| Year | Citation | Score | |||
|---|---|---|---|---|---|
| 2024 | Khan YA, De Pace R, Jungreis I, Carancini G, Mudge JM, Wang J, Kellis M, Atkins JF, Baranov PV, Firth AE, Bonifacino JS, Loughran G. Programmed ribosomal frameshifting during mRNA decoding generates a constitutively active mediator of kinesin-1-dependent lysosome transport. Biorxiv : the Preprint Server For Biology. PMID 39372779 DOI: 10.1101/2024.08.30.610563 | 0.497 | |||
| 2024 | Caracci MO, Pizarro H, Alarcón-Godoy C, Fuentealba LM, Farfán P, De Pace R, Santibañez N, Cavieres VA, Pástor TP, Bonifacino JS, Mardones GA, Marzolo MP. Corrigendum to "The Reelin receptor ApoER2 is a cargo for the adaptor protein complex AP-4: Implications for hereditary spastic paraplegia" [Progr. Neurobiol. 234(2024)102575]. Progress in Neurobiology. 102662. PMID 39294072 DOI: 10.1016/j.pneurobio.2024.102662 | 0.508 | |||
| 2024 | De Pace R, Ghosh S, Ryan VH, Sohn M, Jarnik M, Rezvan Sangsari P, Morgan NY, Dale RK, Ward ME, Bonifacino JS. Messenger RNA transport on lysosomal vesicles maintains axonal mitochondrial homeostasis and prevents axonal degeneration. Nature Neuroscience. PMID 38600167 DOI: 10.1038/s41593-024-01619-1 | 0.506 | |||
| 2024 | Caracci MO, Pizarro H, Alarcón-Godoy C, Fuentealba LM, Farfán P, De Pace R, Santibañez N, Cavieres VA, Pástor TP, Bonifacino JS, Mardones GA, Marzolo MP. The Reelin Receptor ApoER2 is a Cargo for the Adaptor Protein Complex AP-4: Implications for Hereditary Spastic Paraplegia. Progress in Neurobiology. 102575. PMID 38281682 DOI: 10.1016/j.pneurobio.2024.102575 | 0.593 | |||
| 2023 | De Pace R, Maroofian R, Paimboeuf A, Zamani M, Zaki MS, Sadeghian S, Azizimalamiri R, Galehdari H, Zeighami J, Williamson CD, Fleming E, Zhou D, Gannon JL, Thiffault I, Roze E, et al. Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics. Brain : a Journal of Neurology. PMID 38128568 DOI: 10.1093/brain/awad427 | 0.507 | |||
| 2023 | Chen X, Dong T, Hu Y, De Pace R, Mattera R, Eberhardt K, Ziegler M, Pirovolakis T, Sahin M, Bonifacino JS, Ebrahimi-Fakhari D, Gray SJ. Intrathecal AAV9/AP4M1 gene therapy for hereditary spastic paraplegia 50 shows safety and efficacy in preclinical studies. The Journal of Clinical Investigation. PMID 36951961 DOI: 10.1172/JCI164575 | 0.402 | |||
| 2023 | De Pace R, Bonifacino JS. Phagocytosis: Phagolysosome vesiculation promotes cell corpse degradation. Current Biology : Cb. 33: R143-R146. PMID 36854271 DOI: 10.1016/j.cub.2023.01.017 | 0.422 | |||
| 2022 | Mattera R, De Pace R, Bonifacino JS. The adaptor protein chaperone AAGAB stabilizes AP-4 complex subunits. Molecular Biology of the Cell. mbcE22050177. PMID 35976721 DOI: 10.1091/mbc.E22-05-0177 | 0.584 | |||
| 2022 | Williamson CD, Guardia CM, De Pace R, Bonifacino JS, Saric A. Measurement of Lysosome Positioning by Shell Analysis and Line Scan. Methods in Molecular Biology (Clifton, N.J.). 2473: 285-306. PMID 35819772 DOI: 10.1007/978-1-0716-2209-4_19 | 0.686 | |||
| 2022 | Januário YC, Eden J, de Oliveira LS, De Pace R, Tavares LA, da Silva-Januário ME, Apolloni VB, Wilby EL, Altmeyer R, Burgos PV, Corrêa SAL, Gershlick DC, daSilva LLP. Clathrin adaptor AP-1-mediated Golgi export of amyloid precursor protein is crucial for the production of neurotoxic amyloid fragments. The Journal of Biological Chemistry. 102172. PMID 35753347 DOI: 10.1016/j.jbc.2022.102172 | 0.676 | |||
| 2021 | Prabhu AV, Kang I, De Pace R, Wassif CA, Fujiwara H, Kell P, Jiang X, Ory DS, Bonifacino JS, Ward ME, Porter FD. A human iPSC-derived inducible neuronal model of Niemann-Pick disease, type C1. Bmc Biology. 19: 218. PMID 34592985 DOI: 10.1186/s12915-021-01133-x | 0.492 | |||
| 2020 | Mattera R, De Pace R, Bonifacino JS. The role of AP-4 in cargo export from the trans-Golgi network and hereditary spastic paraplegia. Biochemical Society Transactions. PMID 33084855 DOI: 10.1042/BST20190664 | 0.583 | |||
| 2020 | De Pace R, Britt DJ, Mercurio J, Foster AM, Djavaherian L, Hoffmann V, Abebe D, Bonifacino JS. Synaptic Vesicle Precursors and Lysosomes Are Transported by Different Mechanisms in the Axon of Mammalian Neurons. Cell Reports. 31: 107775. PMID 32553155 DOI: 10.1016/J.Celrep.2020.107775 | 0.528 | |||
| 2019 | Guardia CM, De Pace R, Sen A, Saric A, Jarnik M, Kolin DA, Kunwar A, Bonifacino JS. Reversible association with motor proteins (RAMP): A streptavidin-based method to manipulate organelle positioning. Plos Biology. 17: e3000279. PMID 31100061 DOI: 10.1371/Journal.Pbio.3000279 | 0.692 | |||
| 2018 | Di Lorenzo G, Voltolini Velho R, Winter D, Thelen M, Ahmadi S, Schweizer M, De Pace R, Cornils K, Yorgan TA, Grüb S, Hermans-Borgmeyer I, Schinke T, Müller-Loennies S, Braulke T, Pohl S. Lysosomal proteome and secretome analysis identifies missorted enzymes and their non-degraded substrates in mucolipidosis III mouse cells. Molecular & Cellular Proteomics : McP. PMID 29773673 DOI: 10.1074/Mcp.Ra118.000720 | 0.667 | |||
| 2018 | De Pace R, Skirzewski M, Damme M, Mattera R, Mercurio J, Foster AM, Cuitino L, Jarnik M, Hoffmann V, Morris HD, Han TU, Mancini GMS, Buonanno A, Bonifacino JS. Altered distribution of ATG9A and accumulation of axonal aggregates in neurons from a mouse model of AP-4 deficiency syndrome. Plos Genetics. 14: e1007363. PMID 29698489 DOI: 10.1371/Journal.Pgen.1007363 | 0.565 | |||
| 2018 | Guardia CM, De Pace R, Mattera R, Bonifacino JS. Neuronal functions of adaptor complexes involved in protein sorting. Current Opinion in Neurobiology. 51: 103-110. PMID 29558740 DOI: 10.1016/J.Conb.2018.02.021 | 0.731 | |||
| 2017 | Mattera R, Park SY, De Pace R, Guardia CM, Bonifacino JS. AP-4 mediates export of ATG9A from the trans-Golgi network to promote autophagosome formation. Proceedings of the National Academy of Sciences of the United States of America. 114: E10697-E10706. PMID 29180427 DOI: 10.1073/Pnas.1717327114 | 0.722 | |||
| 2017 | Velho RV, De Pace R, Klünder S, Di Lorenzo G, Schweizer M, Braulke T, Pohl S. Site-1 protease and lysosomal homeostasis. Biochimica Et Biophysica Acta. 1864: 2162-2168. PMID 28693924 DOI: 10.1016/j.bbamcr.2017.06.023 | 0.664 | |||
| 2017 | Farías GG, Guardia CM, De Pace R, Britt DJ, Bonifacino JS. BORC/kinesin-1 ensemble drives polarized transport of lysosomes into the axon. Proceedings of the National Academy of Sciences of the United States of America. PMID 28320970 DOI: 10.1073/Pnas.1616363114 | 0.689 | |||
| 2016 | Velho RV, De Pace R, Tidow H, Braulke T, Pohl S. Identification of the interaction domains between α- and γ-subunits of GlcNAc-1-phosphotransferase. Febs Letters. 590: 4287-4295. PMID 27736005 DOI: 10.1002/1873-3468.12456 | 0.668 | |||
| 2015 | De Pace R, Velho RV, Encarnação M, Marschner K, Braulke T, Pohl S. Subunit interactions of the disease-related hexameric GlcNAc-1-phosphotransferase complex. Human Molecular Genetics. 24: 6826-35. PMID 26385638 DOI: 10.1093/hmg/ddv387 | 0.675 | |||
| 2015 | Velho RV, De Pace R, Klünder S, Sperb-Ludwig F, Lourenço CM, Schwartz IV, Braulke T, Pohl S. Analyses of disease-related GNPTAB mutations define a novel GlcNAc-1-phosphotransferase interaction domain and an alternative site-1 protease cleavage site. Human Molecular Genetics. 24: 3497-505. PMID 25788519 DOI: 10.1093/hmg/ddv100 | 0.671 | |||
| 2014 | De Pace R, Coutinho MF, Koch-Nolte F, Haag F, Prata MJ, Alves S, Braulke T, Pohl S. Mucolipidosis II-related mutations inhibit the exit from the endoplasmic reticulum and proteolytic cleavage of GlcNAc-1-phosphotransferase precursor protein (GNPTAB). Human Mutation. 35: 368-76. PMID 24375680 DOI: 10.1002/humu.22502 | 0.657 | |||
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