Webcast - Prof Nicholas Wood - Advances in Genetic Understanding of Parkinson's Disease.

Video: Advances in Genetic Understanding of Parkinson's Disease

Webcast of the presentation entitled ‘Advances in Genetic Understanding of Parkinson's Disease’ given by Nicholas Wood (University College London, United Kingdom) presented at the Biochemical Society Hot Topic event, PINK1-Parkin Signalling in Parkinson’s Disease and Beyond, held in December 2014. More...

Pedigrees and I-FP-CIT SPECT scan images of the four families with GCH1 mutations involved in this study.

GCH1 gene and Parkinson's risk

A study published in Brain, led by researchers at UCL Institute of Neurology, has shown that genetic mutations which cause a decrease in dopamine production in the brain and lead to a form of childhood-onset Dystonia, also play a role in the development of Parkinson’s disease.

Leonard Wolfson Experimental Neurology Centre (LWENC)

The new Leonard Wolfson Experimental Neurology Centre (LWENC) has opened for clinical studies and trials


Audioslide presentation on Claudia Manzoni's paper examining how fibroblasts with LRRK2 mutations react to starvation conditions and the possible deficits that they have in autophagy.

LRRK2 and autophagy in fibroblasts

In this paper Claudia Manzoni studies how fibroblast cells from people with Parkinson’s disease caused by mutations in LRRK2 react to starvation. Although the changes are quite subtle, there are differences between the way that fibroblasts that contain mutant LRRK2 respond to being starved – suggesting that there may be changes in the way that these cells regulate a key process called autophagy (a term which comes from the greek meaning to eat yourself, and is one of the ways that cells get rid of waste and recycle proteins and organellles).

Drosophila fly model - University of Sheffield

Genetic mutations linked to Parkinson's disease

Research led by consortium researchers Dr Helene Plun-Favreau (UCL Institute of Neurology) and Dr Alex Whitworth (University of Sheffield), and collaborator Dr Heike Laman (University of Cambridge), has discovered how genetic mutations linked to Parkinson’s disease might play a key role in the death of brain cells, potentially paving the way for the development of more effective drug treatments. In the new study, published in Nature Neuroscience, the team of cross-institutional researchers showed how defects in the Parkinson’s gene Fbxo7 cause problems with mitophagy. More...

Laura Osellame

(Former Research Associate)

Laura Osellame

Mitochondrial Morphology and distribution. Apoptosis, autophagy and mitochondrial electron transport chain function in relation to Parkinson’s Disease.


Contact details

Lab website

Link to Publications RSS button
Jump to: 2013 | 2012 | 2011 | 2008 | NULL
Number of items: 7.


Osellame, LD; Rahim, AA; Hargreaves, IP; Gegg, ME; Richard-Londt, A; Brandner, S; ... Duchen, MR; + view all (2013) Mitochondria and quality control defects in a mouse model of Gaucher Disease-links to Parkinson's Disease. Cell Metabolism , 17 (6) pp. 941-953. 10.1016/j.cmet.2013.04.014. Green open access


Osellame, LD; Blacker, TS; Duchen, MR; (2012) Cellular and molecular mechanisms of mitochondrial function. Best Pract Res Clin Endocrinol Metab , 26 (6) 711 - 723. 10.1016/j.beem.2012.05.003. Gold open access

Osellame, LD; Rahim, A; Gegg, ME; Waddington, S; Schapira, AHV; Duchen, MR; (2012) Accumulation of damaged mitochondria in neuropathic Gaucher disease, the most prevalent risk factor for Parkinson's disease, is due to defective cellular degradation machinery. In: BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS. (pp. S79 - S80).


Palmer, CS; Osellame, LD; Laine, D; Koutsopoulos, OS; Frazier, AE; Ryan, MT; (2011) MiD49 and MiD51, new components of the mitochondrial fission machinery. EMBO REP , 12 (6) 565 - 573. 10.1038/embor.2011.54.

Palmer, CS; Osellame, LD; Stojanovski, D; Ryan, MT; (2011) The regulation of mitochondrial morphology: Intricate mechanisms and dynamic machinery. CELL SIGNAL , 23 (10) 1534 - 1545. 10.1016/j.cellsig.2011.05.021.


Osellame, LD; Koutsopoulos, OS; Laine, D; Frazier, AE; Ryan, MT; (2008) MiD51 and MiD49: New mediators of mammalian mitochondrial distribution. In: BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS. (pp. S57 - S57). ELSEVIER SCIENCE BV


Koutsopoulos, OS; Laine, D; Osellame, L; Chudakov, DM; Parton, RG; Frazier, AE; Ryan, MT; Human Miltons associate with mitochondria and induce microtubule-dependent remodeling of mitochondrial networks. Biochim Biophys Acta , 1803 (5) 564 - 574. 10.1016/j.bbamcr.2010.03.006.

This list was generated on Mon Mar 30 00:08:20 2015 BST.

Page last modified on 12 feb 14 14:42