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Publication DateNeuron (Cambridge, Mass.), ISSN 0896-6273, 02/2014, Volume 81, Issue 3, pp. 536 - 543
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Axonal Transport - genetics | Humans | RNA, Messenger - metabolism | Cerebral Cortex - cytology | Motor Neurons - ultrastructure | SOXB1 Transcription Factors - metabolism | Octamer Transcription Factor-3 - genetics | SOXB1 Transcription Factors - genetics | Kruppel-Like Transcription Factors - metabolism | Animals, Genetically Modified | Amyotrophic Lateral Sclerosis - genetics | Drosophila | Cells, Cultured | Mitochondria - metabolism | DNA-Binding Proteins - genetics | Mutation - genetics | Motor Neurons - metabolism | Amyotrophic Lateral Sclerosis - pathology | Animals | Octamer Transcription Factor-3 - metabolism | Luminescent Proteins - genetics | Mice | Drosophila Proteins - genetics | Kruppel-Like Transcription Factors - genetics | RNA-Binding Proteins - metabolism | Messenger RNA | Amyotrophic lateral sclerosis | Genetic aspects | Genetic transcription | Ophthalmology | Protein binding | Neurons | Stem cells | Neurophysiology | Proteins | Disease | Insects | Software | Mutation | Index Medicus
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Loading RightsGene therapy, ISSN 0969-7128, 03/2013, Volume 20, Issue 3, pp. 348 - 352
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Genetics & Heredity | Biotechnology & Applied Microbiology | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Dependovirus - genetics | Axonal Transport | Thalamus - metabolism | Species Specificity | Humans | Green Fluorescent Proteins - genetics | Corpus Striatum - cytology | Corpus Striatum - metabolism | Brain - metabolism | Huntington Disease - therapy | Transduction, Genetic - methods | Serotyping | Green Fluorescent Proteins - metabolism | Brain - cytology | Rats | Neurodegenerative Diseases - genetics | Neurodegenerative Diseases - therapy | Dependovirus - classification | Rats, Sprague-Dawley | Genetic Vectors - genetics | Animals | Fluorescent Antibody Technique | Huntington Disease - genetics | Thalamus - cytology | Genetic Therapy - methods | Brain | Care and treatment | Genetic vectors | Huntington's chorea | Viral genetics | Adenoviruses | Physiological aspects | Genetic aspects | Research | Gene therapy | Health aspects | Huntingtons disease | Gene expression | Neurons | Index Medicus | AAV2 | Huntington’s disease | retrograde transport | AAV6
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Loading RightsAnnual review of neuroscience, ISSN 0147-006X, 2008, Volume 31, Issue 1, pp. 151 - 173
Amyotrophic lateral sclerosis | Parkinson's disease | Huntington's disease | Alzheimer's disease | Charcot-Marie-tooth disease | Motor neuron disease | Neurology | Organic mental disorders. Neuropsychology | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Psychopathology. Psychiatry | Biological and medical sciences | Medical sciences | Axonal Transport - genetics | Central Nervous System - metabolism | Humans | Central Nervous System - pathology | Charcot-Marie-Tooth Disease - genetics | Motor Neuron Disease - metabolism | Motor Neuron Disease - genetics | Parkinson Disease - metabolism | Motor Neuron Disease - physiopathology | Charcot-Marie-Tooth Disease - metabolism | Huntington Disease - physiopathology | Alzheimer Disease - physiopathology | Axons - metabolism | Neurodegenerative Diseases - genetics | Neurodegenerative Diseases - metabolism | Parkinson Disease - genetics | Parkinson Disease - physiopathology | Huntington Disease - metabolism | Animals | Neurodegenerative Diseases - physiopathology | Axons - pathology | Alzheimer Disease - metabolism | Huntington Disease - genetics | Central Nervous System - physiopathology | Charcot-Marie-Tooth Disease - physiopathology | Alzheimer Disease - genetics | Nervous system | Degeneration | Axonal transport | Analysis | Index Medicus
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Loading RightsThe Journal of cell biology, ISSN 0021-9525, 2015, Volume 209, Issue 3, pp. 419 - 433
Life Sciences & Biomedicine | Science & Technology | Cell Biology | Axonal Transport | Peptide Fragments - metabolism | Humans | tau Proteins - metabolism | Glycogen Synthase Kinase 3 beta | Glycogen Synthase Kinase 3 - metabolism | Mice, Knockout | Proto-Oncogene Proteins c-fyn - genetics | Animals | Proto-Oncogene Proteins c-fyn - metabolism | tau Proteins - genetics | Glycogen Synthase Kinase 3 - genetics | Amyloid beta-Peptides - genetics | Alzheimer Disease - metabolism | Amyloid beta-Peptides - metabolism | Mice | Alzheimer Disease - genetics | Enzyme Activation - genetics | Peptide Fragments - genetics | Index Medicus
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Loading RightsNeuron (Cambridge, Mass.), ISSN 0896-6273, 04/2012, Volume 74, Issue 2, pp. 331 - 343
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | RNA, Small Interfering - genetics | Immunoprecipitation | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Cercopithecus aethiops | Neurons - cytology | Axons - physiology | Ganglia, Spinal - cytology | DNA-Binding Proteins - metabolism | Transfection | Nuclear Proteins - genetics | Photobleaching | Glycine - genetics | Lysosome-Associated Membrane Glycoproteins - metabolism | Cells, Cultured | Dynactin Complex | Nuclear Proteins - metabolism | Protein Structure, Tertiary - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Protein Transport - genetics | Microscopy, Confocal | Animals | Analysis of Variance | Lysosome-Associated Membrane Glycoproteins - genetics | Mice | RNA, Small Interfering - metabolism | Nervous system diseases | Analysis | Dynein | Proteins | Hypotheses | Statistical methods | Motility | Neurons | Index Medicus | CAP-Gly | Perry syndrome | Hereditary Motor Neuropathy 7B | Dynactin | cytoplasmic dynein | axonal transport | p150Glued | distal Spinal and Bulbar Muscular Atrophy
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Loading RightsThe Journal of cell biology, ISSN 0021-9525, 10/2017, Volume 216, Issue 10, pp. 3291 - 3305
Life Sciences & Biomedicine | Science & Technology | Cell Biology | Amyloid Precursor Protein Secretases - genetics | Axonal Transport | Lysosomes - genetics | Presenilin-2 - metabolism | Aspartic Acid Endopeptidases - genetics | Alzheimer Disease - pathology | Lysosomes - metabolism | Amyloid beta-Peptides - genetics | Amyloid beta-Peptides - metabolism | Lysosomes - pathology | Disease Models, Animal | Plaque, Amyloid - pathology | Axons - metabolism | Nerve Tissue Proteins - genetics | Mice, Knockout | Plaque, Amyloid - genetics | Nerve Tissue Proteins - metabolism | Amyloid Precursor Protein Secretases - metabolism | Animals | Presenilin-2 - genetics | Aspartic Acid Endopeptidases - metabolism | Axons - pathology | Adaptor Proteins, Signal Transducing - genetics | Alzheimer Disease - metabolism | Plaque, Amyloid - metabolism | Mice | Adaptor Proteins, Signal Transducing - metabolism | Alzheimer Disease - genetics | Amyloidogenesis | b-Site APP cleaving enzyme 1 | Neurodegenerative diseases | Lysosomes | JNK protein | Amyloid precursor protein | Haploinsufficiency | Proteins | Pathology | Axons | Cellular biology | Presenilin 2 | Alzheimers disease | Transport | Axonal transport | Alzheimer's disease | Plaques | Index Medicus | 19 | 34 | s | 43
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Loading RightsHuman molecular genetics, ISSN 0964-6906, 05/2012, Volume 21, Issue 9, pp. 1979 - 1988
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Neurology | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Axonal Transport - genetics | Calcium - metabolism | Vesicular Transport Proteins - metabolism | Humans | Homeostasis | Mitochondrial Proteins - genetics | Time-Lapse Imaging | Tubulin - metabolism | Transfection | Mitochondrial Proteins - metabolism | Base Sequence | HEK293 Cells | Plasmids - genetics | Neurons - metabolism | Recombinant Proteins - metabolism | Movement | Mutagenesis, Site-Directed | rho GTP-Binding Proteins - genetics | Amyotrophic Lateral Sclerosis - genetics | Vesicular Transport Proteins - genetics | Mutant Proteins - genetics | Rats | Axonal Transport - physiology | Mutant Proteins - metabolism | Mitochondria - metabolism | Recombinant Proteins - genetics | Kinesin - metabolism | Animals | rho GTP-Binding Proteins - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Amino Acid Substitution | Mitochondria | Tubulin | Motor neuron disease | protein B | Amyotrophic lateral sclerosis | Calcium transport | Axonal transport | Calcium homeostasis | Membrane proteins | Index Medicus
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Loading RightsNature reviews. Neuroscience, ISSN 1471-003X, 10/2007, Volume 8, Issue 10, pp. 776 - 789
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Vertebrates: nervous system and sense organs | Glaucoma and intraocular pressure | Biological and medical sciences | General aspects. Models. Methods | Medical sciences | Ophthalmology | Dendrites - metabolism | Neuronal Plasticity - genetics | Animals | RNA Transport - physiology | Humans | RNA, Messenger - genetics | RNA, Messenger - physiology | Protein Biosynthesis - physiology | Protein Biosynthesis - genetics | RNA, Messenger - metabolism | Dendrites - genetics | Physiological aspects | Messenger RNA | Research | Genetic transcription | Axonal transport | Genetic translation | Index Medicus
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