Fine mapping of interactions between eEF1α protein and 3′UTR of metallothionein-1 mRNA

por Fan, Kunbo, Chrzanowska-Lightowlers, Zofia M.A., Hesketh, John E.
Publicado 2009

The process of mammalian mitochondrial protein synthesis

por Mai, Nicole, Chrzanowska-Lightowlers, Zofia M. A., Lightowlers, Robert N.
Publicado 2016

Structure based hypothesis of a mitochondrial ribosome rescue mechanism

por Huynen, Martijn A, Duarte, Isabel, Chrzanowska-Lightowlers, Zofia M A, Nabuurs, Sander B
Publicado 2012

Overcoming stalled translation in human mitochondria

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

Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunit

por Dennerlein, Sven, Rozanska, Agata, Wydro, Mateusz, Chrzanowska-Lightowlers, Zofia M. A., Lightowlers, Robert N.
Publicado 2010

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

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

REXO2 Is an Oligoribonuclease Active in Human Mitochondria

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

High-resolution imaging reveals compartmentalization of mitochondrial protein synthesis in cultured human cells

por Zorkau, Matthew, Albus, Christin A., Berlinguer-Palmini, Rolando, Chrzanowska-Lightowlers, Zofia M. A., Lightowlers, Robert N.
Publicado 2021

SLIRP stabilizes LRPPRC via an RRM–PPR protein interface

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

Using mitoribosomal profiling to investigate human mitochondrial translation

por Gao, Fei, Wesolowska, Maria, Agami, Reuven, Rooijers, Koos, Loayza-Puch, Fabricio, Lawless, Conor, Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M. A.
Publicado 2018

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

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

Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants

por 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.
Publicado 2006

Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNA(Val) carrying the pathogenic C25U mutation

por Rorbach, Joanna, Yusoff, Abdul Aziz, Tuppen, Helen, Abg-Kamaludin, Dyg P., Chrzanowska-Lightowlers, Zofia M.A., Taylor, Robert W., Turnbull, Douglass M., McFarland, Robert, Lightowlers, Robert N.
Publicado 2008

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

por 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
Publicado 2014

The human mitochondrial ribosome recycling factor is essential for cell viability

por Rorbach, Joanna, Richter, Ricarda, Wessels, Hans J., Wydro, Mateusz, Pekalski, Marcin, Farhoud, Murtada, Kühl, Inge, Gaisne, Mauricette, Bonnefoy, Nathalie, Smeitink, Jan A., Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M.A.
Publicado 2008

Defective mitochondrial protease LonP1 can cause classical mitochondrial disease

por Peter, Bradley, Waddington, Christie L, Oláhová, Monika, Sommerville, Ewen W, Hopton, Sila, Pyle, Angela, Champion, Michael, Ohlson, Monica, Siibak, Triinu, Chrzanowska-Lightowlers, Zofia M A, Taylor, Robert W, Falkenberg, Maria, Lightowlers, Robert N
Publicado 2018

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

por 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.
Publicado 2014

Pathogenic variants in HTRA2 cause an early-onset mitochondrial syndrome associated with 3-methylglutaconic aciduria

por Oláhová, Monika, Thompson, Kyle, Hardy, Steven A., Barbosa, Inês A., Besse, Arnaud, Anagnostou, Maria-Eleni, White, Kathryn, Davey, Tracey, Simpson, Michael A., Champion, Michael, Enns, Greg, Schelley, Susan, Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M. A., McFarland, Robert, Deshpande, Charu, Bonnen, Penelope E., Taylor, Robert W.
Publicado 2016

The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families

por Tuppen, Helen A. L., Hogan, Vanessa E., He, Langping, Blakely, Emma L., Worgan, Lisa, Al-Dosary, Mazhor, Saretzki, Gabriele, Alston, Charlotte L., Morris, Andrew A., Clarke, Michael, Jones, Simon, Devlin, Anita M., Mansour, Sahar, Chrzanowska-Lightowlers, Zofia M. A., Thorburn, David R., McFarland, Robert, Taylor, Robert W.
Publicado 2010

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

por 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
Publicado 2011