Mark R. Cookson, PhD, University of Salford 1995
Affiliations: | Cell Biology and Gene Expression | National Institute of Aging, Cabanatuan City, Central Luzon, Philippines |
Area:
http://www.biomedexperts.com/Profile.bme/1998006/Mark_CooksonWebsite:
http://neuroscience.nih.gov/Lab.asp?Org_ID=519Google:
"Mark Cookson"Bio:
http://www.grc.nia.nih.gov/branches/irp/mcookson.htm
Cross-listing: Neurotree - Alzheimer's Tree
Children
Sign in to add trainee| David N Hauser | grad student | 2010-2015 | (Neurotree) |
| Salvatore Novello | grad student | 2018-2018 | National Institute on Aging Intramural Research Program (Neurotree) |
| Megan F Duffy | post-doc | 2018- | National Institute on Aging Intramural Research Program (Neurotree) |
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Publications
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| Soutar MPM, Melandri D, O'Callaghan B, et al. (2022) Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 loci. Brain : a Journal of Neurology |
| Langston RG, Beilina A, Reed X, et al. (2022) Association of a common genetic variant with Parkinson's disease is mediated by microglia. Science Translational Medicine. 14: eabp8869 |
| Kedariti M, Frattini E, Baden P, et al. (2022) LRRK2 kinase activity regulates GCase level and enzymatic activity differently depending on cell type in Parkinson's disease. Npj Parkinson's Disease. 8: 92 |
| Fernández B, Chittoor-Vinod VG, Kluss JH, et al. (2022) Evaluation of Current Methods to Detect Cellular Leucine-Rich Repeat Kinase 2 (LRRK2) Kinase Activity. Journal of Parkinson's Disease |
| Mamais A, Kluss JH, Bonet-Ponce L, et al. (2021) Mutations in LRRK2 linked to Parkinson disease sequester Rab8a to damaged lysosomes and regulate transferrin-mediated iron uptake in microglia. Plos Biology. 19: e3001480 |
| Nalls MA, Blauwendraat C, Sargent L, et al. (2021) Evidence for connecting multiple neurodegenerative diseases. Brain Communications. 3: fcab095 |
| Lake J, Reed X, Langston RG, et al. (2021) Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk. Movement Disorders : Official Journal of the Movement Disorder Society |
| Johnson JO, Chia R, Miller DE, et al. (2021) Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis. Jama Neurology |
| Mazza MC, Beilina A, Roosen DA, et al. (2021) Generation of iPSC line from a Parkinson patient with PARK7 mutation and CRISPR-edited Gibco human episomal iPSC line to mimic PARK7 mutation. Stem Cell Research. 55: 102506 |
| Bonet-Ponce L, Cookson MR. (2021) LRRK2 recruitment, activity, and function in organelles. The Febs Journal |