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The DNA double-strand break response is abnormal in myeloblasts from patients with therapy-related acute myeloid leukemia

Leukemia, 2014-06, Vol.28 (6), p.1242-1251

2014

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High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

Leukemia, 2006-05, Vol.20 (5), p.840-846

2006

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Genetic heterogeneity of BCR/ABL+ adult B-cell precursor acute lymphoblastic leukemia : impact on the clinical, biological and immunophenotypical disease characteristics

Leukemia, 2005-05, Vol.19 (5), p.713-720

2005

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Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T γ/δ lymphoma

Leukemia, 1996-09, Vol.10 (9), p.1453-1455

1996

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Clonal evolution to acute myeloblastic leukemia with MLL gene rearrangement from trisomy 8 clone

Leukemia, 1997-08, Vol.11 (8), p.1380-1382

1997

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Clinical and molecular characterization of patients with acute myeloid leukemia and sole trisomies of chromosomes 4, 8, 11, 13 or 21

Leukemia, 2020-02, Vol.34 (2), p.358-368

2020

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Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells

Leukemia, 2010-04, Vol.24 (4), p.756-764

2010

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Impact of trisomy 8 on treatment response and survival of patients with chronic myelogenous leukemia in the era of tyrosine kinase inhibitors

Leukemia, 2015-11, Vol.29 (11), p.2263-2266

2015

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Clonal relationship between langerhans cell histiocytosis and myeloid sarcoma

Leukemia, 2012-07, Vol.26 (7), p.1707-1710

2012

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Leukemia-related chromosomal loss detected in hematopoietic progenitor cells of benzene-exposed workers

Leukemia, 2012-12, Vol.26 (12), p.2494-2498

2012

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Cytogenetic profile of de novo acute myeloid leukemia: a study based on 1432 patients in a single institution of China

Leukemia, 2009-10, Vol.23 (10), p.1801-1806

2009

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IDH mutations and trisomy 8 in myelodysplastic syndromes and acute myeloid leukemia

Leukemia, 2010-12, Vol.24 (12), p.2120-2122

2010

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Genomic gains and losses influence expression levels of genes located within the affected regions: a study on acute myeloid leukemias with trisomy 8, 11, or 13, monosomy 7, or deletion 5q

Leukemia, 2005-07, Vol.19 (7), p.1224-1228

2005

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Gene expression analysis reveals HOX gene upregulation in trisomy 8 AML

Leukemia, 2010-06, Vol.24 (6), p.1239-1243

2010

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Demonstration of Philadelphia chromosome negative abnormal clones in patients with chronic myelogenous leukemia during major cytogenetic responses induced by imatinib mesylate

Leukemia, 2003-03, Vol.17 (3), p.481-487

2003

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Characteristics of t(8;21) acute myeloid leukemia (AML) with additional chromosomal abnormality: concomitant trisomy 4 may constitute a distinctive subtype of t(8;21) AML

Leukemia, 2003-04, Vol.17 (4), p.731-737

2003

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Clonal Ph-negative hematopoiesis in CML after therapy with imatinib mesylate is frequently characterized by trisomy 8

Leukemia, 2002-07, Vol.16 (7), p.1390-1393

2002

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Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype

Leukemia, 2002-09, Vol.16 (9), p.1745-1751

2002

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JAK2V617F as progression marker in CMPD and as cooperative mutation in AML with trisomy 8 and t(8;21): a comparative study on 1103 CMPD and 269 AML cases

Leukemia, 2007-08, Vol.21 (8), p.1843-1845

2007

Volltextzugriff (PDF)

Monocytes are activated in patients with myelodysplastic syndromes and can contribute to bone marrow failure through CD40-CD40L interactions with T helper cells

Leukemia, 2007-12, Vol.21 (12), p.2411-2419

2007

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The genetics of familial leukemia

Leukemia, 1997-08, Vol.11 (8), p.1347-1359

HORWITZ, M

1997

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Clonal evolution in Philadelphia chromosome negative cells following successful treatment with Imatinib of a CML patient: clinical and biological features of a myelodysplastic syndrome

Leukemia, 2004-02, Vol.18 (2), p.361-362

2004

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Novel genomic imbalances and chromosome translocations involving c-myc gene in Burkitt's lymphoma

Leukemia, 2001-10, Vol.15 (10), p.1582-1588

2001

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The DNA double-strand break response is abnormal in myeloblasts from patients with therapy-related acute myeloid leukemia

High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

Genetic heterogeneity of BCR/ABL+ adult B-cell precursor acute lymphoblastic leukemia : impact on the clinical, biological and immunophenotypical disease characteristics

Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T γ/δ lymphoma

Clonal evolution to acute myeloblastic leukemia with MLL gene rearrangement from trisomy 8 clone

Clinical and molecular characterization of patients with acute myeloid leukemia and sole trisomies of chromosomes 4, 8, 11, 13 or 21

Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells

Impact of trisomy 8 on treatment response and survival of patients with chronic myelogenous leukemia in the era of tyrosine kinase inhibitors

Prognostic gene mutations and distinct gene- and microRNA-expression signatures in acute myeloid leukemia with a sole trisomy 8

Clonal relationship between langerhans cell histiocytosis and myeloid sarcoma

Leukemia-related chromosomal loss detected in hematopoietic progenitor cells of benzene-exposed workers

Cytogenetic profile of de novo acute myeloid leukemia: a study based on 1432 patients in a single institution of China

IDH mutations and trisomy 8 in myelodysplastic syndromes and acute myeloid leukemia

Report of 34 patients with clonal chromosomal abnormalities in Philadelphia-negative cells during imatinib treatment of Philadelphia-positive chronic myeloid leukemia

Genomic gains and losses influence expression levels of genes located within the affected regions: a study on acute myeloid leukemias with trisomy 8, 11, or 13, monosomy 7, or deletion 5q

Gene expression analysis reveals HOX gene upregulation in trisomy 8 AML

Demonstration of Philadelphia chromosome negative abnormal clones in patients with chronic myelogenous leukemia during major cytogenetic responses induced by imatinib mesylate

Characteristics of t(8;21) acute myeloid leukemia (AML) with additional chromosomal abnormality: concomitant trisomy 4 may constitute a distinctive subtype of t(8;21) AML

Clonal Ph-negative hematopoiesis in CML after therapy with imatinib mesylate is frequently characterized by trisomy 8

Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype

JAK2V617F as progression marker in CMPD and as cooperative mutation in AML with trisomy 8 and t(8;21): a comparative study on 1103 CMPD and 269 AML cases

Monocytes are activated in patients with myelodysplastic syndromes and can contribute to bone marrow failure through CD40-CD40L interactions with T helper cells

The genetics of familial leukemia

Clonal evolution in Philadelphia chromosome negative cells following successful treatment with Imatinib of a CML patient: clinical and biological features of a myelodysplastic syndrome

Novel genomic imbalances and chromosome translocations involving c-myc gene in Burkitt's lymphoma

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