Familial polycythemia vera with non-germline JAK2(V617F) mutation sparing the abnormal and clonal granulopoiesis (Q80599622)

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2 January 2020

title

Familial polycythemia vera with non-germline JAK2(V617F) mutation sparing the abnormal and clonal granulopoiesis (English)

1 reference

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2 January 2020

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Hussein K

1

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2 January 2020

Bock O

2

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2 January 2020

Ballmaier M

3

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2 January 2020

Göhring G

4

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2 January 2020

Steinemann D

5

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2 January 2020

Lehmann U

6

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2 January 2020

Kemper J

7

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2 January 2020

Buhr T

8

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2 January 2020

Kreipe H

9

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2 January 2020

publication date

12 July 2007

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2 January 2020

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2 January 2020

volume

21

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2 January 2020

issue

12

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2 January 2020

page(s)

2566-2568

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https://scigraph.springernature.com/pub.10.1038/sj.leu.2404846

2 January 2020

exact match

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cites work

Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders

1 reference

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7 January 2021

Detection of the single hotspot mutation in the JH2 pseudokinase domain of Janus kinase 2 in bone marrow trephine biopsies derived from chronic myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404846

7 January 2021

Biomarker analysis in polycythemia vera under interferon-alpha treatment: clonality, EEC, PRV-1, and JAK2 V617F.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404846

7 January 2021

The polycythaemia rubra vera‐1 gene is constitutively expressed by bone marrow cells and does not discriminate polycythaemia vera from reactive and other chronic myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404846

7 January 2021

Assessment of differentiation and progression of hepatic tumors using array-based comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404846

7 January 2021

B-CLL developing in a patient with PV is not affected by V617F mutation of the Janus kinase 2

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404846

7 January 2021

JAK2V617F mutation can occur exclusively in the erythroid lineage and be absent in granulocytes and progenitor cells in classic myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404846

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404846

7 January 2021