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

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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

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

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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

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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.

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

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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

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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

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Mitochondrial DNA clonality in the dock: can surveillance swing the case? von Elson, Joanna L., Lightowlers, Robert N.

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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

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

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Investigation of a pathogenic mtDNA microdeletion reveals a translation-dependent deadenylation decay pathway in human mitochondria von Temperley, Richard J., Seneca, Sara H., Tonska, Katarzyna, Bartnik, Ewa, Bindoff, Laurence A., Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M.A.

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

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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.

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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. 

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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

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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

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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.

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Mismatch repair activity in mammalian mitochondria von Mason, Penelope A., Matheson, Elizabeth C., Hall, Andrew G., Lightowlers, Robert N.

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The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both? von Chinnery, Patrick F, Thorburn, David R, Samuels, David C, White, Sarah L, Dahl, Hans-Heinrik M, Turnbull, Doug M, Lightowlers, Robert N, Howell, Neil

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