-
1
-
-
0001639195
-
Some speculations on the myeloproliferative syndromes
-
14820991
-
Dameshek W (1951) Some speculations on the myeloproliferative syndromes. Blood 6:372-375
-
(1951)
Blood
, vol.6
, pp. 372-375
-
-
Dameshek, W.1
-
2
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signaling causes polycythemia vera
-
15793561 10.1038/nature03546
-
James C, Ugo V, Le Couédic JP et al (2005) A unique clonal JAK2 mutation leading to constitutive signaling causes polycythemia vera. Nature 434:1144-1148
-
(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
-
15858187 10.1056/NEJMoa051113
-
Kralovics R, Passamonti F, Buser AS et al (2005) A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med 352:1779-1790
-
(2005)
N Engl J Med
, vol.352
, pp. 1779-1790
-
-
Kralovics, R.1
Passamonti, F.2
Buser, A.S.3
-
4
-
-
20244369569
-
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia and myeloid metaplasia with myelofibrosis
-
15837627 10.1016/j.ccr.2005.03.023
-
Levine RL, Wadleigh M, Cools J et al (2005) Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia and myeloid metaplasia with myelofibrosis. Cancer Cell 7:387-397
-
(2005)
Cancer Cell
, vol.7
, pp. 387-397
-
-
Levine, R.L.1
Wadleigh, M.2
Cools, J.3
-
5
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
-
15781101 10.1016/S0140-6736(05)71142-9
-
Baxter EJ, Scott LM, Campbell PJ et al (2005) Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet 365:1054-1061
-
(2005)
Lancet
, vol.365
, pp. 1054-1061
-
-
Baxter, E.J.1
Scott, L.M.2
Campbell, P.J.3
-
6
-
-
63449099560
-
JAK2 haplotype is a major risk factor for the development of myeloproliferrative neoplasms
-
19287382 10.1038/ng.334
-
Jones AV, Chase A, Silver RT et al (2009) JAK2 haplotype is a major risk factor for the development of myeloproliferrative neoplasms. Nat Genet 41:446-449
-
(2009)
Nat Genet
, vol.41
, pp. 446-449
-
-
Jones, A.V.1
Chase, A.2
Silver, R.T.3
-
7
-
-
63449134208
-
A common JAK2 haplotype confers susceptibility to myeloproliferative neoplasms
-
19287385 10.1038/ng.341
-
Olcaydu D, Harutyunyan A, Jäger R et al (2009) A common JAK2 haplotype confers susceptibility to myeloproliferative neoplasms. Nat Genet 41:450-454
-
(2009)
Nat Genet
, vol.41
, pp. 450-454
-
-
Olcaydu, D.1
Harutyunyan, A.2
Jäger, R.3
-
8
-
-
63449127583
-
A germline JAK2 SNP is associated with predisposition to the development of JAK2 (V617F)-positive myeloproliferative neoplasms
-
3676425 19287384 10.1038/ng.342
-
Kilpivaara O, Mukherjee S, Schram AM et al (2009) A germline JAK2 SNP is associated with predisposition to the development of JAK2 (V617F)-positive myeloproliferative neoplasms. Nat Genet 41:455-459
-
(2009)
Nat Genet
, vol.41
, pp. 455-459
-
-
Kilpivaara, O.1
Mukherjee, S.2
Schram, A.M.3
-
9
-
-
74249123815
-
JAK2 germline genetic variation affects disease susceptibility in primary myelofibrosis regardless of V617F mutational status: Nullizygosity for the JAK2 46/1 haplotype is associated with inferior survival
-
19847199 10.1038/leu.2009.225
-
Tefferi A, Lasho TL, Patnaik MM et al (2010) JAK2 germline genetic variation affects disease susceptibility in primary myelofibrosis regardless of V617F mutational status: nullizygosity for the JAK2 46/1 haplotype is associated with inferior survival. Leukemia 24:105-109
-
(2010)
Leukemia
, vol.24
, pp. 105-109
-
-
Tefferi, A.1
Lasho, T.L.2
Patnaik, M.M.3
-
10
-
-
84881481843
-
JAK2V617F allele burden, JAK2 46/1 haplotype and clinical features of Chinese with myeloproliferative neoplasms
-
23337930 10.1038/leu.2013.21
-
Wang J, Xu Z, Liu L et al (2013) JAK2V617F allele burden, JAK2 46/1 haplotype and clinical features of Chinese with myeloproliferative neoplasms. Leukemia 27:1763-1767
-
(2013)
Leukemia
, vol.27
, pp. 1763-1767
-
-
Wang, J.1
Xu, Z.2
Liu, L.3
-
11
-
-
77955713863
-
Frequency and clinical correlates of JAK2 46/1 (GGCC) haplotype in primary myelofibrosis
-
20520633 10.1038/leu.2010.126
-
Guglielmelli P, Biamonte F, Spolverini A et al (2010) Frequency and clinical correlates of JAK2 46/1 (GGCC) haplotype in primary myelofibrosis. Leukemia 24:1533-1537
-
(2010)
Leukemia
, vol.24
, pp. 1533-1537
-
-
Guglielmelli, P.1
Biamonte, F.2
Spolverini, A.3
-
12
-
-
34548042964
-
Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: Recommendations from an ad hoc international expert panel
-
17488875 10.1182/blood-2007-04-083501
-
Tefferi A, Thiele J, Orazi A et al (2007) Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: Recommendations from an ad hoc international expert panel. Blood 110:1092-1097
-
(2007)
Blood
, vol.110
, pp. 1092-1097
-
-
Tefferi, A.1
Thiele, J.2
Orazi, A.3
-
13
-
-
0032697583
-
Initial (prefibrotic) stages of idiopathic (primary) myelofibrosis (IMF) - A clinicopathological study
-
10557047 10.1038/sj.leu.2401553
-
Thiele J, Kvasnicka HM, Boeltken B, Zankovich R, Diehl V, Fischer R (1999) Initial (prefibrotic) stages of idiopathic (primary) myelofibrosis (IMF) - a clinicopathological study. Leukemia 13:1741-1748
-
(1999)
Leukemia
, vol.13
, pp. 1741-1748
-
-
Thiele, J.1
Kvasnicka, H.M.2
Boeltken, B.3
Zankovich, R.4
Diehl, V.5
Fischer, R.6
-
14
-
-
38049188368
-
Bone marrow pathology in essential thrombocythemia: Interobserver reliability and utility for identifying disease subtypes
-
17885079 10.1182/blood-2007-05-091850
-
Wilkins BS, Erber WN, Bareford D et al (2008) Bone marrow pathology in essential thrombocythemia: interobserver reliability and utility for identifying disease subtypes. Blood 111:60-70
-
(2008)
Blood
, vol.111
, pp. 60-70
-
-
Wilkins, B.S.1
Erber, W.N.2
Bareford, D.3
-
15
-
-
39149112773
-
Proposed criteria for the diagnosis of post-polycythemia vera and post-essential thrombocythemia myelofibrosis: A consensus statement from the International Working Group for Myelofibrosis Research and Treatment
-
10.1038/sj.leu.2404915
-
Barosi G, Mesa RA, Thiele J et al (2008) Proposed criteria for the diagnosis of post-polycythemia vera and post-essential thrombocythemia myelofibrosis: a consensus statement from the International Working Group for Myelofibrosis Research and Treatment. Leukemia 22:438-439
-
(2008)
Leukemia
, vol.22
, pp. 438-439
-
-
Barosi, G.1
Mesa, R.A.2
Thiele, J.3
-
16
-
-
63849328927
-
A new prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment
-
18988864 10.1182/blood-2008-07-170449
-
Cervantes F, Dupriez B, Pereira A et al (2009) A new prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment. Blood 113:2895-3001
-
(2009)
Blood
, vol.113
, pp. 2895-3001
-
-
Cervantes, F.1
Dupriez, B.2
Pereira, A.3
-
17
-
-
33744490974
-
Expression of Jak2V617F causes a polycythemia vera-like disease with associated myelofibrosis in a murine bone marrow transplant model
-
1895786 16478879 10.1182/blood-2005-12-4824
-
Wernig G, Mercher T, Okabe R et al (2006) Expression of Jak2V617F causes a polycythemia vera-like disease with associated myelofibrosis in a murine bone marrow transplant model. Blood 107:4274-4281
-
(2006)
Blood
, vol.107
, pp. 4274-4281
-
-
Wernig, G.1
Mercher, T.2
Okabe, R.3
-
18
-
-
0242493826
-
Clonal hematopoiesis in familial polycythemia vera suggests the involvement of multiple mutational events in the early pathogenesis of the disease
-
12829587 10.1182/blood-2003-03-0885
-
Kralovics R, Stockton DW, Prchal JT (2003) Clonal hematopoiesis in familial polycythemia vera suggests the involvement of multiple mutational events in the early pathogenesis of the disease. Blood 102:3793-3796
-
(2003)
Blood
, vol.102
, pp. 3793-3796
-
-
Kralovics, R.1
Stockton, D.W.2
Prchal, J.T.3
-
19
-
-
33745623666
-
Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders
-
10.1182/blood-2005-12-4852
-
Bellanné-Chantelot Chaumarel I, Labopin M et al (2006) Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders. Blood 108:346-352
-
(2006)
Blood
, vol.108
, pp. 346-352
-
-
Bellanné-Chantelot Chaumarel, I.1
Labopin, M.2
-
20
-
-
84984760593
-
Somatic and germline genetics at the JAK2 locus
-
19338077 10.1038/ng0409-385
-
Campbell PJ (2009) Somatic and germline genetics at the JAK2 locus. Nat Genet 41:385-386
-
(2009)
Nat Genet
, vol.41
, pp. 385-386
-
-
Campbell, P.J.1
-
21
-
-
70350111160
-
The 'GGCC' haplotype of JAK2 confers susceptibility to JAK2 exon 12 mutation-positive polycythemia vera
-
19440215 10.1038/leu.2009.110
-
Olcaydu D, Skoda RC, Looser R et al (2009) The 'GGCC' haplotype of JAK2 confers susceptibility to JAK2 exon 12 mutation-positive polycythemia vera. Leukemia 23:1924-1926
-
(2009)
Leukemia
, vol.23
, pp. 1924-1926
-
-
Olcaydu, D.1
Skoda, R.C.2
Looser, R.3
-
22
-
-
74249121458
-
The JAK2 46/1 haplotype confers susceptibility to essential thrombocythemia regardless of JAK2V617F mutational status - Clinical correlates in a study of 226 consecutive patients
-
19847198 10.1038/leu.2009.226
-
Pardanani A, Lasho TL, Finke CM et al (2010) The JAK2 46/1 haplotype confers susceptibility to essential thrombocythemia regardless of JAK2V617F mutational status - clinical correlates in a study of 226 consecutive patients. Leukemia 24:110-114
-
(2010)
Leukemia
, vol.24
, pp. 110-114
-
-
Pardanani, A.1
Lasho, T.L.2
Finke, C.M.3
-
23
-
-
77953925295
-
The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms
-
3145114 20304805 10.1182/blood-2009-08-236448
-
Jones AV, Campbell PJ, Beer PA et al (2010) The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms. Blood 115:4517-4523
-
(2010)
Blood
, vol.115
, pp. 4517-4523
-
-
Jones, A.V.1
Campbell, P.J.2
Beer, P.A.3
-
24
-
-
77950921110
-
MPL mutation effect on JAK2 46/1 haplotype frequency in JAK2V617F-negative myeloproliferative neoplasms
-
20111067 10.1038/leu.2010.1
-
Patnaik MM, Lasho TL, Finke CM et al (2010) MPL mutation effect on JAK2 46/1 haplotype frequency in JAK2V617F-negative myeloproliferative neoplasms. Leukemia 24:859-860
-
(2010)
Leukemia
, vol.24
, pp. 859-860
-
-
Patnaik, M.M.1
Lasho, T.L.2
Finke, C.M.3
-
25
-
-
84865263436
-
Improving survival trends in primary myelofibrosis: An international study
-
22826273 10.1200/JCO.2012.42.0240
-
Cervantes F, Dupriez B, Passamonti F et al (2012) Improving survival trends in primary myelofibrosis: an international study. J Clin Oncol 30:2981-2987
-
(2012)
J Clin Oncol
, vol.30
, pp. 2981-2987
-
-
Cervantes, F.1
Dupriez, B.2
Passamonti, F.3
-
26
-
-
77950352432
-
A dynamic prognostic model to predict survival in primary myelofibrosis: A study by the International Working Group for Myeloproliferative Neoplasms Research and Treatment
-
20008785 10.1182/blood-2009-09-245837
-
Passamonti F, Cervantes F, Vannucchi A et al (2010) A dynamic prognostic model to predict survival in primary myelofibrosis: a study by the International Working Group for Myeloproliferative Neoplasms Research and Treatment. Blood 115:1703-1708
-
(2010)
Blood
, vol.115
, pp. 1703-1708
-
-
Passamonti, F.1
Cervantes, F.2
Vannucchi, A.3
-
27
-
-
79952087335
-
DIPSS-Plus: A refined dynamic international prognostic scoring system (DIPSS) for primary myelofibrosis that incorporates prognostic information from karyotype, platelet count and transfusion status
-
21149668 10.1200/JCO.2010.32.2446
-
Gangat N, Pardanani A, Hanson CA et al (2011) DIPSS-Plus: a refined dynamic international prognostic scoring system (DIPSS) for primary myelofibrosis that incorporates prognostic information from karyotype, platelet count and transfusion status. J Clin Oncol 29:392-397
-
(2011)
J Clin Oncol
, vol.29
, pp. 392-397
-
-
Gangat, N.1
Pardanani, A.2
Hanson, C.A.3
-
28
-
-
84883742034
-
Mutations and prognosis in primary myelofibrosis
-
23619563 10.1038/leu.2013.119
-
Vannucchi AM, Lasho TL, Guglielmelli P et al (2013) Mutations and prognosis in primary myelofibrosis. Leukemia 27(9):1861-1869
-
(2013)
Leukemia
, vol.27
, Issue.9
, pp. 1861-1869
-
-
Vannucchi, A.M.1
Lasho, T.L.2
Guglielmelli, P.3
-
29
-
-
42449124578
-
Low JAK2V617F allele burden in primary myelofibrosis, compared to either a higher allele burden or unmutated status, is associated with inferior overall and leukemia-free survival
-
18216871 10.1038/sj.leu.2405097
-
Tefferi A, Lasho TL, Huang J et al (2008) Low JAK2V617F allele burden in primary myelofibrosis, compared to either a higher allele burden or unmutated status, is associated with inferior overall and leukemia-free survival. Leukemia 22:756-761
-
(2008)
Leukemia
, vol.22
, pp. 756-761
-
-
Tefferi, A.1
Lasho, T.L.2
Huang, J.3
-
30
-
-
70349580685
-
Identification of patients with poorer survival in primary myelofibrosis based on the burden of JAK2V617F mutated allele
-
19549988 10.1182/blood-2009-04-216044
-
Guglielmelli P, Barosi G, Specchia G et al (2009) Identification of patients with poorer survival in primary myelofibrosis based on the burden of JAK2V617F mutated allele. Blood 114:1477-1483
-
(2009)
Blood
, vol.114
, pp. 1477-1483
-
-
Guglielmelli, P.1
Barosi, G.2
Specchia, G.3
|