Resultados de procura - Aleksandra Pajak

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  1. 1
    Resolving chaperone-assisted protein folding on the ribosome at the peptide level

    Resolving chaperone-assisted protein folding on the ribosome at the peptide level por Thomas E. Wales, Aleksandra Pajak, Alžběta Roeselová, Santosh Shivakumaraswamy, Steven Howell, Svend Kjær, F. Ulrich Hartl, John R. Engen, David Balchin

    Publicado 2024
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  2. 2
    A functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosome

    A functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosome por Ricarda Richter, Joanna Rorbach, Aleksandra Pajak, Paul Smith, Hans J. C. T. Wessels, Martijn A. Huynen, Jan Smeitink, Robert N. Lightowlers, Zofia M. Chrzanowska‐Lightowlers

    Publicado 2010
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  3. 3
    Modulation of mtDNA copy number ameliorates the pathological consequences of a heteroplasmic mtDNA mutation in the mouse

    Modulation of mtDNA copy number ameliorates the pathological consequences of a heteroplasmic mtDNA mutation in the mouse por Roberta Filograna, Camilla Koolmeister, Mamta Upadhyay, Aleksandra Pajak, Paula Clemente, Rolf Wibom, Marie‐Lune Simard, Anna Wredenberg, Christoph Freyer, James B. Stewart, Nils‐Göran Larsson

    Publicado 2019
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  4. 4
    C7orf30 specifically associates with the large subunit of the mitochondrial ribosome and is involved in translation

    C7orf30 specifically associates with the large subunit of the mitochondrial ribosome and is involved in translation por Bas F.J. Wanschers, Radek Szklarczyk, Aleksandra Pajak, Mariël A.M. van den Brand, Jolein Gloerich, Richard J. Rodenburg, Robert N. Lightowlers, Leo Nijtmans, Martijn A. Huynen

    Publicado 2012
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  5. 5
    Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivo

    Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivo por Aleksandra Pajak, Isabelle Laine, Paula Clemente, Najla El-Fissi, F. Schober, Camilla Maffezzini, Javier Calvo‐Garrido, Rolf Wibom, Roberta Filograna, Ashish Dhir, Anna Wedell, Christoph Freyer, Anna Wredenberg

    Publicado 2019
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  6. 6
    Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26

    Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26 por Yoshihito Kishita, Aleksandra Pajak, Nikhita Bolar, C Marobbio, Camilla Maffezzini, Daniela Valeria Miniero, Magnus Monné, Masakazu Kohda, Henrik Stranneheim, Kei Murayama, K Naess, Nicole Lesko, Helene Bruhn, Arnaud Mourier, Rolf Wibom, Inger Nennesmo, Ann Jespers, Paul Govaert, Akira Ohtake, Lut Van Laer, Bart Loeys, Christoph Freyer, Ferdinando Palmieri, Anna Wredenberg, Yasushi Okazaki, Anna Wedell

    Publicado 2015
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