-
1
-
-
0012384465
-
Chronic myeloproliferative diseases
-
Jaffe ES, Harris NL, Stein H, Vardiman JW eds, IARC Press: Lyon
-
Vardiman JW, Brunning RD, Harris NL. Chronic myeloproliferative diseases. In: Jaffe ES, Harris NL, Stein H, Vardiman JW (eds). Tumors of Haematopoietic and Lymphoid Tissues. IARC Press: Lyon, 2001, pp 15-59.
-
(2001)
Tumors of Haematopoietic and Lymphoid Tissues
, pp. 15-59
-
-
Vardiman, J.W.1
Brunning, R.D.2
Harris, N.L.3
-
2
-
-
33645280589
-
Inherited predispositions and hyperactive Ras in myeloid leukemogenesis
-
Lauchle JO, Braun BS, Loh ML, Shannon K. Inherited predispositions and hyperactive Ras in myeloid leukemogenesis. Pediatr Blood Cancer 2006; 46: 579-585.
-
(2006)
Pediatr Blood Cancer
, vol.46
, pp. 579-585
-
-
Lauchle, J.O.1
Braun, B.S.2
Loh, M.L.3
Shannon, K.4
-
3
-
-
0024998851
-
RAS mutations are rare events in Philadelphia chromosome-negative/bcr gene rearrangement-negative chronic myelogenous leukemia, but are prevalent in chronic myelomonocytic leukemia
-
Hirsch-Ginsberg C, LeMaistre AC, Kantarjian H, Talpaz M, Cork A, Freireich EJ et al. RAS mutations are rare events in Philadelphia chromosome-negative/bcr gene rearrangement-negative chronic myelogenous leukemia, but are prevalent in chronic myelomonocytic leukemia. Blood 1990; 76: 1214-1219.
-
(1990)
Blood
, vol.76
, pp. 1214-1219
-
-
Hirsch-Ginsberg, C.1
LeMaistre, A.C.2
Kantarjian, H.3
Talpaz, M.4
Cork, A.5
Freireich, E.J.6
-
4
-
-
13844298936
-
Acquired PTPN11 mutations occur rarely in adult patients with myelodysplastic syndromes and chronic myelomonocytic leukemia
-
Loh ML, Martinelli S, Cordeddu V, Reynolds MG, Vattikuti S, Lee CM et al. Acquired PTPN11 mutations occur rarely in adult patients with myelodysplastic syndromes and chronic myelomonocytic leukemia. Leuk Res 2005; 29: 459-462.
-
(2005)
Leuk Res
, vol.29
, pp. 459-462
-
-
Loh, M.L.1
Martinelli, S.2
Cordeddu, V.3
Reynolds, M.G.4
Vattikuti, S.5
Lee, C.M.6
-
5
-
-
0028279317
-
Absence of rearrangement of the neurofibromatosis 1 (NF1) gene in myelodysplastic syndromes and acute myeloid leukemia
-
Quesnel B, Preudhomme C, Van rumbeke M, Vachee A, Lai JL, Fenaux P. Absence of rearrangement of the neurofibromatosis 1 (NF1) gene in myelodysplastic syndromes and acute myeloid leukemia. Leukemia 1994; 8: 878-880.
-
(1994)
Leukemia
, vol.8
, pp. 878-880
-
-
Quesnel, B.1
Preudhomme, C.2
Van rumbeke, M.3
Vachee, A.4
Lai, J.L.5
Fenaux, P.6
-
6
-
-
0028224348
-
Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation
-
Golub TR, Barker GF, Lovett M, Gilliland DG. Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 1994; 77: 307-316.
-
(1994)
Cell
, vol.77
, pp. 307-316
-
-
Golub, T.R.1
Barker, G.F.2
Lovett, M.3
Gilliland, D.G.4
-
7
-
-
35048848955
-
FLT3 mutations confer enhanced proliferation and survival properties to multipotent progenitors in a murine model of chronic myelomonocytic leukemia
-
Lee BH, Tothova Z, Levine RL, Anderson K, Buza-Vidas N, Cullen DE et al. FLT3 mutations confer enhanced proliferation and survival properties to multipotent progenitors in a murine model of chronic myelomonocytic leukemia. Cancer Cell 2007; 12: 367-380.
-
(2007)
Cancer Cell
, vol.12
, pp. 367-380
-
-
Lee, B.H.1
Tothova, Z.2
Levine, R.L.3
Anderson, K.4
Buza-Vidas, N.5
Cullen, D.E.6
-
8
-
-
25844518265
-
The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia
-
Levine RL, Loriaux M, Huntly BJ, Loh ML, Beran M, Stoffregen E et al. The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia. Blood 2005; 106: 3377-3379.
-
(2005)
Blood
, vol.106
, pp. 3377-3379
-
-
Levine, R.L.1
Loriaux, M.2
Huntly, B.J.3
Loh, M.L.4
Beran, M.5
Stoffregen, E.6
-
9
-
-
33747113568
-
Mutational analysis of the KIT gene in myelodysplastic syndrome (MDS) and MDS-derived leukemia
-
Lorenzo F, Nishii K, Monma F, Kuwagata S, Usui E, Shiku H. Mutational analysis of the KIT gene in myelodysplastic syndrome (MDS) and MDS-derived leukemia. Leuk Res 2006; 30: 1235-1239.
-
(2006)
Leuk Res
, vol.30
, pp. 1235-1239
-
-
Lorenzo, F.1
Nishii, K.2
Monma, F.3
Kuwagata, S.4
Usui, E.5
Shiku, H.6
-
10
-
-
17344371122
-
RAS, FMS and p53 mutations and poor clinical outcome in myelodysplasias: A 10-year follow-up
-
Padua RA, Guinn BA, Al-Sabah AI, Smith M, Taylor C, Pettersson T et al. RAS, FMS and p53 mutations and poor clinical outcome in myelodysplasias: A 10-year follow-up. Leukemia 1998; 12: 887-892.
-
(1998)
Leukemia
, vol.12
, pp. 887-892
-
-
Padua, R.A.1
Guinn, B.A.2
Al-Sabah, A.I.3
Smith, M.4
Taylor, C.5
Pettersson, T.6
-
11
-
-
0032170974
-
Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome
-
Reiter A, Sohal J, Kulkarni S, Chase A, Macdonald DH, Aguiar RC et al. Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome. Blood 1998; 92: 1735-1742.
-
(1998)
Blood
, vol.92
, pp. 1735-1742
-
-
Reiter, A.1
Sohal, J.2
Kulkarni, S.3
Chase, A.4
Macdonald, D.H.5
Aguiar, R.C.6
-
12
-
-
0036234698
-
Cooperativity between mutations in tyrosine kinases and in hematopoietic transcription factors in AML
-
Deguchi K, Gilliland DG. Cooperativity between mutations in tyrosine kinases and in hematopoietic transcription factors in AML. Leukemia 2002; 16: 740-744.
-
(2002)
Leukemia
, vol.16
, pp. 740-744
-
-
Deguchi, K.1
Gilliland, D.G.2
-
13
-
-
47049105417
-
High-throughput sequence analysis of the tyrosine kinome in acute myeloid leukemia
-
Loriaux MM, Levine RL, Tyner JW, Frohling S, Scholl C, Stoffregen EP et al. High-throughput sequence analysis of the tyrosine kinome in acute myeloid leukemia. Blood 2008; 111: 4788-4796.
-
(2008)
Blood
, vol.111
, pp. 4788-4796
-
-
Loriaux, M.M.1
Levine, R.L.2
Tyner, J.W.3
Frohling, S.4
Scholl, C.5
Stoffregen, E.P.6
-
14
-
-
33749993417
-
The consensus coding sequences of human breast and colorectal cancers
-
Sjoblom T, Jones S, Wood LD, Parsons DW, Lin J, Barber TD et al. The consensus coding sequences of human breast and colorectal cancers. Science 2006; 314: 268-274.
-
(2006)
Science
, vol.314
, pp. 268-274
-
-
Sjoblom, T.1
Jones, S.2
Wood, L.D.3
Parsons, D.W.4
Lin, J.5
Barber, T.D.6
-
15
-
-
47149087181
-
Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia
-
Tomasson MH, Xiang Z, Walgren R, Zhao Y, Kasai Y, Miner T et al. Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia. Blood 2008; 111: 4797-4808.
-
(2008)
Blood
, vol.111
, pp. 4797-4808
-
-
Tomasson, M.H.1
Xiang, Z.2
Walgren, R.3
Zhao, Y.4
Kasai, Y.5
Miner, T.6
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