(Q43685807)

English

SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations

scientific article published on 30 April 2013

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scholarly article

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Europe PubMed Central

PubMed publication ID

25 November 2017

SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations (English)

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Europe PubMed Central

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25 November 2017

atypical chronic myeloid leukemia

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Carlo Gambacorti-Passerini

6

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Europe PubMed Central

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25 November 2017

Torsten Haferlach

7

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T Haferlach

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25 November 2017

Claudia Haferlach

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C Haferlach

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25 November 2017

Susanne Schnittger

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S Schnittger

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25 November 2017

author name string

M Meggendorfer

1

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25 November 2017

U Bacher

2

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25 November 2017

T Alpermann

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25 November 2017

W Kern

5

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25 November 2017

language of work or name

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publication date

30 April 2013

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25 November 2017

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25 November 2017

27

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25 November 2017

9

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25 November 2017

1852-1860

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25 November 2017

https://scigraph.springernature.com/pub.10.1038/leu.2013.133

0 references

Atypical chronic myeloid leukemia as defined in the WHO classification is a JAK2 V617F negative neoplasm

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Distribution of cytogenetic abnormalities in myelodysplastic syndromes, Philadelphia negative myeloproliferative neoplasms, and the overlap MDS/MPN category

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

SETBP1 overexpression is a novel leukemogenic mechanism that predicts adverse outcome in elderly patients with acute myeloid leukemia.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

SETBP1 and miR_4319 dysregulation in primary myelofibrosis progression to acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12).

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

A method and server for predicting damaging missense mutations

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

MutationTaster evaluates disease-causing potential of sequence alterations

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Detection of JAK2 exon 12 mutations in 15 patients with JAK2V617F negative polycythemia vera

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

A novel hierarchical prognostic model of AML solely based on molecular mutations

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

High frequencies of SF3B1 and JAK2 mutations in refractory anemia with ring sideroblasts associated with marked thrombocytosis strengthen the assignment to the category of myelodysplastic/myeloproliferative neoplasms

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Activating CBL mutations are associated with a distinct MDS/MPN phenotype

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/myeloproliferative disorders: an analysis of 636 cases

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Mutational spectrum analysis of chronic myelomonocytic leukemia includes genes associated with epigenetic regulation: UTX, EZH2, and DNMT3A.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

The role of chromatin modifiers in normal and malignant hematopoiesis

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Setbp1 promotes the self-renewal of murine myeloid progenitors via activation of Hoxa9 and Hoxa10

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

21 January 2018

Proposals for standardized protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

7 January 2021

based on heuristic

inferred from DOI database lookup

Report on two novel nucleotide exchanges in the JAK2 pseudokinase domain: D620E and E627E

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of an MPLW515 mutation in a case with features of both essential thrombocythemia and refractory anemia with ringed sideroblasts and thrombocytosis

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.133

7 January 2021

based on heuristic

inferred from DOI database lookup

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10.1038/LEU.2013.133

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

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