Neuroscience
Potassium Channel
100%
Episodic Ataxia
51%
Ion Channel
40%
Voltage-Gated Potassium Channel
35%
Kv1.1
35%
Pervasive Developmental Disorder
28%
Inward-Rectifier Potassium Ion Channel
25%
Dopaminergic
21%
C-Terminus
17%
In Vivo
17%
Cell Migration
16%
Migraine
15%
Spectrum Disorder
14%
Medial Vestibular Nucleus
14%
Locus Coeruleus
14%
Glioblastoma Multiforme
14%
Auras
11%
Excitability
10%
Potassium Current
10%
Cell pH
9%
Channel Gating
9%
Cell Death
8%
Neurodegeneration
8%
Ataxia
8%
Potassium Channel Kv1.4
8%
Cell Swelling
8%
Channelopathy
8%
Potassium Channel Kv1.1
7%
Point Mutation
7%
Sphingolipid Activator Protein 2
7%
Lorcaserin
7%
Cerebral Palsy
7%
Tyrosine Hydroxylase
7%
Nociceptor
7%
Protein Tyrosine Phosphatase
7%
Valine
7%
Isoleucine
7%
Antibodies
7%
Amino Acid
7%
In Situ Hybridization
7%
Nerve Cell Differentiation
7%
Pediatric Epilepsy
7%
Phosphatase
7%
Calcium Channel
7%
Excitation Contraction Coupling
7%
Neuroscience
7%
5-HT2C Receptor
7%
Amino Acid Substitution
7%
Protein Binding
7%
Cell Plasticity
7%
8-OH-DPAT
7%
Phytochemical
7%
Megalencephalic Leukoencephalopathy with Subcortical Cysts
7%
BK Channel
7%
Proline
7%
Cell Survival
7%
Muscle Disorder
7%
Thiol
7%
Tobacco Dependence
7%
Cell Function
7%
Ganglion
7%
Sensory Neuron
7%
Serotonin
7%
Levosulpiride
7%
Sulpiride
7%
Inwardly Rectifying Potassium Channel
7%
Protein Aggregate
7%
KCNA4
7%
Inflammatory Bowel Disease
7%
Anion Channel
7%
Calcium Calmodulin Dependent Protein Kinase II
7%
KCNT1
7%
Calmodulin
7%
Ischemia
7%
Trace Amine
7%
Microdialysis
7%
KCNJ10
6%
Skeletal Muscle
6%
Niflumic Acid
6%
Neurological Disorder
6%
Nucleus Accumbens
5%
Striatum
5%
Metabolic Pathway
5%
Substantia Nigra Pars Compacta
5%
Biochemistry, Genetics and Molecular Biology
Potassium Channel
78%
Episodic Ataxia
52%
Kv1.1
31%
Electric Potential
31%
Inward-Rectifier Potassium Ion Channel
21%
Wild Type
21%
Voltage-Gated Potassium Channel
20%
Genetics
14%
Transmembrane Domain
14%
KCNJ10
14%
Cystic Fibrosis
14%
C-Terminus
12%
Channel Gating
11%
Autosomal Dominant Inheritance
11%
Conductance
10%
Animal Model
10%
Morphology
10%
Xenopus
10%
Missense Mutation
9%
Founder Effect
7%
Knockout Mouse
7%
Tyrosine Hydroxylase
7%
Intellectual Disability
7%
Peptide Sequence
7%
Breed
7%
Muscarine
7%
KCNA4
7%
Isoleucine
7%
Protein Tyrosine Phosphatase
7%
Calsequestrin
7%
Potassium Channels
7%
Exome Sequencing
7%
Proline
7%
Weaver Mouse
7%
Serotonergic
7%
Prevalence
7%
Q-Type Calcium Channel
7%
Excitation Contraction Coupling
7%
Tubulin
7%
Cell Migration
7%
Membrane Potential
7%
Mouse
7%
Amino Acids
7%
Testis Development
7%
Valine
7%
BK Channel
7%
Mouse Strain
7%
Wild Type Mouse
7%
Actin
7%
Missense
7%
G Protein
7%
MLC1
7%
Dopaminergic
7%
KCNT1
7%
Flagellum
7%
Spermatogonium
7%
Kir2.1
7%
Potassium Current
7%
Current Amplitude
6%
Xenopus laevis
6%
Skeletal Muscle
6%
Point Mutation
6%
Channelopathy
5%
Oxidation Reduction Reaction
5%
Thiol
5%
Homeostasis
5%
Keyphrases
Single Molecule
14%
Thymosin
14%
Cystic Fibrosis
14%
Gating Properties
10%
Episodic Ataxia
9%
Kv1.1
8%
Italian Families
7%
5-HT2CR
7%
Kv1.4
7%
Renal Tubular Epithelium
7%
Lorcaserin
7%
ClC Channels
7%
ClC-1
7%
Chloride Channel
7%
Spastic Cerebral Palsy
7%
Spectrum Disorder
7%
Molecular Profile
7%
Kv1.2
7%
CaMKII
7%
Volume-regulated Anion Channel
7%
Redox Sensitivity
7%
Skeletal Disorders
7%
Receptor Protein Tyrosine Phosphatase
7%
Neuron Firing
7%
CASQ1
7%
HyperCKaemia
7%
Amino Acid Sequence
7%
Human Glioblastoma
7%
Weaver
7%
Heteromeric Channel
7%
Channel Formation
7%
Cav2.1
7%
Childhood Epilepsy
7%
Epilepsy Onset
7%
CACNA1A Gene
7%
Episodic Ataxia Type 2
7%
Kir4.1
7%
KCa3.1 Channel
7%
KCNJ10
7%
Tubulin
7%
Short-term Potentiation
7%
Medial Vestibular nucleus
7%
Granular Cells
7%
Cell Plasticity
7%
KCNK18
7%
Migraine Disability
7%
TRESK
7%
Unitary Conductance
7%
Positional Effect
7%
Megalencephalic Leukoencephalopathy with Subcortical Cysts
7%
MLC1
7%
Kcnj16
7%
Therapy Mechanism
7%
Partial Pressure of CO2 (pCO2)
7%
Glioblastoma multiforme
7%
Kir5.1
7%
Surface Affinity
7%
Kir4.2
7%
Intestinal Fibrosis
7%
Inhibitory Interactions
7%
Kir2.1 Channel
7%
Kir2.1
7%
Functional Characterization
7%
Cation Current
7%
Isoform Sequencing
7%
Digenic mutation
7%
KCNT1
7%
Time-dependent Changes
7%
Volume Cell
7%
Trace Amines
7%
Glioblastoma Cell Lines
7%
Online Methods
7%
Swelling-activated
7%
Trigeminal Ganglion Neurons
7%
Actin
7%
Age-dependent Expression
7%
Pore Region
7%
Higher Order mutation
7%
Blotting
7%
Abnormal Spermatozoa
7%
Dyshomeostasis
7%
ERG Channels
5%