Iuso Arcangela

From Bioblast
Name Iuso Arcangela,
Institution Institut fΓΌr Humangenetik

Helmholtz Zentrum MΓΌnchen - Deutsches Forschungszentrum fΓΌr Gesundheit und Umwelt

Address IngolstΓ€dter Landstr. 1, 85764
City Neuherberg
State/Province
Country Germany
Email
Weblink
O2k-Network Lab


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Publications

 PublishedReference
Catania 2019 Orphanet J Rare Dis2019Catania A, Iuso A, Bouchereau J, Kremer LS, Paviolo M, Terrile C, BΓ©nit P, Rasmusson AG, Schwarzmayr T, Tiranti V, Rustin P, Rak M, Prokisch H, Schiff M (2019) Arabidopsis thaliana alternative dehydrogenases: a potential therapy for mitochondrial complex I deficiency? Perspectives and pitfalls. Orphanet J Rare Dis 14:236. doi: 10.1186/s13023-019-1185-3
Yepez 2018 PLOS One2018YΓ©pez VA, Kremer LS, Iuso A, Gusic M, Kopajtich R, KoňaΕ™Γ­kovΓ‘ E, Nadel A, Wachutka L, Prokisch H, Gagneur J (2018) OCR-Stats: Robust estimation and statistical testing of mitochondrial respiration activities using Seahorse XF Analyzer. https://doi.org/10.1371/journal.pone.0199938
Haack 2010 Nat Genet2010Haack TB, Danhauser K, Haberberger B, Hoser J, Strecker V, Boehm D, Uziel G, Lamantea E, Invernizzi F, Poulton J, Rolinski B, Iuso A, Biskup S, Schmidt T, Mewes HW, Wittig I, Meitinger T, Zeviani M, Prokisch H (2010) Exome sequencing identifies ACAD9 mutations as a cause of Complex I deficiency. Nat Genet 42:1131-4.
Ahting 2009 Biochim Biophys Acta2009Ahting U, Floss T, Uez N, Schneider-Lohmar I, Becker L, Kling E, Iuso A, Bender A, de Angelis MH, Gailus-Durner V, Fuchs H, Meitinger T, Wurst W, Prokisch H, Klopstock T (2009) Neurological phenotype and reduced lifespan in heterozygous Tim23 knockout mice, the first mouse model of defective mitochondrial import. Biochim Biophys Acta 1787:371-76.

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