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7. Dysfunction of X-linked inhibitor of apoptosis protein (XIAP) triggers neuropathological processes via altered p53 activity in Huntington’s disease

9. Modulation of SETDB1 activity by APQ ameliorates heterochromatin condensation, motor function, and neuropathology in a Huntington’s disease mouse model

11. Personalized iPSC-Derived Dopamine Progenitor Cells for Parkinson’s Disease

13. Human autologous iPSC–derived dopaminergic progenitors restore motor function in Parkinson’s disease models

15. Dysfunction of X-linked inhibitor of apoptosis protein (XIAP) leads to neuronal damage via altered p53 activity in Huntington's disease

20. Cell-Penetrating Peptide-Patchy Deformable Polymeric Nanovehicles with Enhanced Cellular Uptake and Transdermal Delivery

31. LRRK2 G2019S mutation attenuates microglial motility by inhibiting focal adhesion kinase

33. Increased TRPC5 glutathionylation contributes to striatal neuron loss in Huntington’s disease

49. Pharmacological Rescue of Mitochondrial Deficits in iPSC-Derived Neural Cells from Patients with Familial Parkinson’s Disease

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