-
1
-
-
33745728731
-
The 2001 World Health Organization and Updated European Clinical and Pathological Criteria for the Diagnosis, Classification, and Staging of the Philadelphia Chromosome-Negative Chronic Myeloproliferative Disorders
-
Michiels JJ, De Raeve H, Berneman Z, et al. The 2001 World Health Organization and Updated European Clinical and Pathological Criteria for the Diagnosis, Classification, and Staging of the Philadelphia Chromosome-Negative Chronic Myeloproliferative Disorders. Semin Thromb Hemost. 2006;32:307-340.
-
(2006)
Semin Thromb Hemost
, vol.32
, pp. 307-340
-
-
Michiels, J.J.1
De Raeve, H.2
Berneman, Z.3
-
2
-
-
0842309105
-
Multiple signaling pathways are involved in erythropoietin-independent differentiation of erythroid progenitors in polycythemia vera
-
Ugo V, Marzac C, Teyssandier I, et al. Multiple signaling pathways are involved in erythropoietin-independent differentiation of erythroid progenitors in polycythemia vera. Exp Hematol. 2004;32:179-187.
-
(2004)
Exp Hematol
, vol.32
, pp. 179-187
-
-
Ugo, V.1
Marzac, C.2
Teyssandier, I.3
-
4
-
-
0842287505
-
JAK2 contributes to the intrinsic capacity of primary hematopoietic cells to respond to stem cell factor
-
Radosevic N, Winterstein D, Keller JR, et al. JAK2 contributes to the intrinsic capacity of primary hematopoietic cells to respond to stem cell factor. Exp Hematol. 2004;32:149-156.
-
(2004)
Exp Hematol
, vol.32
, pp. 149-156
-
-
Radosevic, N.1
Winterstein, D.2
Keller, J.R.3
-
5
-
-
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
-
6
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signaling causes polycythemia vera
-
James C, Ugo V, Le Couedic J-P, et al. A unique clonal JAK2 mutation leading to constitutive signaling causes polycythemia vera. Nature. 2005;434:1144-1148.
-
(2005)
Nature
, vol.434
, pp. 1144-1148
-
-
James, C.1
Ugo, V.2
Le Couedic, J.-P.3
-
7
-
-
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
-
8
-
-
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
-
9
-
-
25844447519
-
JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia
-
Jelinek J, Oki Y, Gharibyan V, et al. JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia. Blood. 2005;106:3370-3373.
-
(2005)
Blood
, vol.106
, pp. 3370-3373
-
-
Jelinek, J.1
Oki, Y.2
Gharibyan, V.3
-
10
-
-
33646240825
-
Diagnostic assays for the JAK2 V617F mutation in chronic myeloproliferative disorders
-
Greiner TC. Diagnostic assays for the JAK2 V617F mutation in chronic myeloproliferative disorders. Am J Clin Pathol. 2006;125:651-653.
-
(2006)
Am J Clin Pathol
, vol.125
, pp. 651-653
-
-
Greiner, T.C.1
-
11
-
-
33748592820
-
JAK2 V617F in myeloid disorders: Molecular diagnostic techniques and their clinical utility
-
Steensma D. JAK2 V617F in myeloid disorders: molecular diagnostic techniques and their clinical utility. J Mol Diagn. 2006;8:397-411.
-
(2006)
J Mol Diagn
, vol.8
, pp. 397-411
-
-
Steensma, D.1
-
12
-
-
33745966245
-
V617F mutation in myeloproliferative disorders by melting curve analysis using the LightCycler system
-
V617F mutation in myeloproliferative disorders by melting curve analysis using the LightCycler system. Arch Pathol Lab Med. 2006;130:997-1003.
-
(2006)
Arch Pathol Lab Med
, vol.130
, pp. 997-1003
-
-
Olsen, R.J.1
Tang, Z.2
Farkas, D.H.3
-
13
-
-
33747603881
-
Genetic heterogeneity of granulocytes for the JAK2 V617F mutation in essential thrombocythaemia: Implications for mutation detection in peripheral blood
-
Stevenson WS, Hoyt R, Bell A, et al. Genetic heterogeneity of granulocytes for the JAK2 V617F mutation in essential thrombocythaemia: implications for mutation detection in peripheral blood. Pathology. 2006;38:336-342.
-
(2006)
Pathology
, vol.38
, pp. 336-342
-
-
Stevenson, W.S.1
Hoyt, R.2
Bell, A.3
-
14
-
-
33645545371
-
Identification of the JAK2 V617F mutation in chronic myeloproliferative disorders using FRET probes and melting curve analysis
-
Murugesan G, Aboudola S, Szpurka H, et al. Identification of the JAK2 V617F mutation in chronic myeloproliferative disorders using FRET probes and melting curve analysis. Am J Clin Pathol. 2006;125:625-633.
-
(2006)
Am J Clin Pathol
, vol.125
, pp. 625-633
-
-
Murugesan, G.1
Aboudola, S.2
Szpurka, H.3
-
15
-
-
33644969827
-
Validation of two clinically useful assays for evaluation of JAK2 V617F mutation in chronic myeloproliferative disorders
-
McClure R, Mai M, Lasho T. Validation of two clinically useful assays for evaluation of JAK2 V617F mutation in chronic myeloproliferative disorders. Leukemia. 2006;20:168-171.
-
(2006)
Leukemia
, vol.20
, pp. 168-171
-
-
McClure, R.1
Mai, M.2
Lasho, T.3
-
16
-
-
21344467318
-
Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
-
Jones AV, Kreil S, Zoi K, et al. Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. Blood. 2005;106:2162-2168.
-
(2005)
Blood
, vol.106
, pp. 2162-2168
-
-
Jones, A.V.1
Kreil, S.2
Zoi, K.3
-
17
-
-
33744484499
-
V617F mutation in myeloproliferative disorders by ARMS-PCR and capillary electrophoresis
-
V617F mutation in myeloproliferative disorders by ARMS-PCR and capillary electrophoresis. Leukemia. 2006;20:1055-1060.
-
(2006)
Leukemia
, vol.20
, pp. 1055-1060
-
-
Vannucchi, A.M.1
Pancrazzi, A.2
Bogani, C.3
-
18
-
-
33746026365
-
Detection of the JAK2 V617F mutation by LightCycler PCR and probe dissociation analysis
-
Lay M, Mariappan R, Gotlib J, et al. Detection of the JAK2 V617F mutation by LightCycler PCR and probe dissociation analysis. J Mol Diagn. 2006;8:330-334.
-
(2006)
J Mol Diagn
, vol.8
, pp. 330-334
-
-
Lay, M.1
Mariappan, R.2
Gotlib, J.3
-
19
-
-
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
-
20
-
-
23844544647
-
Rapid polymerase chain reaction-based detection of epidermal growth factor receptor gene mutations in lung adenocarcinomas
-
Pan Q, Pao W, Ladanyi M. Rapid polymerase chain reaction-based detection of epidermal growth factor receptor gene mutations in lung adenocarcinomas. J Mol Diagn. 2005;7:396-403.
-
(2005)
J Mol Diagn
, vol.7
, pp. 396-403
-
-
Pan, Q.1
Pao, W.2
Ladanyi, M.3
-
21
-
-
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
-
22
-
-
33747599596
-
The JAK2V617F mutation is detectable at a very low level in peripheral blood of healthy donors [letter]
-
Sidon P, El Housni EI, Dessars B, et al. The JAK2V617F mutation is detectable at a very low level in peripheral blood of healthy donors [letter]. Leukemia. 2006;20:1622.
-
(2006)
Leukemia
, vol.20
, pp. 1622
-
-
Sidon, P.1
El Housni, E.I.2
Dessars, B.3
-
23
-
-
33846012829
-
V617F: Prevalence in a large Chinese hospital population
-
V617F: prevalence in a large Chinese hospital population. Blood. 2007;109:339-342.
-
(2007)
Blood
, vol.109
, pp. 339-342
-
-
Xu, X.1
Luo, J.2
Xing, S.3
-
24
-
-
0028786297
-
Detection of major bcr-abl gene expression at a very low level in blood cells of some healthy individuals
-
Biernaux C, Loos M, Sels A, et al. Detection of major bcr-abl gene expression at a very low level in blood cells of some healthy individuals. Blood. 1995;86:3118-3122.
-
(1995)
Blood
, vol.86
, pp. 3118-3122
-
-
Biernaux, C.1
Loos, M.2
Sels, A.3
-
25
-
-
0032211172
-
The presence of typical and atypical bcr-abl fusion genes in leukocytes of normal individuals: Biologic significance and implications for the assessment of minimal residual disease
-
Bose S, Deininger M, Gora-Tybor J, et al. The presence of typical and atypical bcr-abl fusion genes in leukocytes of normal individuals: biologic significance and implications for the assessment of minimal residual disease. Blood. 1998;9:3362-3367.
-
(1998)
Blood
, vol.9
, pp. 3362-3367
-
-
Bose, S.1
Deininger, M.2
Gora-Tybor, J.3
-
26
-
-
33746043322
-
The role of Janus kinases in haemopoiesis and haematological malignancy
-
Khwaja A. The role of Janus kinases in haemopoiesis and haematological malignancy. Br J Haematol. 2006;134:366-384.
-
(2006)
Br J Haematol
, vol.134
, pp. 366-384
-
-
Khwaja, A.1
-
27
-
-
33745635723
-
Hemizygous/homozygous and heterozygous JAK2 mutation detected in plasma of patients with myeloproliferative diseases: Correlation with clinical behaviour
-
Ma W, Kantarjian H, Verstovsek S, et al. Hemizygous/homozygous and heterozygous JAK2 mutation detected in plasma of patients with myeloproliferative diseases: correlation with clinical behaviour. Br J Haematol. 2006;134:340-350.
-
(2006)
Br J Haematol
, vol.134
, pp. 340-350
-
-
Ma, W.1
Kantarjian, H.2
Verstovsek, S.3
-
28
-
-
33744814083
-
JAK2 V617F: A single mutation in the myeloproliferative group of disorders
-
McLornan D, Percy M, McMullin MF. JAK2 V617F: a single mutation in the myeloproliferative group of disorders. Ulster Med J. 2006;75:112-119.
-
(2006)
Ulster Med J
, vol.75
, pp. 112-119
-
-
McLornan, D.1
Percy, M.2
McMullin, M.F.3
-
31
-
-
33745686457
-
New insights into the pathogenesis of JAK2 V617F-positive myeloproliferative disorders and consequences for the management of patients
-
Villeval J-L, James C, Pisani DF, et al. New insights into the pathogenesis of JAK2 V617F-positive myeloproliferative disorders and consequences for the management of patients. Semin Thromb Hemost. 2006;32:341-351.
-
(2006)
Semin Thromb Hemost
, vol.32
, pp. 341-351
-
-
Villeval, J.-L.1
James, C.2
Pisani, D.F.3
|