Keyphrases
Mouse Model
100%
Synaptic Dysfunction
100%
Spinocerebellar Ataxia
100%
Purkinje Cell
100%
Parallel Fiber
100%
Fn14
42%
Purkinje Neuron
42%
Neuronal Synapses
42%
Human Disease
28%
Spontaneous Excitatory Postsynaptic Current (sEPSC)
28%
Molecular Study
14%
Glutamate
14%
Receptor-mediated
14%
Cultured Neurons
14%
Genomic Deletion
14%
Induced Response
14%
Dominant-negative mutant
14%
Synapse
14%
AMPA Receptor (AMPAR)
14%
Autosomal Dominant Disorder
14%
Cognitive Impairment
14%
Decreased Expression
14%
Littermate
14%
Motor Impairment
14%
Na +
14%
Voltage Gating
14%
Sr2+
14%
Metabotropic Glutamate Receptor
14%
Ca2+ Channels
14%
Paired-pulse Facilitation
14%
Whole-cell Voltage Clamp
14%
Slice Preparation
14%
Short-term Plasticity
14%
Presynaptic Function
14%
Cerebellar Slice
14%
Glucose Transporter 1 (GLUT1)
14%
Synaptic Cleft
14%
Function Type
14%
MGluR1 Receptors
14%
Inherited mutation
14%
Biochemistry, Genetics and Molecular Biology
Mouse Model
100%
Synapse
100%
Purkinje Cell
100%
Fibroblast Growth Factor
75%
Wild Type
50%
Calcium Channel
25%
Animal Model
25%
Gene Deletion
25%
Whole Cell
25%
Allele
25%
Pulse Rate
25%
Electric Potential
25%
Autosomal Dominant Inheritance
25%
Voltage Clamp
25%
Nerve Cell Culture
25%
Excitatory Postsynaptic Potential
25%
Slice Preparation
25%
AMPA Receptor
25%
Vesicular Glutamate Transporter 1
25%
Glutamic Acid
25%
Neuroscience
Spinocerebellar Ataxia
100%
Purkinje Cell
100%
Parallel Fiber
100%
Synapse
57%
Fibroblast Growth Factor 14
42%
Calcium Channel
14%
In Vitro
14%
Glutamic Acid
14%
Cognitive Disorders
14%
AMPA Receptor
14%
Autosomal Dominant Disorder
14%
Stereotypic Movement Disorder
14%
Cleft
14%
Excitatory Postsynaptic Potential
14%
Gene Deletion
14%
Vesicular Glutamate Transporter 1
14%
Receptor
14%
Voltage Clamp
14%