AAAAAA
Results:
1-12
|
Results: 12
Authors:
Borkhardt, A
Teigler-Schlegel, A
Fuchs, U
Keller, C
Konig, M
Harbott, J
Haas, OA
Citation: A. Borkhardt et al., An ins(X;11)(q24;q23) fuses the MLL and the septin 6/KIAA0128 gene in an infant with AML-M2, GENE CHROM, 32(1), 2001, pp. 82-88
Authors:
Ferrari, T
Weber, B
Pils, S
Harbott, J
Borkhardt, A
Citation: T. Ferrari et al., Absence of point mutations within the AML-1 gene in patients with MDS/AML and loss of chromosome 5q or 7, ANN HEMATOL, 80(2), 2001, pp. 72-73
Authors:
Fuchs, U
Rehkamp, G
Haas, OA
Slany, R
Konig, M
Bojesen, S
Bohle, RM
Damm-Welk, C
Ludwig, WD
Harbott, J
Borkhardt, A
Citation: U. Fuchs et al., The human formin-binding protein 17 (FBP17) interacts with sorting nexin, SNX2, and is an MLL-fusion partner in acute myelogeneous leukemia, P NAS US, 98(15), 2001, pp. 8756-8761
Authors:
Fasching, K
Panzer, S
Haas, OA
Borkhardt, A
Marschalek, R
Griesinger, F
Panzer-Grumayer, ER
Citation: K. Fasching et al., Presence of N regions in the clonotypic DJ rearrangements of the immunoglobulin heavy-chain genes indicates an exquisitely short latency in t(4;11)-positive infant acute lymphoblastic leukemia, BLOOD, 98(7), 2001, pp. 2272-2274
Authors:
Wuchter, C
Harbott, J
Schoch, C
Schnittger, S
Borkhardt, A
Karawajew, L
Ratei, R
Ruppert, V
Haferlach, T
Creutzig, U
Dorken, B
Ludwig, WD
Citation: C. Wuchter et al., Detection of acute leukemia cells with mixed lineage leukemia (MLL) gene rearrangements by flow cytometry using monoclonal antibody 7.1, LEUKEMIA, 14(7), 2000, pp. 1232-1238
Authors:
Gortner, L
Borkhardt, A
Reiss, I
Citation: L. Gortner et al., Consequences of scientific reports of complications, LANCET, 356(9246), 2000, pp. 2015-2015
Authors:
Reiss, I
Borkhardt, A
Fussle, R
Sziegoleit, A
Gortner, L
Citation: I. Reiss et al., Disinfectant contaminated with Klebsiella oxytoca as a source of sepsis inbabies, LANCET, 356(9226), 2000, pp. 310-310
Authors:
Borkhardt, A
Bojesen, S
Haas, OA
Fuchs, U
Bartelheimer, D
Loncarevic, IF
Bohle, RM
Harbott, J
Repp, R
Jaeger, U
Viehmann, S
Henn, T
Korth, P
Scharr, D
Lampert, F
Citation: A. Borkhardt et al., The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q, P NAS US, 97(16), 2000, pp. 9168-9173
Authors:
Loncarevic, IF
Roitzheim, B
Ritterbach, J
Viehmann, S
Borkhardt, A
Lampert, F
Harbott, L
Citation: If. Loncarevic et al., Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AMLI gene fusion, GENE CHROM, 24(3), 1999, pp. 272-277
Authors:
Gillert, E
Leis, T
Repp, R
Reichel, M
Hosch, A
Breitenlohner, I
Angermuller, S
Borkhardt, A
Harbott, J
Lampert, F
Griesinger, F
Greil, J
Fey, GH
Marschalek, R
Citation: E. Gillert et al., A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells, ONCOGENE, 18(33), 1999, pp. 4663-4671
Authors:
Viehmann, S
Borkhardt, A
Lampert, F
Harbott, J
Citation: S. Viehmann et al., Multiplex PCR - a rapid screening method for detection of gene rearrangements in childhood acute lymphoblastic leukemia, ANN HEMATOL, 78(4), 1999, pp. 157-162
Authors:
Dordelmann, M
Reiter, A
Borkhardt, A
Ludwig, WD
Gotz, N
Viehmann, S
Gadner, H
Riehm, H
Schrappe, M
Citation: M. Dordelmann et al., Prednisone response is the strongest predictor of treatment outcome in infant acute lymphoblastic leukemia, BLOOD, 94(4), 1999, pp. 1209-1217
Risultati:
1-12
|