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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_Cookson
Website:
http://neuroscience.nih.gov/Lab.asp?Org_ID=519
Google:
"Mark Cookson"
Bio:

http://www.grc.nia.nih.gov/branches/irp/mcookson.htm

Mean distance: 19.3 (cluster 28)
 
Cross-listing: Alzheimer's Tree - Cell Biology Tree

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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
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