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Competitive edge at the imprinted Prader-Willi/Angelman region?
scientific article published in March 1998
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
title
Competitive edge at the imprinted Prader-Willi/Angelman region?
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
author
Tamara Caspary
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
author name string
Tilghman SM
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
Ingram RS
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
language of work or name
English
0 references
publication date
1 March 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
volume
18
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
page(s)
206-208
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
cites work
Competition--a common motif for the imprinting mechanism?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental imprinting and human disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of imprinting caused by deletion of the H19 gene region in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
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%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
UBE3A/E6-AP mutations cause Angelman syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0398-206
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0398-206
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
Dimensions Publication ID
1014590238
0 references
PubMed publication ID
9500535
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9500535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9500535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
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