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Science (New York, N.Y.)|June 22, 2023
Perforin-2 is a pore-forming effector of endocytic escape in cross-presenting dendritic cellsPablo Rodríguez-Silvestre, Marco Laub, Patrycja A Krawczyk, et al.Nature Communications|January 17, 2024
High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegiaAfshin Saffari, Barbara Brechmann, Cedric Böger, et al.Brain Communications|November 3, 2021
High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegiaDarius Ebrahimi-Fakhari, Julian E Alecu, Barbara Brechmann, et al.EMBO Molecular Medicine|October 2, 2024
Pre-clinical development of AP4B1 gene replacement therapy for hereditary spastic paraplegia type 47Jessica P Wiseman, Joseph M Scarrott, João Alves-Cruzeiro, et al.Human Molecular Genetics|January 10, 2020
Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein traffickingRobert Behne, Julian Teinert, Miriam Wimmer, et al.Pageof 2