Tissue-specific mtDNA lesions and radical-associated mitochondrial dysfunction in human hearts exposed to doxorubicin von Lebrecht, Dirk, Kokkori, Aikaterini, Ketelsen, Uwe-Peter, Setzer, Bernhard, Walker, Ulrich A.

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Time-dependent and tissue-specific accumulation of mtDNA and respiratory chain defects in chronic doxorubicin cardiomyopathy von LEBRECHT, Dirk, SETZER, Bernhard, KETELSEN, Uwe-Peter, HABERSTROH, Jörg, WALKER, Ulrich A

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Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4 von Stendel, Claudia, Roos, Andreas, Deconinck, Tine, Pereira, Jorge, Castagner, François, Niemann, Axel, Kirschner, Janbernd, Korinthenberg, Rudolf, Ketelsen, Uwe-Peter, Battaloglu, Esra, Parman, Yesim, Nicholson, Garth, Ouvrier, Robert, Seeger, Jürgen, De Jonghe, Peter, Weis, Joachim, Krüttgen, Alexander, Rudnik-Schöneborn, Sabine, Bergmann, Carsten, Suter, Ueli, Zerres, Klaus, Timmerman, Vincent, Relvas, João B., Senderek, Jan

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The 6‐maleimidocaproyl hydrazone derivative of doxorubicin (DOXO‐EMCH) is superior to free doxorubicin with respect to cardiotoxicity and mitochondrial damage von Lebrecht, Dirk, Geist, Andrea, Ketelsen, Uwe‐Peter, Haberstroh, Jörg, Setzer, Bernhard, Kratz, Felix, Walker, Ulrich A.

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Evidence of Nucleoside Analogue Reverse Transcriptase Inhibitor-Associated Genetic and Structural Defects of Mitochondria in Adipose Tissue of HIV-Infected Patients von Walker, Ulrich A, Bickel, Markus, Volksbeck, Severine I. Lütke, Ketelsen, Uwe-Peter, Schöfer, Helmut, Setzer, Bernhard, Venhoff, Nils, Rickerts, Volker, Staszewski, Schlomo

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p.S143F mutation in lamin A/C: A new phenotype combining myopathy and progeria von Kirschner, Janbernd, Brune, Thomas, Wehnert, Manfred, Denecke, Jonas, Wasner, Christina, Feuer, Anja, Marquardt, Thorsten, Ketelsen, Uwe-Peter, Wieacker, Peter, Bönnemann, Carsten G., Korinthenberg, Rudolf

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Autosomal recessive rippling muscle disease with homozygous CAV3 mutations von Kubisch, Christian, Ketelsen, Uwe-Peter, Goebel, Ingrid, Omran, Heymut

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Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation von Ibañez-Tallon, Inés, Pagenstecher, Axel, Fliegauf, Manfred, Olbrich, Heike, Kispert, Andreas, Ketelsen, Uwe-Peter, North, Alison, Heintz, Nathaniel, Omran, Heymut

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Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients von Kley, Rudolf A., Hellenbroich, Yorck, van der Ven, Peter F. M., Fürst, Dieter O., Huebner, Angela, Bruchertseifer, Vera, Peters, Sören A., Heyer, Christoph M., Kirschner, Janbernd, Schröder, Rolf, Fischer, Dirk, Müller, Klaus, Tolksdorf, Karen, Eger, Katharina, Germing, Alfried, Brodherr, Turgut, Reum, Conny, Walter, Maggie C., Lochmüller, Hanns, Ketelsen, Uwe-Peter, Vorgerd, Matthias

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Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15 von Senderek, Jan, Bergmann, Carsten, Weber, Susanne, Ketelsen, Uwe-Peter, Schorle, Hubert, Rudnik-Schöneborn, Sabine, Büttner, Reinhard, Buchheim, Eckhard, Zerres, Klaus

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Myogenin (Myf4) upregulation in trans-differentiating fibroblasts from a congenital myopathy with arrest of myogenesis and defects of myotube formation von Weise, Claudia, Dai, Fangping, Pröls, Felicitas, Uwe-Peter Ketelsen, Dohrmann, Ulrike, Kirsch, Mathias, Brand-Saberi, Beate

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Axonal Neuropathy and Predominance of Type II Myofibers in Infantile Spinal Muscular Atrophy von Omran, Heymut, Ketelsen, Uwe-Peter, Heinen, Florian, Sauer, Manfred, Rudnik-Schönebom, Sabine, Wirth, Brunhilde, Zerres, Klaus, Kratzer, Wilfried, Korinthenberg, Rudolf

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Neonatal type IV glycogen storage disease associated with “null” mutations in glycogen branching enzyme 1 von Janecke, Andreas R., Dertinger, Susanne, Ketelsen, Uwe-Peter, Bereuter, Lothar, Simma, Burkhard, Müller, Thomas, Vogel, Wolfgang, Offner, Felix A.

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Homozygosity Mapping of a Gene Locus for Primary Ciliary Dyskinesia on Chromosome 5p and Identification of the Heavy Dynein Chain DNAH5 as a Candidate Gene von Omran, Heymut, Haffner, Karsten, Volkel, Alexander, Kuehr, Joachim, Ketelsen, Uwe-Peter, Ross, Uwe-Henning, Konietzko, Nikolaus, Wienker, Thomas, Brandis, Matthias, Hildebrandt, Friedhelm

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Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiency von Kottlors, Michael, Jaksch, Michaela, Ketelsen, Uwe-Peter, Weiner, Stefan, Glocker, Franz Xaver, Lücking, Carl-Hermann

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Cytochrome C oxidase deficiency and Long-Chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy von Reichmann, Heinz, Scheel, Helmut, Bier, Bert, Ketelsen, Uwe-Peter, Zabransky, Siegfried

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Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15 von Senderek, Jan, Bergmann, Carsten, Weber, Susanne, Ketelsen, Uwe-Peter, Schorle, Hubert, Rudnik-Schöneborn, Sabine, Büttner, Reinhard, Buchheim, Eckhard, Zerres, Klaus

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INTRATHYMIC PATHOGENESIS AND DUAL GENETIC CONTROL OF MYASTHENIA GRAVIS von Wekerle, Hartmut, Ketelsen, Uwe-Peter

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Abundant minute myotubes in a patient who later developed centronuclear myopathy von WÖCKEL, L, KETELSEN, U.-P, STÖTTER, M, LAULE, S, MEYERMANN, R, BORNEMANN, A

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Thymic nurse cells-Ia-bearing epithelium involved in T-lymphocyte differentiation? von Wekerle, Hartmut, Ketelsen, Uwe-Peter

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