How cell death shapes cancer von Labi, V, Erlacher, M

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SH2B3 alterations in a novel genetic condition, juvenile myelomonocytic leukemia, and myeloproliferative neoplasia von Niemeyer, Charlotte M, Erlacher, Miriam

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BH3-only proteins in cell death initiation, malignant disease and anticancer therapy von Labi, V, Erlacher, M, Kiessling, S, Villunger, A

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Corneal Donor Profile and Evolution of Corneal Donation in a Brazilian State Where the Number of Individuals on the Waiting List Reached Zero But Increased Again von Freitas, L.S.M., Rocon, P.C., de Almeida, A.V., Erlacher, R.G.N., Paro, F.M.

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P816: TRANSIENT MONOSOMY 7 IN SAMD9/9L SYNDROMES: IS IT SAFE TO WATCH AND WAIT? von Erlacher, M., Andresen, F., Yoshimi, A., Sukova, M., Stary, J., Moerloose, B., Dworzak, M., Polychronopoulou, S., Göhring, G., Kratz, C., Werff ten Bosch, J., Seidel, M., Strahm, B., Wlodarski, M., Niemeyer, C.

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Analysing cell-free plasma DNA and SLE disease activity von Atamaniuk, Johanna, Hsiao, Yu-Yang, Mustak, Monika, Bernhard, Duhm, Erlacher, Ludwig, Fodinger, Manuela, Tiran, Beate, Stuhlmeier, Karl M.

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S274: A NOVEL SUBTYPE OF ANEMIA CAUSED BY MUTATIONS IN TFRC GENE von Colucci, S., Venturi, V., Nicole, F., Jové Solavera, D., Zimon, M., Richter‐Pechanska, P., Hernandez, G., Unal, S., Gumruk, F., Diaz‐Conradi, A., Romero‐Cortadellas, L., Ferrer‐Cortès, X., Olivella, M., Erlacher, M., Niemeyer, C., Wiesel, T., Pepperkok, R., Fleming, M. D., Kulozik, A. E., Sanchez, M., Muckenthaler, M. U.

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Troubles de sommeil dans le sport de haut niveau von Vorster, Albrecht, Erlacher, Daniel, Barrazoni, Fabrizio, Hossner, Ernst-Joachim, Bassetti, Claudio

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intact ribose moiety at A2602 of 23S rRNA is key to trigger peptidyl-tRNA hydrolysis during translation termination von Amort, Melanie, Wotzel, Brigitte, Bakowska-Zywicka, Kamilla, Erlacher, Matthias D, Micura, Ronald, Polacek, Norbert

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Lucid dreaming frequency and personality von Schredl, Michael, Erlacher, Daniel

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Chemical engineering of the peptidyl transferase center reveals an important role of the 2′-hydroxyl group of A2451 von Erlacher, Matthias D., Lang, Kathrin, Shankaran, Nisha, Wotzel, Brigitte, Hüttenhofer, Alexander, Micura, Ronald, Mankin, Alexander S., Polacek, Norbert

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Pitot-tube flowmeter for quantification of airflow during sleep von Kirkness, J P, Verma, M, McGinley, B M, Erlacher, M, Schwartz, A R, Smith, P L, Wheatley, J R, Patil, S P, Amis, T C, Schneider, H

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Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7 von Pastor, Victor B, Sahoo, Sushree S, Boklan, Jessica, Schwabe, Georg C, Saribeyoglu, Ebru, Strahm, Brigitte, Lebrecht, Dirk, Voss, Matthias, Bryceson, Yenan T, Erlacher, Miriam, Ehninger, Gerhard, Niewisch, Marena, Schlegelberger, Brigitte, Baumann, Irith, Achermann, John C, Shimamura, Akiko, Hochrein, Jochen, Tedgård, Ulf, Nilsson, Lars, Hasle, Henrik, Boerries, Melanie, Busch, Hauke, Niemeyer, Charlotte M, Wlodarski, Marcin W

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BH3-only proteins Puma and Bim are rate-limiting for γ-radiation– and glucocorticoid-induced apoptosis of lymphoid cells in vivo von Erlacher, Miriam, Michalak, Ewa M., Kelly, Priscilla N., Labi, Verena, Niederegger, Harald, Coultas, Leigh, Adams, Jerry M., Strasser, Andreas, Villunger, Andreas

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Novel findings in two patients with late-diagnosed afibrinogenaemia: intraosseous haemorrhage and fingertip necrosis von ERLACHER, M., HEISS, J., HAINMANN, I., UHL, M., BUDDE, U., OLDENBURG, J., IVASKEVICIUS, V., AL-JAMALI, J., ZAJONC, H., SUPERTI-FURGA, A., ZIEGER, B.

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Death squads enlisted by the tumour suppressor p53 von Michalak, Ewa, Villunger, Andreas, Erlacher, Miriam, Strasser, Andreas

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Topic: AS04-MDS Biology and Pathogenesis/AS04c-MDS Mouse models (GEMMS, PDX) von Fernandez-Orth, J., Weiss, J., Geoffroy, A., Gonzalez-Mendez, I., Steinemann, D., Quintanilla-Martinez, L., Boerries, M., Niemeyer, C., Erlacher, M.

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O26 - Topic: AS04-MDS Biology and Pathogenesis/AS04c-MDS Mouse models (GEMMS, PDX): LEUKEMOGENESIS IN GATA2 HAPLOINSUFFICIENT MICE IS A SECONDARY EVENT AFTER BONE MARROW FAILURE von Fernandez-Orth, J., Weiss, J., Geoffroy, A., Gonzalez-Mendez, I., Steinemann, D., Quintanilla-Martinez, L., Boerries, M., Niemeyer, C., Erlacher, M.

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Topic: AS04-MDS Biology and Pathogenesis/AS04d-Somatic mutations: THE EVOLVING GENETIC LANDSCAPE OF PEDIATRIC MDS-EB von Erlacher, M., Yoshimi, A., Stasik, S., Ramamoorthy, S., Lebrecht, D., Noellke, P., Goehring, G., De Haas, V., Starý, J., Masetti, R., Ussowicz, M., Barzilai-Birenboim, S., De Moerloose, B., Kállay, K., Buechner, J., Dworzak, M., Catala, A., Hasle, H., Schmugge, M., Polychronopoulou, S., Boďová, I., Jahnukainen, K., Smith, O., Kavcic, M., Turkiewicz, D., Kjollerstrom, P., Locatelli, F., Wlodarski, M., Thiede, C., Strahm, B., Niemeyer, C.

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Enzymatic synthesis of Tinuvin von Schroeder, M., Pereira, L., Couto, Susana Rodríguez, Erlacher, A., Schoening, K.-U., Cavaco-Paulo, A., Guebitz, G.M.

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