(Q33823844)

29 July 2017

title

A new spontaneous mouse mutation in the Kcne1 gene (English)

1 reference

29 July 2017

V A Letts

1

1 reference

29 July 2017

A Valenzuela

2

1 reference

29 July 2017

C Dunbar

3

1 reference

29 July 2017

Q Y Zheng

4

1 reference

29 July 2017

K R Johnson

5

1 reference

29 July 2017

W N Frankel

6

1 reference

29 July 2017

publication date

1 October 2000

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29 July 2017

number of pages

5

1 reference

inferred from page(s)

published in

Mammalian Genome

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29 July 2017

volume

11

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29 July 2017

issue

10

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29 July 2017

page(s)

831-835

1 reference

Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

Mutation of the Gene for I sK Associated With Both Jervell and Lange-Nielsen and Romano-Ward Forms of Long-QT Syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

KCNE1 mutations cause Jervell and Lange-Nielsen syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

Inner ear defects induced by null mutation of the isk gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

Developmental changes in ionic channel activity in the embryonic murine heart

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

Pathology of the Ear in the Cardio-Auditory Syndrome of Jervell and Lange-Nielsen (Recessive Deafness with Electrocardiographic Abnormalities)

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

Alteration of channel activities and gating by mutations of slow ISK potassium channel

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

ISK, a slowly activating voltage-sensitive K+ channel. Characterization of multiple cDNAs and gene organization in the mouse

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

Involvement of IsK-Associated K + Channel in Heart Rate Control of Repolarization in a Murine Engineered Model of Jervell and Lange-Nielsen Syndrome

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

Subunit composition of minK potassium channels.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2862908

The MEV mouse linkage testing stock: mapping 30 novel proviral insertions and establishment of an improved stock

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11003695

12 December 2020

inferred from PubMed ID database lookup

Intracisternal A-type particle elements as genetic markers: detection by repeat element viral element amplified locus-PCR

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11003695

12 December 2020

inferred from PubMed ID database lookup

Adult KCNE1-knockout mice exhibit a mild cardiac cellular phenotype

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11003695

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S003350010178

1 reference

29 July 2017

1 reference

29 July 2017

1 reference