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Journal Article
Andersson, E. I., Puetzer, S., Yadav, B., Dufva, O., Khan, S., He, L., Sellner, L., Schrader, A., Crispatzu, G., Oles, M., Zhang, H., Adnan-Awad, S., Lagstrom, S., Bellanger, D., Mpindi, J. P., Eldfors, S., Pemovska, T., Pietarinen, P., Lauhio, A., Tomska, K., Cuesta-Mateos, C., Faber, E., Koschmieder, S., Bruemmendorf, T. H., Kytola, S., Savolainen, E-R, Siitonen, T., Ellonen, P., Kallioniemi, O., Wennerberg, K., Ding, W., Stern, M-H, Huber, W., Anders, S., Tang, J., Aittokallio, T., Zenz, T., Herling, M. and Mustjoki, S. (2018). Discovery of novel drug sensitivities in T-PLL by high-throughput ex vivo drug testing and mutation profiling. Leukemia, 32 (3). S. 774 - 788. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5551
Berger, A., Weber, I., Khan, S., Chiemlewski, M., Abken, H., Theobald, M. and Hartwig, U. F. (2016). GENERATION OF CHIMERIC ANTIGEN RECEPTOR - MODIFIED MEMORY STEM CELL CD8+T LYMPHOCYTES FROM NAIVE PRECURSORS BY MODULATION OF WNT/BETA-CATENIN PATHWAY OR INHIBITION OF AKT-SIGNALING. Haematologica, 101. S. 192 - 193. PAVIA: FERRATA STORTI FOUNDATION. ISSN 0390-6078
Howell, J., Atkinson, S., PInato, D. J., Knapp, S., Ward, C., Minisini, R., Burlone, M., Leutner, M., Pirisi, M., Khan, S., Odenthal, M., Thursz, M. and Sharma, R. (2017). Identification of actionable mutations in circulating cell-free tumour DNA as a prognostic biomarker in hepatocellular carcinoma. J. Hepatol., 66 (1). S. S449 - 1. AMSTERDAM: ELSEVIER SCIENCE BV. ISSN 1600-0641
Iqbal, M., Baig, S. M., Abdullah, U., Makhdoom, E. U. H., Ali, Z., Khan, S., Jameel, M., Noegel, A. A., Nuernberg, P., Osmond, M. and Hussain, M. S. (2020). Mutations of PCDHGC4 encoding protocadherin gamma-C4 cause primary microcephaly and intellectual disability. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 399 - 401. LONDON: SPRINGERNATURE. ISSN 1476-5438