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Rolf J R J Janssen

Showing results (1-10 of 8) with videos related to

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Expert Review of Molecular Diagnostics|March 6, 2004
Genetic defects in the oxidative phosphorylation (OXPHOS) systemRolf J R J Janssen, Lambert P van den Heuvel, Jan A M Smeitink
Journal of Inherited Metabolic Disease|July 14, 2006
Mitochondrial complex I: structure, function and pathologyRolf J R J Janssen, Leo G Nijtmans, Lambert P van den Heuvel, et al.
Human Molecular Genetics|January 30, 2004
Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiencyCristina Ugalde, Rolf J R J Janssen, Lambert P van den Heuvel, et al.
Molecular Nutrition & Food Research|November 19, 2013
Thermoneutrality results in prominent diet-induced body weight differences in C57BL/6J mice, not paralleled by diet-induced metabolic differencesFemke P M Hoevenaars, Melissa Bekkenkamp-Grovenstein, Rolf J R J Janssen, et al.
The FEBS Journal|October 13, 2005
Human mitochondrial complex I assembly is mediated by NDUFAF1Rutger O Vogel, Rolf J R J Janssen, Cristina Ugalde, et al.
American Journal of Human Genetics|June 3, 2008
NDUFA2 complex I mutation leads to Leigh diseaseSaskia J G Hoefs, Cindy E J Dieteren, Felix Distelmaier, et al.
Human Molecular Genetics|June 16, 2009
Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorderRolf J R J Janssen, Felix Distelmaier, Roel Smeets, et al.
Genes & Development|March 9, 2007
Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assemblyRutger O Vogel, Rolf J R J Janssen, Mariël A M van den Brand, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Expert Review of Molecular Diagnostics|March 6, 2004
Genetic defects in the oxidative phosphorylation (OXPHOS) systemRolf J R J Janssen, Lambert P van den Heuvel, Jan A M Smeitink
Journal of Inherited Metabolic Disease|July 14, 2006
Mitochondrial complex I: structure, function and pathologyRolf J R J Janssen, Leo G Nijtmans, Lambert P van den Heuvel, et al.
Human Molecular Genetics|January 30, 2004
Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiencyCristina Ugalde, Rolf J R J Janssen, Lambert P van den Heuvel, et al.
Molecular Nutrition & Food Research|November 19, 2013
Thermoneutrality results in prominent diet-induced body weight differences in C57BL/6J mice, not paralleled by diet-induced metabolic differencesFemke P M Hoevenaars, Melissa Bekkenkamp-Grovenstein, Rolf J R J Janssen, et al.
The FEBS Journal|October 13, 2005
Human mitochondrial complex I assembly is mediated by NDUFAF1Rutger O Vogel, Rolf J R J Janssen, Cristina Ugalde, et al.
American Journal of Human Genetics|June 3, 2008
NDUFA2 complex I mutation leads to Leigh diseaseSaskia J G Hoefs, Cindy E J Dieteren, Felix Distelmaier, et al.
Human Molecular Genetics|June 16, 2009
Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorderRolf J R J Janssen, Felix Distelmaier, Roel Smeets, et al.
Genes & Development|March 9, 2007
Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assemblyRutger O Vogel, Rolf J R J Janssen, Mariël A M van den Brand, et al.
Pageof 1