-
1
-
-
0036786901
-
The World Health Organization (WHO) classification of the myeloid neoplasms
-
Vardiman JW, Harris NL, Brunning RD: The World Health Organization (WHO) classification of the myeloid neoplasms. Blood 2002, 100:2292-2302
-
(2002)
Blood
, vol.100
, pp. 2292-2302
-
-
Vardiman, J.W.1
Harris, N.L.2
Brunning, R.D.3
-
2
-
-
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
-
Tefferi A, Thiele J, Orazi A, Kvasnicka HM, Barbui T, Hanson CA, Barosi G, Verstovsek S, Birgegard G, Mesa R, Reilly JT, Gisslinger H, Vannucchi AM, Cervantes F, Finazzi G, Hoffman R, Gilliland DG, Bloomfield CD, Vardiman JW: 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 2007, 110:1092-1097
-
(2007)
Blood
, vol.110
, pp. 1092-1097
-
-
Tefferi, A.1
Thiele, J.2
Orazi, A.3
Kvasnicka, H.M.4
Barbui, T.5
Hanson, C.A.6
Barosi, G.7
Verstovsek, S.8
Birgegard, G.9
Mesa, R.10
Reilly, J.T.11
Gisslinger, H.12
Vannucchi, A.M.13
Cervantes, F.14
Finazzi, G.15
Hoffman, R.16
Gilliland, D.G.17
Bloomfield, C.D.18
Vardiman, J.W.19
-
3
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
-
James C, Ugo V, Le Couedic JP, Staerk J, Delhommeau F, Lacout C, Garcon L, Raslova H, Berger R, Bennaceur-Griscelli A, Villeval JL, Constantinescu SN, Casadevall N, Vainchenker W: 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
Staerk, J.4
Delhommeau, F.5
Lacout, C.6
Garcon, L.7
Raslova, H.8
Berger, R.9
Bennaceur-Griscelli, A.10
Villeval, J.L.11
Constantinescu, S.N.12
Casadevall, N.13
Vainchenker, W.14
-
4
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
-
Baxter EJ, Scott LM, Campbell PJ, East C, Fourouclas N, Swanton S, Vassiliou GS, Bench AJ, Boyd EM, Curtin N, Scott MA, Erber WN, Green AR: 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
East, C.4
Fourouclas, N.5
Swanton, S.6
Vassiliou, G.S.7
Bench, A.J.8
Boyd, E.M.9
Curtin, N.10
Scott, M.A.11
Erber, W.N.12
Green, A.R.13
-
5
-
-
20244369569
-
Activating mutation in the tyrosine kinase JAK2 In polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
-
Levine RL, Wadleigh M, Cools J, Ebert BL, Wernig G, Huntly BJ, Boggon TJ, Wlodarska I, Clark JJ, Moore S, Adelsperger J, Koo S, Lee JC, Gabriel S, Mercher T, D'Andrea A, Frohling S, Dohner K, Marynen P, Vandenberghe P, Mesa RA, Tefferi A, Griffin JD, Eck MJ, Sellers WR, Meyerson M, Golub TR, Lee SJ, Gilliland DG: 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
Ebert, B.L.4
Wernig, G.5
Huntly, B.J.6
Boggon, T.J.7
Wlodarska, I.8
Clark, J.J.9
Moore, S.10
Adelsperger, J.11
Koo, S.12
Lee, J.C.13
Gabriel, S.14
Mercher, T.15
D'Andrea, A.16
Frohling, S.17
Dohner, K.18
Marynen, P.19
Vandenberghe, P.20
Mesa, R.A.21
Tefferi, A.22
Griffin, J.D.23
Eck, M.J.24
Sellers, W.R.25
Meyerson, M.26
Golub, T.R.27
Lee, S.J.28
Gilliland, D.G.29
more..
-
6
-
-
17644424955
-
A gain-of-function mutation of JAK2 In myeloproliferative disorders
-
Kralovics R, Passamonti F, Buser AS, Teo SS, Tiedt R, Passweg JR, Tichelli A, Cazzola M, Skoda RC: 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
Teo, S.S.4
Tiedt, R.5
Passweg, J.R.6
Tichelli, A.7
Cazzola, M.8
Skoda, R.C.9
-
7
-
-
33846660947
-
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis
-
Scott LM, Tong W, Levine RL, Scott MA, Beer PA, Stratton MR, Futreal PA, Erber WN, McMullin MF, Harrison CN, Warren AJ, Gilliland DG, Lodish HF, Green AR: JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis. N Engl J Med 2007, 356:459-468
-
(2007)
N Engl J Med
, vol.356
, pp. 459-468
-
-
Scott, L.M.1
Tong, W.2
Levine, R.L.3
Scott, M.A.4
Beer, P.A.5
Stratton, M.R.6
Futreal, P.A.7
Erber, W.N.8
McMullin, M.F.9
Harrison, C.N.10
Warren, A.J.11
Gilliland, D.G.12
Lodish, H.F.13
Green, A.R.14
-
8
-
-
0036191941
-
Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera
-
Kralovics R, Guan Y, Prchal JT: Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera. Exp Hematol 2002, 30:229-236
-
(2002)
Exp Hematol
, vol.30
, pp. 229-236
-
-
Kralovics, R.1
Guan, Y.2
Prchal, J.T.3
-
9
-
-
34547953018
-
Clinical profile of homozygous JAK2V617F mutation in patients with polycythemia vera or essential thrombocythemia
-
Vannucchi AM, Antonioli E, Guglielmelli P, Rambaldi A, Barosi G, Marchioli R, Marfisi RM, Finazzi G, Guerini V, Fabris F, Randi ML, De Stefano V, Caberlon S, Tafuri A, Ruggeri M, Specchia G, Liso V, Rossi E, Pogliani E, Gugliotta L, Bosi A, Barbui T: Clinical profile of homozygous JAK2V617F mutation in patients with polycythemia vera or essential thrombocythemia. Blood 2007, 110:840-846
-
(2007)
Blood
, vol.110
, pp. 840-846
-
-
Vannucchi, A.M.1
Antonioli, E.2
Guglielmelli, P.3
Rambaldi, A.4
Barosi, G.5
Marchioli, R.6
Marfisi, R.M.7
Finazzi, G.8
Guerini, V.9
Fabris, F.10
Randi, M.L.11
De Stefano, V.12
Caberlon, S.13
Tafuri, A.14
Ruggeri, M.15
Specchia, G.16
Liso, V.17
Rossi, E.18
Pogliani, E.19
Gugliotta, L.20
Bosi, A.21
Barbui, T.22
more..
-
10
-
-
31544477194
-
The clinical phenotype of wild-type, heterozygous, and homozygous JAK2V617F in polycythemia vera
-
Tefferi A, LashoTL, SchwagerSM, Strand JS, Elliott M, Mesa R, Li CY, Wadleigh M, Lee SJ, Gilliland DG: 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
Strand, J.S.4
Elliott, M.5
Mesa, R.6
Li, C.Y.7
Wadleigh, M.8
Lee, S.J.9
Gilliland, D.G.10
-
11
-
-
34548136101
-
Prospective identification of high-risk polycythemia vera patients based on JAK2(V617F) allele burden
-
Vannucchi AM, Antonioli E, Guglielmelli P, Longo G, Pancrazzi A, Ponziani V, Bogani C, Ferrini PR, Rambaldi A, Guerini V, Bosi A, Barbui T: Prospective identification of high-risk polycythemia vera patients based on JAK2(V617F) allele burden. Leukemia 2007, 21:1952-1959
-
(2007)
Leukemia
, vol.21
, pp. 1952-1959
-
-
Vannucchi, A.M.1
Antonioli, E.2
Guglielmelli, P.3
Longo, G.4
Pancrazzi, A.5
Ponziani, V.6
Bogani, C.7
Ferrini, P.R.8
Rambaldi, A.9
Guerini, V.10
Bosi, A.11
Barbui, T.12
-
12
-
-
37049039725
-
JAK2 V617F mutational status predicts progression to large splenomegaly and leukemic transformation in primary myelofibrosis
-
Barosi G, Bergamaschi G, Marchetti M, Vannucchi AM, Guglielmelli P, Antonioli E, Massa M, Rosti V, Campanelli R, Villani L, Viarengo G, Gattoni E, Gerli G, Specchia G, Tinelli C, Rambaldi A, Barbui T: JAK2 V617F mutational status predicts progression to large splenomegaly and leukemic transformation in primary myelofibrosis. Blood 2007, 110:4030-4036
-
(2007)
Blood
, vol.110
, pp. 4030-4036
-
-
Barosi, G.1
Bergamaschi, G.2
Marchetti, M.3
Vannucchi, A.M.4
Guglielmelli, P.5
Antonioli, E.6
Massa, M.7
Rosti, V.8
Campanelli, R.9
Villani, L.10
Viarengo, G.11
Gattoni, E.12
Gerli, G.13
Specchia, G.14
Tinelli, C.15
Rambaldi, A.16
Barbui, T.17
-
13
-
-
33845755386
-
Polycythemia vera is not initiated by JAK2V617F mutation
-
Nussenzveig RH, Swierczek SI, Jelinek J, Gaikwad A, Liu E, Verstovsek S, Prchal JF, Prchal JT: Polycythemia vera is not initiated by JAK2V617F mutation. Exp Hematol 2007, 35:32-38
-
(2007)
Exp Hematol
, vol.35
, pp. 32-38
-
-
Nussenzveig, R.H.1
Swierczek, S.I.2
Jelinek, J.3
Gaikwad, A.4
Liu, E.5
Verstovsek, S.6
Prchal, J.F.7
Prchal, J.T.8
-
14
-
-
27144443646
-
Clinical implications of the JAK2 V617F mutation in essential thrombocythemia
-
Antonioli E, Guglielmelli P, Pancrazzi A, Bogani C, Verrucci M, Ponziani V, Longo G, Bosi A, Vannucchi AM: 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
Bogani, C.4
Verrucci, M.5
Ponziani, V.6
Longo, G.7
Bosi, A.8
Vannucchi, A.M.9
-
15
-
-
33846883073
-
Long-term serial analysis of X-chromosome inactivation patterns and JAK2 V617F mutant levels in patients with essential thrombocythemia show that minor mutantpositive 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 mutantpositive 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
-
16
-
-
34548836555
-
X-linked clonality testing: Interpretation and limitations
-
Chen GL, Prchal JT: X-linked clonality testing: interpretation and limitations. Blood 2007, 110:1411-1419
-
(2007)
Blood
, vol.110
, pp. 1411-1419
-
-
Chen, G.L.1
Prchal, J.T.2
-
17
-
-
33746437130
-
MPLW515L Is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia
-
Pikman Y, Lee BH, Mercher T, McDowell E, Ebert BL, Gozo M, Cuker A, Wernig G, Moore S, Galinsky I, DeAngelo DJ, Clark JJ, Lee SJ, Golub TR, Wadleigh M, Gilliland DG, Levine RL: MPLW515L Is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia. PLoS Med 2006, 3:e270
-
(2006)
PLoS Med
, vol.3
-
-
Pikman, Y.1
Lee, B.H.2
Mercher, T.3
McDowell, E.4
Ebert, B.L.5
Gozo, M.6
Cuker, A.7
Wernig, G.8
Moore, S.9
Galinsky, I.10
DeAngelo, D.J.11
Clark, J.J.12
Lee, S.J.13
Golub, T.R.14
Wadleigh, M.15
Gilliland, D.G.16
Levine, R.L.17
-
18
-
-
31044439372
-
The molecular mechanisms that control thrombopoiesis
-
Kaushansky K: The molecular mechanisms that control thrombopoiesis. J Clin Invest 2005, 115:3339-3347
-
(2005)
J Clin Invest
, vol.115
, pp. 3339-3347
-
-
Kaushansky, K.1
-
19
-
-
0030718597
-
High thrombopoietin production by hematopoietic cells induces a fatal myeloproliferative syndrome in mice
-
Villeval JL, Cohen-Solal K, Tulliez M, Giraudier S, Guichard J, Burstein SA, Cramer EM, Vainchenker W, Wendling F: High thrombopoietin production by hematopoietic cells induces a fatal myeloproliferative syndrome in mice. Blood 1997, 90:4369-4383
-
(1997)
Blood
, vol.90
, pp. 4369-4383
-
-
Villeval, J.L.1
Cohen-Solal, K.2
Tulliez, M.3
Giraudier, S.4
Guichard, J.5
Burstein, S.A.6
Cramer, E.M.7
Vainchenker, W.8
Wendling, F.9
-
20
-
-
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, Chen Y, Fletcher F, Hawley RG, McNiece IK: 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
Chen, Y.4
Fletcher, F.5
Hawley, R.G.6
McNiece, I.K.7
-
21
-
-
33344455687
-
An amphipathic motif at the transmembrane-cytoplasmic junction prevents autonomous activation of the thrombopoietin receptor
-
Staerk J, Lacout C, Sato T, Smith SO, Vainchenker W, Constantinescu SN: An amphipathic motif at the transmembrane-cytoplasmic junction prevents autonomous activation of the thrombopoietin receptor. Blood 2006, 107:1864-1871
-
(2006)
Blood
, vol.107
, pp. 1864-1871
-
-
Staerk, J.1
Lacout, C.2
Sato, T.3
Smith, S.O.4
Vainchenker, W.5
Constantinescu, S.N.6
-
22
-
-
34247473543
-
Haematopoietic cell lineage distribution of MPLW515L/K mutations in patients with idiopathic myelofibrosis
-
Hu WY, Zhao Y, Ishii T, Sozer S, Shi J, Zhang W, Bruno E, Hoffman R, Xu M: Haematopoietic cell lineage distribution of MPLW515L/K mutations in patients with idiopathic myelofibrosis. Br J Haematol 2007, 137:378-379
-
(2007)
Br J Haematol
, vol.137
, pp. 378-379
-
-
Hu, W.Y.1
Zhao, Y.2
Ishii, T.3
Sozer, S.4
Shi, J.5
Zhang, W.6
Bruno, E.7
Hoffman, R.8
Xu, M.9
-
23
-
-
34548786770
-
Demonstration of MPLW515K, but not JAK2V617F, in in vitro expanded CD4+ T lymphocytes
-
Pardanani A, Lasho TL, Finke C, Markovic SN, Tefferi A: Demonstration of MPLW515K, but not JAK2V617F, in in vitro expanded CD4+ T lymphocytes. Leukemia 2007, 21:2206-2207
-
(2007)
Leukemia
, vol.21
, pp. 2206-2207
-
-
Pardanani, A.1
Lasho, T.L.2
Finke, C.3
Markovic, S.N.4
Tefferi, A.5
-
24
-
-
36348999273
-
Evidence for MPL W515L/K mutations in hematopoietic stem cells in primitive myelofibrosis
-
Chaligne R, James C, Tonetti C, Besancenot R, Le Couedic JP, Fava F, Mazurier F, Godin I, Maloum K, Larbret F, Lecluse Y, Vainchenker W, Giraudier S: Evidence for MPL W515L/K mutations in hematopoietic stem cells in primitive myelofibrosis. Blood 2007, 110:3735-3743
-
(2007)
Blood
, vol.110
, pp. 3735-3743
-
-
Chaligne, R.1
James, C.2
Tonetti, C.3
Besancenot, R.4
Le Couedic, J.P.5
Fava, F.6
Mazurier, F.7
Godin, I.8
Maloum, K.9
Larbret, F.10
Lecluse, Y.11
Vainchenker, W.12
Giraudier, S.13
-
25
-
-
33750534561
-
MPL515 mutations in myeloproliferative and other myeloid disorders: A study of 1182 patients
-
Pardanani AD, Levine RL, Lasho T, Pikman Y, Mesa RA, Wadleigh M, Steensma DP, Elliott MA, Wolanskyj AP, Hogan WJ, McClure RF, Litzow MR, Gilliland DG, Tefferi A: MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients. Blood 2006, 108:3472-3476
-
(2006)
Blood
, vol.108
, pp. 3472-3476
-
-
Pardanani, A.D.1
Levine, R.L.2
Lasho, T.3
Pikman, Y.4
Mesa, R.A.5
Wadleigh, M.6
Steensma, D.P.7
Elliott, M.A.8
Wolanskyj, A.P.9
Hogan, W.J.10
McClure, R.F.11
Litzow, M.R.12
Gilliland, D.G.13
Tefferi, A.14
-
26
-
-
34047211223
-
Anaemia characterises patients with myelofibrosis harbouring Mpl mutation
-
Guglielmelli P, Pancrazzi A, Bergamaschi G, Rosti V, Villani L, Antonioli E, Bosi A, Barosi G, Vannucchi AM: Anaemia characterises patients with myelofibrosis harbouring Mpl mutation. Br J Haematol 2007, 137:244-247
-
(2007)
Br J Haematol
, vol.137
, pp. 244-247
-
-
Guglielmelli, P.1
Pancrazzi, A.2
Bergamaschi, G.3
Rosti, V.4
Villani, L.5
Antonioli, E.6
Bosi, A.7
Barosi, G.8
Vannucchi, A.M.9
-
27
-
-
37749011577
-
MPL W515 and JAK2 V617 mutation analysis in patients with refractory anemia with ringed sideroblasts and an eievated platelet count
-
Steensma DP, Caudill JS, Pardanani A, McClure RF, Lasho TL, Tefferi A: MPL W515 and JAK2 V617 mutation analysis in patients with refractory anemia with ringed sideroblasts and an eievated platelet count. Haematologica 2006, 91:ECR57
-
(2006)
Haematologica
, vol.91
-
-
Steensma, D.P.1
Caudill, J.S.2
Pardanani, A.3
McClure, R.F.4
Lasho, T.L.5
Tefferi, A.6
-
28
-
-
33750550297
-
Concurrent MPL515 and JAK2V617F mutations in myelofibrosis: Chronology of clonal emergence and changes in mutant allele burden over time
-
Lasho TL, Pardanani A, McClure RF, Mesa RA, Levine RL, Gilliland DG, Tefferi A: Concurrent MPL515 and JAK2V617F mutations in myelofibrosis: chronology of clonal emergence and changes in mutant allele burden over time. Br J Haematol 2006, 135:683-687
-
(2006)
Br J Haematol
, vol.135
, pp. 683-687
-
-
Lasho, T.L.1
Pardanani, A.2
McClure, R.F.3
Mesa, R.A.4
Levine, R.L.5
Gilliland, D.G.6
Tefferi, A.7
-
29
-
-
38349053791
-
JAK2 inhibitor therapy in myeloproliferative disorders: Rationale, preclinical studies and ongoing clinical trials
-
Pardanani A: JAK2 inhibitor therapy in myeloproliferative disorders: rationale, preclinical studies and ongoing clinical trials. Leukemia 2008, 22:23-30
-
(2008)
Leukemia
, vol.22
, pp. 23-30
-
-
Pardanani, A.1
-
30
-
-
0242352640
-
Design considerations and effects of LNA in PCR primers
-
Latorra D, Arar K, Hurley JM: Design considerations and effects of LNA in PCR primers. Mol Cell Probes 2003, 17:253-259
-
(2003)
Mol Cell Probes
, vol.17
, pp. 253-259
-
-
Latorra, D.1
Arar, K.2
Hurley, J.M.3
-
31
-
-
0038723184
-
Enhanced allele-specific PCR discrimination in SNP genotyping using 3' locked nucleic acid (LNA) primers
-
Latorra D, Campbell K, Wolter A, Hurley JM: Enhanced allele-specific PCR discrimination in SNP genotyping using 3' locked nucleic acid (LNA) primers. Hum Mutat 2003, 22:79-85
-
(2003)
Hum Mutat
, vol.22
, pp. 79-85
-
-
Latorra, D.1
Campbell, K.2
Wolter, A.3
Hurley, J.M.4
-
32
-
-
50949127379
-
Characteristics And Clinical Correlates of Mpl 515W>L/K Mutation In Essential Thrombocythemia
-
June 2, Epub ahead of print
-
Vannucchi AM, Antonioli E, Guglielmelli P, Pancrazzi A, Guerini V, Barosi G, Ruggeri M, Specchia G, LoCoco F, Delfini F, Villani L, Fiotto S, Ammatuna E, Alterini R, Carrai V, Capaccioli G, Di Lolo S, Liso V, Rambaldi A, Bosi A, Barbui T: Characteristics And Clinical Correlates of Mpl 515W>L/K Mutation In Essential Thrombocythemia, BLOOD 2008: June 2, [Epub ahead of print]
-
(2008)
BLOOD
-
-
Vannucchi, A.M.1
Antonioli, E.2
Guglielmelli, P.3
Pancrazzi, A.4
Guerini, V.5
Barosi, G.6
Ruggeri, M.7
Specchia, G.8
LoCoco, F.9
Delfini, F.10
Villani, L.11
Fiotto, S.12
Ammatuna, E.13
Alterini, R.14
Carrai, V.15
Capaccioli, G.16
Di Lolo, S.17
Liso, V.18
Rambaldi, A.19
Bosi, A.20
Barbui, T.21
more..
-
33
-
-
34247647062
-
Comparison of whole blood vs purified blood granulocytes for the detection and quantitation of JAK2(V617F)
-
Hermouet S, Dobo I, Lippert E, Boursier MC, Ergand L, Perrault-Hu F, Pineau D: Comparison of whole blood vs purified blood granulocytes for the detection and quantitation of JAK2(V617F). Leukemia 2007, 21:1128-1130
-
(2007)
Leukemia
, vol.21
, pp. 1128-1130
-
-
Hermouet, S.1
Dobo, I.2
Lippert, E.3
Boursier, M.C.4
Ergand, L.5
Perrault-Hu, F.6
Pineau, D.7
-
34
-
-
47649123488
-
Clinical correlates of JAK2V617F presence or alelle burden in myeloproliferative neoplasms: A critical reappraisal
-
Vannucchi AM, Antonioli E, Guglielmelli P, Pardanani A, Tefferi A: Clinical correlates of JAK2V617F presence or alelle burden in myeloproliferative neoplasms: a critical reappraisal. Leukemia 2008, 22:1299-1307
-
(2008)
Leukemia
, vol.22
, pp. 1299-1307
-
-
Vannucchi, A.M.1
Antonioli, E.2
Guglielmelli, P.3
Pardanani, A.4
Tefferi, A.5
-
35
-
-
33846880278
-
Monitoring of the JAK2-V617F mutation by highly sensitive quantitative real-time PCR after allogeneic stem cell transplantation in patients with myelofibrosis
-
Kroger N, Badbaran A, Holler E, Hahn J, Kobbe G, Bornhauser M, Reiter A, Zabelina T, Zander AR, Fehse B: Monitoring of the JAK2-V617F mutation by highly sensitive quantitative real-time PCR after allogeneic stem cell transplantation in patients with myelofibrosis. Blood 2007, 109:1316-1321
-
(2007)
Blood
, vol.109
, pp. 1316-1321
-
-
Kroger, N.1
Badbaran, A.2
Holler, E.3
Hahn, J.4
Kobbe, G.5
Bornhauser, M.6
Reiter, A.7
Zabelina, T.8
Zander, A.R.9
Fehse, B.10
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