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COST Action CA15203 (2016-2021): MitoEAGLE
Evolution-Age-Gender-Lifestyle-Environment: mitochondrial fitness mapping
Spinazzi Marco
MitoPedia topics: EAGLE
Name | Spinazzi Marco, MD, PhD |
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Institution | Ingénieur hospitalier
Biochimie Métabolique et Hormonologie Département de Biochimie et Génétique |
Address | IBS - CHU Angers
BNVI CNRS 6214 / INSERM U771 02.41.35.77.04, |
City | Angers |
State/Province | |
Country | France |
Marco.Spinazzi@chu-angers.fr | |
Weblink | |
O2k-Network Lab | BE Leuven Spinazzi M, FR Angers Gueguen N |
Bioenergetics Communications
- Marco Spinazzi is Associate Editor of the journal Bioenergetics Communications
- Keywords: mitochondria, neurodegeneration, neurological disorders, brain, muscle
MitoEAGLE
- Benefits for COST and for the COST Action MitoEAGLE
- I believe it will be a very useful contribution if we’ll be able to finalize in a next future a consensus paper on mitochondrial function terminology as we discussed.
Participated at
Visiting scientist in the Oroboros O2k-Laboratory
Marco Spinazzi: Visiting scientist at the Oroboros O2k-Laboratory
- October 21 to October 22 2015
Labels:
Publications
Published | Reference | |
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Kanellopoulos 2020 Cell | 2020 | Kanellopoulos AK, Mariano V, Spinazzi M, Woo YJ, McLean C, Pech U, Li KW, Armstrong JD, Giangrande A, Callaerts P, Smit AB, Abrahams BS, Fiala A, Achsel T, Bagni C (2020) Aralar sequesters GABA into hyperactive mitochondria, causing social behavior deficits. Cell 180:1178-97. |
BEC 2020.1 doi10.26124bec2020-0001.v1 | 2020 | Gnaiger E et al ― MitoEAGLE Task Group (2020) Mitochondrial physiology. https://doi.org/10.26124/bec:2020-0001.v1 |
Cornelissen 2020 Hum Mol Genet | 2020 | Cornelissen 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 A | 2019 | Spinazzi M, Radaelli E, Horré 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 Nature | 2016 | Leucci 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. |
Spinazzi 2014 Neuropathol Appl Neurobiol | 2014 | Spinazzi M, Sghirlanzoni A, Salviati L, Angelini C (2014) Impaired copper and iron metabolism in blood cells and muscles of patients affected by copper deficiency myeloneuropathy. Neuropathol Appl Neurobiol 40:888-98. |
Spinazzi 2012 Nat Protoc | 2012 | Spinazzi M, Casarin A, Pertegato V, Salviati L, Angelini C (2012) Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells. Nat Protoc 7:1235-46. |