The function of orthologues of the human Parkinson's disease gene LRRK2 across species: implications for disease modelling in preclinical research von Langston, Rebekah G, Rudenko, Iakov N, Cookson, Mark R

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The G2385R risk factor for Parkinson's disease enhances CHIP-dependent intracellular degradation of LRRK2 von Rudenko, Iakov N, Kaganovich, Alice, Langston, Rebekah G, Beilina, Aleksandra, Ndukwe, Kelechi, Kumaran, Ravindran, Dillman, Allissa A, Chia, Ruth, Cookson, Mark R

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

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Use of a Modified STROOP Test to Assess Color Discrimination Deficit in Parkinson's Disease von Langston, Rebekah G, Virmani, Tuhin

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Generation of fourteen isogenic cell lines for Parkinson’s disease-associated leucine-rich repeat kinase (LRRK2) von Beylina, Aleksandra, Langston, Rebekah G., Rosen, Dorien, Reed, Xylena, Cookson, Mark R.

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Hexokinases link DJ-1 to the PINK1/parkin pathway von 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

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Characteristics and career outcomes of Neurosurgery Research and Education Foundation research fellowship recipients von Wilson, Taylor A., Langston, Rebekah G., Wong, Ka Hin, Rodriguez, Analiz

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Recent trends in NIH funding for top surgeon-scientists von Langston, Rebekah G., Zhao, Edward H., Wong, Ka Hin, Rodriguez, Analiz

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Mutations in LRRK2 linked to Parkinson disease sequester Rab8a to damaged lysosomes and regulate transferrin-mediated iron uptake in microglia von Mamais, Adamantios, Kluss, Jillian, Bonet-Ponce, Luis C., Landeck, Natalie, Langston, Rebekah, Smith, Nathan, Beilina, Alexandra R., Kaganovich, Alice, Ghosh, Manik C., Pellegrini, Laura, Kumaran, Ravindran J., Papazoglou, Ioannis C., Heaton, George R., Bandopadhyay, Rina, Maio, Nunziata, Kim, Changyoun, LaVoie, Matthew, Gershlick, David, Cookson, Mark

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Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk von Lake, Julie, Reed, Xylena, Langston, Rebekah G., Nalls, Mike A., Gan‐Or, Ziv, Cookson, Mark R., Singleton, Andrew B., Blauwendraat, Cornelis, Leonard, Hampton L.

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Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types von 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., Chio, Adriano, Traynor, Bryan J.

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Intracranial hematolymphoid malignancies: A case series with molecular characterization von Langston, Rebekah G., Pinckard-Dover, Heather, Guzman, Grace, Wardell, Christopher P., Gokden, Murat, Morris, T.W., Day, J.D., Rodriguez, Analiz

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Differences in Stability, Activity and Mutation Effects Between Human and Mouse Leucine-Rich Repeat Kinase 2 von Langston, Rebekah G., Rudenko, Iakov N., Kumaran, Ravindran, Hauser, David N., Kaganovich, Alice, Ponce, Luis Bonet, Mamais, Adamantios, Ndukwe, Kelechi, Dillman, Allissa A., Al-Saif, Amr M., Beilina, Aleksandra, Cookson, Mark R.

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Evaluating N-benzylgalactonoamidines as putative transition state analogs for β-galactoside hydrolysis von Fan, Qiu-Hua, Striegler, Susanne, Langston, Rebekah G, Barnett, James D

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Primary glioblastoma of the cauda equina with molecular and histopathological characterization: Case report von Langston, Rebekah G, Wardell, Christopher P, Palmer, Angela, Scott, Hayden, Gokden, Murat, Pait, T Glenn, Rodriguez, Analiz

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The Polg Mutator Phenotype Does Not Cause Dopaminergic Neurodegeneration in DJ-1-Deficient Mice von Hauser, David N, Primiani, Christopher T, Langston, Rebekah G, Kumaran, Ravindran, Cookson, Mark R

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

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

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Evaluating N-benzylgalactonoamidines as putative transition state analogs for β-galactoside hydrolysisElectronic supplementary information (ESI) available: 1H and 13C NMR spectra o... von Fan, Qiu-Hua, Striegler, Susanne, Langston, Rebekah G, Barnett, James D

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The Polg Mutator Phenotype Does Not Cause Dopaminergic Neurodegeneration in DJ-1-Deficient Mice1,2,3 von Hauser, David N., Primiani, Christopher T., Langston, Rebekah G., Kumaran, Ravindran, Cookson, Mark R.

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