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English
Breaking the silence in Rett syndrome
scientific article published on 01 October 1999
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
title
Breaking the silence in Rett syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
main subject
Rett syndrome
0 references
author
Brian Hendrich
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
author name string
Willard HF
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
publication date
1 October 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
volume
23
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
page(s)
127-128
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/13751
0 references
cites work
Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13751
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13751
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Patterns of X chromosome inactivation in the Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13751
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13751
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%2F13751
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA methylation and chromatin modification.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13751
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA methylation and imprinting: why bother?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13751
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%2F13751
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%2F13751
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%2F13751
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and characterization of a family of mammalian methyl-CpG binding proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13751
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprinting in Prader-Willi and Angelman syndromes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13751
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13751
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Requirement of Rsk-2 for epidermal growth factor-activated phosphorylation of histone H3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13751
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/13751
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PubMed ID
10508498
1 reference
stated in
Europe PubMed Central
PubMed ID
10508498
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508498%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
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