Proline affects brain function in 22q11DS children with the low activity COMT 158 allele (Q30483462)

18 October 2017

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

1 reference

18 October 2017

11

Herman van Engeland

1 reference

18 October 2017

12

Chantal Kemner

1 reference

18 October 2017

2

Bruce I Turetsky

1 reference

18 October 2017

10

René S Kahn

1 reference

18 October 2017

Jacob A S Vorstman

1

1 reference

18 October 2017

Monique E J Sijmens-Morcus

3

1 reference

18 October 2017

Monique G de Sain

4

1 reference

18 October 2017

Bert Dorland

5

1 reference

18 October 2017

Mirjam Sprong

6

1 reference

18 October 2017

Eric F Rappaport

7

1 reference

18 October 2017

Frits A Beemer

8

1 reference

18 October 2017

Beverly S Emanuel

9

1 reference

18 October 2017

language of work or name

English

0 references

publication date

3 September 2008

1 reference

18 October 2017

Neuropsychopharmacology

1 reference

18 October 2017

34

1 reference

18 October 2017

3

1 reference

18 October 2017

739-746

1 reference

Neurophysiological endophenotypes across bipolar and schizophrenia psychosis

18 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic women

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Towards a functional topography of sensory gating areas: invasive P50 recording and electrical stimulation mapping in epilepsy surgery candidates.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Neurophysiological endophenotypes of schizophrenia: the viability of selected candidate measures

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Lower prepulse inhibition in children with the 22q11 deletion syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Functional consequences of PRODH missense mutations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Catechol O -methyltransferase val 158 -met genotype and individual variation in the brain response to amphetamine

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Catechol O-methyltransferase mRNA expression in human and rat brain: evidence for a role in cortical neuronal function

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Stress activation of glutamate neurotransmission in the prefrontal cortex: implications for dopamine-associated psychiatric disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Neuropsychiatric disorders in the 22q11 deletion syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

A common molecular basis for rearrangement disorders on chromosome 22q11

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Prefrontal cortex regulates inhibition and excitation in distributed neural networks

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

The mammalian brain high-affinity L-proline transporter is enriched preferentially in synaptic vesicles in a subpopulation of excitatory nerve terminals in rat forebrain.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Proline-induced inhibition of glutamate release in hippocampal area CA1.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Proline-induced potentiation of glutamate transmission

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Normalization by nicotine of deficient auditory sensory gating in the relatives of schizophrenics

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

NMDA receptor-mediated depolarizing action of proline on CA1 pyramidal cells

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Effects of bromocriptine and haloperidol on prepulse inhibition of the acoustic startle response in man.

20 June 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Prepulse inhibition and P50 suppression are both deficient but not correlated in schizophrenia patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Localization of the brain-specific high-affinity l-proline transporter in cultured hippocampal neurons: molecular heterogeneity of synaptic terminals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Neuronal substrates of sensory gating within the human brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Effect of d-amphetamine on prepulse inhibition of the startle reflex in humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Mitochondrial toxin 3-nitropropionic acid produces startle reflex abnormalities and striatal damage in rats that model some features of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Cortical mechanisms of retinal and extraretinal smooth pursuit eye movements to different target velocities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Concurrent assessment of acoustic startle and auditory P50 evoked potential measures of sensory inhibition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Effects of nicotine on hippocampal and cingulate activity during smooth pursuit eye movement in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Catechol O-methyltransferase polymorphism and eye tracking in schizophrenia: a preliminary report

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Neurobiology of smooth pursuit eye movement deficits in schizophrenia: an fMRI study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPP.2008.132

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2817942

Normalization of auditory physiology by cigarette smoking in schizophrenic patients

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18769474

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18769474

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18769474

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NPP.2008.132

1 reference

Dimensions Publication ID

18 October 2017

0 references

1 reference

18 October 2017

1 reference