UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (1396) 1396
life sciences & biomedicine (1310) 1310
humans (1196) 1196
neurosciences & neurology (951) 951
animals (935) 935
neurosciences (890) 890
tau proteins - metabolism (821) 821
tau proteins - genetics (761) 761
alzheimer's disease (738) 738
tauopathy (635) 635
tauopathies - pathology (560) 560
tauopathies - metabolism (538) 538
tauopathies - genetics (518) 518
mice (508) 508
disease models, animal (460) 460
tau (444) 444
mice, transgenic (425) 425
male (416) 416
pathology (385) 385
phosphorylation (385) 385
tau protein (383) 383
clinical neurology (382) 382
female (350) 350
neurodegeneration (339) 339
neurodegenerative diseases (338) 338
tauopathies (336) 336
brain - pathology (328) 328
brain - metabolism (319) 319
proteins (293) 293
mutation (272) 272
mental disorders (270) 270
biochemistry & molecular biology (265) 265
alzheimer’s disease (264) 264
neurology (261) 261
dementia (237) 237
alzheimer disease - metabolism (231) 231
neurons (231) 231
neurons - metabolism (224) 224
analysis (220) 220
brain (217) 217
aged (215) 215
alzheimer disease - pathology (208) 208
middle aged (186) 186
neurons - pathology (182) 182
nervous system diseases (177) 177
frontotemporal dementia (173) 173
research (169) 169
alzheimer disease - genetics (166) 166
tauopathies - physiopathology (164) 164
genetic engineering (158) 158
cell biology (156) 156
alzheimers disease (153) 153
nervous system (152) 152
neurofibrillary tangles - pathology (148) 148
progressive supranuclear palsy (146) 146
mice, inbred c57bl (144) 144
tau proteins - chemistry (142) 142
rodents (141) 141
aged, 80 and over (132) 132
neurofibrillary tangles (129) 129
mutation - genetics (127) 127
immunohistochemistry (125) 125
genetic aspects (121) 121
neurofibrillary tangles - metabolism (121) 121
tau proteins (119) 119
physiological aspects (108) 108
degeneration (106) 106
tauopathies - drug therapy (106) 106
alzheimer disease (104) 104
transgenic mice (95) 95
geriatrics & gerontology (94) 94
aging (93) 93
gene expression (93) 93
medicine & public health (92) 92
neuroscience (91) 91
rats (90) 90
cells, cultured (89) 89
animal models (87) 87
disease progression (87) 87
amyloid beta-peptides - metabolism (86) 86
science & technology - other topics (85) 85
hippocampus - pathology (84) 84
multidisciplinary sciences (84) 84
dementia - genetics (81) 81
neurodegenerative diseases - genetics (80) 80
kinases (79) 79
hippocampus - metabolism (78) 78
neurodegenerative diseases - pathology (78) 78
neuropathology (78) 78
research article (78) 78
cognitive ability (76) 76
health aspects (76) 76
hippocampus (75) 75
amyloid (74) 74
nerve degeneration - pathology (74) 74
parkinson's disease (74) 74
corticobasal degeneration (73) 73
dementia disorders (72) 72
adult (70) 70
neurodegenerative diseases - metabolism (69) 69
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1700) 1700
Japanese (8) 8
French (3) 3
German (3) 3
Portuguese (3) 3
Korean (1) 1
Spanish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Neuron (Cambridge, Mass.), ISSN 0896-6273, 08/2012, Volume 75, Issue 4, pp. 618 - 632
Mitochondrial abnormalities have been documented in Alzheimer’s disease and related neurodegenerative disorders, but the causal relationship between... 
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurons - pathology | Microtubule-Associated Proteins - genetics | Tauopathies - genetics | Cytoskeletal Proteins - genetics | Gelsolin - metabolism | Microtubule-Associated Proteins - metabolism | Humans | Actins - metabolism | Tauopathies - pathology | Cytoplasm - metabolism | MicroRNAs - metabolism | Green Fluorescent Proteins - genetics | Mitochondrial Proteins - genetics | Drosophila Proteins - metabolism | GTP-Binding Proteins - genetics | Nerve Degeneration - metabolism | Neurons - ultrastructure | tau Proteins - genetics | Cell Death - genetics | Mitochondria - genetics | Mitochondrial Proteins - metabolism | ATP Synthetase Complexes - metabolism | Cell Cycle Proteins - genetics | Tauopathies - complications | Cytoskeletal Proteins - metabolism | Myosins - metabolism | Cytoplasm - genetics | RNA Interference - physiology | Disease Models, Animal | In Situ Nick-End Labeling | Green Fluorescent Proteins - metabolism | Animals, Genetically Modified | Gene Expression Regulation - genetics | Drosophila | Cell Cycle Proteins - metabolism | Mitochondria - metabolism | Mitochondria - pathology | Mutation - genetics | Animals | GTP Phosphohydrolases - metabolism | Analysis of Variance | GTP Phosphohydrolases - genetics | Gelsolin - genetics | Mice | Drosophila Proteins - genetics | Nerve Degeneration - etiology | Voltage-Dependent Anion Channels - metabolism | GTP-Binding Proteins - metabolism | Nervous system diseases | Actin | Neurons | Utrophin | Myosin | Mitochondrial DNA | Alzheimer's disease | Proteins | Phosphorylation | Mitochondria | Neurotoxicity | Insects | Microscopy | Neurodegeneration | Pathogenesis | Morphology | Mutation | Defects | Index Medicus | Neurodegenerative diseases | Tau protein | Cell death | Elongation
Journal Article
Nature genetics, ISSN 1546-1718, 06/2011, Volume 43, Issue 7, pp. 699 - 705
Journal Article
Annual review of genetics, ISSN 0066-4197, 11/2013, Volume 47, Issue 1, pp. 601 - 623
Prions are proteins that acquire alternative conformations that become self-propagating. Transformation of proteins into prions is generally accompanied by an... 
neurodegeneration | prion | Neurodegeneration | Prion | Fungal Proteins - chemistry | Synucleins - physiology | Amyloidogenic Proteins - classification | Prion Diseases - genetics | Prions - genetics | Transcription Factors - chemistry | Tauopathies - genetics | Neurodegenerative Diseases - etiology | Humans | Virulence | mRNA Cleavage and Polyadenylation Factors - chemistry | Amyloidogenic Proteins - physiology | Amyloidogenic Proteins - chemistry | Neurofibrillary Tangles | mRNA Cleavage and Polyadenylation Factors - classification | Tauopathies - etiology | Plaque, Amyloid | Inclusion Bodies | tau Proteins - genetics | tau Proteins - physiology | Saccharomyces cerevisiae Proteins - classification | Peptide Termination Factors - physiology | Models, Molecular | Neurodegenerative Diseases - genetics | Fungal Proteins - classification | Mammals | Transcription Factors - classification | Peptide Termination Factors - classification | Fungal Proteins - physiology | Animals | Prions - physiology | Prion Diseases - etiology | Age of Onset | Protein Conformation | Peptide Termination Factors - chemistry | Saccharomyces cerevisiae Proteins - physiology | Neurodegenerative Diseases - epidemiology | Saccharomyces cerevisiae Proteins - chemistry | Prions | Physiological aspects | Causes of | Nervous system | Degeneration | Genetic aspects | Health aspects | Proteins | Fungi | Pathogenesis | Neurological disorders | Index Medicus
Journal Article
Nature medicine, ISSN 1546-170X, 07/2014, Volume 20, Issue 8, pp. 881 - 885
Journal Article