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Mitochondrion|November 17, 2016
Investigating Leber's hereditary optic neuropathy: Cell models and future perspectivesElona Jankauskaitė, Ewa Bartnik, Agata KodrońBiochimica Et Biophysica Acta|March 10, 2010
Genotype-phenotype correlations in Leber hereditary optic neuropathyKatarzyna Tońska, Agata Kodroń, Ewa BartnikPharmacological Research|October 16, 2020
The ubiquitin-proteasome system and its crosstalk with mitochondria as therapeutic targets in medicineAgata Kodroń, Ben Hur Mussulini, Iwona Pilecka, et al.Journal of Clinical Pathology|April 22, 2014
m.3635G>A mutation as a cause of Leber hereditary optic neuropathyAgata Kodroń, Maciej R Krawczyński, Katarzyna Tońska, et al.Archiwum Medycyny Sadowej I Kryminologii|August 26, 2011
[Population data analysis of miniSTR loci: D10S1248, D14S1434 and D22S1045 in the Pomerania-Kujawy region of Poland]Agata Kodroń, Edyta Rychlicka, Iwona Milewska, et al.Acta Biochimica Polonica|October 5, 2019
Analysis of BNIP3 and BNIP3L/Nix expression in cybrid cell lines harboring two LHON-associated mutationsAgata Kodroń, Parvana Hajieva, Agata Kulicka, et al.Journal of Applied Genetics|March 12, 2020
Testosterone increases apoptotic cell death and decreases mitophagy in Leber's hereditary optic neuropathy cellsElona Jankauskaitė, Anna Maria Ambroziak, Parvana Hajieva, et al.Acta Biochimica Polonica|March 12, 2017
Mitochondrial DNA in pediatric leukemia patientsAgata Kodroń, Magda Ghanim, Katarzyna K Krawczyk, et al.Journal of Molecular Biology|May 25, 2025
Immunoproteasome-specific Subunit Alterations as a Potential Therapeutic Target for MitochondriopathiesAgata Kodroń, Konrad Kowalski, Ben Hur Marins Mussulini, et al.Nature Communications|July 11, 2023
Immunoproteasome-specific subunit PSMB9 induction is required to regulate cellular proteostasis upon mitochondrial dysfunctionMinji Kim, Remigiusz A Serwa, Lukasz Samluk, et al.Pageof 1