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Uwe Ahting

Showing results (11-20 of 36) with videos related to

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Neurogenetics|January 22, 2013
Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosisDennis Lal, Kerstin Becker, Susanne Motameny, et al.
Mitochondrion|October 11, 2016
Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G>A and m.14484T>C of the mitochondrial DNAClaudia B Catarino, Uwe Ahting, Mirjana Gusic, et al.
American Journal of Human Genetics|December 14, 2011
Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathwayJohannes A Mayr, Peter Freisinger, Kurt Schlachter, et al.
Journal of Neurology|February 21, 2008
Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutationJügen Prestel, Klaus Gempel, Till-Karsten Hauser, et al.
Journal of Inherited Metabolic Disease|May 7, 2019
Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial diseaseMatias Wagner, Riccardo Berutti, Bettina Lorenz-Depiereux, et al.
Molecular Biology of the Cell|December 12, 2003
Reconstituted TOM core complex and Tim9/Tim10 complex of mitochondria are sufficient for translocation of the ADP/ATP carrier across membranesAndreja Vasiljev, Uwe Ahting, Frank E Nargang, et al.
Proteomics|November 19, 2005
Proteome analysis of mitochondrial outer membrane from Neurospora crassaSimone Schmitt, Holger Prokisch, Tilman Schlunck, et al.
Journal of Inherited Metabolic Disease|March 18, 2015
Spectrum of combined respiratory chain defectsJohannes A Mayr, Tobias B Haack, Peter Freisinger, et al.
Plos One|October 8, 2013
Alterations of red cell membrane properties in neuroacanthocytosisClaudia Siegl, Patricia Hamminger, Herbert Jank, et al.
Biochimica Et Biophysica Acta|December 30, 2008
Neurological phenotype and reduced lifespan in heterozygous Tim23 knockout mice, the first mouse model of defective mitochondrial importUwe Ahting, Thomas Floss, Nikolas Uez, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Neurogenetics|January 22, 2013
Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosisDennis Lal, Kerstin Becker, Susanne Motameny, et al.
Mitochondrion|October 11, 2016
Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G>A and m.14484T>C of the mitochondrial DNAClaudia B Catarino, Uwe Ahting, Mirjana Gusic, et al.
American Journal of Human Genetics|December 14, 2011
Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathwayJohannes A Mayr, Peter Freisinger, Kurt Schlachter, et al.
Journal of Neurology|February 21, 2008
Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutationJügen Prestel, Klaus Gempel, Till-Karsten Hauser, et al.
Journal of Inherited Metabolic Disease|May 7, 2019
Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial diseaseMatias Wagner, Riccardo Berutti, Bettina Lorenz-Depiereux, et al.
Molecular Biology of the Cell|December 12, 2003
Reconstituted TOM core complex and Tim9/Tim10 complex of mitochondria are sufficient for translocation of the ADP/ATP carrier across membranesAndreja Vasiljev, Uwe Ahting, Frank E Nargang, et al.
Proteomics|November 19, 2005
Proteome analysis of mitochondrial outer membrane from Neurospora crassaSimone Schmitt, Holger Prokisch, Tilman Schlunck, et al.
Journal of Inherited Metabolic Disease|March 18, 2015
Spectrum of combined respiratory chain defectsJohannes A Mayr, Tobias B Haack, Peter Freisinger, et al.
Plos One|October 8, 2013
Alterations of red cell membrane properties in neuroacanthocytosisClaudia Siegl, Patricia Hamminger, Herbert Jank, et al.
Biochimica Et Biophysica Acta|December 30, 2008
Neurological phenotype and reduced lifespan in heterozygous Tim23 knockout mice, the first mouse model of defective mitochondrial importUwe Ahting, Thomas Floss, Nikolas Uez, et al.
Pageof 4