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Results: 6,128
Number of items: 6,128
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Gonçalves, S., de Munck, J. C., Heethaar, R. M., Lopes da Silva, F. H., & van Dijk, B. W. (2000). The application of electrical impedance tomography to reduce systematic errors in the EEG inverse problem: a simulation study. Physiological Measurement, 21(3), 379-393. https://doi.org/10.1088/0967-3334/21/3/304
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Spelbrink, J. N., Toivonen, J. M., Hakkaart, G. A. J., Kurkela, J. M., Cooper, H. M., Lehtinen, S. K., Lecrenier, N., Back, J. W., Speijer, D., Foury, F., & Jacobs, H. T. (2000). In vivo functional analysis of the human mitochondrial DNA polymerase POLG expressed in cultured human cells. The Journal of Biological Chemistry, 275(32), 24815-24828.
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Teusink, B., & Westerhoff, H. V. (2000). 'Slave' metabolites and enzymes. A rapid way of delineating metabolic control. European Journal of Biochemistry, 267, 1889-1893. https://doi.org/10.1046/j.1432-1327.2000.01220.x
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Kloosterman, F., Haeften van, T., & Lopes da Silva, F. H. (2000). Functional characterization of hippocampal output to the Entorhinal cortex in the rat. In H. E. Scharfmann, M. P. Witter, & R. Schwarcz (Eds.), The parahippocampal region. Implications for Neurological and psychiatric diseases (Vol. 911, pp. 459-461).
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Teusink, B., Passarge, J., Reijenga, C. A., Esgalhado, E., van der Weijden, C. C., Schepper, M. G. J., Walsh, M. C., Bakker, B. M., van Dam, K., Westerhoff, H. V., & Snoep, J. L. (2000). Can yeast glycolysis be understood in terms of in vitro kinetics of the constituent enzymes? Testing biochemistry. European Journal of Biochemistry, 267, 5313-5329. https://doi.org/10.1046/j.1432-1327.2000.01527.x
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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
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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
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