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B Obermaier

Showing results (51-60 of 67) with videos related to

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European Journal of Pediatrics|June 1, 1996
Successful treatment of heart failure with enoximone in a patient with cytochrome c oxidase deficiencyA Timnik, S Mühlbauer, A Merkenschlager, et al.
The Journal of Physiology|August 3, 2001
Differential expression and regulation of AE2 anion exchanger subtypes in rabbit parietal and mucous cellsH Rossmann, O Bachmann, Z Wang, et al.
Diabete & Metabolisme|July 1, 1987
Insulin receptor kinase defects as a possible cause of cellular insulin resistanceH Häring, B Obermaier, B Ermel, et al.
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.
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.
American Journal of Human Genetics|November 1, 1994
Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathyB Obermaier-Kusser, B Lorenz, S Schubring, et al.
Nucleic Acids Research|October 25, 1989
Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndromeI Nelson, F Degoul, B Obermaier-Kusser, et al.
Trends in Cell Biology|February 1, 1997
BIME joins the destruction teamY M Yamashita, J M Peters, R W King, et al.
IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society|August 6, 2003
Graz-BCI: state of the art and clinical applicationsG Pfurtscheller, C Neuper, G R Müller, et al.
Genome Research|March 7, 2001
Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAsS Wiemann, B Weil, R Wellenreuther, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
European Journal of Pediatrics|June 1, 1996
Successful treatment of heart failure with enoximone in a patient with cytochrome c oxidase deficiencyA Timnik, S Mühlbauer, A Merkenschlager, et al.
The Journal of Physiology|August 3, 2001
Differential expression and regulation of AE2 anion exchanger subtypes in rabbit parietal and mucous cellsH Rossmann, O Bachmann, Z Wang, et al.
Diabete & Metabolisme|July 1, 1987
Insulin receptor kinase defects as a possible cause of cellular insulin resistanceH Häring, B Obermaier, B Ermel, et al.
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.
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.
American Journal of Human Genetics|November 1, 1994
Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathyB Obermaier-Kusser, B Lorenz, S Schubring, et al.
Nucleic Acids Research|October 25, 1989
Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndromeI Nelson, F Degoul, B Obermaier-Kusser, et al.
Trends in Cell Biology|February 1, 1997
BIME joins the destruction teamY M Yamashita, J M Peters, R W King, et al.
IEEE Transactions on Neural Systems and Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society|August 6, 2003
Graz-BCI: state of the art and clinical applicationsG Pfurtscheller, C Neuper, G R Müller, et al.
Genome Research|March 7, 2001
Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAsS Wiemann, B Weil, R Wellenreuther, et al.
Pageof 7