Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

302 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
The Reelin receptor ApoER2 is a cargo for the adaptor protein complex AP-4: Implications for Hereditary Spastic Paraplegia.
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. Caracci MO, et al. Among authors: bonifacino js. Prog Neurobiol. 2024 Mar;234:102575. doi: 10.1016/j.pneurobio.2024.102575. Epub 2024 Jan 26. Prog Neurobiol. 2024. PMID: 38281682
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia.
Diarra S, Ghosh S, Cissé L, Coulibaly T, Yalcouyé A, Harmison G, Diallo S, Diallo SH, Coulibaly O, Schindler A, Cissé CAK, Maiga AB, Bamba S, Samassekou O, Khokha MK, Mis EK, Lahkani SA, Donovan FX, Jacobson S, Blackstone C, Guinto CO, Landouré G, Bonifacino JS, Fischbeck KH, Grunseich C. Diarra S, et al. Among authors: bonifacino js. Neurobiol Dis. 2024 May 19:106537. doi: 10.1016/j.nbd.2024.106537. Online ahead of print. Neurobiol Dis. 2024. PMID: 38772452
The Reelin Receptor ApoER2 is a Cargo for the Adaptor Protein Complex AP-4: Implications for Hereditary Spastic Paraplegia.
Caracci MO, Pizarro H, Alarcón-Godoy C, Fuentealba LM, Farfán P, Pace R, Santibañez N, Cavieres VA, Pástor TP, Bonifacino JS, Mardones GA, Marzolo MP. Caracci MO, et al. Among authors: bonifacino js. bioRxiv [Preprint]. 2023 Dec 22:2023.12.21.572896. doi: 10.1101/2023.12.21.572896. bioRxiv. 2023. PMID: 38187774 Free PMC article. Updated. Preprint.
Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics.
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, Suri M, Zifarelli G, Bauer P, Houlden H, Severino M, Patten SA, Farrow E, Bonifacino JS. De Pace R, et al. Among authors: bonifacino js. Brain. 2024 May 3;147(5):1751-1767. doi: 10.1093/brain/awad427. Brain. 2024. PMID: 38128568 Free PMC article.
Architecture of the ESCPE-1 membrane coat.
Lopez-Robles C, Scaramuzza S, Astorga-Simon EN, Ishida M, Williamson CD, Baños-Mateos S, Gil-Carton D, Romero-Durana M, Vidaurrazaga A, Fernandez-Recio J, Rojas AL, Bonifacino JS, Castaño-Díez D, Hierro A. Lopez-Robles C, et al. Among authors: bonifacino js. Nat Struct Mol Biol. 2023 Jul;30(7):958-969. doi: 10.1038/s41594-023-01014-7. Epub 2023 Jun 15. Nat Struct Mol Biol. 2023. PMID: 37322239 Free PMC article.
Inhibition of endolysosome fusion increases exosome secretion.
Shelke GV, Williamson CD, Jarnik M, Bonifacino JS. Shelke GV, et al. Among authors: bonifacino js. J Cell Biol. 2023 Jun 5;222(6):e202209084. doi: 10.1083/jcb.202209084. Epub 2023 May 22. J Cell Biol. 2023. PMID: 37213076 Free PMC article.
302 results