Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology von Grünewald, A., Gegg, M.E., Taanman, J.-W., King, R.H., Kock, N., Klein, C., Schapira, A.H.V.

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Biochemical abnormalities and excitotoxicity in Huntington's disease brain von Tabrizi, S. J., Cleeter, M. W. J., Xuereb, J., Taanman, J.-W., Cooper, J. M., Schapira, A. H. V.

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Mitochondria in the etiology and pathogenesis of parkinson's disease von Schapira, A. H. V., Gu, M., Taanman, J.-W., Tabrizi, S. J., Seaton, T., Cleeter, M., Cooper, J. M.

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Subunit composition of respiratory chain complex 1 and its responses to oxygen in mitochondria from human donor livers von Khorsandi, S E, Taanman, J W, Heaton, N

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Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease von Gu, M., Cooper, J. M., Taanman, J. W., Schapira, A. H. V.

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A mutation in the human heme A:farnesyltransferase gene (COX10) causes cytochrome c oxidase deficiency von VALNOT, I, VON KLEIST-RETZOW, J.-C, BARRIENTOS, A, GORBATYUK, M, TAANMAN, J.-W, MEHAYE, B, RUSTIN, P, TZAGOLOFF, A, MUNNICH, A, RÖTIG, A

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A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure von Tzagoloff, Alexander, Niaudet, Patrick, Barrientos, Antoni, Munnich, Arnold, Rustin, Pierre, Taanman, Jan-Willem, Chrétien, Dominique, Kadhom, Noman, Rötig, Agnès, Benayoun, Emmanuel, Lombès, Anne, Valnot, Isabelle, de Lonlay, Pascale, Gorbatyuk, Marina, de Baulny, Hélène Ogier

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The mitochondrial genome: structure, transcription, translation and replication von Taanman, Jan-Willem

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Expression of mutant α-synuclein causes increased susceptibility to dopamine toxicity von TABRIZI, Sarah J, ORTH, Michael, WILKINSON, J. Max, TAANMAN, Jan-Willem, WARNER, Thomas T, COOPER, J. Mark, SCHAPIRA, Anthony H. V

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Remodelling of bioenergetic pathways in human fibroblasts with carbohydrates von Protasoni, M, Taanman, J.-W

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Mitochondrial DNA depletion can be prevented by dGMP and dAMP supplementation in a resting culture of deoxyguanosine kinase-deficient fibroblasts von Taanman, Jan-Willem, Muddle, John R., Muntau, Ania C.

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Cytochrome c Oxidase subunit I microdeletion in a patient with motor neuron disease von Comi, Giacomo P., Bordoni, Andreina, Salani, Sabrina, Franceschina, Liliana, Sciacco, Monica, Prelle, Alessandro, Fortunato, Francesco, Zeviani, Massimo, Napoli, Laura, Bresolin, Nereo, Moggio, Maurizio, Ausenda, Carlo D., Taanman, Jan-Willem, Scarlato, Guglielmo

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Mutations in the mitochondrial complex I assembly factor NDUFAF1 cause fatal infantile hypertrophic cardiomyopathy von Fassone, Elisa, Taanman, Jan-Willem, Hargreaves, Iain P, Sebire, Neil J, Cleary, Maureen A, Burch, Michael, Rahman, Shamima

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A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome von TIRANTI, Valeria, CORONA, Paola, GRECO, Marilena, TAANMAN, Jan-Willem, CARRARA, Franco, LAMANTEA, Eleonora, NIJTMANS, Leo, UZIEL, Graziella, ZEVIANI, Massimo

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Influence of zinc and zinc chelator on HT-29 colorectal cell line von Gurusamy, K. S, Farooqui, N, Loizidou, M, Dijk, S, Taanman, J. W, Whiting, S, Farquharson, M. J, Fuller, B. J, Davidson, B. R

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Molecular Mechanisms in Mitochondrial DNA Depletion Syndrome von Taanman, J.-W., Bodnar, A. G., Cooper, J. M., Morris, A. A. M., Clayton, P. T., Leonard, J. V., Schapira, A. H. V.

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Decreased brain protein levels of cytochrome oxidase subunits in Alzheimer's disease and in hereditary spinocerebellar ataxia disorders : A nonspecific change? von KISH, S. J, MASTROGIACOMO, F, GUTTMAN, M, FURUKAWA, Y, TAANMAN, J.-W, DOZIC, S, PANDOLFO, M, LAMARCHE, J, DISTEFANO, L, CHANG, L.-J

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A Missense Mutation of Cytochrome Oxidase Subunit II Causes Defective Assembly and Myopathy von Rahman, Shamima, Taanman, Jan-Willem, Cooper, J. Mark, Nelson, Isabelle, Hargreaves, Ian, Meunier, Brigitte, Hanna, Michael G, García, José J., Capaldi, Roderick A., Lake, Brian D., Leonard, James V., Schapira, Anthony H.V.

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POG01 Anti-thymidine phosphorylase antibodies in the diagnosis of mitochondrial neurogastrointestinal encephalomyopathy von Ginsberg, L, Taanman, J W

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Diagnostic Value of Succinate Ubiquinone Reductase Activity in the Identification of Patients with Mitochondrial DNA Depletion von Hargreaves, I. P., Rahman, S., Guthrie, P., Taanman, J‐W., Leonard, J. V., Land, J. M., Heales, S. J. R.

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