Keyphrases
Potassium Channel
83%
Ion Channels
74%
AMP-activated Protein Kinase
66%
Calmodulin
66%
Kv1.4
66%
Abnormal Repolarization
66%
Ca2+
66%
Protein Kinase
66%
Conductance
66%
Atrial Fibrillation
66%
SKA3
66%
NEDD4
47%
SCN5A
44%
Loss Function
44%
Na+ Current
44%
Left Bundle Branch Block
44%
Surface Expression
38%
Epilepsy Patients
33%
KCNC1
33%
Pharmacological Activation
26%
SCN5A Gene
22%
Patch Clamp
22%
Long QT Syndrome
22%
Cardiac Phenotype
22%
Channelopathy
22%
Diagnostic Criteria
22%
Brugada Syndrome
22%
Arrhythmia
22%
Inactivation Kinetics
22%
Clinical Manifestations
22%
Biophysical Properties
22%
Genetic Variation
22%
Persistent Atrial Fibrillation
22%
Structural Abnormalities
22%
Voltage-gated Sodium Channel
22%
Associated Phenotypes
22%
Proband
22%
Underlining
22%
Ubiquitin Ligase
19%
Xenopus Oocytes
19%
Serum and Glucocorticoid-regulated Kinase 1
19%
Phosphatidylinositol 4-phosphate 5-kinase (PIP5K)
19%
Myoclonus
16%
Current Amplitude
16%
Ataxia
16%
Membrane Potential
16%
Channel Activation
16%
Seizure Disorder
16%
GABAergic Interneurons
16%
Activation Kinetics
16%
Biochemistry, Genetics and Molecular Biology
Potassium Channel
100%
Repolarization
100%
Ion Channel
74%
Atrial Fibrillation
66%
Calmodulin
66%
SK3
66%
AMP-activated Protein Kinase
66%
Conductance
66%
calcium activated,phospholipid dependent protein kinase
66%
Kinase
53%
Phosphotransferase
53%
Left Bundle Branch Block
44%
Long QT Syndrome
37%
Electric Potential
35%
Cell Membrane
33%
Membrane Potential
33%
Current Amplitude
33%
Action Potential
33%
Interneuron
33%
Cardiac Dysrhythmia
29%
Ubiquitin Ligase
26%
Xenopus laevis
26%
Glucocorticoid
26%
Brugada Syndrome
22%
Patch Clamp
22%
Sodium Channel
22%
Channelopathy
22%
Electrocardiogram
22%
Genetic Variation
22%
Proband
22%
T Wave
22%
Medicine and Dentistry
Repolarization
83%
Lafora Disease
66%
Ion Channel
66%
Potassium Channel Kv1.4
66%
Atrial Fibrillation
66%
Myocardial Disease
66%
Left Bundle Branch Block
66%
Sodium Ion
66%
Cardiac Dysrhythmia
33%
In Vitro
33%
Diagnosis
33%
Patch Clamp
33%
KCNC1
33%
Voltage Gated Sodium Channel
33%
Brugada Syndrome
33%
Channelopathy
33%
Persistent Atrial Fibrillation
33%
Electrocardiogram
33%
Long QT Syndrome
33%
Genetic Variation
33%
Phosphatidylinositol 4,5 Bisphosphate 3 Kinase
26%
Serum and Glucocorticoid Regulated Kinase 1
26%
Tonic-Clonic Seizure
16%
Interneuron
16%
Potassium Channel
16%
Membrane Potential
16%
Epileptic Seizure
16%
Cell Membrane
16%
Action Potential
16%
Disease
16%
Myoclonus
16%
Ataxia
16%