Mutation analysis of ASXL1, CBL, DNMT3A, IDH1, IDH2, JAK2, MPL, NF1, SF3B1, SUZ12, and TET2 in myeloproliferative neoplasms. (Q54518446)

30 May 2018

title

Mutation analysis of ASXL1, CBL, DNMT3A, IDH1, IDH2, JAK2, MPL, NF1, SF3B1, SUZ12, and TET2 in myeloproliferative neoplasms. (English)

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12

Borhane Slama

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author name string

Mandy Brecqueville

1

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Jérôme Rey

2

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François Bertucci

3

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Emilie Coppin

4

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Pascal Finetti

5

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Nadine Carbuccia

6

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Nathalie Cervera

7

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Véronique Gelsi-Boyer

8

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Christine Arnoulet

9

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Olivier Gisserot

10

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Denis Verrot

11

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Norbert Vey

13

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Marie-Joelle Mozziconacci

14

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Daniel Birnbaum

15

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Anne Murati

16

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publication date

9 April 2012

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Genes, Chromosomes and Cancer

published in

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volume

51

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issue

8

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page(s)

743-755

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Genetic analysis of transforming events that convert chronic myeloproliferative neoplasms to leukemias

cites work

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DNMT3A mutational analysis in primary myelofibrosis, chronic myelomonocytic leukemia and advanced phases of myeloproliferative neoplasms

21 January 2018

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Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms

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Rare mutations in DNMT3A in myeloproliferative neoplasms and myelodysplastic syndromes.

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Mutations and deletions of the SUZ12 polycomb gene in myeloproliferative neoplasms

21 January 2018

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Mutations of ASXL1 gene in myeloproliferative neoplasms.

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Mutual exclusion of ASXL1 and NPM1 mutations in a series of acute myeloid leukemias.

21 January 2018

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Additional sex comb-like 1 (ASXL1), in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor

21 January 2018

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Mutation in TET2 in myeloid cancers

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Molecular aspects of myeloproliferative neoplasms.

21 January 2018

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Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

21 January 2018

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Characterization of Asxl1, a murine homolog of Additional sex combs, and analysis of the Asx-like gene family

21 January 2018

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DIPSS plus: a refined Dynamic International Prognostic Scoring System for primary myelofibrosis that incorporates prognostic information from karyotype, platelet count, and transfusion status

21 January 2018

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Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms

21 January 2018

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DNMT3A Mutations in Acute Myeloid Leukemia

21 January 2018

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Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignancies.

21 January 2018

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TET2, ASXL1, IDH1, IDH2, and c-CBL genes in JAK2- and MPL-negative myeloproliferative neoplasms

21 January 2018

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ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN Favorable genetic category

21 January 2018

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Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes

21 January 2018

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Myeloid blastic transformation of myeloproliferative neoplasms—A review of 112 cases

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Novel mutations in the inhibitory adaptor protein LNK drive JAK-STAT signaling in patients with myeloproliferative neoplasms.

21 January 2018

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Janus kinase 2 mutations in Philadelphia negative chronic myeloproliferative disorders: clinical implications

21 January 2018

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Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts

21 January 2018

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IDH1 and IDH2 mutation analysis in chronic- and blast-phase myeloproliferative neoplasms.

21 January 2018

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LNK mutation studies in blast-phase myeloproliferative neoplasms, and in chronic-phase disease with TET2, IDH, JAK2 or MPL mutations

21 January 2018

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MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia

21 January 2018

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ASXL1 mutations in primary and secondary myelofibrosis

21 January 2018

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Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias

21 January 2018

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Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB

21 January 2018

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Inactivation of polycomb repressive complex 2 components in myeloproliferative and myelodysplastic/myeloproliferative neoplasms

21 January 2018

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JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis

21 January 2018

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Sex differences in the JAK2 V617F allele burden in chronic myeloproliferative disorders.

21 January 2018

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Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes

21 January 2018

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Spectrum of mutations in RARS-T patients includes TET2 and ASXL1 mutations

21 January 2018

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Novel mutations and their functional and clinical relevance in myeloproliferative neoplasms: JAK2, MPL, TET2, ASXL1, CBL, IDH and IKZF1

21 January 2018

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Primary myelofibrosis: 2012 update on diagnosis, risk stratification, and management

21 January 2018

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TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis

21 January 2018

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IDH1 and IDH2 mutation studies in 1473 patients with chronic-, fibrotic- or blast-phase essential thrombocythemia, polycythemia vera or myelofibrosis.

21 January 2018

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The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes

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Frequent pathway mutations of splicing machinery in myelodysplasia

21 January 2018

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Myelodysplastic syndromes: lost between two states?

21 January 2018

1 reference

7 January 2021

Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia

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7 January 2021

Distinct clinical and biological features of de novo acute myeloid leukemia with additional sex comb-like 1 (ASXL1) mutations

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7 January 2021

ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia

1 reference

7 January 2021

Deletion of the tumor-suppressor gene NF1 occurs in 5% of myeloid malignancies and is accompanied by a mutation in the remaining allele in half of the cases

1 reference

7 January 2021

SF3B1 mutations in primary myelofibrosis: clinical, histopathology and genetic correlates among 155 patients

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7 January 2021

DNMT3A mutations in myeloproliferative neoplasms

1 reference

7 January 2021

Mutation in TET2 in myeloid cancers

1 reference

7 January 2021

SF3B1, a splicing factor is frequently mutated in refractory anemia with ring sideroblasts

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.21960

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30 May 2018

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30 May 2018