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American Journal of Physiology - Endocrinology and Metabolism, ISSN 0193-1849, 2016, Volume 311, Issue 5, pp. E836 - E849
Alcohol ingestion decreases postexercise rates of muscle protein synthesis, but the mechanism( s) (e.g., increased protein breakdown) underlying this... 
Alcohol | Exercise | Autophagy | Protein | Apoptosis | alcohol | ACTIVATION | PHYSIOLOGY | autophagy | MITOCHONDRIAL BIOGENESIS | INCREASES | exercise | apoptosis | HUMAN SKELETAL-MUSCLE | MTOR | CELL-DEATH | DIRECT PHOSPHORYLATION | P53 | MESSENGER-RNA | RESISTANCE EXERCISE | protein | ENDOCRINOLOGY & METABOLISM | Molecular Chaperones - metabolism | Apoptosis - drug effects | Humans | Male | Autophagy - physiology | Alcohol Drinking | Carrier Proteins - drug effects | Autophagy - drug effects | Electron Transport Complex IV - metabolism | Transcription Factors - drug effects | Central Nervous System Depressants - pharmacology | Mitochondrial Proteins - drug effects | Young Adult | Organelle Biogenesis | Mitochondrial Proteins - metabolism | Dietary Proteins - pharmacology | Nuclear Respiratory Factor 1 - metabolism | Mitochondrial Proton-Translocating ATPases - drug effects | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - drug effects | Voltage-Dependent Anion Channel 1 - drug effects | Mitochondrial Degradation - physiology | Mitochondrial Proton-Translocating ATPases - metabolism | Cross-Over Studies | Signal Transduction - drug effects | Mitochondrial Degradation - drug effects | Adolescent | Electron Transport Complex IV - drug effects | Membrane Proteins - drug effects | Exercise - physiology | RNA-Binding Proteins - metabolism | Protein Kinases - metabolism | Muscle Fibers, Skeletal - drug effects | Healthy Volunteers | DNA-Binding Proteins - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - metabolism | Adult | Molecular Chaperones - drug effects | Membrane Proteins - metabolism | DNA Fragmentation - drug effects | Muscle Fibers, Skeletal - physiology | Proto-Oncogene Proteins - metabolism | Protein Kinases - drug effects | Proto-Oncogene Proteins - drug effects | Dietary Carbohydrates - pharmacology | DNA-Binding Proteins - drug effects | Tumor Suppressor Protein p53 - metabolism | Voltage-Dependent Anion Channel 1 - metabolism | Tumor Suppressor Protein p53 - drug effects | Nuclear Respiratory Factor 1 - drug effects | RNA-Binding Proteins - drug effects | Transcription Factors - metabolism | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - drug effects | Ethanol - pharmacology | Carrier Proteins - metabolism | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism | Apoptosis - physiology | Autophagy (Cytology) | Cell research | Alcoholic beverages | Physiological aspects | Cellular signal transduction | Research
Journal Article
British Journal of Cancer, ISSN 0007-0920, 05/2009, Volume 100, Issue 9, pp. 1425 - 1433
Curcumin has been shown to inhibit the growth of various types of cancer cells; however, at concentrations much above the clinically achievable levels in... 
Curcumin | Chk1 | G2/M arrest | DNA damage | Pancreatic cancer | CARCINOMA-CELLS | DNA-DAMAGE | DOWN-REGULATION | REGULATED GENE-PRODUCTS | FACTOR-KAPPA-B | BENZYL ISOTHIOCYANATE | I CLINICAL-TRIAL | pancreatic cancer | ONCOLOGY | PROSTATE-CANCER | CHEMOPREVENTIVE AGENT | curcumin | Cell Cycle Proteins - drug effects | Protein Kinases - metabolism | Gene Expression Regulation, Enzymologic - drug effects | Protein Kinases - genetics | Gene Silencing - drug effects | Apoptosis - drug effects | Humans | Caspase 3 - metabolism | Collagen Type XI - metabolism | DNA-Binding Proteins - metabolism | Pancreatic Neoplasms - drug therapy | Transfection | Tumor Suppressor Proteins - genetics | Caspase 3 - drug effects | Cell Cycle Proteins - genetics | Gene Expression Regulation, Neoplastic - drug effects | Protein-Serine-Threonine Kinases - metabolism | DNA Damage - drug effects | Protein Kinases - drug effects | Tumor Suppressor Proteins - metabolism | Collagen Type XI - drug effects | Pancreatic Neoplasms - pathology | Cell Cycle Proteins - metabolism | Curcumin - pharmacology | DNA-Binding Proteins - drug effects | Pancreatic Neoplasms - enzymology | Protein-Serine-Threonine Kinases - genetics | Ataxia Telangiectasia Mutated Proteins | DNA-Binding Proteins - genetics | Cell Division - drug effects | Protein-Serine-Threonine Kinases - drug effects | Cell Line, Tumor | Checkpoint Kinase 1 | Tumor Suppressor Proteins - drug effects | Cell Cycle - drug effects | Translational Therapeutics | M arrest
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 6/2006, Volume 173, Issue 5, pp. 673 - 683
In late mitosis and early G1, replication origins are licensed for subsequent use by loading complexes of the minichromosome maintenance proteins 2-7 (Mcm2-7).... 
Replication origin | Molecules | Chromatin | Spermatozoa | DNA replication | Gels | Interphase | DNA | Small interfering RNA | Ova | CYCLIN-DEPENDENT KINASES | REPLICON INITIATION | RECOGNITION COMPLEX | XENOPUS EGG EXTRACTS | PREREPLICATION COMPLEX | EUKARYOTIC DNA-REPLICATION | MINICHROMOSOME MAINTENANCE PROTEINS | ULTRAVIOLET-LIGHT | SACCHAROMYCES-CEREVISIAE | S-PHASE CHECKPOINT | CELL BIOLOGY | Cell Cycle Proteins - drug effects | Chromatin - metabolism | Hydroxyurea - pharmacology | DNA Replication - drug effects | Oxidative Stress - physiology | Adenosine Triphosphatases - drug effects | Minichromosome Maintenance Complex Component 7 | Carrier Proteins - drug effects | Minichromosome Maintenance Complex Component 2 | Minichromosome Maintenance Complex Component 3 | Minichromosome Maintenance Complex Component 4 | DNA-Binding Proteins - metabolism | Aphidicolin - pharmacology | Time Factors | Caffeine - pharmacology | Nuclear Proteins - drug effects | Chromatin - drug effects | Cell Survival - drug effects | Xenopus Proteins - drug effects | Caenorhabditis elegans - growth & development | Xenopus laevis | Cell Cycle Proteins - metabolism | DNA-Binding Proteins - drug effects | Adenosine Triphosphatases - metabolism | Nuclear Proteins - metabolism | Animals | Caenorhabditis elegans - drug effects | Carrier Proteins - metabolism | DNA Replication - physiology | Replication Origin | Xenopus Proteins - metabolism | Dormancy (Biology) | Research
Journal Article
Molecular Endocrinology, ISSN 0888-8809, 03/2004, Volume 18, Issue 3, pp. 653 - 665
Growth differentiation factor-9 (GDF-9) is an oocyte-derived growth factor and a member of the TGF-β superfamily that includes TGF-β, activin, and bone... 
ALK7 SIGNALS | BONE MORPHOGENETIC PROTEIN | MAD-RELATED PROTEIN | ENDOCRINOLOGY & METABOLISM | OSTEOGENIC PROTEIN-1 | FOLLICULAR-GROWTH | TGF-BETA RECEPTOR | OVARIAN GRANULOSA-CELLS | IDENTIFICATION | HOMOLOG GDF-9B | LUTEAL CELLS | Phosphorylation | Receptors, Transforming Growth Factor beta - genetics | Trans-Activators - drug effects | Protein-Serine-Threonine Kinases | Activin Receptors - drug effects | Activins - metabolism | COS Cells - drug effects | Activin Receptors - genetics | Granulosa Cells - drug effects | Granulosa Cells - metabolism | COS Cells - metabolism | DNA-Binding Proteins - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Bone Morphogenetic Proteins - metabolism | Growth Differentiation Factor 9 | Trans-Activators - genetics | Female | Smad7 Protein | Promoter Regions, Genetic | Signal Transduction | Smad6 Protein | Cells, Cultured | DNA-Binding Proteins - drug effects | Rats | Activin Receptors, Type I - metabolism | DNA-Binding Proteins - genetics | Activin Receptors, Type I - genetics | Rats, Sprague-Dawley | Activin Receptors, Type I - drug effects | Transforming Growth Factor beta - pharmacology | Bone Morphogenetic Protein 15 | Smad3 Protein | Activin Receptors - metabolism | Animals | Activins - pharmacology | Receptors, Transforming Growth Factor beta - drug effects | Receptors, Transforming Growth Factor beta - metabolism | Intercellular Signaling Peptides and Proteins - pharmacology | Smad Proteins | Trans-Activators - metabolism | RNA, Small Interfering | Transforming Growth Factor beta - metabolism | Smad2 Protein
Journal Article
Molecular Cell, ISSN 1097-2765, 02/2014, Volume 53, Issue 3, pp. 369 - 379
Journal Article
Neuron, ISSN 0896-6273, 05/2009, Volume 62, Issue 3, pp. 335 - 348
Journal Article
Oncogene, ISSN 0950-9232, 05/2007, Volume 26, Issue 24, pp. 3473 - 3481
MDM2 is a critical negative regulator of the p53 tumor suppressor protein. Recently, small-molecule antagonists of MDM2, the Nutlins, have been developed to... 
E2F1 | MDM2 | Nutlin-3a | DNA damage | Apoptosis | ONCOPROTEIN | MDM2 ANTAGONISTS | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | DNA-DAMAGE | apoptosis | P73 | UBIQUITIN LIGASE ACTIVITY | CELL BIOLOGY | E2F-1-INDUCED APOPTOSIS | ONCOLOGY | PATHWAY | GENETICS & HEREDITY | S-PHASE | DEGRADATION | nutlin-3a | Apoptosis - drug effects | Humans | Apoptosis - genetics | Piperazines - metabolism | Tumor Suppressor Protein p53 - genetics | DNA-Binding Proteins - metabolism | Proto-Oncogene Proteins c-bcl-2 - metabolism | Transcription, Genetic | Antineoplastic Agents - pharmacology | Nuclear Proteins - drug effects | Tumor Cells, Cultured | Proto-Oncogene Proteins c-mdm2 - metabolism | Imidazoles - metabolism | Tumor Suppressor Proteins - metabolism | DNA-Binding Proteins - drug effects | Tumor Suppressor Protein p53 - metabolism | Nuclear Proteins - metabolism | Imidazoles - pharmacology | Cisplatin - pharmacology | E2F1 Transcription Factor - metabolism | Piperazines - pharmacology | Tumor Suppressor Protein p53 - drug effects | Tumor Protein p73 | Animals | Proto-Oncogene Proteins c-bcl-2 - drug effects | Mice | Tumor Suppressor Proteins - drug effects | Carboplatin - pharmacology | E2F1 Transcription Factor - genetics | Doxorubicin - pharmacology | Chemotherapy | Enzyme inhibitors | Leukemia | Genetic aspects | Research | Chemical properties | Drug therapy | Health aspects | Cancer | Proteins | Cellular biology | Rodents | Genetics | Tumors
Journal Article
Journal Article