Progress and prospects: gene therapy for mitochondrial DNA disease von Kyriakouli, D S, Boesch, P, Taylor, R W, Lightowlers, R N

Volltext

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA von Turnbull, Douglass M, Andrews, Richard M, Kubacka, Iwona, Chinnery, Patrick F, Lightowlers, Robert N, Howell, Neil

Volltext

Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement von Betts, J., Jaros, E., Perry, R. H., Schaefer, A. M., Taylor, R. W., Abdel-All, Z., Lightowlers, R. N., Turnbull, D. M.

Volltext

Transmission of mitochondrial DNA disorders: possibilities for the future von Brown, DT, Herbert, M, Lamb, VK, Chinnery, PF, Taylor, RW, Lightowlers, RN, Craven, L, Cree, L, Gardner, JL, Turnbull, DM

Volltext

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

Volltext

Molecular pathology of MELAS and MERRF the relationship between mutation load and clinical phenotypes von CHINNERY, P. F, HOWELL, N, LIGHTOWLERS, R. N, TURNBULL, D. M

Volltext

Mammalian mitochondrial genetics: heredity, heteroplasmy and disease von Lightowlers, Robert N., Chinnery, Patrick F., Turnbull, Douglass M., Howell, Neil

Volltext

Analysis of European mtDNAs for Recombination von Elson, J.L., Andrews, R.M., Chinnery, P.F., Lightowlers, R.N., Turnbull, D.M., Howell, Neil

Volltext

Transmitochondrial embryonic stem cells containing pathogenic mtDNA mutations are compromised in neuronal differentiation von Kirby, D. M. , Rennie, K. J. , Smulders-Srinivasan, T. K. , Acin-Perez, R. , Whittington, M. , Enriquez, J.-A. , Trevelyan, A. J. , Turnbull, D. M. , Lightowlers, R. N. 

Volltext

Role of mitochondrial DNA mutations in human aging: Implications for the central nervous system and muscle von Brierley, Elizabeth J., Johnson, Margaret A., Lightowlers, Robert N., James, Oliver F. W., Turnbull, Douglass M.

Volltext

175th ENMC International Workshop: Mitochondrial protein synthesis in health and disease, 25–27th June 2010, Naarden, The Netherlands von Chrzanowska-Lightowlers, Z.M.A, Horvath, R, Lightowlers, R.N

Volltext

Potential compounds for the treatment of mitochondrial disease von Rai, P K, Russell, O M, Lightowlers, R N, Turnbull, D M

Volltext

Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids von Taylor, Robert W, Chinnery, Patrick F, Turnbull, Douglass M, Lightowlers, Robert N

Volltext

An mtDNA Mutation in the Initiation Codon of the Cytochrome C Oxidase Subunit II Gene Results in Lower Levels of the Protein and a Mitochondrial Encephalomyopathy von Clark, Kim M., Taylor, Robert W., Johnson, Margaret A., Chinnery, Patrick F., Chrzanowska-Lightowlers, Zofia M.A., Andrews, Richard M., Nelson, Isobel P., Wood, Nicholas W., Lamont, Phillipa J., Hanna, Michael G., Lightowlers, Robert N., Turnbull, Douglass M.

Volltext

Mitochondrial DNA deletion in “identical” twin brothers von Blakely, E L, He, L, Taylor, R W, Chinnery, P F, Lightowlers, R N, Schaefer, A M, Turnbull, D M

Volltext

MELAS and MERRF : The relationship between maternal mutation load and the frequency of clinically affected offspring von CHINNERY, P. F, HOWELL, N, LIGHTOWLERS, R. N, TURNBULL, D. M

Volltext

Why do mammalian mitochondria possess a mismatch repair activity? von Mason, P.A., Lightowlers, R.N.

Volltext

Defective mitochondrial protease LonP1 can cause classical mitochondrial disease von 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

Volltext

Absence of expression from RNA internalised into electroporated mammalian mitochondria von McGregor, A, Temperley, R, Chrzanowska-Lightowlers, Z M, Lightowlers, R N

Volltext

Peptide nucleic acid delivery to human mitochondria von CHINNERY, P. F, TAYLOR, R. W, DIEKERT, K, LILL, R, TURNBULL, D. M, LIGHTOWLERS, R. N

Volltext