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Somatic SETBP1 mutations in myeloid malignancies

Somatic SETBP1 mutations in myeloid malignancies

http://www.wikidata.org/entity/Q37060418

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Therapeutic approaches in myelofibrosis and myelodysplastic/myeloproliferative overlap syndromes Cytogenetic and molecular abnormalities in chronic myelomonocytic leukemia Chronic neutrophilic leukemia: a clinical perspective Therapy-Related Myeloid Neoplasms Chronic neutrophilic leukemia 2014: Update on diagnosis, molecular genetics, and management Emerging patterns of somatic mutations in cancer Evaluation of a father and son with atypical chronic myeloid leukemia with SETBP1 mutations and a review of the literature Clinical and biological implications of ancestral and non-ancestral IDH1 and IDH2 mutations in myeloid neoplasms A novel BCR-ABL1 fusion gene with genetic heterogeneity indicates a good prognosis in a chronic myeloid leukemia case.ASXL1 mutations are frequent and prognostically detrimental in CSF3R-mutated chronic neutrophilic leukemia.Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation Tet2 loss leads to hypermutagenicity in haematopoietic stem/progenitor cells.Clinical and genetic predictors of prognosis in myelodysplastic syndromes.Molecular features of early onset adult myelodysplastic syndrome Prioritization of neurodevelopmental disease genes by discovery of new mutations.From the Biology of PP2A to the PADs for Therapy of Hematologic Malignancies Refining analyses of copy number variation identifies specific genes associated with developmental delay Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage.PRPF8 defects cause missplicing in myeloid malignancies.Clonal evolution in myelodysplastic syndromes Pathogenesis of myelodysplastic syndromes: an overview of molecular and non-molecular aspects of the disease.Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia Mutational landscape of gastric adenocarcinoma in Chinese: implications for prognosis and therapy.The molecular basis of myeloid malignancies.SETBP1 mutations drive leukemic transformation in ASXL1-mutated MDS.Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia.Prognostic significance of SETBP1 mutations in myelodysplastic syndromes, chronic myelomonocytic leukemia, and chronic neutrophilic leukemia: A meta-analysis.Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.Whole-exome and targeted sequencing identify ROBO1 and ROBO2 mutations as progression-related drivers in myelodysplastic syndromes.Myelodysplastic syndromes, version 2.2015 Runx1 repression by histone deacetylation is critical for Setbp1-induced mouse myeloid leukemia development Relapse after Allogeneic Hematopoietic Cell Transplantation for Myelodysplastic Syndromes: Analysis of Late Relapse Using Comparative Karyotype and Chromosome Genome Array Testing Clonality of neutrophilia associated with plasma cell neoplasms: report of a SETBP1 mutation and analysis of a single institution series.An International MDS/MPN Working Group's perspective and recommendations on molecular pathogenesis, diagnosis and clinical characterization of myelodysplastic/myeloproliferative neoplasms.Myeloid neoplasms with isolated isochromosome 17q demonstrate a high frequency of mutations in SETBP1, SRSF2, ASXL1 and NRAS.The multi-omic landscape of transcription factor inactivation in cancer.BRCC3 mutations in myeloid neoplasms.Peripheral blood cell-free DNA is an alternative tumor DNA source reflecting disease status in myelodysplastic syndromes.Diagnosis and treatment of primary myelodysplastic syndromes in adults: recommendations from the European LeukemiaNet.

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Somatic SETBP1 mutations in myeloid malignancies

http://www.wikidata.org/entity/Q37060418

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 07 July 2013

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Somatic SETBP1 mutations in myeloid malignancies

@en

Somatic SETBP1 mutations in myeloid malignancies.

@nl

type

label

Somatic SETBP1 mutations in myeloid malignancies

@en

Somatic SETBP1 mutations in myeloid malignancies.

@nl

prefLabel

Somatic SETBP1 mutations in myeloid malignancies

@en

Somatic SETBP1 mutations in myeloid malignancies.

@nl

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Nature Genetics

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Somatic SETBP1 mutations in myeloid malignancies

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Andres Jerez

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Bartlomiej Przychodzen

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Hideki Makishima

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Hideki Muramatsu

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Hiraku Mori

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Hiroko Tanaka

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Hirotoshi Sakaguchi

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Ines Gomez-Segui

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Jaroslaw P Maciejewski

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Kathryn Guinta

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Impaired hydroxylation of 5-methylcytosine in myeloid cancers with mutant TET2

Heterodimers of the SnoN and Ski oncoproteins form preferentially over homodimers and are more potent transforming agents

Recurring mutations found by sequencing an acute myeloid leukemia genome

Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML

DNMT3A Mutations in Acute Myeloid Leukemia

Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia

Identification and characterization of SEB, a novel protein that binds to the acute undifferentiated leukemia-associated protein SET

International scoring system for evaluating prognosis in myelodysplastic syndromes

Integrative genomics viewer

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942-946

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scholarly article

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10.1038/NG.2696

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8

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45

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Kenichi Yoshida

Bandana A Vishwakarma

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2013-07-07T00:00:00Z

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247157032

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23832012

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