cached image

Mark R. Cookson, PhD, University of Salford 1995

Cell Biology and Gene Expression National Institute of Aging, Cabanatuan City, Central Luzon, Philippines 
"Mark Cookson"

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

BETA: Related 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
See more...