A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis (Q35370222)

8 August 2017

title

A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis (English)

1 reference

8 August 2017

7

Stephen C. Cannon

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21881211

11 December 2024

author name string

Fenfen Wu

1

1 reference

8 August 2017

Wentao Mi

2

1 reference

8 August 2017

Yu Fu

4

1 reference

8 August 2017

Dennis K. Burns

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21881211

11 December 2024

Hillery F. Gray

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21881211

11 December 2024

Arie F. Struyk

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21881211

11 December 2024

language of work or name

English

0 references

publication date

1 September 2011

1 reference

full work available at URL

8 August 2017

http://www.jci.org/articles/view/57398/files/pdf

file format

Portable Document Format

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21881211

https://europepmc.org/articles/PMC3195470

11 December 2024

file format

HyperText Markup Language

content deliverer

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21881211

https://europepmc.org/articles/PMC3195470?pdf=render

11 December 2024

file format

Portable Document Format

content deliverer

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21881211

https://doi.org/10.1172/jci57398

11 December 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21881211

Journal of Clinical Investigation

11 December 2024

published in

1 reference

8 August 2017

volume

121

1 reference

8 August 2017

issue

10

1 reference

8 August 2017

page(s)

4082-4094

1 reference

Leaky sodium channels from voltage sensor mutations in periodic paralysis, but not paramyotonia

8 August 2017

cites work

1 reference

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Voltage-sensor mutations in channelopathies of skeletal muscle

12 July 2018

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K -dependent paradoxical membrane depolarization and Na overload, major and reversible contributors to weakness by ion channel leaks

12 July 2018

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Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis

12 July 2018

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Gating pore currents in DIIS4 mutations of NaV1.4 associated with periodic paralysis: saturation of ion flux and implications for disease pathogenesis

12 July 2018

1 reference

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Targeted mutation of mouse skeletal muscle sodium channel produces myotonia and potassium-sensitive weakness.

12 July 2018

1 reference

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A Na channel mutation linked to hypokalemic periodic paralysis exposes a proton-selective gating pore

12 July 2018

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Pathomechanisms in channelopathies of skeletal muscle and brain

12 July 2018

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The primary periodic paralyses: diagnosis, pathogenesis and treatment

12 July 2018

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Histidine scanning mutagenesis of basic residues of the S4 segment of the shaker k channel

12 July 2018

1 reference

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The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation.

12 July 2018

1 reference

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Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current

12 July 2018

1 reference

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Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H

12 July 2018

1 reference

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Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis

12 July 2018

1 reference

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Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

12 July 2018

1 reference

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Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families

12 July 2018

1 reference

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Hypokalemic periodic paralysis: In vitro investigation of muscle fiber membrane parameters

12 July 2018

1 reference

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Barium-treated mammalian skeletal muscle: similarities to hypokalaemic periodic paralysis

12 July 2018

1 reference

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Role of the anomalous rectifier in determining membrane potentials of mouse muscle fibres at low extracellular K .

12 July 2018

1 reference

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Gating behaviour of sodium currents in adult mouse muscle recorded with an improved two-electrode voltage clamp.

12 July 2018

1 reference

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Paradoxical depolarization of BA2 - treated muscle exposed to low extracellular K : insights into resting potential abnormalities in hypokalemic paralysis.

26 September 2018

1 reference

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Gating pore current in an inherited ion channelopathy

26 September 2018

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Isoprenaline-stimulated differential adrenergic response of K channels in skeletal muscle under hypokalaemic conditions

26 September 2018

1 reference

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Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.

26 September 2018

1 reference

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A novel sodium channel mutation in a family with hypokalemic periodic paralysis

26 September 2018

1 reference

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Insulin modulation of ATP-sensitive K channel of rat skeletal muscle is impaired in the hypokalaemic state.

26 September 2018

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Acetazolamide Prophylaxis in Hypokalemic Periodic Paralysis

26 September 2018

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A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation

26 September 2018

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12 December 2020

Differential diagnosis of periodic paralysis aided by in vitro myography

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12 December 2020

CLINICAL AND ELECTROMYOGRAPHIC STUDIES IN A PATIENT WITH PRIMARY HYPOKALEMIC PERIODIC PARALYSIS

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12 December 2020

Homozygosity for dominant mutations increases severity of muscle channelopathies

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12 December 2020

The role of K channels in the force recovery elicited by Na -K pump stimulation in Ba2 -paralysed rat skeletal muscle

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12 December 2020

Evolution and content of vacuoles in primary hypokalemic periodic paralysis

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12 December 2020

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12 December 2020

Primary midline developmental field. I. Clinical and epidemiological characteristics

https://api.crossref.org/works/10.1172/JCI57398

5

1 reference

11 December 2024

Identifiers

DOI

10.1172/JCI57398

1 reference

8 August 2017

1 reference

8 August 2017

1 reference