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Author/Creator Cookson, Mark R.

1. [P4–443]: PARKINSON's DISEASE‐ASSOCIATED MUTATIONS IN LRRK2 CAUSE CENTROSOMAL DEFECTS VIA RAB8A PHOSPHORYLATION. (1st July 2017)

Authors:
Madero‐Pérez, Jesús; Fdez, Elena; Fernández, Belén; Lara Ordóñez, Antonio J.; Ramírez, Marian Blanca; Gómez‐Suaga, Patricia; Waschbüsch, Dieter; Lobbestael, Evy; Baekelandt, Veerle; Nairn, Angus C.; Ruiz‐Martínez, Javier; Aiastui, Ana; de Munaín, Adolfo López; Lis, Pawel; Comptdaer, Thomas; Tayma...
Journal:
Alzheimer's & dementia
Issue:
Volume 13:Supplement 7S(2017)Part 31
Page Start:
P1501
Record Type:
Journal Article
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2. A comprehensive analysis of SNCA‐related genetic risk in sporadic parkinson disease. Issue 1 (26th August 2018)

Authors:
Pihlstrøm, Lasse; Blauwendraat, Cornelis; Cappelletti, Chiara; Berge‐Seidl, Victoria; Langmyhr, Margrete; Henriksen, Sandra Pilar; van de Berg, Wilma D. J.; Gibbs, J. Raphael; Cookson, Mark R.; Singleton, Andrew B.; Nalls, Mike A.; Toft, Mathias
Journal:
Annals of neurology
Issue:
Volume 84:Issue 1(2018)
Page Start:
117
Record Type:
Journal Article
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9. Differential protein–protein interactions of LRRK1 and LRRK2 indicate roles in distinct cellular signaling pathways. (14th July 2014)

Authors:
Reyniers, Lauran; Del Giudice, Maria Grazia; Civiero, Laura; Belluzzi, Elisa; Lobbestael, Evy; Beilina, Alexandra; Arrigoni, Giorgio; Derua, Rita; Waelkens, Etienne; Li, Yan; Crosio, Claudia; Iaccarino, Ciro; Cookson, Mark R.; Baekelandt, Veerle; Greggio, Elisa; Taymans, Jean‐Marc
Journal:
Journal of neurochemistry
Issue:
Volume 131:Number 2(2014:Oct.)
Page Start:
239
Record Type:
Journal Article
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