JAK2 mutation and disease phenotype: a double L611V/V617F in cis mutation of JAK2 is associated with isolated erythrocytosis and increased activation of AKT and ERK1/2 rather than STAT5. (Q43150782)
Jump to navigation
Jump to search
scientific article published on 25 February 2010
Language | Label | Description | Also known as |
---|---|---|---|
English | JAK2 mutation and disease phenotype: a double L611V/V617F in cis mutation of JAK2 is associated with isolated erythrocytosis and increased activation of AKT and ERK1/2 rather than STAT5. |
scientific article published on 25 February 2010 |
Statements
1 reference
JAK2 mutation and disease phenotype: a double L611V/V617F in cis mutation of JAK2 is associated with isolated erythrocytosis and increased activation of AKT and ERK1/2 rather than STAT5. (English)
1 reference
1 reference
J Jelinek
1 reference
F Girodon
1 reference
M Boissinot
1 reference
T Ponge
1 reference
J-L Harousseau
1 reference
J-P Issa
1 reference
S Hermouet
1 reference
25 February 2010
1 reference
1 reference
24
1 reference
5
1 reference
1069-1073
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference