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K D Gerbitz

Showing results (51-60 of 63) with videos related to

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Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|April 1, 1990
Mutations of the mitochondrial DNA: the contribution of DNA techniques to the diagnosis of mitochondrial encephalomyopathiesK D Gerbitz, B Obermaier-Kusser, P Lestienne, et al.
Journal of Molecular Biology|May 26, 1999
Genetic and structural characterization of the human mitochondrial inner membrane translocaseM F Bauer, K Gempel, A S Reichert, et al.
Nucleic Acids Research|December 10, 1998
MITOP: database for mitochondria-related proteins, genes and diseasesC Scharfe, P Zaccaria, K Hoertnagel, et al.
Journal of Medical Genetics|October 5, 2001
Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficienciesM Jaksch, S Kleinle, C Scharfe, et al.
Journal of Medical Genetics|December 1, 1998
A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathyM Jaksch, S Hofmann, S Kleinle, et al.
Diabetes Care|November 1, 1984
Clinical utility of nonenzymatically glycosylated blood proteins as an index of glucose controlE D Schleicher, K D Gerbitz, R Dolhofer, et al.
Annals of Neurology|October 20, 1998
Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) geneM Jaksch, T Klopstock, G Kurlemann, et al.
Neurogenetics|March 29, 2000
Novel mutations of mitochondrial complex I in pathologically proven Parkinson diseaseS Kösel, E M Grasbon-Frodl, U Mautsch, et al.
Human Molecular Genetics|March 4, 2000
Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patientsG V Börner, M Zeviani, V Tiranti, et al.
Nucleic Acids Research|December 11, 1999
MITOP, the mitochondrial proteome database: 2000 updateC Scharfe, P Zaccaria, K Hoertnagel, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|April 1, 1990
Mutations of the mitochondrial DNA: the contribution of DNA techniques to the diagnosis of mitochondrial encephalomyopathiesK D Gerbitz, B Obermaier-Kusser, P Lestienne, et al.
Journal of Molecular Biology|May 26, 1999
Genetic and structural characterization of the human mitochondrial inner membrane translocaseM F Bauer, K Gempel, A S Reichert, et al.
Nucleic Acids Research|December 10, 1998
MITOP: database for mitochondria-related proteins, genes and diseasesC Scharfe, P Zaccaria, K Hoertnagel, et al.
Journal of Medical Genetics|October 5, 2001
Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficienciesM Jaksch, S Kleinle, C Scharfe, et al.
Journal of Medical Genetics|December 1, 1998
A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathyM Jaksch, S Hofmann, S Kleinle, et al.
Diabetes Care|November 1, 1984
Clinical utility of nonenzymatically glycosylated blood proteins as an index of glucose controlE D Schleicher, K D Gerbitz, R Dolhofer, et al.
Annals of Neurology|October 20, 1998
Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) geneM Jaksch, T Klopstock, G Kurlemann, et al.
Neurogenetics|March 29, 2000
Novel mutations of mitochondrial complex I in pathologically proven Parkinson diseaseS Kösel, E M Grasbon-Frodl, U Mautsch, et al.
Human Molecular Genetics|March 4, 2000
Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patientsG V Börner, M Zeviani, V Tiranti, et al.
Nucleic Acids Research|December 11, 1999
MITOP, the mitochondrial proteome database: 2000 updateC Scharfe, P Zaccaria, K Hoertnagel, et al.
Pageof 7