13 results on '"Keagle, Pamela J."'
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2. Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia
3. Systematic rare variant analyses identify RAB32as a susceptibility gene for familial Parkinson’s disease
4. Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia
5. Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia
6. ATXN2 intermediate expansions in amyotrophic lateral sclerosis.
7. Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
8. A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts
9. Characterization of FUS Mutations in Amyotrophic Lateral Sclerosis Using RNA-Seq
10. Paraoxonase gene mutations in amyotrophic lateral sclerosis
11. ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of function.
12. Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia.
13. ATXN2 intermediate expansions in amyotrophic lateral sclerosis.
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