Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

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Mutation spectra of histone methyltransferases with canonical SET domains and EZH2-targeted therapy.The H3K4 methyltransferase Setd1b is essential for hematopoietic stem and progenitor cell homeostasis in mice.

P2860

Q38594002-F91BB74F-CA53-4021-B156-241D69068AFD Q55437673-3A3EF38A-C81C-49EC-A7D8-42C55D876178

P2860

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

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http://www.wikidata.org/entity/Q50481525

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

@wuu

2014年学术文章

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2014年学术文章

@zh-cn

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@zh-hans

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2014年學術文章

@zh-hant

name

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

@en

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

@nl

type

Item

label

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

@en

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

@nl

prefLabel

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

@en

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

@nl

P1476

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

@en

P2093

Alessandro M Vannucchi

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

Chiara Paoli

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

Giulia Daniele

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

Terra Lasho

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

P2860

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia

Presence of unfavorable cytogenetic abnormalities is the strongest predictor of poor survival in secondary myelofibrosis.

DIPSS plus: a refined Dynamic International Prognostic Scoring System for primary myelofibrosis that incorporates prognostic information from karyotype, platelet count, and transfusion status.

Survival and prognosis among 1545 patients with contemporary polycythemia vera: an international study.

The diagnosis and management of polycythemia vera in the era since the Polycythemia Vera Study Group: a survey of American Society of Hematology members' practice patterns.

Identification of submicroscopic genetic changes and precise breakpoint mapping in myelofibrosis using high resolution mate-pair sequencing.

Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert panel.

Somatic SETBP1 mutations in myeloid malignancies

Conventional cytogenetics in myelofibrosis: literature review and discussion.

New mutations and pathogenesis of myeloproliferative neoplasms.

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438-442

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P31

scholarly article

P356

10.1002/AJH.23659

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P433

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

P478

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Lisa Pieri

Clelia Tiziana Storlazzi

Ayalew Tefferi

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2014-04-01T00:00:00Z

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P5875

259559911

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24382738

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P921

karyotype

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

about

P2860

P2860

Complex karyotype in a polycythemia vera patient with a novel SETD1B/GTF2H3 fusion gene.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921