(Q30459881)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

title

Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

main subject

autism spectrum disorder

0 references

0 references

0 references

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

author name string

Takeshi Hiramoto

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Gina Kang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Yasushi Satoh

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Raju Kucherlapati

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Yasuhiro Watanabe

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

Noboru Hiroi

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

publication date

9 September 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

issue

24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

page(s)

4775-4785

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

Enriched environment and physical activity reduce microglia and influence the fate of NG2 cells in the amygdala of adult mice

12 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Solving the autism puzzle a few pieces at a time

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Patterns of cardiac and extracardiac anomalies in adults with tetralogy of fallot

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Disruption of Adult Neurogenesis in the Olfactory Bulb Affects Social Interaction but not Maternal Behavior

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Prefrontal cortical inputs to the basal amygdala undergo pruning during late adolescence in the rat.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Constitutional mechanisms of vulnerability and resilience to nicotine dependence

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

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.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Neurodevelopment and executive function in autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Ultrasonic vocalizations: a tool for behavioural phenotyping of mouse models of neurodevelopmental disorders.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Unusual repertoire of vocalizations in the BTBR T+tf/J mouse model of autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Mechanisms and functional implications of adult neurogenesis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Structural variation of chromosomes in autism spectrum disorder

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Mouse behavioral assays relevant to the symptoms of autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Can neuroscience be integrated into the DSM-V?

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Dopamine D2 receptor stimulation promotes the proliferation of neural progenitor cells in adult mouse hippocampus

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Social skills and executive function deficits in children with the 22q11 Deletion Syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Neuron number decreases in the rat ventral, but not dorsal, medial prefrontal cortex between adolescence and adulthood

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Inhibitory control in high-functioning autism: decreased activation and underconnectivity in inhibition networks

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Ablation of hippocampal neurogenesis impairs contextual fear conditioning and synaptic plasticity in the dentate gyrus

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Phenotypic and functional characterization of adult brain neuropoiesis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Arrested neuronal proliferation and impaired hippocampal function following fractionated brain irradiation in the adult rat.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

The neurobiological basis of spontaneous alternation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

The 22q11 deletion syndromes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Communication disorders in the 22Q11.2 microdeletion syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

The Emanuel Miller Memorial Lecture 1997. Change and continuity in the development of children with autism

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

22q11 deletion syndrome in adults with schizophrenia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Autism as a strongly genetic disorder: evidence from a British twin study

14 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

14 July 2018

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Velo-cardio-facial syndrome: language and psychological profiles.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.

14 July 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Communication issues in 22q11.2 deletion syndrome: children at risk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Executive functions and memory abilities in children with 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

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/10.1093%2FHMG%2FDDR404

Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Changes in molecular composition of rat medial prefrontal cortex synapses during adolescent development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Increasing Interaction of amygdalar afferents with GABAergic interneurons between birth and adulthood

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Neurogenesis decreases during brain maturation from adolescence to adulthood

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Pleiotropic impact of constitutive fosB inactivation on nicotine-induced behavioral alterations and stress-related traits in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Environmental enrichment stimulates progenitor cell proliferation in the amygdala.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Electroconvulsive seizures stimulate glial proliferation and reduce expression of Sprouty2 within the prefrontal cortex of rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Electroconvulsive seizures induce proliferation of NG2-expressing glial cells in adult rat amygdala

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Electroconvulsive seizure treatment increases cell proliferation in rat frontal cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Inhibition of adult hippocampal neurogenesis disrupts contextual learning but spares spatial working memory, long-term conditional rule retention and spatial reversal.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Monoamine oxidase A knockout mice exhibit impaired nicotine preference but normal responses to novel stimuli

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR404

Risk factors for the emergence of psychotic disorders in adolescents with 22q11.2 deletion syndrome.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3221538

Comparing phenotypes in patients with idiopathic autism to patients with velocardiofacial syndrome (22q11 DS) with and without autism

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21908517

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21908517

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Effects of isolation, handling and novelty on the pituitary--adrenal response in the mouse

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21908517

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDR404

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21908517%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

PubMed publication ID

21908517

1 reference