(Q52196602)

26 April 2018

title

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements (English)

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26 April 2018

Beckwith-Wiedemann syndrome

main subject

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4

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26 April 2018

author name string

M P Lee

series ordinal

1

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26 April 2018

R J Hu

series ordinal

2

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26 April 2018

L A Johnson

series ordinal

3

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26 April 2018

language of work or name

English

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publication date

1 February 1997

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26 April 2018

published in

Nature Genetics

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26 April 2018

volume

15

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26 April 2018

issue

2

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26 April 2018

page(s)

181-185

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26 April 2018

Relaxation of imprinted genes in human cancer

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Parental genomic imprinting of the human IGF2 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Monoallelic expression of the human H19 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

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%2FNG0297-181

7 January 2021

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Epigenetic lesions at the H19 locus in Wilms' tumour patients

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

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%2FNG0297-181

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%2FNG0297-181

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Increased exon-trapping efficiency through modifications to the pSPL3 splicing vector

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Basic local alignment search tool

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-181

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%2FNG0297-181

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%2FNG0297-181

7 January 2021

Identifiers

DOI

10.1038/NG0297-181

1 reference

26 April 2018

1 reference

26 April 2018