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PLoS ONE, ISSN 1932-6203, 04/2012, Volume 7, Issue 4, p. e34653
Background: Shedding microvesicles are membrane released vesicles derived directly from the plasma membrane. Exosomes are released membrane vesicles of late... 
CA2&-STIMULATED ADENOSINE-TRIPHOSPHATASE | HUMAN PROSTATIC FLUID | EPITHELIAL-CELLS | MEMBRANE-VESICLES | BIOLOGY | HUMAN SEMEN | SPERMATOZOA | EXTRACELLULAR ORGANELLES PROSTASOMES | SECRETION | TUMOR-DERIVED EXOSOMES | HUMAN SPERM | Exosomes - metabolism | Cell Line | NIH 3T3 Cells | Microscopy, Electron, Transmission - methods | Secretory Vesicles - metabolism | DNA - metabolism | RNA, Messenger - metabolism | Clathrin - metabolism | Animals | Cell Nucleus - metabolism | Biological Transport | Myocytes, Cardiac - metabolism | Cytosol - metabolism | Cell Membrane - metabolism | Membrane Proteins - metabolism | Mice | Annexin A2 - metabolism | Caveolin 3 - metabolism | Fibroblasts - metabolism | RNA - metabolism | Clathrin | RNA | Genes | Hostages | Nucleotide sequencing | Gene expression | DNA sequencing | Heart | Flow cytometry | Sperm | Centrifugation | Lung cancer | Ultracentrifugation | Biochemistry | Exosomes | Cytosol | Nuclei | Muscular dystrophy | Gene sequencing | Vesicles | Rodents | Penicillin | Fibroblasts | Public health | Deoxyribonucleic acid--DNA | Messages | Nucleotide sequence | Caveolin | Membrane vesicles | Cardiomyocytes | Electron microscopy | Metabolism | Medicine | Polymerase | DNA nucleotidylexotransferase | Cytometry | Hospitals | Transmission electron microscopy | Ribonucleic acids | MicroRNAs | Media (differential) | Biochemical characteristics | Clinical medicine | Mutation | Prostate | Cell and Molecular Biology | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Cell- och molekylärbiologi | Medicinska och farmaceutiska grundvetenskaper | Deoxyribonucleic acid | DNA
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2014, Volume 9, Issue 3, p. e91997
Introduction: Brown adipose tissue (BAT) is a potential therapeutic target to reverse obesity. The purpose of this study was to determine whether primary... 
THERMOGENESIS | ACTIVATION | MESSENGER-RNA | COLD-EXPOSURE | METABOLISM | MULTIDISCIPLINARY SCIENCES | INCREASES | ADULT HUMANS | ADIPOGENESIS | EXPRESSION | BROWN FAT | Adipocytes, Brown - metabolism | LIM-Homeodomain Proteins - metabolism | Homeodomain Proteins - metabolism | Humans | Ion Channels - genetics | Male | Mitochondrial Proteins - genetics | Tumor Necrosis Factor Receptor Superfamily, Member 9 - genetics | Fatty Acid-Binding Proteins - metabolism | PPAR gamma - metabolism | Obesity - genetics | Case-Control Studies | Subcutaneous Fat - metabolism | Mitochondrial Proteins - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Adult | Cell Differentiation | Nuclear Proteins - genetics | PPAR gamma - genetics | Biomarkers - metabolism | Adipocytes, Brown - pathology | Gene Expression | Retinoblastoma Protein - metabolism | Nuclear Proteins - metabolism | Tumor Necrosis Factor Receptor Superfamily, Member 9 - metabolism | Transcription Factors - genetics | Fatty Acid-Binding Proteins - genetics | Subcutaneous Fat - pathology | Homeodomain Proteins - genetics | Obesity - metabolism | Obesity - pathology | Transcription Factors - metabolism | LIM-Homeodomain Proteins - genetics | Adipocytes, White - pathology | Ion Channels - metabolism | Retinoblastoma Protein - genetics | Primary Cell Culture | Uncoupling Protein 1 | Adipocytes, White - metabolism | Adipose tissues | Obesity | Gene expression | Health aspects | Genes | Heart | Adipose tissue | Laboratories | Adipocytes | Males | Tissues | Proteins | Uncoupling protein 1 | Rodents | Penicillin | Physiology | Cardiology | Adipose tissue (brown) | CD137 antigen | Markers | Preadipocytes | Cultures | Metabolism | Insulin | Lipolysis | Abdomen | Musculoskeletal system | Weight control | Thermogenesis | Cell lines | Stem cells | Diabetes | Peroxisome proliferator-activated receptors | Differentiation
Journal Article
Drug Metabolism and Disposition, ISSN 0090-9556, 12/2007, Volume 35, Issue 12, pp. 2166 - 2176
Olmesartan, a novel angiotensin II AT1-receptor antagonist, is excreted into both bile and urine, with minimal metabolism. Because olmesartan is a hydrophilic... 
PHARMACOKINETICS | INVOLVEMENT | PHARMACOLOGY & PHARMACY | RESISTANCE-ASSOCIATED PROTEIN-4 | ORGANIC ANION TRANSPORTERS | EXCRETION | IDENTIFICATION | MEDOXOMIL | EXPRESSION | OATP1B1 | BLOCKER | ATP Binding Cassette Transporter, Sub-Family G, Member 2 | Humans | ATP-Binding Cassette, Sub-Family B, Member 1 - metabolism | Membrane Transport Proteins - drug effects | Hepatocytes - metabolism | Imidazoles - pharmacokinetics | Neoplasm Proteins - metabolism | Angiotensin II Type 1 Receptor Blockers - pharmacokinetics | Sincalide - metabolism | Angiotensin II Type 1 Receptor Blockers - metabolism | Organic Anion Transporters - metabolism | Prodrugs - metabolism | Tetrazoles - metabolism | Dose-Response Relationship, Drug | Kidney - metabolism | Protein Isoforms - metabolism | Transfection | Liver - drug effects | Membrane Transport Proteins - genetics | Organic Anion Transporters, Sodium-Independent - metabolism | Adenosine Triphosphate - metabolism | ATP-Binding Cassette Transporters - metabolism | Female | Membrane Transport Proteins - metabolism | Hepatocytes - drug effects | Solute Carrier Organic Anion Transporter Family Member 1B3 | Imidazoles - metabolism | Olmesartan Medoxomil | Cell Line | Liver - metabolism | Probenecid - pharmacology | Penicillin G - pharmacology | Mice, Knockout | p-Aminohippuric Acid - pharmacology | Animals | Estrone - analogs & derivatives | Multidrug Resistance-Associated Proteins - deficiency | Prodrugs - pharmacokinetics | Estrone - metabolism | Dogs | Protein Binding | ATP Binding Cassette Transporter, Sub-Family B | Mice | Kinetics | In Vitro Techniques | Solute Carrier Organic Anion Transporter Family Member 1b1 | Multidrug Resistance-Associated Proteins - metabolism | Tetrazoles - pharmacokinetics
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2010, Volume 5, Issue 2, p. e9367
Background: Mitochondrial dysfunction and degradation takes a central role in current paradigms of neurodegeneration in Parkinson's disease (PD). Loss of DJ-1... 
PINK1 | FUSION | GENE | MULTIDISCIPLINARY SCIENCES | ENERGETIC DEPRESSION | CYSTEINE-SULFINIC ACID | MUSCLE | DEGRADATION | MUTATIONS | PATHOLOGY | FISSION | Oncogene Proteins - genetics | Phosphorylation | Reactive Oxygen Species - metabolism | Humans | Intracellular Signaling Peptides and Proteins - metabolism | Autophagy | Fibroblasts - ultrastructure | Lysosomes - metabolism | Intracellular Signaling Peptides and Proteins - genetics | Fibroblasts - metabolism | Parkinson Disease - pathology | Oncogene Proteins - metabolism | Oxidative Phosphorylation | Mitochondria - metabolism | Parkinson Disease - genetics | Microscopy, Electron | Blotting, Western | Mice, Knockout | Peroxiredoxins | Lysosomes - ultrastructure | Protein Deglycase DJ-1 | Animals | Fibroblasts - cytology | Mice | Mutation | Mitogen-Activated Protein Kinase 1 - metabolism | Genes | Genetic aspects | Oxidative stress | Cell culture | Reactive oxygen species | Animal models | Parkinson's disease | Laboratories | Downstream effects | Parkinsons disease | Homeostasis | Lysosomes | Kinases | Accumulation | Degradation | Proteins | Mitochondria | Neurodegeneration | Penicillin | Fibroblasts | Aging | Physiology | Membrane potential | Movement disorders | Neurodegenerative diseases | Extracellular signal-regulated kinase | Organelles | PARK7 protein | Neurology | Brain research | Hypoxia | Electron transport | Respiration | Alzheimers disease | Phagocytosis | Apoptosis | Integrity
Journal Article
Nature Reviews Microbiology, ISSN 1740-1526, 12/2005, Volume 3, Issue 12, pp. 937 - 947
Journal Article