Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q24311799)
Watch
English
UBE3A/E6-AP mutations cause Angelman syndrome
scientific article
In more languages
default for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
0 references
title
UBE3A/E6-AP mutations cause Angelman syndrome
(English)
0 references
main subject
Ubiquitin protein ligase E3A
1 reference
stated in
GOA release 2020-03-11
brain development
1 reference
stated in
GOA release 2020-03-11
Angelman syndrome
1 reference
based on heuristic
inferred from title
author name string
T Kishino
series ordinal
1
0 references
M Lalande
series ordinal
2
0 references
J Wagstaff
series ordinal
3
0 references
language of work or name
English
0 references
publication date
January 1997
0 references
published in
Nature Genetics
0 references
volume
15
0 references
issue
1
0 references
page(s)
70-3
0 references
cites work
Angelman syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Uniparental paternal disomy in Angelman's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
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%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
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%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The critical region for Angelman syndrome lies between D15S122 and D15S113
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Physical mapping studies at D15S10: implications for candidate gene identification in the Angelman syndrome/Prader-Willi syndrome chromosome region of 15q11-q13
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning and expression of the cDNA for E6-AP, a protein that mediates the interaction of the human papillomavirus E6 oncoprotein with p53.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental imprinting of the mouse insulin-like growth factor II gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue- and developmental stage-specific imprinting of the mouse proinsulin gene, Ins2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of imprinting in U2AFBPL, a human homologue of the imprinted mouse gene U2afbp-rs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The MAS proto-oncogene is not imprinted in humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Promoter-specific imprinting of the human insulin-like growth factor-II gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protein ubiquitination involving an E1-E2-E3 enzyme ubiquitin thioester cascade
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Drosophila bendless gene encodes a neural protein related to ubiquitin-conjugating enzymes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The ubiquitin-proteasome pathway is required for processing the NF-kappa B1 precursor protein and the activation of NF-kappa B
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of genes from complex sources of mammalian genomic DNA using exon amplification
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-70
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0197-70
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
889960
Dimensions Publication ID
1012945311
0 references
Fatcat ID
release_g3yobb3o3ffdzmkue5lkjdlfd4
0 references
OpenCitations bibliographic resource ID
889960
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
889960
PubMed publication ID
8988171
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
889960
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit