Homocystinuria (HCU) is an inborn error of metabolism and a conformational disorder chiefly caused by the missense mutations in the cystathionine beta-synthase (CBS) gene. These mutations often cause CBS destabilization, misfolding and dysfunction resulting in CBS deficiency and pathological accumulation of homocystein...
Ela Mijatovic, T. M. Philipp, Karim Zuhra et al.· Free Radical Biology & Medic...· 0 citations
The transfer of mitochondrial cargo through extracellular vesicles (EVs) has been reported in several model systems and cell types, yet a detailed characterization of mitochondrial components across different EV populations remains limited. Here, we characterized the mitochondrial cargo of small EVs (sEVs) and large EV...
Finn Brigger, A. Kitanovic, Sébastien Meurant et al.· International journal of pha...· 0 citations
This work integrates transcriptomics with whole-cell and purified mitochondrial proteomics to profile lipopolysaccharide (LPS)/interferon-γ (IFN-γ)– and interleukin-4 (IL-4)/IL-13–stimulated macrophages and identifies mtDNA expression, intramitochondrial translation, and mitochondrial membrane potential as critical, dr...
Joan Blanco-Fernández, Miriam Lisci, Mads M. Foged et al.· Science Advances· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.