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Journal of Neurochemistry, ISSN 0022-3042, 08/2010, Volume 114, Issue 4, pp. 1177 - 1192
J. Neurochem. (2010) 114, 1177–1192. Peripherin is a type III intermediate filament protein that is up‐regulated during neuronal injury and is a major... 
inclusion | intermediate filament | sciatic crush | alternative splicing | amyotrophic lateral sclerosis | stroke | NERVOUS-SYSTEM | B-LYMPHOCYTES | DIFFERENTIAL EXPRESSION | BIOCHEMISTRY & MOLECULAR BIOLOGY | AMYOTROPHIC-LATERAL-SCLEROSIS | NEUROSCIENCES | INTERMEDIATE-FILAMENT PROTEIN | FAMILIAL ALS | NEUROFILAMENT HEAVY GENE | TRANSGENIC MOUSE MODEL | SUPEROXIDE-DISMUTASE | CEREBRAL-ISCHEMIA | Membrane Glycoproteins - metabolism | Membrane Glycoproteins - biosynthesis | Male | Brain Injuries - physiopathology | Motor Neuron Disease - metabolism | Motor Neuron Disease - genetics | Intermediate Filament Proteins - genetics | Nerve Tissue Proteins - biosynthesis | Motor Neuron Disease - physiopathology | Disease Models, Animal | Biomarkers - metabolism | Peripherins | Sciatic Nerve - pathology | Amyotrophic Lateral Sclerosis - genetics | Mice, Inbred C57BL | Gene Expression Regulation - physiology | Intermediate Filament Proteins - biosynthesis | Mice, Transgenic | Nerve Tissue Proteins - genetics | Nerve Crush - methods | Membrane Glycoproteins - genetics | Mice, Knockout | Nerve Tissue Proteins - metabolism | Amyotrophic Lateral Sclerosis - pathology | Animals | Protein Isoforms - biosynthesis | Amyotrophic Lateral Sclerosis - metabolism | Proteomics | Mice | Brain Injuries - etiology | Intermediate Filament Proteins - metabolism | Protein Isoforms - genetics | Amyotrophic lateral sclerosis | Neurons | Intermediate filament proteins | Analysis | Proteins | Neurology | Biochemistry | Rodents
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 05/2004, Volume 24, Issue 19, pp. 4585 - 4595
Journal Article
Science, ISSN 0036-8075, 3/2000, Volume 287, Issue 5460, pp. 2032 - 2036
Journal Article
Journal Article
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 08/2006, Volume 98, Issue 3, pp. 926 - 938
Peripherin is a type III neuronal intermediate filament detected in motor neuron inclusions of amyotrophic lateral sclerosis (ALS) patients. We previously... 
axonal transport | peripherin | neurofilaments | intermediate filaments | Neurofilaments | Peripherin | Axonal transport | Intermediate filaments | MOTOR-NEURONS | ALPHA-INTERNEXIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | AMYOTROPHIC-LATERAL-SCLEROSIS | MUTANT SUPEROXIDE-DISMUTASE | NEUROSCIENCES | INTERMEDIATE-FILAMENT PROTEIN | NF-L | MOUSE MODEL | IN-VIVO | GENE-EXPRESSION | TRANSGENIC MICE | Neurons - pathology | Axonal Transport - genetics | Humans | Membrane Glycoproteins - biosynthesis | Spheroids, Cellular - pathology | Ganglia, Spinal - cytology | Neurofilament Proteins - antagonists & inhibitors | Neurofilament Proteins - genetics | Membrane Glycoproteins - physiology | Intermediate Filament Proteins - genetics | Nerve Tissue Proteins - biosynthesis | Neurons - metabolism | Organ Culture Techniques | Cell Line | Peripherins | Nerve Tissue Proteins - physiology | Intermediate Filament Proteins - biosynthesis | Intermediate Filament Proteins - physiology | Mice, Transgenic | Up-Regulation - genetics | Nerve Tissue Proteins - genetics | Membrane Glycoproteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Animals | Amyotrophic Lateral Sclerosis - metabolism | Cell Line, Tumor | Mice | Neurofilament Proteins - classification | Neurofilament Proteins - metabolism | Ganglia, Spinal - metabolism | Proteins | Physiological aspects | Neurons | Amyotrophic lateral sclerosis | Biochemistry | Gene expression | Transgenic animals | Up-Regulation | Axonal Transport | Biochemistry, Molecular Biology | Nerve Tissue Proteins | Life Sciences | Amyotrophic Lateral Sclerosis | Neurofilament Proteins | Membrane Glycoproteins | Spheroids, Cellular | Ganglia, Spinal | Intermediate Filament Proteins
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 11/2003, Volume 163, Issue 4, pp. 901 - 910
Profilaggrin is a large epidermal polyprotein that is proteolytically processed during keratinocyte differentiation to release multiple filaggrin monomer,... 
Newborns | Antibodies | Keratinocytes | Epidermis | Lipids | Skin diseases | Skin | Mice | Monomers | Ichthyosis | Membrane serine protease | Lipid lamellar bodies | Stratum corneum | Profilaggrin | Barrier function | ICHTHYOSIS VULGARIS | STRUCTURAL PROTEINS | CORNIFIED CELL ENVELOPES | HUMAN STRATUM-CORNEUM | LAMELLAR GRANULES | SERINE-PROTEASE | SKIN BARRIER FUNCTION | PERMEABILITY BARRIER | IDENTIFICATION | HARLEQUIN ICHTHYOSIS | CELL BIOLOGY | Peptide Hydrolases - genetics | Extracellular Matrix - metabolism | Peptide Hydrolases - deficiency | Epidermis - growth & development | Cell Differentiation - genetics | Extracellular Matrix - genetics | Ichthyosis - pathology | Ichthyosis - genetics | Serine Endopeptidases - genetics | Trypsin - genetics | Epidermis - enzymology | Skin Abnormalities - pathology | Keratinocytes - enzymology | Keratinocytes - ultrastructure | Skin Abnormalities - enzymology | Epidermis - pathology | Serine Endopeptidases - deficiency | Dehydration - enzymology | Trypsin - deficiency | Intermediate Filament Proteins - biosynthesis | Lipid Metabolism | S100 Proteins - metabolism | Permeability | Microscopy, Electron | Mice, Knockout | Protein Precursors - metabolism | Membrane Proteins | Keratinocytes - pathology | Animals | Intermediate Filament Proteins - deficiency | Skin Abnormalities - genetics | Ichthyosis - enzymology | Extracellular Matrix - pathology | Intermediate Filament Proteins - metabolism | Cell research | Serine | Calcium compounds | Cell differentiation | Genetic regulation | Proteases | Analysis | Physiological aspects | Genetic aspects | Binding proteins | Matriptase | filaggrin | MT-SP1 protein | barrier function; lipid lamellar bodies; membrane serine protease; profilaggrin; stratum corneum
Journal Article
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 06/2003, Volume 23, Issue 12, pp. 5131 - 5140
We have investigated the potential of human pluripotent cells to restore function in rats paralyzed with a virus-induced motor neuronopathy. Cells derived from... 
Embryoid body | Trophic factors | Embryonic germ cell | Motor neuron disease | Stem cells | Sindbis virus | trophic factors | PROGENITOR CELLS | MOTONEURON SURVIVAL | MOUSE-BRAIN | stem cells | motor neuron disease | STEM-CELLS | SINDBIS VIRUS-INFECTION | SPINAL-CORD | embryoid body | NEUROSCIENCES | TRANSPLANTATION | embryonic germ cell | GROWTH-FACTOR-ALPHA | CENTRAL-NERVOUS-SYSTEM | SYNAPTOPHYSIN IMMUNOREACTIVITY | Nestin | Encephalitis, Viral - virology | Germ Cells - transplantation | Humans | Rats, Inbred Lew | Neurons - cytology | Transplantation, Heterologous | Encephalitis, Viral - complications | Motor Activity | Recovery of Function | Motor Neuron Disease - virology | Stem Cell Transplantation | Motor Neuron Disease - therapy | Brain-Derived Neurotrophic Factor - biosynthesis | Germ Cells - cytology | Neurons - metabolism | Germ Cells - metabolism | Motor Neuron Disease - physiopathology | Transforming Growth Factor alpha - biosynthesis | Astrocytes - cytology | Pluripotent Stem Cells - cytology | Cell Survival | Intermediate Filament Proteins - biosynthesis | Rats | Graft Survival | Treatment Outcome | Nerve Tissue Proteins | Pluripotent Stem Cells - metabolism | Alphavirus Infections - complications | Antigens, Differentiation - biosynthesis | Alphavirus Infections - virology | Animals | Pluripotent Stem Cells - transplantation | Sindbis Virus - pathogenicity | Astrocytes - metabolism | Plasticity | Development | Repair
Journal Article
Journal Article