Molecular diagnosis of myeloproliferative neoplasms. - Wikidata - awgldk - TriplyDB

Molecular diagnosis of myeloproliferative neoplasms.

Molecular diagnosis of myeloproliferative neoplasms.

http://www.wikidata.org/entity/Q37542270

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Prognostic markers for myeloid neoplasms: a comparative review of the literature and goals for future investigation.

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P2860

Molecular diagnosis of myeloproliferative neoplasms.

http://www.wikidata.org/entity/Q37542270

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on July 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Molecular diagnosis of myeloproliferative neoplasms.

@en

Molecular diagnosis of myeloproliferative neoplasms.

@nl

type

label

Molecular diagnosis of myeloproliferative neoplasms.

@en

Molecular diagnosis of myeloproliferative neoplasms.

@nl

prefLabel

Molecular diagnosis of myeloproliferative neoplasms.

@en

Molecular diagnosis of myeloproliferative neoplasms.

@nl

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Expert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcare

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Molecular diagnosis of myeloproliferative neoplasms.

@en

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Mrinal M Patnaik

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P2860

Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)

8p12 stem cell myeloproliferative disorder: the FOP-fibroblast growth factor receptor 1 fusion protein of the t(6;8) translocation induces cell survival mediated by mitogen-activated protein kinase and phosphatidylinositol 3-kinase/Akt/mTOR pathways

JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis

A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome.

Molecular remission and reversal of myelofibrosis in response to imatinib mesylate treatment in patients with the myeloproliferative variant of hypereosinophilic syndrome.

Characterization of FIM-FGFR1, the fusion product of the myeloproliferative disorder-associated t(8;13) translocation

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

NIN, a gene encoding a CEP110-like centrosomal protein, is fused to PDGFRB in a patient with a t(5;14)(q33;q24) and an imatinib-responsive myeloproliferative disorder

FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome

The t(8;13)(p11;q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP

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481-492

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scholarly article

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10.1586/ERM.09.29

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5

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9

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2009-07-01T00:00:00Z

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19580432

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