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1.
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Grey Matter 150th anniversary of Charcot's description of amyotrophic lateral sclerosis
Brain (London, England : 1878), ISSN 0006-8950, 10/2019, Volume 142, Issue 10, pp. 3306 - 3313
Journal Article
Acta neuropathologica, ISSN 0001-6322, 4/2013, Volume 125, Issue 4, pp. 511 - 522
Pathology | Neurosciences | Medicine & Public Health | Neuropathology | Motor neuron disease | Paget’s disease | FTLD–ALS | p62 | Familial and sporadic ALS | FTLD-ALS | Paget's disease | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Sequestosome-1 Protein | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Ubiquitin - metabolism | Male | Ubiquitin - genetics | DNA-Binding Proteins - genetics | DNA-Binding Proteins - metabolism | Amyotrophic Lateral Sclerosis - pathology | Adaptor Proteins, Signal Transducing - genetics | Aged, 80 and over | Brain - pathology | Adult | Female | Heterozygote | Aged | Mutation | Adaptor Proteins, Signal Transducing - metabolism | Ubiquitin | Amyotrophic lateral sclerosis | Genetic aspects | Gene mutations | Analysis | Genes | Index Medicus
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Scientific reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 2918 - 2918
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Transferrin | Therapeutic applications | DNA damage | Resource allocation | Ferritin | Clinical trials | Lipid peroxidation | Amyotrophic lateral sclerosis | Iron | Interleukin 6 | Cell death | Biomarkers | Oxidation | Hepcidin | Deoxyribonucleic acid--DNA | Apoptosis | Index Medicus | Life Sciences
Journal Article
Nature reviews. Neurology, ISSN 1759-4758, 11/2011, Volume 7, Issue 11, pp. 650 - 654
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neuroprotective Agents - therapeutic use | Animals | Humans | Clinical Trials as Topic | Translational Medical Research - methods | Amyotrophic Lateral Sclerosis - drug therapy | Disease Models, Animal | Amyotrophic lateral sclerosis | Care and treatment | Research | Diagnosis | Risk factors | Index Medicus
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Endothelial Mineralocorticoid Receptor Mediates Diet-Induced Aortic Stiffness in Females
Circulation research, ISSN 0009-7330, 03/2016, Volume 118, Issue 6, pp. 935 - 943
macrophages | nitric oxide | vascular stiffness | inflammation | Western diet | Cardiac & Cardiovascular Systems | Peripheral Vascular Disease | Life Sciences & Biomedicine | Hematology | Cardiovascular System & Cardiology | Science & Technology | Aorta - pathology | Animals | Vascular Stiffness - physiology | Female | Mice | Aorta - physiology | Diet, Western - adverse effects | Endothelium, Vascular - physiology | Mice, Knockout | Receptors, Mineralocorticoid - physiology | Index Medicus | endothelial cell mineralocorticoid receptor | stiffness | endothelial dysfunction | Vascular stiffness
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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
Nature genetics, ISSN 1061-4036, 05/2008, Volume 40, Issue 5, pp. 572 - 574
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Neurology | Cerebrospinal fluid. Meninges. Spinal cord | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Nervous system (semeiology, syndromes) | Amino Acid Sequence | Protein Biosynthesis | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Molecular Sequence Data | Male | Mutation, Missense | DNA-Binding Proteins - genetics | DNA-Binding Proteins - metabolism | Pedigree | Base Sequence | Amyotrophic Lateral Sclerosis - metabolism | Adult | Female | Aged | Motor neurons | Amyotrophic lateral sclerosis | Genetic aspects | Gene mutations | Health aspects | Risk factors | Proteins | Medical research | Data analysis | Genetics | Cystic fibrosis | Amino acids | Mutation | Chromosomes | Neurological disorders | Muscular dystrophy | Index Medicus
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Lancet neurology, ISSN 1474-4422, 2010, Volume 9, Issue 10, pp. 986 - 994
Neurology | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Frontotemporal Dementia - genetics | United States - epidemiology | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Europe - epidemiology | Case-Control Studies | Chromosomes, Human, Pair 9 - genetics | Internationality | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Aged | Genome-Wide Association Study - methods | Frontotemporal Dementia - epidemiology | United Kingdom - epidemiology | Amyotrophic Lateral Sclerosis - epidemiology | Cohort Studies | Genetic research | Amyotrophic lateral sclerosis | Analysis | Genomics | Risk factors | Index Medicus | Fast track
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Nature (London), ISSN 0028-0836, 08/2012, Volume 488, Issue 7412, pp. 499 - 503
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Human | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Humans | Actins - metabolism | Amyotrophic Lateral Sclerosis - diagnosis | Molecular Sequence Data | Male | Jews - genetics | Ubiquitination | Profilins - genetics | Motor Neurons - cytology | Female | Amino Acid Sequence | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Amyotrophic Lateral Sclerosis - genetics | Cells, Cultured | Mutant Proteins - genetics | Axons - metabolism | Models, Molecular | Mutant Proteins - metabolism | Mutation - genetics | Motor Neurons - metabolism | Amyotrophic Lateral Sclerosis - pathology | Exome - genetics | Animals | Growth Cones - metabolism | Pedigree | Axons - pathology | Amyotrophic Lateral Sclerosis - metabolism | Protein Conformation | High-Throughput Nucleotide Sequencing | Mice | Profilins - metabolism | Amyotrophic lateral sclerosis | Genetic aspects | Research | Gene mutations | Health aspects | Risk factors | Proteins | Genomes | Polypeptides | Mutation | Pathogenesis | Genes | Index Medicus
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Hypertension (Dallas, Tex. 1979), ISSN 0194-911X, 07/2015, Volume 66, Issue 1, pp. 99 - 107
vascular stiffness | spironolactone | aldosterone | obesity | Peripheral Vascular Disease | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Pulse Wave Analysis | Receptors, Mineralocorticoid - physiology | Dose-Response Relationship, Drug | Spironolactone - pharmacology | Mineralocorticoid Receptor Antagonists - pharmacology | Female | Aorta - physiopathology | Nitric Oxide Synthase Type III - metabolism | Myocytes, Smooth Muscle - drug effects | Spironolactone - therapeutic use | Arteriosclerosis - etiology | Aorta - drug effects | Femoral Artery - physiopathology | Mice, Inbred C57BL | Obesity - physiopathology | Femoral Artery - drug effects | Diet, Western - adverse effects | Mineralocorticoid Receptor Antagonists - therapeutic use | Arteriosclerosis - prevention & control | Animals | Vascular Stiffness - drug effects | Inflammation - prevention & control | Mice | Oxidative Stress - drug effects | Vasodilation - drug effects | Endothelial Cells - drug effects | Index Medicus | Aldosterone
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Neuron (Cambridge, Mass.), ISSN 0896-6273, 03/2018, Volume 97, Issue 6, pp. 1268 - 1283.e6
WGS | GWAS | WES | KIF5A | ALS | axonal transport | cargo | no | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Amino Acid Sequence | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Amyotrophic Lateral Sclerosis - diagnosis | Male | Young Adult | Aged, 80 and over | Kinesin - genetics | Adult | Female | Aged | Genome-Wide Association Study - methods | Amyotrophic Lateral Sclerosis - epidemiology | Cohort Studies | Loss of Function Mutation - genetics | Genetic research | Genes | Analysis | Genomics | Phenotypes | Disease | Neurodegenerative diseases | Pathogenesis | Homeostasis | Amyotrophic lateral sclerosis | Genomes | Risk factors | Consortia | Hereditary spastic paraplegia | Proteins | Paraplegia | Charcot-Marie-Tooth disease | Cytoskeleton | Mutation | Spastic paraplegia | Index Medicus | Life Sciences
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