Search results
Results: 77,082
Number of items: 77,082
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Burwinkel, B., Maichele, A. J., Aagenaes, O., Bakker, H. D., Lerner, A., Shin, Y. S., Strachan, J. A., & Kilimann, M. W. (1997). Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB). Human Molecular Genetics, 6, 1109-1115. https://doi.org/10.1093/hmg/6.7.1109 -
Ylst, L., Oostheim, W., Ruiter, J. P. N., & Wanders, R. J. A. (1997). Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of two new mutations. Journal of inherited metabolic disease, 20, 420-422. https://doi.org/10.1023/A:1005310903004 -
Coremans, J. M. C. C., Ince, C., Bruining, H. A., & Puppels, G. J. (1997). (Semi-) quantitative analysis of reduced nicotinamide adenine dinucleotide fluorescence images of blood-perfused rat heart. Biophysical Journal, 72, 1849-1860. https://doi.org/10.1016/S0006-3495(97)78831-3 -
Ya, J., Schilham, M. W., Clevers, H., Moorman, A. F. M., & Lamers, W. H. (1997). Animal models of congenital defects in the ventriculoarterial connection of the heart. Journal of Molecular Medicine, 75, 551-566. https://doi.org/10.1007/s001090050140 -
Holmstrom, S. A., Wei, C., Manson, N. B., Martin, J. P. D., Windsor, A. S. M., & Glasbeek, M. (1997). Spin echo at the Rabi frequency in solids. Physical Review Letters, 78, 302-305. https://doi.org/10.1103/PhysRevLett.78.302 -
Breitweg (et al.), J., Bokel, C. H., Botje, M. A. J., Brummer, N. C., Chlebana, F. S., Engelen, J. J., de Kamps, M., Kooijman, P. M., Kruse, A., van Sighem, A. I., Tiecke, H. G. J. M., Verkerke, W., Vossebeld, J. H., Vreeswijk, M., Wiggers, L. W., & de Wolf, E. (1997). Study of photon dissociation in diffractive photoproduction at HERA. Zeitschrift für Physik. C, Particles and Fields, 75, 421. https://doi.org/10.1007/s002880050485 -
Verhagen, C. E., Wierenga, E. A., Buffing, A. A. M., Chand, M. A., Faber, W. R., & Das, P. K. (1997). Reversal reaction in borderline leprosy is associated with a polarized shift to type 1-like Mycobacterium leprae T cell reactivity in lesional skin. A follow-up study. The journal of immunology, 159, 4474-4483. -
van Kuilenburg, A. B. P., Vreken, P., Meinsma, R., van Lenthe, H., Beex, L. V. A. M., de Abreu, R. A., & van Gennip, A. H. (1997). Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity. European Journal of Cancer, 33, 2258-2264. https://doi.org/10.1016/S0959-8049(97)00261-X
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