KVLQT1, the rhythm of imprinting (Q73040757)

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31 October 2019

title

KVLQT1, the rhythm of imprinting (English)

1 reference

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31 October 2019

author name string

Mannens M

series ordinal

1

1 reference

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31 October 2019

Wilde A

series ordinal

2

1 reference

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31 October 2019

publication date

1 February 1997

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31 October 2019

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31 October 2019

volume

15

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31 October 2019

issue

2

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31 October 2019

page(s)

113-115

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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

31 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Long QT and Harvey-ras

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Inner ear defects induced by null mutation of the isk gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Promoter-specific imprinting of the human insulin-like growth factor-II gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Allele-specific gene expression in mammals: the curious case of the imprinted RNAs

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Disruption of imprinting caused by deletion of the H19 gene region in mice

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-113

7 January 2021

Identifiers

DOI

10.1038/NG0297-113

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020829%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1 reference