ETV6: A versatile player in leukemogenesis von Bohlander, Stefan K.

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CCAAT/enhancer-binding protein alpha (CEBPA) gene haploinsufficiency does not alter hematopoiesis or induce leukemia in Lck-CALM/AF10 transgenic mice von Lange, A P, Almeida, L Y, Araújo Silva, C L, Scheucher, P S, Chahud, F, Krause, A, Bohlander, S K, Rego, E M

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Clathrin assembly lymphoid myeloid leukemia (CALM) protein: localization in endocytic-coated pits, interactions with clathrin, and the impact of overexpression on clathrin-mediated... von Tebar, F, Bohlander, S K, Sorkin, A

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Mediation analysis reveals common mechanisms of RUNX1 point mutations and RUNX1/RUNX1T1 fusions influencing survival of patients with acute myeloid leukemia von Hornung, Roman, Jurinovic, Vindi, Batcha, Aarif M. N., Bamopoulos, Stefanos A., Rothenberg-Thurley, Maja, Amler, Susanne, Sauerland, Maria Cristina, Berdel, Wolfgang E., Wörmann, Bernhard J., Bohlander, Stefan K., Braess, Jan, Hiddemann, Wolfgang, Lehmann, Sören, Mareschal, Sylvain, Spiekermann, Karsten, Metzeler, Klaus H., Herold, Tobias, Boulesteix, Anne-Laure

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Block of C/EBP alpha function by phosphorylation in acute myeloid leukemia with FLT3 activating mutations von Radomska, Hanna S, Bassères, Daniela S, Zheng, Rui, Zhang, Pu, Dayaram, Tajhal, Yamamoto, Yukiya, Sternberg, David W, Lokker, Nathalie, Giese, Neill A, Bohlander, Stefan K, Schnittger, Susanne, Delmotte, Marie-Hélène, Davis, Roger J, Small, Donald, Hiddemann, Wolfgang, Gilliland, D Gary, Tenen, Daniel G

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A BCR-JAK2 fusion gene as the result of a t(9;22)(p24;q11.2) translocation in a patient with a clinically typical chronic myeloid leukemia von Griesinger, Frank, Hennig, Heike, Hillmer, Frauke, Podleschny, Martina, Steffens, Rainer, Pies, Andreas, Wörmann, Bernhard, Haase, Detlef, Bohlander, Stefan K.

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Molecular analysis of the CALM/AF10 fusion : identical rearrangements in acute myeloid leukemia, acute lymphoblastic leukemia and malignant lymphoma patients von BOHLANDER, S. K, MUSCHINSKY, V, DREYLING, M. H, SCHRADER, K, SIEBERT, R, SCHLEGELBERGER, B, HARDER, L, SCHEMMEL, V, FONATSCH, C, LUDWIG, W.-D, HIDDEMANN, W

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Fusion of the TEL Gene on 12p13 to the AML1 Gene on 21q22 in Acute Lymphoblastic Leukemia von Golub, Todd R., Barker, George F., Bohlander, Stefan K., Hiebert, Scott W., Ward, David C., Bray-Ward, Patricia, Morgan, Elaine, Raimondi, Susana C., Rowley, Janet D., Gilliland, D. Gary

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Oligomerization of the ABL tyrosine kinase by the Ets protein TEL in human leukemia von Golub, Todd R., Goga, Andrei, Barker, George F., Afar, Daniel E. H., McLaughlin, Jami, Bohlander, Stefan K., Rowley, Janet D., Witte, Owen N., Gilliland, D. Gary

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The t(10;11)(p13;q14) in the U937 Cell Line Results in the Fusion of the AF10 Gene and CALM, Encoding a New Member of the AP-3 Clathrin Assembly Protein Family von Dreyling, M. H., Martinez-Climent, J. A., Zheng, M., Mao, J., Rowley, J. D., Bohlander, S. K.

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SALL1, the gene mutated in Townes-Brocks syndrome, encodes a transcriptional repressor which interacts with TRF1/PIN2 and localizes to pericentromeric heterochromatin von Netzer, C, Rieger, L, Brero, A, Zhang, C D, Hinzke, M, Kohlhase, J, Bohlander, S K

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Fluorescence In Situ Hybridization Mapping of Translocations and Deletions Involving the Short Arm of Human Chromosome 12 in Malignant Hematologic Diseases von Kobayashi, Hirofumi, Montgomery, Kate T., Bohlander, Stefan K., Adra, Chaker N., Lim, Bing L., Kucherlapati, Raju S., Donis-Keller, Helen, Holt, Matthew S., Le Beau, Michelle M., Rowley, Janet D.

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Association of Jacobsen syndrome and bipolar affective disorder in a patient with a de novo 11q terminal deletion von Böhm, D., Hoffmann, K., Laccone, F., Wilken, B., Dechent, P., Frahm, J., Bartels, I., Bohlander, S.K.

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Dual-color split signal fluorescence in situ hybridization assays for the detection of CALM/AF10 in t(10;11)(p13;q14-q21)-positive acute leukemia von La Starza, R, Crescenzi, B, Krause, A, Pierini, V, Specchia, G, Bardi, A, Nieddu, R, Ariola, C, Nanni, M, Diverio, D, Aventin, A, Sborgia, M, Martelli, MF, Bohlander, SK, Mecucci, C

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Homozygous deletions within chromosomal bands 9p21-22 in bladder cancer von STADLER, W. M, SHERMAN, J, BOHLANDER, S. K, ROULSTON, D, DREYLING, M, RUKSTALIS, D, OLOPADE, O. I

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Mutational analysis of the candidate tumor suppressor genes TEL and KIP1 in childhood acute lymphoblastic leukemia von STEGMAIER, K, TAKEUCHI, S, GOLUB, T. R, BOHLANDER, S. K, BARTRAM, C. R, KOEFFLER, H. P, GILLILAND, D. G

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A method for the rapid sequence-independent amplification of microdissected chromosomal material von Bohlander, Stefan K., Espinosa, Rafael, Le Beau, Michelle M., Rowley, Janet D., Díaz, Manuel O.

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TOPORS E3 ligase mediates resistance to hypomethylating agent cytotoxicity in acute myeloid leukemia cells von Truong, P, Shen, S, Joshi, S, Islam, MI, Zhong, L, Raftery, MJ, Afrasiabi, A, Alinejad-Rokny, H, Nguyen, M, Zou, X, Bhuyan, GS, Sarowar, CH, Ghodousi, ES, Stonehouse, O, Mohamed, S, Toscan, CE, Connerty, P, Kakadia, PM, Bohlander, SK, Michie, KA, Larsson, J, Lock, RB, Walkley, CR, Thoms, JAI, Jolly, CJ, Pimanda, JE

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Frequent Loss of Heterozygosity at the TEL Gene Locus in Acute Lymphoblastic Leukemia of Childhood von Stegmaier, Kimberly, Pendse, Shona, Barker, George F., Bray-Ward, Patricia, Ward, David C., Montgomery, Kate T., Krauter, Kenneth S., Reynolds, Carol, Sklar, Jeffrey, Donnelly, Mia, Bohlander, Stefan K., Rowley, Janet D., Sallan, Stephen E., Gilliland, D.Gary, Golub, Todd R.

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Detection of CDKN2 deletions in tumor cell lines and primary glioma by interphase fluorescence in situ hybridization von Dreyling, M H, Bohlander, S K, Adeyanju, M O, Olopade, O I

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