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English
Incriminating gene suspects, Prader-Willi style
scientific article published on 01 October 1999
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10508501
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508501%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
title
Incriminating gene suspects, Prader-Willi style
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10508501
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508501%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
author name string
Nicholls RD
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10508501
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508501%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
publication date
1 October 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10508501
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508501%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10508501
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508501%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
volume
23
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10508501
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508501%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10508501
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508501%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
page(s)
132-134
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10508501
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508501%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/13758
0 references
cites work
Disruption of the mouse necdin gene results in early post-natal lethality
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
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Imprinting in Prader-Willi and Angelman syndromes
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
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An imprinted, mammalian bicistronic transcript encodes two independent proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
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inferred from DOI database lookup
A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
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A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
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A mouse model for Prader-Willi syndrome imprinting-centre mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
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Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
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Mouse models of human genetic disease: which mouse is more like a man?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
based on heuristic
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Know your neighbors: three phenotypes in null mutants of the myogenic bHLH gene MRF4.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
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inferred from DOI database lookup
Limbs move beyond the Radical fringe
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The structural H19 gene is required for transgene imprinting
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13758
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%2F13758
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/13758
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10508501
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508501%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PubMed publication ID
10508501
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10508501
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10508501%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
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