Potential Pitfalls of the Mx1-Cre System: Implications for Experimental Modeling of Normal and Malignant Hematopoiesis

Por Velasco-Hernandez, Talia, Säwén, Petter, Bryder, David, Cammenga, Jörg
Publicado no Stem Cell Reports (2016)

RUNX1 cooperates with FLT3-ITD to induce leukemia

Por Behrens, Kira, Maul, Katrin, Tekin, Nilgün, Kriebitzsch, Neele, Indenbirken, Daniela, Prassolov, Vladimir, Müller, Ursula, Serve, Hubert, Cammenga, Jörg, Stocking, Carol
Publicado no J Exp Med (2017)

AML1-ETO fusion protein up-regulates TRKA mRNA expression in human CD34(+) cells, allowing nerve growth factor-induced expansion

Por Mulloy, James C., Jankovic, Vladimir, Wunderlich, Mark, Delwel, Ruud, Cammenga, Jorg, Krejci, Ondrej, Zhao, Hui, Valk, Peter J. M., Lowenberg, Bob, Nimer, Stephen D.
Publicado em 2005

Young woman with mild bone marrow dysplasia, GATA2 and ASXL1 mutation treated with allogeneic hematopoietic stem cell transplantation

Por Lübking, Anna, Vosberg, Sebastian, Konstandin, Nikola P., Dufour, Annika, Graf, Alexander, Krebs, Stefan, Blum, Helmut, Weber, Axel, Lenhoff, Stig, Ehinger, Mats, Spiekermann, Karsten, Greif, Philipp A., Cammenga, Jörg
Publicado no Leuk Res Rep (2015)

HIF-2α maintains an undifferentiated state in neural crest-like human neuroblastoma tumor-initiating cells

Por Pietras, Alexander, Hansford, Loen M., Johnsson, A. Sofie, Bridges, Esther, Sjölund, Jonas, Gisselsson, David, Rehn, Matilda, Beckman, Siv, Noguera, Rosa, Navarro, Samuel, Cammenga, Jörg, Fredlund, Erik, Kaplan, David R., Påhlman, Sven
Publicado em 2009

Sox4 is a key oncogenic target in C/EBPα mutant Acute Myeloid Leukemia

Por Zhang, Hong, Alberich-Jordà, Meritxell, Amabile, Giovanni, Yang, Henry, Staber, Philipp B., DiRuscio, Annalisa, Welner, Rob, Ebralidze, Alexander, Zhang, Junyan, Levantini, Elena, Lefebvre, Véronique, Valk, Peter J.M., Delwel, Ruud, Hoogenkamp, Maarten, Nerlov, Claus, Cammenga, Jörg, Saez, Borja, Scadden, David T., Bonifer, Constanze, Ye, Min, Tenen, Daniel G.
Publicado em 2013

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms

Por Tesi, Bianca, Davidsson, Josef, Voss, Matthias, Rahikkala, Elisa, Holmes, Tim D., Chiang, Samuel C. C., Komulainen-Ebrahim, Jonna, Gorcenco, Sorina, Rundberg Nilsson, Alexandra, Ripperger, Tim, Kokkonen, Hannaleena, Bryder, David, Fioretos, Thoas, Henter, Jan-Inge, Möttönen, Merja, Niinimäki, Riitta, Nilsson, Lars, Pronk, Cornelis Jan, Puschmann, Andreas, Qian, Hong, Uusimaa, Johanna, Moilanen, Jukka, Tedgård, Ulf, Cammenga, Jörg, Bryceson, Yenan T.
Publicado no Blood (2017)