Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Brischigliaro Michele

From Bioblast
Revision as of 07:30, 18 July 2022 by Beno Marija (talk | contribs) (Created page with "{{Person |lastname=Brischigliaro |firstname=Michele |title= |institution=right|180px|Brischigliaro M Department of Biomedical Sciences, Universit...")
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Name Brischigliaro Michele,
Institution
Brischigliaro M
Department of Biomedical Sciences,

University of Padova, IT

Address Via Ugo Bassi, 58/B, 35131
City Padova
State/Province
Country Italy
Email [email protected]
Weblink
O2k-Network Lab IT Padova Viscomi C


Labels:



Publications

 PublishedReference
Fernandez-Vizarra 2022 Cell Metab2022Fernández-Vizarra E, López-Calcerrada S, Sierra-Magro A, Pérez-Pérez R, Formosa LE, Hock DH, Illescas M, Peñas A, Brischigliaro M, Ding S, Fearnley IM, Tzoulis C, Pitceathly RDS, Arenas J, Martín MA, Stroud DA, Zeviani M, Ryan MT, Ugalde C (2022) Two independent respiratory chains adapt OXPHOS performance to glycolytic switch. https://doi.org/10.1016/j.cmet.2022.09.005
Brischigliaro 2021 Biochim Biophys Acta Bioenerg2021Brischigliaro M, Zeviani M (2021) Cytochrome c oxidase deficiency. Biochim Biophys Acta Bioenerg 1862:148335. doi: 10.1016/j.bbabio.2020.148335
Beninca 2020 J Med Genet2020Beninca C, Zanette V, Brischigliaro M, Johnson M, Reyes A, Valle DAD, Robinson AJ, Degiorgi A, Yeates A, Telles BA, Prudent J, Baruffini E, Santos ML, de Souza RL, Fernandez-Vizarra E, Whitworth A, Zeviani M (2020) Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features. J Med Genet 58:155-67.

Abstracts

Add abstract