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R H Triepels

Showing results (1-10 of 6) with videos related to

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American Journal of Medical Genetics|October 2, 2001
Respiratory chain complex I deficiencyR H Triepels, L P Van Den Heuvel, J M Trijbels, et al.
Human Molecular Genetics|September 15, 1998
Nuclear genes of human complex I of the mitochondrial electron transport chain: state of the artJ A Smeitink, J L Loeffen, R H Triepels, et al.
The Journal of Biological Chemistry|December 22, 2000
Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patternsR H Triepels, B J Hanson, L P van den Heuvel, et al.
Human Mutation|January 29, 2000
Isolated complex I deficiency in children: clinical, biochemical and genetic aspectsJ L Loeffen, J A Smeitink, J M Trijbels, et al.
Biochemical and Biophysical Research Communications|January 8, 1999
cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completedJ L Loeffen, R H Triepels, L P van den Heuvel, et al.
Annals of Neurology|June 9, 1999
Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex IR H Triepels, L P van den Heuvel, J L Loeffen, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics|October 2, 2001
Respiratory chain complex I deficiencyR H Triepels, L P Van Den Heuvel, J M Trijbels, et al.
Human Molecular Genetics|September 15, 1998
Nuclear genes of human complex I of the mitochondrial electron transport chain: state of the artJ A Smeitink, J L Loeffen, R H Triepels, et al.
The Journal of Biological Chemistry|December 22, 2000
Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patternsR H Triepels, B J Hanson, L P van den Heuvel, et al.
Human Mutation|January 29, 2000
Isolated complex I deficiency in children: clinical, biochemical and genetic aspectsJ L Loeffen, J A Smeitink, J M Trijbels, et al.
Biochemical and Biophysical Research Communications|January 8, 1999
cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completedJ L Loeffen, R H Triepels, L P van den Heuvel, et al.
Annals of Neurology|June 9, 1999
Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex IR H Triepels, L P van den Heuvel, J L Loeffen, et al.
Pageof 1