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English
KVLQT1, the rhythm of imprinting
scientific article published on 01 February 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
title
KVLQT1, the rhythm of imprinting
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
author name string
Mannens M
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
Wilde A
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
publication date
1 February 1997
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
volume
15
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
page(s)
113-115
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0297-113
0 references
cites work
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long QT and Harvey-ras
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inner ear defects induced by null mutation of the isk gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
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%2FNG0297-113
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%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Beckwith-Wiedemann syndrome, tumourigenesis and imprinting
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allele-specific gene expression in mammals: the curious case of the imprinted RNAs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-113
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%2FNG0297-113
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0297-113
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PubMed ID
9020829
1 reference
stated in
Europe PubMed Central
PubMed ID
9020829
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
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