Publications

Neureiter, A.; Brändl, B.; Hiber, M.; Tandon, R.; Müller, F.-J.; Steenpass, L.: Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect. Stem Cell Research 33, pp. 20 - 24 (2018)

Tandon, R.; Brändl, B.; Baryshnikova, N.; Landshammer, A.; Steenpaß, L.; Keminer, O.; Pless, O.; Müller, F.-J.: Generation of two human isogenic iPSC lines from fetal dermal fibroblasts. Stem Cell Research 33, pp. 120 - 124 (2018)

Allison, T. F.; Andrews, P. W.; Avior, Y.; Barbaric, I.; Benvenisty, N.; Bock, C.; Brehm, J.; Bruestle, O.; Damjanov, I.; Elefanty, A. et al.; Felkner, D.; Gokhale, P. J.; Halbritter, F.; Healy, L. E.; Hu, T. X.; Knowles, B. B.; Loring, J. F.; Ludwig, T. E.; Mayberry, R.; Micallef, S.; Mohamed, J. S.; Müller, F.-J.; Mummery, C. L.; Nakatsuji, N.; Ng, E. S.; Oh, S. K. W.; O'Shea, O.; Pera, M. F.; Reubinoff, B.; Robson, P.; Rossant, J.; Schuldt, B. M.; Solter, D.; Sourris, K.; Stacey, G.; Stanley, E. G.; Suemori, H.; Takahashi, K.; Yamanaka, S.: Assessment of Established Techniques to Determine Developmental and Malignant Potential of Human Pluripotent Stem Cells. Nature Communications 9 (1), 1925 (2018)

Vögtle, F.-N.; Brändl, B.; Larson, A.; Pendziwiat, M.; Friederich, M. W.; White, S. M.; Basinger, A.; Kücükköse, C.; Muhle, H.; Jähn, J. A. et al.; Keminer, O.; Helbig, K. L.; Delto, C. F.; Myketin, L.; Mossmann, D.; Burger, N.; Miyake, N.; Burnett, A.; van Baalen, A.; Lovell, M. A.; Matsumoto, N.; Walsh, M.; Yu, H.-C.; Deepali N. Shinde, D. N.; Stephani, U.; Van Hove, J. L. K.; Müller, F.-J.; Helbig, I.: Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood. American Journal of Human Genetics 102 (4), pp. 557 - 573 (2018)