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Cooperating gene mutations in acute myeloid leukemia: a review of the literature

Leukemia, 2008-05, Vol.22 (5), p.915-931

2008

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Prognostic significance of DNA methyltransferase 3A mutations in cytogenetically normal acute myeloid leukemia: a study by the Acute Leukemia French Association

Leukemia, 2012-06, Vol.26 (6), p.1247-1254

2012

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Impact of Wilms' tumor 1 expression on outcome of patients undergoing allogeneic stem cell transplantation for AML

Bone marrow transplantation (Basingstoke), 2017-04, Vol.52 (4), p.539-543

2017

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Mutation analysis of TET2, IDH1, IDH2 and ASXL1 in chronic myeloid leukemia

Leukemia, 2011-10, Vol.25 (10), p.1661-1664

2011

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Molecular prognostic factors in acute myeloid leukemia receiving first-line therapy with azacitidine

Leukemia, 2016-06, Vol.30 (6), p.1416-1418

2016

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142 MOLECULAR PROGNOSTIC FACTORS IN HIGHER RISK MDS RECEIVING FIRST LINE AZACYTIDINE (AZA)

Leukemia research, 2015-04, Vol.39, p.S72-S72

2015

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Waved aCGH: to smooth or not to smooth

Nucleic acids research, 2010-04, Vol.38 (7), p.e94-e94

2010

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Wilms' tumor 1 single-nucleotide polymorphism rs16754 does not predict clinical outcome in adult acute myeloid leukemia

Leukemia, 2011-12, Vol.25 (12), p.1918-1921

2011

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P-082 Midostaurin efficacy in a case of CMML with t(9;12)(q22;p12)/TEL-SYK fusion and constitutive activation of the SYK kinase

Leukemia research, 2013-05, Vol.37, p.S58-S59

2013

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Recurrent in-frame insertion in C EBPα TAD2 region is a polymorphism without prognostic value in AML

Leukemia, 2008-03, Vol.22 (3), p.655-657

2008

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Microparticle phenotypes are associated with driver mutations and distinct thrombotic risks in essential thrombocythemia

Haematologica (Roma), 2016-09, Vol.101 (9), p.e365-e368

2016

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260 Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes RUNX1/AML1 lesions

Leukemia research, 2011, Vol.35, p.S102-S102

2011

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Standardization of molecular monitoring of CML: results and recommendations from the European treatment and outcome study

Leukemia, 2022-07, Vol.36 (7), p.1834-1842

2022

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Acute myeloid leukemia with translocation t(3;5): new molecular insights

Haematologica (Roma), 2013-04, Vol.98 (4), p.e52-e54

2013

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Impact of additional genetic alterations on the outcome of patients with NPM1-mutated cytogenetically normal acute myeloid leukemia

Haematologica (Roma), 2015-05, Vol.100 (5), p.e196-e199

2015

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Thalassémie β°/β° avec phénotype « intermédiaire » : un diagnostic rare... auquel il faut penser

Annales de biologie clinique (Paris), 2006, Vol.64 (4), p.341-345

2006

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Un syndrome hyperéosinophilique avec mutation JAK2

Annales de dermatologie et de vénéréologie, 2013-12, Vol.140 (12), p.S606-S606

2013

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CEBPA Methylation and Notch1 Mutations Are Common in Immature T-ALLs but Not M0 AML and Cosegregate with TCRG Rearrangement and the TCRgd Lineage

Blood, 2007-11, Vol.110 (11), p.2788-2788

2007

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Recurrent in-frame insertion in C/EBP[alpha] TAD2 region is a polymorphism without prognostic value in AML

Leukemia, 2008-03, Vol.22 (3), p.655

2008

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Isolated tetrasomy 8 in AML, MDS and MPD

Atlas of genetics and cytogenetics in oncology and haematology, 2011-11 (9)

2011

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Beta(o)/beta(o) thalassemia with a mild phenotype

Annales de biologie clinique (Paris), 2006-07, Vol.64 (4), p.341-345

2006

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Recurrent in-frame insertion in C/EBPalpha TAD2 region is a polymorphism without prognostic value in AML

Leukemia, 2008-03, Vol.22 (3), p.655

2008

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C/EBPα regulated microRNA-34a targets E2F3 during granulopoiesis and is down-regulated in AML with CEBPA mutations

Blood, 2010-12, Vol.116 (25), p.5638-5649

2010

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Cooperating gene mutations in acute myeloid leukemia: a review of the literature

Prognostic significance of DNA methyltransferase 3A mutations in cytogenetically normal acute myeloid leukemia: a study by the Acute Leukemia French Association

Impact of Wilms' tumor 1 expression on outcome of patients undergoing allogeneic stem cell transplantation for AML

Mutation analysis of TET2, IDH1, IDH2 and ASXL1 in chronic myeloid leukemia

Molecular prognostic factors in acute myeloid leukemia receiving first-line therapy with azacitidine

142 MOLECULAR PROGNOSTIC FACTORS IN HIGHER RISK MDS RECEIVING FIRST LINE AZACYTIDINE (AZA)

Waved aCGH: to smooth or not to smooth

Wilms' tumor 1 single-nucleotide polymorphism rs16754 does not predict clinical outcome in adult acute myeloid leukemia

P-082 Midostaurin efficacy in a case of CMML with t(9;12)(q22;p12)/TEL-SYK fusion and constitutive activation of the SYK kinase

Recurrent in-frame insertion in C EBPα TAD2 region is a polymorphism without prognostic value in AML

Microparticle phenotypes are associated with driver mutations and distinct thrombotic risks in essential thrombocythemia

260 Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes RUNX1/AML1 lesions

Standardization of molecular monitoring of CML: results and recommendations from the European treatment and outcome study

Acute myeloid leukemia with translocation t(3;5): new molecular insights

Impact of additional genetic alterations on the outcome of patients with NPM1-mutated cytogenetically normal acute myeloid leukemia

Thalassémie β°/β° avec phénotype « intermédiaire » : un diagnostic rare... auquel il faut penser

Un syndrome hyperéosinophilique avec mutation JAK2

CEBPA Methylation and Notch1 Mutations Are Common in Immature T-ALLs but Not M0 AML and Cosegregate with TCRG Rearrangement and the TCRgd Lineage

Recurrent in-frame insertion in C/EBP[alpha] TAD2 region is a polymorphism without prognostic value in AML

Isolated tetrasomy 8 in AML, MDS and MPD

Beta(o)/beta(o) thalassemia with a mild phenotype

Recurrent in-frame insertion in C/EBPalpha TAD2 region is a polymorphism without prognostic value in AML

C/EBPα regulated microRNA-34a targets E2F3 during granulopoiesis and is down-regulated in AML with CEBPA mutations

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