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Disruption of the mouse necdin gene results in early post-natal lethality
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
10508517
retrieved
31 January 2017
title
Disruption of the mouse necdin gene results in early post-natal lethality
(English)
1 reference
stated in
PubMed
PubMed ID
10508517
retrieved
31 January 2017
main subject
maternal health
0 references
Necdin, MAGE family member
1 reference
stated in
GOA release 2020-03-11
author
Rachel Wevrick
object named as
R. Wevrick
series ordinal
3
0 references
author name string
M. Gérard
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
10508517
retrieved
31 January 2017
L. Hernandez
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
10508517
retrieved
31 January 2017
C. L. Stewart
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
10508517
retrieved
31 January 2017
language of work or name
English
0 references
publication date
1 October 1999
1 reference
stated in
PubMed
PubMed ID
10508517
retrieved
31 January 2017
published in
Nature Genetics
1 reference
stated in
PubMed
PubMed ID
10508517
retrieved
31 January 2017
volume
23
1 reference
stated in
PubMed
PubMed ID
10508517
retrieved
31 January 2017
page(s)
199–202
1 reference
stated in
PubMed
PubMed ID
10508517
retrieved
31 January 2017
issue
2
1 reference
stated in
PubMed
PubMed ID
10508517
retrieved
31 January 2017
cites work
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuronally-expressed necdin gene: an imprinted candidate gene in Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure and function of the human chromosome 15 imprinting center
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
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%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of a HoxD enhancer induces transcriptional heterochrony leading to transposition of the sacrum
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cre-mediated gene deletion in the mammary gland
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of necdin, an embryonal carcinoma-derived nuclear protein, in developing mouse brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Arrest of cell growth by necdin, a nuclear protein expressed in postmitotic neurons
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure and expression of the mouse necdin gene. Identification of a postmitotic neuron-restrictive core promoter
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Necdin, a postmitotic neuron-specific growth suppressor, interacts with viral transforming proteins and cellular transcription factor E2F1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F13828
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%2F13828
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/13828
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1594010
OpenCitations bibliographic resource ID
1594010
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1594010
PubMed ID
10508517
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1594010
Springer Nature article ID
10.1038/13828
0 references
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