JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained (Q58289362)

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19 January 2020

title

JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained (English)

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19 January 2020

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acute myeloid leukemia

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1

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19 January 2020

Scott H Kaufmann

8

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19 January 2020

author name string

R F McClure

2

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19 January 2020

J E Karp

3

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19 January 2020

T L Lasho

5

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19 January 2020

H L Powell

6

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19 January 2020

G W DeWald

7

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19 January 2020

A Tefferi

4

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19 January 2020

publication date

1 June 2006

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19 January 2020

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19 January 2020

volume

20

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19 January 2020

issue

6

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19 January 2020

page(s)

971-978

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https://scigraph.springernature.com/pub.10.1038/sj.leu.2404206

19 January 2020

exact match

0 references

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JAK2 V617F in myeloid disorders: what do we know now, and where are we headed?

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Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders

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

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JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia

21 January 2018

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21 January 2018

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Identifiers

DOI

10.1038/SJ.LEU.2404206

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16598306%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference