(Q50312721)

2 March 2018

title

Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions. (English)

1 reference

2 March 2018

0 references

6

1 reference

2 March 2018

Nagahide Takahashi

3

object named as

Nagahide Takahashi

1 reference

2 March 2018

author name string

Takeshi Sakurai

1

1 reference

2 March 2018

Nathan P Dorr

2

1 reference

2 March 2018

L Alison McInnes

4

1 reference

2 March 2018

Gregory A Elder

5

1 reference

2 March 2018

publication date

3 December 2010

1 reference

2 March 2018

published in

Autism Research

1 reference

2 March 2018

volume

4

1 reference

2 March 2018

issue

1

1 reference

2 March 2018

page(s)

28-39

1 reference

2 March 2018

Partial 7q11.23 deletions further implicate GTF2I and GTF2IRD1 as the main genes responsible for the Williams-Beuren syndrome neurocognitive profile.

cites work

1 reference

Identification of the TFII-I family target genes in the vertebrate genome

21 January 2018

1 reference

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

21 January 2018

1 reference

Increased locomotor activity in mice lacking the low-density lipoprotein receptor

21 January 2018

1 reference

Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development

21 January 2018

1 reference

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

21 January 2018

1 reference

An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.

21 January 2018

1 reference

Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex

21 January 2018

1 reference

Williams-Beuren syndrome-associated transcription factor TFII-I regulates osteogenic marker genes

21 January 2018

1 reference

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

21 January 2018

1 reference

Copy number variants at Williams-Beuren syndrome 7q11.23 region.

21 January 2018

1 reference

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

21 January 2018

1 reference

Animal models of Williams syndrome

21 January 2018

1 reference

Williams-Beuren syndrome.

21 January 2018

1 reference

Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment

21 January 2018

1 reference

Slc25a12 disruption alters myelination and neurofilaments: a model for a hypomyelination syndrome and childhood neurodevelopmental disorders

21 January 2018

1 reference

GTF2IRD1 in craniofacial development of humans and mice

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/AUR.169

1 reference

2 March 2018

PubMed ID

21328569

1 reference

2 March 2018