Somatic mtDNA Mutations Cause Aging Phenotypes without Affecting Reactive Oxygen Species Production by Aleksandra Trifunovic, Hansson, Anna, Wredenberg, Anna, Anja T. Rovio, Dufour, Eric, Ivan Khvorostov, Johannes N. Spelbrink, Wibom, Rolf, Jacobs, Howard T., Larsson, Nils-Göran

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Premature ageing in mice expressing defective mitochondrial DNA polymerase by Trifunovic, Aleksandra, Wredenberg, Anna, Falkenberg, Maria, Spelbrink, Johannes N., Rovio, Anja T., Bruder, Carl E., Bohlooly-Y, Mohammad, Gidlöf, Sebastian, Oldfors, Anders, Wibom, Rolf, Törnell, Jan, Jacobs, Howard T., Larsson, Nils-Göran

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Prevalence of electrocardiographic markers associated with myocardial fibrosis in masters athletes: a cohort study by Kramer, Tilmann, Ventovuori, Ville, Heinonen, Ari, Parkkari, Jari, Korhonen, Marko T, Rovio, Anja, Hoenemann, Jan-Niklas, Möstl, Stefan, Sies, Wolfram, Kaiser-Stolz, Claudia, Chilibeck, Philip, Tanaka, Hirofumi, Kramer, Mira, Rittweger, Joern, Hautala, Arto J

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Mannose-binding lectin 2 gene polymorphism in recurrent herpes simplex virus 2 infection by Seppänen, Mikko, Lokki, Marja-Liisa, Lappalainen, Maija, Hiltunen-Back, Eija, Rovio, Anja T, Kares, Saara, Hurme, Mikko, Aittoniemi, Janne

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Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological states by KAJANDER, Olli A, ROVIO, Anja T, MAJAMAA, Kari, POULTON, Joanna, SPELBRINK, Johannes N, HOLT, Lan J, KARHUNEN, Pekka J, JACOBS, Howard T

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Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness families by Shah, Zahid H., Toompuu, Marina, Hakkinen, Terhi, Rovio, Anja T., van Ravenswaay, Conny, De Leenheer, Els M.R., Smith, Richard J.H., Cremers, Frans P.M., Cremers, Cor W.R.J., Jacobs, Howard T.

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A prevalent POLG CAG microsatellite length allele in humans and African great apes by Rovio, Anja T, Abel, Josef, Ahola, Arja L, Andres, Aida M, Bertranpetit, Jaume, Blancher, Antoine, Bontrop, Ronald E, Chemnick, Leona G, Cooke, Howard J, Cummins, James M, Davis, Heidi A, Elliott, David J, Fritsche, Ellen, Hargreave, Timothy B, Hoffman, Susan M G, Jequier, Anne M, Kao, Shu-Huei, Kim, Heui-Soo, Marchington, David R, Mehmet, Denise, Otting, Nel, Poulton, Joanna, Ryder, Oliver A, Schuppe, Hans-Christian, Takenaka, Osamu, Wei, Yau-Huei, Wichmann, Lars, Jacobs, Howard T

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Molecular Phenotype of a Human Lymphoblastoid Cell-line Homoplasmic for the np 7445 Deafness-associated Mitochondrial Mutation by Reid, Fiona M., Rovio, Anja, Holt, Ian J., Jacobs, Howard T.

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Premature ageing in mice expressing detective mitochondrial DNA polymerase by TRIFUNOVIC, Aleksandra, WREDENBERG, Anna, TÖRNELL, Jan, JACOBS, Howard T, LARSSON, Nils-Göran, FALKENBERG, Maria, SPELBRINK, Johannes N, ROVIO, Anja T, BRUDER, Carl E, BOHLOOLY-Y, Mohammad, GIDLÖF, Sebastian, OLDFORS, Anders, WIBOM, Roll

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Familial mitochondrial DNA depletion in liver : haplotype analysis of candidate genes by SPELBRINK, J. N, VAN GALEN, M. J. M, ZWART, R, BAKKER, H. D, ROVIO, A, JACOBS, H. T, VAN DEN BOGERT, C

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