-
1
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
-
Baxter EJ, Scott LM, Campbell PJ. 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
-
2
-
-
20244369569
-
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thromobocythemia, and myeloid metaplasia with myelofibrosis
-
Levine RL, Wadleigh M, Cools J, Ebert BL, Wernig G, Huntly BJP et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thromobocythemia, 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.P.6
-
3
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
-
James C, Ugo V, LeCouedic JP, Staerk J, Delhommeau F, Lacout C et al. 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
LeCouedic, J.P.3
Staerk, J.4
Delhommeau, F.5
Lacout, C.6
-
4
-
-
17644424955
-
A gain-of-function mutation of JAK2 in myeloproliferative disorders
-
Kralovics R, Passamonti F, Buser AS, Teo SS, Tiedt R, Passweg JR 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
Teo, S.S.4
Tiedt, R.5
Passweg, J.R.6
-
5
-
-
21344467318
-
Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
-
Jones AV, Kreil S, Zoi K, Waghorn K, Curtis C, Zhang L 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
Waghorn, K.4
Curtis, C.5
Zhang, L.6
-
6
-
-
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, Bueso-Ramos C, Prchal JT, Verstovsek S 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
Bueso-Ramos, C.4
Prchal, J.T.5
Verstovsek, S.6
-
7
-
-
21344440357
-
The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both 'atypical' myeloproliferative disorders and the myelodysplastic syndrome
-
Steensma DP, Dewald GW, Lasho TL, Powell HL, McClure RF, Levine RL et al. The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both 'atypical' myeloproliferative disorders and the myelodysplastic syndrome. Blood 2005; 106: 1207-1209.
-
(2005)
Blood
, vol.106
, pp. 1207-1209
-
-
Steensma, D.P.1
Dewald, G.W.2
Lasho, T.L.3
Powell, H.L.4
McClure, R.F.5
Levine, R.L.6
-
8
-
-
25844518265
-
The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia
-
Levine RL, Loriaux M, Huntly BJP, Loh ML, Beran M, Stoffregen E et al. The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia. Blood 2005; 106: 3377-3379.
-
(2005)
Blood
, vol.106
, pp. 3377-3379
-
-
Levine, R.L.1
Loriaux, M.2
Huntly, B.J.P.3
Loh, M.L.4
Beran, M.5
Stoffregen, E.6
-
9
-
-
0032076542
-
Jak2 is essential for signaling through a variety of cytokine receptors
-
Parganas E, Wang D, Stravopodis D, Topham DJ, Marine JC, Teglund S et al. Jak2 is essential for signaling through a variety of cytokine receptors. Cell 1998; 93: 385-395.
-
(1998)
Cell
, vol.93
, pp. 385-395
-
-
Parganas, E.1
Wang, D.2
Stravopodis, D.3
Topham, D.J.4
Marine, J.C.5
Teglund, S.6
-
10
-
-
0030852328
-
Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia
-
Peeters P, Raynaud SD, Cools J, Wlodarska I, Grosgeorge J, Philip P et al. Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia. Blood 1997; 90: 2535-2540.
-
(1997)
Blood
, vol.90
, pp. 2535-2540
-
-
Peeters, P.1
Raynaud, S.D.2
Cools, J.3
Wlodarska, I.4
Grosgeorge, J.5
Philip, P.6
-
11
-
-
17544402395
-
Molecular monitoring of cerebrospinal fluid can predict clinical relapse in acute lymphoblastic leukemia with eosinophilia
-
Nunez CA, Zipf TF, Roberts WM, Medeiros LJ, Hayes K, Bueso-Ramos CE. Molecular monitoring of cerebrospinal fluid can predict clinical relapse in acute lymphoblastic leukemia with eosinophilia. Arch Pathol Lab Med 2003; 127: 601-605.
-
(2003)
Arch Pathol Lab Med
, vol.127
, pp. 601-605
-
-
Nunez, C.A.1
Zipf, T.F.2
Roberts, W.M.3
Medeiros, L.J.4
Hayes, K.5
Bueso-Ramos, C.E.6
-
12
-
-
20144389913
-
The t(8;9)(p22;p24) is a recurrent abnormality in chronic and acute leukemia that fuses PCM1 to JAK2
-
Reiter A, Walz C, Watmore A, Schoch C, Blau I, Schlegelberger B et al. The t(8;9)(p22;p24) is a recurrent abnormality in chronic and acute leukemia that fuses PCM1 to JAK2. Cancer Res 2005; 65: 2662-2667.
-
(2005)
Cancer Res
, vol.65
, pp. 2662-2667
-
-
Reiter, A.1
Walz, C.2
Watmore, A.3
Schoch, C.4
Blau, I.5
Schlegelberger, B.6
-
13
-
-
0003545097
-
-
8th edn. DSMZ: Braunschweig, Germany
-
Drexler HG, Dirks W, MacLeod RAF, Quentmeier H, Steube KG, Uphoff CC. DSMZ Catalogue of Human and Animal Cell Lines, 8th edn. DSMZ: Braunschweig, Germany, 2001.
-
(2001)
DSMZ Catalogue of Human and Animal Cell Lines
-
-
Drexler, H.G.1
Dirks, W.2
MacLeod, R.A.F.3
Quentmeier, H.4
Steube, K.G.5
Uphoff, C.C.6
-
16
-
-
27144501134
-
Cell line OCI/AML3 bears exon-12 NPM gene mutation-A and cytoplasmic expression of nucleophosmin
-
Quentmeier H, Martelli MP, Dirks WG, Bolli N, Liso A, MacLeod RAF et al. Cell line OCI/AML3 bears exon-12 NPM gene mutation-A and cytoplasmic expression of nucleophosmin. Leukemia 2005; 19: 1760-1767.
-
(2005)
Leukemia
, vol.19
, pp. 1760-1767
-
-
Quentmeier, H.1
Martelli, M.P.2
Dirks, W.G.3
Bolli, N.4
Liso, A.5
MacLeod, R.A.F.6
-
17
-
-
0031684409
-
Effects of thrombopoietin, interleukin-3 and the kinase inhibitor K-252a on growth and polyploidization of the megakaryocytic cell line M-07e
-
Quentmeier H, Zaborski M, Drexler HG. Effects of thrombopoietin, interleukin-3 and the kinase inhibitor K-252a on growth and polyploidization of the megakaryocytic cell line M-07e. Leukemia 1998; 12: 1603-1611.
-
(1998)
Leukemia
, vol.12
, pp. 1603-1611
-
-
Quentmeier, H.1
Zaborski, M.2
Drexler, H.G.3
-
18
-
-
0036048240
-
New acute myeloid leukemia-derived cell line: MUTZ-8 with 5q-
-
Hu ZB, MacLeod RAF, Meyer C, Quentmeier H, Drexler HG. New acute myeloid leukemia-derived cell line: MUTZ-8 with 5q-. Leukemia 2002; 16: 1556-1561.
-
(2002)
Leukemia
, vol.16
, pp. 1556-1561
-
-
Hu, Z.B.1
MacLeod, R.A.F.2
Meyer, C.3
Quentmeier, H.4
Drexler, H.G.5
-
19
-
-
0033967383
-
Establishment and characterization of a new human megakaryoblastic cell line (SET-2) that spontaneously matures to megakaryocytes and produces platelet-like particles
-
Uozumi K, Otsuka M, Ohno N, Moriyama T, Suzuki S, Shimotakahara S et al. Establishment and characterization of a new human megakaryoblastic cell line (SET-2) that spontaneously matures to megakaryocytes and produces platelet-like particles. Leukemia 2000; 14: 142-152.
-
(2000)
Leukemia
, vol.14
, pp. 142-152
-
-
Uozumi, K.1
Otsuka, M.2
Ohno, N.3
Moriyama, T.4
Suzuki, S.5
Shimotakahara, S.6
-
20
-
-
0034650193
-
Derivation of a new hematopoietic cell line with endothelial features from a patient with transformed myeloproliferative syndrome
-
Fiedler W, Henke RP, Ergün S, Schumacher U, Gehling UM, Vohwinkel G et al. Derivation of a new hematopoietic cell line with endothelial features from a patient with transformed myeloproliferative syndrome. Cancer 2000; 88: 344-351.
-
(2000)
Cancer
, vol.88
, pp. 344-351
-
-
Fiedler, W.1
Henke, R.P.2
Ergün, S.3
Schumacher, U.4
Gehling, U.M.5
Vohwinkel, G.6
-
21
-
-
33644499331
-
del(5q) in myeloid malignancies
-
Charrin C. del(5q) in myeloid malignancies. Atlas Genet Cytogenet Oncol Haematol 1998, URL: http://www.infobiogen.fr/services/chromcancer/ Anomalies/del5qID1092.html.
-
(1998)
Atlas Genet Cytogenet Oncol Haematol
-
-
Charrin, C.1
-
22
-
-
0031451136
-
Identity of original and late passage Dami megakaryocytes with HEL erythroleukemia cells shown by combined cytogenetics and DNA fingerprinting
-
MacLeod RAF, Dirks WG, Reid YA, Hay RJ, Drexler HG. Identity of original and late passage Dami megakaryocytes with HEL erythroleukemia cells shown by combined cytogenetics and DNA fingerprinting. Leukemia 1997; 11: 2032-2038.
-
(1997)
Leukemia
, vol.11
, pp. 2032-2038
-
-
MacLeod, R.A.F.1
Dirks, W.G.2
Reid, Y.A.3
Hay, R.J.4
Drexler, H.G.5
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