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SP 126 FLT3 is a stratification factor for targeted therapy treatments in adult and pediatric AML phase III trials

European journal of cancer (1990), 2011, Vol.47, p.S4-S4

Meshinchi, S

2011

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NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern

Leukemia, 2013-12, Vol.27 (12), p.2280-2288

2013

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A recurrent immunophenotype at diagnosis independently identifies high-risk pediatric acute myeloid leukemia: a report from Children's Oncology Group

Leukemia, 2016-10, Vol.30 (10), p.2077-2080

2016

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Molecular alterations of the IDH1 gene in AML: a Children's Oncology Group and Southwest Oncology Group study

Leukemia, 2010-05, Vol.24 (5), p.909-913

2010

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Mutations in KIT and RAS are frequent events in pediatric core-binding factor acute myeloid leukemia

Leukemia, 2005-09, Vol.19 (9), p.1536-1542

2005

Volltextzugriff (PDF)

Aberrantly low STAT3 and STAT5 responses are associated with poor outcome and an inflammatory gene expression signature in pediatric acute myeloid leukemia

Clinical & translational oncology, 2021-10, Vol.23 (10), p.2141-2154

2021

Volltextzugriff (PDF)

Ethnic variation of TET2 SNP rs2454206 and association with clinical outcome in childhood AML: a report from the Children's Oncology Group

Leukemia, 2015-12, Vol.29 (12), p.2424-2426

2015

Volltextzugriff (PDF)

Prevalence and clinical implications of NRAS mutations in childhood AML: a report from the Children's Oncology Group

Leukemia, 2011-06, Vol.25 (6), p.1039-1042

2011

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Heterogeneity of clonal expansion and maturation-linked mutation acquisition in hematopoietic progenitors in human acute myeloid leukemia

Leukemia, 2014-10, Vol.28 (10), p.1969-1977

2014

Volltextzugriff (PDF)

Copy-neutral loss of heterozygosity is prevalent and a late event in the pathogenesis of FLT3/ITD AML

Blood cancer journal (New York), 2014-05, Vol.4 (5), p.e208-e208

2014

Volltextzugriff (PDF)

P521: TREATMENT OF BLASTIC PLASMACYTOID DENDRITIC CELL NEOPLASM IN PEDIATRIC PATIENTS WITH TAGRAXOFUSP, A CD123‐TARGETED THERAPY

HemaSphere, 2022-06, Vol.6, p.420-421

2022

Volltextzugriff (PDF)

A retrospective study of 69 patients with t(6;9)(p23;q34) AML emphasizes the need for a prospective, multicenter initiative for rare 'poor prognosis' myeloid malignancies

Leukemia, 2006-07, Vol.20 (7), p.1295-1297

2006

Volltextzugriff (PDF)

PTPN11 mutations in pediatric patients with acute myeloid leukemia: results from the Children's Cancer Group

Leukemia, 2004-11, Vol.18 (11), p.1831-1834

2004

Volltextzugriff (PDF)

The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms

Leukemia, 2022-07, Vol.36 (7), p.1703-1719

2022

Volltextzugriff (PDF)

DNA repair polymorphisms and outcome of chemotherapy for acute myelogenous leukemia: a report from the Children's Oncology Group

Leukemia, 2008-02, Vol.22 (2), p.265-272

2008

Volltextzugriff (PDF)

1144 POSTER Using Single-cell Network Profiling (SCNP) Signatures to Predict Response to Induction Therapy and Relapse Risk in Pediatric Patients With Acute Myeloid Leukemia (AML)

European journal of cancer (1990), 2011, Vol.47, p.S137-S137

2011

Volltextzugriff (PDF)

Description of a novel subtype of acute myeloid leukemia defined by recurrent CBFB insertions

Blood, 2023-02, Vol.141 (7), p.800-805

2023

Volltextzugriff (PDF)

Clinical implications of FLT3 mutations in pediatric AML

Blood, 2006-12, Vol.108 (12), p.3654-3661

2006

Volltextzugriff (PDF)

Size of FLT3 internal tandem duplication has prognostic significance in patients with acute myeloid leukemia

Blood, 2006-05, Vol.107 (9), p.3724-3726

2006

Volltextzugriff (PDF)

Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis

Blood, 2004-03, Vol.103 (6), p.2325-2331

2004

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Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia

Blood, 2001-01, Vol.97 (1), p.89-94

2001

Volltextzugriff (PDF)

Structural and functional reconstitution of the glucocorticoid receptor-hsp90 complex

The Journal of biological chemistry, 1990-12, Vol.265 (35), p.21397-21400

1990

Volltextzugriff (PDF)

FLT3, RAS, and TP53 mutations in elderly patients with acute myeloid leukemia

Blood, 2001-06, Vol.97 (11), p.3589-3595

2001

Volltextzugriff (PDF)

Relationship of the 90-kDa murine heat shock protein to the untransformed and transformed states of the L cell glucocorticoid receptor

The Journal of biological chemistry, 1987-05, Vol.262 (15), p.6986-6991

1987

Volltextzugriff (PDF)

Ethnicity and survival in childhood acute myeloid leukemia: a report from the Children's Oncology Group

Blood, 2006-07, Vol.108 (1), p.74-80

2006

Volltextzugriff (PDF)

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SP 126 FLT3 is a stratification factor for targeted therapy treatments in adult and pediatric AML phase III trials

NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern

A recurrent immunophenotype at diagnosis independently identifies high-risk pediatric acute myeloid leukemia: a report from Children's Oncology Group

Molecular alterations of the IDH1 gene in AML: a Children's Oncology Group and Southwest Oncology Group study

Mutations in KIT and RAS are frequent events in pediatric core-binding factor acute myeloid leukemia

Aberrantly low STAT3 and STAT5 responses are associated with poor outcome and an inflammatory gene expression signature in pediatric acute myeloid leukemia

Ethnic variation of TET2 SNP rs2454206 and association with clinical outcome in childhood AML: a report from the Children's Oncology Group

Prevalence and clinical implications of NRAS mutations in childhood AML: a report from the Children's Oncology Group

Heterogeneity of clonal expansion and maturation-linked mutation acquisition in hematopoietic progenitors in human acute myeloid leukemia

Copy-neutral loss of heterozygosity is prevalent and a late event in the pathogenesis of FLT3/ITD AML

P521: TREATMENT OF BLASTIC PLASMACYTOID DENDRITIC CELL NEOPLASM IN PEDIATRIC PATIENTS WITH TAGRAXOFUSP, A CD123‐TARGETED THERAPY

A retrospective study of 69 patients with t(6;9)(p23;q34) AML emphasizes the need for a prospective, multicenter initiative for rare 'poor prognosis' myeloid malignancies

PTPN11 mutations in pediatric patients with acute myeloid leukemia: results from the Children's Cancer Group

The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms

DNA repair polymorphisms and outcome of chemotherapy for acute myelogenous leukemia: a report from the Children's Oncology Group

1144 POSTER Using Single-cell Network Profiling (SCNP) Signatures to Predict Response to Induction Therapy and Relapse Risk in Pediatric Patients With Acute Myeloid Leukemia (AML)

Description of a novel subtype of acute myeloid leukemia defined by recurrent CBFB insertions

Clinical implications of FLT3 mutations in pediatric AML

Size of FLT3 internal tandem duplication has prognostic significance in patients with acute myeloid leukemia

Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis

Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia

Structural and functional reconstitution of the glucocorticoid receptor-hsp90 complex

FLT3, RAS, and TP53 mutations in elderly patients with acute myeloid leukemia

Relationship of the 90-kDa murine heat shock protein to the untransformed and transformed states of the L cell glucocorticoid receptor

Ethnicity and survival in childhood acute myeloid leukemia: a report from the Children's Oncology Group

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