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BE Leuven Spinazzi M

From Bioblast


BE Leuven Spinazzi M

Oroboros O2k-Network

O2k-Network Lab KU Leuven Center for Human Genetics

Laboratory for the Research on Neurodegenerative Diseases VIB Center for the Biology of Disease

Address Herestraat 49 bus 602, 3000
City Leuven
Country Belgium
Contact Spinazzi Marco
Team previous
Status O2k 2015-2018
Oroboros Events IOC116, IOC100


Cornelissen 2020 Hum Mol Genet2020Cornelissen T, Spinazzi M, Martin S, Imberechts D, Vangheluwe P, Bird M, De Strooper B, Vandenberghe W (2020) CHCHD2 harboring the Parkinson's disease-linked T61I mutation precipitates inside mitochondria and induces precipitation of wild-type CHCHD2. Hum Mol Genet 29:1096-106.
Spinazzi 2019 Proc Natl Acad Sci U S A2019Spinazzi M, Radaelli E, Horrรฉ K, Arranz AM, Gounko NV, Agostinis P, Maia TM, Impens F, Morais VA, Lopez-Lluch G, Serneels L, Navas P, De Strooper B (2019) PARL deficiency in mouse causes Complex III defects, coenzyme Q depletion, and Leigh-like syndrome. Proc Natl Acad Sci U S A 116:277-86.
Leucci 2016 Nature2016Leucci E, Vendramin R, Spinazzi M, Laurette P, Fiers M, Wouters J, Radaelli E, Eyckerman S, Leonelli C, Vanderheyden K, Rogiers A, Hermans E, Baatsen P, Aerts S, Amant F, Van Aelst S, van den Oord J, de Strooper B, Davidson I, Lafontaine DL, Gevaert K, Vandesompele J, Mestdagh P, Marine JC (2016) Melanoma addiction to the long non-coding RNA SAMMSON. Nature 531:518-22.


update please

Visiting scientist in the Oroboros O2k-Laboratory


Marco Spinazzo: Visiting scientist at the Oroboros O2k-Laboratory from October 21 to October 22 2015.