(Q31126823)

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Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12545250%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12545250%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

Janine M. LaSalle

4

1 reference

Europe PubMed Central

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17 December 2019

author name string

Damina Balmer

1

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12545250%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

Jared Goldstine

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12545250%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

Y Manjula Rao

3

1 reference

Europe PubMed Central

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17 December 2019

publication date

19 December 2002

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17 December 2019

Journal of Molecular Medicine

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17 December 2019

81

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17 December 2019

61-68

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17 December 2019

1

1 reference

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17 December 2019

https://scigraph.springernature.com/pub.10.1007/s00109-002-0396-5

0 references

Rett syndrome: clinical update and review of recent genetic advances.

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Decreased dendritic branching in frontal, motor and limbic cortex in Rett syndrome compared with trisomy 21.

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Methyl-CpG-binding protein 2 mutations in Rett syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Mutation screening in Rett syndrome patients.

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2.

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

DNA methylation specifies chromosomal localization of MeCP2.

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Expression pattern of the Rett syndrome gene MeCP2 in primate prefrontal cortex.

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Alternative poly(A) site selection in complex transcription units: means to an end?

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Regulation of gene expression for translation initiation factor eIF-2 alpha: importance of the 3' untranslated region

1 reference

https://api.crossref.org/works/10.1007%2FS00109-002-0396-5

21 January 2018

Selective dendritic alterations in the cortex of Rett syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12545250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Review of Rett syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12545250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12545250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00109-002-0396-5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12545250%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

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1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12545250%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

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