(Q33647411)

English

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

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

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

1 reference

Europe PubMed Central

28 July 2017

Véronique Gelsi-Boyer

11

object named as

Véronique Gelsi-Boyer

0 references

Marie-Joëlle Mozziconacci

12

object named as

Marie-Joelle Mozziconacci

0 references

Sylviane Olschwang

8

object named as

Sylviane Olschwang

1 reference

Europe PubMed Central

28 July 2017

author name string

Julien Rocquain

1

1 reference

Europe PubMed Central

28 July 2017

Nadine Carbuccia

2

1 reference

Europe PubMed Central

28 July 2017

Virginie Trouplin

3

1 reference

Europe PubMed Central

28 July 2017

Stéphane Raynaud

4

1 reference

Europe PubMed Central

28 July 2017

Anne Murati

5

1 reference

Europe PubMed Central

28 July 2017

Meyer Nezri

6

1 reference

Europe PubMed Central

28 July 2017

Zoulika Tadrist

7

1 reference

Europe PubMed Central

28 July 2017

Norbert Vey

9

1 reference

Europe PubMed Central

28 July 2017

Daniel Birnbaum

10

1 reference

Europe PubMed Central

28 July 2017

Marie-Joelle Mozziconacci

12

1 reference

Europe PubMed Central

28 July 2017

language of work or name

0 references

publication date

2 August 2010

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

10

1 reference

Europe PubMed Central

28 July 2017

401

1 reference

Europe PubMed Central

28 July 2017

https://scigraph.springernature.com/pub.10.1186/1471-2407-10-401

0 references

Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

The common feature of leukemia-associated IDH1 and IDH2 mutations is a neomorphic enzyme activity converting alpha-ketoglutarate to 2-hydroxyglutarate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Cancer-associated IDH1 mutations produce 2-hydroxyglutarate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Loss-of-function Additional sex combs like 1 mutations disrupt hematopoiesis but do not cause severe myelodysplasia or leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Recurring mutations found by sequencing an acute myeloid leukemia genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Wilms tumor 1 gene mutations are associated with a higher risk of recurrence in young adults with acute myeloid leukemia: a study from the Acute Leukemia French Association

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Altered nucleophosmin transport in acute myeloid leukaemia with mutated NPM1: molecular basis and clinical implications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Acquired mutations in TET2 are common in myelodysplastic syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Mutation in TET2 in myeloid cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Genetic characterization of TET1, TET2, and TET3 alterations in myeloid malignancies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Detection of mutant TET2 in myeloid malignancies other than myeloproliferative neoplasms: CMML, MDS, MDS/MPN and AML.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1 genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Prognostic implications of gene mutations in acute myeloid leukemia with normal cytogenetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Mutation of the Wilms' tumor 1 gene is a poor prognostic factor associated with chemotherapy resistance in normal karyotype acute myeloid leukemia: the United Kingdom Medical Research Council Adult Leukaemia Working Party

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Nucleophosmin and cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Oxygen‐regulated expression of the Wilms’ tumor suppressorWt1involves hypoxia‐inducible factor‐1 (HIF‐1)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Molecular genetics of human leukemias: new insights into therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

FLT3 signaling in hematopoietic cells involves CBL, SHC and an unknown P115 as prominent tyrosine-phosphorylated substrates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2923633

14 July 2018

Myelodysplastic Syndromes

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-10-401

21 January 2018

Novel TET2 mutations associated with UPD4q24 in myelodysplastic syndrome.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-10-401

21 January 2018

Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-10-401

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-10-401

21 January 2018

Taxing sugar-sweetened beverages

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-10-401

21 January 2018

250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-10-401

21 January 2018

Cancer. Puzzling patterns of predisposition

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-10-401

21 January 2018

AML1/RUNX1 point mutation possibly promotes leukemic transformation in myeloproliferative neoplasms.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-10-401

21 January 2018

Analyses of TET2 mutations in post-myeloproliferative neoplasm acute myeloid leukemias

1 reference

https://pubmed.ncbi.nlm.nih.gov/20678218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myelodysplastic syndromes: lost between two states?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20678218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mutations of IDH1 and IDH2 in the leukemic transformation of myeloproliferative neoplasms

1 reference

https://pubmed.ncbi.nlm.nih.gov/20678218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20678218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome profiling of acute myelomonocytic leukemia: alteration of the MYB locus in MYST3-linked cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/20678218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alterations of NFIA in chronic malignant myeloid diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/20678218

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2407-10-401

1 reference

Europe PubMed Central

28 July 2017

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0 references

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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0 references

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