Articles

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

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (140) 140
life sciences & biomedicine (129) 129
humans (110) 110
neurosciences & neurology (76) 76
female (67) 67
male (67) 67
neurosciences (63) 63
animals (62) 62
neurology (54) 54
clinical neurology (42) 42
mice (40) 40
middle aged (40) 40
mutation (38) 38
adult (35) 35
biological and medical sciences (35) 35
medical sciences (34) 34
aged (32) 32
parkinson's disease (32) 32
genetics & heredity (28) 28
biochemistry & molecular biology (26) 26
proteins (25) 25
cell biology (23) 23
analysis (21) 21
nerve tissue proteins - genetics (20) 20
nervous system (20) 20
parkinson disease - genetics (20) 20
degenerative and inherited degenerative diseases of the nervous system. leukodystrophies. prion diseases (18) 18
genetics (18) 18
pedigree (18) 18
ataxins (17) 17
nervous system diseases (17) 17
neurodegeneration (17) 17
neurons (17) 17
spinocerebellar ataxia (17) 17
spinocerebellar ataxias - genetics (17) 17
biomedicine (16) 16
dopamine (16) 16
genetic aspects (16) 16
mitochondria (16) 16
neurons - metabolism (15) 15
ataxia (14) 14
genotype (14) 14
nerve tissue proteins - metabolism (14) 14
pathology (14) 14
research (14) 14
gene expression (13) 13
mice, knockout (13) 13
mice, transgenic (13) 13
physiological aspects (13) 13
research article (13) 13
spinocerebellar ataxia type 2 (13) 13
young adult (13) 13
adolescent (12) 12
alpha-synuclein (12) 12
alpha-synuclein - metabolism (12) 12
amyotrophic lateral sclerosis (12) 12
ataxin-2 - genetics (12) 12
genetic predisposition to disease (12) 12
medical genetics (12) 12
medicin och hälsovetenskap (12) 12
movement disorders (12) 12
neurodegenerative diseases (12) 12
aged, 80 and over (11) 11
alpha-synuclein - genetics (11) 11
disease models, animal (11) 11
genes (11) 11
genetic linkage (11) 11
molecular sequence data (11) 11
multidisciplinary sciences (11) 11
neurons - pathology (11) 11
parkinson disease - pathology (11) 11
parkinsons disease (11) 11
pink1 (11) 11
protein kinases - genetics (11) 11
science & technology - other topics (11) 11
alleles (10) 10
amino acid sequence (10) 10
biology (10) 10
chromosome mapping (10) 10
genes, dominant (10) 10
molecular biology (10) 10
neurobiology (10) 10
parkinson disease (10) 10
parkinson disease - metabolism (10) 10
sca2 (10) 10
brain - metabolism (9) 9
brain - pathology (9) 9
chemistry (9) 9
human genetics (9) 9
medicine (9) 9
mitochondria - metabolism (9) 9
parkinson’s disease (9) 9
risk factors (9) 9
rna (9) 9
rodents (9) 9
spinocerebellar ataxias - pathology (9) 9
spinocerebellar ataxias - physiopathology (9) 9
synuclein (9) 9
cells, cultured (8) 8
cellular and molecular neuroscience (8) 8
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Spinocerebellar ataxia type 2
by Auburger, Georg W.J
2011, ISBN 9780444518927, Volume 103
Ataxins | Spinocerebellar Ataxias - pathology | Nerve Tissue Proteins - genetics | Humans | Spinocerebellar Ataxias - genetics | Index Medicus
Book Chapter
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice
by Becker, Lindsay A and Huang, Brenda and Bieri, Gregor and Ma, Rosanna and Knowles, David A and Jafar-Nejad, Paymaan and Messing, James and Kim, Hong Joo and Soriano, Armand and Auburger, Georg and Pulst, Stefan M and Taylor, J. Paul and Rigo, Frank and Gitler, Aaron D
Nature (London), ISSN 0028-0836, 04/2017, Volume 544, Issue 7650, pp. 367 - 371
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Central Nervous System - metabolism | Amyotrophic Lateral Sclerosis - physiopathology | Humans | Stress, Physiological | Male | Protein Aggregation, Pathological - therapy | Ataxin-2 - genetics | Gene Knockdown Techniques | DNA-Binding Proteins - metabolism | Cytoplasmic Granules - metabolism | Oligonucleotides, Antisense - therapeutic use | Female | Protein Aggregation, Pathological - genetics | Motor Skills - physiology | Amyotrophic Lateral Sclerosis - therapy | Amyotrophic Lateral Sclerosis - genetics | Mice, Transgenic | Longevity | DNA-Binding Proteins - genetics | DNA-Binding Proteins - chemistry | Disease Progression | Ataxin-2 - deficiency | Mice, Knockout | Animals | Oligonucleotides, Antisense - genetics | Amyotrophic Lateral Sclerosis - metabolism | Survival Analysis | Oligonucleotides, Antisense - administration & dosage | Mice | Proteins | Pathology | Hypotheses | Neurodegeneration | Neurons | Transgenic animals | Rodents | Nervous system | Mutation | Dementia | Recruitment | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text The RNA-binding protein ATXN2 is expressed during megakaryopoiesis and may control timing of gene expression
by Hansen, Marten and Zeddies, Sabrina and Meinders, Marjolein and di Summa, Franca and Rollmann, Ewa and van Alphen, Floris P. J and Hoogendijk, Arjan J and Moore, Kat S and Halbach, Melanie and Gutiérrez, Laura and van den Biggelaar, Maartje and Thijssen-Timmer, Daphne C and Auburger, Georg W. J and van den Akker, Emile and von Lindern, Marieke
International journal of molecular sciences, ISSN 1661-6596, 2020, Volume 21, Issue 3, p. 967
RBP | Spectroscopy | Translation | Molecular Biology | ITGB3 | Megakaryopoiesis | ATAXIN2 | MEG-01 | ATXN2 | Computer Science Applications | Hemostasis | PECAM1 | Catalysis | Inorganic Chemistry | MRNA | Physical and Theoretical Chemistry | Organic Chemistry | Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Life Sciences & Biomedicine | Chemistry, Multidisciplinary | Science & Technology | Index Medicus | meg-01 | itgb3 | rbp | megakaryopoiesis | atxn2 | translation | mrna | pecam1 | hemostasis | ataxin2
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
by Elden, Andrew C and Kim, Hyung-Jun and Hart, Michael P and Chen-Plotkin, Alice S and Johnson, Brian S and Fang, Xiaodong and Armakola, Maria and Geser, Felix and Greene, Robert and Lu, Min Min and Padmanabhan, Arun and Clay-Falcone, Dana and McCluskey, Leo and Elman, Lauren and Juhr, Denise and Gruber, Peter J and Rüb, Udo and Auburger, Georg and Trojanowski, John Q and Lee, Virginia M.-Y and Van Deerlin, Vivianna M and Bonini, Nancy M and Gitler, Aaron D
Nature (London), ISSN 0028-0836, 08/2010, Volume 466, Issue 7310, pp. 1069 - 1075
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Drosophila - drug effects | Neurons - pathology | Saccharomyces cerevisiae - genetics | Humans | Middle Aged | Peptides - genetics | Male | Saccharomyces cerevisiae - drug effects | DNA-Binding Proteins - metabolism | Saccharomyces cerevisiae - metabolism | Young Adult | Ataxins | Aged, 80 and over | Adult | Female | Drosophila - genetics | Cell Line | Genetic Predisposition to Disease | Peptides - chemistry | Amyotrophic Lateral Sclerosis - genetics | DNA-Binding Proteins - toxicity | Risk Factors | Repetitive Sequences, Amino Acid - genetics | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Animals | Aged | Proteins | Yeast | Insects | Pathogenesis | Toxicity | Genes | Genetics | Amyotrophic lateral sclerosis | Mutation | Kinases | Health risk assessment | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Spinocerebellar ataxia 2 (SCA2)
by Lastres-Becker, Isabel and Rüb, Udo and Auburger, Georg
Cerebellum (London, England), ISSN 1473-4222, 6/2008, Volume 7, Issue 2, pp. 115 - 124
Neurology | Neurosciences | Biomedicine | ataxin-2 | spinocerebellar ataxia type 2 | olivo-ponto-cerebellar atrophy | Neurobiology | neurodegeneration | Wadia-Swami or Menzel type of ataxia | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Spinocerebellar Ataxias - diagnosis | Ataxins | Diagnosis, Differential | Genes, Dominant | Cerebellar Cortex - pathology | Humans | Brain - pathology | Spinocerebellar Ataxias - pathology | Nerve Tissue Proteins - genetics | RNA - genetics | RNA - metabolism | Spinocerebellar Ataxias - genetics | Proteins | Medical research | Ataxia | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Sensory neuropathy and nociception in rodent models of Parkinson's disease
by Valek, Lucie and Auburger, Georg and Tegeder, Irmgard
Disease models & mechanisms, ISSN 1754-8403, 06/2019, Volume 12, Issue 6, p. dmm039396
Pathology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Nociception | Sensation | Parkinson Disease - pathology | Animals | Dopaminergic Neurons - pathology | Humans | Motor Activity | Parkinson Disease - physiopathology | Disease Models, Animal | Index Medicus | Pain | 302 | Non-motor Parkinson's disease | Mitogenesis | Sensory neuropathy | Review | Synuclein | Mitophagy | Protein aggregate
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text PINK1 and Parkin Control Localized Translation of Respiratory Chain Component mRNAs on Mitochondria Outer Membrane
by Gehrke, Stephan and Wu, Zhihao and Klinkenberg, Michael and Sun, Yaping and Auburger, Georg and Guo, Su and Lu, Bingwei
Cell metabolism, ISSN 1550-4131, 01/2015, Volume 21, Issue 1, pp. 95 - 108
Endocrinology & Metabolism | Life Sciences & Biomedicine | Science & Technology | Cell Biology | RNA-Binding Proteins - genetics | Protein Biosynthesis | Humans | Drosophila Proteins - metabolism | DNA-Binding Proteins - metabolism | Drosophila melanogaster - metabolism | Ubiquitination | Guanine Nucleotide Exchange Factors - metabolism | HEK293 Cells | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Nuclear Proteins - genetics | Drosophila Proteins - antagonists & inhibitors | Protein-Serine-Threonine Kinases - metabolism | RNA-Binding Proteins - antagonists & inhibitors | Guanine Nucleotide Exchange Factors - genetics | Protein-Serine-Threonine Kinases - genetics | Ubiquitin-Protein Ligases - metabolism | Rats | Nuclear Proteins - metabolism | Electron Transport Chain Complex Proteins - genetics | Mitochondria - metabolism | DNA-Binding Proteins - genetics | Rats, Sprague-Dawley | Mitochondrial Membranes - metabolism | Heterogeneous-Nuclear Ribonucleoprotein Group F-H - metabolism | Animals | Electron Transport Chain Complex Proteins - metabolism | Drosophila Proteins - genetics | Lipid Peroxidation | Ubiquitin-Protein Ligases - genetics | RNA-Binding Proteins - metabolism | RNA, Small Interfering - metabolism | Biosynthesis | Mitochondrial DNA | Messenger RNA | Genetic translation | Genomics | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Mutations in CIZ1 cause adult onset primary cervical dystonia
by Xiao, Jianfeng and Uitti, Ryan J and Zhao, Yu and Vemula, Satya R and Perlmutter, Joel S and Wszolek, Zbigniew K and Maraganore, Demetrius M and Auburger, Georg and Leube, Barbara and Lehnhoff, Katja and LeDoux, Mark S
Annals of neurology, ISSN 0364-5134, 04/2012, Volume 71, Issue 4, pp. 458 - 469
Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Biological and medical sciences | Medical sciences | Diseases of striated muscles. Neuromuscular diseases | Amino Acid Sequence | Genetic Predisposition to Disease - genetics | Humans | Molecular Sequence Data | Genotype | Male | Torticollis - genetics | DNA Mutational Analysis | Pedigree | Adult | Female | Mutation | Nuclear Proteins - genetics | Genetic Linkage | Muscular system | FDA approval | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights