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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
11242117
retrieved
24 January 2017
title
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
(English)
1 reference
stated in
PubMed
PubMed ID
11242117
retrieved
24 January 2017
main subject
Rett syndrome
0 references
Methyl CpG binding protein 2
1 reference
stated in
GOA release 2020-03-11
Methyl-CpG binding domain protein 2
1 reference
stated in
GOA release 2020-03-11
author
Brian Hendrich
object named as
B. Hendrich
series ordinal
2
0 references
Adrian Peter Bird
object named as
A. Bird
series ordinal
5
0 references
author name string
J. Guy
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
11242117
retrieved
24 January 2017
M. Holmes
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
11242117
retrieved
24 January 2017
J. E. Martin
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
11242117
retrieved
24 January 2017
language of work or name
English
0 references
publication date
1 March 2001
1 reference
stated in
PubMed
PubMed ID
11242117
retrieved
24 January 2017
published in
Nature Genetics
1 reference
stated in
PubMed
PubMed ID
11242117
retrieved
24 January 2017
volume
27
1 reference
stated in
PubMed
PubMed ID
11242117
retrieved
24 January 2017
page(s)
322–326
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stated in
PubMed
PubMed ID
11242117
retrieved
24 January 2017
issue
3
1 reference
stated in
PubMed
PubMed ID
11242117
retrieved
24 January 2017
cites work
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MECP2 mutations account for most cases of typical forms of Rett syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the MECP2 gene in a cohort of girls with Rett syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation screening in Rett syndrome patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA methylation specifies chromosomal localization of MeCP2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a mammalian protein that binds specifically to DNA containing methylated CpGs.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Site-specific DNA recombination in mammalian cells by the Cre recombinase of bacteriophage P1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
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7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Closely related proteins MBD2 and MBD3 play distinctive but interacting roles in mouse development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Methylation-mediated transcriptional silencing in euchromatin by methyl-CpG binding protein MBD1 isoforms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Active repression of methylated genes by the chromosomal protein MBD1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional consequences of Rett syndrome mutations on human MeCP2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA recognition by the methyl-CpG binding domain of MeCP2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85899
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/85899
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
636175
OpenCitations bibliographic resource ID
636175
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
636175
PubMed ID
11242117
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
636175
ResearchGate publication ID
12090316
0 references
Springer Nature article ID
10.1038/85899
0 references
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