Add to ORKGDuplication and deletion of a common interval spanning 26 genes on chromosome 7q11.23 cause Dup7q11.23 Syndrome and Williams-Beuren Syndrome, neurodevelopmental disorders with contrasting anxiety phenotypes. The General Transcription Factor 2 I (GTF2I) gene has been implicated in separation anxiety, common in people with Dup7q11.23, and we studied the effects of commonly used anxiolytics on maternal separation-induced USV in mouse models with copy number changes in Gtf2i. Subcutaneous injection of saline affected both USV production and plasma corticosterone levels in a Gtf2i gene-dosage dependent manner. Drugs acting on the glutamate receptors were most effective at attenuating USVs in all genotypes, compared to GABAergic and serotonergic ...
With the advances in genome wide screening arrays and sequencing techniques scientists were enabled ...
Mutations in the coding region of the WFS1 gene cause Wolfram syndrome, a rare multisystem neurodege...
Williams-Beuren Syndrome (WBS) is an autosomal dominant neurodevelopmental disorder caused by hemizy...
Duplication and deletion of a common interval spanning 26 genes on chromosome 7q11.23 cause Dup7q11....
Duplication (dup7q11.23) and deletion (Williams syndrome) of chromosomal region 7q11.23 cause neurod...
Deletion (Williams-Beuren syndrome (WBS)) and duplication (Dup7q11.23) of a common interval spanning...
Williams-Beuren syndrome (WBS) is a neurodevelopmental disorder caused by a heterozygous deletion of...
Williams-Beuren syndrome (WBS) is a rare genetic disorder caused by a hemizygous deletion of around ...
Genomic rearrangements, particularly deletions and duplications, are known to cause many genetic dis...
Abstract Williams-Beuren syndrome (WBS) is a neurodevelopmental disorder caused by the...
Williams–Beuren syndrome (WBS) is a rare genetic disorder caused by a hemizygous deletion of around ...
Williams-Beuren syndrome (WBS)is a complex neurodevelopmental disorder that results from a hemizygou...
Williams Beuren syndrome Syndrome (WBS) and 7q11.23 Duplication Syndrome (Dup7) are rare neurodevelo...
Williams-Beuren Syndrome (WBS) is a genetic neurodevelopmental disorder caused by the deletion of 25...
Anxiety disorders are prevalent and disabling yet understudied from a genetic standpoint, compared w...
With the advances in genome wide screening arrays and sequencing techniques scientists were enabled ...
Mutations in the coding region of the WFS1 gene cause Wolfram syndrome, a rare multisystem neurodege...
Williams-Beuren Syndrome (WBS) is an autosomal dominant neurodevelopmental disorder caused by hemizy...
Duplication and deletion of a common interval spanning 26 genes on chromosome 7q11.23 cause Dup7q11....
Duplication (dup7q11.23) and deletion (Williams syndrome) of chromosomal region 7q11.23 cause neurod...
Deletion (Williams-Beuren syndrome (WBS)) and duplication (Dup7q11.23) of a common interval spanning...
Williams-Beuren syndrome (WBS) is a neurodevelopmental disorder caused by a heterozygous deletion of...
Williams-Beuren syndrome (WBS) is a rare genetic disorder caused by a hemizygous deletion of around ...
Genomic rearrangements, particularly deletions and duplications, are known to cause many genetic dis...
Abstract Williams-Beuren syndrome (WBS) is a neurodevelopmental disorder caused by the...
Williams–Beuren syndrome (WBS) is a rare genetic disorder caused by a hemizygous deletion of around ...
Williams-Beuren syndrome (WBS)is a complex neurodevelopmental disorder that results from a hemizygou...
Williams Beuren syndrome Syndrome (WBS) and 7q11.23 Duplication Syndrome (Dup7) are rare neurodevelo...
Williams-Beuren Syndrome (WBS) is a genetic neurodevelopmental disorder caused by the deletion of 25...
Anxiety disorders are prevalent and disabling yet understudied from a genetic standpoint, compared w...
With the advances in genome wide screening arrays and sequencing techniques scientists were enabled ...
Mutations in the coding region of the WFS1 gene cause Wolfram syndrome, a rare multisystem neurodege...
Williams-Beuren Syndrome (WBS) is an autosomal dominant neurodevelopmental disorder caused by hemizy...