Use of a Modified STROOP Test to Assess Color Discrimination Deficit in Parkinson's Disease

por Langston, Rebekah G., Virmani, Tuhin
Publicado 2018

Generation of fourteen isogenic cell lines for Parkinson’s disease-associated leucine-rich repeat kinase (LRRK2)

por Beylina, Aleksandra, Langston, Rebekah G., Rosen, Dorien, Reed, Xylena, Cookson, Mark R.
Publicado 2021

The Polg Mutator Phenotype Does Not Cause Dopaminergic Neurodegeneration in DJ-1-Deficient Mice1,2,3

por Hauser, David N., Primiani, Christopher T., Langston, Rebekah G., Kumaran, Ravindran, Cookson, Mark R.
Publicado 2015

Primary glioblastoma of the cauda equina with molecular and histopathological characterization: Case report

por Langston, Rebekah G, Wardell, Christopher P, Palmer, Angela, Scott, Hayden, Gokden, Murat, Pait, T Glenn, Rodriguez, Analiz
Publicado 2021

Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk

por Lake, Julie, Reed, Xylena, Langston, Rebekah G., Nalls, Mike A., Gan‐Or, Ziv, Cookson, Mark R., Singleton, Andrew B., Blauwendraat, Cornelis, Leonard, Hampton L.
Publicado 2021

Divergent patterns of healthy aging across human brain regions at single-cell resolution reveal links to neurodegenerative disease

por Duffy, Megan F., Ding, Jinhui, Langston, Rebekah G., Shah, Syed I., Nalls, Mike A., Scholz, Sonja W., Whitaker, D. Thad, Auluck, Pavan K., Marenco, Stefano, Gibbs, J. Raphael, Cookson, Mark R.
Publicado 2023

Hexokinases link DJ-1 to the PINK1/parkin pathway

por Hauser, David N., Mamais, Adamantios, Conti, Melissa M., Primiani, Christopher T., Kumaran, Ravindran, Dillman, Allissa A., Langston, Rebekah G., Beilina, Alexandra, Garcia, Joseph H., Diaz-Ruiz, Alberto, Bernier, Michel, Fiesel, Fabienne C., Hou, Xu, Springer, Wolfdieter, Li, Yan, de Cabo, Rafael, Cookson, Mark R.
Publicado 2017

Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types

por Saez-Atienzar, Sara, Bandres-Ciga, Sara, Langston, Rebekah G., Kim, Jonggeol J., Choi, Shing Wan, Reynolds, Regina H., Abramzon, Yevgeniya, Dewan, Ramita, Ahmed, Sarah, Landers, John E., Chia, Ruth, Ryten, Mina, Cookson, Mark R., Nalls, Michael A., Chiò, Adriano, Traynor, Bryan J.
Publicado 2021

Mutations in LRRK2 linked to Parkinson disease sequester Rab8a to damaged lysosomes and regulate transferrin-mediated iron uptake in microglia

por Mamais, Adamantios, Kluss, Jillian H., Bonet-Ponce, Luis, Landeck, Natalie, Langston, Rebekah G., Smith, Nathan, Beilina, Alexandra, Kaganovich, Alice, Ghosh, Manik C., Pellegrini, Laura, Kumaran, Ravindran, Papazoglou, Ioannis, Heaton, George R., Bandopadhyay, Rina, Maio, Nunziata, Kim, Changyoun, LaVoie, Matthew J., Gershlick, David C., Cookson, Mark R.
Publicado 2021

Correction: Mutations in LRRK2 linked to Parkinson disease sequester Rab8a to damaged lysosomes and regulate transferrin-mediated iron uptake in microglia

por Mamais, Adamantios, Kluss, Jillian H., Bonet-Ponce, Luis, Landeck, Natalie, Langston, Rebekah G., Smith, Nathan, Beilina, Alexandra, Kaganovich, Alice, Ghosh, Manik C., Pellegrini, Laura, Kumaran, Ravindran, Papazoglou, Ioannis, Heaton, George R., Harvey, Kirsten, Bandopadhyay, Rina, Maio, Nunziata, Kim, Changyoun, LaVoie, Matthew J., Gershlick, David C., Cookson, Mark R.
Publicado 2022

LAG3 is not expressed in human and murine neurons and does not modulate α‐synucleinopathies

por Emmenegger, Marc, De Cecco, Elena, Hruska‐Plochan, Marian, Eninger, Timo, Schneider, Matthias M, Barth, Melanie, Tantardini, Elena, de Rossi, Pierre, Bacioglu, Mehtap, Langston, Rebekah G, Kaganovich, Alice, Bengoa‐Vergniory, Nora, Gonzalez‐Guerra, Andrès, Avar, Merve, Heinzer, Daniel, Reimann, Regina, Häsler, Lisa M, Herling, Therese W, Matharu, Naunehal S, Landeck, Natalie, Luk, Kelvin, Melki, Ronald, Kahle, Philipp J, Hornemann, Simone, Knowles, Tuomas P J, Cookson, Mark R, Polymenidou, Magdalini, Jucker, Mathias, Aguzzi, Adriano
Publicado 2021