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Neuron, ISSN 0896-6273, 04/2013, Volume 78, Issue 1, pp. 57 - 64
Valosin-containing protein (VCP) is a highly expressed member of the type II AAA+ ATPase family. mutations are the cause of inclusion body myopathy, Paget’s... 
LIPID-PEROXIDATION | SPINAL-CORD PATHOLOGY | MOUSE MODEL | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | DYSFUNCTION | BONE | NEUROSCIENCES | PAGET-DISEASE | TRANSGENIC MICE | REVEALS | RNA, Small Interfering - genetics | Humans | Middle Aged | Male | Frontotemporal Dementia - metabolism | Neurons - ultrastructure | Muscular Dystrophies, Limb-Girdle - genetics | Adenosine Triphosphate - metabolism | Membrane Potential, Mitochondrial - genetics | Muscular Dystrophies, Limb-Girdle - pathology | NAD - metabolism | Fibroblasts - metabolism | Animals, Newborn | Frontotemporal Dementia - genetics | Magnesium - metabolism | Mitochondria - pathology | Fibroblasts - pathology | Mutation - genetics | Myositis, Inclusion Body - genetics | Osteitis Deformans - pathology | Muscular Dystrophies, Limb-Girdle - metabolism | Analysis of Variance | Luminescent Proteins - genetics | Adenosine Triphosphatases - genetics | Mice | Lipid Peroxidation - genetics | RNA, Small Interfering - metabolism | Valosin Containing Protein | Osteitis Deformans - metabolism | Family Health | Cerebral Cortex - cytology | Case-Control Studies | Osteitis Deformans - genetics | Transfection | Mitochondria - genetics | Cell Cycle Proteins - genetics | Myositis, Inclusion Body - pathology | Adult | Female | Neuroblastoma - pathology | Frontotemporal Dementia - pathology | Adenosine Triphosphatases - deficiency | Mice, Inbred C57BL | Cells, Cultured | Cell Cycle Proteins - deficiency | Mitochondria - metabolism | Animals | Oxygen Consumption - genetics | Myositis, Inclusion Body - metabolism | Aged | Nervous system diseases | Neurosciences | Genes | Amyotrophic lateral sclerosis | Genetic aspects | Adenosine triphosphatase | Dementia | Proteins | Medical research | Phosphorylation | Biomedical research | Disease | Rodents | Respiration | Experiments | Patients | Index Medicus | Report
Journal Article
Drug Metabolism and Disposition, ISSN 0090-9556, 07/2012, Volume 40, Issue 7, pp. 1366 - 1379
The transcription factors aryl hydrocarbon receptor (AhR), constitutive androstane receptor (CAR), pregnane X receptor (PXR), peroxisome proliferator-activated... 
TRANSCRIPTION FACTORS | PRIMARY HUMAN HEPATOCYTES | ANTIOXIDANT RESPONSE ELEMENT | MESSENGER-RNA EXPRESSION | CONSTITUTIVE ANDROSTANE RECEPTOR | BILIARY-EXCRETION | PROLIFERATOR-ACTIVATED RECEPTOR | MOUSE-LIVER | PHARMACOLOGY & PHARMACY | MICROSOMAL-ENZYME INDUCERS | PREGNANE-X-RECEPTOR | Inactivation, Metabolic | Receptors, Steroid - metabolism | Cytochrome P-450 Enzyme System - metabolism | Male | NAD(P)H Dehydrogenase (Quinone) - genetics | Organic Anion Transporters - metabolism | Glucuronosyltransferase - genetics | Organic Anion Transporters - genetics | Glutathione Transferase - genetics | Receptors, Aryl Hydrocarbon - metabolism | Female | NF-E2-Related Factor 2 - genetics | Sulfotransferases - metabolism | Aldehyde Dehydrogenase - metabolism | Sulfotransferases - genetics | Liver - metabolism | Mice, Inbred C57BL | RNA, Messenger - genetics | Receptors, Aryl Hydrocarbon - genetics | Glutathione Transferase - metabolism | Aldehyde Dehydrogenase - genetics | PPAR alpha - genetics | Receptors, Cytoplasmic and Nuclear - genetics | Transcription Factors - genetics | Mice, Knockout | Gene Expression Regulation, Enzymologic | Transcription Factors - metabolism | Animals | Glucuronosyltransferase - metabolism | Receptors, Steroid - genetics | NF-E2-Related Factor 2 - metabolism | Cytochrome P-450 Enzyme System - genetics | NAD(P)H Dehydrogenase (Quinone) - metabolism | Mice | PPAR alpha - metabolism | Multidrug Resistance-Associated Proteins | Receptors, Cytoplasmic and Nuclear - metabolism | Index Medicus
Journal Article
Genome Research, ISSN 1088-9051, 12/2012, Volume 22, Issue 12, pp. 2409 - 2417
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 03/2011, Volume 286, Issue 11, pp. 9856 - 9864
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 09/2013, Volume 288, Issue 36, pp. 25938 - 25949
NAD(+) is mainly synthesized in human cells via the "salvage" pathways starting from nicotinamide, nicotinic acid, or nicotinamide riboside (NR). The... 
NAMPT INHIBITION | IN-VITRO | CYCLIC-ADP-RIBOSE | CHS 828 | ENZYME | BIOCHEMISTRY & MOLECULAR BIOLOGY | GROWTH | NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE | CD38 | FK866 | LYMPHOCYTES | 5'-Nucleotidase - genetics | Gene Expression Regulation, Enzymologic - drug effects | Humans | Membrane Glycoproteins - biosynthesis | GPI-Linked Proteins - biosynthesis | Neoplasm Proteins - antagonists & inhibitors | Neoplasm Proteins - metabolism | Nicotinamide Phosphoribosyltransferase - antagonists & inhibitors | Neoplasms - genetics | Nicotinamide Phosphoribosyltransferase - metabolism | Piperidines - pharmacology | NAD - biosynthesis | Cell Death - drug effects | Gene Expression Regulation, Neoplastic - drug effects | Neoplasm Proteins - genetics | Acrylamides - pharmacology | Cytokines - genetics | Gene Expression Regulation, Neoplastic - genetics | 5'-Nucleotidase - biosynthesis | NAD - genetics | ADP-ribosyl Cyclase 1 - genetics | Cytokines - metabolism | Gene Silencing | Neoplasms - enzymology | Down-Regulation - drug effects | Down-Regulation - genetics | Membrane Glycoproteins - genetics | Neoplasms - drug therapy | Nicotinamide Phosphoribosyltransferase - genetics | Gene Expression Regulation, Enzymologic - genetics | ADP-ribosyl Cyclase 1 - biosynthesis | Cell Line, Tumor | Cytokines - antagonists & inhibitors | Nicotinamide Mononucleotide - biosynthesis | Nicotinamide Mononucleotide - genetics | GPI-Linked Proteins - genetics | NAD | Cancer Therapy | CD73 | Nicotinamide Riboside | NAD Biosynthesis | Signal Transduction | Cell Death | Nicotinamide Mononucleotide | Nicotinamide
Journal Article
Aging Cell, ISSN 1474-9718, 08/2017, Volume 16, Issue 4, pp. 837 - 846
Summary Kallistatin, an endogenous protein, protects against vascular injury by inhibiting oxidative stress and inflammation in hypertensive rats and enhancing... 
sirtuin 1 | kallistatin | vascular senescence | aging | microRNA‐34a | oxidative stress | microRNA-34a | NECROSIS-FACTOR-ALPHA | TISSUE KALLIKREIN INHIBITOR | BINDING PROTEIN | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | ORGAN INJURY | CAENORHABDITIS-ELEGANS | PROTECTIVE ROLE | PROGENITOR-CELL SENESCENCE | ENDOTHELIAL-CELLS | RENAL INJURY | Sirtuin 1 - metabolism | Diabetes Mellitus, Experimental - drug therapy | Endothelial Progenitor Cells - cytology | MicroRNAs - antagonists & inhibitors | Streptozocin | Humans | Diabetes Mellitus, Experimental - genetics | NADPH Oxidases - metabolism | Caenorhabditis elegans Proteins - metabolism | Cellular Senescence - drug effects | Male | MicroRNAs - metabolism | Sirtuin 1 - genetics | Telomerase - genetics | Plasminogen Activator Inhibitor 1 - metabolism | Superoxides - metabolism | beta-Galactosidase - metabolism | NADPH Oxidases - genetics | Telomerase - metabolism | Diabetes Mellitus, Experimental - chemically induced | Superoxides - antagonists & inhibitors | Nitric Oxide Synthase Type III - metabolism | Plasminogen Activator Inhibitor 1 - genetics | Diabetes Mellitus, Experimental - metabolism | Sirtuins - genetics | Endothelial Progenitor Cells - metabolism | Cellular Senescence - genetics | Caenorhabditis elegans - metabolism | Caenorhabditis elegans - genetics | Catalase - genetics | Endothelial Progenitor Cells - drug effects | Cells, Cultured | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Nitric Oxide Synthase Type III - genetics | Serpins - pharmacology | Catalase - metabolism | Tumor Necrosis Factor-alpha - pharmacology | Animals | Caenorhabditis elegans - drug effects | Genistein - pharmacology | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Mice | MicroRNAs - genetics | beta-Galactosidase - genetics | Caenorhabditis elegans Proteins - genetics | Sirtuins - metabolism | Tumor Necrosis Factor-alpha - antagonists & inhibitors | Gene expression | MicroRNA | Oxidative stress | Senescence | Genistein | INK4a protein | Kinases | NAD(P)H oxidase | Catalase | Rodents | Aging | Aorta | Telomerase | Protein-tyrosine kinase | Tyrosine | Enzymes | Diabetes mellitus | p16 Protein | MiRNA | Superoxide | SIRT1 protein | Life span | Tumor necrosis factor | MicroRNAs | Stem cells | Nematodes | Diabetes | Original
Journal Article
Journal Article
Nature Cell Biology, ISSN 1465-7392, 2014, Volume 16, Issue 4, pp. 357 - 366
The YAP and TAZ mediators of the Hippo pathway ( hereafter called YAP/TAZ) promote tissue proliferation and organ growth. However, how their biological... 
ORGAN GROWTH | CHOLESTEROL | YAP/TAZ | TRANSCRIPTION | HIPPO PATHWAY | STATINS | CELL BIOLOGY | Phosphorylation - physiology | Cell Proliferation | Active Transport, Cell Nucleus - physiology | Humans | Intracellular Signaling Peptides and Proteins - metabolism | Drosophila Proteins - metabolism | Phosphoproteins - metabolism | Sterol Regulatory Element Binding Proteins - genetics | Breast Neoplasms - metabolism | Drosophila melanogaster - metabolism | RNA Interference | Tumor Suppressor Proteins - genetics | HEK293 Cells | Trans-Activators - genetics | Female | Transcription, Genetic | Hydroxymethylglutaryl-CoA Reductases, NAD-Dependent - metabolism | Nuclear Proteins - genetics | Protein-Serine-Threonine Kinases - metabolism | Signal Transduction | HCT116 Cells | Protein-Serine-Threonine Kinases - genetics | Nuclear Proteins - metabolism | Sterol Regulatory Element Binding Proteins - metabolism | Transcription Factors - genetics | Mevalonic Acid - metabolism | Polyisoprenyl Phosphates - metabolism | Transcription Factors - metabolism | Animals | Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology | rho GTP-Binding Proteins - metabolism | Trans-Activators - metabolism | Mice | Polyisoprenyl Phosphates - biosynthesis | Pyridines - pharmacology | RNA, Small Interfering | Drosophila Proteins - genetics | Adaptor Proteins, Signal Transducing - metabolism | Cell metabolism | Genetic research | Genetic aspects | Research | Cellular control mechanisms
Journal Article
CELL, ISSN 0092-8674, 08/2002, Volume 110, Issue 3, pp. 361 - 371
During photosynthesis, plants must control the utilization of light energy in order to avoid photoinhibition. We isolated an Arabidopsis mutant, pgr5 (proton... 
CHLOROPHYLL-FLUORESCENCE | PHOTOACOUSTIC MEASUREMENTS | TRANSPORT | BIOCHEMISTRY & MOLECULAR BIOLOGY | NAD(P)H DEHYDROGENASE | LEAVES | CHLOROPLASTS | ENERGY-STORAGE | NDHB GENE | NADH-DEHYDROGENASE | TOBACCO | CELL BIOLOGY | Chlorophyll - radiation effects | Photosynthetic Reaction Center Complex Proteins - metabolism | Photosystem II Protein Complex | Electron Transport - radiation effects | Electron Transport - genetics | Oxidation-Reduction - radiation effects | Molecular Sequence Data | Cell Respiration - radiation effects | Amino Acid Sequence - genetics | Chlorophyll - genetics | Oxygen - metabolism | Photic Stimulation - adverse effects | Cell Respiration - genetics | Photosynthesis - genetics | Photosynthetic Reaction Center Complex Proteins - genetics | Photosynthetic Reaction Center Complex Proteins - radiation effects | Thylakoids - genetics | Light-Harvesting Protein Complexes | NADP - metabolism | Photosynthesis - radiation effects | Arabidopsis Proteins - genetics | Base Sequence - genetics | Gene Expression Regulation, Plant - radiation effects | Carbon Dioxide - metabolism | NADP - radiation effects | Mutation - radiation effects | Arabidopsis - cytology | Light - adverse effects | Chlorophyll - metabolism | Mutation - genetics | Thylakoids - radiation effects | Thylakoids - metabolism | Arabidopsis - metabolism | Arabidopsis Proteins - radiation effects | Macromolecular Substances | Photosystem I Protein Complex | Arabidopsis - genetics | Arabidopsis Proteins - isolation & purification | Gene Expression Regulation, Plant - physiology | NADP - genetics | Photosynthetic Reaction Center Complex Proteins - isolation & purification | Cell research | Gene mutations | Arabidopsis | Analysis | Photosynthesis research | Physiological aspects | Genetic aspects | Hydrogen-ion concentration | Cells
Journal Article
Journal of Biotechnology, ISSN 0168-1656, 04/2012, Volume 158, Issue 4, pp. 184 - 191
► Cofactor-imbalance is a problem in xylose metabolism by recombinant ► NADH-preferable XR, NAD-dependent XDH and XK were overexpressed in Balanced expression... 
Xylose | NADH-preferable xylose reductase | Ethanol | Saccharomyces cerevisiae | STRAINS | XYLITOL DEHYDROGENASE | CONVERSION | PICHIA-STIPITIS | XYLULOKINASE ACTIVITY | PATHWAY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GLUCOSE | GROWTH | FERMENTATION | IMPROVEMENT | Aldehyde Reductase - genetics | D-Xylulose Reductase - genetics | Saccharomyces cerevisiae - genetics | Saccharomyces cerevisiae Proteins - biosynthesis | D-Xylulose Reductase - metabolism | Pichia - enzymology | Xylose - genetics | Saccharomyces cerevisiae - metabolism | Pichia - metabolism | Recombination, Genetic | Aldehyde Reductase - metabolism | Genes, Fungal | NADP - metabolism | NAD - metabolism | Transaldolase - genetics | Gene Expression | Metabolic Engineering - methods | NAD - genetics | Xylose - metabolism | Aerobiosis | Ethanol - metabolism | Phosphotransferases (Alcohol Group Acceptor) - genetics | Aldehyde Oxidoreductases - genetics | Saccharomyces cerevisiae Proteins - genetics | Fermentation | Mutation - genetics | Transaldolase - metabolism | Aldehyde Oxidoreductases - metabolism | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Xylitol - genetics | D-Xylulose Reductase - biosynthesis | Pichia - genetics | Saccharomyces cerevisiae Proteins - metabolism | Saccharomyces cerevisiae - enzymology | Xylitol - metabolism | NADP - genetics | Enzymes | Xylitol | Alcohol, Denatured | Alcohol | Sugars | Production data | Monosaccharides
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2006, Volume 78, Issue 1, pp. 15 - 27
An efficient testing strategy called the “focused interaction testing framework” (FITF) was developed to identify susceptibility genes involved in epistatic... 
S-TRANSFERASE M1 | BREAST-CANCER | MULTIFACTOR-DIMENSIONALITY REDUCTION | OXIDATIVE STRESS | POLYMORPHISMS | DISEASE | COMPLEXITY | GENETICS & HEREDITY | RECEPTOR | HYPERTENSION | GENOTYPE-PHENOTYPE ASSOCIATIONS | Gene expression | Research | Genetic epistasis
Journal Article
PLoS Genetics, ISSN 1553-7390, 10/2013, Volume 9, Issue 10, p. e1003871