activated Protein Kinase Kinases - biosynthesis | Receptor, Notch1 - biosynthesis | Biflavonoids - administration & dosage | Signal Transduction - drug effects | Neovascularization, Pathologic - drug therapy | Cell Line, Tumor | Carcinoma - genetics | Neovascularization, Pathologic - genetics | Catechin - analogs & derivatives | Proto-Oncogene Proteins c-myc - genetics | Receptor, Notch1 - genetics | Polyphenols | Development and progression | Care and treatment | Neovascularization | Health aspects | Ovarian cancer | Immunoglobulins | Phosphorylation | Transcription factors | Kinases | Cancer therapies | Eggs | Studies | Proteins | Tea | Angiogenesis | Cell growth | Chemotherapy | Cell cycle | Vascular endothelial growth factor | Tumors | Index Medicus
Journal Article
Biogerontology, ISSN 1389-5729, 2013, Volume 14, Issue 3, pp. 303 - 323
During ageing skeletal muscles undergo a process of structural and functional remodelling that leads to sarcopenia, a syndrome characterized by loss of muscle... 
Life Sciences | Sarcopenia | FoxO | Geriatrics/Gerontology | Ageing | mTOR | IGF1 | Akt | Developmental Biology | Cell Biology | LIFE-SPAN | IGF-I | ALPHA-V-BETA-3 INTEGRIN | PLASMINOGEN-ACTIVATOR INHIBITOR-1 | GERIATRICS & GERONTOLOGY | GROWTH-HORMONE | MESSENGER-RNA | GENETIC-DETERMINANTS | FAST-TWITCH | CELL-CYCLE | S6 KINASE | Microtubule-Associated Proteins - genetics | SKP Cullin F-Box Protein Ligases - genetics | Humans | SKP Cullin F-Box Protein Ligases - physiology | Male | Forkhead Transcription Factors - physiology | Ubiquitin-Protein Ligases - physiology | Tripartite Motif Proteins | Young Adult | Aged, 80 and over | Adult | Female | Mice, Inbred DBA | Models, Animal | TOR Serine-Threonine Kinases - physiology | Muscle Proteins - physiology | Serpin E2 - physiology | Mice, Inbred C57BL | Mice, Transgenic | Proto-Oncogene Proteins c-akt - physiology | Muscle, Skeletal - physiology | Mice, Knockout | Microtubule-Associated Proteins - physiology | Muscle Proteins - genetics | Autophagy-Related Protein 7 | Sarcopenia - physiopathology | Serpin E2 - genetics | Animals | Aging - physiology | Insulin-Like Growth Factor I - physiology | Adolescent | Signal Transduction - physiology | Aged | Forkhead Box Protein O1 | Mice | Ubiquitin-Protein Ligases - genetics | Ubiquitin | Muscles | Ligases | Proteolysis | Analysis | Index Medicus | SKP Cullin F-Box Protein Ligases | Muscle Proteins | Aging | Serpin E2 | Signal Transduction | Biochemistry, Molecular Biology | Microtubule-Associated Proteins | Insulin-Like Growth Factor I | Proto-Oncogene Proteins c-akt | Ubiquitin-Protein Ligases | TOR Serine-Threonine Kinases | Muscle, Skeletal | Forkhead Transcription Factors | Clinical Medicine | Neurology | Neurologi | Medical and Health Sciences | Medicin och hälsovetenskap | Clinical Neurophysiology | Klinisk neurofysiologi | Klinisk medicin
Journal Article
BMC Medical Genomics, ISSN 1755-8794, 2010, Volume 3, Issue 1, pp. 26 - 26
Background: Hyperactivation of the Ras signaling pathway is a driver of many cancers, and RAS pathway activation can predict response to targeted therapies.... 
CELL LUNG-CANCER | CETUXIMAB | SIGNALING PATHWAYS | METAANALYSIS | GENOMIC STRATEGY | IN-VIVO | GROWTH | GENETICS & HEREDITY | MUTATIONS | IDENTIFICATION | METASTATIC COLORECTAL-CANCER | Neoplasms - metabolism | Lung Neoplasms - drug therapy | ras Proteins - genetics | Proto-Oncogene Proteins p21(ras) | Colorectal Neoplasms - genetics | Humans | Gene Expression Regulation, Neoplastic | Databases, Genetic | ras Proteins - metabolism | Antibodies, Monoclonal - therapeutic use | Drug Resistance, Neoplasm | Antineoplastic Agents - therapeutic use | Gene Expression Profiling | Phosphatidylinositol 3-Kinases - metabolism | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Antibodies, Monoclonal, Humanized | Mitogen-Activated Protein Kinase Kinases - metabolism | RNA Interference | Colorectal Neoplasms - drug therapy | Female | Cetuximab | Proto-Oncogene Proteins c-akt - metabolism | Lung Neoplasms - genetics | Proto-Oncogene Proteins - metabolism | Proto-Oncogene Proteins - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors | ras Proteins - antagonists & inhibitors | Proto-Oncogene Proteins - genetics | Breast Neoplasms - drug therapy | Breast Neoplasms - genetics | Signal Transduction - drug effects | Cell Line, Tumor | Mutation | Proto-Oncogene Proteins c-akt - antagonists & inhibitors | RNA, Small Interfering - metabolism | Ras genes | Physiological aspects | Genetic aspects | Research | Gene expression | Protein kinases | Risk factors | Cancer | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 04/2006, Volume 281, Issue 15, pp. 10105 - 10117
Journal Article
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 07/2011, Volume 121, Issue 7, pp. 2693 - 2708
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 06/2014, Volume 124, Issue 6, pp. 2651 - 2667
Duchenne muscular dystrophy (DMD) is caused by mutations in the gene encoding dystrophin, which results in dysfunctional signaling pathways within muscle.... 
MEDICINE, RESEARCH & EXPERIMENTAL | SKELETAL-MUSCLE | MDX MOUSE | MESSENGER-RNAS | CENTRONUCLEAR MYOPATHY | GLYCOPROTEIN COMPLEX | C2C12 MYOBLAST | TUMOR-SUPPRESSOR | CELL-PROLIFERATION | MYOBLAST FUSION | PROTEIN-KINASE B | Muscular Dystrophy, Animal - genetics | Up-Regulation | Humans | Male | MicroRNAs - metabolism | Muscle, Skeletal - metabolism | Muscle Fibers, Skeletal - metabolism | Muscular Dystrophy, Animal - pathology | Guanine Nucleotide Exchange Factors - metabolism | Base Sequence | Mice, Inbred mdx | Muscular Dystrophy, Animal - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Cell Line | Guanine Nucleotide Exchange Factors - genetics | Signal Transduction | Mice, Inbred C57BL | PTEN Phosphohydrolase - metabolism | Mice, Transgenic | Muscular Dystrophy, Duchenne - pathology | Nerve Tissue Proteins - genetics | Sequence Homology, Nucleic Acid | Nerve Tissue Proteins - metabolism | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Muscle Fibers, Skeletal - pathology | Mice | MicroRNAs - genetics | Muscular Dystrophy, Duchenne - metabolism | Muscle, Skeletal - pathology | Muscular Dystrophy, Duchenne - genetics | MicroRNA | Cellular signal transduction | Genetic aspects | Diagnosis | Properties | Genetic regulation | Muscular dystrophy | Muscular system | Mutation | Rodents | Index Medicus | Abridged Index Medicus
Journal Article