(Q54650456)

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Clinical implications of the JAK2 V617F mutation in essential thrombocythemia.

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Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

Clinical implications of the JAK2 V617F mutation in essential thrombocythemia. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

Paola Guglielmelli

2

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Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

author name string

Antonioli E

1

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Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

Pancrazzi A

3

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Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

Bogani C

4

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Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

Verrucci M

5

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

Ponziani V

6

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

Longo G

7

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

Bosi A

8

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

Vannucchi AM

9

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Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

publication date

1 October 2005

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Europe PubMed Central

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2 June 2018

http://europepmc.org/abstract/MED/16079890

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

19

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Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

10

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Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

1847-1849

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Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

On the molecular origins of the chronic myeloproliferative disorders: it all makes sense

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403902

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403902

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%2FSJ.LEU.2403902

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403902

21 January 2018

Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403902

21 January 2018

PRV-1, erythroid colonies and platelet Mpl are unrelated to thrombosis in essential thrombocythaemia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403902

21 January 2018

Identifiers

10.1038/SJ.LEU.2403902

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/16079890

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