Molecular basis of myelodysplastic/myeloproliferative neoplasms. - Wikidata - wikimedia - TriplyDB

Molecular basis of myelodysplastic/myeloproliferative neoplasms.

Molecular basis of myelodysplastic/myeloproliferative neoplasms.

http://www.wikidata.org/entity/Q42956279

about

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia Cytogenetic risk stratification in chronic myelomonocytic leukemia.Molecular similarity between myelodysplastic form of chronic myelomonocytic leukemia and refractory anemia with ring sideroblasts Clinical management of myelodysplastic syndrome/myeloproliferative neoplasm overlap syndromes.Clinical overview of cutaneous features in hypereosinophilic syndrome.Molecular pathogenesis of atypical CML, CMML and MDS/MPN-unclassifiable.Centrosomal targeting of tyrosine kinase activity does not enhance oncogenicity in chronic myeloproliferative disorders.Chelation efficacy and erythroid response during deferasirox treatment in patients with myeloproliferative neoplasms in fibrotic phase.Characteristics of the four subtypes of myelodysplastic/myeloproliferative neoplasms.TET2 gene is not deleted in chronic myelomonocytic leukemia: a FISH retrospective study.Risk assessment in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms.Specific molecular mutation patterns delineate chronic neutrophilic leukemia, atypical chronic myeloid leukemia, and chronic myelomonocytic leukemia.New prognostic markers, determined using gene expression analyses, reveal two distinct subtypes of chronic myelomonocytic leukaemia patients.Successful transplantation of ethnically mismatched cord blood in a boy with atypical chronic myeloid leukemia.De novo childhood myelodysplastic/myeloproliferative disease with unique molecular characteristics.The mutational landscape of 18 investigated genes clearly separates four subtypes of myelodysplastic/myeloproliferative neoplasms.SRSF2 mutations in myelodysplasia/myeloproliferative neoplasms

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Molecular basis of myelodysplastic/myeloproliferative neoplasms.

http://www.wikidata.org/entity/Q42956279

description

2009 nî lūn-bûn

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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2009年论文

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2009年论文

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name

Molecular basis of myelodysplastic/myeloproliferative neoplasms.

@en

Molecular basis of myelodysplastic/myeloproliferative neoplasms.

@nl

type

label

Molecular basis of myelodysplastic/myeloproliferative neoplasms.

@en

Molecular basis of myelodysplastic/myeloproliferative neoplasms.

@nl

prefLabel

Molecular basis of myelodysplastic/myeloproliferative neoplasms.

@en

Molecular basis of myelodysplastic/myeloproliferative neoplasms.

@nl

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HAEMATOL.2009.014001

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P1476

Molecular basis of myelodysplastic/myeloproliferative neoplasms.

@en

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Andreas Reiter

http://www.w3.org/2001/XMLSchema#string

Mario Cazzola

http://www.w3.org/2001/XMLSchema#string

Rosangela Invernizzi

http://www.w3.org/2001/XMLSchema#string

P2860

Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1

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

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

Mutation in TET2 in myeloid cancers

The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts.

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

Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia.

Acquired mutations in TET2 are common in myelodysplastic syndromes.

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

Frequent TET2 mutations in systemic mastocytosis: clinical, KITD816V and FIP1L1-PDGFRA correlates.

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10.3324/HAEMATOL.2009.014001

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