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Nature (London), ISSN 0028-0836, 2014, Volume 505, Issue 7483, pp. 361 - 366
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Brain - anatomy & histology | Humans | Middle Aged | Male | Brain - abnormalities | Case-Control Studies | Iceland | Brain - metabolism | Young Adult | Fertility - genetics | Schizophrenia - genetics | Cognition - physiology | Adult | Female | Autistic Disorder - genetics | Chromosome Deletion | Genetic Predisposition to Disease | Chromosomes, Human - genetics | DNA Copy Number Variations - genetics | Chromosomes, Human, Pair 15 - genetics | Dyslexia - genetics | Neuropsychological Tests | Magnetic Resonance Imaging | Phenotype | Adolescent | Heterozygote | Learning Disorders - genetics | Aged | Autism | Copy number variations | Physiological aspects | Schizophrenia | Dyslexia | Genetic aspects | Cognition | Research | Population | Cognition & reasoning | Disease | Memory | Index Medicus
Journal Article
American journal of medical genetics. Part B, Neuropsychiatric genetics, ISSN 1552-4841, 01/2018, Volume 177, Issue 1, pp. 21 - 34
Humans | Family/psychology | Genetic Predisposition to Disease/genetics | Male | schizophrenia | bipolar disorder | Polymorphism, Single Nucleotide/genetics | Psychotic Disorders/genetics | Adult | Female | Event-Related Potentials, P300 | Endophenotypes/blood | Schizophrenia/genetics | GENOME-WIDE ASSOCIATION | European Continental Ancestry Group/genetics | cognition | WHITE-MATTER | EEG | Europe | Risk Factors | UNAFFECTED 1ST-DEGREE RELATIVES | Brain/physiology | Multifactorial Inheritance/genetics | Bipolar Disorder/genetics | Neuropsychological Tests | MAUDSLEY FAMILY | single nucleotide polymorphism (SNP) | EVENT-RELATED POTENTIALS | PSYCHIATRIC-DISORDERS | GENETIC OVERLAP | EDINBURGH HIGH-RISK | Cognition/physiology | Australia | WORKING-MEMORY | Genetics & Heredity | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Family - psychology | Multifactorial Inheritance - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Bipolar Disorder - genetics | Brain - physiology | Psychotic Disorders - genetics | Schizophrenia - genetics | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Endophenotypes - blood | Medical research | Usage | Schizophrenia | Medicine, Experimental | Bipolar disorder | Genetic aspects | Risk factors | Statistical analysis | Mental disorders | Cognitive ability | Event-related potentials | Auditory evoked potentials | Genetic diversity | Psychosis | Genetic variance | Genotyping | Auditory discrimination learning | Ventricle | Structure-function relationships | Index Medicus
Journal Article
Neurology, ISSN 0028-3878, 05/2012, Volume 78, Issue 18, pp. 1434 - 1440
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Biological and medical sciences | Medical sciences | Diseases of striated muscles. Neuromuscular diseases | Olfaction Disorders - genetics | Glucosylceramidase - genetics | Genetic Testing | Memory Disorders - genetics | Humans | Middle Aged | Dementia - diagnosis | Male | Memory Disorders - diagnosis | Olfaction Disorders - diagnosis | Dementia - genetics | Basal Ganglia Diseases - genetics | DNA Mutational Analysis | beta-Glucosidase - genetics | Basal Ganglia Diseases - diagnosis | Mental Status Schedule | Adult | Cognitive Dysfunction - genetics | Female | Cognitive Dysfunction - diagnosis | Depressive Disorder - genetics | Depressive Disorder - diagnosis | Protein-Serine-Threonine Kinases - genetics | Genotype | Parkinson Disease - genetics | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 | Neuropsychological Tests | Phenotype | Parkinson Disease - diagnosis | Ubiquitin-Protein Ligases - genetics | Genetic Carrier Screening | Index Medicus | Abridged Index Medicus | Executive function | Demography | Parkinson's disease | Neurodegenerative diseases | Memory | spatial memory | Attention | Cognitive ability | Risk factors | Dementia disorders | Glucosylceramidase | Parkin protein | Mutation | LRRK2 protein | Age | Genotypes | Movement disorders | 165 | 201 | 205
Journal Article
2009, The extraordinary brain series, ISBN 1848728433, xxxiii, 343
Book
Neuropharmacology, ISSN 0028-3908, 05/2014, Volume 80, pp. 18 - 27
Intellectual disability disorder | Long-term potentiation | Epigenetics | Long-term memory | Nucleosome remodeling | Autism spectrum disorder | Chromatin remodeling | Pharmacology & Pharmacy | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Memory Disorders - physiopathology | Autistic Disorder - physiopathology | Autistic Disorder - metabolism | Memory Disorders - genetics | Epigenesis, Genetic | Humans | Memory | Actins - metabolism | Brain - enzymology | Memory Disorders - metabolism | Cognition Disorders - metabolism | Actins - genetics | Brain - metabolism | DNA-Binding Proteins - metabolism | Nucleosomes - enzymology | Neurons - metabolism | Nuclear Proteins - genetics | DNA Helicases - genetics | Autistic Disorder - genetics | Cognition Disorders - physiopathology | Chromosomal Proteins, Non-Histone - metabolism | Gene Expression Regulation | Chromatin Assembly and Disassembly | Nucleosomes - metabolism | Nuclear Proteins - metabolism | Cognition Disorders - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Chromosomal Proteins, Non-Histone - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | DNA Helicases - metabolism | Animals | Models, Biological | Neuronal Plasticity | Neurons - enzymology | Intellectual Disability - etiology | Mutation | Chromatin | Neurons | Genes | Histones | Schizophrenia | Gene expression | Index Medicus | chromatin remodeling | intellectual disability disorder | autism spectrum disorder | nucleosome remodeling | long-term memory | epigenetics | long-term potentiation
Journal Article
Molecular neurobiology, ISSN 0893-7648, 5/2016, Volume 53, Issue 4, pp. 2451 - 2467
Cerebrovascular pathology | Neurology | Neurosciences | Biomedicine | Blood–brain barrier dysfunction | Alzheimer’s disease | Neurobiology | Homocysteine | Cell Biology | Dementia | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Memory - drug effects | Glial Fibrillary Acidic Protein - genetics | Cadherins - metabolism | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Blood-Brain Barrier - physiopathology | Claudin-5 - metabolism | Microvessels - pathology | Male | Synapses - pathology | Glial Fibrillary Acidic Protein - metabolism | RNA, Messenger - metabolism | Antigens, CD - genetics | Alzheimer Disease - pathology | Antigens, CD - metabolism | Matrix Metalloproteinase 9 - metabolism | Cadherins - genetics | Synapses - drug effects | Alzheimer Disease - physiopathology | Hydrogen Sulfide - pharmacology | Cerebrovascular Circulation - drug effects | Matrix Metalloproteinase 2 - metabolism | Mice, Inbred C57BL | RNA, Messenger - genetics | Alzheimer Disease - drug therapy | Microvessels - drug effects | Claudin-5 - genetics | Cystathionine beta-Synthase - metabolism | Permeability | Blood-Brain Barrier - drug effects | Nerve Tissue Proteins - genetics | Blood-Brain Barrier - metabolism | Gene Expression Regulation - drug effects | Nerve Tissue Proteins - metabolism | Blood-Brain Barrier - pathology | Hydrogen Sulfide - therapeutic use | Intercellular Adhesion Molecule-1 - metabolism | Animals | Intercellular Adhesion Molecule-1 - genetics | Avoidance Learning - drug effects | Alzheimer Disease - genetics | Dizocilpine Maleate - pharmacology | Hydrogen sulfide | Methyl aspartate | Brain | RNA | Neurons | Intermediate filament proteins | Alzheimer's disease | Index Medicus | cerebrovascular pathology | dementia | blood brain barrier dysfunction
Journal Article