Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3 (Q29616516)

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30 April 2017

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9

Zoghbi H

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6

Noebels J

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author name string

Shahbazian M

1

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Young J

2

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Yuva-Paylor L

3

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30 April 2017

Spencer C

4

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Antalffy B

5

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Armstrong D

7

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Paylor R

8

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language of work or name

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publication date

18 July 2002

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volume

35

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issue

2

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page(s)

243-54

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

30 April 2017

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Social Dominance in Inbred Mouse Strains

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A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males

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Altered chromatin structure associated with methylation-induced gene silencing in cancer cells: correlation of accessibility, methylation, MeCP2 binding and acetylation

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

636199

636199

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12160743

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017