(Q33823844)

29 July 2017

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

1 October 2000

1 reference

29 July 2017

5

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

29 July 2017

11

1 reference

29 July 2017

831-835

1 reference

29 July 2017

10

1 reference

https://scigraph.springernature.com/pub.10.1007/s003350010178

29 July 2017

0 references

cites work

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

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 IsK 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 IKs 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