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Genes & cancer, ISSN 1947-6027, 04/2014, Volume 5, Issue 1-2, pp. 15 - 21
Journal Article
PloS one, ISSN 1932-6203, 03/2015, Volume 10, Issue 3, pp. e0118649 - e0118649
Late-onset neurodegenerative diseases remain poorly understood as search continues for the perceived pathogenic protein species. Previously, variants in... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Superoxide Dismutase - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Genotype | Neurodegenerative Diseases - metabolism | RNA, Messenger - metabolism | Protein Folding | Motor Neurons - metabolism | Superoxide Dismutase - chemistry | Amyotrophic Lateral Sclerosis - pathology | Phenotype | Protein Isoforms - metabolism | Adolescent | Amyotrophic Lateral Sclerosis - metabolism | Survival Analysis | Adult | Aged | Mutation | Superoxide Dismutase-1 | Proteome - metabolism | Superoxide Dismutase - metabolism | Protein Isoforms - genetics | Proteins | Nervous system diseases | Analysis | Physiological aspects | Amyotrophic lateral sclerosis | Genetic aspects | Superoxide | Oxidative stress | Copy number | Superoxide dismutase | mRNA | Risk factors | Protein turnover | Genotype & phenotype | Mitochondria | Protein folding | Rodents | Age | Neurological disorders | Genotypes | Pathogens | Motor neurons | Phenotypes | Statistical analysis | Stability | Neurodegenerative diseases | Neurons | Washout | Energy expenditure | Exponential functions | Metabolism | Risk analysis | Ribonucleic acid--RNA | Proteasome inhibitors | Neurological diseases | Pathogenicity | Nursing | Exhaustion | Neuromuscular junctions | Proteomes | Index Medicus | RNA | Ribonucleic acid
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 9/2016, Volume 113, Issue 36, pp. 10198 - 10203
Mutations in superoxide dismutase (SOD1) cause amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disease characterized by the loss of upper and... 
ALS|mutant sod1 mouse | Mutant sod1|misfolded sod1|mif | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Brain | Spinal cord | Membranes | Neurons | Rodents | Amyotrophic lateral sclerosis | Cytoplasm | Index Medicus | mutant SOD1 | ALS | Biological Sciences | misfolded SOD1 | MIF | mutant SOD1 mouse
Journal Article
Experimental neurology, ISSN 0014-4886, 04/2018, Volume 302, pp. 129 - 135
Mutations in Cu/Zn-superoxide dismutase (SOD1) cause familial forms of amyotrophic lateral sclerosis (ALS), a fatal disorder characterized by the progressive... 
Amyotrophic lateral sclerosis | GCLM | SOD1 | Glutathione | Index Medicus
Journal Article
Neurotoxicity research, ISSN 1029-8428, 2/2017, Volume 31, Issue 2, pp. 230 - 244
The aim of the present study was to evaluate the therapeutic effect of the novel neuroprotective multitarget brain permeable monoamine oxidase inhibitor/iron... 
Neurochemistry | Neurology | Neurosciences | Biomedicine | Mitochondrial biogenesis | Neurobiology | Amyotrophic lateral sclerosis | Multifunctional iron chelator | Pharmacology/Toxicology | Cell Biology | SOD1 G93A mice | mice | SOD1 | Index Medicus
Journal Article
Neurochemical research, ISSN 1573-6903, 01/2018, Volume 44, Issue 1, pp. 228 - 233
Impaired interactions between Calcineurin (Cn) and (Cu/Zn) superoxide dismutase (SOD1) are suspected to be responsible for the formation of hyperphosphorylated... 
Neurochemistry | Biochemistry, general | Neurology | SOD1 G93A | Neurosciences | Spinal cord | Biomedicine | TDP-43 | Calcineurin | ALS | Cell Biology | SOD1 | Animal models | Stability | Serine | Superoxide dismutase | Amyotrophic lateral sclerosis | Thorax | Agglomeration | Zinc | Proteins | Sacrum | Rodents | Copper | Protein interaction | Index Medicus | Original Paper | SOD1G93A
Journal Article
Neurotherapeutics, ISSN 1933-7213, 08/2012, Volume 9, Issue 4, pp. 814 - 826
Amyotrophic lateral sclerosis is a neurodegenerative disorder characterized by progressive weakness, muscle atrophy, and paralysis due to the loss of upper and... 
Neurology | Neurosciences | Biomedicine | Motoneuron disease | PRE-084 | Neurobiology | Amyotrophic lateral sclerosis | Neurosurgery | Sigma-1 receptor | SOD1 G93A mice | mice | SOD1 | Pharmacology & Pharmacy | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Immunohistochemistry | Superoxide Dismutase - genetics | Amyotrophic Lateral Sclerosis - physiopathology | Cell Survival | Humans | Electrophysiology | Morpholines - pharmacology | Motor Activity - drug effects | Male | Mice, Transgenic | Receptors, sigma - agonists | Amyotrophic Lateral Sclerosis - drug therapy | Blotting, Western | Motor Neurons - pathology | Motor Neurons - metabolism | Amyotrophic Lateral Sclerosis - pathology | Animals | Neuroprotective Agents - pharmacology | Amyotrophic Lateral Sclerosis - metabolism | Female | Mice | Superoxide Dismutase-1 | Motor Neurons - drug effects | Disease Models, Animal | Methyl aspartate | Nervous system diseases | Analysis | Cells | Index Medicus | Motor neurons | Phosphorylation | Spinal cord | Neurodegenerative diseases | Glutamic acid receptors (ionotropic) | Central nervous system | Muscles | N-Methyl-D-aspartic acid receptors | Glutamic acid receptors | Survival | Calcium influx | Western blotting | Atrophy | Locomotion | Ischemia | Paralysis | Frontotemporal dementia | Age | SOD1G93A mice | Original
Journal Article