Anzahl der Publikationen: 3
Zeitschriftenartikel
Delgado Herran, Hilda de la
ORCID: https://orcid.org/0000-0003-2506-6172; Vecellio Reane, Denis
ORCID: https://orcid.org/0000-0003-1275-0370; Cheng, Yiming
ORCID: https://orcid.org/0009-0006-4270-7292; Katona, Máté
ORCID: https://orcid.org/0000-0002-2426-8939; Hosp, Fabian; Greotti, Elisa
ORCID: https://orcid.org/0000-0003-3702-4789; Wettmarshausen, Jennifer; Patron, Maria
ORCID: https://orcid.org/0000-0003-1165-597X; Mohr, Hermine
ORCID: https://orcid.org/0000-0002-3061-1166; Prudente Mello, Natalia de
ORCID: https://orcid.org/0000-0002-2343-7884; Chudenkova, Margarita; Gorza, Matteo; Walia, Safal; Feng, Michael Sheng-Fu
ORCID: https://orcid.org/0000-0001-8050-998X; Leimpek, Anja
ORCID: https://orcid.org/0009-0009-7965-5416; Mielenz, Dirk
ORCID: https://orcid.org/0000-0002-1135-0642; Pellegata, Natalia S; Langer, Thomas; Hajnóczky, György; Mann, Matthias
ORCID: https://orcid.org/0000-0003-1292-4799; Murgia, Marta
ORCID: https://orcid.org/0000-0001-6244-3358 und Perocchi, Fabiana
ORCID: https://orcid.org/0000-0002-1102-6500
(2024):
Systematic mapping of mitochondrial calcium uniporter channel (MCUC)-mediated calcium signaling networks.
In: EMBO Journal, Bd. 43, Nr. 21: S. 5288-5326
[PDF, 9MB]
Haack, Tobias B.; Ignatius, Erika; Calvo-Garrido, Javier; Iuso, Arcangela; Isohanni, Pirjo; Maffezzini, Camilla; Lönnqvist, Tuula; Suomalainen, Anu; Gorza, Matteo; Kremer, Laura S.; Graf, Elisabeth; Hartig, Monika; Berutti, Riccardo; Paucar, Martin; Svenningsson, Per; Stranneheim, Henrik; Brandberg, Göran; Wedell, Anna; Kurian, Manju A.; Hayflick, Susan A.; Venco, Paola; Tiranti, Valeria; Strom, Tim M.; Dichgans, Martin; Horvath, Rita; Holinski-Feder, Elke; Freyer, Christoph; Meitinger, Thomas; Prokisch, Holger; Senderek, Jan; Wredenberg, Anna; Carroll, Christopher J. und Klopstock, Thomas
(2016):
Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy.
In: American Journal of Human Genetics, Bd. 99, Nr. 3: S. 735-743
Haack, Tobias B.; Haberberger, Birgit; Frisch, Eva-Maria; Wieland, Thomas; Iuso, Arcangela; Gorza, Matteo; Strecker, Valentina; Graf, Elisabeth; Mayr, Johannes A.; Herberg, Ulrike; Hennermann, Julia B.; Klopstock, Thomas; Kuhn, Klaus A.; Ahting, Uwe; Sperl, Wolfgang; Wilichowski, Ekkehard; Hoffmann, Georg F.; Tesarova, Marketa; Hansikova, Hana; Zeman, Jiri; Plecko, Barbara; Zeviani, Massimo; Wittig, Ilka; Strom, Tim M.; Schuelke, Markus; Freisinger, Peter; Meitinger, Thomas und Prokisch, Holger
(April 2012):
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.
In: Journal of medical genetics, Bd. 49, Nr. 4: S. 277-283
[PDF, 372kB]
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