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English
Methylation gets SMRT. Functional insights into Rett syndrome
scientific article published on 01 September 2003
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12967552
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967552%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
title
Methylation gets SMRT. Functional insights into Rett syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12967552
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967552%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
main subject
Rett syndrome
0 references
author name string
Monica L Vetter
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12967552
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967552%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
publication date
1 September 2003
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12967552
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967552%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
number of pages
2
1 reference
based on heuristic
inferred from page(s)
published in
Developmental Cell
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12967552
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967552%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
volume
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12967552
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967552%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12967552
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967552%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
page(s)
359-360
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12967552
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967552%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
cites work
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/10.1016%2FS1534-5807%2803%2900267-3
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/10.1016%2FS1534-5807%2803%2900267-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vertebrate hairy and Enhancer of split related proteins: transcriptional repressors regulating cellular differentiation and embryonic patterning
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1534-5807%2803%2900267-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular targets of vertebrate segmentation: two mechanisms control segmental expression of Xenopus hairy2 during somite formation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1534-5807%2803%2900267-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1534-5807%2803%2900267-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A histone deacetylase corepressor complex regulates the Notch signal transduction pathway
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1534-5807%2803%2900267-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA methylation in animal development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1534-5807%2803%2900267-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome and MeCP2: linking epigenetics and neuronal function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1534-5807%2803%2900267-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1534-5807%2803%2900267-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Methyl CpG-binding proteins and transcriptional repression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1534-5807%2803%2900267-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1534-5807(03)00267-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12967552
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967552%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
PubMed publication ID
12967552
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12967552
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967552%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
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