(Q33905573)

29 July 2017

Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice (English)

1 reference

29 July 2017

E J Young

1

1 reference

29 July 2017

T Lipina

2

1 reference

29 July 2017

E Tam

3

1 reference

29 July 2017

A Mandel

4

1 reference

29 July 2017

S J Clapcote

5

1 reference

29 July 2017

A R Bechard

6

1 reference

29 July 2017

J Chambers

7

1 reference

29 July 2017

H T J Mount

8

1 reference

29 July 2017

P J Fletcher

9

1 reference

29 July 2017

J C Roder

10

1 reference

29 July 2017

L R Osborne

11

1 reference

29 July 2017

language of work or name

English

0 references

publication date

3 August 2007

1 reference

Genes, Brain and Behavior

29 July 2017

1 reference

29 July 2017

7

1 reference

29 July 2017

224-234

1 reference

29 July 2017

2

1 reference

Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Analysis of knock-out mice to determine the role of HPC-1/syntaxin 1A in expressing synaptic plasticity.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Serotonin 1A and 2A receptor densities, neurochemical and behavioural characteristics in two closely related mice strains after long-term isolation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

GTF2IRD1 in craniofacial development of humans and mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

stathmin, a gene enriched in the amygdala, controls both learned and innate fear

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Severe expressive-language delay related to duplication of the Williams-Beuren locus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

TFII-I, a candidate gene for Williams syndrome cognitive profile: parallels between regional expression in mouse brain and human phenotype

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Partial deletion of the critical 1.5 Mb interval in Williams-Beuren syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Mutational mechanisms of Williams-Beuren syndrome deletions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Essential role of Fkbp6 in male fertility and homologous chromosome pairing in meiosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Anxiety, Fears, and Phobias in Persons With Williams Syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

The social deficits of the oxytocin knockout mouse

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Targeted mutation of Cyln2 in the Williams syndrome critical region links CLIP-115 haploinsufficiency to neurodevelopmental abnormalities in mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Prevalence estimation of Williams syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Biochemistry and biology of the inducible multifunctional transcription factor TFII-I.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Structure-function analysis of TFII-I. Roles of the N-terminal end, basic region, and I-repeats

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Features of the genetically defined anxiety in mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Dysfunction in the neural circuitry of emotion regulation--a possible prelude to violence.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Williams syndrome: cognition, personality, and adaptive behavior

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Alternatively spliced isoforms of TFII-I. Complex formation, nuclear translocation, and differential gene regulation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Novel arterial pathology in mice and humans hemizygous for elastin

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Polymorphism in serotonin transporter gene associated with susceptibility to major depression.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Derivation of completely cell culture-derived mice from early-passage embryonic stem cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Parachlorophenylalanine-induced serotonin depletion increases offensive but not defensive aggression in male rats.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

The primate amygdala and the neurobiology of social behavior: implications for understanding social anxiety

5 July 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Differential role of the 5-HT1A receptor in aggressive and non-aggressive mice: an across-strain comparison.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Effects of the rd1 mutation and host strain on hippocampal learning in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

5-HT(1B) receptors, ventral orbitofrontal cortex, and aggressive behavior in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

The early embryonic expression of TFII-I during mouse preimplantation development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Comparison of the effects of bilateral orbital prefrontal cortex lesions and amygdala lesions on emotional responses in rhesus monkeys.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Distinctive Personality Characteristics of 8-, 9-, and 10-Year-Olds With Williams Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Abnormal spine morphology and enhanced LTP in LIMK-1 knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Neural correlates of genetically abnormal social cognition in Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Increased social fear and decreased fear of objects in monkeys with neonatal amygdala lesions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Anxiolytic-like effect of (S)-WAY 100135, a 5-HT1A receptor antagonist, in the murine elevated plus-maze test.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

Dynamic changes of brain serotonergic and dopaminergic activities during development of anxious depression: experimental study

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Progressive sensorimotor impairment is not associated with reduced dopamine and high energy phosphate donors in a model of ataxia-telangiectasia.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883608

Methods to rapidly and accurately screen a large number of ENU mutagenized mice for abnormal motor phenotypes

29 October 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-183X.2007.00343.X

"Everybody in the world is my friend" hypersociability in young children with Williams syndrome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17680805

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Statural growth in Williams-Beuren syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17680805

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The Williams syndrome cognitive profile

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17680805

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1601-183X.2007.00343.X

1 reference

29 July 2017

1 reference

29 July 2017

1 reference