Search Results - "Baranowska, Emilia"

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    Analysis of MT-ATP8 gene variants reported in patients by modeling in silico and in yeast model organism by Panja, Chiranjit, Niedzwiecka, Katarzyna, Baranowska, Emilia, Poznanski, Jaroslaw, Kucharczyk, Roza

    Published in Scientific reports (20-06-2023)
    “…Defects in ATP synthase functioning due to the substitutions in its two mitochondrially encoded subunits a and 8 lead to untreatable mitochondrial diseases…”
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  2. 2

    ATP synthase interactome analysis identifies a new subunit l as a modulator of permeability transition pore in yeast by Panja, Chiranjit, Wiesyk, Aneta, Niedźwiecka, Katarzyna, Baranowska, Emilia, Kucharczyk, Roza

    Published in Scientific reports (07-03-2023)
    “…The mitochondrial ATP synthase, an enzyme that synthesizes ATP and is involved in the formation of the mitochondrial mega-channel and permeability transition,…”
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  3. 3

    ATP Synthase Subunit a Supports Permeability Transition in Yeast Lacking Dimerization Subunits and Modulates yPTP Conductance by Niedzwiecka, Katarzyna, Baranowska, Emilia, Panja, Chiranjit, Kucharczyk, Roza

    Published in Cellular physiology and biochemistry (27-02-2020)
    “…Mitochondrial ATP synthase, in addition to being involved in ATP synthesis, is involved in permeability transition pore (PTP) formation, which precedes…”
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    Probing the pathogenicity of patient-derived variants of MT-ATP6 in yeast by Baranowska, Emilia, Niedzwiecka, Katarzyna, Panja, Chiranjit, Charles, Camille, Dautant, Alain, Poznanski, Jarosław, di Rago, Jean-Paul, Tribouillard-Tanvier, Déborah, Kucharczyk, Roza

    Published in Disease models & mechanisms (01-04-2023)
    “…The list of mitochondrial DNA (mtDNA) variants detected in individuals with neurodegenerative diseases is constantly growing. Evaluating their functional…”
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    Molecular basis of diseases induced by the mitochondrial DNA mutation m.9032T>C by Baranowska, Emilia, Niedzwiecka, Katarzyna, Panja, Chiranjit, Charles, Camille, Dautant, Alain, di Rago, Jean-Paul, Tribouillard-Tanvier, Déborah, Kucharczyk, Roza

    Published in Human molecular genetics (06-04-2023)
    “…Abstract The mitochondrial DNA mutation m.9032T>C was previously identified in patients presenting with NARP (Neuropathy Ataxia Retinitis Pigmentosa). Their…”
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