Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice (Q30479118)

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English	Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice	scientific article

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scholarly article

1 reference

Europe PubMed Central

19 August 2017

Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice (English)

1 reference

Europe PubMed Central

19 August 2017

object named as

Go Suzuki

1

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Kathryn M Harper

object named as

Kathryn M Harper

2

0 references

Bernice E. Morrow

object named as

Bernice Morrow

10

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Pekka T. Männistö

object named as

Pekka T Männistö

11

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author name string

Takeshi Hiramoto

3

1 reference

Europe PubMed Central

19 August 2017

Birgit Funke

4

1 reference

Europe PubMed Central

19 August 2017

MoonSook Lee

5

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Europe PubMed Central

19 August 2017

Gina Kang

6

1 reference

Europe PubMed Central

19 August 2017

Mahalah Buell

7

1 reference

Europe PubMed Central

19 August 2017

Mark A Geyer

8

1 reference

Europe PubMed Central

19 August 2017

Raju Kucherlapati

9

1 reference

Europe PubMed Central

19 August 2017

Soh Agatsuma

12

1 reference

Europe PubMed Central

19 August 2017

Noboru Hiroi

13

1 reference

Europe PubMed Central

19 August 2017

publication date

19 July 2009

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Europe PubMed Central

19 August 2017

Human Molecular Genetics

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Europe PubMed Central

19 August 2017

18

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Europe PubMed Central

19 August 2017

20

1 reference

Europe PubMed Central

19 August 2017

3914-3925

1 reference

Europe PubMed Central

19 August 2017

Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice

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A 15q13.3 microdeletion segregating with autism

1 reference

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Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.

1 reference

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Failure of neuronal homeostasis results in common neuropsychiatric phenotypes

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Modeling genetic inheritance of copy number variations.

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Genetic dissection of the role of catechol-O-methyltransferase in cognition and stress reactivity in mice

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Clinical variability of the 22q11.2 duplication syndrome.

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Large recurrent microdeletions associated with schizophrenia

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Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

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Structural variation of chromosomes in autism spectrum disorder

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No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics

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20 June 2018

Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplication

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20 June 2018

Paired-end mapping reveals extensive structural variation in the human genome

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20 June 2018

Strong association of de novo copy number mutations with autism

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The influence of visual ability on learning and memory performance in 13 strains of mice

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DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features.

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Repeated social defeat causes increased anxiety-like behavior and alters splenocyte function in C57BL/6 and CD-1 mice

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Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

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Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond

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A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice

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Microduplication and triplication of 22q11.2: a highly variable syndrome

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

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Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia

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The catechol-O-methyltransferase polymorphism: relations to the tonic-phasic dopamine hypothesis and neuropsychiatric phenotypes

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A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome

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A comprehensive analysis of 22q11 gene expression in the developing and adult brain

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Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

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

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Retinal degeneration mutants in the mouse

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A common molecular basis for rearrangement disorders on chromosome 22q11

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Distribution of catechol-O-methyltransferase expression in human central nervous system.

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Lesions of the frontal cortex, hippocampus, and intralaminar thalamic nuclei have distinct effects on remembering in rats.

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Determination of catechol-O-methyltransferase activity by high-performance liquid chromatography with electrochemical detection.

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20 June 2018

Autistic disorder and 22q11.2 duplication.

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Effect of COMT Val158Met polymorphism on the Continuous Performance Test, Identical Pairs Version: tuning rather than improving performance

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Association study of a functional catechol-O-methyltransferase-gene polymorphism and cognitive function in healthy females

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Prefrontal cortex and hippocampus in posttraumatic functional recovery: spatial delayed alternation by rats subjected to transection of the fimbria-fornix and/or ablation of the prefrontal cortex.

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Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study.

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Microduplication 22q11.2: a benign polymorphism or a syndrome with a very large clinical variability and reduced penetrance?--Report of two families.

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Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.

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Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flow.

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12 December 2020

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10.1093/HMG/DDP334

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

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