Difference between revisions of "Spinazzi Marco"
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[[Image:O2k-Network.png|left|40px|link=O2k-Network|O2k-Network]] Visiting scientist at the [[OROBOROS | [[Image:O2k-Network.png|left|40px|link=O2k-Network|O2k-Network]] Visiting scientist at the [[OROBOROS MitoFit lab: visiting scientists |OROBOROS MitoFit Laboratory]] from October 21 to October 22 2015. | ||
Revision as of 17:14, 12 February 2016
| Name | Spinazzi Marco, MD, PhD |
|---|---|
| Institution |  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 |
| State/Province | |
| Country | Belgium |
| [email protected] | |
| Weblink | |
| O2k-Network Lab | BE Leuven Spinazzi M, FR Angers Gueguen N |
Labels:
Publications
| Published | Reference | |
|---|---|---|
| Radaelli 2023 Elife | 2023 | Radaelli E, Assenmacher CA, Verrelle J, Banerjee E, Manero F, Khiati S, Girona A, Lopez-Lluch G, Navas P, Spinazzi M (2023) Mitochondrial defects caused by PARL deficiency lead to arrested spermatogenesis and ferroptosis. https://doi.org/10.7554/elife.84710 |
| 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. Bioenerg Commun 2020.1. 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. 10.1073/pnas.1811938116 |
| 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. |
Abstracts
Participated at
Visiting scientist at the OROBOROS MitoFit Laboratory from October 21 to October 22 2015.
