未登录Standardisation and consensus guidelines for minimal residual disease assessment in Philadelphia-positive acute lymphoblastic leukemia (Ph+ALL) by real-time quantitative reverse transcriptase PCR of e1a2 BCR-ABL1 (vol 32, pg 345, 2019)
Pfeifer, H.; Cazzaniga, G.; van der Velden, V. H. J.; Cayuela, J. M.; Schafer, B.; Spinelli, O.; Akiki, S.; Avigad, S.; Bendit, I.; Borg, K.; Cave, H.; Elia, L.; Reshmi, S. C.; Gerrard, G.; Hayette, S.; Hermanson, M.; Juh, A.; Jurcek, T.; Chillon, M. C.; Homburg, C.; Martinelli, G.; Kairisto, V.; Lange, T.; Lion, T.; Mueller, M. C.; Pane, F.; Rai, L.; Damm-Welk, C.; Sacha, T.; Schnittger, S.; Touloumenidou, T.; Valerhaugen, H.; Vandenberghe, P.; Zuna, J.; Serve, H.; Herrmann, E.; Markovic, S.; van Dongen, J. J. M.; Ottmann, O. G. .png)
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收藏Standardisation and consensus guidelines for minimal residual disease assessment in Philadelphia-positive acute lymphoblastic leukemia (Ph plus ALL) by real-time quantitative reverse transcriptase PCR of e1a2 BCR-ABL1Pfeifer, H.; Cazzaniga, G.; van der Velden, V. H. J.; Cayuele, J. M.; Schafer, B.; Spinelli, O.; Akiki, S.; Avigad, S.; Bendit, I; Borg, K.; Cave, H.; Elia, L.; Reshmi, S. C.; Gerrard, G.; Hayette, S.; Hermanson, M.; Juh, A.; Jurcek, T.; Chillon, M. C.; Homburg, C.; Martinelli, G.; Kairisto, V; Langen, T.; Lion, T.; Mueller, M. C.; Pane, F.; Rai, L.; Damm-Welk, C.; Sacha, T.; Schnittger, S.; Touloumenidou, T.; Valerhaugen, H.; Vandenberghe, P.; Zuna, J.; Server, H.; Herrmann, E.; Markovic, S.; van Dongen, J. J. M.; Ottmann, O. G. 分享 收藏 分享 收藏 Age, not therapy intensity, determines outcomes of adults with acute myeloid leukemiaBuechner, T.; Krug, U. O.; Gale, R. Peter; Heinecke, A.; Sauerland, M. C.; Haferlach, C.; Schnittger, S.; Haferlach, T.; Mueller-Tidow, C.; Stelljes, M.; Mesters, R. M.; Serve, H. L.; Braess, J.; Spiekermann, K.; Staib, P.; Grueneisen, A.; Reichle, A.; Balleisen, L.; Eimermacher, H.; Giagounidis, A.; Rasche, H.; Lengfelder, E.; Goerlich, D.; Faldum, A.; Koepcke, W.; Hehlmann, R.; Woermann, B. J.; Berdel, W. E.; Hiddemann, W. 分享 收藏 Gain of Chromosome 21 or Amplification of Chromosome Arm 21q Is One Mechanism for Increased ERG Expression in Acute Myeloid LeukemiaWeber, Simone; Haferlach, Claudia; Jeromin, Sabine; Nadarajah, Niroshan; Dicker, Frank; Noel, Louisa; Zenger, Melanie; Alpermann, Tamara; Kern, Wolfgang; Haferlach, Torsten; Schnittger, Susanne 分享 收藏 分享 收藏 Molecular subtypes of NPM1 mutations have different clinical profiles, specific patterns of accompanying molecular mutations and varying outcomes in intermediate risk acute myeloid leukemiaNPM1突变的分子亚型在中危急性髓细胞白血病中具有不同的临床特征，伴随的分子突变的特定模式和不同的结局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 分享 收藏 Additional mutations in SRSF2, ASXL1 and/or RUNX1 identify a high-risk group of patients with KIT D816V+advanced systemic mastocytosisJawhar, M.; Schwaab, J.; Schnittger, S.; Meggendorfer, M.; Pfirrmann, M.; Sotlar, K.; Horny, H-P; Metzgeroth, G.; Kluger, S.; Naumann, N.; Haferlach, C.; Haferlach, T.; Valent, P.; Hofmann, W-K; Fabarius, A.; Cross, N. C. P.; Reiter, A. 分享 收藏 分享 收藏 Array CGH identifies copy number changes in 11% of 520 MDS patients with normal karyotype and uncovers prognostically relevant deletionsVolkert, S.; Haferlach, T.; Holzwarth, J.; Zenger, M.; Kern, W.; Staller, M.; Nagata, Y.; Yoshida, K.; Ogawa, S.; Schnittger, S.; Haferlach, C. 分享 收藏 Fusion of PDGFRB to MPRIP, CPSF6, and GOLGB1 in Three Patients with Eosinophilia-Associated Myeloproliferative NeoplasmsNaumann, Nicole; Schwaab, Juliana; Metzgeroth, Georgia; Jawhar, Mohamad; Haferlach, Claudia; Goehring, Gudrun; Schlegelberger, Brigitte; Dietz, Christian T.; Schnittger, Susanne; Lotfi, Sina; Gaertner, Michael; Tu-Anh Dang; Hofmann, Wolf-Karsten; Cross, Nicholas C. P.; Reiter, Andreas; Fabarius, Alice 分享 收藏 分享 收藏 KIT D816V and JAK2 V617F mutations are seen recurrently in hypereosinophilia of unknown significanceSchwaab, Juliana; Umbach, Roland; Metzgeroth, Georgia; Naumann, Nicole; Jawhar, Mohamad; Sotlar, Karl; Horny, Hans-Peter; Gaiser, Timo; Hofmann, Wolf-Karsten; Schnittger, Susanne; Cross, Nicholas C. P.; Fabarius, Alice; Reiter, Andreas 分享 收藏 Next-generation deep-sequencing detects multiple clones of CALR mutations in patients with BCR-ABL1 negative MPNJeromin, S.; Kohlmann, A.; Meggendorfer, M.; Schindela, S.; Perglerova, K.; Nadarajah, N.; Kern, W.; Haferlach, C.; Haferlach, T.; Schnittger, S. 分享 收藏 Rare FLT3 deletion mutants may provide additional treatment options to patients with AML: an approach to individualized medicineChatain, N.; Perera, R. C.; Rossetti, G.; Rosso, J.; Carloni, P.; Schemionek, M.; Haferlach, T.; Brummendorf, T. H.; Schnittger, S.; Koschmieder, S. 分享 收藏 BRCC3 mutations in myeloid neoplasmsHuang, Dayong; Nagata, Yasunobu; Grossmann, Vera; Radivoyevitch, Tomas; Okuno, Yusuke; Nagae, Genta; Hosono, Naoko; Schnittger, Susanne; Sanada, Masashi; Przychodzen, Bartlomiej; Kon, Ayana; Polprasert, Chantana; Shen, Wenyi; Clemente, Michael J.; Phillips, James G.; Alpermann, Tamara; Yoshida, Kenichi; Nadarajah, Niroshan; Sekeres, Mikkael A.; Oakley, Kevin; Nhu Nguyen; Shiraishi, Yuichi; Shiozawa, Yusuke; Chiba, Kenichi; Tanaka, Hiroko; Koeffler, H. Phillip; Klein, Hans-Ulrich; Dugas, Martin; Aburatani, Hiroyuki; Miyano, Satoru; Haferlach, Claudia; Kern, Wolfgang; Haferlach, Torsten; Du, Yang; Ogawa, Seishi; Makishima, Hideki 分享 收藏 Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasmsTapper, William; Jones, Amy V.; Kralovics, Robert; Harutyunyan, Ashot S.; Zoi, Katerina; Leung, William; Godfrey, Anna L.; Guglielmelli, Paola; Callaway, Alison; Ward, Daniel; Aranaz, Paula; White, Helen E.; Waghorn, Katherine; Lin, Feng; Chase, Andrew; Baxter, E. Joanna; Maclean, Cathy; Nangalia, Jyoti; Chen, Edwin; Evans, Paul; Short, Michael; Jack, Andrew; Wallis, Louise; Oscier, David; Duncombe, Andrew S.; Schuh, Anna; Mead, Adam J.; Griffiths, Michael; Ewing, Joanne; Gale, Rosemary E.; Schnittger, Susanne; Haferlach, Torsten; Stegelmann, Frank; Doehner, Konstanze; Grallert, Harald; Strauch, Konstantin; Tanaka, Toshiko; Bandinelli, Stefania; Giannopoulos, Andreas; Pieri, Lisa; Mannarelli, Carmela; Gisslinger, Heinz; Barosi, Giovanni; Cazzola, Mario; Reiter, Andreas; Harrison, Claire; Campbell, Peter; Green, Anthony R.; Vannucchi, Alessandro; Cross, Nicholas C. P. 分享 收藏 Molecular profiling of myeloid progenitor cells in multi-mutated advanced systemic mastocytosis identifies KIT D816V as a distinct and late eventJawhar, M.; Schwaab, J.; Schnittger, S.; Sotlar, K.; Horny, H-P; Metzgeroth, G.; Mueller, N.; Schneider, S.; Naumann, N.; Walz, C.; Haferlach, T.; Valent, P.; Hofmann, W-K; Cross, N. C. P.; Fabarius, A.; Reiter, A. 分享 收藏 分享 收藏 Refractory anemia with ring sideroblasts and marked thrombocytosis cases harbor mutations in SF3B1 or other spliceosome genes accompanied by JAK2V617F and ASXL1 mutationsJeromin, Sabine; Haferlach, Torsten; Weissmann, Sandra; Meggendorfer, Manja; Eder, Christiane; Nadarajah, Niroshan; Alpermann, Tamara; Kohlmann, Alexander; Kern, Wolfgang; Haferlach, Claudia; Schnittger, Susanne 分享 收藏 
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