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Clinical Biochemistry|October 1, 1995
Screening for mitochondrial DNA (mtDNA) point mutations using nonradioactive single strand conformation polymorphism (SSCP) analysisM Jaksch, K D Gerbitz, C KilgerFEBS Letters|April 26, 1993
Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) geneK D Gerbitz, A Paprotta, M Jaksch, et al.Biochimica Et Biophysica Acta|May 24, 1995
Mitochondrial diabetes mellitus: a reviewK D Gerbitz, J M van den Ouweland, J A Maassen, et al.Molecular and Cellular Biochemistry|October 6, 1997
Analysis of the mitochondrial DNA from patients with Wolfram (DIDMOAD) syndromeS Hofmann, R Bezold, M Jaksch, et al.Clinical Chemistry and Laboratory Medicine|December 22, 1999
Mitochondrial disorders. A diagnostic challenge in clinical chemistryM F Bauer, K Gempel, S Hofmann, et al.Human Molecular Genetics|September 25, 1997
Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with diseaseS Hofmann, M Jaksch, R Bezold, et al.Human Molecular Genetics|April 6, 2000
Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiencyM Jaksch, I Ogilvie, J Yao, et al.Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|November 1, 1977
Human alkaline phosphatases. II. Metalloenzyme properties of the enzyme from human liverK D GerbitzJournal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|June 1, 1980
[Pancreatic B cell peptides: kinetic behaviour and concentrations of proinsulin, insulin and C-peptide in plasma and urine, problems of assay methods, clinical significance and literature review (author's transl)]K D GerbitzBiochemical and Biophysical Research Communications|October 12, 2000
Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiencyR Horvath, H Lochmüller, R Stucka, et al.Pageof 9