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1. Full Text Cardiomyocyte microvesicles contain DNA/RNA and convey biological messages to target cells
by Waldenström, Anders and Gennebäck, Nina and Hellman, Urban and Ronquist, Gunnar and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Kardiologi and Umeå universitet
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
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2. Full Text From the regulation of peptidoglycan synthesis to bacterial growth and morphology
by Typas, Athanasios and Banzhaf, Manuel and Gross, Carol A and Vollmer, Waldemar
Nature Reviews Microbiology, ISSN 1740-1526, 02/2012, Volume 10, Issue 2, pp. 123 - 136
How bacteria grow and divide while retaining a defined shape is a fundamental question in microbiology, but technological advances are now driving a new... 
D-AMINO ACIDS | ATOMIC-FORCE MICROSCOPY | ESCHERICHIA-COLI-CELLS | GRAM-NEGATIVE BACTERIA | DIVISION PROTEIN FTSN | BACILLUS-SUBTILIS | DAUGHTER CELL-SEPARATION | CAULOBACTER-CRESCENTUS | PENICILLIN-BINDING PROTEINS | TOL-PAL COMPLEX | MICROBIOLOGY | Amidohydrolases - metabolism | Endopeptidases - metabolism | Bacteria - metabolism | Escherichia coli Proteins - metabolism | Gram-Negative Bacteria - metabolism | Hydrolysis | N-Acetylmuramoyl-L-alanine Amidase - metabolism | Peptidoglycan - biosynthesis | Bacteria - growth & development | Bacterial Outer Membrane Proteins - metabolism | Cell Wall - metabolism | Escherichia coli - metabolism | Gram-Negative Bacteria - growth & development | Cytoskeleton - metabolism | Bacterial Proteins - metabolism | Cytoskeletal Proteins - metabolism | Escherichia coli - growth & development | Gene Expression Regulation, Bacterial | Enzymes | Bacterial growth | Peptidoglycans | Physiological aspects | Bacteria | Hydrolases | Research
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3. Full Text Regulation of fungal secondary metabolism
by Brakhage, Axel A
Nature Reviews Microbiology, ISSN 1740-1526, 01/2013, Volume 11, Issue 1, pp. 21 - 32
Fungi produce a multitude of low-molecular-mass compounds known as secondary metabolites, which have roles in a range of cellular processes such as... 
NATURAL-PRODUCT | NONRIBOSOMAL PEPTIDE SYNTHETASE | CCAAT-BINDING COMPLEX | ACREMONIUM-CHRYSOGENUM | PENICILLIN BIOSYNTHESIS GENE | ASPERGILLUS-NIDULANS | AFLATOXIN PATHWAY | FINGER TRANSCRIPTION FACTOR | MICROBIOLOGY | BETA-LACTAM BIOSYNTHESIS | FILAMENTOUS FUNGI | Gene Expression Regulation, Fungal | Metabolic Networks and Pathways - genetics | Multigene Family | Biological Products - metabolism | Genes, Fungal | Transcription, Genetic | Fungi - metabolism | Fungi - genetics | Fungi | Physiological aspects | Genetic aspects
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4. Full Text Reduced UCP-1 content in in vitro differentiated beige/ brite adipocytes derived from preadipocytes of human subcutaneous white adipose tissues in obesity
by Carey, Andrew L and Vorlander, Camilla and Reddy-Luthmoodoo, Medini and Natoli, Alaina K and Formosa, Melissa F and Bertovic, David A and Anderson, Mitchell J and Duffy, Stephen J and Kingwell, Bronwyn A
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
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5. Full Text Multiple Human Isoforms of Drug Transporters Contribute to the Hepatic and Renal Transport of Olmesartan, a Selective Antagonist of the Angiotensin II AT1-Receptor
by Akihiro Yamada and Kazuya Maeda and Emi Kamiyama and Daisuke Sugiyama and Tsunenori Kondo and Yoshiyuki Shiroyanagi and Hayakazu Nakazawa and Teruo Okano and Masashi Adachi and John D. Schuetz and Yasuhisa Adachi and Zhuohan Hu and Hiroyuki Kusuhara and Yuichi Sugiyama
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
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6. Full Text Reduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1
by Krebiehl, Guido and Ruckerbauer, Sabine and Burbulla, Lena F and Kieper, Nicole and Maurer, Brigitte and Waak, Jens and Wolburg, Hartwig and Gizatullina, Zemfira and Gellerich, Frank N and Woitalla, Dirk and Riess, Olaf and Kahle, Philipp J and Proikas-Cezanne, Tassula and Krüger, Rejko
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
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7. Full Text Fungal secondary metabolism - from biochemistry to genomics
by Turner, Geoffrey and Bennett, Joan W and Keller, Nancy P
Nature Reviews Microbiology, ISSN 1740-1526, 12/2005, Volume 3, Issue 12, pp. 937 - 947
Much of natural product chemistry concerns a group of compounds known as secondary metabolites. These low-molecular-weight metabolites often have potent... 
ASPERGILLUS-PARASITICUS DEFICIENT | BIOSYNTHETIC GENE-CLUSTER | AFLATOXIN BIOSYNTHESIS | MICROBIOLOGY | TRANSCRIPTION FACTOR | REGULATORY GENE | GIBBERELLA-FUJIKUROI | FILAMENTOUS FUNGI | PEPTIDE SYNTHETASE | FUSARIUM-SPOROTRICHIOIDES | PLANT-PATHOGENIC FUNGUS | Aflatoxins - metabolism | Penicillins - biosynthesis | Molecular Weight | Terpenes - metabolism | Genome, Fungal | Ergot Alkaloids - metabolism | Epigenesis, Genetic | Genomics | Genes, Fungal | Macrolides - metabolism | Fungi - metabolism
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8. Full Text Metabolism shapes the cell
by Sperber, Anthony M and Herman, Jennifer K
Journal of Bacteriology, ISSN 0021-9193, 06/2017, Volume 199, Issue 11
More than 5 decades of work support the idea that cell envelope synthesis, including the inward growth of cell division, is tightly coordinated with DNA... 
FtsZ | MreB | UDP-glucose | Cell division | Metabolism | Morphogenesis, peptidoglycan, phosphoenolpyruvate, undecaprenyl phosphate | Gluconeogenesis | CAULOBACTER-CRESCENTUS | PENICILLIN-BINDING PROTEIN-2 | ESCHERICHIA-COLI | cell division | MICROBIOLOGY | gluconeogenesis | UNDECAPRENYL-PHOSPHATE | undecaprenyl phosphate | INTERACTION NETWORK | peptidoglycan | morphogenesis | phosphoenolpyruvate | BACILLUS-SUBTILIS | MORPHOLOGICAL DEFECTS | MEMBRANE-BOUND GLUCOSYLTRANSFERASE | GENE-EXPRESSION | metabolism | STAPHYLOCOCCUS-AUREUS | Bacteria - growth & development | Bacteria - metabolism | Cell Division | Bacterial Proteins - genetics | Bacterial Proteins - metabolism | Gene Expression Regulation, Bacterial | Bacteria - genetics | Morphogenesis | Research
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