-
2
-
-
0024361278
-
Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome
-
Abe K, Kajii T, Niikawa N (1989): Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome. Hum Genet 82:313-316.
-
(1989)
Hum Genet
, vol.82
, pp. 313-316
-
-
Abe, K.1
Kajii, T.2
Niikawa, N.3
-
3
-
-
0030669455
-
Fusion of the platelet-derived growth factor receptor beta to a novel gene CEV14 in acute myelogenous leukemia after clonal evolution
-
Abe A, Emi N, Tanimoto M, Terasaki H, Marunouchi T, Saito H (1997): Fusion of the platelet-derived growth factor receptor beta to a novel gene CEV14 in acute myelogenous leukemia after clonal evolution. Blood 90:4271-4277.
-
(1997)
Blood
, vol.90
, pp. 4271-4277
-
-
Abe, A.1
Emi, N.2
Tanimoto, M.3
Terasaki, H.4
Marunouchi, T.5
Saito, H.6
-
4
-
-
17144378549
-
Gains on 9p are common genomic aberrations in idiopathic myelofibrosis: a comparative genomic hybridization study
-
Al Assar O, Ul-Hassan A, Brown R, Wilson GA, Hammond DW, Reilly JT (2005): Gains on 9p are common genomic aberrations in idiopathic myelofibrosis: a comparative genomic hybridization study. Br J Haematol 129:66-71.
-
(2005)
Br J Haematol
, vol.129
, pp. 66-71
-
-
Al Assar, O.1
Ul-Hassan, A.2
Brown, R.3
Wilson, G.A.4
Hammond, D.W.5
Reilly, J.T.6
-
5
-
-
0036697796
-
Frequency of structural abnormalities of the long arm of chromosome 12 in myelofibrosis with myeloid metaplasia
-
Andrieux J, Demory JL, Morel P, Plantier I, Dupriez B, Caulier MT, Bauters F, Lai JL (2002): Frequency of structural abnormalities of the long arm of chromosome 12 in myelofibrosis with myeloid metaplasia. Cancer Genet Cytogenet 137:68-71.
-
(2002)
Cancer Genet Cytogenet
, vol.137
, pp. 68-71
-
-
Andrieux, J.1
Demory, J.L.2
Morel, P.3
Plantier, I.4
Dupriez, B.5
Caulier, M.T.6
Bauters, F.7
Lai, J.L.8
-
6
-
-
0344420249
-
Dysregulation and overexpression of HMGA2 in myelofibrosis with myeloid metaplasia
-
Andrieux J, Demory JL, Dupriez B, Quief S, Plantier I, Roumier C, Bauters F, Lai JL, Kerckaert JP (2004): Dysregulation and overexpression of HMGA2 in myelofibrosis with myeloid metaplasia. Genes Chromosomes Cancer 39:82-87.
-
(2004)
Genes Chromosomes Cancer
, vol.39
, pp. 82-87
-
-
Andrieux, J.1
Demory, J.L.2
Dupriez, B.3
Quief, S.4
Plantier, I.5
Roumier, C.6
Bauters, F.7
Lai, J.L.8
Kerckaert, J.P.9
-
7
-
-
34548674206
-
Bone morphogenetic protein antagonist gene NOG is involved in myeloproliferative disease associated with myelofibrosis
-
Andrieux J, Roche-Lestienne C, Geffroy S, Desterke C, Grardel N, Plantier I, Selleslag D, Demory JL, Lai JL, Leleu X, Bousse-Kerdiles C, Vandenberghe P (2007): Bone morphogenetic protein antagonist gene NOG is involved in myeloproliferative disease associated with myelofibrosis. Cancer Genet Cytogenet 178:11-16.
-
(2007)
Cancer Genet Cytogenet
, vol.178
, pp. 11-16
-
-
Andrieux, J.1
Roche-Lestienne, C.2
Geffroy, S.3
Desterke, C.4
Grardel, N.5
Plantier, I.6
Selleslag, D.7
Demory, J.L.8
Lai, J.L.9
Leleu, X.10
Bousse-Kerdiles, C.11
Vandenberghe, P.12
-
8
-
-
18744373593
-
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia
-
Ang SO, Chen H, Hirota K, Gordeuk VR, Jelinek J, Guan Y, Liu E, Sergueeva AI, Miasnikova GY, Mole D, Maxwell PH, Stockton DW, Semenza GL, Prchal JT (2002): Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia. Nat Genet 32:614-621.
-
(2002)
Nat Genet
, vol.32
, pp. 614-621
-
-
Ang, S.O.1
Chen, H.2
Hirota, K.3
Gordeuk, V.R.4
Jelinek, J.5
Guan, Y.6
Liu, E.7
Sergueeva, A.I.8
Miasnikova, G.Y.9
Mole, D.10
Maxwell, P.H.11
Stockton, D.W.12
Semenza, G.L.13
Prchal, J.T.14
-
9
-
-
15844431788
-
Conventional cytogenetics of myeloproliferative diseases other than CML contribute valid information
-
Bacher U, Haferlach T, Kern W, Hiddemann W, Schnittger S, Schoch C (2005): Conventional cytogenetics of myeloproliferative diseases other than CML contribute valid information. Ann Hematol 84:250-257.
-
(2005)
Ann Hematol
, vol.84
, pp. 250-257
-
-
Bacher, U.1
Haferlach, T.2
Kern, W.3
Hiddemann, W.4
Schnittger, S.5
Schoch, C.6
-
10
-
-
0038487039
-
Cytogenetic and molecular genetic aspects of eosinophilic leukaemias
-
Bain BJ (2003): Cytogenetic and molecular genetic aspects of eosinophilic leukaemias. Br] Haematol 122:173-179.
-
(2003)
Br] Haematol
, vol.122
, pp. 173-179
-
-
Bain, B.J.1
-
11
-
-
0025298698
-
Monosomy-7 in childhood hemopoietic disorders
-
Baranger L, Baruchel A, Leverger G, Schaison G, Berger R (1990): Monosomy-7 in childhood hemopoietic disorders. Leukemia 4:345-349.
-
(1990)
Leukemia
, vol.4
, pp. 345-349
-
-
Baranger, L.1
Baruchel, A.2
Leverger, G.3
Schaison, G.4
Berger, R.5
-
12
-
-
70350186921
-
The t(4;22)(qI2;ql 1) in atypical chronic myeloid leukaemia fuses BCR to PDGFRA
-
Baxter EJ, Hochhaus A, Bolufer P, Reiter A, Fernandez JM, Senent L, Cervera J, Moscardo F, Sanz MA, Cross NC (2002): The t(4;22)(qI2;ql 1) in atypical chronic myeloid leukaemia fuses BCR to PDGFRA. Hum Mol Genet 11:1391-1397.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1391-1397
-
-
Baxter, E.J.1
Hochhaus, A.2
Bolufer, P.3
Reiter, A.4
Fernandez, J.M.5
Senent, L.6
Cervera, J.7
Moscardo, F.8
Sanz, M.A.9
Cross, N.C.10
-
13
-
-
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 (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
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
-
14
-
-
33745623666
-
Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders
-
Bellanne-Chantelot C, Chaumarel I, Labopin M, Bellanger F, Barbu V, De Toma C, Delhommeau F, Casadevall N, Vainchenker W, Thomas G, Najman A (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
-
-
Bellanne-Chantelot, C.1
Chaumarel, I.2
Labopin, M.3
Bellanger, F.4
Barbu, V.5
De Toma, C.6
Delhommeau, F.7
Casadevall, N.8
Vainchenker, W.9
Thomas, G.10
Najman, A.11
-
15
-
-
19944432120
-
8pl 1 myeloproliferative syndrome with a novel t(7;8) translocation leading to fusion of the FGFRl and TIF1 genes
-
Belloni E, Trubia M, Gasparini P, Micucci C, Tapinassi C, Confalonieri S, Nuciforo P, Martino B, Lo-Coco F, Pelicci PG, Di Fiore PP (2005): 8pl 1 myeloproliferative syndrome with a novel t(7;8) translocation leading to fusion of the FGFRl and TIF1 genes. Genes Chromosomes Cancer 42:320-325.
-
(2005)
Genes Chromosomes Cancer
, vol.42
, pp. 320-325
-
-
Belloni, E.1
Trubia, M.2
Gasparini, P.3
Micucci, C.4
Tapinassi, C.5
Confalonieri, S.6
Nuciforo, P.7
Martino, B.8
Lo-Coco, F.9
Pelicci, P.G.10
Di Fiore, P.P.11
-
16
-
-
25844494941
-
Chromosomal abnormalities and molecular markers in myeloproliferative disorders
-
Bench AJ, Pahl HL (2005): Chromosomal abnormalities and molecular markers in myeloproliferative disorders. Semin Hematol 42:196-205.
-
(2005)
Semin Hematol
, vol.42
, pp. 196-205
-
-
Bench, A.J.1
Pahl, H.L.2
-
18
-
-
0034632693
-
Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes UK Cancer Cytogenetics Group (UKCCG)
-
Bench AJ, Nacheva EP, Hood TL, Holden JL, French L, Swanton S, Champion KM, Li J, Whittaker P, Stavrides G, Hunt AR, Huntly BJ, Campbell LJ, Bentley DR, Deloukas P, Green AR (2000): Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes. UK Cancer Cytogenetics Group (UKCCG). Oncogene 19:3902-3913.
-
(2000)
Oncogene
, vol.19
, pp. 3902-3913
-
-
Bench, A.J.1
Nacheva, E.P.2
Hood, T.L.3
Holden, J.L.4
French, L.5
Swanton, S.6
Champion, K.M.7
Li, J.8
Whittaker, P.9
Stavrides, G.10
Hunt, A.R.11
Huntly, B.J.12
Campbell, L.J.13
Bentley, D.R.14
Deloukas, P.15
Green, A.R.16
-
19
-
-
0021268319
-
Chromosome studies in polycythemia vera patients
-
Berger R, Bernheim A, Le Coniat M, Vecchione D, Flandrin G, Dresch C, Najean Y (1984): Chromosome studies in polycythemia vera patients. Cancer Genet Cytogenet 12:217-223.
-
(1984)
Cancer Genet Cytogenet
, vol.12
, pp. 217-223
-
-
Berger, R.1
Bernheim, A.2
Le Coniat, M.3
Vecchione, D.4
Flandrin, G.5
Dresch, C.6
Najean, Y.7
-
20
-
-
0345373976
-
Evidence of clonality in chronic neutrophilic leukaemia
-
Bohm J, Kock S, Schaefer HE, Fisch P (2003): Evidence of clonality in chronic neutrophilic leukaemia. / Clin Pathol 56:292-295.
-
(2003)
J Clin Pathol
, vol.56
, pp. 292-295
-
-
Bohm, J.1
Kock, S.2
Schaefer, H.E.3
Fisch, P.4
-
21
-
-
9644262495
-
Cryptic translocations involving chromosome 20 in polycythemia vera
-
Busson M, Romana S, Nguyen Khac F, Bernard O, Berger R (2004): Cryptic translocations involving chromosome 20 in polycythemia vera. Ann Genet 47:365-371.
-
(2004)
Ann Genet
, vol.47
, pp. 365-371
-
-
Busson, M.1
Romana, S.2
Nguyen Khac, F.3
Bernard, O.4
Berger, R.5
-
22
-
-
0027954472
-
The prognostic significance of deletion of the long arm of chromosome 20 in myeloid disorders
-
Campbell LJ, Garson OM (1994): The prognostic significance of deletion of the long arm of chromosome 20 in myeloid disorders. Leukemia 8:67-71.
-
(1994)
Leukemia
, vol.8
, pp. 67-71
-
-
Campbell, L.J.1
Garson, O.M.2
-
23
-
-
33344471678
-
V6i 7F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis
-
Campbell PJ, Griesshammer M, Dohner K, Dohner H, Kusec R, Hasselbalch HC, Larsen TS, Pallisgaard N, Giraudier S, Bousse-Kerdiles MC, Desterke C, Guerton B, Dupriez B, Bordessoule D, Fenaux P, Kiladjian JJ, Viallard JF, Briere J, Harrison CN, Green AR, Reilly JT (2006): V6i 7F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis. Blood 107:2098-2100.
-
(2006)
Blood
, vol.107
, pp. 2098-2100
-
-
Campbell, P.J.1
Griesshammer, M.2
Dohner, K.3
Dohner, H.4
Kusec, R.5
Hasselbalch, H.C.6
Larsen, T.S.7
Pallisgaard, N.8
Giraudier, S.9
Bousse-Kerdiles, M.C.10
Desterke, C.11
Guerton, B.12
Dupriez, B.13
Bordessoule, D.14
Fenaux, P.15
Kiladjian, J.J.16
Viallard, J.F.17
Briere, J.18
Harrison, C.N.19
Green, A.R.20
Reilly, J.T.21
more..
-
24
-
-
14144251673
-
GATA1 mutation and trisomy 21 are required only in haematopoietic cells for development of transient myeloproliferative disorder
-
Carpenter E, Valverde-Garduno V, Sternberg A, Mitchell C, Roberts I, Vyas P, Vora A (2005): GATA1 mutation and trisomy 21 are required only in haematopoietic cells for development of transient myeloproliferative disorder. Br J Haematol 128:548-551.
-
(2005)
Br J Haematol
, vol.128
, pp. 548-551
-
-
Carpenter, E.1
Valverde-Garduno, V.2
Sternberg, A.3
Mitchell, C.4
Roberts, I.5
Vyas, P.6
Vora, A.7
-
25
-
-
0031798991
-
Gain of 9p in the pathogenesis of polycythemia vera
-
Chen Z, Notohamiprodjo M, Guan XY, Paietta E, Blackwell S, Stout K, Turner A, Richkind K, Trent JM, Lamb A, Sandberg AA (1998): Gain of 9p in the pathogenesis of polycythemia vera. Genes Chromosomes Cancer 22:321-324.
-
(1998)
Genes Chromosomes Cancer
, vol.22
, pp. 321-324
-
-
Chen, Z.1
Notohamiprodjo, M.2
Guan, X.Y.3
Paietta, E.4
Blackwell, S.5
Stout, K.6
Turner, A.7
Richkind, K.8
Trent, J.M.9
Lamb, A.10
Sandberg, A.A.11
-
26
-
-
0344987881
-
A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome
-
Cools J, DeAngelo DJ, Gotlib J, Stover EH, Legare RD, Cortes J, Kutok J, Clark J, Galinsky I, Griffin JD, Cross NC, Tefferi A, Malone J, Alam R, Schrier SL, Schmid J, Rose M, Vandenberghe P, Verhoef G, Boogaerts M, Wlodarska I, Kantarjian H, Marynen P, Coutre SE, Stone R, Gilliland DG (2003): A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome. N EnglJ Med 348:1201-1214.
-
(2003)
N EnglJ Med
, vol.348
, pp. 1201-1214
-
-
Cools, J.1
DeAngelo, D.J.2
Gotlib, J.3
Stover, E.H.4
Legare, R.D.5
Cortes, J.6
Kutok, J.7
Clark, J.8
Galinsky, I.9
Griffin, J.D.10
Cross, N.C.11
Tefferi, A.12
Malone, J.13
Alam, R.14
Schrier, S.L.15
Schmid, J.16
Rose, M.17
Vandenberghe, P.18
Verhoef, G.19
Boogaerts, M.20
Wlodarska, I.21
Kantarjian, H.22
Marynen, P.23
Coutre, S.E.24
Stone, R.25
Gilliland, D.G.26
more..
-
27
-
-
0036045381
-
Tyrosine kinase fusion genes in chronic myeloproliferative diseases
-
Cross NC, Reiter A (2002): Tyrosine kinase fusion genes in chronic myeloproliferative diseases. Leukemia 16:1207-1212.
-
(2002)
Leukemia
, vol.16
, pp. 1207-1212
-
-
Cross, N.C.1
Reiter, A.2
-
28
-
-
34250007662
-
Two novel imatinib-responsive PDGFRA fusion genes in chronic eosinophilic leukaemia
-
Curtis CE, Grand FH, Musto P, Clark A, Murphy J, Perla G, Minervini MM, Stewart J, Reiter A, Cross NC (2007): Two novel imatinib-responsive PDGFRA fusion genes in chronic eosinophilic leukaemia. Br J Haematol 138:77-81.
-
(2007)
Br J Haematol
, vol.138
, pp. 77-81
-
-
Curtis, C.E.1
Grand, F.H.2
Musto, P.3
Clark, A.4
Murphy, J.5
Perla, G.6
Minervini, M.M.7
Stewart, J.8
Reiter, A.9
Cross, N.C.10
-
29
-
-
0025064343
-
Monosomy 7 syndrome Clinical heterogeneity in children and adolescents
-
Daghistani D, Toledano SR, Curless R (1990): Monosomy 7 syndrome. Clinical heterogeneity in children and adolescents. Cancer Genet Cytogenet 44:263-269.
-
(1990)
Cancer Genet Cytogenet
, vol.44
, pp. 263-269
-
-
Daghistani, D.1
Toledano, S.R.2
Curless, R.3
-
30
-
-
0023726101
-
Cytogenetic studies and their prognostic significance in agnogenic myeloid metaplasia: a report on 47 cases
-
Demory JL, Dupriez B, Fenaux P, Lai JL, Beuscart R, Jouet JP, Deminatti M, Bauters F (1988): Cytogenetic studies and their prognostic significance in agnogenic myeloid metaplasia: a report on 47 cases. Blood 72:855-859.
-
(1988)
Blood
, vol.72
, pp. 855-859
-
-
Demory, J.L.1
Dupriez, B.2
Fenaux, P.3
Lai, J.L.4
Beuscart, R.5
Jouet, J.P.6
Deminatti, M.7
Bauters, F.8
-
32
-
-
2542502506
-
Familial essential thrombocythemia associated with a dominant-positive activating mutation of the c-MPL gene, which encodes for the receptor for thrombopoietin
-
Ding J, Komatsu H, Wakita A, Kato-Uranishi M, Ito M, Satoh A, Tsuboi K, Nitta M, Miyazaki H, Iida S, Ueda R (2004): Familial essential thrombocythemia associated with a dominant-positive activating mutation of the c-MPL gene, which encodes for the receptor for thrombopoietin. Blood 103:4198^200.
-
(2004)
Blood
, vol.103
, pp. 4198-4200
-
-
Ding, J.1
Komatsu, H.2
Wakita, A.3
Kato-Uranishi, M.4
Ito, M.5
Satoh, A.6
Tsuboi, K.7
Nitta, M.8
Miyazaki, H.9
Iida, S.10
Ueda, R.11
-
33
-
-
24944565419
-
Der(6)t(l;6)(q21-23;p21 3): aspecific cytogenetic abnormality in myelofibrosis with myeloid metaplasia
-
Dingli D, Grand FH, Mahaffey V, Spurbeck J, Ross FM, Watmore AE, Reilly JT, Cross NC, Dewald GW, Tefferi A (2005): Der(6)t(l;6)(q21-23;p21.3): aspecific cytogenetic abnormality in myelofibrosis with myeloid metaplasia. Br J Haematol 130:229-232.
-
(2005)
Br J Haematol
, vol.130
, pp. 229-232
-
-
Dingli, D.1
Grand, F.H.2
Mahaffey, V.3
Spurbeck, J.4
Ross, F.M.5
Watmore, A.E.6
Reilly, J.T.7
Cross, N.C.8
Dewald, G.W.9
Tefferi, A.10
-
34
-
-
30844463437
-
Presence of unfavorable cytogenetic abnormalities is the strongest predictor of poor survival in secondary myelofibrosis
-
Dingli D, Schwager SM, Mesa RA, Li CY, Dewald GW, Tefferi A (2006): Presence of unfavorable cytogenetic abnormalities is the strongest predictor of poor survival in secondary myelofibrosis. Cancer 106:1985-1989.
-
(2006)
Cancer
, vol.106
, pp. 1985-1989
-
-
Dingli, D.1
Schwager, S.M.2
Mesa, R.A.3
Li, C.Y.4
Dewald, G.W.5
Tefferi, A.6
-
35
-
-
33846697877
-
Cytogenetics of agnogenic myeloid metaplasia: a study of 61 patients
-
Djordjevic V, Dencic-Fekete M, Jovanovic J, Bizic S, Jankovic G, Bogdanovic A, Cemerikic-Martinovic V, Gotic M (2007): Cytogenetics of agnogenic myeloid metaplasia: a study of 61 patients. Cancer Genet Cytogenet 173:57-62.
-
(2007)
Cancer Genet Cytogenet
, vol.173
, pp. 57-62
-
-
Djordjevic, V.1
Dencic-Fekete, M.2
Jovanovic, J.3
Bizic, S.4
Jankovic, G.5
Bogdanovic, A.6
Cemerikic-Martinovic, V.7
Gotic, M.8
-
36
-
-
0029767865
-
Prognostic factors in agnogenic myeloid metaplasia: a report on 195 cases with a new scoring system
-
Dupriez B, Morel P, Demory JL, Lai JL, Simon M, Plantier I, Bauters F (1996): Prognostic factors in agnogenic myeloid metaplasia: a report on 195 cases with a new scoring system. Blood 88:1013-1018.
-
(1996)
Blood
, vol.88
, pp. 1013-1018
-
-
Dupriez, B.1
Morel, P.2
Demory, J.L.3
Lai, J.L.4
Simon, M.5
Plantier, I.6
Bauters, F.7
-
37
-
-
0025146168
-
Trisomy 21 in transient myeloproliferative disorder
-
Faed MJ, Robertson J, Todd AS, Sivakumaran M, Tarnow-Mordi WO (1990): Trisomy 21 in transient myeloproliferative disorder. Cancer Genet Cytogenet 48:259-264.
-
(1990)
Cancer Genet Cytogenet
, vol.48
, pp. 259-264
-
-
Faed, M.J.1
Robertson, J.2
Todd, A.S.3
Sivakumaran, M.4
Tarnow-Mordi, W.O.5
-
38
-
-
0019818299
-
Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell
-
Fialkow PJ, Faguet GB, Jacobson RJ, Vaidya K, Murphy S (1981): Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell. Blood 58:916-919.
-
(1981)
Blood
, vol.58
, pp. 916-919
-
-
Fialkow, P.J.1
Faguet, G.B.2
Jacobson, R.J.3
Vaidya, K.4
Murphy, S.5
-
39
-
-
0035159831
-
Fusion of the BCR and the (ibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(pl 1;q 11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL
-
Fioretos T, Panagopoulos I, Lassen C, Swedin A, Billstrom R, Isaksson M, Strombeck B, Olofsson T, Mitelman F, Johansson B (2001): Fusion of the BCR and the (ibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(pl 1;q 11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL. Genes Chromosomes Cancer 32:302-310.
-
(2001)
Genes Chromosomes Cancer
, vol.32
, pp. 302-310
-
-
Fioretos, T.1
Panagopoulos, I.2
Lassen, C.3
Swedin, A.4
Billstrom, R.5
Isaksson, M.6
Strombeck, B.7
Olofsson, T.8
Mitelman, F.9
Johansson, B.10
-
40
-
-
33749368009
-
KIT mutation in mast cells and other bone marrow hematopoietic cell lineages in systemic mast cell disorders: a prospective study of the Spanish Network on Mastocytosis (REMA) in a series of 113 patients
-
Garcia-Montero AC, Jara-Acevedo M, Teodosio C, Sanchez ML, Nunez R, Prados A, Aldanondo I, Sanchez L, Dominguez M, Botana LM, Sanchez-Jimenez F, Sotlar K, Almeida J, Escribano L, Orfao A (2006): KIT mutation in mast cells and other bone marrow hematopoietic cell lineages in systemic mast cell disorders: a prospective study of the Spanish Network on Mastocytosis (REMA) in a series of 113 patients. Blood 108:2366-2372.
-
(2006)
Blood
, vol.108
, pp. 2366-2372
-
-
Garcia-Montero, A.C.1
Jara-Acevedo, M.2
Teodosio, C.3
Sanchez, M.L.4
Nunez, R.5
Prados, A.6
Aldanondo, I.7
Sanchez, L.8
Dominguez, M.9
Botana, L.M.10
Sanchez-Jimenez, F.11
Sotlar, K.12
Almeida, J.13
Escribano, L.14
Orfao, A.15
-
41
-
-
0028224348
-
Fusion of PDGF receptor beta to a novel ets-like gene, tej, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation
-
Golub TR, Barker GF, Lovett M, Gilliland DG (1994): Fusion of PDGF receptor beta to a novel ets-like gene, tej, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 77:307-316.
-
(1994)
Cell
, vol.77
, pp. 307-316
-
-
Golub, T.R.1
Barker, G.F.2
Lovett, M.3
Gilliland, D.G.4
-
42
-
-
21344440247
-
Molecular classification and pathogenesis of eosinophilic disorders: 2005 update
-
Gotlib J (2005): Molecular classification and pathogenesis of eosinophilic disorders: 2005 update. Acta Haematol 114:7-25.
-
(2005)
Acta Haematol
, vol.114
, pp. 7-25
-
-
Gotlib, J.1
-
43
-
-
1942422114
-
Identification of a novel gene, FGFRJOP2, fused to FGFR1 in 8p 11 myeloproliferative syndrome
-
Grand EK, Grand FH, Chase AJ, Ross FM, Corcoran MM, Oscier DG, Cross NC (2004a): Identification of a novel gene, FGFRJOP2, fused to FGFR1 in 8p 11 myeloproliferative syndrome. Genes Chromosomes Cancer 40:78-83.
-
(2004)
Genes Chromosomes Cancer
, vol.40
, pp. 78-83
-
-
Grand, E.K.1
Grand, F.H.2
Chase, A.J.3
Ross, F.M.4
Corcoran, M.M.5
Oscier, D.G.6
Cross, N.C.7
-
44
-
-
5644271514
-
p53-Binding protein 1 is fused to the platelet-derived growth factor receptor beta in a patient with a t(5; 15)(q33;q22) and an imatinib-responsive eosinophilic myeloproliferative disorder
-
Grand FH, Burgstaller S, Kuhr T, Baxter EJ, Webersinke G, Thaler J, Chase AJ, Cross NC (2004b): p53-Binding protein 1 is fused to the platelet-derived growth factor receptor beta in a patient with a t(5; 15)(q33;q22) and an imatinib-responsive eosinophilic myeloproliferative disorder. Cancer Res 64:7216-7219.
-
(2004)
Cancer Res
, vol.64
, pp. 7216-7219
-
-
Grand, F.H.1
Burgstaller, S.2
Kuhr, T.3
Baxter, E.J.4
Webersinke, G.5
Thaler, J.6
Chase, A.J.7
Cross, N.C.8
-
45
-
-
25844469587
-
A BCR-JAK2 fusion gene as the result of a t(9;22)(p24;q 11 2) translocation in a patient with a clinically typical chronic myeloid leukemia
-
Griesinger F, Hennig H, Hillmer F, Podleschny M, Steffens R, Pies A, Wormann B, Haase D, Bohlander SK (2005): A BCR-JAK2 fusion gene as the result of a t(9;22)(p24;q 11.2) translocation in a patient with a clinically typical chronic myeloid leukemia. Genes Chromosomes Cancer 44:329-333.
-
(2005)
Genes Chromosomes Cancer
, vol.44
, pp. 329-333
-
-
Griesinger, F.1
Hennig, H.2
Hillmer, F.3
Podleschny, M.4
Steffens, R.5
Pies, A.6
Wormann, B.7
Haase, D.8
Bohlander, S.K.9
-
46
-
-
0023689044
-
Cytogenetics of acutely transformed chronic myeloproliferative syndromes without a Philadelphia chromosome. A multicenter study of 55 patients
-
Groupe Franijais de Cytogenetique Hematologique
-
Groupe Franijais de Cytogenetique Hematologique (1988): Cytogenetics of acutely transformed chronic myeloproliferative syndromes without a Philadelphia chromosome. A multicenter study of 55 patients. Cancer Genet Cytogenet 32:157-168.
-
(1988)
Cancer Genet Cytogenet
, vol.32
, pp. 157-168
-
-
-
47
-
-
0034161335
-
FGFR1 is fused to the centrosome-associated protein CEP110 in the 8pl2 stem cell myeloproliferative disorder with t(8;9)(pl2;q33)
-
Guasch G, Mack GJ, Popovici C, Dastugue N, Birnbaum D, Rattner JB, Pebusque MJ (2000): FGFR1 is fused to the centrosome-associated protein CEP110 in the 8pl2 stem cell myeloproliferative disorder with t(8;9)(pl2;q33). Blood 95:1788-1796.
-
(2000)
Blood
, vol.95
, pp. 1788-1796
-
-
Guasch, G.1
Mack, G.J.2
Popovici, C.3
Dastugue, N.4
Birnbaum, D.5
Rattner, J.B.6
Pebusque, M.J.7
-
48
-
-
0037216062
-
Endogenous retro viral sequence is fused to FGFR1 kinase in the 8pl 2 stem-cell myeloproliferative disorder with t(8;19)(pl2;ql3 3)
-
Guasch G, Popovici C, Mugneret F, Chaffanet M, Pontarotti P, Birnbaum D, Pebusque MJ (2003): Endogenous retro viral sequence is fused to FGFR1 kinase in the 8pl 2 stem-cell myeloproliferative disorder with t(8;19)(pl2;ql3.3). Blood 101:286-288.
-
(2003)
Blood
, vol.101
, pp. 286-288
-
-
Guasch, G.1
Popovici, C.2
Mugneret, F.3
Chaffanet, M.4
Pontarotti, P.5
Birnbaum, D.6
Pebusque, M.J.7
-
49
-
-
0347597750
-
FOP- FGFR1 tyrosine kinase, the product of a t(6;8) translocation, induces a fatal myeloproliferative disease in mice
-
Guasch G, Delaval B, Arnoulet C, Xie MJ, Xerri L, Sainty D, Birnbaum D, Pebusque MJ (2004): FOP- FGFR1 tyrosine kinase, the product of a t(6;8) translocation, induces a fatal myeloproliferative disease in mice. Blood 103:309-312.
-
(2004)
Blood
, vol.103
, pp. 309-312
-
-
Guasch, G.1
Delaval, B.2
Arnoulet, C.3
Xie, M.J.4
Xerri, L.5
Sainty, D.6
Birnbaum, D.7
Pebusque, M.J.8
-
50
-
-
33745213401
-
The JAK2 V617F mutation identifies a subgroup of MDS patients with isolated deletion 5q and a proliferative bone marrow
-
Ingram W, Lea NC, Cervera J, Germing U, Fenaux P, Cassinat B, Kiladjian JJ, Varkonyi J, Antunovic P, Westwood NB, Arno MJ, Mohamedali A, Gaken J, Kontou T, Czepulkowski BH, Twine NA, Tamaska J, Csomer J, Benedek S, Gattermann N, Zipperer E, Giagounidis A, Garcia-Casado Z, Sanz G, Mufti GJ (2006): The JAK2 V617F mutation identifies a subgroup of MDS patients with isolated deletion 5q and a proliferative bone marrow. Leukemia 20:1319-1321.
-
(2006)
Leukemia
, vol.20
, pp. 1319-1321
-
-
Ingram, W.1
Lea, N.C.2
Cervera, J.3
Germing, U.4
Fenaux, P.5
Cassinat, B.6
Kiladjian, J.J.7
Varkonyi, J.8
Antunovic, P.9
Westwood, N.B.10
Arno, M.J.11
Mohamedali, A.12
Gaken, J.13
Kontou, T.14
Czepulkowski, B.H.15
Twine, N.A.16
Tamaska, J.17
Csomer, J.18
Benedek, S.19
Gattermann, N.20
Zipperer, E.21
Giagounidis, A.22
Garcia-Casado, Z.23
Sanz, G.24
Mufti, G.J.25
more..
-
51
-
-
0017812507
-
Agnogenic myeloid metaplasia: a clonal proliferation of hematopoietic stem cells with secondary myelofibrosis
-
Jacobson RJ, Salo A, Fialkow PJ (1978): Agnogenic myeloid metaplasia: a clonal proliferation of hematopoietic stem cells with secondary myelofibrosis. Blood 51:189-194.
-
(1978)
Blood
, vol.51
, pp. 189-194
-
-
Jacobson, R.J.1
Salo, A.2
Fialkow, P.J.3
-
52
-
-
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 (2005): A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature 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
-
53
-
-
34249732053
-
Low-dose imatinib mesylate leads to rapid induction of major molecular responses and achievement of complete molecular remission in FIP1L1 -PDGFRA-positive chronic eosinophilic leukemia
-
Jovanovic JV, Score J, Waghorn K, Cilloni D, Gottardi E, Metzgeroth G, Erben P, Popp H, Walz C, Hochhaus A, Roche-Lestienne C, Preudhomme C, Solomon E, Apperley J, Rondoni M, Ottaviani E, Martinelli G, Brito-Babapulle F, Saglio G, Hehhnann R, Cross NC, Reiter A, Grimwade D (2007): Low-dose imatinib mesylate leads to rapid induction of major molecular responses and achievement of complete molecular remission in FIP1L1 -PDGFRA-positive chronic eosinophilic leukemia. Blood 109:4635-^640.
-
(2007)
Blood
, vol.109
, pp. 4635-4640
-
-
Jovanovic, J.V.1
Score, J.2
Waghorn, K.3
Cilloni, D.4
Gottardi, E.5
Metzgeroth, G.6
Erben, P.7
Popp, H.8
Walz, C.9
Hochhaus, A.10
Roche-Lestienne, C.11
Preudhomme, C.12
Solomon, E.13
Apperley, J.14
Rondoni, M.15
Ottaviani, E.16
Martinelli, G.17
Brito-Babapulle, F.18
Saglio, G.19
Hehhnann, R.20
Cross, N.C.21
Reiter, A.22
Grimwade, D.23
more..
-
54
-
-
0038792233
-
Elevated serum tryptase levels identify a subset of patients with a myeloproliferative variant of idiopathic hypereosinophilic syndrome associated with tissue fibrosis, poor prognosis, and imatinib responsiveness
-
Klion AD, Noel P, Akin C, Law MA, Gilliland DG, Cools J, Metcalfe DD, Nutman TB (2003): Elevated serum tryptase levels identify a subset of patients with a myeloproliferative variant of idiopathic hypereosinophilic syndrome associated with tissue fibrosis, poor prognosis, and imatinib responsiveness. Blood 101:4660-4666.
-
(2003)
Blood
, vol.101
, pp. 4660-4666
-
-
Klion, A.D.1
Noel, P.2
Akin, C.3
Law, M.A.4
Gilliland, D.G.5
Cools, J.6
Metcalfe, D.D.7
Nutman, T.B.8
-
55
-
-
0030954685
-
Two new EPO receptor mutations: truncated EPO receptors are most frequently associated with primary familial and congenital polycythemias
-
Kralovics R, Indrak K, Stopka T, Berman BW, Prchal JF, Prchal JT (1997): Two new EPO receptor mutations: truncated EPO receptors are most frequently associated with primary familial and congenital polycythemias. Blood 90:2057-2061.
-
(1997)
Blood
, vol.90
, pp. 2057-2061
-
-
Kralovics, R.1
Indrak, K.2
Stopka, T.3
Berman, B.W.4
Prchal, J.F.5
Prchal, J.T.6
-
56
-
-
0036191941
-
Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera
-
Kralovics R, Guan Y, Prchal JT (2002): Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera. Exp Hematol 30:229-236.
-
(2002)
Exp Hematol
, vol.30
, pp. 229-236
-
-
Kralovics, R.1
Guan, Y.2
Prchal, J.T.3
-
57
-
-
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 (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
Teo, S.S.4
Tiedt, R.5
Passweg, J.R.6
Tichelli, A.7
Cazzola, M.8
Skoda, R.C.9
-
58
-
-
0031975407
-
Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies
-
La Starza R, Wlodarska I, Aventin A, Falzetti D, Crescenzi B, Martelli MF, Van den Berghe H, Mecucci C (1998): Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies. Blood 91:231-237.
-
(1998)
Blood
, vol.91
, pp. 231-237
-
-
La Starza, R.1
Wlodarska, I.2
Aventin, A.3
Falzetti, D.4
Crescenzi, B.5
Martelli, M.F.6
Van Den Berghe, H.7
Mecucci, C.8
-
59
-
-
33745721197
-
JAK2V617F expression in murine hematopoietic cells leads to MPD mimicking human PV with secondary myelofibrosis
-
Lacout C, Pisani DF, Tulliez M, Gachelin FM, Vainchenker W, Villeval JL (2006): JAK2V617F expression in murine hematopoietic cells leads to MPD mimicking human PV with secondary myelofibrosis. Blood 108:1652-1660.
-
(2006)
Blood
, vol.108
, pp. 1652-1660
-
-
Lacout, C.1
Pisani, D.F.2
Tulliez, M.3
Gachelin, F.M.4
Vainchenker, W.5
Villeval, J.L.6
-
60
-
-
38549089581
-
Activity of imatinib in systemic mastocytosis with chronic basophilic leukemia and a PRKG2-PDGFRB fusion
-
Lahortiga I, Akin C, Cools J, Wilson TM, Mentens N, Arthur DC, Marie I, Noel P, Kocabas C, Marynen P, Lessin LS, Wlodarska I, Robyn J, Metcalfe DD (2008): Activity of imatinib in systemic mastocytosis with chronic basophilic leukemia and a PRKG2-PDGFRB fusion. Haematologica 93:49-56.
-
(2008)
Haematologica
, vol.93
, pp. 49-56
-
-
Lahortiga, I.1
Akin, C.2
Cools, J.3
Wilson, T.M.4
Mentens, N.5
Arthur, D.C.6
Marie, I.7
Noel, P.8
Kocabas, C.9
Marynen, P.10
Lessin, L.S.11
Wlodarska, I.12
Robyn, J.13
Metcalfe, D.D.14
-
61
-
-
0018978059
-
Cytogenetic studies in Philadelphia chromosome-negative myeloproliferative disorders, particularly polycythaemia rubra vera
-
Lawler SD (1980): Cytogenetic studies in Philadelphia chromosome-negative myeloproliferative disorders, particularly polycythaemia rubra vera. Clin Haematol 9:159-174.
-
(1980)
Clin Haematol
, vol.9
, pp. 159-174
-
-
Lawler, S.D.1
-
62
-
-
25844518265
-
The JAK2 V617F 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 BJ, Loh ML, Beran M, Stoffregen E, Berger R, Clark JJ, Willis SG, Nguyen KT, Flores NJ, Estey E, Gattermann N, Armstrong S, Look AT, Griffin JD, Bernard OA, Heinrich MC, Gilliland DG, Druker B, Deininger MW (2005a): The JAK2 V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia. Blood 106:3377-3379.
-
(2005)
Blood
, vol.106
, pp. 3377-3379
-
-
Levine, R.L.1
Loriaux, M.2
Huntly, B.J.3
Loh, M.L.4
Beran, M.5
Stoffregen, E.6
Berger, R.7
Clark, J.J.8
Willis, S.G.9
Nguyen, K.T.10
Flores, N.J.11
Estey, E.12
Gattermann, N.13
Armstrong, S.14
Look, A.T.15
Griffin, J.D.16
Bernard, O.A.17
Heinrich, M.C.18
Gilliland, D.G.19
Druker, B.20
Deininger, M.W.21
more..
-
63
-
-
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 (2005b): 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
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..
-
64
-
-
11844290650
-
K1AA1509 is a novel PDGFRB fusion partner in imatinib-responsive myeloproliferative disease associated with a t(5; 14)(q33;q32)
-
Levine RL, Wadleigh M, Sternberg DW, Wlodarska I, Galinsky I, Stone RM, DeAngelo DJ, Gilliland DG, Cools J (2005c): K1AA1509 is a novel PDGFRB fusion partner in imatinib-responsive myeloproliferative disease associated with a t(5; 14)(q33;q32). Leukemia 19:27-30.
-
(2005)
Leukemia
, vol.19
, pp. 27-30
-
-
Levine, R.L.1
Wadleigh, M.2
Sternberg, D.W.3
Wlodarska, I.4
Galinsky, I.5
Stone, R.M.6
DeAngelo, D.J.7
Gilliland, D.G.8
Cools, J.9
-
65
-
-
0009013631
-
Somatic c-KIT activating mutation in urticaria pigmentosa and aggressive mastocytosis: establishment of clonality in a human mast cell neoplasm
-
Longley BJ, Tyrrell L, Lu SZ, Ma YS, Langley K, Ding TG, Duffy T, Jacobs P, Tang LH, Modlin I (1996): Somatic c-KIT activating mutation in urticaria pigmentosa and aggressive mastocytosis: establishment of clonality in a human mast cell neoplasm. Nat Genet 12:312-314.
-
(1996)
Nat Genet
, vol.12
, pp. 312-314
-
-
Longley, B.J.1
Tyrrell, L.2
Lu, S.Z.3
Ma, Y.S.4
Langley, K.5
Ding, T.G.6
Duffy, T.7
Jacobs, P.8
Tang, L.H.9
Modlin, I.10
-
66
-
-
0033555976
-
Myelodysplastic and myeloproliferative disorders of childhood: a study of 167 patients
-
Luna-Fineman S, Shannon KM, Atwater SK, Davis J, Masterson M, Ortega J, Sanders J, Steinherz P, Weinberg V, Lange BJ (1999): Myelodysplastic and myeloproliferative disorders of childhood: a study of 167 patients. Blood 93:459-466.
-
(1999)
Blood
, vol.93
, pp. 459-466
-
-
Luna-Fineman, S.1
Shannon, K.M.2
Atwater, S.K.3
Davis, J.4
Masterson, M.5
Ortega, J.6
Sanders, J.7
Steinherz, P.8
Weinberg, V.9
Lange, B.J.10
-
67
-
-
0036493872
-
The c-KIT mutation causing human mastocytosis is resistant to STI571 and dther KIT kinase inhibitors; kinases with enzymatic site mutations show different inhibitor sensitivity profiles than wild-type kinases and those with regulatory-type mutations
-
Ma Y, Zeng S, Metcalfe DD, Akin C, Dimitrijevic S, Butterfield JH, McMahon G, Longley BJ (2002): The c-KIT mutation causing human mastocytosis is resistant to STI571 and dther KIT kinase inhibitors; kinases with enzymatic site mutations show different inhibitor sensitivity profiles than wild-type kinases and those with regulatory-type mutations. Blood 99:1741-1744.
-
(2002)
Blood
, vol.99
, pp. 1741-1744
-
-
Ma, Y.1
Zeng, S.2
Metcalfe, D.D.3
Akin, C.4
Dimitrijevic, S.5
Butterfield, J.H.6
McMahon, G.7
Longley, B.J.8
-
68
-
-
0036202064
-
The 8pl I myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1
-
Macdonald D, Reiter A, Cross NC (2002): The 8pl I myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1. Acta Haematol 107:101-107.
-
(2002)
Acta Haematol
, vol.107
, pp. 101-107
-
-
Macdonald, D.1
Reiter, A.2
Cross, N.C.3
-
69
-
-
0035849797
-
Identification of candidate genes on chromosome band 20ql2 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines
-
MacGrogan D, Alvarez S, DeBlasio T, Jhanwar SC, Nimer SD (2001): Identification of candidate genes on chromosome band 20ql2 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines. Oncogene 20:4150-4160.
-
(2001)
Oncogene
, vol.20
, pp. 4150-4160
-
-
MacGrogan, D.1
Alvarez, S.2
DeBlasio, T.3
Jhanwar, S.C.4
Nimer, S.D.5
-
70
-
-
0035889128
-
Rabaptin-5 is a novel fusion partner to platelet-derived growth factor beta receptor in chronic myelomonocytic leukemia
-
Magnusson MK, Meade KE, Brown KE, Arthur DC, Krueger LA, Barrett AJ, Dunbar CE (2001): Rabaptin-5 is a novel fusion partner to platelet-derived growth factor beta receptor in chronic myelomonocytic leukemia. Blood 98:2518-2525.
-
(2001)
Blood
, vol.98
, pp. 2518-2525
-
-
Magnusson, M.K.1
Meade, K.E.2
Brown, K.E.3
Arthur, D.C.4
Krueger, L.A.5
Barrett, A.J.6
Dunbar, C.E.7
-
71
-
-
0025848934
-
Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature
-
Mertens F, Johansson B, Heim S, Kristoffersson U, Mitelman F (1991): Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature. Leukemia 5:214-220.
-
(1991)
Leukemia
, vol.5
, pp. 214-220
-
-
Mertens, F.1
Johansson, B.2
Heim, S.3
Kristoffersson, U.4
Mitelman, F.5
-
72
-
-
5644284103
-
HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t(5;17)(q33;pl 1
-
Morerio C, Acquila M, Rosanda C, Rapella A, Dufour C, Locatelli F, Maserati E, Pasquali F, Panarello C (2004): HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t(5;17)(q33;pl 1.2). Cancer Res 64:2649-2651.
-
(2004)
2). Cancer Res
, vol.64
, pp. 2649-2651
-
-
Morerio, C.1
Acquila, M.2
Rosanda, C.3
Rapella, A.4
Dufour, C.5
Locatelli, F.6
Maserati, E.7
Pasquali, F.8
Panarello, C.9
-
73
-
-
0029031073
-
Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes
-
Nacheva E, Holloway T, Carter N, Grace C, White N, Green AR (1995): Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes. Cancer Genet Cytogenet 80:87-94.
-
(1995)
Cancer Genet Cytogenet
, vol.80
, pp. 87-94
-
-
Nacheva, E.1
Holloway, T.2
Carter, N.3
Grace, C.4
White, N.5
Green, A.R.6
-
74
-
-
0036439588
-
Exploring polycythaemia vera with fluorescence in situ hybridization: additional cryptic 9p is the most frequent abnormality detected
-
Najfeld V, Montella L, Scalise A, Fruchtman S (2002): Exploring polycythaemia vera with fluorescence in situ hybridization: additional cryptic 9p is the most frequent abnormality detected. Br J Haematol 119:558-566.
-
(2002)
Br J Haematol
, vol.119
, pp. 558-566
-
-
Najfeld, V.1
Montella, L.2
Scalise, A.3
Fruchtman, S.4
-
75
-
-
10744228486
-
CHIC2 deletion, a surrogate for FIPIL1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy
-
Pardanani A, Ketterling RP, Brockman SR, Flynn HC, Paternoster SF, Shearer BM, Reeder TL, Li CY, Cross NC, Cools J, Gilliland DG, Dewald GW, Tefferi A (2003a): CHIC2 deletion, a surrogate for FIPIL1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy. Blood 102:3093-3096.
-
(2003)
Blood
, vol.102
, pp. 3093-3096
-
-
Pardanani, A.1
Ketterling, R.P.2
Brockman, S.R.3
Flynn, H.C.4
Paternoster, S.F.5
Shearer, B.M.6
Reeder, T.L.7
Li, C.Y.8
Cross, N.C.9
Cools, J.10
Gilliland, D.G.11
Dewald, G.W.12
Tefferi, A.13
-
77
-
-
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 (2006): MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients. Blood 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
-
78
-
-
34447627350
-
TG101209, a small molecule JAK2-selective kinase inhibitor potently inhibits myeloproliferative disorder-associated JAK2V617F and MPLW515L/K mutations
-
Pardanani A, Hood J, Lasho T, Levine RL, Martin MB, Noronha G, Finke C, Mak CC, Mesa R, Zhu H, Soil R, Gilliland DG, Tefferi A (2007a): TG101209, a small molecule JAK2-selective kinase inhibitor potently inhibits myeloproliferative disorder-associated JAK2V617F and MPLW515L/K mutations. Leukemia 21:1658-1668.
-
(2007)
Leukemia
, vol.21
, pp. 1658-1668
-
-
Pardanani, A.1
Hood, J.2
Lasho, T.3
Levine, R.L.4
Martin, M.B.5
Noronha, G.6
Finke, C.7
Mak, C.C.8
Mesa, R.9
Zhu, H.10
Soil, R.11
Gilliland, D.G.12
Tefferi, A.13
-
79
-
-
34548128326
-
Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera
-
Pardanani A, Lasho TL, Finke C, Hanson CA, Tefferi A (2007b): Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera. Leukemia 21:1960-1963.
-
(2007)
Leukemia
, vol.21
, pp. 1960-1963
-
-
Pardanani, A.1
Lasho, T.L.2
Finke, C.3
Hanson, C.A.4
Tefferi, A.5
-
80
-
-
0029080356
-
Genetic analysis of chromosome 13 deletions in BCR/ABL negative chronic myeloproliferative disorders
-
Pastore C, Nomdedeu J, Volpe G, Guerrasio A, Rege-Cambrin G, Parvis G, Pautasso M, Daglio C, Mazza U, Saglio G (1995): Genetic analysis of chromosome 13 deletions in BCR/ABL negative chronic myeloproliferative disorders. Genes Chromosomes Cancer 14:106-111.
-
(1995)
Genes Chromosomes Cancer
, vol.14
, pp. 106-111
-
-
Pastore, C.1
Nomdedeu, J.2
Volpe, G.3
Guerrasio, A.4
Rege-Cambrin, G.5
Parvis, G.6
Pautasso, M.7
Daglio, C.8
Mazza, U.9
Saglio, G.10
-
81
-
-
0037441601
-
Mutations in the VHL gene in sporadic apparently congenital polycythemia
-
Pastore YD, Jelinek J, Ang S, Guan Y, Liu E, Jedlickova K, Krishnamurti L, Prchal JT (2003): Mutations in the VHL gene in sporadic apparently congenital polycythemia. Blood 101:1591-1595.
-
(2003)
Blood
, vol.101
, pp. 1591-1595
-
-
Pastore, Y.D.1
Jelinek, J.2
Ang, S.3
Guan, Y.4
Liu, E.5
Jedlickova, K.6
Krishnamurti, L.7
Prchal, J.T.8
-
82
-
-
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, Monpoux F, Van Rompaey L, Baens M, Van den Berghe H, Marynen P (1997): 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 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
Monpoux, F.7
Van Rompaey, L.8
Baens, M.9
Van Den Berghe, H.10
Marynen, P.11
-
83
-
-
0033558253
-
The t(6;8)(q27;p 11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1
-
Popovici C, Zhang B, Gregoire MJ, Jonveaux P, Lafage-Pochitaloff M, Bimbaum D, Pebusque MJ (1999): The t(6;8)(q27;p 11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1. Blood 93A3SI-US9.
-
(1999)
Blood
-
-
Popovici, C.1
Zhang, B.2
Gregoire, M.J.3
Jonveaux, P.4
Lafage-Pochitaloff, M.5
Bimbaum, D.6
Pebusque, M.J.7
-
84
-
-
0021956939
-
Evidence for the involvement of B lymphoid cells in polycythemia vera and essential thrombocythemia
-
Raskind WH, Jacobson R, Murphy S, Adamson JW, Fialkow PJ (1985): Evidence for the involvement of B lymphoid cells in polycythemia vera and essential thrombocythemia. J Clin Invest 75:1388-1390.
-
(1985)
J Clin Invest
, vol.75
, pp. 1388-1390
-
-
Raskind, W.H.1
Jacobson, R.2
Murphy, S.3
Adamson, J.W.4
Fialkow, P.J.5
-
85
-
-
0023092651
-
A chromosomal profile of polycythemia vera
-
Rege-Cambrin G, Mecucci C, Tricot G, Michaux JL, Louwagie A, Van Hove W, Francart H, Van den Berghe H (1987): A chromosomal profile of polycythemia vera. Cancer Genet Cytogenet 25:233-245.
-
(1987)
Cancer Genet Cytogenet
, vol.25
, pp. 233-245
-
-
Rege-Cambrin, G.1
Mecucci, C.2
Tricot, G.3
Michaux, J.L.4
Louwagie, A.5
Van Hove, W.6
Francart, H.7
Van Den Berghe, H.8
-
86
-
-
0026342824
-
Extra translocation + der(lq9p) is a prognostic indicator in myeloproliferative disorders
-
Rege-Cambrin G, Speleman F, Kerim S, Scaravaglio P, Carozzi F, Dal Cin P, Michaux JL, Offner F, Saglio G, Van den Berghe H (1991): Extra translocation + der(lq9p) is a prognostic indicator in myeloproliferative disorders. Leukemia 5:1059-1063.
-
(1991)
Leukemia
, vol.5
, pp. 1059-1063
-
-
Rege-Cambrin, G.1
Speleman, F.2
Kerim, S.3
Scaravaglio, P.4
Carozzi, F.5
Dal Cin, P.6
Michaux, J.L.7
Offner, F.8
Saglio, G.9
Van Den Berghe, H.10
-
87
-
-
0030748326
-
Cytogenetic abnormalities and their prognostic significance in idiopathic myelofibrosis: a study of 106 cases
-
Reilly JT, Snowden JA, Spearing RL, Fitzgerald PM, Jones N, Watmore A, Potter A (1997): Cytogenetic abnormalities and their prognostic significance in idiopathic myelofibrosis: a study of 106 cases. Br J Haematol 98:96-102.
-
(1997)
Br J Haematol
, vol.98
, pp. 96-102
-
-
Reilly, J.T.1
Snowden, J.A.2
Spearing, R.L.3
Fitzgerald, P.M.4
Jones, N.5
Watmore, A.6
Potter, A.7
-
88
-
-
0032170974
-
Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(pl I;ql2) myeloproliferative syndrome
-
Reiter A, Sohal J, Kulkarni S, Chase A, Macdonald DH, Aguiar RC, Goncalves C, Hernandez JM, Jennings BA, Goldman JM, Cross NC (1998): Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(pl I;ql2) myeloproliferative syndrome. Blood 92:1735-1742.
-
(1998)
Blood
, vol.92
, pp. 1735-1742
-
-
Reiter, A.1
Sohal, J.2
Kulkarni, S.3
Chase, A.4
Macdonald, D.H.5
Aguiar, R.C.6
Goncalves, C.7
Hernandez, J.M.8
Jennings, B.A.9
Goldman, J.M.10
Cross, N.C.11
-
89
-
-
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, Berger U, Telford N, Aruliah S, Yin JA, Vanstraelen D, Barker HF, Taylor PC, O'Driscoll A, Benedetti F, Rudolph C, Kolb HJ, Hochhaus A, Hehlmann R, Chase A, Cross NC (2005): The t(8;9)(p22;p24) is a recurrent abnormality in chronic and acute leukemia that fuses PCM1 to JAK2. Cancer Res 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
Berger, U.7
Telford, N.8
Aruliah, S.9
Yin, J.A.10
Vanstraelen, D.11
Barker, H.F.12
Taylor, P.C.13
O'Driscoll, A.14
Benedetti, F.15
Rudolph, C.16
Kolb, H.J.17
Hochhaus, A.18
Hehlmann, R.19
Chase, A.20
Cross, N.C.21
more..
-
90
-
-
33846828831
-
Cytogenetics and molecular genetics in myelofibrosis with myeloid metaplasia and polycythemia vera
-
Roche-Lestienne C, Andrieux J (2007): Cytogenetics and molecular genetics in myelofibrosis with myeloid metaplasia and polycythemia vera. Pathol Biol 55:49-55.
-
(2007)
Pathol Biol
, vol.55
, pp. 49-55
-
-
Roche-Lestienne, C.1
Andrieux, J.2
-
91
-
-
34249799656
-
PDGFRB fuses to TPM3 in the t(l;5)(q23;q33) of chronic eosinophilic leukemia and to NDE1 in the t(5;16)(q33;pl3) of chronic myelomonocytic leukemia
-
Rosati R, La Starza R, Bardi A, Luciano L, Matteucci C, Pierini V (2006a): PDGFRB fuses to TPM3 in the t(l;5)(q23;q33) of chronic eosinophilic leukemia and to NDE1 in the t(5;16)(q33;pl3) of chronic myelomonocytic leukemia. Haematologica 91(Suppl 1): 214.
-
(2006)
Haematologica
, vol.91
, Issue.SUPPL 1
, pp. 214
-
-
Rosati, R.1
La Starza, R.2
Bardi, A.3
Luciano, L.4
Matteucci, C.5
Pierini, V.6
-
92
-
-
33747602537
-
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia
-
Rosati R, La Starza R, Luciano L, Gorello P, Matteucci C, Pierini V, Romoli S, Crescenzi B, Rotoli B, Martelli MF, Pane F, Mecucci C (2006b): TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia. Leukemia 20:1623-1624.
-
(2006)
Leukemia
, vol.20
, pp. 1623-1624
-
-
Rosati, R.1
La Starza, R.2
Luciano, L.3
Gorello, P.4
Matteucci, C.5
Pierini, V.6
Romoli, S.7
Crescenzi, B.8
Rotoli, B.9
Martelli, M.F.10
Pane, F.11
Mecucci, C.12
-
93
-
-
0031864246
-
Fusion of Huntingtin interacting protein 1 to platelet-derived growth factor beta receptor (PDGFbetaR) in chronic myelomonocytic leukemia with t(5;7)(q33;ql 1
-
Ross TS, Bernard OA, Berger R, Gilliland DG (1998): Fusion of Huntingtin interacting protein 1 to platelet-derived growth factor beta receptor (PDGFbetaR) in chronic myelomonocytic leukemia with t(5;7)(q33;ql 1.2). Blood 91:4419-4426.
-
(1998)
2). Blood
, vol.91
, pp. 4419-4426
-
-
Ross, T.S.1
Bernard, O.A.2
Berger, R.3
Gilliland, D.G.4
-
94
-
-
0027375437
-
Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20
-
Roulston D, Espinosa R III, Stoffel M, Bell GI, Le Beau MM (1993): Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20. Blood 82:3424-3429.
-
(1993)
Blood
, vol.82
, pp. 3424-3429
-
-
Roulston, D.1
Espinosa III, R.2
Stoffel, M.3
Bell, G.I.4
Le Beau, M.M.5
-
95
-
-
0035877975
-
H4(DIOS17O), a gene frequently rearranged in papillary thyroid carcinoma, is fused to the platelet-derived growth factor receptor beta gene in atypical chronic myeloid leukemia with t(5;10)(q33;q22)
-
Schwaller J, Anastasiadou E, Cain D, Kutok J, Wojiski S, Williams IR, La Starza R, Crescenzi B, Sternberg DW, Andreasson P, Schiavo R, Siena S, Mecucci C, Gilliland DG (2001): H4(DIOS17O), a gene frequently rearranged in papillary thyroid carcinoma, is fused to the platelet-derived growth factor receptor beta gene in atypical chronic myeloid leukemia with t(5;10)(q33;q22). Blood 97:3910-3918.
-
(2001)
Blood
, vol.97
, pp. 3910-3918
-
-
Schwaller, J.1
Anastasiadou, E.2
Cain, D.3
Kutok, J.4
Wojiski, S.5
Williams, I.R.6
La Starza, R.7
Crescenzi, B.8
Sternberg, D.W.9
Andreasson, P.10
Schiavo, R.11
Siena, S.12
Mecucci, C.13
Gilliland, D.G.14
-
96
-
-
33646152550
-
Identification of a novel imatinib responsive KIF5B-PDGFRA fusion gene following screening for PDGFRA overexpression in patients with hypereosinophilia
-
Score J, Curtis C, Waghorn K, Stalder M, Jotterand M, Grand FH, Cross NC (2006): Identification of a novel imatinib responsive KIF5B-PDGFRA fusion gene following screening for PDGFRA overexpression in patients with hypereosinophilia. Leukemia 20:827-832.
-
(2006)
Leukemia
, vol.20
, pp. 827-832
-
-
Score, J.1
Curtis, C.2
Waghorn, K.3
Stalder, M.4
Jotterand, M.5
Grand, F.H.6
Cross, N.C.7
-
97
-
-
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 (2007): JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis. N Engl J Med 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
-
98
-
-
0024460062
-
Cytogenetic analysis in essential thrombocythemia at diagnosis and at transformation
-
Sessarego M, Defferrari R, Dejana AM, Rebuttato AM, Fugazza G, Salvidio E, Ajmar F (1989): Cytogenetic analysis in essential thrombocythemia at diagnosis and at transformation. A 12-year study. Cancer Genet Cytogenet 43:57-65.
-
(1989)
A 12-year study. Cancer Genet Cytogenet
, vol.43
, pp. 57-65
-
-
Sessarego, M.1
Defferrari, R.2
Dejana, A.M.3
Rebuttato, A.M.4
Fugazza, G.5
Salvidio, E.6
Ajmar, F.7
-
99
-
-
0026655447
-
Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7
-
Shannon KM, Turhan AG, Rogers PC, Kan YW (1992): Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7. Genomics 14:121-125.
-
(1992)
Genomics
, vol.14
, pp. 121-125
-
-
Shannon, K.M.1
Turhan, A.G.2
Rogers, P.C.3
Kan, Y.W.4
-
100
-
-
0035015773
-
Fluorescence in situ hybridization analysis of 25 cases of idiopathic myelofibrosis and two cases of secondary myelofibrosis: monoallelic loss of RBI D13S319 and D13S25 loci associated with cytogenetic deletion and translocation involving 13ql4
-
Sinclair EJ, Forrest EC, Reilly JT, Watmore AE, Potter AM (2001): Fluorescence in situ hybridization analysis of 25 cases of idiopathic myelofibrosis and two cases of secondary myelofibrosis: monoallelic loss of RBI, D13S319 and D13S25 loci associated with cytogenetic deletion and translocation involving 13ql4. Br J Haematol 113:365-368.
-
(2001)
Br J Haematol
, vol.113
, pp. 365-368
-
-
Sinclair, E.J.1
Forrest, E.C.2
Reilly, J.T.3
Watmore, A.E.4
Potter, A.M.5
-
101
-
-
21344440357
-
The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes
-
Steensma DP, Dewald GW, Lasho TL, Powell HL, McClure RF, Levine RL, Gilliland DG, Tefferi A (2005): The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes. Blood 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
Gilliland, D.G.7
Tefferi, A.8
-
102
-
-
0031982894
-
Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea: high proportion of cases with I7p deletion
-
Sterkers Y, Preudhomme C, Lai JL, Demory JL, Caulier MT, Watte! E, Bordessoule D, Bauters F, Fenaux P (1998): Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea: high proportion of cases with I7p deletion. Blood 91:616-622.
-
(1998)
Blood
, vol.91
, pp. 616-622
-
-
Sterkers, Y.1
Preudhomme, C.2
Lai, J.L.3
Demory, J.L.4
Caulier, M.T.5
Watte!, E.6
Bordessoule, D.7
Bauters, F.8
Fenaux, P.9
-
103
-
-
33744484267
-
Activation of FIP1L1 -PDGFRalpha requires disruption of the juxtamembrane domain of PDGFRalpha and is FIPlLl-independent
-
Stover EH, Chen J, Folens C, Lee BH, Mentens N, Marynen P, Williams IR, Gilliland DG, Cools J (2006): Activation of FIP1L1 -PDGFRalpha requires disruption of the juxtamembrane domain of PDGFRalpha and is FIPlLl-independent. Proc NatlAcadSci USA 103:8078-8083.
-
(2006)
Proc NatlAcadSci USA
, vol.103
, pp. 8078-8083
-
-
Stover, E.H.1
Chen, J.2
Folens, C.3
Lee, B.H.4
Mentens, N.5
Marynen, P.6
Williams, I.R.7
Gilliland, D.G.8
Cools, J.9
-
104
-
-
0023008771
-
Trisomy lq in polycythemia vera and its relation to disease transition
-
Swolin B, Weinfeld A, Westin J (1986): Trisomy lq in polycythemia vera and its relation to disease transition. Am J Hematol 22:155-167.
-
(1986)
Am J Hematol
, vol.22
, pp. 155-167
-
-
Swolin, B.1
Weinfeld, A.2
Westin, J.3
-
105
-
-
0023713372
-
A prospective long-term cytogenetic study in polycythemia vera in relation to treatment and clinical course
-
Swolin B, Weinfeld A, Westin J (1988): A prospective long-term cytogenetic study in polycythemia vera in relation to treatment and clinical course. Blood 72:386-395.
-
(1988)
Blood
, vol.72
, pp. 386-395
-
-
Swolin, B.1
Weinfeld, A.2
Westin, J.3
-
106
-
-
0343893612
-
Cytogenetic studies in patients with mastocytosis
-
Swolin B, Rodjer S, Roupe G (2000): Cytogenetic studies in patients with mastocytosis. Cancer Genet Cytogenel 120:131-135.
-
(2000)
Cancer Genet Cytogenel
, vol.120
, pp. 131-135
-
-
Swolin, B.1
Rodjer, S.2
Roupe, G.3
-
107
-
-
0036328608
-
Trisomies 8 and 9 not detected with FISH in patients with mastocytosis
-
Swolin B, Rodjer S, Ogard I, Roupe G (2002): Trisomies 8 and 9 not detected with FISH in patients with mastocytosis. Am J Hematol 70:324-325.
-
(2002)
Am J Hematol
, vol.70
, pp. 324-325
-
-
Swolin, B.1
Rodjer, S.2
Ogard, I.3
Roupe, G.4
-
108
-
-
33947328520
-
Oncogenes in myeloproliferative disorders
-
Tefferi A, Gilliland DG (2007): Oncogenes in myeloproliferative disorders. Cell Cycle 6:550-566.
-
(2007)
Cell Cycle
, vol.6
, pp. 550-566
-
-
Tefferi, A.1
Gilliland, D.G.2
-
109
-
-
38349101871
-
Classification and diagnosis of myeloproliferative neoplasms: the 2008 World Health Organization criteria and point-of-care diagnostic algorithms
-
Tefferi A, Vardiman JW (2008): Classification and diagnosis of myeloproliferative neoplasms: the 2008 World Health Organization criteria and point-of-care diagnostic algorithms. Leukemia 22:14-22.
-
(2008)
Leukemia
, vol.22
, pp. 14-22
-
-
Tefferi, A.1
Vardiman, J.W.2
-
110
-
-
0034988764
-
Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia
-
Tefferi A, Mesa RA, Schroeder G, Hanson CA, Li CY, Dewald GW (2001): Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia. Br J Haematol 113:763-771.
-
(2001)
Br J Haematol
, vol.113
, pp. 763-771
-
-
Tefferi, A.1
Mesa, R.A.2
Schroeder, G.3
Hanson, C.A.4
Li, C.Y.5
Dewald, G.W.6
-
111
-
-
34047236618
-
Markers of myeloproliferative diseases in childhood polycythemia vera and essential thrombocythemia
-
Teofili L, Giona F, Martini M, Cenci T, Guidi F, Torti L, Palumbo G, Amendola A, Foa R, Larocca LM (2007): Markers of myeloproliferative diseases in childhood polycythemia vera and essential thrombocythemia. J Clin Oncol 25:1048-1053.
-
(2007)
J Clin Oncol
, vol.25
, pp. 1048-1053
-
-
Teofili, L.1
Giona, F.2
Martini, M.3
Cenci, T.4
Guidi, F.5
Torti, L.6
Palumbo, G.7
Amendola, A.8
Foa, R.9
Larocca, L.M.10
-
112
-
-
0019631494
-
Report on essential thrombocythemia
-
Third International Workshop on Chromosomes in Leukemia
-
Third International Workshop on Chromosomes in Leukemia (1981): Report on essential thrombocythemia. Cancer Genet Cytogenet 4:138-142.
-
(1981)
Cancer Genet Cytogenet
, vol.4
, pp. 138-142
-
-
-
113
-
-
43249084493
-
Ratio of mutant JAK2-V617F to wild type JAK2 determines the MPD phenotypes in transgenic mice
-
Tiedt R, Hao-Shen H, Sobas MA, Looser R, Dimhofer S, Schwaller J, Skoda RC (2008): Ratio of mutant JAK2-V617F to wild type JAK2 determines the MPD phenotypes in transgenic mice. Blood 111:3931-3940.
-
(2008)
Blood
, vol.111
, pp. 3931-3940
-
-
Tiedt, R.1
Hao-Shen, H.2
Sobas, M.A.3
Looser, R.4
Dimhofer, S.5
Schwaller, J.6
Skoda, R.C.7
-
114
-
-
0035210554
-
Leukemic transformation of polycythemia vera after treatment with hydroxyurea with abnormalities of chromosome 17
-
Tothova E, Fricova M, Stecova N, Hlebaskova ML Kafkova A, Raffac S, Guman T, Svorcova E, Nebesnakova E (2001): Leukemic transformation of polycythemia vera after treatment with hydroxyurea with abnormalities of chromosome 17. Neoplasma 48:389-392.
-
(2001)
Neoplasma
, vol.48
, pp. 389-392
-
-
Tothova, E.1
Fricova, M.2
Stecova, N.3
Hlebaskova, M.L.4
Kafkova, A.5
Raffac, S.6
Guman, T.7
Svorcova, E.8
Nebesnakova, E.9
-
115
-
-
3042678647
-
Clinical and molecular features of FIP1L1 -PDFGRA (+) chronic eosinophilic leukemias
-
Vandenberghe P, Wlodarska I, Michaux L, Zachee P, Boogaerts M, Vanstraelen D, Herregods MC, Van Hoof A, Selleslag D, Roufosse F, Maerevoet M, Verhoef G, Cools J, Gilliland DG, Hagemeijer A, Marynen P (2004): Clinical and molecular features of FIP1L1 -PDFGRA (+) chronic eosinophilic leukemias. Leukemia 18:734-742.
-
(2004)
Leukemia
, vol.18
, pp. 734-742
-
-
Vandenberghe, P.1
Wlodarska, I.2
Michaux, L.3
Zachee, P.4
Boogaerts, M.5
Vanstraelen, D.6
Herregods, M.C.7
Van Hoof, A.8
Selleslag, D.9
Roufosse, F.10
Maerevoet, M.11
Verhoef, G.12
Cools, J.13
Gilliland, D.G.14
Hagemeijer, A.15
Marynen, P.16
-
116
-
-
34547953018
-
Clinical profile of homozygous JAK2 617V >F 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 SV, Caberlon S, Tafuri A, Ruggeri M, Specchia G, Liso V, Rossi E, Pogliani E, Gugliotta L, Bosi A, Barbui T (2007): Clinical profile of homozygous JAK2 617V >F mutation in patients with polycythemia vera or essential thrombocythemia. Blood 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, S.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..
-
117
-
-
0036786901
-
The World Health Organization (WHO) classification of the myeloid neoplasms
-
Vardiman JW, Harris NL, Brunning RD (2002): The World Health Organization (WHO) classification of the myeloid neoplasms. Blood 100:2292-2302.
-
(2002)
Blood
, vol.100
, pp. 2292-2302
-
-
Vardiman, J.W.1
Harris, N.L.2
Brunning, R.D.3
-
118
-
-
5644251199
-
NIN, a gene encoding a CEP110-like centrosomal protein, is fused to PDGFRB in a patient with a t(5;14)(q33;q24) and an imatinib-responsive myeloproliferative disorder
-
Vizmanos JL, Novo FJ, Roman JP, Baxter EJ, Lahortiga I, Larrayoz MJ, Odero MD, Giraldo P, Calasanz MJ, Cross NC (2004): NIN, a gene encoding a CEP110-like centrosomal protein, is fused to PDGFRB in a patient with a t(5;14)(q33;q24) and an imatinib-responsive myeloproliferative disorder. Cancer Res 64:2673-2676.
-
(2004)
Cancer Res
, vol.64
, pp. 2673-2676
-
-
Vizmanos, J.L.1
Novo, F.J.2
Roman, J.P.3
Baxter, E.J.4
Lahortiga, I.5
Larrayoz, M.J.6
Odero, M.D.7
Giraldo, P.8
Calasanz, M.J.9
Cross, N.C.10
-
119
-
-
20844443647
-
The t(8; 17)(p 11;q23) in the 8p 11 myeloproliferative syndrome fuses MYO18A to FGFR1
-
Walz C, Chase A, Schoch C, Weisser A, Schlegel F, Hochhaus A, Fuchs R, Schmitt-Graff A, Hehlmann R, Cross NC, Reiter A (2005): The t(8; 17)(p 11;q23) in the 8p 11 myeloproliferative syndrome fuses MYO18A to FGFR1. Leukemia 19:1005-1009.
-
(2005)
Leukemia
, vol.19
, pp. 1005-1009
-
-
Walz, C.1
Chase, A.2
Schoch, C.3
Weisser, A.4
Schlegel, F.5
Hochhaus, A.6
Fuchs, R.7
Schmitt-Graff, A.8
Hehlmann, R.9
Cross, N.C.10
Reiter, A.11
-
120
-
-
33748491495
-
Transient response to imatinib in a chronic eosinophilic leukemia associated with ins(9;4)(q33;ql2q25) and a CDK5RAP2-PDGFRA fusion gene
-
Walz C, Curtis C, Schnittger S, Schultheis B, Metzgeroth G, Schoch C, Lengfelder E, Erben P, Muller MC, Haferlach T, Hochhaus A, Hehlmann R, Cross NC, Reiter A (2006): Transient response to imatinib in a chronic eosinophilic leukemia associated with ins(9;4)(q33;ql2q25) and a CDK5RAP2-PDGFRA fusion gene. Genes Chromosomes Cancer 45:950-956.
-
(2006)
Genes Chromosomes Cancer
, vol.45
, pp. 950-956
-
-
Walz, C.1
Curtis, C.2
Schnittger, S.3
Schultheis, B.4
Metzgeroth, G.5
Schoch, C.6
Lengfelder, E.7
Erben, P.8
Muller, M.C.9
Haferlach, T.10
Hochhaus, A.11
Hehlmann, R.12
Cross, N.C.13
Reiter, A.14
-
121
-
-
33947543336
-
Characterization of three new imatinib-responsive fusion genes in chronic myeloproliferative disorders generated by disruption of the platelet-derived growth factor receptor beta gene
-
Walz C, Metzgeroth G, Haferlach C, Schmitt-Graeff A, Fabarius A, Hagen V, Prummer O, Rauh S, Hehlmann R, Hochhaus A, Cross NC, Reiter A (2007): Characterization of three new imatinib-responsive fusion genes in chronic myeloproliferative disorders generated by disruption of the platelet-derived growth factor receptor beta gene. Haematologica 92:163-169.
-
(2007)
Haematologica
, vol.92
, pp. 163-169
-
-
Walz, C.1
Metzgeroth, G.2
Haferlach, C.3
Schmitt-Graeff, A.4
Fabarius, A.5
Hagen, V.6
Prummer, O.7
Rauh, S.8
Hehlmann, R.9
Hochhaus, A.10
Cross, N.C.11
Reiter, A.12
-
122
-
-
0026533908
-
Cytogenetic studies of bone marrow fibroblasts cultured from patients with myelofibrosis and myeloid metaplasia
-
Wang JC, Lang HD, Lichter S, Weinstein M, Benn P (1992): Cytogenetic studies of bone marrow fibroblasts cultured from patients with myelofibrosis and myeloid metaplasia. Br J Haematol 80:184-188.
-
(1992)
Br J Haematol
, vol.80
, pp. 184-188
-
-
Wang, J.C.1
Lang, H.D.2
Lichter, S.3
Weinstein, M.4
Benn, P.5
-
123
-
-
0344826038
-
Cloning of the t (I;5)(q23;q33) in a myeloproliferative disorder associated with eosinophilia: involvement of PDGFRB and response to imatinib
-
Wilkinson K, Velloso ER, Lopes LF, Lee C, Aster JC, Shipp MA, Aguiar RC (2003): Cloning of the t (I;5)(q23;q33) in a myeloproliferative disorder associated with eosinophilia: involvement of PDGFRB and response to imatinib. Blood 102:4187-4190.
-
(2003)
Blood
, vol.102
, pp. 4187-4190
-
-
Wilkinson, K.1
Velloso, E.R.2
Lopes, L.F.3
Lee, C.4
Aster, J.C.5
Shipp, M.A.6
Aguiar, R.C.7
-
124
-
-
33744458176
-
Physical association of the patient-specific GATA1 mutants with RUNX1 in acute megakaryoblastic leukemia accompanying Down syndrome
-
Xu G, Kanezaki R, Toki T, Watanabe S, Takahashi Y, Terui K, Kitabayashi I, Ito E (2006): Physical association of the patient-specific GATA1 mutants with RUNX1 in acute megakaryoblastic leukemia accompanying Down syndrome. Leukemia 20:1002-1008.
-
(2006)
Leukemia
, vol.20
, pp. 1002-1008
-
-
Xu, G.1
Kanezaki, R.2
Toki, T.3
Watanabe, S.4
Takahashi, Y.5
Terui, K.6
Kitabayashi, I.7
Ito, E.8
-
125
-
-
0018147073
-
A chromosomal abnormality in primary thrombocythemia
-
Zaccaria A, Tura S (1978): A chromosomal abnormality in primary thrombocythemia. N EnglJ Med 298:1422-1423.
-
(1978)
N EnglJ Med
, vol.298
, pp. 1422-1423
-
-
Zaccaria, A.1
Tura, S.2
-
126
-
-
0037355255
-
Transient leukaemia: a benign form of leukaemia in newborn infants with trisomy 21
-
Zipursky A (2003): Transient leukaemia: a benign form of leukaemia in newborn infants with trisomy 21. Br J Haematol 120:930-938.
-
(2003)
Br J Haematol
, vol.120
, pp. 930-938
-
-
Zipursky, A.1
|