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Biorxiv : the Preprint Server for Biology|January 31, 2024
Development and characterization of phospho-ubiquitin antibodies to monitor PINK1-PRKN signaling in cells and tissueJens O Watzlawik, Xu Hou, Tyrique Richardson, et al.Plos Biology|December 16, 2021
Mutations in LRRK2 linked to Parkinson disease sequester Rab8a to damaged lysosomes and regulate transferrin-mediated iron uptake in microgliaAdamantios Mamais, Jillian H Kluss, Luis Bonet-Ponce, et al.Plos Biology|May 4, 2022
Correction: Mutations in LRRK2 linked to Parkinson disease sequester Rab8a to damaged lysosomes and regulate transferrin-mediated iron uptake in microgliaAdamantios Mamais, Jillian H Kluss, Luis Bonet-Ponce, et al.Proceedings of the National Academy of Sciences of the United States of America|February 11, 2014
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson diseaseAlexandria Beilina, Iakov N Rudenko, Alice Kaganovich, et al.Nature Protocols|December 17, 2024
A consensus platform for antibody characterizationRiham Ayoubi, Joel Ryan, Sara Gonzalez Bolivar, et al.Brain : a Journal of Neurology|November 23, 2019
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementiaCornelis Blauwendraat, Xylena Reed, Lynne Krohn, et al.JAMA Neurology|August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral SclerosisJanel O Johnson, Ruth Chia, Danny E Miller, et al.Pageof 3