Keyphrases
Amyotrophic Lateral Sclerosis
100%
Proteostasis Network
100%
Motor Neuron
100%
Degradation Dynamics
20%
Protein Degradation
20%
Vesicular Transport
10%
Genetic mutation
10%
Reduced Protein
10%
Mutant SOD1
10%
Genetic Variants
10%
Neuropathological Proteins
10%
Genetic Studies
10%
Isogenic Controls
10%
Cell Behavior
10%
Motor Neuron Degeneration
10%
Intervention Strategies
10%
Synthesis Rate
10%
Protein Quality Control
10%
Molecular Pathways
10%
Family Forms
10%
Mass Spectrometry Analysis
10%
Neuronal Control
10%
Strategic Advantage
10%
Protein Substrate
10%
Neurodegenerative Diseases
10%
Lower Motor Neuron
10%
RNA Processing
10%
Therapeutic Target
10%
Mitochondrial Function
10%
Proteome-wide
10%
Therapeutic Intervention
10%
Upper Motor Neuron
10%
Cytoskeletal Regulation
10%
Global Analysis
10%
Mitochondrial Proteins
10%
Cellular Mechanisms
10%
Protein Aggregates
10%
Protein Homeostasis
10%
C9orf72
10%
Initiating Event
10%
Neurodegeneration
10%
Superoxide Dismutase 1 (SOD1)
10%
Patient-derived
10%
Biochemistry, Genetics and Molecular Biology
Protein Homeostasis
100%
Motor Neuron
100%
Protein Catabolism
50%
Dynamics
50%
SOD1
50%
Vesicular Transporter
25%
C9orf72
25%
Genetic Divergence
25%
Protein Characterization
25%
Quality Control
25%
Genetics
25%
Proteome
25%
Gene Mutation
25%
Nerve Cell Degeneration
25%
Cell Function
25%
Upper Motor Neuron
25%
RNA Processing
25%
Lower Motor Neuron
25%
Neuroscience
Amyotrophic Lateral Sclerosis
100%
SOD1
20%
Mitochondrial Function
10%
Upper Motor Neuron
10%
Lower Motor Neuron
10%
Neurodegenerative Disorder
10%
Nerve Cell Degeneration
10%
Vesicular Transporter
10%
Gene Mutation
10%
Cell Function
10%
Mass Spectrometry
10%
RNA Processing
10%
Protein Aggregate
10%
Neurodegeneration
10%
Proteome
10%