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
Mean distance: 19.3 (cluster 28)
Cross-listing: Alzheimer's Tree - Cell Biology Tree
Children
Sign in to add traineeDavid N Hauser | grad student | 2010-2015 | |
Salvatore Novello | grad student | 2018-2018 | National Institute on Aging Intramural Research Program |
Megan F Duffy | post-doc | 2018- | National Institute on Aging Intramural Research Program |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
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 |