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R J Rodenburg

Showing results (11-20 of 34) with videos related to

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Clinical Genetics|December 2, 2016
A lethal neonatal phenotype of mitochondrial short-chain enoyl-CoA hydratase-1 deficiencyF Al Mutairi, H E Shamseldin, M Alfadhel, et al.
Journal of Inherited Metabolic Disease|October 19, 2013
Sequence variants in four candidate genes (NIPSNAP1, GBAS, CHCHD1 and METT11D1) in patients with combined oxidative phosphorylation system deficienciesP Smits, R J Rodenburg, J A M Smeitink, et al.
Molecular Reproduction and Development|August 1, 1993
Transcriptional regulation of the major promoters of the human IGF-II geneP Holthuizen, M A Van Dijk, R J Rodenburg, et al.
Journal of Immunological Methods|January 23, 1999
Peripheral blood monocytes of rheumatoid arthritis patients do not express elevated TNF alpha, IL-1beta, and IL-8 mRNA levels. A comparison of monocyte isolation proceduresR J Rodenburg, F H van den Hoogen, L B van de Putte, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 5, 2007
Early cardiac involvement in children carrying the A3243G mtDNA mutationS B Wortmann, R J Rodenburg, A P Backx, et al.
Arthritis and Rheumatism|October 3, 2000
The antiinflammatory drug sulfasalazine inhibits tumor necrosis factor alpha expression in macrophages by inducing apoptosisR J Rodenburg, A Ganga, P L van Lent, et al.
JIMD Reports|February 23, 2013
Infantile Progressive Hepatoencephalomyopathy with Combined OXPHOS Deficiency due to Mutations in the Mitochondrial Translation Elongation Factor Gene GFM1S Balasubramaniam, Y S Choy, A Talib, et al.
Annals of the Rheumatic Diseases|September 24, 1999
Superinduction of interleukin 8 mRNA in activated monocyte derived macrophages from rheumatoid arthritis patientsR J Rodenburg, F H van Den Hoogen, P Barrera, et al.
Neurobiology of Disease|March 20, 2012
The role of mitochondrial OXPHOS dysfunction in the development of neurologic diseasesM E Breuer, W J Koopman, S Koene, et al.
Neurology|November 30, 2006
Mitochondrial disease criteria: diagnostic applications in childrenE Morava, L van den Heuvel, F Hol, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Clinical Genetics|December 2, 2016
A lethal neonatal phenotype of mitochondrial short-chain enoyl-CoA hydratase-1 deficiencyF Al Mutairi, H E Shamseldin, M Alfadhel, et al.
Journal of Inherited Metabolic Disease|October 19, 2013
Sequence variants in four candidate genes (NIPSNAP1, GBAS, CHCHD1 and METT11D1) in patients with combined oxidative phosphorylation system deficienciesP Smits, R J Rodenburg, J A M Smeitink, et al.
Molecular Reproduction and Development|August 1, 1993
Transcriptional regulation of the major promoters of the human IGF-II geneP Holthuizen, M A Van Dijk, R J Rodenburg, et al.
Journal of Immunological Methods|January 23, 1999
Peripheral blood monocytes of rheumatoid arthritis patients do not express elevated TNF alpha, IL-1beta, and IL-8 mRNA levels. A comparison of monocyte isolation proceduresR J Rodenburg, F H van den Hoogen, L B van de Putte, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 5, 2007
Early cardiac involvement in children carrying the A3243G mtDNA mutationS B Wortmann, R J Rodenburg, A P Backx, et al.
Arthritis and Rheumatism|October 3, 2000
The antiinflammatory drug sulfasalazine inhibits tumor necrosis factor alpha expression in macrophages by inducing apoptosisR J Rodenburg, A Ganga, P L van Lent, et al.
JIMD Reports|February 23, 2013
Infantile Progressive Hepatoencephalomyopathy with Combined OXPHOS Deficiency due to Mutations in the Mitochondrial Translation Elongation Factor Gene GFM1S Balasubramaniam, Y S Choy, A Talib, et al.
Annals of the Rheumatic Diseases|September 24, 1999
Superinduction of interleukin 8 mRNA in activated monocyte derived macrophages from rheumatoid arthritis patientsR J Rodenburg, F H van Den Hoogen, P Barrera, et al.
Neurobiology of Disease|March 20, 2012
The role of mitochondrial OXPHOS dysfunction in the development of neurologic diseasesM E Breuer, W J Koopman, S Koene, et al.
Neurology|November 30, 2006
Mitochondrial disease criteria: diagnostic applications in childrenE Morava, L van den Heuvel, F Hol, et al.
Pageof 4