Mitochondrial disease in adults: a scale to monitor progression and treatment von Schaefer, A M, Phoenix, C, Elson, J L, McFarland, R, Chinnery, P F, Turnbull, D M

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RRM2B MUTATIONS ARE FREQUENT IN FAMILIAL PEO WITH MULTIPLE mtDNA DELETIONS von FRATTER, C, RAMAN, P, POULTON, J, BRIERLEY, C, STAUNTON, T. G, TURNPENNY, P. D, SCHAEFER, A. M, CHINNERY, P. F, HORVATH, R, TURNBULL, D. M, GORMAN, G. S, TAYLOR, R. W, ALSTON, C. L, BLAKELY, E. L, CRAIG, K, SMITH, C, EVANS, J, SELLER, A, CZERMIN, B, HANNA, M. G

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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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Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO) von AGOSTINO, A, VALLETTA, L, CHINNERY, P. F, FERRARI, G, CARRARA, F, TAYLOR, R. W, SCHAEFER, A. M, TURNBULL, D. M, TIRANTI, V, ZEVIANI, M

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Prevalence and progression of diabetes in mitochondrial disease von Whittaker, R. G, Schaefer, A. M, McFarland, R, Taylor, R. W, Walker, M, Turnbull, D. M

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Homoplasmy, heteroplasmy, and mitochondrial dystonia von MCFARLAND, R, CHINNERY, P. F, TAYLOR, R. W, BLAKELY, E. L, SCHAEFER, A. M, MORRIS, A. A. M, FOSTER, S. M, TUPPEN, H. A. L, RAMESH, V, DORMAN, P. J, TURNBULL, D. M

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Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions von Betts-Henderson, J., Jaros, E., Krishnan, K. J., Perry, R. H., Reeve, A. K., Schaefer, A. M., Taylor, R. W., Turnbull, D. M.

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GASTROINTESTINAL TRACT INVOLVEMENT ASSOCIATED WITH THE 3243A>G MITOCHONDRIAL DNA MUTATION von BETTS, J, BARRON, M. J, NEEDHAM, S. J, SCHAEFER, A. M, TAYLOR, R. W, TURNBULL, D. M

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Occurrence of blood parasites in seabirds admitted for rehabilitation in the Western Cape, South Africa, 2001–2013 von Parsons, N.J., Voogt, N.M., Schaefer, A.M., Peirce, M.A., Vanstreels, R.E.T.

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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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POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions von Hudson, G, Deschauer, M, Taylor, R W, Hanna, M G, Fialho, D, Schaefer, A M, He, L-P, Blakely, E, Turnbull, D M, Chinnery, P F

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Hematological and serum biochemical profile of farm emus (Dromaius novaehollandiae) at the onset of their breeding season von Menon, D. G., Bennett, D. C., Schaefer, A. M., Cheng, K. M.

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Stimulation of the chemosensory TRPA1 cation channel by volatile toxic substances promotes cell survival of small cell lung cancer cells von Schaefer, Eva A.M., Stohr, Stefanie, Meister, Michael, Aigner, Achim, Gudermann, Thomas, Buech, Thomas R.H.

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Differential investment in pre‐ vs. post‐copulatory sexual selection reinforces a cross‐continental reversal of sexual size dimorphism in Sepsis punctum (Diptera: Sepsidae) von Puniamoorthy, N., Blanckenhorn, W. U., Schäfer, M. A.

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Catastrophic presentation of mitochondrial disease due to a mutation in the tRNA(His) gene von Taylor, R W, Schaefer, A M, McDonnell, M T, Petty, R K H, Thomas, A M, Blakely, E L, Hayes, C M, McFarland, R, Turnbull, D M

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The bHLH protein Dimmed controls neuroendocrine cell differentiation in Drosophila von Hewes, Randall S, Park, Dongkook, Gauthier, Sebastien A, Schaefer, Anneliese M, Taghert, Paul H

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rpm-1, A Conserved Neuronal Gene that Regulates Targeting and Synaptogenesis in C. elegans von Schaefer, Anneliese M., Hadwiger, Gayla D., Nonet, Michael L.

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Cytochrome c oxidase deficient muscle fibres: Substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathy von Barron, M.J., Chinnery, P.F., Howel, D., Blakely, E.L., Schaefer, A.M., Taylor, R.W., Turnbull, D.M.

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Mutations in Caenorhabditis elegans Cytoplasmic Dynein Components Reveal Specificity of Neuronal Retrograde Cargo von Koushika, Sandhya P, Schaefer, Anneliese M, Vincent, Rose, Willis, John H, Bowerman, Bruce, Nonet, Michael L

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No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation von Deschauer, M, Chinnery, P F, Schaefer, A M, Turnbull, D M, Taylor, R W, Zierz, S, Shanske, S, DiMauro, S, Majamaa, K, Wilichowski, E, Thorburn, D R

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