LRRK2 impairs PINK1/Parkin-dependent mitophagy via its kinase activity: pathologic insights into Parkinson’s disease

Author:

Bonello Fiona1234,Hassoun Sidi-Mohamed1234,Mouton-Liger François1234,Shin Yea Seul5,Muscat Adeline1234,Tesson Christelle1234,Lesage Suzanne1234,Beart Philip M5,Brice Alexis12346,Krupp Johannes7,Corvol Jean-Christophe12348,Corti Olga1234

Affiliation:

1. Institut du Cerveau et de la Moelle épinière, ICM, Paris, France

2. Inserm, Paris, France

3. CNRS, UMR, Paris, France

4. Sorbonne Universités, Paris, France

5. Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia

6. AP-HP, Hôpital de la Pitié-Salpêtrière, Department of Genetics, Paris, France

7. Ipsen Innovation, Les Ulis, France

8. AP-HP, Hôpital de la Pitié-Salpêtrière, Clinical Investigation Center for Neurology (CIC), Department of Neurology, Hôpital Pitié-Salpêtrière, Paris, France

Funder

Institut National de la Santé et de la Recherche Médicale

Association France Parkinson

Innovative Medicines Initiative

European Union Seventh Framework Programme

European Federation of Pharmaceutical Industries and Associations

Association Nationale Recherche Technologie and Association France Parkinson

International Union of Biochemistry and Molecular Biology

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Reference80 articles.

1. The genetics of Parkinson disease;Deng;Ageing Res. Rev.,2017

2. Genetic screening for a single common LRRK2 mutation in familial Parkinson’s disease;Nichols;Lancet Lond. Engl.,2005

3. A common LRRK2 mutation in idiopathic Parkinson’s disease;Gilks;Lancet Lond. Engl.,2005

4. Parkinson’s disease-related LRRK2 G2019S mutation results from independent mutational events in humans;Lesage;Hum. Mol. Genet.,2010

5. What genetics tells us about the causes and mechanisms of Parkinson’s disease;Corti;Physiol. Rev.,2011

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