(Q81381426)

English

The JAK2 V617F tyrosine kinase mutation in myelodysplastic syndromes (MDS) developing myelofibrosis indicates the myeloproliferative nature in a subset of MDS patients

scientific article published on 01 December 2005

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16239910%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

The JAK2 V617F tyrosine kinase mutation in myelodysplastic syndromes (MDS) developing myelofibrosis indicates the myeloproliferative nature in a subset of MDS patients (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16239910%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

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Ohyashiki K

1

1 reference

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8 January 2020

Aota Y

2

1 reference

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8 January 2020

Akahane D

3

1 reference

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8 January 2020

Gotoh A

4

1 reference

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8 January 2020

Miyazawa K

5

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8 January 2020

Kimura Y

6

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8 January 2020

Ohyashiki JH

7

1 reference

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8 January 2020

publication date

1 December 2005

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8 January 2020

1 reference

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8 January 2020

19

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8 January 2020

12

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8 January 2020

2359-2360

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8 January 2020

https://scigraph.springernature.com/pub.10.1038/sj.leu.2403989

0 references

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403989

7 January 2021

based on heuristic

inferred from DOI database lookup

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.2403989

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403989

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403989

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical and cytogenetic characteristics of myelodysplastic syndromes developing myelofibrosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403989

7 January 2021

based on heuristic

inferred from DOI database lookup

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