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Results: 13
Number of items: 13
  • Artal Sanz, M., Tsang, W. Y., Willems, E. M., Grivell, L. A., Lemire, B. D., van der Spek, J. C., Nijtmans, L. G. J., & Sanz, M. A. (2003). The mitochondrial prohibition complex is essential for embryonic viability and germline function in Caenorhabditis elegans. The Journal of Biological Chemistry, 278, 32091-32099. https://doi.org/10.1074/jbc.M304877200
  • Open Access
    Artal Sanz, M. (2003). The role of the PHB complex in mitochondrial biogenesis. [Thesis, fully internal, Universiteit van Amsterdam].
  • Nijtmans, L. G. J., Artal Sanz, M., Grivell, L. A., & Coates, P. J. (2002). The mitochondrial PHB complex: roles in mitochondrial respiratory complex assembly, ageing and degenerative disease. Cellular and Molecular Life Sciences, 59(1), 143-155. https://doi.org/10.1007/s00018-002-8411-0
  • Nijtmans, L. G. J., Artal Sanz, M., Bucko, M., Farhoud, M. H., Feenstra, M., Hakkaart, G. A. J., Zeviani, M., & Grivell, L. A. (2001). Shy1p occurs in a high molecular weight complex and is required for efficient assembly of cytochrome c oxidase in yeast. FEBS Letters, 498(1), 46-51. https://doi.org/10.1016/S0014-5793(01)02447-4
  • Nijtmans, L. G. J., de Jong, L., Artal Sanz, M., Coates, P. J., Berden, J. A., Back, J. W., Muijsers, A. O., van der Spek, J. C., & Grivell, L. A. (2000). Prohibitins act as a membrane-bound chaperone for the stabilization of mitochondrial proteins. EMBO Journal, 19, 2444-2451. https://doi.org/10.1093/emboj/19.11.2444
  • Henderson, N. S., Nijtmans, L. G. J., Lindsay, J. G., Lamantea, E., Zeviani, M., & Holt, I. J. (2000). Separation of intact pyruvate dehydrogenase complex using blue native agarose gel electrophoresis. Electrophoresis, 21, 2925-2931. https://doi.org/10.1002/1522-2683(20000801)21:14<2925::AID-ELPS2925>3.0.CO;2-2
  • Vreken, P., Valianpour, F., Nijtmans, L. G. J., Grivell, L. A., Plecko, B., Wanders, R. J. A., & Barth, P. G. (2000). Defective remodeling of cardiolipin and phosphatidylglycerol in barth syndrome. Biochemical and Biophysical Research Communications, 279, 378-382. https://doi.org/10.1006/bbrc.2000.3952
  • Tiranti, V., Corona, P., Greco, M., Taanman, J. W., Carrara, F., Lamantea, E., Nijtmans, L. G. J., Uziel, G., & Zeviani, M. (2000). A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by leigh-like syndrome. Human Molecular Genetics, 9, 2733-2742. https://doi.org/10.1093/hmg/9.18.2733
  • Coenen, M. J. H., van den Heuvel, L. P., Nijtmans, L. G. J., Morava, E., Marquardt, I., Girschick, H., Trijbels, F. J. M., Grivell, L. A., & Smeitink, J. A. M. (1999). Surfeit-1 gene analysis in COX deficiency. Biochemical and Biophysical Research Communications, 265, 339-344. https://doi.org/10.1006/bbrc.1999.1662
  • Vergani, L., Barile, M., Angelini, C., Burlina, A. B., Nijtmans, L. G. J., Freda, M. P., Brizio, C., Zerbetto, E., & Dabbeni-Sala, F. (1999). Riboflavin therapy: biochemical heterogeneity in two adult lipid storage myophathies. Brain, 122, 2401-2411. https://doi.org/10.1093/brain/122.12.2401
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