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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
1997 5
1998 7
1999 12
2000 7
2001 10
2002 12
2003 11
2004 11
2005 13
2006 12
2007 14
2008 14
2009 11
2010 16
2011 3
2012 5
2013 12
2014 5
2015 8
2016 5
2017 7
2018 4
2020 1
2022 1
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198 results
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Page 1
Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation.
Madero-Pérez J, Fdez E, Fernández B, Lara Ordóñez AJ, Blanca Ramírez M, Gómez-Suaga P, Waschbüsch D, Lobbestael E, Baekelandt V, Nairn AC, Ruiz-Martínez J, Aiastui A, López de Munain A, Lis P, Comptdaer T, Taymans JM, Chartier-Harlin MC, Beilina A, Gonnelli A, Cookson MR, Greggio E, Hilfiker S. Madero-Pérez J, et al. Mol Neurodegener. 2018 Jan 23;13(1):3. doi: 10.1186/s13024-018-0235-y. Mol Neurodegener. 2018. PMID: 29357897 Free PMC article.
198 results