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2017, Methods in molecular biology, ISBN 9178149396937, Volume 1595.
Web Resource
2013, Sub-cellular biochemistry, ISBN 9789400768895, Volume 69
Web Resource
PPAR research, ISSN 1687-4757, 2006
Journal
04/2017, Methods in Molecular Biology Ser., ISBN 1493969358, Volume 1595
Annotation This volume provides easily accessible and comprehensive collection of methods, techniques, and strategies to investigate the molecular and cellular... 
Peroxisomes | Science
Web Resource
Chest, ISSN 0012-3692, 07/2016, Volume 150, Issue 1, pp. 91 - 101
Background OSA is a highly prevalent condition that is associated with a wide range of long-term morbidities including metabolic, cardiovascular, and cognitive... 
DNA methylation | peroxisome proliferation-activated receptor γ | monocytes | OSA | positive air pressure | OBSTRUCTIVE SLEEP-APNEA | OXIDATIVE STRESS | ACTIVATION | RESISTANT HYPERTENSION | OLDER-ADULTS | MACROPHAGES | peroxisome proliferation-activated receptor gamma | WHITE ADIPOSE-TISSUE | RESPIRATORY SYSTEM | INSULIN-RESISTANCE | INFLAMMATION | GENE-EXPRESSION | CRITICAL CARE MEDICINE | Peroxisome Proliferator-Activated Receptors - genetics | Epigenesis, Genetic | Humans | Middle Aged | Obesity Hypoventilation Syndrome - metabolism | Gene Expression Profiling - methods | Male | Monocytes - metabolism | Treatment Outcome | Statistics as Topic | Continuous Positive Airway Pressure - methods | DNA Methylation | Obesity Hypoventilation Syndrome - therapy | Peroxisome Proliferator-Activated Receptors - metabolism | Adult | Female | Overweight persons | Care and treatment | Usage | Obesity hypoventilation syndrome | DNA | Research | Methylation | Index Medicus | Abridged Index Medicus | HTN, hypertension | OHS, obesity hypoventilation syndrome | peroxisome proliferation-activated receptor γ | PPARG, peroxisome proliferation-activated receptor γ | PPARE, peroxisome proliferation-activated receptor-responsive element | MeDIP, methylated DNA immunoprecipitation | AHI, apnea-hypopnea index | DMR, differentially methylated region | Sleep Disorder | PAP, positive airway pressure | PPAR, peroxisome proliferation-activated receptor
Journal Article
Lipids, ISSN 0024-4201, 10/2016, Volume 51, Issue 10, pp. 1127 - 1136
Leucine modulates synthetic and degradative pathways in muscle, possibly providing metabolic benefits for both athletes and diseased populations. Leucine has... 
Life Sciences | Neurochemistry | Medicinal Chemistry | PPARα (peroxisome proliferator-activated receptor alpha) | PPARβ/δ (peroxisome proliferator-activated receptor beta/delta) | Lipidology | Nutrition | Microbial Genetics and Genomics | Lipid oxidation | Medical Biochemistry | PPARγ (peroxisome proliferator-activated receptor gamma) | Fatty acid synthesis | PPARα (peroxisome proliferator‐activated receptor alpha) | PPARβ/δ (peroxisome proliferator‐activated receptor beta/delta) | PPARγ (peroxisome proliferator‐activated receptor gamma) | MAMMALIAN TARGET | RAPAMYCIN | PATHWAYS | PPAR gamma (peroxisome proliferator-activated receptor gamma) | BIOCHEMISTRY & MOLECULAR BIOLOGY | PPAR beta/delta (peroxisome proliferator-activated receptor beta/delta) | SUPPLEMENTATION | METHYLBUTYRATE HMB | NUTRITION & DIETETICS | INHIBITION | SKELETAL-MUSCLE CELLS | PPAR alpha (peroxisome proliferator-activated receptor alpha) | LEUCINE | EXPRESSION | C2C12 CELLS | Cell Line | Cell Survival - drug effects | PPAR-beta - metabolism | PPAR alpha - genetics | Mitochondria - metabolism | Mitochondria - drug effects | Muscle Fibers, Skeletal - drug effects | Muscle Fibers, Skeletal - metabolism | PPAR-beta - genetics | Valerates - pharmacology | Oxygen - metabolism | Gene Expression Regulation - drug effects | Organelle Biogenesis | Animals | Lipid Metabolism - drug effects | Glucose - metabolism | Muscle Fibers, Skeletal - cytology | Mice | Lipids - analysis | PPAR alpha - metabolism | PPAR delta - metabolism | PPAR delta - genetics | Index Medicus
Journal Article
Reproductive Toxicology, ISSN 0890-6238, 07/2012, Volume 33, Issue 4, pp. 491 - 505
► Perfluorooctanoic acid (PFOA) exposure induces neonatal mortality and growth deficits in mice. ► PFOA activates peroxisome proliferator-activated... 
Peroxisome proliferator activated receptor-beta (PPARβ) | Developmental toxicity | Perfluorooctanoic acid (PFOA) | Peroxisome proliferator activated receptor-alpha (PPARα) | Peroxisome proliferator activated receptor-gamma (PPARγ) | RAT-LIVER | GAMMA | PERFLUOROALKYL ACIDS | Peroxisome proliferator activated receptor-beta (PPAR beta) | MECHANISMS | PREGNANCY | TARGET GENES | REPRODUCTIVE BIOLOGY | Peroxisome proliferator activated receptor-alpha (PPAR alpha) | ALPHA EXPRESSION | Peroxisome proliferator activated receptor-gamma (PPAR gamma) | MICE | TOXICOLOGY | EXPOSURE | Fluorocarbons - toxicity | Environmental Pollutants - pharmacokinetics | Male | Caprylates - pharmacokinetics | Environmental Pollutants - blood | Fluorocarbons - blood | Aging - genetics | Female | Fetal Development - genetics | Environmental Pollutants - toxicity | Real-Time Polymerase Chain Reaction | Animals, Newborn | Peroxisome Proliferator-Activated Receptors - genetics | Caprylates - toxicity | Fetal Development - drug effects | Gene Expression Regulation, Developmental - drug effects | Fluorocarbons - pharmacokinetics | Mice, Inbred Strains | Organ Specificity | Gestational Age | Blotting, Western | Prenatal Exposure Delayed Effects - metabolism | Pregnancy | Prenatal Exposure Delayed Effects - genetics | Animals | Mice | Caprylates - blood | Prenatal Exposure Delayed Effects - chemically induced | Aging - metabolism | Pregnant women | Genes | Patient outcomes | Physiological aspects | Genetic research | Infants | Glucose | Ammonium perfluorooctanoate | Dextrose | Index Medicus | Heart | Spleen | Neonates | Stomach | RNA | Toxicity | Fetuses | Liver | Lung | Mortality | Lipids | perfluorooctanoic acid | Gene expression | Metabolism | Survival | Kidney | Western blotting | Thymus | Contaminants | Intestine | Peroxisome proliferator-activated receptors | Age
Journal Article
European Journal of Pharmacology, ISSN 0014-2999, 01/2015, Volume 746, pp. 56 - 62
Curcumin exerts an inhibitory effect on hepatic stellate cell (HSC) activation, a key step for liver fibrogenesis, and on liver fibrosis by up-regulation of... 
Curcumin (PubChem CID: 969516) | Curcumin | Hepatic stellate cell | Peroxisome proliferator-activated receptor-γ coactivator-1α | Adenosine monophosphate-activated protein kinase | Peroxisome proliferator-activated receptor-γ | Curcumin Peroxisome proliferator-activated receptor-γ | kinase | Adenosine monophosphate-activated protein | FIBROSIS | OXIDATIVE STRESS | SIGNALING PATHWAYS | PGC-1-ALPHA | ALPHA | Peroxisome proliferator-activated receptor-gamma | COLLAGEN-SYNTHESIS | GENE-EXPRESSION | PPAR-GAMMA | PHARMACOLOGY & PHARMACY | MICE | Peroxisome proliferator-activated receptor-gamma coactiyator-1 alpha | INHIBIT | Transcription, Genetic - drug effects | AMP-Activated Protein Kinases - metabolism | Superoxide Dismutase - genetics | RNA, Messenger - genetics | Transcriptional Activation - drug effects | Curcumin - pharmacology | Hepatic Stellate Cells - enzymology | Hepatic Stellate Cells - metabolism | Rats | Transcription Factors - genetics | Enzyme Activation - drug effects | RNA, Messenger - metabolism | Hepatic Stellate Cells - cytology | Orphan Nuclear Receptors - genetics | Rats, Sprague-Dawley | Gene Expression Regulation - drug effects | Up-Regulation - drug effects | Animals | Collagen Type I - genetics | Signal Transduction - drug effects | Liver X Receptors | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Hepatic Stellate Cells - drug effects | Index Medicus
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 09/2016, Volume 214, Issue 6, pp. 677 - 690
Peroxisomes are metabolic organelles necessary for anabolic and catabolic lipid reactions whose numbers are highly dynamic based on the metabolic need of the... 
MAMMALIAN PEROXISOMES | RAT-LIVER PEROXISOMES | IMPORT | AUTOPHAGIC DEGRADATION | MITOCHONDRIA | SIGNALS | RECEPTOR | MEMBRANE POLYPEPTIDES | PROTEIN-ENERGY MALNUTRITION | SELECTIVE AUTOPHAGY | CELL BIOLOGY | TOR Serine-Threonine Kinases - metabolism | Humans | Male | Autophagy - drug effects | Mechanistic Target of Rapamycin Complex 1 | Peroxisomes - drug effects | Protein-Energy Malnutrition - enzymology | TOR Serine-Threonine Kinases - antagonists & inhibitors | Multiprotein Complexes - metabolism | Peroxisomal Biogenesis Factor 2 | Ubiquitination | Transfection | RNA Interference | Time Factors | Proteolysis | HEK293 Cells | ATP-Binding Cassette Transporters - metabolism | Membrane Proteins - metabolism | Disease Models, Animal | Peroxisomes - pathology | Protein-Energy Malnutrition - pathology | Signal Transduction | Membrane Proteins - genetics | Mice, Inbred C57BL | Protein-Energy Malnutrition - genetics | Rats | Amino Acids - deficiency | Sirolimus - pharmacology | Animals | Proteins - metabolism | Peroxisome-Targeting Signal 1 Receptor | HeLa Cells | Peroxisomes - enzymology | Receptors, Cytoplasmic and Nuclear - metabolism | Ubiquitin | Ligases | Cells | Membrane proteins | Physiological aspects | Autophagy (Cytology) | Observations | Proteins | Enzymes | Lipids | Amino acids | Cellular biology | Mammals | Index Medicus
Journal Article
Traffic, ISSN 1398-9219, 01/2012, Volume 13, Issue 1, pp. 168 - 183
During biogenesis of the peroxisome, a subcellular organelle, the peroxisomal‐targeting signal 1 (PTS1) receptor Pex5 functions as a shuttling receptor for... 
AWP1 zinc‐finger protein | peroxisome‐cytoplasmic recycling | peroxin | ubiquitination | ATPase cycle | Pex5 | peroxisome‐targeting signal 1 receptor | peroxisome biogenesis | protein import | AAA ATPase | Peroxisome-targeting signal 1 receptor | Ubiquitination | AWP1 zinc-finger protein | Peroxisome-cytoplasmic recycling | Protein import | Peroxin | Peroxisome biogenesis | MAMMALIAN-CELL MUTANT | IN-VITRO IMPORT | CYCLING RECEPTOR | MATRIX PROTEIN IMPORT | MEMBRANE-PROTEIN | PTS2 RECEPTOR PEX7P | SACCHAROMYCES-CEREVISIAE | ZINC-FINGER DOMAIN | CELL BIOLOGY | peroxisome-cytoplasmic recycling | peroxisome-targeting signal 1 receptor | PEROXISOME-TARGETING SIGNAL | NF-KAPPA-B | Cell Fractionation | Immunoprecipitation | Cricetulus | Humans | Molecular Sequence Data | Transfection | Base Sequence | Protein Stability | CHO Cells | Amino Acid Sequence | ATPases Associated with Diverse Cellular Activities | Cricetinae | Zinc Fingers | Electrophoresis, Polyacrylamide Gel | Liver - metabolism | Adenosine Triphosphatases - metabolism | Rats | Receptors, Cytoplasmic and Nuclear - genetics | Peroxisomes - metabolism | Protein Transport | Animals | Models, Biological | Peroxisome-Targeting Signal 1 Receptor | Adaptor Proteins, Signal Transducing - genetics | Cytosol - metabolism | Adenosine Triphosphatases - genetics | Liver - cytology | Mice | HeLa Cells | Adaptor Proteins, Signal Transducing - metabolism | Microscopy, Fluorescence | Receptors, Cytoplasmic and Nuclear - metabolism | Proteins | Biosynthesis | Universities and colleges | RNA | Adenosine triphosphatase | Index Medicus
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 04/2016, Volume 93, pp. 177 - 189
Diurnal oscillations in the expression of antioxidant genes imply that protection against oxidative stress is circadian-gated. We hypothesized that... 
Oxidative stress | Mitochondria | Energy metabolism | Bioenergetics | Peroxisome proliferator‐activated receptor gamma coactivator 1‐alpha (PGC‐1α)(PPARGC1A) | NR1D1 | Circadian | Preconditioning | Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α)(PPARGC1A) | LIFE-SPAN | MITOCHONDRIAL BIOGENESIS | REDOX HOMEOSTASIS | AUTOPHAGY RHYTHM | BIOCHEMISTRY & MOLECULAR BIOLOGY | Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1 alpha) (PPARGC1A) | SKELETAL-MUSCLE | SHIFT WORK | IN-VIVO | ENDOCRINOLOGY & METABOLISM | NEONATAL MICE | NURSES HEALTH | CLOCK | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics | Heme Oxygenase-1 - biosynthesis | Nuclear Receptor Subfamily 1, Group D, Member 1 - genetics | Superoxide Dismutase - biosynthesis | Antioxidants - metabolism | Oxidative Stress - genetics | Mice, Transgenic | Mitochondria - metabolism | Hydrogen Peroxide - metabolism | Animals | Mitochondria - genetics | Mice | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - biosynthesis | Catalase - biosynthesis | Energy Metabolism - genetics | Nuclear Receptor Subfamily 1, Group D, Member 1 - metabolism | Fibroblasts - metabolism | Index Medicus | circadian | bioenergetics | mitochondria | Peroxisome proliferator- activated receptor gamma coactivator 1- alpha (PGC- 1α)(PPARGC1A) | oxidative stress | energy metabolism | preconditioning
Journal Article
Traffic, ISSN 1398-9219, 08/2011, Volume 12, Issue 8, pp. 1067 - 1083
Pex5p is the cytosolic receptor for peroxisome matrix proteins with peroxisome‐targeting signal (PTS) type 1 and shuttles between the cytosol and peroxisomes.... 
dominant‐negative mutant | peroxisome‐targeting signal | peroxin | ubiquitination | PTS1 receptor | Pex5p | CHO cell mutant | peroxisome biogenesis | protein import | Peroxisome-targeting signal | Ubiquitination | Dominant-negative mutant | Protein import | Peroxin | Peroxisome biogenesis | FUNCTIONAL COMPLEMENTATION | BIOGENESIS DISORDERS | ANIMAL-CELL MUTANTS | CYCLING RECEPTOR | MATRIX PROTEIN IMPORT | peroxisome-targeting signal | TYPE-1 RECEPTOR | RHIZOMELIC CHONDRODYSPLASIA PUNCTATA | CELL BIOLOGY | CONSERVED CYSTEINE | dominant-negative mutant | ZELLWEGER-SYNDROME | Cricetulus | Humans | Cysteine - genetics | Cysteine - metabolism | Membrane Proteins - metabolism | Tumor Cells, Cultured | Ubiquitination - physiology | Repressor Proteins - metabolism | CHO Cells | Dithiothreitol - pharmacology | Protein Structure, Tertiary | Peroxisomes - genetics | Cricetinae | Peroxisomal Targeting Signal 2 Receptor | Membrane Proteins - genetics | Cells, Cultured | Rats | Receptors, Cytoplasmic and Nuclear - genetics | Peroxisomes - metabolism | Amino Acid Motifs | Protein Transport | Animals | Peroxisome-Targeting Signal 1 Receptor | Protein Binding | Cytosol - metabolism | HeLa Cells | Mutation | Receptors, Cytoplasmic and Nuclear - metabolism | Ubiquitin | Cysteine | Thiols | Recycling (Waste, etc.) | Biosynthesis | Universities and colleges | Cystine | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 03/2015, Volume 112, Issue 13, pp. 4158 - 4163
Lipid droplets/oil bodies (OBs) are lipid-storage organelles that play a crucial role as an energy resource in a variety of eukaryotic cells. Lipid stores are... 
Peroxisome | Oil bodies | SDP1 lipase | Retromer | Protein trafficking | STORAGE | MUTANT | COMPLEX | protein trafficking | MOBILIZATION | MULTIDISCIPLINARY SCIENCES | TRAFFICKING | peroxisome | retromer | THALIANA | SEED | PURIFICATION | oil bodies | <