Myeloproliferative neoplasms: contemporary diagnosis using histology and genetics (Q37608910)

21 August 2017

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title

Myeloproliferative neoplasms: contemporary diagnosis using histology and genetics (English)

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21 August 2017

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1

Ayalew Tefferi

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21 August 2017

3

James W Vardiman

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21 August 2017

Radek Skoda

2

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21 August 2017

language of work or name

English

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publication date

6 October 2009

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Nature Reviews Clinical Oncology

21 August 2017

published in

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21 August 2017

volume

6

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21 August 2017

issue

11

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21 August 2017

page(s)

627-637

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Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

21 August 2017

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Conventional cytogenetics in myelofibrosis: literature review and discussion

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

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Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining

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A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia

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Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22

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A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera

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A gain-of-function mutation of JAK2 in myeloproliferative disorders

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The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes

31 March 2020

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Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders

31 March 2020

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High occurrence of JAK2 V617 mutation in refractory anemia with ringed sideroblasts associated with marked thrombocytosis

31 March 2020

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JAK2V617F mutation status identifies subtypes of refractory anemia with ringed sideroblasts associated with marked thrombocytosis

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Expression of Jak2V617F causes a polycythemia vera-like disease with associated myelofibrosis in a murine bone marrow transplant model

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Acquisition of the V617F mutation of JAK2 is a late genetic event in a subset of patients with myeloproliferative disorders.

31 March 2020

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Extending Jak2V617F and MplW515 mutation analysis to single hematopoietic colonies and B and T lymphocytes.

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Host genetic variation contributes to phenotypic diversity in myeloproliferative disorders

31 March 2020

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JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms

31 March 2020

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A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms

31 March 2020

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A common JAK2 haplotype confers susceptibility to myeloproliferative neoplasms.

31 March 2020

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JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis

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Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera.

31 March 2020

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Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders

31 March 2020

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

31 March 2020

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

31 March 2020

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Anaemia characterises patients with myelofibrosis harbouring Mpl mutation.

31 March 2020

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MPL mutations in myeloproliferative disorders: analysis of the PT-1 cohort.

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRCLINONC.2009.149

Evidence for MPL W515L/K mutations in hematopoietic stem cells in primitive myelofibrosis

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRCLINONC.2009.149

Demonstration of MPLW515K, but not JAK2V617F, in in vitro expanded CD4+ T lymphocytes

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRCLINONC.2009.149

Concurrent MPL515 and JAK2V617F mutations in myelofibrosis: chronology of clonal emergence and changes in mutant allele burden over time.

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRCLINONC.2009.149

Clonal diversity in the myeloproliferative neoplasms: independent origins of genetically distinct clones

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRCLINONC.2009.149

Identification of mutations in the coding sequence of the proto-oncogene c-kit in a human mast cell leukemia cell line causing ligand-independent activation of c-kit product

31 March 2020

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KIT mutation in mast cells and other bone marrow hematopoietic cell lineages in systemic mast cell disorders: a prospective study of the Spanish Network on Mastocytosis (REMA) in a series of 113 patients

31 March 2020

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Mastocytosis in mice expressing human Kit receptor with the activating Asp816Val mutation

31 March 2020

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Constitutively active mutant D816VKit induces megakayocyte and mast cell differentiation of early haemopoietic cells from murine foetal liver.

31 March 2020

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The complete evaluation of erythrocytosis: congenital and acquired

31 March 2020

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Serum erythropoietin values in erythrocytoses and in primary thrombocythaemia

31 March 2020

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Classification and diagnosis of myeloproliferative neoplasms: the 2008 World Health Organization criteria and point-of-care diagnostic algorithms

31 March 2020

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Clinical correlates of JAK2V617F allele burden in essential thrombocythemia

31 March 2020

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Eosinophilia: secondary, clonal and idiopathic

31 March 2020

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Some speculations on the myeloproliferative syndromes.

31 March 2020

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12 December 2020

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10.1038/NRCLINONC.2009.149

Identifiers

DOI

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21 August 2017

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