Number of items: 4.
2022
Thomalla, D.,
Beckmann, L. ,
Grimm, C. ,
Oliverio, M. ,
Meder, L.,
Herling, C. D.,
Nieper, P.,
Feldmann, T.,
Merkel, O.,
Lorsy, E.,
da Palma Guerreiro, A.,
von Jan, J.,
Kisis, I. ,
Wasserburger, E.,
Claasen, J.,
Faitschuk-Meyer, E.,
Altmüller, J.,
Nürnberg, P.,
Yang, T.-P.,
Lienhard, M.,
Herwig, R. ,
Kreuzer, K.-A.,
Pallasch, C. P. ,
Büttner, R.,
Schäfer, S. C.,
Hartley, J.,
Abken, H.,
Peifer, M.,
Kashkar, H.,
Knittel, G.,
Eichhorst, B.,
Ullrich, R. T.,
Herling, M.,
Reinhardt, H. C.,
Hallek, M. ,
Schweiger, M. R. and
Frenzel, L. P.
(2022)
Deregulation and epigenetic modification of BCL2-family genes cause resistance to venetoclax in hematologic malignancies.
Blood 140 (20), pp. 2113-2126.
Fulltext not available.
2018
Wagener, R.,
Seufert, J.,
Raimondi, F.,
Bens, S.,
Kleinheinz, K.,
Nagel, I.,
Altmueller, J.,
Thiele, H.,
Huebschmann, D.,
Kohler, Christian,
Nürnberg, P.,
Au-Yeung, R.,
Burkhardt, B.,
Horn, H.,
Leoncini, L.,
Jaffe, E. S.,
Ott, G.,
Rymkiewicz, G. ,
Schlesner, M. ,
Russell, R. B. ,
Klapper, W. and
Siebert, R.
(2018)
The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma.
Blood.
Fulltext not available.
2016
Nieuwenhuis, M. A.,
Siedlinski, M. ,
van den Berge, M.,
Granell, R.,
Li, X.,
Niens, M.,
van der Vlies, P.,
Altmüller, J.,
Nürnberg, P.,
Kerkhof, M.,
van Schayck, O. C.,
Riemersma, R. A.,
van der Molen, T.,
de Monchy, J. G.,
Bossé, Y.,
Sandford, A.,
Bruijnzeel-Koomen, C. A.,
Gerth van Wijk, R.,
ten Hacken, N. H.,
Timens, W.,
Boezen, H. M.,
Henderson, J.,
Kabesch, M.,
Vonk, J. M.,
Postma, D. S. and
Koppelman, G. H.
(2016)
Combining genomewide association study and lung eQTL analysis provides evidence for novel genes associated with asthma.
Allergy 71 (12), pp. 1712-1720.
Fulltext not available.
2011
Krumbiegel, M.,
Pasutto, F.,
Schlötzer-Schrehardt, U.,
Uebe, S.,
Zenkel, M.,
Mardin, C. Y.,
Weisschuh, N.,
Paoli, D.,
Gramer, E.,
Becker, C.,
Ekici, A. B.,
Weber, Bernhard H. F. ,
Nürnberg, P.,
Kruse, F. E. and
Reis, A.
(2011)
Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome.
European Journal of Human Genetics 19 (2), pp. 186-193.
Fulltext not available.
This list was generated on Thu Dec 5 18:13:49 2024 CET.