-
1
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
-
James C, Ugo V, Le Couedic JP, et al. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature. 2005;434:1144-1148.
-
(2005)
Nature
, vol.434
, pp. 1144-1148
-
-
James, C.1
Ugo, V.2
Le Couedic, J.P.3
-
2
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
-
Baxter EJ, Scott LM, Campbell PJ, et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet. 2005;365:1054-1061.
-
(2005)
Lancet
, vol.365
, pp. 1054-1061
-
-
Baxter, E.J.1
Scott, L.M.2
Campbell, P.J.3
-
3
-
-
17644424955
-
A gain-of-function mutation of Jak2 in myeloproliferative disorders
-
Kralovics R, Passamonti F, Buser A, et al. A gain-of-function mutation of Jak2 in myeloproliferative disorders. N Engl J Med. 2005;352:1779-1790.
-
(2005)
N Engl J Med
, vol.352
, pp. 1779-1790
-
-
Kralovics, R.1
Passamonti, F.2
Buser, A.3
-
4
-
-
20244369569
-
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and agnogenic myeloid metaplasia
-
Levine RL, Wadleigh M, Cools J, et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and agnogenic myeloid metaplasia. Cancer Cell. 2005;7:387-397.
-
(2005)
Cancer Cell
, vol.7
, pp. 387-397
-
-
Levine, R.L.1
Wadleigh, M.2
Cools, J.3
-
5
-
-
21344444103
-
The JAK2V617F tyrosine kinase mutation in myeloproliferative disorders: Status report and immediate implications for disease classification and diagnosis
-
Tefferi A, Gilliland DG. The JAK2V617F tyrosine kinase mutation in myeloproliferative disorders: status report and immediate implications for disease classification and diagnosis. Mayo Clin Proc. 2005;80:947-958.
-
(2005)
Mayo Clin Proc
, vol.80
, pp. 947-958
-
-
Tefferi, A.1
Gilliland, D.G.2
-
6
-
-
21344467318
-
Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
-
Jones AV, Kreil S, Zoi K, et al. Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. Blood. 2005;106:2162-2168.
-
(2005)
Blood
, vol.106
, pp. 2162-2168
-
-
Jones, A.V.1
Kreil, S.2
Zoi, K.3
-
7
-
-
21344440357
-
The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes
-
Steensma DP, Dewald GW, Lasho TL, et al. The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes. Blood. 2005;106:1207-1209.
-
(2005)
Blood
, vol.106
, pp. 1207-1209
-
-
Steensma, D.P.1
Dewald, G.W.2
Lasho, T.L.3
-
8
-
-
2342578680
-
Suppressor screen in Mpl-/- mice: C-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signaling
-
U S A
-
Carpinelli MR, Hilton DJ, Metcalf D, et al. Suppressor screen in Mpl-/- mice: c-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signaling. Proc Natl Acad Sci U S A. 2004;101:6553-6558.
-
(2004)
Proc Natl Acad Sci
, vol.101
, pp. 6553-6558
-
-
Carpinelli, M.R.1
Hilton, D.J.2
Metcalf, D.3
-
9
-
-
18244383783
-
Anomalous megakaryocytopoiesis in mice with mutations in the c-Myb gene
-
Metcalf D, Carpinelli MR, Hyland C, et al. Anomalous megakaryocytopoiesis in mice with mutations in the c-Myb gene. Blood. 2005;105:3480-3487.
-
(2005)
Blood
, vol.105
, pp. 3480-3487
-
-
Metcalf, D.1
Carpinelli, M.R.2
Hyland, C.3
-
10
-
-
0037126308
-
A transcription-factor-binding surface of coactivator p300 is required for haematopoiesis
-
Kasper LH, Boussouar F, Ney PA, et al. A transcription-factor-binding surface of coactivator p300 is required for haematopoiesis. Nature. 2002;419:738-743.
-
(2002)
Nature
, vol.419
, pp. 738-743
-
-
Kasper, L.H.1
Boussouar, F.2
Ney, P.A.3
-
11
-
-
0025821494
-
A functional c-myb gene is required for normal murine fetal hepatic hematopoiesis
-
Mucenski ML, McLain K, Kier AB, et al. A functional c-myb gene is required for normal murine fetal hepatic hematopoiesis. Cell. 1991;65:677-689.
-
(1991)
Cell
, vol.65
, pp. 677-689
-
-
Mucenski, M.L.1
McLain, K.2
Kier, A.B.3
-
12
-
-
0029010475
-
v-Myb DNA binding is required to block thrombocytic differentiation of Myb-Ets-transformed multipotent haematopoietic progenitors
-
Frampton J, McNagny K, Sieweke M, Philip A, Smith G, Graf T. v-Myb DNA binding is required to block thrombocytic differentiation of Myb-Ets-transformed multipotent haematopoietic progenitors. EMBO J. 1995;14:2866-2875.
-
(1995)
EMBO J
, vol.14
, pp. 2866-2875
-
-
Frampton, J.1
McNagny, K.2
Sieweke, M.3
Philip, A.4
Smith, G.5
Graf, T.6
-
13
-
-
0029956149
-
A model of myelofibrosis and osteosclerosis in mice induced by overexpressing thrombopoietin (mpl ligand): Reversal of disease by bone marrow transplantation
-
Yan XQ, Lacey D, Hill D, et al. A model of myelofibrosis and osteosclerosis in mice induced by overexpressing thrombopoietin (mpl ligand): reversal of disease by bone marrow transplantation. Blood. 1996;88:402-409.
-
(1996)
Blood
, vol.88
, pp. 402-409
-
-
Yan, X.Q.1
Lacey, D.2
Hill, D.3
-
14
-
-
3042606722
-
Impaired GATA-1 expression and myelofibrosis in an animal model
-
Paris
-
Vannucchi AM, Bianchi L, Paoletti F, Di Giacomo V, Migliaccio G, Migliaccio AR. Impaired GATA-1 expression and myelofibrosis in an animal model. Pathol Biol (Paris). 2004;52:275-279.
-
(2004)
Pathol Biol
, vol.52
, pp. 275-279
-
-
Vannucchi, A.M.1
Bianchi, L.2
Paoletti, F.3
Di Giacomo, V.4
Migliaccio, G.5
Migliaccio, A.R.6
-
15
-
-
0037103206
-
Development of myelofibrosis in mice genetically impaired for GATA-1 expression (GATA-1(low) mice)
-
Vannucchi AM, Bianchi L, Cellai C, et al. Development of myelofibrosis in mice genetically impaired for GATA-1 expression (GATA-1(low) mice). Blood. 2002;100:1123-1132.
-
(2002)
Blood
, vol.100
, pp. 1123-1132
-
-
Vannucchi, A.M.1
Bianchi, L.2
Cellai, C.3
-
16
-
-
0023052242
-
Studies of the human c-myb gene and its product in human acute leukemias
-
Slamon DJ, Boone TC, Murdock DC, et al. Studies of the human c-myb gene and its product in human acute leukemias. Science. 1986;233:347-351.
-
(1986)
Science
, vol.233
, pp. 347-351
-
-
Slamon, D.J.1
Boone, T.C.2
Murdock, D.C.3
|