X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2100) 2100
Book Review (202) 202
Publication (131) 131
Newsletter (34) 34
Book Chapter (12) 12
Book / eBook (8) 8
Conference Proceeding (3) 3
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (2030) 2030
humans (1814) 1814
male (1246) 1246
schizophrenia (1200) 1200
schizophrenia - enzymology (1154) 1154
female (1032) 1032
adult (868) 868
middle aged (653) 653
neurosciences (582) 582
psychiatry (562) 562
animals (535) 535
schizophrenia - genetics (487) 487
schizophrenia - drug therapy (343) 343
blood platelets - enzymology (293) 293
brain - enzymology (287) 287
aged (275) 275
monoamine oxidase - blood (259) 259
rats (259) 259
brain (256) 256
pharmacology & pharmacy (245) 245
adolescent (243) 243
genotype (238) 238
schizophrenia - blood (200) 200
mice (189) 189
case-control studies (188) 188
genetics & heredity (180) 180
antipsychotic agents - therapeutic use (176) 176
bipolar disorder - enzymology (174) 174
schizophrenia - metabolism (174) 174
bipolar disorder (171) 171
abridged index medicus (169) 169
enzymes (168) 168
catechol o-methyltransferase - genetics (167) 167
biochemistry & molecular biology (163) 163
clinical neurology (144) 144
association (140) 140
chronic disease (140) 140
dopamine (132) 132
genetic predisposition to disease (131) 131
prefrontal cortex (130) 130
alleles (129) 129
mental disorders (126) 126
schizophrenic psychology (124) 124
physiological aspects (123) 123
antipsychotic agents - pharmacology (119) 119
expression (118) 118
analysis (117) 117
polymorphism, genetic (117) 117
polymorphism (114) 114
gene frequency (113) 113
neurons (111) 111
research (111) 111
schizophrenia - physiopathology (110) 110
risk factors (106) 106
oxidative stress (105) 105
genetic aspects (102) 102
polymorphism, single nucleotide (102) 102
schizophrenia - diagnosis (102) 102
rats, sprague-dawley (101) 101
genetics (100) 100
gene expression (97) 97
prefrontal cortex - enzymology (97) 97
neurons - enzymology (94) 94
metabolism (89) 89
psychotic disorders - enzymology (89) 89
schizophrenia - pathology (89) 89
dopamine - metabolism (87) 87
proteins (87) 87
neurology (85) 85
rat-brain (82) 82
genes (81) 81
psychiatric status rating scales (81) 81
reference values (81) 81
antipsychotic agents - adverse effects (79) 79
article (79) 79
mental disorders - enzymology (79) 79
brain - metabolism (78) 78
cell biology (78) 78
erythrocytes - enzymology (78) 78
multidisciplinary sciences (77) 77
young adult (75) 75
catechol-o-methyltransferase (74) 74
kinetics (74) 74
research article (74) 74
child (73) 73
haloperidol (73) 73
schizophrenia, paranoid - enzymology (73) 73
sex factors (73) 73
monoamine oxidase - metabolism (72) 72
bipolar disorder - genetics (71) 71
comt (71) 71
dose-response relationship, drug (71) 71
polymorphism, single nucleotide - genetics (71) 71
risk (71) 71
psychosis (70) 70
aged, 80 and over (69) 69
brain - drug effects (69) 69
gene (69) 69
medicine (69) 69
alzheimers-disease (68) 68
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1961) 1961
Russian (80) 80
German (25) 25
Polish (23) 23
Chinese (17) 17
Japanese (10) 10
French (7) 7
Spanish (6) 6
Italian (4) 4
Czech (3) 3
Hungarian (3) 3
Croatian (1) 1
Finnish (1) 1
Hebrew (1) 1
Portuguese (1) 1
Romanian (1) 1
Slovak (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Molecular Neurobiology, ISSN 0893-7648, 10/2015, Volume 52, Issue 2, pp. 826 - 836
The carnitine palmitoyl transferase (CPT) system is a multiprotein complex with catalytic activity localized within a core represented by CPT1 and CPT2 in the... 
Metabolic-cognitive syndrome | Neurology | Neurosciences | Biomedicine | Oxidative phosphorylation | Nutrition | Neurobiology | AMP-activated protein kinase | Malonyl-CoA | Cell Biology | OXIDATIVE STRESS | ACETYL-L-CARNITINE | FATTY-ACID-METABOLISM | AMP-activated | ENDOPLASMIC-RETICULUM STRESS | PALMITOYLTRANSFERASE-I | NEUROSCIENCES | protein kinase | ENERGY HOMEOSTASIS | INSULIN-RESISTANCE | MITOCHONDRIAL DYSFUNCTION | REGULATES FOOD-INTAKE | PARKINSONS-DISEASE | Endocannabinoids - metabolism | Mitochondria - enzymology | Carnitine O-Palmitoyltransferase - genetics | Humans | Brain - enzymology | Carnitine - metabolism | Cardiovascular Diseases - enzymology | Eating - physiology | Malonyl Coenzyme A - metabolism | Carnitine O-Palmitoyltransferase - deficiency | Energy Metabolism - physiology | Fatty Acids - metabolism | Metabolic Syndrome - enzymology | Ceramides - metabolism | Mitochondria, Muscle - enzymology | Oxidation-Reduction | Diabetes Mellitus, Type 2 - enzymology | Carnitine O-Palmitoyltransferase - physiology | Hypoglycemia | Mitochondria, Liver - enzymology | Disease Progression | Learning - physiology | Insulin - metabolism | Animals | Multienzyme Complexes - physiology | Protein Isoforms | Lipid Metabolism, Inborn Errors | Neurodegenerative Diseases - enzymology | Proteins | Nervous system diseases | Schizophrenia | Mitochondrial DNA | Fatty acids | Alzheimer's disease | Carnitine | Neurophysiology | Enzymes | Neuropsychology | Neurological disorders | Index Medicus
Journal Article
FEBS Journal, ISSN 1742-464X, 2014, Volume 281, Issue 3, pp. 708 - 723
Human D-amino acid oxidase (EC 1.4.3.3; hDAAO) is a peroxisomal flavoenzyme significantly enriched in the mammalian brain. hDAAO has been proposed to play... 
Schizophrenia | Regulation | D-serine | Neuromodulator | Degradation pathway | GENE G72 | NMDA RECEPTORS | UBIQUITIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLYCINE SITE | degradation pathway | schizophrenia | D-ASPARTATE RECEPTOR | RACEMASE | ASTROCYTES | neuromodulator | PREFRONTAL CORTEX | PROTEASOME-DEPENDENT DEGRADATION | regulation | Mitochondria - enzymology | Humans | Brain - enzymology | Lysosomes - enzymology | Green Fluorescent Proteins - genetics | Endosomes - metabolism | Recombinant Fusion Proteins | Brain - metabolism | Cytosol - enzymology | Protease Inhibitors - pharmacology | Proteolysis - drug effects | Lysosomes - metabolism | Proteasome Endopeptidase Complex - drug effects | Ubiquitination - drug effects | Endosomes - drug effects | Neurons - metabolism | D-Amino-Acid Oxidase - metabolism | Neurons - drug effects | Lysosomes - drug effects | Green Fluorescent Proteins - metabolism | Bacterial Proteins - genetics | D-Amino-Acid Oxidase - genetics | Mitochondria - metabolism | Nerve Tissue Proteins - genetics | Peroxisomes - metabolism | Brain - drug effects | Nerve Tissue Proteins - metabolism | Carrier Proteins - genetics | Carrier Proteins - metabolism | Neurons - enzymology | Protein Stability - drug effects | Cell Line, Tumor | Bacterial Proteins - metabolism | Cytosol - metabolism | Luminescent Proteins - genetics | Endosomes - enzymology | Peroxisomes - enzymology | Luminescent Proteins - metabolism | Oxidases | Ubiquitin | Ammonium compounds | Brain | Gliomas | Ammonium paratungstate | Fluorescence | Amino acids | Glutamate | Biodegradation | Proteins | Enzymes | Metabolism | Molecular biology | Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2018, Volume 102, Issue 2, pp. 278 - 295
Copy-number variations (CNVs) are strong risk factors for neurodevelopmental and psychiatric disorders. The 15q13.3 microdeletion syndrome region contains up... 
15q13.3 microdeletion syndrome | neurodevelopmental disorder | copy-number variation | OTUD7A | dendrite | dendritic spine | synapse | schizophrenia | autism spectrum disorder | deubiquitinase | DE-NOVO MUTATIONS | MENTAL-RETARDATION | COPY-NUMBER | RECEPTOR KNOCKOUT MICE | MOUSE MODEL | NEUROPSYCHIATRIC DISEASES | GENETICS & HEREDITY | AUTISM SPECTRUM DISORDER | 16P11.2 DELETION | DEVELOPMENTAL DELAY | GENOME-WIDE ASSOCIATION | Seizures - genetics | Humans | Deubiquitinating Enzymes - physiology | Male | Dendritic Spines - metabolism | Neurodevelopmental Disorders - genetics | Intellectual Disability - genetics | Chromosome Disorders - enzymology | Gene Deletion | Intellectual Disability - enzymology | Female | Neurodevelopmental Disorders - enzymology | Prosencephalon - pathology | Chromosome Deletion | Autism Spectrum Disorder - genetics | Endopeptidases - metabolism | Seizures - enzymology | Genetic Association Studies | Chromosomes, Human, Pair 15 - genetics | Deubiquitinating Enzymes - genetics | Phenotype | Animals | Endopeptidases - genetics | Mice | Chromosomes, Human, Pair 15 - enzymology | Chromosome Disorders - genetics | Usage | Copy number variations | Pervasive developmental disorders | Nucleotide sequencing | Research | Gene expression | Health aspects | Risk factors | DNA sequencing | Index Medicus
Journal Article
Journal Article
Journal Article
The International Journal of Neuropsychopharmacology, ISSN 1461-1457, 9/2011, Volume 14, Issue 8, pp. 1069 - 1074
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2012, Volume 7, Issue 5, pp. e38172 - e38172
We previously identified a significant bipolar spectrum disorder linkage peak on 15q25-26 using 35 extended families with a broad clinical phenotype, including... 
CELL-ADHESION MOLECULE | DIAGNOSTIC INTERVIEW | EMBRYONIC FORM | MULTIDISCIPLINARY SCIENCES | BIPOLAR AFFECTIVE-DISORDER | GENOME-WIDE SCAN | SCHIZOPHRENIA | LINKAGE | ASSOCIATION | POLYSIALYLTRANSFERASE | POLYSIALIC ACID | Haplotypes | Mood Disorders - enzymology | Mood Disorders - genetics | Humans | Middle Aged | Genetic Loci - genetics | Male | Prefrontal Cortex - growth & development | Case-Control Studies | Schizophrenia - genetics | Base Sequence | Adult | Female | Schizophrenia - enzymology | Prefrontal Cortex - enzymology | Psychotic Disorders - enzymology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Sialyltransferases - genetics | Chromosome Mapping | Chromosomes, Human, Pair 15 - genetics | Bipolar Disorder - genetics | Psychotic Disorders - genetics | Gene Expression Regulation, Enzymologic - genetics | Polymorphism, Single Nucleotide - genetics | Bipolar Disorder - enzymology | Cohort Studies | Enzymes | Brain | Depression, Mental | Genes | Disease susceptibility | Genetic aspects | Gene expression | Neurosciences | Network formation | Mental disorders | Schizophrenia | Risk | Bipolar disorder | Single-nucleotide polymorphism | Mental depression | Variance analysis | Cell adhesion & migration | Plasticity (neural) | Proteins | Studies | Autism | Mood | Coding | Plasticity | Gene mapping | Chromosome 15 | Chromosomes | Index Medicus
Journal Article
Neuropsychopharmacology, ISSN 0893-133X, 03/2016, Volume 41, Issue 4, pp. 1080 - 1092
Journal Article