(Q34777768)

4 August 2017

title

Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome (English)

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4 August 2017

7

Alexandre Reymond

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4 August 2017

2

Paulina Carmona-Mora

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4 August 2017

8

Katherina Walz

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4 August 2017

6

James R Lupski

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4 August 2017

Jessica Molina

1

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4 August 2017

Jacqueline Chrast

series ordinal

3

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4 August 2017

Paola M Krall

series ordinal

4

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4 August 2017

César P Canales

series ordinal

5

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4 August 2017

publication date

10 May 2008

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4 August 2017

published in

Human Molecular Genetics

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4 August 2017

volume

17

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4 August 2017

issue

16

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4 August 2017

page(s)

2486-2495

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Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion

4 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Mutations in RAI1 associated with Smith-Magenis syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

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/10.1093%2FHMG%2FDDN148

Anxiety in high-functioning children with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Automated apparatus for quantitation of social approach behaviors in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Effects of age on brain volume and head circumference in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

The amygdala is enlarged in children but not adolescents with autism; the hippocampus is enlarged at all ages.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Complexin 1 knockout mice exhibit marked deficits in social behaviours but appear to be cognitively normal

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Advances in behavioral genetics: mouse models of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Fmr1 KO mice as a possible model of autistic features.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Rett syndrome: of girls and mice--lessons for regression in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Side effects of genome structural changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

affy--analysis of Affymetrix GeneChip data at the probe level

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

Social Dominance in Inbred Mouse Strains

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN148

21 January 2018

Identifiers

DOI

10.1093/HMG/DDN148

1 reference

4 August 2017

1 reference