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Pediatrics in Review, ISSN 0191-9601, 01/2016, Volume 37, Issue 1, pp. 3 - 17
Journal Article
Journal Article
Developmental Biology, ISSN 0012-1606, 11/2014, Volume 395, Issue 1, pp. 84 - 95
Peroxisome biogenesis disorders (PBD) are autosomal recessive disorders in humans characterized by skeletal, eye and brain abnormalities. Despite the fact that... 
Peroxisome | Synapse formation | Neuromuscular junction | Acetylcholine receptor | Axon integrity | MYELINATION | DEVELOPMENTAL BIOLOGY | TANDEM MASS-SPECTROMETRY | X-LINKED ADRENOLEUKODYSTROPHY | GLIAL-CELLS | OLIGODENDROCYTES | IMPORT | AXONAL LOSS | GENE | ZELLWEGER-SYNDROME | SCHWANN-CELLS | Immunohistochemistry | Humans | Molecular Sequence Data | Male | Muscle, Skeletal - innervation | Mice, 129 Strain | Motor Endplate - physiology | Sciatic Nerve - embryology | Embryo, Mammalian - metabolism | Sciatic Nerve - metabolism | Spinal Cord Diseases - metabolism | Peroxins | Muscle, Skeletal - embryology | Peripheral Nervous System Diseases - genetics | Embryo, Mammalian - ultrastructure | Disease Models, Animal | Amino Acid Sequence | Microscopy, Electron, Transmission | Peripheral Nervous System Diseases - embryology | Mice, Inbred C57BL | Cells, Cultured | Peroxisomal Disorders - metabolism | Receptors, Cytoplasmic and Nuclear - genetics | Peroxisomal Disorders - embryology | Peroxisomes - metabolism | Mice, Knockout | Spinal Cord Diseases - genetics | Action Potentials - physiology | Peripheral Nervous System Diseases - metabolism | Sequence Homology, Amino Acid | Microscopy, Confocal | Motor Activity - genetics | Animals | Embryo, Mammalian - cytology | Peroxisomal Disorders - genetics | Spinal Cord Diseases - embryology | Peroxisomes - ultrastructure | Receptors, Cytoplasmic and Nuclear - metabolism | Proteins | Nervous system diseases | Growth | Analysis | Fetus | Biosynthesis | Cells | Medical colleges | Stem cells | Index Medicus | peroxisome | neuromuscular junction | axon integrity | synapse formation
Journal Article
Journal Article
Journal Article
Journal of Cell Science, ISSN 0021-9533, 02/2012, Volume 125, Issue 3, pp. 589 - 602
Peroxisome division is regulated by several factors, termed fission factors, as well as the conditions of the cellular environment. Over the past decade, the... 
Fis1 | Peroxin pex11p | Fatty acid β-oxidation | Dynamin-like protein 1 | Division | Peroxisome morphogenesis | Elongation | Fission | DYNAMIN-LIKE PROTEIN-1 | Fatty acid beta-oxidation | FUNCTIONAL COMPLEMENTATION | BIOGENESIS DISORDERS | X-LINKED ADRENOLEUKODYSTROPHY | MAMMALIAN-CELLS | CELL BIOLOGY | Peroxin Pex11p | ZELLWEGER-SYNDROME | D-BIFUNCTIONAL PROTEIN | ACYL-COA OXIDASE | CDNA CLONING | CHO-CELL MUTANT | Isomerases - deficiency | RNA, Small Interfering - genetics | Acyl-CoA Oxidase - metabolism | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Humans | 3-Hydroxyacyl CoA Dehydrogenases - metabolism | Multienzyme Complexes - metabolism | Mitochondrial Proteins - genetics | GTP Phosphohydrolases - antagonists & inhibitors | Acyl-CoA Oxidase - deficiency | Fibroblasts - ultrastructure | Time-Lapse Imaging | Peroxisomes - drug effects | Microtubules - metabolism | Multienzyme Complexes - deficiency | Mitochondrial Proteins - metabolism | Base Sequence | Microtubules - ultrastructure | Membrane Proteins - metabolism | Enoyl-CoA Hydratase - deficiency | Fatty Acids - metabolism | Fibroblasts - metabolism | Oxidation-Reduction | Enoyl-CoA Hydratase - metabolism | Mitochondrial Proteins - antagonists & inhibitors | Cells, Cultured | Peroxisomal Disorders - metabolism | Microtubule-Associated Proteins - antagonists & inhibitors | Peroxisomes - metabolism | Docosahexaenoic Acids - pharmacology | GTP Phosphohydrolases - metabolism | Membrane Proteins - chemistry | Peroxisomal Disorders - pathology | GTP Phosphohydrolases - genetics | Models, Biological | Fibroblasts - drug effects | Peroxisomal Bifunctional Enzyme | 3-Hydroxyacyl CoA Dehydrogenases - deficiency | Isomerases - metabolism | Peroxisomes - ultrastructure | Protein Multimerization - drug effects | Docosahexaenoic Acids - metabolism | Index Medicus
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 11/2007, Volume 114, Issue 5, pp. 481 - 489
A number of the lysosomal storage diseases that have now been characterized are associated with intra-lysosomal accumulation of lipids, caused by defective... 
Pathology | Medicine & Public Health | Lysosome | Peroxisome | Lipid storage | α-synuclein | Neuronal nuclei | Lipidstorage | DEMENTIA | ALZHEIMERS-DISEASE | peroxisome | NEURODEGENERATION | lipid storage | PATHOLOGY | alpha-synuclein | LYSOSOMAL STORAGE DISORDERS | NEUROSCIENCES | CLINICAL NEUROLOGY | PATHOPHYSIOLOGY | neuronal nuclei | MULTIPLE SYSTEM ATROPHY | lysosome | LEWY BODIES | BRAIN | Neurons - pathology | Synucleins - analysis | Lysosomal Storage Diseases, Nervous System - physiopathology | Sandhoff Disease - pathology | Antigens, Nuclear - metabolism | Neuroglia - pathology | Humans | Middle Aged | Sandhoff Disease - metabolism | Child, Preschool | Lipidoses - pathology | Male | Lysosomal Storage Diseases, Nervous System - pathology | Brain - metabolism | Adult | Brain Diseases, Metabolic, Inborn - pathology | Lipid Metabolism - genetics | Neurons - metabolism | Brain Diseases, Metabolic, Inborn - metabolism | Brain - physiopathology | Peroxisomal Disorders - metabolism | Lysosomal Storage Diseases, Nervous System - metabolism | Lipidoses - physiopathology | Brain Diseases, Metabolic, Inborn - physiopathology | Synucleins - metabolism | Nerve Tissue Proteins - metabolism | Sandhoff Disease - physiopathology | Peroxisomal Disorders - pathology | Brain - pathology | Neuroglia - metabolism | Peroxisomal Disorders - physiopathology | beta-Synuclein - metabolism | Lipidoses - metabolism | alpha-Synuclein - metabolism | Cohort Studies | Index Medicus
Journal Article
Journal Article
Journal Article