Immunoproteasome-specific subunit PSMB9 induction is required to regulate cellular proteostasis upon mitochondrial dysfunction von Kim, Minji, Serwa, Remigiusz A., Samluk, Lukasz, Suppanz, Ida, Kodroń, Agata, Stępkowski, Tomasz M., Elancheliyan, Praveenraj, Tsegaye, Biniyam, Oeljeklaus, Silke, Wasilewski, Michal, Warscheid, Bettina, Chacinska, Agnieszka

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Testosterone increases apoptotic cell death and decreases mitophagy in Leber’s hereditary optic neuropathy cells von Jankauskaitė, Elona, Ambroziak, Anna Maria, Hajieva, Parvana, Ołdak, Monika, Tońska, Katarzyna, Korwin, Magdalena, Bartnik, Ewa, Kodroń, Agata

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The ubiquitin-proteasome system and its crosstalk with mitochondria as therapeutic targets in medicine von Kodroń, Agata, Mussulini, Ben Hur, Pilecka, Iwona, Chacińska, Agnieszka

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Investigating Leber's hereditary optic neuropathy: Cell models and future perspectives von Jankauskaitė, Elona, Bartnik, Ewa, Kodroń, Agata

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Analysis of BNIP3 and BNIP3L/Nix expression in cybrid cell lines harboring two LHON-associated mutations von Kodroń, Agata, Hajieva, Parvana, Kulicka, Agata, Paterczyk, Bohdan, Jankauskaite, Elona, Bartnik, Ewa

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Genotype–phenotype correlations in Leber hereditary optic neuropathy von Tońska, Katarzyna, Kodroń, Agata, Bartnik, Ewa

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Mitochondrial DNA in pediatric leukemia patients von Kodroń, Agata, Ghanim, Magda, Krawczyk, Katarzyna K., Stelmaszczyk-Emmel, Anna, Tońska, Katarzyna, Demkow, Urszula, Bartnik, Ewa

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m.3635G>A mutation as a cause of Leber hereditary optic neuropathy von Kodroń, Agata, Krawczyński, Maciej R, Tońska, Katarzyna, Bartnik, Ewa

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Genotype–phenotype correlation in Leber hereditary optic neuropathy von Tońska, Katarzyna, Kodroń, Agata, Bartnik, Ewa

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Mitochondrial encephalopathy in a patient with a 13042G>A de novo mutation von Slawek, Jaroslaw, Kierdaszuk, Biruta, Tonska, Katarzyna, Kodron, Agata, Schinwelski, Michal, Sitek, Emilia Jadwiga, Bartnik, Ewa, Kaminska, Anna, Kwiecinski, Hubert

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USE OF IMMUNOPROTEASOME SUBUNIT INHIBITORS FOR TREATMENT OR PREVENTION OF MITOCHONDRIOPATHIES von CHACINSKA, Agnieszka, NGATI, Sonia Aleksandra, WASILEWSKI, Michal, KODRON, Agata Krystyna, KIM, Minji

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USE OF IMMUNOPROTEASOME INHIBITORS FOR TREATMENT OR PREVENTION OF MITOCHONDRIOPATHIES von CHACINSKA, Agnieszka, NGATI, Sonia Aleksandra, WASILEWSKI, Michal, KODRON, Agata Krystyna, KIM, Minji

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Mitochondrial encephalopathy in a patient with a 13042G>A de novo mutation von Slawek, Jaroslaw, Kierdaszuk, Biruta, Tonska, Katarzyna, Kodron, Agata, Schinwelski, Michal, Sitek, Emilia Jadwiga, Bartnik, Ewa, Kaminska, Anna, Kwiecinski, Hubert

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