Serum-deprivation stimulates cap-binding by PARN at the expense of eIF4E, consistent with the observed decrease in mRNA stability

by Seal, Ruth, Temperley, Richard, Wilusz, Jeffrey, Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M. A.
Published 2005

Structure based hypothesis of a mitochondrial ribosome rescue mechanism

by Huynen, Martijn A, Duarte, Isabel, Chrzanowska-Lightowlers, Zofia M A, Nabuurs, Sander B
Published 2012

REXO2 Is an Oligoribonuclease Active in Human Mitochondria

by Bruni, Francesco, Gramegna, Pasqua, Oliveira, Jorge M. A., Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M. A.
Published 2013

Overcoming stalled translation in human mitochondria

by Wesolowska, Maria T., Richter-Dennerlein, Ricarda, Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M. A.
Published 2014

Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants

by Pye, Deborah, Kyriakouli, Dimitra S., Taylor, Geoffrey A., Johnson, Riem, Elstner, Matthias, Meunier, Brigitte, Chrzanowska-Lightowlers, Zofia M. A., Taylor, Robert W., Turnbull, Douglass M., Lightowlers, Robert N.
Published 2006

SLIRP stabilizes LRPPRC via an RRM–PPR protein interface

by Spåhr, Henrik, Rozanska, Agata, Li, Xinping, Atanassov, Ilian, Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M. A., Rackham, Oliver, Larsson, Nils-Göran
Published 2016

The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease

by Elson, Joanna L., Smith, Paul M., Greaves, Laura C., Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M.A., Taylor, Robert W., Vila-Sanjurjo, Antón
Published 2015

The role of the mitochondrial ribosome in human disease: searching for mutations in 12S mitochondrial rRNA with high disruptive potential

by Smith, Paul M., Elson, Joanna L., Greaves, Laura C., Wortmann, Saskia B., Rodenburg, Richard J.T., Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M.A., Taylor, Robert W., Vila-Sanjurjo, Antón
Published 2014

Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency☆

by Almalki, Abdulraheem, Alston, Charlotte L., Parker, Alasdair, Simonic, Ingrid, Mehta, Sarju G., He, Langping, Reza, Mojgan, Oliveira, Jorge M.A., Lightowlers, Robert N., McFarland, Robert, Taylor, Robert W., Chrzanowska-Lightowlers, Zofia M.A.
Published 2014

Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency

by Kemp, John P., Smith, Paul M., Pyle, Angela, Neeve, Vivienne C. M., Tuppen, Helen A. L., Schara, Ulrike, Talim, Beril, Topaloglu, Haluk, Holinski-Feder, Elke, Abicht, Angela, Czermin, Birgit, Lochmüller, Hanns, McFarland, Robert, Chinnery, Patrick F., Chrzanowska-Lightowlers, Zofia M.A., Lightowlers, Robert N., Taylor, Robert W., Horvath, Rita
Published 2011

A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression

by Wilson, William C., Hornig-Do, Hue-Tran, Bruni, Francesco, Chang, Jeong Ho, Jourdain, Alexis A., Martinou, Jean-Claude, Falkenberg, Maria, Spåhr, Henrik, Larsson, Nils-Göran, Lewis, Richard J., Hewitt, Lorraine, Baslé, Arnaud, Cross, Harold E., Tong, Liang, Lebel, Robert R., Crosby, Andrew H., Chrzanowska-Lightowlers, Zofia M. A., Lightowlers, Robert N.
Published 2014

LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population

by Oláhová, Monika, Hardy, Steven A., Hall, Julie, Yarham, John W., Haack, Tobias B., Wilson, William C., Alston, Charlotte L., He, Langping, Aznauryan, Erik, Brown, Ruth M., Brown, Garry K., Morris, Andrew A. M., Mundy, Helen, Broomfield, Alex, Barbosa, Ines A., Simpson, Michael A., Deshpande, Charu, Moeslinger, Dorothea, Koch, Johannes, Stettner, Georg M., Bonnen, Penelope E., Prokisch, Holger, Lightowlers, Robert N., McFarland, Robert, Chrzanowska-Lightowlers, Zofia M. A., Taylor, Robert W.
Published 2015