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SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia

Oncogene, 2015-01, Vol.34 (5), p.631-638

2015

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Quantitative HOX expression in chromosomally defined subsets of acute myelogenous leukemia

Leukemia, 2002-02, Vol.16 (2), p.186-195

2002

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ETV6 (TEL) gene amplification in a myelodysplastic syndrome with excess of blasts

Leukemia, 2004-08, Vol.18 (8), p.1436-1438

2004

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Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders : rearrangements of DNA satellite II and new recurrent translocations

Leukemia, 1999-12, Vol.13 (12), p.1975-1981

1999

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Persistence of Transcriptionally Silent BCR-ABL Rearrangements in Chronic Myeloid Leukemia Patients in Sustained Complete Cytogenetic Remission

Leukemia & lymphoma, 2001, Vol.42 (5), p.933-944

2001

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Detection of monosomy 7 and trisomies 8 and 11 in myelodysplastic disorders by interphase fluorescent in situ hybridization. Comparison with acute non-lymphocytic leukemias

Leukemia, 1994-06, Vol.8 (6), p.1005-1011

1994

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Abnormalities of the short arm of chromosome 12 in T cell prolymphocytic leukemia

Leukemia, 1998-06, Vol.12 (6), p.972-975

1998

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Bile Salt Anion Sorption by Polymeric Resins: Comparison of a Functionalized Polyacrylamide Resin with Cholestyramine

Journal of colloid and interface science, 2000-12, Vol.232 (2), p.282-288

2000

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Does BCR-ABL genomic rearrangement persist in CML patients in complete remission after interferon α therapy?

Leukemia, 1998-07, Vol.12 (7), p.1076-1080

1998

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CO-43 – Anomalies cytogénétiques additionnelles et variants au diagnostic dans la leucemie myeloïde chronique de l'enfant: description et impact pronostique

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2015-05, Vol.22 (5), p.221-221

2015

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Interstitial telomere repeats in translocations of hematopoietic disorders

Leukemia, 2000-09, Vol.14 (9), p.1630-1633

2000

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Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T‐prolymphocytic leukaemia: four new cases and a review of the literature

British journal of haematology, 1994-04, Vol.86 (4), p.780-785

1994

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Persistence of BCR-ABL genomic rearrangement in chronic myeloid leukemia patients in complete and sustained cytogenetic remission after interferon-α therapy or allogeneic bone marrow transplantation

Blood, 2000-01, Vol.95 (2), p.404-409

2000

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Indolent course as a relatively frequent presentation in T‐prolymphocytic leukaemia

British journal of haematology, 1998-11, Vol.103 (2), p.488-494

1998

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p190(BCR-ABL) rearrangement as a secondary change in a case of acute myelo-monocytic leukemia with inv(16)(p13q22)

Leukemia research, 2004-01, Vol.28 (1), p.97-99

2004

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A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia

Genes chromosomes & cancer, 2001-07, Vol.31 (3), p.248-254

2001

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Human LPP gene is fused to MLL in a secondary acute leukemia with a t(3;11) (q28;q23)

Genes chromosomes & cancer, 2001-08, Vol.31 (4), p.382-389

2001

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Ovarian sarcoma and acute myelogenous leukaemia

The hematology journal : the official journal of the European Haematology Association, 2001, Vol.2 (6), p.404

2001

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Binding of Bile Acids by Polymerized Cyclodextrin Resins

Journal of macromolecular science. Part A, Pure and applied chemistry, 1997-02, Vol.34 (2), p.335-347

1997

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Therapy-related acute lymphoblastic leukemia with MLL rearrangement following treatment of Burkitt's leukemia

Leukemia & lymphoma, 2005-06, Vol.46 (6), p.925-927

2005

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Comparison of M-FISH and conventional cytogenetic analysis in accelerated and acute phases of CML

Leukemia research, 2004-04, Vol.28 (4), p.345-348

2004

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Proliferative Response of B Chronic Lymphocytic Leukemia Lymphocytes Stimulated with IL2 and Soluble CD23

Leukemia & lymphoma, 1994, Vol.14 (3-4), p.311-318

1994

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p190 super(BCR-ABL) rearrangement as a secondary change in a case of acute myelo-monocytic leukemia with inv(16)(p13q22)

Leukemia research, 2004-01, Vol.28 (1), p.97-99

2004

Volltextzugriff (PDF)

Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome–acute myeloid leukemia actually differ?

Cancer genetics and cytogenetics, 2007-07, Vol.176 (1), p.1-21

2007

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Aml1/ETO and Pml/RARA Rearrangements in a Case of AML-M2 Acute Myeloblastic Leukemia with t(15;17)

Leukemia & lymphoma, 1999, Vol.33 (3-4), p.403-406

1999

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SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia

Quantitative HOX expression in chromosomally defined subsets of acute myelogenous leukemia

ETV6 (TEL) gene amplification in a myelodysplastic syndrome with excess of blasts

Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders : rearrangements of DNA satellite II and new recurrent translocations

Persistence of Transcriptionally Silent BCR-ABL Rearrangements in Chronic Myeloid Leukemia Patients in Sustained Complete Cytogenetic Remission

Detection of monosomy 7 and trisomies 8 and 11 in myelodysplastic disorders by interphase fluorescent in situ hybridization. Comparison with acute non-lymphocytic leukemias

Abnormalities of the short arm of chromosome 12 in T cell prolymphocytic leukemia

Bile Salt Anion Sorption by Polymeric Resins: Comparison of a Functionalized Polyacrylamide Resin with Cholestyramine

Does BCR-ABL genomic rearrangement persist in CML patients in complete remission after interferon α therapy?

CO-43 – Anomalies cytogénétiques additionnelles et variants au diagnostic dans la leucemie myeloïde chronique de l'enfant: description et impact pronostique

Interstitial telomere repeats in translocations of hematopoietic disorders

Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T‐prolymphocytic leukaemia: four new cases and a review of the literature

Persistence of BCR-ABL genomic rearrangement in chronic myeloid leukemia patients in complete and sustained cytogenetic remission after interferon-α therapy or allogeneic bone marrow transplantation

Indolent course as a relatively frequent presentation in T‐prolymphocytic leukaemia

p190(BCR-ABL) rearrangement as a secondary change in a case of acute myelo-monocytic leukemia with inv(16)(p13q22)

A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia

Human LPP gene is fused to MLL in a secondary acute leukemia with a t(3;11) (q28;q23)

Ovarian sarcoma and acute myelogenous leukaemia

Binding of Bile Acids by Polymerized Cyclodextrin Resins

Therapy-related acute lymphoblastic leukemia with MLL rearrangement following treatment of Burkitt's leukemia

Comparison of M-FISH and conventional cytogenetic analysis in accelerated and acute phases of CML

Proliferative Response of B Chronic Lymphocytic Leukemia Lymphocytes Stimulated with IL2 and Soluble CD23

p190 super(BCR-ABL) rearrangement as a secondary change in a case of acute myelo-monocytic leukemia with inv(16)(p13q22)

Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome–acute myeloid leukemia actually differ?

Aml1/ETO and Pml/RARA Rearrangements in a Case of AML-M2 Acute Myeloblastic Leukemia with t(15;17)

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