-
1
-
-
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;352:1779-1790.
-
(2005)
N Engl J Med
, vol.352
, pp. 1779-1790
-
-
Kralovics, R.1
Passamonti, F.2
Buser, A.S.3
-
2
-
-
33748684367
-
The JAK2-V617F mutation is frequently present at diagnosis in patients with essential thrombocythemia and polycythemia vera
-
Lippert E, Boissinot M, Kralovics R, et al. The JAK2-V617F mutation is frequently present at diagnosis in patients with essential thrombocythemia and polycythemia vera. Blood. 2006;108:1865-1867.
-
(2006)
Blood
, vol.108
, pp. 1865-1867
-
-
Lippert, E.1
Boissinot, M.2
Kralovics, R.3
-
3
-
-
27744606173
-
JAK2 mutation in essential thrombocythaemia: Clinical associations and long-term prognostic relevance
-
Wolanskyj AP, Lasho TL, Schwager SM, et al. JAK2 mutation in essential thrombocythaemia: clinical associations and long-term prognostic relevance. Br J Haematol. 2005;131:208-213.
-
(2005)
Br J Haematol
, vol.131
, pp. 208-213
-
-
Wolanskyj, A.P.1
Lasho, T.L.2
Schwager, S.M.3
-
4
-
-
28244442441
-
Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: A prospective study
-
Campbell PJ, Scott LM, Buck G, et al. Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study. Lancet. 2005;366:1945-1953.
-
(2005)
Lancet
, vol.366
, pp. 1945-1953
-
-
Campbell, P.J.1
Scott, L.M.2
Buck, G.3
-
5
-
-
33746858555
-
JAK2V617F mutation in platelets from essential thrombocythemia patients: Correlation with clinical features and analysis of STAT5 phosphorylation status
-
Heller PG, Lev PR, Salim JP, et al. JAK2V617F mutation in platelets from essential thrombocythemia patients: correlation with clinical features and analysis of STAT5 phosphorylation status. Eur J Haematol. 2006;77:210-216.
-
(2006)
Eur J Haematol
, vol.77
, pp. 210-216
-
-
Heller, P.G.1
Lev, P.R.2
Salim, J.P.3
-
6
-
-
27144443646
-
Clinical implications of the JAK2 V617F mutation in essential thrombocythemia
-
Antonioli E, Guglielmelli P, Pancrazzi A, et al. Clinical implications of the JAK2 V617F mutation in essential thrombocythemia. Leukemia. 2005;19:1847-1849.
-
(2005)
Leukemia
, vol.19
, pp. 1847-1849
-
-
Antonioli, E.1
Guglielmelli, P.2
Pancrazzi, A.3
-
7
-
-
33644826144
-
The presence of the JAK2 V617F mutation is associated with a higher haemoglobin and increased risk of thrombosis in essential thrombocythaemia
-
Cheung B, Radia D, Pantelidis P, Yadegarfar G, Harrison C. The presence of the JAK2 V617F mutation is associated with a higher haemoglobin and increased risk of thrombosis in essential thrombocythaemia. Br J Haematol. 2006;132:244-245.
-
(2006)
Br J Haematol
, vol.132
, pp. 244-245
-
-
Cheung, B.1
Radia, D.2
Pantelidis, P.3
Yadegarfar, G.4
Harrison, C.5
-
8
-
-
33947262701
-
Leukocytosis is a risk factor for thrombosis in essential thrombocythemia: Interaction with treatment, standard risk factors and Jak2 mutation status
-
Carobbio A, Finazzi G, Guerini V et al. Leukocytosis is a risk factor for thrombosis in essential thrombocythemia: interaction with treatment, standard risk factors and Jak2 mutation status. Blood. 2007;109:2310-2313.
-
(2007)
Blood
, vol.109
, pp. 2310-2313
-
-
Carobbio, A.1
Finazzi, G.2
Guerini, V.3
-
9
-
-
33645400695
-
X-inactivation-based clonality analysis and quantitative JAK2V617F assessment reveal a strong association between clonality and JAK2V617F in PV but not ET/MMM, and identifies a subset of JAK2V617F-negative ET and MMM patients with clonal hematopoiesis
-
Levine RL, Belisle C, Wadleigh M, et al. X-inactivation-based clonality analysis and quantitative JAK2V617F assessment reveal a strong association between clonality and JAK2V617F in PV but not ET/MMM, and identifies a subset of JAK2V617F-negative ET and MMM patients with clonal hematopoiesis. Blood. 2006;107:4139-4141.
-
(2006)
Blood
, vol.107
, pp. 4139-4141
-
-
Levine, R.L.1
Belisle, C.2
Wadleigh, M.3
-
10
-
-
30844456807
-
WHO histological classification of chronic myeloproliferative diseases
-
Jaffe ES, Harris NL, Stein H, Vardiman JW, editors, Lyon, France: International Agency for Research on Cancer (IARC) Press;
-
Vardiman JW, Brunning RD, Harris NL. WHO histological classification of chronic myeloproliferative diseases. In: Jaffe ES, Harris NL, Stein H, Vardiman JW, editors. World Health Organization Classification of Tumours: Tumours of the Haematopoietic and Lymphoid Tissues. Lyon, France: International Agency for Research on Cancer (IARC) Press; 2001:17-44.
-
(2001)
World Health Organization Classification of Tumours: Tumours of the Haematopoietic and Lymphoid Tissues
, pp. 17-44
-
-
Vardiman, J.W.1
Brunning, R.D.2
Harris, N.L.3
-
11
-
-
32944477304
-
Concomitant neutrophil JAK2 mutation screening and PRV-1 expression analysis in myeloproliferative disorders and secondary polycythaemia
-
Tefferi A, Sirhan S, Lasho TL, et al. Concomitant neutrophil JAK2 mutation screening and PRV-1 expression analysis in myeloproliferative disorders and secondary polycythaemia. Br J Haematol. 2005;131:166-171.
-
(2005)
Br J Haematol
, vol.131
, pp. 166-171
-
-
Tefferi, A.1
Sirhan, S.2
Lasho, T.L.3
-
12
-
-
33744505451
-
Prevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome
-
Patel RK, Lea NC, Heneghan MA, et al. Prevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome. Gastroenterology. 2006;130:2031-2038.
-
(2006)
Gastroenterology
, vol.130
, pp. 2031-2038
-
-
Patel, R.K.1
Lea, N.C.2
Heneghan, M.A.3
-
13
-
-
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
-
14
-
-
20244369569
-
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
-
Levine RL, Wadleigh M, Cools J, et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell. 2005;7:387-397.
-
(2005)
Cancer Cell
, vol.7
, pp. 387-397
-
-
Levine, R.L.1
Wadleigh, M.2
Cools, J.3
-
15
-
-
31444439623
-
Detection of JAK2 V617F as a first intention diagnostic test for erythrocytosis
-
James C, Delhommeau F, Marzac C, et al. Detection of JAK2 V617F as a first intention diagnostic test for erythrocytosis. Leukemia. 2006;20:350-353.
-
(2006)
Leukemia
, vol.20
, pp. 350-353
-
-
James, C.1
Delhommeau, F.2
Marzac, C.3
-
16
-
-
33645740979
-
Minimal molecular response in polycythemia vera patients treated with imatinib or interferon alpha
-
Jones AV Silver RT, Waghorn K, et al. Minimal molecular response in polycythemia vera patients treated with imatinib or interferon alpha. Blood. 2006;107:3339-3341.
-
(2006)
Blood
, vol.107
, pp. 3339-3341
-
-
Jones, A.V.1
Silver, R.T.2
Waghorn, K.3
-
17
-
-
32144461605
-
Essential thrombocythemia beyond the first decade: Life expectancy, long-term complication rates, and prognostic factors
-
Wolanskyj AR Schwager SM, McClure RF, Larson DR, Tefferi A. Essential thrombocythemia beyond the first decade: life expectancy, long-term complication rates, and prognostic factors. Mayo Clin Proc. 2006;81:159-166.
-
(2006)
Mayo Clin Proc
, vol.81
, pp. 159-166
-
-
Wolanskyj, A.R.1
Schwager, S.M.2
McClure, R.F.3
Larson, D.R.4
Tefferi, A.5
-
18
-
-
33947208087
-
Leukocytosis as a major thrombotic risk factor in patients with polycythemia vera
-
Landolfi R, Di Gennaro L, Barbui T, et al. Leukocytosis as a major thrombotic risk factor in patients with polycythemia vera. Blood. 2007;109:2446-2452.
-
(2007)
Blood
, vol.109
, pp. 2446-2452
-
-
Landolfi, R.1
Di Gennaro, L.2
Barbui, T.3
-
19
-
-
34249007698
-
Influence of the Jak2V617F mutational load at diagnosis on major clinical aspects in patients with polycythemia vera
-
Abstract 5
-
Vannucchi AM, Antonioli E, Guglielmelli P, et al. Influence of the Jak2V617F mutational load at diagnosis on major clinical aspects in patients with polycythemia vera. Blood. 2006;108. Abstract 5.
-
(2006)
Blood
, pp. 108
-
-
Vannucchi, A.M.1
Antonioli, E.2
Guglielmelli, P.3
-
20
-
-
31544477194
-
The clinical phenotype of wild-type, heterozygous, and homozygous JAK2V617F in polycythemia vera
-
Tefferi A, Lasho TL, Schwager SM, et al. The clinical phenotype of wild-type, heterozygous, and homozygous JAK2V617F in polycythemia vera. Cancer. 2006;106:631-635.
-
(2006)
Cancer
, vol.106
, pp. 631-635
-
-
Tefferi, A.1
Lasho, T.L.2
Schwager, S.M.3
-
21
-
-
33846883073
-
Long-term serial analysis of X-chromosome inactivation patterns and JAK2 V617F mutant levels in patients with essential thrombocythemia show that minor mutant-positive clones can remain stable for many years
-
Gale RE, Allen AJ, Nash MJ, Linch DC. Long-term serial analysis of X-chromosome inactivation patterns and JAK2 V617F mutant levels in patients with essential thrombocythemia show that minor mutant-positive clones can remain stable for many years. Blood. 2007;109:1241-1243.
-
(2007)
Blood
, vol.109
, pp. 1241-1243
-
-
Gale, R.E.1
Allen, A.J.2
Nash, M.J.3
Linch, D.C.4
-
22
-
-
27244432586
-
Mutation studies in CD3+, CD19+ and CD34+ cell fractions in myeloproliferative disorders with homozygous JAK2(V617F) in granulocytes
-
Lasho TL, Mesa R, Gilliland DG, Tefferi A. Mutation studies in CD3+, CD19+ and CD34+ cell fractions in myeloproliferative disorders with homozygous JAK2(V617F) in granulocytes. Br J Haematol. 2005;130:797-799.
-
(2005)
Br J Haematol
, vol.130
, pp. 797-799
-
-
Lasho, T.L.1
Mesa, R.2
Gilliland, D.G.3
Tefferi, A.4
|