Functional polypeptides can be synthesized from human mitochondrial transcripts lacking termination codons.

Por Chrzanowska-Lightowlers, Zofia M A, Temperley, Richard J, Smith, Paul M, Seneca, Sara H, Lightowlers, Robert N
Publicado em 2004

Foetal bile pigment handling after administration of [(14)C] haemin

Por Jackson, Benjamin T., Lester, Roger, Little, Joanna M., Piasecki, George J., Rauschecker, Helmut F. J., Smith, Paul M.
Publicado em 1973

Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency

Por Boczonadi, Veronika, Smith, Paul M., Pyle, Angela, Gomez-Duran, Aurora, Schara, Ulrike, Tulinius, Mar, Chinnery, Patrick F., Horvath, Rita
Publicado em 2013

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 no Mitochondrion (2015)

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

Por Richter, Ricarda, Rorbach, Joanna, Pajak, Aleksandra, Smith, Paul M, Wessels, Hans J, Huynen, Martijn A, Smeitink, Jan A, Lightowlers, Robert N, Chrzanowska-Lightowlers, Zofia M
Publicado em 2010

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 em 2014

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 em 2011

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy

Por Horvath, Rita, Kemp, John P., Tuppen, Helen A. L., Hudson, Gavin, Oldfors, Anders, Marie, Suely K. N., Moslemi, Ali-Reza, Servidei, Serenella, Holme, Elisabeth, Shanske, Sara, Kollberg, Gittan, Jayakar, Parul, Pyle, Angela, Marks, Harold M., Holinski-Feder, Elke, Scavina, Mena, Walter, Maggie C., Çoku, Jorida, Günther-Scholz, Andrea, Smith, Paul M., McFarland, Robert, Chrzanowska-Lightowlers, Zofia M. A., Lightowlers, Robert N., Hirano, Michio, Lochmüller, Hanns, Taylor, Robert W., Chinnery, Patrick F., Tulinius, Mar, DiMauro, Salvatore
Publicado em 2009