Keyphrases
Amyotrophic Lateral Sclerosis
100%
TAR DNA-binding Protein 43 (TDP-43)
100%
SOD1 mutation
100%
Mutant SOD1
41%
Superoxide Dismutase 1 (SOD1)
33%
Familial ALS
25%
Glia
16%
SOD1G93A Mice
16%
Transfected Cells
8%
Phosphorylation
8%
Physical Interaction
8%
Spinal Cord
8%
Overexpression
8%
Insolubility
8%
Co-immunoprecipitation (co-IP)
8%
Neurodegenerative Diseases
8%
Detergent
8%
Cell Apoptosis
8%
Immunoprecipitation Assay
8%
Pathologic
8%
Motor Neuron
8%
Age-dependent
8%
Insoluble Fraction
8%
Zn-superoxide Dismutase
8%
Motor Neuron Disease
8%
Neuronal Cytotoxicity
8%
SOD1G93A
8%
C-terminal Fragments
8%
Adult-onset
8%
Human Tissue Model
8%
IPSC-derived Neurons
8%
ALS Patients
8%
Human Cell Models
8%
Cytoplasmic Inclusions
8%
Neuroscience
Amyotrophic Lateral Sclerosis
100%
SOD1
100%
TAR DNA Binding Protein
100%
Motor Neuron
25%
Glia
16%
Cell Line
8%
Neurodegenerative Disorder
8%
C-Terminus
8%
Immunoprecipitation
8%
Cytotoxicity
8%
Copper Zinc Superoxide Dismutase
8%
Biochemistry, Genetics and Molecular Biology
TAR DNA Binding Protein
100%
SOD1
100%
Motor Neuron
25%
Superoxide Dismutase
8%
C-Terminus
8%
Animal Model
8%
Solubility
8%
Immunoprecipitation
8%
Cytotoxicity
8%
Induced Pluripotent Stem Cell
8%