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Results: 77,061
Number of items: 77,061
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Satijn, D. P. E., Olson, D. J., van der Vlag, J., Hamer, C. M., Lambrechts, C., Masselink, H., Gunster, M. J., Sewalt, R. G. A. B., van Driel, R., & Otte, A. P. (1997). Interference with the expression of a novel human Polycomb protein, hPc2, results in cellular transformation and apoptosis. Molecular and Cellular Biology, (17), 6076-6086. -
Schoorlemmer, J., Marcos-Gutierrez, C., Were, F., Martinez, R., Garcia-Mendoza, E., Satijn, D. P. E., Otte, A. P., & Vidal, M. (1997). Ring1A is a transcriptional repressor that interacts with the Polycomb-M33 protein and is expressed at rhombomere boundaries in the mouse hindbrain. EMBO Journal, (16), 5930-5942. -
Horrevoets, A. J. G., Pannekoek, H., & Nesheim, M. E. (1997). A steady-state template model that describes the kinetics of fibrin-stimulated [Glu1]- and [Lys78] plasminogen activation by native tissue-type plasminigen activator and variants that lack either the finger of kringle-2 domain. The Journal of Biological Chemistry, 272(4), 2183-2191. -
Hop, C. C. E. M., de Waard, V., van Mourik, J. A., & Pannekoek, H. (1997). Lack of gradual regulation of tetracycline-controlled gene expression by the tetracyclin-repressor/VP16 transactivator (tTA) in cultured cells. FEBS Letters, 405, 167-171. https://doi.org/10.1016/S0014-5793(97)00179-8 -
Vreken, P., van Kuilenburg, A. B. P., Meinsma, R., & van Gennip, A. H. (1997). Dihydropyrimidine dehydrogenase (DPD) deficiency: identification and expression of missense mutations C29R, R886H and R235W. Human Genetics, 101, 333-338. https://doi.org/10.1007/s004390050637 -
Wanders, R. J. A., Romeijn, G. J., Wijburg, F. A., Hennekam, R. C. M., de Jong, J. G. N., Wevers, R., & Dacremont, G. (1997). Smith-Lemli-Opitz syndrome: deficient delta7-reductase activity in cultured skin fibroblasts and chorionic villus fibroblasts and its application to pre- and postnatal detection. Journal of inherited metabolic disease, 20, 432-436. https://doi.org/10.1023/A:1005371104822
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