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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

BETA: Related publications

Publications

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Billingsley KJ, Ding J, Alvarez Jerez P, et al. (2023) Genome-wide analysis of Structural Variants in Parkinson's Disease. Annals of Neurology
Pantazis CB, Yang A, Lara E, et al. (2022) A reference human induced pluripotent stem cell line for large-scale collaborative studies. Cell Stem Cell. 29: 1685-1702.e22
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
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