Channel:  Aligning Science Across Parkinson's (ASAP)

448 Articles

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Nova-ST: Nano-Patterned Ultra-Dense platform for spatial transcriptomics
Poovathingal, S., Davie, K., Vandepoel, R., Poulvellarie, N., Verfaillie, A., Corthout, N., Aerts, S.
10.1101/2024.02.22.581576 — Posted: 2024-04-10
Understanding monogenic Parkinson's disease at a global scale
Junker, J., Lange, L. M., Vollstedt, E.-J., Roopnarain, K., Doquenia, M. L. M., Ahmad-Annuar, A., Avenali, M., Bardien, S., Bahr, N., Ellis, M., Galandra, C., Gasser, T., Heutink, P., Illarionova, A., Kanana, Y., Keller Sarmiento, I. J., Kumar, K. R., Lim, S.-Y., Madoev, H., Mata, I., Mencacci, N. E., Nalls, M. A., Padmanabhan, S., Shambetova, C., Solle, J., Tan, A.-H., Trinh, J., Valente, E. M., Singleton, A., Blauwendraat, C., Lohmann, K., Fang, Z.-H., Klein, C., the Global Parkinson's Genetics Program (GP2)
10.1101/2024.03.12.24304154 — Posted: 2024-04-09
Alpha-synuclein aggregates are phosphatase resistant
Choi, S. G., Prada, D. A. G., Tittle, T., Kordower, J. H., Melki, R., Killinger, B. A.
10.1101/2023.11.20.567854 — Posted: 2024-04-09
SARM1 activation induces reversible mitochondrial dysfunction and can be prevented in human neurons by antisense oligonucleotides
Loreto, A., Cramb, K. M. L., McDermott, L. A., Antoniou, C., Cirilli, I., Caiazza, M. C., Merlini, E., Arthur-Farra, P., Mock, E. D., Zhao, H. T., Bennett, D. L., Orsomando, G., Coleman, M. P., Wade-Martins, R.
10.1101/2024.04.02.587827 — Posted: 2024-04-03
Combined detrimental effect of male sex and GBA1 variants on cognitive decline in Parkinson's Disease
Caminiti, S. P., Avenali, M., Galli, A., Malito, R., Cuconato, G., Pilotto, A., Padovani, A., Blandini, F. P., Perani, D., Tassorelli, C., Valente, E. M.
10.1101/2024.04.02.24305191 — Posted: 2024-04-03
Detecting rhythmic spiking through the power spectra of point process model residuals
Cox, K. M., Kase, D., Znati, T., Turner, R. S.
10.1101/2023.09.08.556120 — Posted: 2024-03-25
Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathies
Nazeen, S., Wang, X., Zielinski, D., Lam, I., Hallacli, E., Xu, P., Ethier, E., Strom, R., Zanella, C. A., Nithianandam, V., Ritter, D., Henderson, A., Saurat, N., Afroz, J., Nutter-Upham, A., Benyamini, H., Copty, J., Ravishankar, S., Morrow, A., Mitchel, J., Neavin, D., Gupta, R., Farbehi, N., Grundman, J., Myers, R. H., Scherzer, C. R., Trojanowski, J. Q., Van Deerlin, V. M., Cooper, A. A., Lee, E. B., Erlich, Y., Lindquist, S., Peng, J., Geschwind, D. H., Powell, J., Studer, L., Feany, M. B., Sunyaev, S. R., Khurana, V.
10.1101/2024.03.03.583145 — Posted: 2024-03-07
LRRK2 G2019S mutation suppresses differentiation of Th9 and Treg cells via JAK/STAT3
Zheng, N., Jaffery, R., Guerrero, A., Hou, J., Pan, Y., Zhou, F., Chen, S., Xu, C., Egan, N. A., Bohat, R., Chen, K., Schwarzschild, M. A., Chen, X., Peng, W.
10.1101/2024.02.28.582561 — Posted: 2024-03-03
Adoptive transfer of mitochondrial antigen-specific CD8+ T-cells in mice causes parkinsonism and compromises the dopamine system
Elemeery, M. N., Tchung, A., Boulet, S., Mukherjee, S., Giguere, N., Daudelin, J.-F., Hetu-Arbour, R., Matheoud, D., STRATTON, J. A., Labrecque, N., Trudeau, L.-E.
10.1101/2024.02.26.582098 — Posted: 2024-02-28
Comparative study of enriched dopaminergic neurons from siblings with Gaucher disease discordant for parkinsonism
Hertz, E., Perez, G., Hao, Y., Rytel, K., Ma, C., Kirby, M., Anderson, S., Wincovitch, S., Andersh, K., Ahfeldt, T., Blanchard, J., Qi, Y. A., Lopez, G., Tayebi, N., Sidransky, E., Chen, Y.
10.1101/2024.02.25.581985 — Posted: 2024-02-28

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