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Genomics|January 1, 1997
Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypesS Hofmann, R Bezold, M Jaksch, et al.Nucleic Acids Research|December 10, 1998
MITOP: database for mitochondria-related proteins, genes and diseasesC Scharfe, P Zaccaria, K Hoertnagel, et al.European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|January 1, 1991
Biochemistry and molecular genetics of muscle diseasesT Deufel, K D GerbitzJournal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|July 1, 1985
Pancreatic B-cell peptides as parameters for diagnosis and localisation of hormone secreting tumoursK D Gerbitz, F SpelsbergJournal 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.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.Biological Chemistry Hoppe-Seyler|August 1, 1990
Effect of nonenzymatic glycation on the structure of immunoglobulin GR Dolhofer-Bliesener, K D GerbitzAnnals 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.Scandinavian Journal of Clinical and Laboratory Investigation|November 1, 1990
Impairment by glycation of immunoglobulin G Fc fragment functionR Dolhofer-Bliesener, K D GerbitzKlinische Wochenschrift|September 15, 1988
Pathobiochemical aspects of diabetic nephropathyE Schleicher, A Nerlich, K D GerbitzPageof 9