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Genetic vs. pharmacological inactivation of COMT influences cannabinoid-induced expression of schizophrenia-related phenotypes.
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- International Journal of Neuropsychopharmacology, 2012, v. 15, n. 9, p. 1331, doi. 10.1017/S1461145711001581
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- Article
Analysis of prepulse inhibition in mouse lines overexpressing 22q11.2 orthologues.
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- International Journal of Neuropsychopharmacology, 2009, v. 12, n. 7, p. 983, doi. 10.1017/S1461145709000492
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- Publication type:
- Article
Family history identifies sporadic schizoaffective disorder as a subtype for genetic studies.
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- South African Journal of Psychiatry, 2020, v. 26, p. 1, doi. 10.4102/sajpsychiatry.v26i0.1393
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- Publication type:
- Article
Decreased Phosphorylation of NMDA Receptor Type 1 at Serine 897 in Brains of Patients with Schizophrenia.
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- Journal of Neuroscience, 2004, v. 24, n. 7, p. 1561, doi. 10.1523/JNEUROSCI.4650-03.2004
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- Article
Combined small-molecule inhibition accelerates the derivation of functional cortical neurons from human pluripotent stem cells.
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- Nature Biotechnology, 2017, v. 35, n. 2, p. 154, doi. 10.1038/nbt.3777
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- Article
De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.
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- Nature Genetics, 2012, v. 44, n. 12, p. 1365, doi. 10.1038/ng.2446
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- Article
Exome sequencing supports a de novo mutational paradigm for schizophrenia.
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- Nature Genetics, 2011, v. 43, n. 9, p. 864, doi. 10.1038/ng.902
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- Article
Strong association of de novo copy number mutations with sporadic schizophrenia.
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- Nature Genetics, 2008, v. 40, n. 7, p. 880, doi. 10.1038/ng.162
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- Article
Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model.
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- Nature Genetics, 2008, v. 40, n. 6, p. 751, doi. 10.1038/ng.138
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- Article
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.
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- Nature Genetics, 2006, v. 38, n. 5, p. 556, doi. 10.1038/ng1770
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- Article
Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia.
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- Nature Genetics, 2004, v. 36, n. 7, p. 725, doi. 10.1038/ng1375
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- Publication type:
- Article
Convergent evidence for impaired AKT1-GSK3ß signaling in schizophrenia.
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- Nature Genetics, 2004, v. 36, n. 2, p. 131, doi. 10.1038/ng1296
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- Article
Advancing drug discovery for schizophrenia.
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- Annals of the New York Academy of Sciences, 2011, v. 1236, n. 1, p. 30, doi. 10.1111/j.1749-6632.2011.06216.x
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- Article
Clinical Characteristics of an Afrikaner Founder Population Recruited for a Schizophrenia Genetic Study.
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- Annals of the New York Academy of Sciences, 2009, v. 1151, p. 85, doi. 10.1111/j.1749-6632.2008.03453.x
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- Article
Costly Genes.
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- PLoS Genetics, 2020, v. 16, n. 8, p. 1, doi. 10.1371/journal.pgen.1008889
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- Article
Schizophrenia genetics: uncovering positional candidate genes.
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- European Journal of Human Genetics, 2006, v. 14, n. 5, p. 512, doi. 10.1038/sj.ejhg.5201587
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- Publication type:
- Article
Site-Specific Role of Catechol-O-Methyltransferase in Dopamine Overflow within Prefrontal Cortex and Dorsal Striatum.
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- Journal of Neuroscience, 2007, v. 27, n. 38, p. 10196, doi. 10.1523/JNEUROSCI.0665-07.2007
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- Publication type:
- Article
Lack of increased oxidative stress in catechol-O-methyltransferase (COMT)-deficient mice.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2004, v. 370, n. 4, p. 279, doi. 10.1007/s00210-004-0967-9
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- Article
Impaired hippocampal–prefrontal synchrony in a genetic mouse model of schizophrenia.
- Published in:
- Nature, 2010, v. 464, n. 7289, p. 763, doi. 10.1038/nature08855
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- Article
Fine Mapping on Chromosome 13q32-34 and Brain Expression Analysis Implicates MYO16 in Schizophrenia.
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- Neuropsychopharmacology, 2014, v. 39, n. 4, p. 934, doi. 10.1038/npp.2013.293
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- Article
Chronic Adolescent Exposure to Delta-9-Tetrahydrocannabinol in COMT Mutant Mice: Impact on Indices of Dopaminergic, Endocannabinoid and GABAergic Pathways.
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- Neuropsychopharmacology, 2012, v. 37, n. 7, p. 1773, doi. 10.1038/npp.2012.24
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- Publication type:
- Article
Chronic Adolescent Exposure to Δ-9-Tetrahydrocannabinol in COMT Mutant Mice: Impact on Psychosis-Related and Other Phenotypes.
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- Neuropsychopharmacology, 2010, v. 35, n. 11, p. 2262, doi. 10.1038/npp.2010.100
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- Publication type:
- Article
d-Amphetamine responses in catechol-O-methyltransferase (COMT) disrupted mice.
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- Psychopharmacology, 2004, v. 172, n. 1, p. 1, doi. 10.1007/s00213-003-1627-3
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- Article
Quantitative role of COMT in dopamine clearance in the prefrontal cortex of freely moving mice.
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- Journal of Neurochemistry, 2010, v. 114, n. 6, p. 1745, doi. 10.1111/j.1471-4159.2010.06889.x
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- Publication type:
- Article
A Transient Inhibition and Permanent Lack of Catechol- O-Methyltransferase have Minor Effects on Feeding Pattern of Female Rodents.
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- Basic & Clinical Pharmacology & Toxicology, 2012, v. 110, n. 4, p. 307, doi. 10.1111/j.1742-7843.2011.00783.x
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- Publication type:
- Article
Increase in Free Choice Oral Ethanol Self-Administration in Catechol- O-Methyltransferase Gene-Disrupted Male Mice.
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- Basic & Clinical Pharmacology & Toxicology, 2008, v. 103, n. 4, p. 297, doi. 10.1111/j.1742-7843.2008.00267.x
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- Publication type:
- Article
Stress-Induced Analgesia and Morphine Responses Are Changed in Catechol- O-methyltransferase-Deficient Male Mice.
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- Basic & Clinical Pharmacology & Toxicology, 2008, v. 103, n. 4, p. 367, doi. 10.1111/j.1742-7843.2008.00289.x
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- Publication type:
- Article
Brain catecholamine metabolism in catechol-O -methyltransferase (COMT)-deficient mice.
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- European Journal of Neuroscience, 2002, v. 15, n. 2, p. 246, doi. 10.1046/j.0953-816x.2001.01856.x
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- Article
22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
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- 2010
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- Publication type:
- journal article
Diverse types of genetic variation converge on functional gene networks involved in schizophrenia.
- Published in:
- Nature Neuroscience, 2012, v. 15, n. 12, p. 1723, doi. 10.1038/nn.3261
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- Article
The best of times, the worst of times for psychiatric disease.
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- Nature Neuroscience, 2012, v. 15, n. 6, p. 811, doi. 10.1038/nn.3115
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- Article
Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion.
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- Nature Neuroscience, 2008, v. 11, n. 11, p. 1302, doi. 10.1038/nn.2204
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- Article
Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice.
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- Nature Neuroscience, 2005, v. 8, n. 11, p. 1586, doi. 10.1038/nn1562
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- Publication type:
- Article
Family history identifies sporadic schizoaffective disorder as a subtype for genetic studies.
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- South African Journal of Obstetrics & Gynaecology, 2020, v. 26, p. 1, doi. 10.4102/sajpsychiatry.v26i0.1393
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- Publication type:
- Article
The gene encoding proline dehydrogenase modulates sensorimotor gating in mice.
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- Nature Genetics, 1999, v. 21, n. 4, p. 434, doi. 10.1038/7777
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- Article
Neuromotor deficits in children with the 22q11 deletion syndrome.
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- Movement Disorders, 2006, v. 21, n. 12, p. 2082, doi. 10.1002/mds.21103
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- Article
The 22q11.2 microdeletion: Fifteen years of insights into the genetic and neural complexity of psychiatric disorders
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- International Journal of Developmental Neuroscience, 2011, v. 29, n. 3, p. 259, doi. 10.1016/j.ijdevneu.2010.09.007
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- Article
The Pattern of Cortical Dysfunction in a Mouse Model of a Schizophrenia-Related Microdeletion.
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- Journal of Neuroscience, 2013, v. 33, n. 37, p. 14825, doi. 10.1523/JNEUROSCI.1611-13.2013
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- Publication type:
- Article