Author Title [ Type(Desc)] Year
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Journal Article
Li, D., Secher, J., Hyttel, P., Ivask, M., Kolko, M., Hall, V.Jane, and Freude, K.K. (2018). Generation of transgene-free porcine intermediate type induced pluripotent stem cells.Cell Cycle.
Hall, V.J., Lindblad, M.M., Jakobsen, J.E., Gunnarsson, A., Schmidt, M., Rasmussen, M.A., Volke, D., Zuchner, T., and Hyttel, P. (2015). Impaired APP activity and altered tau splicing in embryonic stem cell-derived astrocytes derived from the APPsw transgenic minipig.Dis Model Mech.
Kobolák, J., Molnár, K., Varga, E., Bock, I., Jezsó, B., Téglási, A., Zhou, S., Giudice, M.Lo, Hoogeveen-Westerveld, M., Pijnappel, W.Pim, et al. (2019). Modelling the neuropathology of lysosomal storage disorders through disease-specific human induced pluripotent stem cells.Exp Cell Res.
Valleh, M.Vafaye, Tahmoorespur, M., Joupari, M.Daliri, Dehghani, H., Rasmussen, M.Aabech, Hyttel, P., and Strøbech, L. (2014). Paternal breed effects on expression of IGF-II, BAK1 and BCL2-L1 in bovine preimplantation embryos.Zygote1-10.
Ostrup, O., Olbricht, G., Ostrup, E., Hyttel, P., Collas, P., and Cabot, R. (2013). RNA Profiles of Porcine Embryos during Genome Activation Reveal Complex Metabolic Switch Sensitive to In Vitro Conditions.Plos One8, e61547.
Petkov, S., Hyttel, P., and Niemann, H. (2014). The Small Molecule Inhibitors PD0325091 and CHIR99021 Reduce Expression of Pluripotency-Related Genes in Putative Porcine Induced Pluripotent Stem Cells.Cell Reprogram.