(Q22010246)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

title

Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

Potassium voltage-gated channel subfamily Q member 1

10 December 2019

main subject

1 reference

Potassium voltage-gated channel subfamily E regulatory subunit 1

GOA release 2020-03-11

1 reference

delayed rectifier potassium channel activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

5

C Napolitano

C

Napolitano

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

7

R Bryskin

R

Bryskin

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

8

P J Schwartz

P J

Schwartz

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

L Bianchi

1

L

Bianchi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

Z Shen

2

Z

Shen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

A T Dennis

3

A T

Dennis

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

S G Priori

4

S G

Priori

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

E Ronchetti

6

E

Ronchetti

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

A M Brown

9

A M

Brown

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

language of work or name

English

0 references

publication date

1 August 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

page(s)

1499-1507

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10400998%20AND%20SRC:MED&resulttype=core&format=json

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

10 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

Induction of endogenous channels by high levels of heterologous membrane proteins in Xenopus oocytes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

Properties of HERG channels stably expressed in HEK 293 cells studied at physiological temperature

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

Cardiac potassium channels in health and disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

The conduction pore of a cardiac potassium channel

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

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/10.1093%2FHMG%2F8.8.1499

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/10.1093%2FHMG%2F8.8.1499

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

Molecular mechanism and functional significance of the MinK control of the KvLQT1 channel activity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021

A recessive variant of the Romano-Ward long-QT syndrome?

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1499

7 January 2021