(Q24602261)

21 June 2017

Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice (English)

1 reference

21 June 2017

Williams-Beuren syndrome

1 reference

13

Karl Deisseroth

0 references

author name string

Hong Hua Li

1

1 reference

21 June 2017

Madhuri Roy

2

1 reference

21 June 2017

Unsal Kuscuoglu

3

1 reference

21 June 2017

Corinne M Spencer

4

1 reference

21 June 2017

Birgit Halm

5

1 reference

21 June 2017

Katharine C Harrison

6

1 reference

21 June 2017

Joseph H Bayle

7

1 reference

21 June 2017

Alessandra Splendore

8

1 reference

21 June 2017

Feng Ding

9

1 reference

21 June 2017

Leslie A Meltzer

10

1 reference

21 June 2017

Elena Wright

11

1 reference

21 June 2017

Richard Paylor

12

1 reference

21 June 2017

Uta Francke

14

1 reference

21 June 2017

language of work or name

English

0 references

publication date

1 April 2009

1 reference

21 June 2017

EMBO Molecular Medicine

1 reference

21 June 2017

1

1 reference

21 June 2017

1

1 reference

21 June 2017

50-65

1 reference

SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice

21 June 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Physical and functional interactions of histone deacetylase 3 with TFII-I family proteins and PIASxbeta

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

WSTF-ISWI chromatin remodeling complex targets heterochromatic replication foci

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

GTF2IRD1 in craniofacial development of humans and mice

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Frizzled 9 knock-out mice have abnormal B-cell development

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Action of TFII-I outside the nucleus as an inhibitor of agonist-induced calcium entry

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Protamine-Cre recombinase transgenes efficiently recombine target sequences in the male germ line of mice, but not in embryonic stem cells

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Fronto-parietal and cerebellar contributions to motor dysfunction in Williams syndrome: a review and future directions

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

An optical neural interface: in vivo control of rodent motor cortex with integrated fiberoptic and optogenetic technology

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

TFII-I down-regulates a subset of estrogen-responsive genes through its interaction with an initiator element and estrogen receptor alpha.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

The WSTF-SNF2h chromatin remodeling complex interacts with several nuclear proteins in transcription

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Hyperacusis in Williams syndrome: characteristics and associated neuroaudiologic abnormalities

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Discriminating power of localized three-dimensional facial morphology

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Altered anxiety-related and social behaviors in the Fmr1 knockout mouse model of fragile X syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Relative sparing of primary auditory cortex in Williams Syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Neurocranial morphology and growth in Williams syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Automated apparatus for quantitation of social approach behaviors in mice.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Use of the "partition" test in behavioral and pharmacological experiments

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Williams (Williams Beuren) syndrome: a distinct neurobehavioral disorder

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Williams-Beuren syndrome: genes and mechanisms

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements in mice

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Chromosome engineering in mice

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

In-depth analysis of spatial cognition in Williams syndrome: A critical assessment of the role of the LIMK1 gene

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Mutational mechanisms of Williams-Beuren syndrome deletions

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Hyperacusis in Williams syndrome: a sample survey study.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3378107

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.

30 May 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

Williams syndrome: neuronal size and neuronal-packing density in primary visual cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

Reduced parietal and visual cortical activation during global processing in Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

The use of behavioral test batteries, II: effect of test interval.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

Abnormal cortical complexity and thickness profiles mapped in Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

Behavioral characterization of mouse models for Smith-Magenis syndrome and dup(17)(p11.2p11.2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.200900003

Cytoarchitectonic anomalies in a genetically based disorder: Williams 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=3378107

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

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20049703

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/EMMM.200900003

1 reference

OpenCitations bibliographic resource ID

21 June 2017

4959816

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference