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Stephen C Cannon Selected Research

Hypokalemic Periodic Paralysis (Periodic Paralysis, Hypokalemic)

1/2022Voltage-dependent Ca2+ release is impaired in hypokalemic periodic paralysis caused by CaV1.1-R528H but not by NaV1.4-R669H.
11/2021Gating pore currents occur in CaV1.1 domain III mutants associated with HypoPP.
1/2018Stac3 enhances expression of human CaV1.1 in Xenopus oocytes and reveals gating pore currents in HypoPP mutant channels.
8/2014Disrupted coupling of gating charge displacement to Na+ current activation for DIIS4 mutations in hypokalemic periodic paralysis.
3/2013Bumetanide prevents transient decreases in muscle force in murine hypokalemic periodic paralysis.
12/2012A calcium channel mutant mouse model of hypokalemic periodic paralysis.
10/2011A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis.
5/2011Leaky sodium channels from voltage sensor mutations in periodic paralysis, but not paramyotonia.
6/2010Voltage-sensor mutations in channelopathies of skeletal muscle.
10/2008Gating pore currents in DIIS4 mutations of NaV1.4 associated with periodic paralysis: saturation of ion flux and implications for disease pathogenesis.
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Stephen C Cannon Research Topics

Disease

11Hypokalemic Periodic Paralysis (Periodic Paralysis, Hypokalemic)
01/2022 - 07/2007
11Channelopathies
01/2022 - 07/2002
11Myotonia
01/2020 - 07/2002
11Paralysis (Palsy)
01/2020 - 08/2002
3Muscular Diseases (Myopathy)
01/2019 - 01/2016
2Epilepsy (Aura)
09/2019 - 01/2010
2Myotonic Dystrophy (Dystrophia Myotonica)
12/2004 - 07/2002
1Myoclonic Epilepsies (Myoclonic Encephalopathy)
01/2021
1Brain Diseases (Brain Disorder)
01/2021
1Arthrogryposis
01/2020
1Bronchial Spasm
01/2020
1Seizures (Absence Seizure)
09/2019
1Acidosis
01/2019
1Malignant Hyperthermia
01/2017
1Muscle Hypotonia (Hypotonia)
03/2016
1Myotonia Congenita (Thomsen Disease)
03/2014
1Rare Diseases (Rare Disease)
03/2014
1Muscle Weakness
12/2013
1Hyperkalemic Periodic Paralysis
03/2013
1Limb-Girdle Muscular Dystrophies (Limb-Girdle Muscular Dystrophy)
10/2011
1Limb-girdle muscular dystrophy type 2H
10/2011
1Bardet-Biedl Syndrome (Syndrome, Bardet-Biedl)
10/2011
1Dystonia (Limb Dystonia)
07/2004
1Dystonia 12
07/2004

Drug/Important Bio-Agent (IBA)

16Sodium Channels (Sodium Channel)IBA
01/2022 - 06/2005
8Arginine (L-Arginine)FDA Link
01/2022 - 07/2007
7Calcium Channels (Calcium Channel)IBA
01/2022 - 06/2010
4PotassiumIBA
11/2021 - 04/2008
4SodiumIBA
01/2021 - 06/2010
4Chloride Channels (Chloride Channel)IBA
04/2015 - 07/2002
4ChloridesIBA
03/2014 - 07/2002
4Ion Channels (Ion Channel)IBA
06/2010 - 08/2002
3Proteins (Proteins, Gene)FDA Link
09/2019 - 12/2004
2Protons (Proton)IBA
01/2018 - 07/2007
2CalciumIBA
01/2018 - 12/2012
2Potassium Channels (Potassium Channel)IBA
01/2018 - 04/2015
2Bumetanide (Bumex)FDA LinkGeneric
12/2013 - 03/2013
2Protein Isoforms (Isoforms)IBA
10/2008 - 07/2007
2RNA Precursors (Precursor, mRNA)IBA
12/2004 - 07/2002
1Indicators and Reagents (Reagents)IBA
01/2022
1Oregon Green 488 carboxylic acidIBA
01/2022
1L-Type Calcium Channels (Dihydropyridine Receptor)IBA
11/2021
1Carbamazepine (Tegretol)FDA LinkGeneric
01/2020
1Lysine (L-Lysine)FDA Link
01/2020
1MagnesiumIBA
01/2017
1Dantrolene (Dantrium)FDA LinkGeneric
01/2017
1Insulin (Novolin)FDA Link
12/2013
1Glucose (Dextrose)FDA LinkGeneric
12/2013
1Cysteine (L-Cysteine)FDA Link
07/2013
1Tripartite Motif ProteinsIBA
10/2011
1Voltage-Gated Sodium ChannelsIBA
03/2008
1Ligand-Gated Ion ChannelsIBA
01/2006
1Messenger RNA (mRNA)IBA
12/2004
1Adenosine Triphosphatases (ATPase)IBA
07/2004
1RNA (Ribonucleic Acid)IBA
07/2002

Therapy/Procedure

2Therapeutics
01/2020 - 12/2013
1Drug Therapy (Chemotherapy)
09/2019
1Transcutaneous Electric Nerve Stimulation (TENS)
01/2019