N., Jordan, R., Luzzani, C., Miriuka, S., Radrizzani, M., Donadeu, F.
In vitro and in vivo development of horse cloned embryos generated with i PSCs, mesenchymal stromal cells and fetal or adult fibroblasts as nuclear donors. | Ortiz-Escribano, N., Bogado Pascottini, O., Woelders, H., Vandenberghe, L., De Schauwer, C., Govaere, J., Van den Abbeel, E., Vullers, T., Ververs, C., Roels, K., Van De Velde, M., Van Soom, A., and Smits, K. An improved vitrification protocol for equine immature oocytes, resulting in a first live foal.
In ‘Proceedings of the IETS Equine Reproduction Symposium’, 9–10 January 2015, France.
Acceptability of biotechnologies in the horse industry in Europe.
Interest in equine somatic cell nuclear transfer technology has increased significantly since the first equid clones were produced in 2003.
Activation of cumulus-free equine oocytes: effect of maturation medium, calcium ionophore concentration and duration of cycloheximide exposure.
Production of a mitochondrial-DNA identical cloned foal using oocytes recovered from immature follicles of selected mares.
Developmental potential of bovine hand-made clone embryos reconstructed by aggregation or fusion with distinct cytoplasmic volumes.
| Lagutina, I., Lazzari, G., Duchi, R., Colleoni, S., Ponderato, N., Turini, P., Crotti, G., and Galli, C. Somatic cell nuclear transfer in horses: effect of oocyte morphology, embryo reconstruction method and donor cell type.
Cloned foal derived from in vivo matured horse oocytes aspirated by the short disposable needle system.