(Q50346631)

2 July 2018

title

Mecp2 truncation in male mice promotes affiliative social behavior. (English)

1 reference

2 July 2018

author

Brandon L. Pearson

1

1 reference

PubMed publication ID

21909962

5 March 2018

http://europepmc.org/abstract/MED/21909962

author name string

E B Defensor

2

1 reference

2 July 2018

R L H Pobbe

3

1 reference

2 July 2018

L H L Yamamoto

4

1 reference

2 July 2018

V J Bolivar

5

1 reference

2 July 2018

D C Blanchard

6

1 reference

2 July 2018

R J Blanchard

7

1 reference

2 July 2018

language of work or name

English

0 references

publication date

11 September 2011

1 reference

2 July 2018

published in

Behavior Genetics

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2 July 2018

volume

42

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2 July 2018

issue

2

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2 July 2018

page(s)

299-312

1 reference

2 July 2018

https://scigraph.springernature.com/pub.10.1007/s10519-011-9501-2

exact match

0 references

cites work

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Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice

3 July 2018

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3 July 2018

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

3 July 2018

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3 July 2018

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3 July 2018

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3 July 2018

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3 July 2018

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3 July 2018

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3 July 2018

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3 July 2018

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3 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843946

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

14 August 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843946

De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastia.

14 August 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843946

A Rett syndrome MECP2 mutation that causes mental retardation in men.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843946

MECP2 mutation in male patients with non-specific X-linked mental retardation.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843946

MECP2 mutations account for most cases of typical forms of Rett syndrome.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5843946

Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males

14 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10519-011-9501-2

A pinch or a lesion: a reconceptualization of biting consequences in mice

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21909962

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hair-nibbling and whisker-trimming as indicators of social hierarchy in mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21909962

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10519-011-9501-2

1 reference

2 July 2018

PMC publication ID

5843946

1 reference

2 July 2018

PubMed publication ID

21909962

1 reference

2 July 2018