Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy

Keyphrases

• Amyotrophic Lateral Sclerosis 100%
• TAR DNA-binding Protein 43 (TDP-43) 100%
• Motor Neuropathy 100%
• Stathmin-2 100%
• Neuromuscular Junction 30%
• Denervation 20%
• Knock-in Mouse Model 10%
• Excision 10%
• Early Onset 10%
• Axonal Degeneration 10%
• Spinal Cord 10%
• Slowly Progressive 10%
• RNA Splicing 10%
• Functional Deficits 10%
• Neuropathy 10%
• Sensory Neuropathy 10%
• Motor Behavior 10%
• Partial Loss 10%
• Motor Unit 10%
• Heterozygous Mice 10%
• Motoneuron 10%
• TDP-43 Pathology 10%
• Motoneuron Degeneration 10%

Neuroscience

• Amyotrophic Lateral Sclerosis 100%
• Stathmin 100%
• Neuropathy 100%
• Neuromuscular Junction 30%
• Denervation 20%
• Behavior (Neuroscience) 10%
• Motor Unit 10%
• RNA Splicing 10%
• Axon 10%

Biochemistry, Genetics and Molecular Biology

• Transactive Response Dna Binding Protein-43 100%
• Stathmin 100%
• Knockout Mouse 10%
• Axon 10%
• RNA Splicing 10%
• Locomotion 10%