(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

PubMed publication ID

18769474

1 reference