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Showing results (21-30 of 39) with videos related to

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The New England Journal of Medicine|October 20, 1988
Prenatal diagnosis of cytochrome c oxidase deficiency by biopsy of chorionic villiW Ruitenbeek, R Sengers, M Albani, et al.
Biochemical and Biophysical Research Communications|July 2, 1998
cDNA sequence and chromosomal localization of the remaining three human nuclear encoded iron sulphur protein (IP) subunits of complex I: the human IP fraction is completedJ Loeffen, L van den Heuvel, R Smeets, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patientsJ Loeffen, R Smeets, J Smeitink, et al.
Human Genetics|October 6, 1998
Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex IJ Smeitink, J Loeffen, R Smeets, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
The human nuclear-encoded acyl carrier subunit (NDUFAB1) of the mitochondrial complex I in human pathologyR Triepels, J Smeitink, J Loeffen, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Thiopurine treatment in childhood leukemia. Metabolic aspects and sensitivityR A De Abreu, J P Bokkerink, C W Keuzenkamp-Jansen, et al.
Annals of Clinical Biochemistry|May 1, 1992
Maturation of mitochondrial and other isoenzymes of creatine kinase in skeletal muscle of preterm born infantsJ Smeitink, W Ruitenbeek, T van Lith, et al.
Annals of Clinical Biochemistry|March 1, 1992
A method for quantitative measurement of mitochondrial creatine kinase in human skeletal muscleJ Smeitink, R Wevers, J Hulshof, et al.
Nature Genetics|March 18, 1999
Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsyM Schuelke, J Smeitink, E Mariman, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
The X-chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: tissue expression and mutation detectionJ Loeffen, R Smeets, J Smeitink, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
The New England Journal of Medicine|October 20, 1988
Prenatal diagnosis of cytochrome c oxidase deficiency by biopsy of chorionic villiW Ruitenbeek, R Sengers, M Albani, et al.
Biochemical and Biophysical Research Communications|July 2, 1998
cDNA sequence and chromosomal localization of the remaining three human nuclear encoded iron sulphur protein (IP) subunits of complex I: the human IP fraction is completedJ Loeffen, L van den Heuvel, R Smeets, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patientsJ Loeffen, R Smeets, J Smeitink, et al.
Human Genetics|October 6, 1998
Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex IJ Smeitink, J Loeffen, R Smeets, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
The human nuclear-encoded acyl carrier subunit (NDUFAB1) of the mitochondrial complex I in human pathologyR Triepels, J Smeitink, J Loeffen, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Thiopurine treatment in childhood leukemia. Metabolic aspects and sensitivityR A De Abreu, J P Bokkerink, C W Keuzenkamp-Jansen, et al.
Annals of Clinical Biochemistry|May 1, 1992
Maturation of mitochondrial and other isoenzymes of creatine kinase in skeletal muscle of preterm born infantsJ Smeitink, W Ruitenbeek, T van Lith, et al.
Annals of Clinical Biochemistry|March 1, 1992
A method for quantitative measurement of mitochondrial creatine kinase in human skeletal muscleJ Smeitink, R Wevers, J Hulshof, et al.
Nature Genetics|March 18, 1999
Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsyM Schuelke, J Smeitink, E Mariman, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
The X-chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: tissue expression and mutation detectionJ Loeffen, R Smeets, J Smeitink, et al.
Pageof 4