 | Up a level |
Chirico, N., Kessler, E. L., Maas, R. G. C., Fang, J., Qin, J., Dokter, I, Ciccone, S., Saric, T., Buikema, J. W., Lei, Z., Doevendans, P., Sluijter, J. P. G. and Van Mil, A. (2022). Small molecule-mediated rapid maturation of human induced pluripotent stem cell derived cardiomyocytes. Cardiovasc. Res., 118 (SUPPL 1). OXFORD: OXFORD UNIV PRESS. ISSN 1755-3245
Cunha, D. L., Eckl, K. M., Gupta, M., Lingenhel, A., Schmuth, M., Zschocke, J., Saric, T. and Hennies, H. C. (2018). Induced pluripotent stem cell-derived keratinocytes for disease modelling of autosomal recessive congenital ichthyosis and other inherited skin diseases. Br. J. Dermatol., 178 (6). S. E430 - 1. HOBOKEN: WILEY. ISSN 1365-2133
Cunha, D. L., Eckl, K. M., Rauch, M., Casper, R., Gupta, M., Nurnberg, P., Schmuth, M., Zschocke, J., Saric, T. and Hennies, H. C. (2014). Generation and characterization of induced Pluripotent Stem (iPS) cells from Autosomal Recessive Congenital Ichthyosis patients - a new model system to study rare keratinization disorders. J. Invest. Dermatol., 134. S. S34 - 1. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1523-1747
Dreher, L., Perrech, M., Roehn, G., Goldbrunner, R., Saric, T. and Timmer, M. (2014). Evaluation of stem cell markers and different stemness genes in glioblastoma cell lines. Oncol. Res. Treat., 37. S. 119 - 120. BASEL: KARGER. ISSN 2296-5262
Eckl, K., Cunha, D., Saric, T., Plank, R. and Hennies, H. (2016). Patient-specific induced pluripotent stem cell-derived melanocytes for three-dimensional monogenic disease modelling. Br. J. Dermatol., 174 (5). S. E62 - 1. HOBOKEN: WILEY-BLACKWELL. ISSN 1365-2133
Frobel, J., Hemeda, H., Lenz, M., Denecke, B., Saric, T., Zenke, M. and Wagner, W. (2014). Epigenetic rejuvenation of human mesenchymal stromal cells by derivation from induced pluripotent stem cells. Oncol. Res. Treat., 37. S. 304 - 306. BASEL: KARGER. ISSN 2296-5262
Garcia-Perez, A., Zhang, X. H., Telugu, N., Saric, T., Morad, M. and Izsvak, Z. (2017). Using non-viral gene delivery by Sleeping Beauty to generate hHCN4-expressing hiPSCs as platform for pacemaker cardiomyocytes differentiation. Hum. Gene Ther., 28 (12). S. A120 - 1. NEW ROCHELLE: MARY ANN LIEBERT, INC. ISSN 1557-7422
Hennies, H. C., Cunha, D. de Lima, Barragan Vazquez, I., Saric, T. and Eckl, K. M. (2018). TP63 is expressed in adult epidermal and induced pluripotent stem cell-derived melanocytes, furthering the role of Delta Np63 in ectodermal gatekeeping and cell migration to the epidermis. Br. J. Dermatol., 178 (6). S. E415 - 1. HOBOKEN: WILEY. ISSN 1365-2133
Peinkofer, G., Klinke, A., Maass, M., Urban, K., Lange, M., Saric, T., Mueller-Ehmsen, J., Baldus, S., Hescheler, J. and Halbach, M. (2015). Arrhythmic risk after transplantation of induced pluripotent stem cell derived cardiomyocytes into infarcted mouse hearts. Eur. Heart J., 36. S. 709 - 710. OXFORD: OXFORD UNIV PRESS. ISSN 1522-9645
Peinkofer, G., Klinke, A., Maass, M., Urban, K., Lange, M., Saric, T., Mueller-Ehmsen, J., Baldus, S., Hescheler, J. and Halbach, M. (2016). Susceptibility to induced ventricular tachycardias increases with time after transplantation of induced pluripotent stem cell-derived cardiomyocytes into infarcted mouse hearts. Eur. Heart J., 37. S. 834 - 835. OXFORD: OXFORD UNIV PRESS. ISSN 1522-9645
Peinkofer, G., Maass, M., Burkert, K., Saric, T., Baldus, S., Hescheler, J. and Halbach, M. (2017). Electrical integration and persistence of transplanted induced pluripotent stem cell-derived cardiomyocytes from different developmental stages. Eur. Heart J., 38. S. 532 - 534. OXFORD: OXFORD UNIV PRESS. ISSN 1522-9645