ouabain and Familial Hypokalemic Periodic Paralysis

ouabain has been researched along with Familial Hypokalemic Periodic Paralysis in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Burns, DK; Cannon, SC; Fu, Y; Gray, HF; Mi, W; Struyk, AF; Wu, F	1

Other Studies

1 other study(ies) available for ouabain and Familial Hypokalemic Periodic Paralysis

Article	Year
A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis. The Journal of clinical investigation, 2011, Volume: 121, Issue:10 Topics: Amino Acid Substitution; Animals; Disease Models, Animal; Female; Gene Knock-In Techniques; Glucose; Homozygote; Humans; Hypokalemic Periodic Paralysis; Insulin; Isometric Contraction; Male; Mice; Mice, Mutant Strains; Mutagenesis, Site-Directed; Mutant Proteins; NAV1.4 Voltage-Gated Sodium Channel; Ouabain; Phenotype; Potassium; Sodium Channels	2011

Article

Year

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

The Journal of clinical investigation, 2011, Volume: 121, Issue:10

Topics: Amino Acid Substitution; Animals; Disease Models, Animal; Female; Gene Knock-In Techniques; Glucose; Homozygote; Humans; Hypokalemic Periodic Paralysis; Insulin; Isometric Contraction; Male; Mice; Mice, Mutant Strains; Mutagenesis, Site-Directed; Mutant Proteins; NAV1.4 Voltage-Gated Sodium Channel; Ouabain; Phenotype; Potassium; Sodium Channels

2011