Channel:  Aligning Science Across Parkinson's (ASAP)

462 Articles

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Generation of knock-in Cre and FlpO mouse lines for precise targeting of striatal projection neurons and dopaminergic neurons
Albarran, E., Fushiki, A., Nelson, A., Ng, D., Chaimowitz, C., Nikoobakht, L., Sippy, T., Peterka, D. S., Costa, R. M.
10.1101/2025.06.15.659794 — Posted: 2025-06-15
Single-cell multiomics identifies both shared and unique features of immune dysfunction in Parkinson's disease and inflammatory bowel disease colon, plasma and stool
Bolen, M. L., Buendia, M., Shi, J., Staley, H., Kachergus, J. M., Efron, P. A., Park, G., Nagpal, R., Alvarez, S. D., Xue, Q.-S., McFarland, N. R., Zimmermann, E. M., Forsmark, C. E., Menees, K. B., Salas, A., Thompson, E. A., Tansey, M. G.
10.1101/2025.04.29.651228 — Posted: 2025-06-11
Internalized α-synuclein fibrils become truncated and resist degradation in neurons while glial cells rapidly degrade α-synuclein fibrils.
Karim, M. R., Tiegs, E., Gasparini, E., Schlichte, R., Vermilyea, S. C., Lee, M. K.
10.1101/2024.06.05.597615 — Posted: 2025-06-11
The age at onset of LRRK2 p.Gly2019Ser Parkinson's disease across ancestries and countries of origin
Lüth, T., Laabs, B.-H., Sendel, S., König, I. R., Caliebe, A., Noyce, A. J., Screven, L. A., Bardien, S., Farrer, M., Hentati, F., Klein, C., Ben Sassi, S., Trinh, J., Global Parkinson's Genetics Program (GP2)
10.1101/2025.06.04.25327685 — Posted: 2025-06-09
JIP4 deficiency causes a novel lysosome storage disease arising from impaired cystine efflux
Nassar, L. M., Shi, x., Roczniak-Ferguson, A., Shen, H., Ferguson, S. M.
10.1101/2025.06.06.657909 — Posted: 2025-06-09
Genetic modulation of immune gene co-expression in the aged mouse hippocampus by the Apbb1ip locus
Tomkins, J. E., Methi, A., Bouland, G., Doludda, B., Murphy, K., Miller, J. A., Overall, R. W., Mozhui, K.
10.1101/2025.06.04.657838 — Posted: 2025-06-08
Parkinson's disease-vulnerable and -resilient dopamine neurons display opposite responses to excitatory input
Hadjas, L. C., Kollman, G. J., Linderhof, L., Xia, M., Mansur, S., Saint-Pierre, M., Lim, B., Lee, E. B., Cicchetti, F., Awatramani, R., Hollon, N. G., Hnasko, T. S.
10.1101/2025.06.03.657460 — Posted: 2025-06-07
Bridging Pleiotropic Mechanisms in Leprosy Type-1 Reactions and Neurodegenerative diseases
Fava, V. M., Perico, J., Orlova, M., Dallmann-Sauer, M., Xu, Y. Z., Van Thuc, N., Thai, V. H., Belone, A. F., Latini, A. C. P., Schurr, E.
10.1101/2025.06.05.25329059 — Posted: 2025-06-06
RAB32-linked Parkinson's disease: Deep phenotyping, MDSGene literature review, and application of SynNeurGe criteria
Kleinz, T., Cavallieri, F., Borsche, M., Toschi, G., Valzania, F., Fioravanti, V., Valente, E. M., Mitrotti, P., Avenali, M., Zittel, S., Born, R., Matarazzo, M., Di Fonzo, A., Monfrini, E., Radefeldt, M., Santinelli, L., Griebner, N., Shambetova, C., Brand, M., Gabbert, C., Blauwendraat, C., Trinh, J., Beetz, C., Bauer, P., Brueggemann, N., Global Parkinson's Genetics Program (GP2), , Klein, C.
10.1101/2025.06.03.25328628 — Posted: 2025-06-03
Genetically Encoded and Modular SubCellular Organelle Probes (GEM-SCOPe) reveal lysosomal and mitochondrial dysfunction driven by PRKN knockout
Goldman, C., Kareva, T., Sarrafha, L., Sahasrabudhe, A., Schuldt, B. R., Ahfeldt, T., Blanchard, J. W.
10.1101/2024.05.21.594886 — Posted: 2025-06-02

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