Proline affects brain function in 22q11DS children with the low activity COMT 158 allele - Wikidata - wikimedia - TriplyDB

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

http://www.wikidata.org/entity/Q30483462

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Early interventions in risk groups for schizophrenia: what are we waiting for?Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome Cytosolic Accumulation of L-Proline Disrupts GABA-Ergic Transmission through GAD Blockade Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.Psychophysiological markers of vulnerability to psychopathology in men with an extra X chromosome (XXY).22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.Proline and COMT status affect visual connectivity in children with 22q11.2 deletion syndrome.Velo-Cardio-Facial Syndrome.The development of cognitive control in children with chromosome 22q11.2 deletion syndrome Proton magnetic resonance spectroscopy in 22q11 deletion syndrome.Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes Association of variants in DRD2 and GRM3 with motor and cognitive function in first-episode psychosis Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome.Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome Effects of the val(158)met catechol-O-methyltransferase gene polymorphism on olfactory processing in schizophrenia.Glutamatergic markers, age, intellectual functioning and psychosis in 22q11 deletion syndrome.COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.22q11.2 deletion syndrome A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndrome Evidence that COMT genotype and proline interact on negative-symptom outcomes in schizophrenia and bipolar disorder.Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion.The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.Disrupted working memory circuitry and psychotic symptoms in 22q11.2 deletion syndrome.Behavioral and neurochemical effects of proline.Child development and structural variation in the human genome.Improving patient tolerability in immunoglobulin treatment: focus on stabilizer effects.Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications.PRODH rs450046 and proline x COMT Val¹⁵⁸ Met interaction effects on intelligence and startle in adults with 22q11 deletion syndrome.Executive functions and memory abilities in children with 22q11.2 deletion syndrome.Critical region within 22q11.2 linked to higher rate of autism spectrum disorder.Striatal D₂ receptor binding in 22q11 deletion syndrome: an [¹²³I]IBZM SPECT study.Auditory Verbal Hallucinations in Schizophrenia from a Levels of Explanation Perspective.Long-term proline exposure alters nucleotide catabolism and ectonucleotidase gene expression in zebrafish brain.Startle reactivity and prepulse inhibition of the acoustic startle response are modulated by catechol-O-methyl-transferase Val(158) Met polymorphism in adults with 22q11 deletion syndrome.The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2.Profiling of Amino Acids and Their Derivatives Biogenic Amines Before and After Antipsychotic Treatment in First-Episode Psychosis.Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia – relationship with COMT Val108/158 Met polymorphism, gender and symptomatology

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P2860

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

http://www.wikidata.org/entity/Q30483462

description

2008 nî lūn-bûn

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2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

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Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

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type

label

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

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Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

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prefLabel

Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

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Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

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Neuropsychopharmacology

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Proline affects brain function in 22q11DS children with the low activity COMT 158 allele

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Bert Dorland

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Beverly S Emanuel

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Eric F Rappaport

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Frits A Beemer

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Jacob A S Vorstman

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Mirjam Sprong

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Monique E J Sijmens-Morcus

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Monique G de Sain

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P2860

The dopamine D(3) receptor Ser9Gly polymorphism modulates prepulse inhibition of the acoustic startle reflex

Functional consequences of PRODH missense mutations

Impaired prepulse inhibition of acoustic and tactile startle response in patients with Huntington's disease.

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

A common molecular basis for rearrangement disorders on chromosome 22q11

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

Molecular cloning and expression of a high affinity L-proline transporter expressed in putative glutamatergic pathways of rat brain

The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10

Lower prepulse inhibition in children with the 22q11 deletion syndrome.

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739-746

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scholarly article

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10.1038/NPP.2008.132

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3

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34

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Herman van Engeland

Bruce I Turetsky

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2008-09-03T00:00:00Z

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23234007

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1019042379

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18769474

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2817942

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