Klaus-Dieter Gerbitz
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Advanced Glycation End Products research, Diabetes and associated disorders
Most-Cited Works
- → Mitochondria and Diabetes: Genetic, Biochemical, and Clinical Implications of the Cellular Energy Circuit(1996)285 cited
- → Mitochondrial diabetes mellitus: a review(1995)220 cited
- → Population Genetics and Disease Susceptibility: Characterization of Central European Haplogroups By mtDNA Gene Mutations, Correlation with D Loop Variants and Association With Disease(1997)168 cited
- → Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochromec oxidase deficiency(1999)119 cited
- → Genetic and structural characterization of the human mitochondrial inner membrane translocase 1 1Edited by J. Karn(1999)116 cited
- → Role of the Deafness Dystonia Peptide 1 (DDP1) in Import of Human Tim23 into the Inner Membrane of Mitochondria(2001)103 cited
- → The C66W Mutation in the Deafness Dystonia Peptide 1 (DDP1) Affects the Formation of Functional DDP1·TIM13 Complexes in the Mitochondrial Intermembrane Space(2002)93 cited
- → Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease(1998)85 cited
- → The mitochondrial TIM22 preprotein translocase is highly conserved throughout the eukaryotic kingdom(1999)85 cited
- → Myoadenylate deaminase deficiency: Successful symptomatic therapy by high dose oral administration of ribose(1986)84 cited