Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice (Q28585784)

22 June 2017

title

Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice (English)

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Potassium voltage-gated channel, subfamily Q, member 1

22 June 2017

main subject

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GOA release 2020-03-11

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M P Lee

1

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22 June 2017

J D Ravenel

2

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22 June 2017

R J Hu

3

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22 June 2017

L R Lustig

4

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22 June 2017

G Tomaselli

5

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22 June 2017

R D Berger

6

1 reference

22 June 2017

S A Brandenburg

7

1 reference

22 June 2017

T J Litzi

8

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22 June 2017

T E Bunton

9

1 reference

22 June 2017

C Limb

10

1 reference

22 June 2017

H Francis

11

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22 June 2017

M Gorelikow

12

1 reference

22 June 2017

H Gu

13

1 reference

22 June 2017

K Washington

14

1 reference

22 June 2017

P Argani

15

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22 June 2017

J R Goldenring

16

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22 June 2017

R J Coffey

17

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22 June 2017

A P Feinberg

18

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22 June 2017

language of work or name

English

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publication date

1 December 2000

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Journal of Clinical Investigation

22 June 2017

published in

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22 June 2017

volume

106

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22 June 2017

issue

12

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22 June 2017

page(s)

1447-1455

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A constitutively open potassium channel formed by KCNQ1 and KCNE3

22 June 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

A minK-HERG complex regulates the cardiac potassium current I(Kr)

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Detection of the SYT-SSX chimeric RNA of synovial sarcoma in paraffin-embedded tissue and its application in problematic cases

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Targeted disruption of the murine Na+/H+ exchanger isoform 2 gene causes reduced viability of gastric parietal cells and loss of net acid secretion

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Inner ear defects induced by null mutation of the isk gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Developmental changes in ionic channel activity in the embryonic murine heart

29 September 2017

1 reference

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Dynamics of epithelial cells in the corpus of the mouse stomach. III. Inward migration of neck cells followed by progressive transformation into zymogenic cells

29 September 2017

1 reference

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Pathways of processing of the gastrin precursor in rat antral mucosa

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Anti-minK Antisense Decreases the Amplitude of the Rapidly Activating Cardiac Delayed Rectifier K + Current

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Olfactory neuroblastoma is not related to the Ewing family of tumors: absence of EWS/FLI1 gene fusion and MIC2 expression

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Projections from the ventral cochlear nucleus to the dorsal cochlear nucleus in rats

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Developmental changes in the delayed rectifier K+ channels in mouse heart.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Overexpression of transforming growth factor-alpha alters differentiation of gastric cell lineages

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Otopathology in a case of multichannel cochlear implantation.

3 June 2018

1 reference

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An efficient algorithm for spectral analysis of heart rate variability

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Replacement by homologous recombination of the minK gene with lacZ reveals restriction of minK expression to the mouse cardiac conduction system.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Imprinting of mouse Kvlqt1 is developmentally regulated.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Beat-to-beat QT interval variability: novel evidence for repolarization lability in ischemic and nonischemic dilated cardiomyopathy.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

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

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

Hypertrophic gastropathy in Helicobacter felis-infected wild-type C57BL/6 mice and p53 hemizygous transgenic mice.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=387258

In vivo cardiac electrophysiology studies in the mouse

27 November 2018

1 reference

12 December 2020

Adult KCNE1-knockout mice exhibit a mild cardiac cellular phenotype

1 reference

12 December 2020

Gastric H+, K+-adenosine triphosphatase β subunit is required for normal function, development, and membrane structure of mouse parietal cells

1 reference

12 December 2020

KVLQT1, the rhythm of imprinting

1 reference

12 December 2020

Electrophysiological properties of neonatal mouse cardiac myocytes in primary culture

1 reference

12 December 2020

Loss of imprinting in human cancer

1 reference

12 December 2020

Identification and characteristics of delayed rectifier K+ current in fetal mouse ventricular myocytes

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI10897

1 reference

OpenCitations bibliographic resource ID

22 June 2017

2723062

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2723062

1 reference