(Q48573215)

12 February 2018

title

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

1 reference

12 February 2018

0 references

5

1 reference

12 February 2018

author name string

Paolo Moretti

1

1 reference

12 February 2018

J Adriaan Bouwknecht

2

1 reference

12 February 2018

Ryan Teague

3

1 reference

12 February 2018

Richard Paylor

4

1 reference

12 February 2018

publication date

17 November 2004

1 reference

12 February 2018

published in

Human Molecular Genetics

1 reference

12 February 2018

volume

14

1 reference

12 February 2018

issue

2

1 reference

12 February 2018

page(s)

205-220

1 reference

12 February 2018

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Rett's syndrome: characterization of respiratory patterns and sleep

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Features of autism in Rett syndrome and severe mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Rett syndrome: qualitative and quantitative differentiation from autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Development. New hints into the biological basis of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

The Screening and Diagnosis of Autistic Spectrum Disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Rett syndrome. Current status and new vistas

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Identification of MeCP2 mutations in a series of females with autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Mutation analysis of the coding sequence of the MECP2 gene in infantile autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Occurrence of Rett syndrome in boys.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

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%2FDDI016

X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Influence of running wheel activity on free-running sleep/wake and drinking circadian rhythms in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Activity Feedback to the Mammalian Circadian Pacemaker: Influence on Observed Measures of Rhythm Period Length

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Dopamine production in the caudate putamen restores feeding in dopamine-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Expanded characterization of the social interaction abnormalities in mice lacking Dvl1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

A proposed test battery and constellations of specific behavioral paradigms to investigate the behavioral phenotypes of transgenic and knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

The Rett Syndrome Behaviour Questionnaire (RSBQ): refining the behavioural phenotype of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Associated medical disorders and disabilities in children with autistic disorder: a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Neuropsychiatric problems in tuberous sclerosis complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Autism in Angelman syndrome: an exploration of comorbidity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Cognitive and adaptive behavior profiles of children with Angelman syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Differential functions of mPer1, mPer2, and mPer3 in the SCN circadian clock

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

Social Dominance in Inbred Mouse Strains

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI016

21 January 2018

Identifiers

DOI

10.1093/HMG/DDI016

1 reference

12 February 2018

1 reference

12 February 2018