The HUWE1-HAPSTR1-USP7 complex is established as a key ubiquitin code modifier, providing a molecular rationale for HUWE1 dysregulation in neurodevelopmental disorders and cancer.
S. Yatskevich, Jugal Mohapatra, R. Mroue et al.· Molecules and Cells· 0 citations
The development of scalable iPSC-neuron models enables tauopathy drug discovery and reconstructs progressive Tau seeding, fibrillization and synaptic dysfunction, and establishes a physiologically relevant, scalable platform for therapeutic screening that connects Tau seed uptake, site-specific phosphorylation, fibril...
J. Lipka, Xiwei Shan, Qiao Zhang et al.· bioRxiv· 0 citations
It is shown that depletion of these AD risk genes disrupts baseline morpho-transcriptomic coupling and fundamentally alters microglial phagocytic capacity, revealing how AD GWAS genes may drive microglia into dysfunctional states characterized by altered morphology, distinct multi-omic signatures, and impaired function...
Ying-Jie Zhang, Ai Zhang, Sang Seo et al.· bioRxiv· 0 citations
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