Publikationen von Alexandra K. Davies

Saffari, A.; Brechmann, B.; Böger, C.; Saber, W. A.; Jumo, H.; Whye, D.; Wood, D.; Wahlster, L.; Alecu, J. E.; Ziegler, M. et al.; Scheffold, M.; Winden, K.; Hubbs, J.; Buttermore, E. D.; Barrett, L.; Borner, G. H. H.; Davies, A. K.; Ebrahimi-Fakhari, D.; Sahin, M.: High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia. Nature Communications 15, 584 (2024)

Schessner, J. P.; Albrecht, V.; Davies, A. K.; Sinitcyn, P.; Borner, G. H. H.: Deep and fast label-free Dynamic Organellar Mapping. Nature Communications 14 (1), 5252 (2023)

Rodriguez-Silvestre, P.; Laub, M.; Krawczyk, P. A.; Davies, A. K.; Schessner, J. P.; Parveen, R.; Tuck, B. J.; McEwan, W. A.; Borner, G. H.; Kozik, P.: Perforin-2 is a pore-forming effector of endocytic escape in cross-presenting dendritic cells. Science 380 (6651), S. 1258 - 1265 (2023)

Davies, A. K.; Alecu, J. E.; Ziegler, M.; Vasilopoulou, C. G.; Merciai, F.; Jumo, H.; Afshar-Saber, W.; Sahin, M.; Ebrahimi-Fakhari, D.; Borner, G. H. H.: AP-4-mediated axonal transport controls endocannabinoid production in neurons. Nature Communications 13 (1), 1058 (2022)

Ebrahimi-Fakhari, D.; Alecu, J. E.; Brechmann, B.; Ziegler, M.; Eberhardt, K.; Jumo, H.; D'Amore, A.; Habibzadeh, P.; Faghihi, M. A.; De Bleecker, J. L. et al.; Vuillaumier-Barrot, S.; Auvin, S.; Santorelli, F. M.; Neuser, S.; Popp, B.; Yang, E.; Barrett, L.; Davies, A. K.; Saffari, A.; Hirst, J.; Sahin, M.: High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegia. Brain Communications 3 (4), fcab221 (2021)

Behne, R.; Teinert, J.; Wimmer, M.; D'Amore, A.; Davies, A. K.; Scarrott, J. M.; Eberhardt, K.; Brechmann, B.; Chen, I. P.-F.; Buttermore, E. D. et al.; Barrett, L.; Dwyer, S.; Chen, T.; Hirst, J.; Wiesener, A.; Segal, D.; Martinuzzi, A.; Duarte, S. T.; Bennett, J. T.; Bourinaris, T.; Houlden, H.; Roubertie, A.; Santorelli, F. M.; Robinson, M.; Azzouz, M.; Lipton, J. O.; Borner, G. H. H.; Sahin, M.; Ebrahimi-Fakhari, D.: Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking. HUMAN MOLECULAR GENETICS 29 (2), S. 320 - 334 (2020)

Ebrahimi-Fakhari, D.; Brechmann, B.; Ziegler, M.; Alecu, J. E.; Eberhardt, K.; Jumo, H.; D'Amore, A.; Davies, A. K.; Neuser, S.; Popp, B. et al.; Yang, E.; Barrett, L.; Hirst, J.; Sahin, M.: High-Throughput Imaging of ATG9A Distribution as a Diagnostic Functional Assay for Adaptor Protein Complex 4 - Associated Hereditary Spastic Paraplegia. In Annals of Neurology, 90 (S27), K-211, S. S195 - S195. 146th Annual Meeting American Neurological Association, ELECTR NETWORK, 17. Oktober 2021 - 19. Oktober 2021. American Neurological Association, Boston (2021)