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1MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences,University of Dundee, 2The Michael J. Fox Foundation for Parkinson’s Research, 3Department of Medical and Molecular Genetics,Indiana University School of Medicine, 4Morton and Gloria Shulman Movement Disorders Centre and the Edmond J. Safra Program in Parkinson’s Disease, Toronto Western Hospital,University of Toronto, 5Division of Cell Signalling and Immunology, School of Life Sciences,University of Dundee, 6Division of Molecular and Clinical Medicine, School of Medicine, Ninewells Hospital and Medical School,University of Dundee
Chapitres
- 00:01Introduction
- 00:48Neutrophil Isolation from Human Peripheral Blood
- 07:18LRRK2 Kinase Inhibitor Treatment
- 10:33Résultats
- 12:14Conclusion
Las mutaciones en el gen de la quinasa 2 de la leucina rica causan la enfermedad de Parkinson hereditaria. Hemos desarrollado un método fácil y robusto para evaluar la fosforilación controlada por LRRK2 de Rab10 en neutrófilos de sangre periférica humana. Esto puede ayudar a identificar a las personas con aumento de la actividad de la vía de la quinasa LRRK2.
