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The Journal of Cell Biology, ISSN 0021-9525, 9/2009, Volume 186, Issue 6, pp. 805 - 816
The dynamin-related guanosine triphosphatase Drp1 mediates the division of mitochondria and peroxisomes. To understand the in vivo function of Drp1, complete... 
Cerebellum | Mitochondria | Peroxisomes | Neurons | Antibodies | Cytochromes | Reports | Mice | Giant cells | Embryos | Apoptosis | OUTER-MEMBRANE | APOPTOSIS | DOMINANT OPTIC ATROPHY | FUSION | MITOCHONDRIAL FISSION MACHINERY | SYNAPSE FORMATION | CYTOCHROME-C RELEASE | PROTEIN DLP1 | DIVISION | CELL-DEATH | CELL BIOLOGY | Mitochondria - enzymology | Trophoblasts - ultrastructure | Fibroblasts - enzymology | Giant Cells - enzymology | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Trophoblasts - enzymology | Cerebellum - enzymology | Fibroblasts - ultrastructure | Mitochondria - ultrastructure | Purkinje Cells - enzymology | Cerebellum - embryology | Myocytes, Cardiac - enzymology | Adenosine Triphosphate - metabolism | Ultrasonography | Microtubule-Associated Proteins - deficiency | Purkinje Cells - diagnostic imaging | Mice, Inbred C57BL | Cells, Cultured | Dynamins | Gestational Age | Mice, Knockout | Organogenesis | Animals | GTP Phosphohydrolases - metabolism | GTP Phosphohydrolases - genetics | GTP Phosphohydrolases - deficiency | Peroxisomes - enzymology | Cerebellum - ultrastructure | Mitochondrial Size | Myocytes, Cardiac - ultrastructure | Organelle Shape | Peroxisomes - ultrastructure | Giant Cells - ultrastructure | Physiological aspects | Brain | Embryonic development | Research | Guanosine triphosphatase
Journal Article
Journal of Histochemistry and Cytochemistry, ISSN 0022-1554, 02/2006, Volume 54, Issue 2, pp. 191 - 199
Journal Article
The Plant Cell, ISSN 1040-4651, 8/2011, Volume 23, Issue 8, pp. 2895 - 2908
Postgerminative growth of seed plants requires specialized metabolism, such as gluconeogenesis, to support heterotrophic growth of seedlings until the... 
Hydrolysis | Cotyledons | Cell growth | Phenotypes | Germination | Alleles | Proton pump inhibitors | Plants | Seedlings | Plant cells | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | LEAF DEVELOPMENT | TRANSLOCATING INORGANIC PYROPHOSPHATASE | PLANT SCIENCES | CELL BIOLOGY | ORGAN SIZE | MUTANTS | CELL EXPANSION | ACID BETA-OXIDATION | THALIANA | GROWTH | PLANT VACUOLES | Darkness | Vacuoles - enzymology | Diphosphates - metabolism | Arabidopsis - enzymology | Arabidopsis - growth & development | Saccharomyces cerevisiae - genetics | Seedlings - genetics | Sucrose - pharmacology | Heterotrophic Processes | Inorganic Pyrophosphatase - metabolism | Seedlings - enzymology | Seedlings - growth & development | Arabidopsis Proteins - metabolism | Cytosol - enzymology | Plants, Genetically Modified | Gene Expression Regulation, Plant | Gluconeogenesis | Arabidopsis Proteins - genetics | Oxidation-Reduction | Hypocotyl - growth & development | Saccharomyces cerevisiae Proteins - genetics | Cotyledon - genetics | Peroxisomes - metabolism | Arabidopsis - genetics | Phenotype | Inorganic Pyrophosphatase - genetics | Cotyledon - enzymology | Saccharomyces cerevisiae Proteins - metabolism | Cotyledon - growth & development | Saccharomyces cerevisiae - enzymology | Vacuoles - metabolism | Cytosol - metabolism | Mutation | Hydrogen-Ion Concentration
Journal Article
The Plant Journal, ISSN 0960-7412, 08/2012, Volume 71, Issue 3, pp. 353 - 365
Summary The psychoactive and analgesic cannabinoids (e.g. Δ9‐tetrahydrocannabinol (THC)) in Cannabis sativa are formed from the short‐chain fatty acyl‐coenzyme... 
acyl‐CoA | acyl‐activating enzyme | Cannabis sativa | marijuana | hexanoate | cannabinoid | acyl-CoA | acyl-activating enzyme | POLYKETIDE SYNTHASE | ACID SYNTHASE | QUANTITATIVE-ANALYSIS | FUNCTIONAL GENOMICS | PLANT SCIENCES | COENZYME-A SYNTHETASE | ARABIDOPSIS CONTAINS | DICTYOSTELIUM-DISCOIDEUM | TARGETING SIGNALS | GLANDULAR TRICHOMES | JASMONIC ACID | Acyl Coenzyme A - biosynthesis | Coenzyme A Ligases - genetics | Molecular Sequence Data | Plant Roots - genetics | Flowers - chemistry | Phylogeny | Plant Stems - genetics | Cannabinoids - biosynthesis | Coenzyme A Ligases - metabolism | Cannabis - genetics | Cannabis - chemistry | Base Sequence | Plant Proteins - metabolism | Plant Stems - chemistry | Caproates - metabolism | Plant Leaves - enzymology | Cannabis - enzymology | Plant Leaves - chemistry | Amino Acid Sequence | Cytoplasm - enzymology | Gene Library | Flowers - enzymology | Transcriptome - genetics | Organ Specificity | Plant Stems - enzymology | Plant Proteins - genetics | Sequence Alignment | Plant Leaves - genetics | Plant Roots - chemistry | Plant Roots - enzymology | Kinetics | Peroxisomes - enzymology | Flowers - genetics | Unsaturated fatty acids | Cannabinoids | Analgesics | Ligases | Analysis | Physiological aspects | Esters | Marijuana | Flowers | Plant biology | Enzymes | Biosynthesis | Fatty acids
Journal Article
Antioxidants & Redox Signaling, ISSN 1523-0864, 01/2013, Volume 18, Issue 1, pp. 5 - 18
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2008, Volume 105, Issue 46, pp. 17712 - 17717
Refsum disease is caused by a deficiency of phytanoyl-CoA hydroxylase (PHYH), the first enzyme of the peroxisomal a-oxidation system, resulting in the... 
Cerebellum | Peroxisomes | Diet | Gait | Purkinje cells | Alleles | Central nervous system | Mice | Fatty acids | Refsum disease | Fatty acid oxidation | Metabolic disorder | PPAR-ALPHA | RAT | MULTIDISCIPLINARY SCIENCES | PRISTANIC ACID | ACTIVATED RECEPTOR-ALPHA | ASTROCYTES | GAS-CHROMATOGRAPHY | METABOLISM | CHAIN FATTY-ACIDS | metabolic disorder | peroxisomes | MICE | fatty acid oxidation | PHYTANIC ACID | Mixed Function Oxygenases - deficiency | Central Nervous System - abnormalities | Central Nervous System - pathology | Lipidoses - pathology | Male | Purkinje Cells - enzymology | Refsum Disease - enzymology | Behavior, Animal - drug effects | Peripheral Nervous System Diseases - pathology | Purkinje Cells - drug effects | Spermatogonia - pathology | Ataxia - pathology | Disease Models, Animal | Spermatogonia - drug effects | Ataxia - physiopathology | Gene Targeting | Automation | Refsum Disease - pathology | Peripheral Nervous System Diseases - enzymology | Lipidoses - enzymology | Gait - drug effects | Phenotype | Phytol - pharmacology | Animals | Ataxia - enzymology | Refsum Disease - physiopathology | Central Nervous System - drug effects | Spermatogonia - enzymology | Genetic Vectors | Mixed Function Oxygenases - genetics | Phytol - administration & dosage | Dietary Supplements | Purkinje Cells - pathology | Central Nervous System - enzymology | Phytanic Acid - blood | Ataxia | Models | Biological oxidation (Metabolism) | Research | Properties | Health aspects | Biological Sciences
Journal Article
The FEBS Journal, ISSN 1742-464X, 02/2014, Volume 281, Issue 3, pp. 708 - 723
Human d‐amino acid oxidase (EC 1.4.3.3; hDAAO) is a peroxisomal flavoenzyme significantly enriched in the mammalian brain. hDAAO has been proposed to play... 
degradation pathway | schizophrenia | regulation | neuromodulator | d‐serine | Schizophrenia | Regulation | D-serine | Neuromodulator | Degradation pathway | GENE G72 | NMDA RECEPTORS | UBIQUITIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLYCINE SITE | D-ASPARTATE RECEPTOR | RACEMASE | ASTROCYTES | PREFRONTAL CORTEX | PROTEASOME-DEPENDENT DEGRADATION | Mitochondria - enzymology | Humans | Brain - enzymology | Lysosomes - enzymology | Green Fluorescent Proteins - genetics | Endosomes - metabolism | Recombinant Fusion Proteins | Brain - metabolism | Cytosol - enzymology | Protease Inhibitors - pharmacology | Proteolysis - drug effects | Lysosomes - metabolism | Proteasome Endopeptidase Complex - drug effects | Ubiquitination - drug effects | Endosomes - drug effects | Neurons - metabolism | D-Amino-Acid Oxidase - metabolism | Neurons - drug effects | Lysosomes - drug effects | Green Fluorescent Proteins - metabolism | Bacterial Proteins - genetics | D-Amino-Acid Oxidase - genetics | Mitochondria - metabolism | Nerve Tissue Proteins - genetics | Peroxisomes - metabolism | Brain - drug effects | Nerve Tissue Proteins - metabolism | Carrier Proteins - genetics | Carrier Proteins - metabolism | Neurons - enzymology | Protein Stability - drug effects | Cell Line, Tumor | Bacterial Proteins - metabolism | Cytosol - metabolism | Luminescent Proteins - genetics | Endosomes - enzymology | Peroxisomes - enzymology | Luminescent Proteins - metabolism | Oxidases | Ubiquitin | Ammonium compounds | Brain | Gliomas | Ammonium paratungstate | Fluorescence | Amino acids | Glutamate | Biodegradation | Proteins | Enzymes | Metabolism | Molecular biology
Journal Article
Journal Article
Biochemical Society Transactions, ISSN 0300-5127, 2001, Volume 29, Issue 2, pp. 250 - 267
Peroxisomes are subcellular organelles with an indispensable role in cellular metabolism. The importance of peroxisomes for humans is stressed by the existence... 
Genetic diseases | Membrane transport | Peroxisomes
Journal Article