Alexandra K Davies

9PUBLICATIONS
40CO-AUTHORS
Neurology and neuromuscular diseasesMedical devicesMedical molecular engineering of nucleic acids and proteinsAutomated software engineeringInnate immunity
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Publications (9)

|Oct 02, 2024
Pre-clinical development of AP4B1 gene replacement therapy for hereditary spastic paraplegia type 47.

Jessica P Wiseman, Joseph M Scarrott, João Alves-Cruzeiro

|Apr 05, 2024
The role of the AP-1 adaptor complex in outgoing and incoming membrane traffic.

Margaret S Robinson, Robin Antrobus, Anneri Sanger

|Jan 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 paraplegia.

Afshin Saffari, Barbara Brechmann, Cedric Böger

|Aug 29, 2023
Deep and fast label-free Dynamic Organellar Mapping.

Julia P Schessner, Vincent Albrecht, Alexandra K Davies

|Jul 03, 2023
High-Content Small Molecule Screen Identifies a Novel Compound That Restores AP-4-Dependent Protein Trafficking in Neuronal Models of AP-4-Associated Hereditary Spastic Paraplegia.

Afshin Saffari, Barbara Brechmann, Cedric Boeger

|Jun 22, 2023
Perforin-2 is a pore-forming effector of endocytic escape in cross-presenting dendritic cells.

Pablo Rodríguez-Silvestre, Marco Laub, Patrycja A Krawczyk

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Frequent Collaborators

6 joint publications

Georg H H Borner

4 joint publications

Mustafa Sahin

4 joint publications

Darius Ebrahimi-Fakhari

3 joint publications

Wardiya Afshar-Saber