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Frontiers in Genetics|March 18, 2022
Current Status of Next-Generation Sequencing Approaches for Candidate Gene Discovery in Familial Parkinson´s DiseaseNikita Simone Pillay, Owen A Ross, Alan Christoffels, et al.
Neuroscience Letters|July 6, 2002
Normal localization of deltaF323-Y328 mutant torsinA in transfected human cellsCasey O'Farrell, Dena G Hernandez, Crystal Evey, et al.
Annals of Human Genetics|June 4, 2009
Parkinson's disease and low frequency alleles found together throughout LRRK2Coro Paisán-Ruiz, Nicole Washecka, Priti Nath, et al.
Human Mutation|January 24, 2008
Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controlsCoro Paisán-Ruíz, Priti Nath, Nicole Washecka, et al.
Frontiers in Aging Neuroscience|November 7, 2022
Genetic architecture of Parkinson's disease subtypes - Review of the literatureJarosław Dulski, Ryan J Uitti, Owen A Ross, et al.
BMC Genomics|November 14, 2012
Cell population-specific expression analysis of human cerebellumAlexandre Kuhn, Azad Kumar, Alexandra Beilina, et al.
Neurobiology of Aging|July 28, 2005
Assessment of PINK1 (PARK6) polymorphisms in Finnish PDJordi Clarimón, Johanna Eerola, Olli Hellström, et al.
Neuroscience Letters|April 9, 2008
Association between AKT1 gene and Parkinson's disease: a protective haplotypeGeorgia Xiromerisiou, Georgios M Hadjigeorgiou, Alexandros Papadimitriou, et al.
BMC Neurology|December 26, 2006
A common genetic factor for Parkinson disease in ethnic Chinese population in TaiwanHon-Chung Fung, Chiung-Mei Chen, John Hardy, et al.
Experimental Gerontology|May 8, 2004
Hypothetical soluble KIR2DS4 natural killer cell receptor molecule does not associate with successful ageing in the IrishOwen A Ross, Lynn D Maxwell, I Maeve Rea, et al.
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