-
2
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
-
James C, Ugo V, Le Couédic JP, et al. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature 2005;434:1144-8.
-
(2005)
Nature
, vol.434
, pp. 1144-1148
-
-
James, C.1
Ugo, V.2
Le Couédic, J.P.3
-
3
-
-
17644424955
-
A gain-of-function mutation of JAK2 in myeloproliferative disorders
-
Kralovics R, Passamonti F, Buser AS, et al. A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med 2005;352:1779-90.
-
(2005)
N Engl J Med
, vol.352
, pp. 1779-1790
-
-
Kralovics, R.1
Passamonti, F.2
Buser, A.S.3
-
4
-
-
33845436745
-
The myeloproliferative disorders
-
Campbell PJ, Green AR. The myeloproliferative disorders. N Engl J Med 2006;355:2452-66.
-
(2006)
N Engl J Med
, vol.355
, pp. 2452-2466
-
-
Campbell, P.J.1
Green, A.R.2
-
5
-
-
33846660947
-
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis
-
Scott LM, Tong W, Levine RL, et al. JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis. N Engl J Med 2007;356:459-68.
-
(2007)
N Engl J Med
, vol.356
, pp. 459-468
-
-
Scott, L.M.1
Tong, W.2
Levine, R.L.3
-
6
-
-
79551607979
-
Molecular and clinical features of the myeloproliferative neoplasm associated with JAK2 exon 12 mutations
-
Passamonti F, Elena C, Schnittger S, et al. Molecular and clinical features of the myeloproliferative neoplasm associated with JAK2 exon 12 mutations. Blood 2011;117:2813-6.
-
(2011)
Blood
, vol.117
, pp. 2813-2816
-
-
Passamonti, F.1
Elena, C.2
Schnittger, S.3
-
7
-
-
33746437130
-
MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia
-
Pikman Y, Lee BH, Mercher T, et al. MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia. PLoS Med 2006;3(7):e270.
-
(2006)
PLoS Med
, vol.3
, Issue.7
-
-
Pikman, Y.1
Lee, B.H.2
Mercher, T.3
-
8
-
-
84880595307
-
Acquired copy-neutral loss of heterozygosity of chromosome 1p as a molecular event associated with marrow fibrosis in MPL-mutated myeloproliferative neoplasms
-
Rumi E, Pietra D, Guglielmelli P, et al. Acquired copy-neutral loss of heterozygosity of chromosome 1p as a molecular event associated with marrow fibrosis in MPL-mutated myeloproliferative neoplasms. Blood 2013;121:4388-95.
-
(2013)
Blood
, vol.121
, pp. 4388-4395
-
-
Rumi, E.1
Pietra, D.2
Guglielmelli, P.3
-
9
-
-
77956439565
-
A prospective study of 338 patients with polycythemia vera: The impact of JAK2 (V617F) allele burden and leukocytosis on fibrotic or leukemic disease transformation and vascular complications
-
Passamonti F, Rumi E, Pietra D, et al. A prospective study of 338 patients with polycythemia vera: the impact of JAK2 (V617F) allele burden and leukocytosis on fibrotic or leukemic disease transformation and vascular complications. Leukemia 2010;24:1574-9.
-
(2010)
Leukemia
, vol.24
, pp. 1574-1579
-
-
Passamonti, F.1
Rumi, E.2
Pietra, D.3
-
11
-
-
67349124376
-
TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis
-
Tefferi A, Pardanani A, Lim KH, et al. TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis. Leukemia 2009;23:905-11.
-
(2009)
Leukemia
, vol.23
, pp. 905-911
-
-
Tefferi, A.1
Pardanani, A.2
Lim, K.H.3
-
12
-
-
67650401377
-
Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms
-
Grand FH, Hidalgo-Curtis CE, Ernst T, et al. Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms. Blood 2009;113:6182-92.
-
(2009)
Blood
, vol.113
, pp. 6182-6192
-
-
Grand, F.H.1
Hidalgo-Curtis, C.E.2
Ernst, T.3
-
13
-
-
68949124841
-
Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms
-
Sanada M, Suzuki T, Shih LY, et al. Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms. Nature 2009;460:904-8.
-
(2009)
Nature
, vol.460
, pp. 904-908
-
-
Sanada, M.1
Suzuki, T.2
Shih, L.Y.3
-
14
-
-
77955085750
-
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders
-
Ernst T, Chase AJ, Score J, et al. Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders. Nat Genet 2010;42:722-6.
-
(2010)
Nat Genet
, vol.42
, pp. 722-726
-
-
Ernst, T.1
Chase, A.J.2
Score, J.3
-
15
-
-
81055126771
-
EZH2 mutational status predicts poor survival in myelofibrosis
-
Guglielmelli P, Biamonte F, Score J, et al. EZH2 mutational status predicts poor survival in myelofibrosis. Blood 2011;118:5227-34.
-
(2011)
Blood
, vol.118
, pp. 5227-5234
-
-
Guglielmelli, P.1
Biamonte, F.2
Score, J.3
-
16
-
-
79960248721
-
DNMT3A mutational analysis in primary myelofibrosis, chronic myelomonocytic leukemia and advanced phases of myeloproliferative neoplasms
-
Abdel-Wahab O, Pardanani A, Rampal R, Lasho TL, Levine RL, Tefferi A. DNMT3A mutational analysis in primary myelofibrosis, chronic myelomonocytic leukemia and advanced phases of myeloproliferative neoplasms. Leukemia 2011;25:1219-20.
-
(2011)
Leukemia
, vol.25
, pp. 1219-1220
-
-
Abdel-Wahab, O.1
Pardanani, A.2
Rampal, R.3
Lasho, T.L.4
Levine, R.L.5
Tefferi, A.6
-
17
-
-
70450239681
-
Mutations of ASXL1 gene in myeloproliferative neoplasms
-
Carbuccia N, Murati A, Trouplin V, et al. Mutations of ASXL1 gene in myeloproliferative neoplasms. Leukemia 2009;23:2183-6.
-
(2009)
Leukemia
, vol.23
, pp. 2183-2186
-
-
Carbuccia, N.1
Murati, A.2
Trouplin, V.3
-
18
-
-
54049123194
-
Genetic complexity of myeloproliferative neoplasms
-
Kralovics R. Genetic complexity of myeloproliferative neoplasms. Leukemia 2008;22:1841-8.
-
(2008)
Leukemia
, vol.22
, pp. 1841-1848
-
-
Kralovics, R.1
-
19
-
-
79960145108
-
Genome integrity of myeloproliferative neoplasms in chronic phase and during disease progression
-
Klampfl T, Harutyunyan A, Berg T, et al. Genome integrity of myeloproliferative neoplasms in chronic phase and during disease progression. Blood 2011;118:167-76.
-
(2011)
Blood
, vol.118
, pp. 167-176
-
-
Klampfl, T.1
Harutyunyan, A.2
Berg, T.3
-
21
-
-
84883742034
-
Mutations and prognosis in primary myelofibrosis
-
Vannucchi AM, Lasho TL, Guglielmelli P, et al. Mutations and prognosis in primary myelofibrosis. Leukemia 2013;27:1861-9.
-
(2013)
Leukemia
, vol.27
, pp. 1861-1869
-
-
Vannucchi, A.M.1
Lasho, T.L.2
Guglielmelli, P.3
-
22
-
-
84869786872
-
SRSF2 mutations in primary myelofibrosis: Significant clustering with IDH mutations and independent association with inferior overall and leukemia-free survival
-
Lasho TL, Jimma T, Finke CM, et al. SRSF2 mutations in primary myelofibrosis: significant clustering with IDH mutations and independent association with inferior overall and leukemia-free survival. Blood 2012;120:4168-71.
-
(2012)
Blood
, vol.120
, pp. 4168-4171
-
-
Lasho, T.L.1
Jimma, T.2
Finke, C.M.3
-
23
-
-
0027166881
-
Kaplan-Meier, marginal or conditional probability curves in summarizing competing risks failure time data?
-
Pepe MS, Mori M. Kaplan-Meier, marginal or conditional probability curves in summarizing competing risks failure time data? Stat Med 1993;12:737-51.
-
(1993)
Stat Med
, vol.12
, pp. 737-751
-
-
Pepe, M.S.1
Mori, M.2
-
24
-
-
0018080123
-
The analysis of failure times in the presence of competing risks
-
Prentice RL, Kalbfleisch JD, Peterson AV Jr, Flournoy N, Farewell VT, Breslow NE. The analysis of failure times in the presence of competing risks. Biometrics 1978;34:541-54.
-
(1978)
Biometrics
, vol.34
, pp. 541-554
-
-
Prentice, R.L.1
Kalbfleisch, J.D.2
Peterson Jr., A.V.3
Flournoy, N.4
Farewell, V.T.5
Breslow, N.E.6
-
25
-
-
70449486011
-
Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis
-
Malcovati L, Della Porta MG, Pietra D, et al. Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis. Blood 2009;114:3538-45.
-
(2009)
Blood
, vol.114
, pp. 3538-3545
-
-
Malcovati, L.1
Della Porta, M.G.2
Pietra, D.3
-
26
-
-
1542615163
-
Thrombocytosis
-
Schafer AI. Thrombocytosis. N Engl J Med 2004;350:1211-9.
-
(2004)
N Engl J Med
, vol.350
, pp. 1211-1219
-
-
Schafer, A.I.1
-
27
-
-
77949879489
-
ERp57 modulates STAT3 signaling from the lumen of the endoplasmic reticulum
-
Coe H, Jung J, Groenendyk J, Prins D, Michalak M. ERp57 modulates STAT3 signaling from the lumen of the endoplasmic reticulum. J Biol Chem 2010;285:6725-38.
-
(2010)
J Biol Chem
, vol.285
, pp. 6725-6738
-
-
Coe, H.1
Jung, J.2
Groenendyk, J.3
Prins, D.4
Michalak, M.5
-
28
-
-
45549108898
-
Activated Ca2+/cal?Mod?Ulin-dependent protein kinase IIgamma is a critical regulator of myeloid leukemia cell proliferation
-
Si J, Collins SJ. Activated Ca2+/cal?mod?ulin-dependent protein kinase IIgamma is a critical regulator of myeloid leukemia cell proliferation. Cancer Res 2008;68:3733-42.
-
(2008)
Cancer Res
, vol.68
, pp. 3733-3742
-
-
Si, J.1
Collins, S.J.2
-
29
-
-
84862879735
-
Hepatitis B virus-induced calreticulin protein is involved in IFN resistance
-
Yue X, Wang H, Zhao F, et al. Hepatitis B virus-induced calreticulin protein is involved in IFN resistance. J Immunol 2012;189:279-86.
-
(2012)
J Immunol
, vol.189
, pp. 279-286
-
-
Yue, X.1
Wang, H.2
Zhao, F.3
-
30
-
-
33344471678
-
V617F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis
-
Campbell PJ, Griesshammer M, Döhner K, et al. V617F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis. Blood 2006;107:2098-100.
-
(2006)
Blood
, vol.107
, pp. 2098-2100
-
-
Campbell, P.J.1
Griesshammer, M.2
Döhner, K.3
-
31
-
-
77950352432
-
A dynamic prognostic model to predict survival in primary myelofibrosis: A study by the IWG-MRT (International Working Group for Myeloproliferative Neoplasms Research and Treatment)
-
Passamonti F, Cervantes F, Vannucchi AM, et al. A dynamic prognostic model to predict survival in primary myelofibrosis: a study by the IWG-MRT (International Working Group for Myeloproliferative Neoplasms Research and Treatment). Blood 2010;115:1703-8.
-
(2010)
Blood
, vol.115
, pp. 1703-1708
-
-
Passamonti, F.1
Cervantes, F.2
Vannucchi, A.M.3
-
32
-
-
84865187605
-
A prognostic model to predict survival in 867 World Health Organization-defined essential thrombocythemia at diagnosis: A study by the International Working Group on Myelofibrosis Research and Treatment
-
Passamonti F, Thiele J, Girodon F, et al. A prognostic model to predict survival in 867 World Health Organization-defined essential thrombocythemia at diagnosis: a study by the International Working Group on Myelofibrosis Research and Treatment. Blood 2012;120:1197-201.
-
(2012)
Blood
, vol.120
, pp. 1197-1201
-
-
Passamonti, F.1
Thiele, J.2
Girodon, F.3
|