AAAAAA

   
Results: 1-22 |
Results: 22
An ins(X;11)(q24;q23) fuses the MLL and the septin 6/KIAA0128 gene in an infant with AML-M2
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
Absence of point mutations within the AML-1 gene in patients with MDS/AML and loss of chromosome 5q or 7
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
Treatment response and residual-disease monitoring in initial and relapsedTEL-AML1 positive childhood ALL
Authors: Seeger, K Viehmann, S Buchwald, D Harbott, J Schrappe, M Stary, J Henze, G Trka, J
Citation: K. Seeger et al., Treatment response and residual-disease monitoring in initial and relapsedTEL-AML1 positive childhood ALL, LEUKEMIA, 15(2), 2001, pp. 280-282
Impact of CD133 (AC133) and CD90 expression analysis for acute leukemia immunophenotyping
Authors: Wuchter, C Ratei, R Spahn, G Schoch, C Harbott, J Schnittger, S Haferlach, T Creutzig, U Sperling, C Karawajew, L Ludwig, WD
Citation: C. Wuchter et al., Impact of CD133 (AC133) and CD90 expression analysis for acute leukemia immunophenotyping, HAEMATOLOG, 86(2), 2001, pp. 154-161
Detection of translocations involving the HOX11/TCL3-locus in 10q24 by interphase fluorescence in situ hybridization
Authors: Kahl, C Gesk, S Harder, L Harbott, J French, L Deloukas, P Grote, W Schlegelberger, B Siebert, R
Citation: C. Kahl et al., Detection of translocations involving the HOX11/TCL3-locus in 10q24 by interphase fluorescence in situ hybridization, CANC GENET, 129(1), 2001, pp. 80-84
Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis
Authors: Scholz, I Popp, S Granzow, M Schoell, B Holtgreve-Grez, H Takeuchi, S Schrappe, M Harbott, J Teigler-Schlegel, A Zimmermann, M Fischer, C Koeffler, HP Bartram, CR Jauch, A
Citation: I. Scholz et al., Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis, CANC GENET, 124(2), 2001, pp. 89-97
The human formin-binding protein 17 (FBP17) interacts with sorting nexin, SNX2, and is an MLL-fusion partner in acute myelogeneous leukemia
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
t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia
Authors: Tosi, S Harbott, J Teigler-Schlegel, A Haas, OA Pirc-Danoewinata, H Harrison, CJ Biondi, A Cazzaniga, G Kempski, H Scherer, SW Kearney, L
Citation: S. Tosi et al., t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia, GENE CHROM, 29(4), 2000, pp. 325-332
Detection of acute leukemia cells with mixed lineage leukemia (MLL) gene rearrangements by flow cytometry using monoclonal antibody 7.1
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
Granulocyte colony-stimulating factor receptor expression and 11q23/MLL genotype in childhood acute lymphoblastic leukemia developing during the first 18 months of life
Authors: Stanulla, M Kasper, B Schrappe, M Viehmann, S Harbott, J Ludwig, WD Welte, K
Citation: M. Stanulla et al., Granulocyte colony-stimulating factor receptor expression and 11q23/MLL genotype in childhood acute lymphoblastic leukemia developing during the first 18 months of life, LEUKEMIA, 14(2), 2000, pp. 337-338
Long-term results of four consecutive trials in childhood ALL performed bythe ALL-BFM study group from 1981 to 1995
Authors: Schrappe, M Reiter, A Zimmermann, M Harbott, J Ludwig, WD Henze, G Gadner, H Odenwald, E Riehm, H
Citation: M. Schrappe et al., Long-term results of four consecutive trials in childhood ALL performed bythe ALL-BFM study group from 1981 to 1995, LEUKEMIA, 14(12), 2000, pp. 2205-2222
Nineteen cases of the t(1;22)(p13;q13) acute megakaryoblastic leukaemia ofinfants/children and a review of 39 cases: report from a t(1;22) study group
Authors: Bernstein, J Dastugue, N Haas, OA Harbott, J Heerema, NA Huret, JL Landman-Parker, J LeBeau, MM Leonard, C Mann, G Pages, MP Perot, C Pirc-Danoewinata, H Roitzheim, B Rubin, CM Slociak, M Viguie, F
Citation: J. Bernstein et al., Nineteen cases of the t(1;22)(p13;q13) acute megakaryoblastic leukaemia ofinfants/children and a review of 39 cases: report from a t(1;22) study group, LEUKEMIA, 14(1), 2000, pp. 216-218
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
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
Constitutive expression levels of CD95 and Bcl-2 as well as CD95 function and spontaneous apoptosis in vitro do not predict the response to inductionchemotherapy and relapse rate in childhood acute lymphoblastic leukaemia
Authors: Wuchter, C Karawajew, L Ruppert, V Schrappe, M Harbott, J Ratei, R Dorken, B Ludwig, WD
Citation: C. Wuchter et al., Constitutive expression levels of CD95 and Bcl-2 as well as CD95 function and spontaneous apoptosis in vitro do not predict the response to inductionchemotherapy and relapse rate in childhood acute lymphoblastic leukaemia, BR J HAEM, 110(1), 2000, pp. 154-160
TEL/AML1 gene fusion is related to in vitro drug sensitivity for L-asparaginase in childhood acute lymphoblastic leukemia
Authors: Ramakers-van Woerden, NL Pieters, R Loonen, AH Hubeek, I van Drunen, E Beverloo, HB Slater, RM Harbott, J Seyfarth, J van Wering, ER Hahlen, K Schmiegelow, K Janka-Schaub, GE Veerman, AJP
Citation: Nl. Ramakers-van Woerden et al., TEL/AML1 gene fusion is related to in vitro drug sensitivity for L-asparaginase in childhood acute lymphoblastic leukemia, BLOOD, 96(3), 2000, pp. 1094-1099
Improved outcome in childhood acute lymphoblastic leukemia despite reduceduse of anthracyclines and cranial radiotherapy: results of trial ALL-BFM 90
Authors: Schrappe, M Reiter, A Ludwig, WD Harbott, J Zimmermann, M Hiddemann, W Niemeyer, C Henze, G Feldges, A Zintl, F Kornhuber, B Ritter, J Welte, K Gadner, H Riehm, H
Citation: M. Schrappe et al., Improved outcome in childhood acute lymphoblastic leukemia despite reduceduse of anthracyclines and cranial radiotherapy: results of trial ALL-BFM 90, BLOOD, 95(11), 2000, pp. 3310-3322
Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q)
Authors: Scheurlen, WG Schwabe, GC Seranski, P Joos, S Harbott, J Metzke, S Dohner, H Poustka, A Wilgenbus, K Haas, OA
Citation: Wg. Scheurlen et al., Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q), GENE CHROM, 25(3), 1999, pp. 230-240
Expression of the c-kit receptor (CD117) is a feature of almost all subtypes of de novo acute myeloblastic leukemia (AML), including cytogenetically good-risk AML, and lacks prognostic significance
Authors: Schwartz, S Heinecke, A Zimmermann, M Creutzig, U Schoch, C Harbott, J Fonatsch, C Loffler, H Buchner, T Ludwig, WD Thiel, E
Citation: S. Schwartz et al., Expression of the c-kit receptor (CD117) is a feature of almost all subtypes of de novo acute myeloblastic leukemia (AML), including cytogenetically good-risk AML, and lacks prognostic significance, LEUK LYMPH, 34(1-2), 1999, pp. 85-94
A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells
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
Multiplex PCR - a rapid screening method for detection of gene rearrangements in childhood acute lymphoblastic leukemia
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
Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7
Authors: Hasle, H Arico, M Basso, G Biondi, A Rajnoldi, AC Creutzig, U Fenu, S Fonatsch, C Haas, OA Harbott, J Kardos, G Kerndrup, G Mann, G Niemeyer, CM Ptoszkova, H Ritter, J Slater, R Stary, J Stollmann-Gibbels, B Testi, AM van Wering, ER Zimmermann, M
Citation: H. Hasle et al., Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7, LEUKEMIA, 13(3), 1999, pp. 376-385
A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q)in childhood acute myeloid leukemia
Authors: Jaju, RJ Haas, OA Neat, M Harbott, J Saha, V Boultwood, J Brown, JM Pirc-Danoewinata, H Krings, BW Muller, U Morris, SW Wainscoat, JS Kearney, L
Citation: Rj. Jaju et al., A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q)in childhood acute myeloid leukemia, BLOOD, 94(2), 1999, pp. 773-780
Risultati: 1-22 |