Nikolay, R.; Hilal, T.; Qin, B.; Mielke, T.; Bürger, J.; Loerke, J.; Textoris-Taube, K.; Nierhaus, K. H.; Spahn, C. M.T.: Structural Visualization of the Formation and Activation of the 50S Ribosomal Subunit during In Vitro Reconstitution. Molecular Cell 70 (5), e3, S. 881 - 893 (2018)

Reddy Devullapally, P.; Bürger, J.; Mielke, T.; Konthur, Z.; Lehrach, H.; Yaspo, M.-L.; Glökler, J.; Warnatz, H.-J.: Simple paired heavy- and light-chain antibody repertoire sequencing using endoplasmic reticulum microsomes. Genome Medicine 10, 10:34 (2018)

Qureshi, B. M.; Schmidt, A.; Behrmann, E.; Bürger, J.; Mielke, T.; Spahn, C. M. T.; Heck, M.; Scheerer, P.: Mechanistic insights into the role of prenyl-binding protein PrBP/δ in membrane dissociation of phosphodiesterase 6. Nature Communications 9 (1), 90 (2018)

Ehmke, N.; Graul-Neumann, L.; Smorag, L.; Koenig, R.; Segebrecht, L.; Magoulas, P.; Scaglia, F.; Kilic, E.; Hennig, A. F.; Adolphs, N. et al.; Saha, N.; Fauler, B.; Kalscheuer, V. M.; Hennig, F.; Altmüller, J.; Netzer, C.; Thiele, H.; Nürnberg, P.; Yigit, G.; Jäger, M.; Hecht, J.; Krüger, U.; Mielke, T.; Krawitz, P. M.; Horn, D.; Schuelke, M.; Mundlos, S.; Bacino, C. A.; Bonnen, P. E.; Wollnik, B.; Fischer-Zirnsak, B.; Kornak, U.: De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. The American Journal of Human Genetics 101 (5), S. 833 - 843 (2017)

Reddy-Alla, S.; Böhme, M. A.; Reynolds, E.; Beis, C.; Grasskamp, A. T.; Mampell, M. M.; Maglione, M.; Jusyte, M.; Rey, U.; Babikir, H. et al.; McCarthy, A. W.; Quentin, C.; Matkovic, T.; Bergeron, D. D.; Mushtaq, Z.; Göttfert, F.; Owald, D.; Mielke, T.; Hell, S. W.; Sigrist, S. J.; Walter, A. M.: Stable positioning of Unc13 restricts synaptic vesicle fusion to defined release sites to promote synchronous neurotransmission. Neuron 95 (6), S. 1350 - 1364 (2017)

Matz, P.; Wruck, W.; Fauler, B.; Herebian, D.; Mielke, T.; Adjaye, J.: Footprint-free human fetal foreskin derived iPSCs: A tool for modeling hepatogenesis associated gene regulatory networks. Scientific Reports 7 (1), 6294 (2017)

Lorenz, C.; Lesimple, P.; Bukowiecki, R.; Zink, A.; Inak, G.; Mlody, B.; Singh, M.; Semtner, M.; Mah, N.; Auré, K. et al.; Leong, M.; Zabiegalov, O.; Lyras, E.-M.; Pfiffer, V.; Fauler, B.; Eichhorst, J.; Wiesner, B.; Huebner, N.; Priller, J.; Mielke, T.; Meierhofer, D.; Izsvák, Z.; Meier, J. C.; Bouillaud, F.; Adjaye, J.; Schuelke, M.; Wanker, E. E.; Lombès, A.; Prigione, A.: Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders. Cell Stem Cell 20 (5), e9, S. 659 - 674 (2017)

Said, N.; Krupp, F.; Anedchenko, E.; Santos, K. F.; Dybkov, O.; Huang, Y. H.; Lee, C. T.; Loll, B.; Behrmann, E.; Buerger, J. et al.; Mielke, T.; Loerke, J.; Urlaub, H.; Spahn, C. M. T.; Weber, G.; Wahl, M. C.: Structural basis for λN-dependent processive transcription antitermination. Nature Microbiology 2, 2:17062 (2017)

Hilal, T.; Yamamoto, H.; Loerke, J.; Bürger, J.; Mielke, T.; Spahn, C. M. T.: Structural insights into ribosomal rescue by Dom34 and Hbs1 at near-atomic resolution. Nature Communications 7, 7:13521 (2016)

Arumughan, A.; Roske, Y.; Barth, C.; Forero, L. L.; Bravo-Rodriguez, K.; Redel, A.; Kostova, S.; McShane, E.; Robert Opitz, R.; Faelber, K. et al.; Rau, K.; Mielke, T.; Daumke, O.; Selbach, M.; Sanchez-Garcia, E.; Rocks, O.; Daniela Panáková, D.; Heinemann, U.; Wanker, E. E.: Quantitative interaction mapping reveals an extended UBX domain in ASPL that disrupts functional p97 hexamers. Nature Communications 7, 7:13047 (2016)