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Small-molecule suppression of calpastatin degradation reduces neuropathology in models of Huntington's disease | Nature Communications
Striatal neurons directly converted from Huntington's disease patient fibroblasts recapitulate age-associated disease phenotypes | Nature Neuroscience
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Cell Type-Specific Transcriptomics Reveals that Mutant Huntingtin Leads to Mitochondrial RNA Release and Neuronal Innate Immune Activation - ScienceDirect
Organ-specific, multimodal, wireless optoelectronics for high-throughput phenotyping of peripheral neural pathways | Nature Communications
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PABPN1 functions as a hub in the assembly of nuclear poly(A) domains that are essential for mouse oocyte development | Science Advances
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