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2021
Rudek, Loreen Sophie, Zimmermann, Katharina, Galla, Melanie, Meyer, Johann, Kuehle, Johannes, Stamopoulou, Andriana, Brand, Daniel, Sandalcioglu, I. Erol, Neyazi, Belal, Moritz, Thomas, Rossig, Claudia, Altvater, Bianca, Falk, Christine S., Abken, Hinrich, Morgan, Michael Alexander and Schambach, Axel (2021). Generation of an NF kappa B-Driven Alpharetroviral All-in-One Vector Construct as a Potent Tool for CAR NK Cell Therapy. Front. Immunol., 12. LAUSANNE: FRONTIERS MEDIA SA. ISSN 1664-3224
2020
Zimmermann, Katharina, Kuehle, Johannes, Dragon, Anna Christina 
ORCID: 0000-0002-5228-7627, Galla, Melanie, Kloth, Christina, Rudek, Loreen Sophie, Sandalcioglu, I. Erol, Neyazi, Belal, Moritz, Thomas, Meyer, Johann, Rossig, Claudia, Altvater, Bianca, Eiz-Vesper, Britta, Morgan, Michael Alexander, Abken, Hinrich and Schambach, Axel
(2020).
Design and Characterization of an All-in-One Lentiviral Vector System Combining Constitutive Anti-G(D2) CAR Expression and Inducible Cytokines.
Cancers, 12 (2).
BASEL:
MDPI.
ISSN 2072-6694
2018
Erger, Florian ORCID: 0000-0002-2768-1702, Burau, Karin, Elsaesser, Michael, Zimmermann, Katharina, Moog, Ute and Netzer, Christian
(2018).
Uniparental isodisomy as a cause of recessive Mendelian disease: a diagnostic pitfall with a quick and easy solution in medium/large NGS analyses.
Eur. J. Hum. Genet., 26 (9).
S. 1392 - 1396.
LONDON:
NATURE PUBLISHING GROUP.
ISSN 1476-5438
2014
Hoyer-Kuhn, Heike, Semler, Oliver ORCID: 0000-0003-0029-7556, Garbes, Lutz, Zimmermann, Katharina, Becker, Jutta, Wollnik, Bernd, Schoenau, Eckhard and Netzer, Christian
(2014).
A Nonclassical IFITM5 Mutation Located in the Coding Region Causes Severe Osteogenesis Imperfecta With Prenatal Onset.
J. Bone Miner. Res., 29 (6).
S. 1387 - 1392.
HOBOKEN:
WILEY.
ISSN 1523-4681