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Prader-Willi and snoRNAs
scientific article published on 01 June 2008
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
18509309
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509309%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
title
Prader-Willi and snoRNAs
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18509309
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509309%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
author name string
Jo Peters
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
18509309
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509309%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
publication date
1 June 2008
1 reference
stated in
Europe PubMed Central
PubMed ID
18509309
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509309%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
18509309
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509309%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
volume
40
1 reference
stated in
Europe PubMed Central
PubMed ID
18509309
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509309%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
issue
6
1 reference
stated in
Europe PubMed Central
PubMed ID
18509309
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509309%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
page(s)
688-689
1 reference
stated in
Europe PubMed Central
PubMed ID
18509309
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509309%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
exact match
https://scigraph.springernature.com/pub.10.1038/ng0608-688
0 references
cites work
Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial interstitial 570 kbp deletion of theUBE3Agene region causing Angelman syndrome but not Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mouse model for Prader-Willi syndrome imprinting-centre mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The imprinted gene Magel2 regulates normal circadian output.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Small Nucleolar RNAs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0608-688
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0608-688
1 reference
stated in
Europe PubMed Central
PubMed ID
18509309
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509309%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
PubMed ID
18509309
1 reference
stated in
Europe PubMed Central
PubMed ID
18509309
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18509309%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
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