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To compare the proteome between PFN1 mutant and PFN1 WT iPSC-microglia under baseline conditions
ORGANISM(S): Homo sapiens (Human) 
2024-02-18 | PXD038943 | Pride
Dominant mutations in profilin-1 (PFN1) are associated with amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disease characterized by motor neuron loss, paralysis, and death from respiratory failure. Our lab recently demonstrated that PFN1 mutant proteins are destabilized—they unfold a...
ORGANISM(S): Homo sapiens (Human) 
2022-02-15 | PXD015602 | Pride
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