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Proceedings of the National Academy of Sciences of the United States of America|April 8, 2003
The G protein-coupled receptor repertoires of human and mouseDemetrios K Vassilatis, John G Hohmann, Hongkui Zeng, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2017
Nurr1:RXRα heterodimer activation as monotherapy for Parkinson's diseaseAthanasios D Spathis, Xenophon Asvos, Despina Ziavra, et al.
Human Molecular Genetics|April 26, 2021
Nurr1 repression mediates cardinal features of Parkinson's disease in α-synuclein transgenic miceMaria Argyrofthalmidou, Athanasios D Spathis, Matina Maniati, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 28, 2007
Large-scale, saturating insertional mutagenesis of the mouse genomeAlexander Gragerov, Kyoji Horie, Maria Pavlova, et al.
Neurobiology of Aging|August 22, 2013
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variantsMichael G Heckman, Alexis Elbaz, Alexandra I Soto-Ortolaza, et al.
The Lancet. Neurology|September 3, 2011
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control studyOwen A Ross, Alexandra I Soto-Ortolaza, Michael G Heckman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 2013
Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) ConsortiumMichael G Heckman, Alexandra I Soto-Ortolaza, Jan O Aasly, et al.
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