Keyphrases
Gene Model
100%
Hereditary Spastic Paraparesis
100%
Genetic Model
100%
Motor Neuron Disease
100%
Amyotrophic Lateral Sclerosis
71%
Alsin
57%
Spastin
42%
Primary Lateral Sclerosis
42%
ALS2
28%
Upper Motor Neuron
28%
Protein-protein Interaction
28%
Specific Intent
28%
ALS Phenotypes
14%
Heterogeneous Disorder
14%
SPG5
14%
Chromosome 8q
14%
Confocal Microscopy Analysis
14%
Dual-labeling
14%
FRET Analysis
14%
Gene Discovery
14%
Causative Gene
14%
High-throughput Sequencing
14%
SPG4
14%
Confocal FRET
14%
Knock-in Mouse Model
14%
Co-immunoprecipitation (co-IP)
14%
X Chromosome
14%
Motor Neuron Degeneration
14%
Related Disorders
14%
Signaling Pathway
14%
Yeast Two-hybrid
14%
Genetic Contribution
14%
Lower Motor Neuron
14%
Interaction Partner
14%
Dementia
14%
Last Five Years
14%
Disease Mechanisms
14%
Bioinformatics
14%
Biochemistry, Genetics and Molecular Biology
Genetic Model
100%
Motor Neuron
100%
Spastin
100%
ALS2
66%
Upper Motor Neuron
66%
Knockout Model
33%
Gene Discovery
33%
X Chromosome
33%
Fluorescence Resonance Energy Transfer
33%
Immunoprecipitation
33%
Genetics
33%
Confocal Microscopy
33%
Protein-Protein Interaction
33%
Protein Interaction
33%
Nerve Cell Degeneration
33%
Chromosome 8q
33%
High Throughput Sequencing
33%
Lower Motor Neuron
33%
Two-Hybrid Screening
33%
Bioinformatics
33%
Neuroscience
Amyotrophic Lateral Sclerosis
100%
Paraparesis
77%
Spastin
33%
Primary Lateral Sclerosis
33%
Upper Motor Neuron
22%
Confocal Microscopy
11%
Lower Motor Neuron
11%
Nerve Cell Degeneration
11%
Protein-Protein Interaction
11%
Protein Interaction
11%
Chromosome 8q
11%
X Chromosome
11%
Immunoprecipitation
11%