Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation. (Q31126823)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.	scientific article

Statements

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

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

17 December 2019

author name string

Damina Balmer

1

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

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

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

17 December 2019

publication date

19 December 2002

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

Journal of Molecular Medicine

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

81

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

61-68

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

1

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

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

Dimensions Publication ID

0 references

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

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q31126823&oldid=1545427305"