Specific molecular mutation patterns delineate chronic neutrophilic leukemia, atypical chronic myeloid leukemia, and chronic myelomonocytic leukemia

Por Meggendorfer, Manja, Haferlach, Torsten, Alpermann, Tamara, Jeromin, Sabine, Haferlach, Claudia, Kern, Wolfgang, Schnittger, Susanne
Publicado no Haematologica (2014)

Stably integrated and expressed retroviral sequences can influence nuclear location and chromatin condensation of the integration locus

Por Nagel, Jens, Groß, Birgit, Meggendorfer, Manja, Preiss, Carolin, Grez, Manuel, Brack-Werner, Ruth, Dietzel, Steffen
Publicado em 2012

Ultra-deep sequencing leads to earlier and more sensitive detection of the tyrosine kinase inhibitor resistance mutation T315I in chronic myeloid leukemia

Por Baer, Constance, Kern, Wolfgang, Koch, Sarah, Nadarajah, Niroshan, Schindela, Sonja, Meggendorfer, Manja, Haferlach, Claudia, Haferlach, Torsten
Publicado no Haematologica (2016)

RAS signaling promotes resistance to JAK inhibitors by suppressing BAD-mediated apoptosis

Por Winter, Peter S., Sarosiek, Kristopher A., Lin, Kevin H., Meggendorfer, Manja, Schnittger, Susanne, Letai, Anthony, Wood, Kris C.
Publicado no Sci Signal (2014)

Karyotype evolution and acquisition of FLT3 or RAS pathway alterations drive progression of myelodysplastic syndrome to acute myeloid leukemia

Por Meggendorfer, Manja, de Albuquerque, Andreia, Nadarajah, Niroshan, Alpermann, Tamara, Kern, Wolfgang, Steuer, Kimberly, Perglerová, Karolína, Haferlach, Claudia, Schnittger, Susanne, Haferlach, Torsten
Publicado no Haematologica (2015)

Refractory anemia with ring sideroblasts and marked thrombocytosis cases harbor mutations in SF3B1 or other spliceosome genes accompanied by JAK2V617F and ASXL1 mutations

Por Jeromin, Sabine, Haferlach, Torsten, Weissmann, Sandra, Meggendorfer, Manja, Eder, Christiane, Nadarajah, Niroshan, Alpermann, Tamara, Kohlmann, Alexander, Kern, Wolfgang, Haferlach, Claudia, Schnittger, Susanne
Publicado no Haematologica (2015)

Molecular subtypes of NPM1 mutations have different clinical profiles, specific patterns of accompanying molecular mutations and varying outcomes in intermediate risk acute myeloid...

Por Alpermann, Tamara, Schnittger, Susanne, Eder, Christiane, Dicker, Frank, Meggendorfer, Manja, Kern, Wolfgang, Schmid, Christoph, Aul, Carlo, Staib, Peter, Wendtner, Clemens-Martin, Schmitz, Norbert, Haferlach, Claudia, Haferlach, Torsten
Publicado no Haematologica (2016)

SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)

Por Meggendorfer, Manja, Roller, Andreas, Haferlach, Torsten, Eder, Christiane, Dicker, Frank, Grossmann, Vera, Kohlmann, Alexander, Alpermann, Tamara, Yoshida, Kenichi, Ogawa, Seishi, Koeffler, H. Phillip, Kern, Wolfgang, Haferlach, Claudia, Schnittger, Susanne
Publicado em 2012

Integrating clinical features and genetic lesions in the risk assessment of patients with chronic myelomonocytic leukemia

Por Elena, Chiara, Gallì, Anna, Such, Esperanza, Meggendorfer, Manja, Germing, Ulrich, Rizzo, Ettore, Cervera, Jose, Molteni, Elisabetta, Fasan, Annette, Schuler, Esther, Ambaglio, Ilaria, Lopez-Pavia, Maria, Zibellini, Silvia, Kuendgen, Andrea, Travaglino, Erica, Sancho-Tello, Reyes, Catricalà, Silvia, Vicente, Ana I., Haferlach, Torsten, Haferlach, Claudia, Sanz, Guillermo F., Malcovati, Luca, Cazzola, Mario
Publicado no Blood (2016)