-
1
-
-
0036202064
-
The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1
-
Macdonald D., Reiter A., and Cross N.C. The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation of FGFR1. Acta Haematol 107 (2002) 101-107
-
(2002)
Acta Haematol
, vol.107
, pp. 101-107
-
-
Macdonald, D.1
Reiter, A.2
Cross, N.C.3
-
2
-
-
0037093259
-
NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15) [Erratum in: Blood 2002;100:1132]
-
Rosati R., La Starza R., Veronese A., Aventin A., Schwienbacher C., Vallespi T., Negrini M., Martelli M.F., and Mecucci C. NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15) [Erratum in: Blood 2002;100:1132]. Blood 99 (2002) 3857-3860
-
(2002)
Blood
, vol.99
, pp. 3857-3860
-
-
Rosati, R.1
La Starza, R.2
Veronese, A.3
Aventin, A.4
Schwienbacher, C.5
Vallespi, T.6
Negrini, M.7
Martelli, M.F.8
Mecucci, C.9
-
3
-
-
0035159831
-
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL
-
Fioretos T., Panagopoulos I., Lassen C., Swedin A., Billström R., Isaksson M., Strömbeck B., Olofsson T., Mitelman F., and Johansson B. Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL. Genes Chromosomes Cancer 32 (2001) 302-310
-
(2001)
Genes Chromosomes Cancer
, vol.32
, pp. 302-310
-
-
Fioretos, T.1
Panagopoulos, I.2
Lassen, C.3
Swedin, A.4
Billström, R.5
Isaksson, M.6
Strömbeck, B.7
Olofsson, T.8
Mitelman, F.9
Johansson, B.10
-
4
-
-
0035895067
-
The t(8;22) in chronic myeloid leukemia fuses BCR to FGFR1: transforming activity and specific inhibition of FGFR1 fusion proteins
-
Demiroglu A., Steer E.J., Heath C., Taylor K., Bentley M., Allen S.L., Koduru P., Brody J.P., Hawson G., Rodwell R., Doody M.L., Carnicero F., Reiter A., Goldman J.M., Melo J.V., and Cross N.C. The t(8;22) in chronic myeloid leukemia fuses BCR to FGFR1: transforming activity and specific inhibition of FGFR1 fusion proteins. Blood 98 (2001) 3778-3783
-
(2001)
Blood
, vol.98
, pp. 3778-3783
-
-
Demiroglu, A.1
Steer, E.J.2
Heath, C.3
Taylor, K.4
Bentley, M.5
Allen, S.L.6
Koduru, P.7
Brody, J.P.8
Hawson, G.9
Rodwell, R.10
Doody, M.L.11
Carnicero, F.12
Reiter, A.13
Goldman, J.M.14
Melo, J.V.15
Cross, N.C.16
-
5
-
-
0036972521
-
A fourth case of BCR-FGFR1 positive CML-like disease with t(8;22) translocation showing an extensive deletion on the derivative chromosome 8p
-
Pini M., Gottardi E., Scaravaglio P., Giugliano E., Libener R., Baraldi A., Muzio A., Cornaglia E., Saglio G., and Levis A. A fourth case of BCR-FGFR1 positive CML-like disease with t(8;22) translocation showing an extensive deletion on the derivative chromosome 8p. Hematol J 3 (2002) 315-316
-
(2002)
Hematol J
, vol.3
, pp. 315-316
-
-
Pini, M.1
Gottardi, E.2
Scaravaglio, P.3
Giugliano, E.4
Libener, R.5
Baraldi, A.6
Muzio, A.7
Cornaglia, E.8
Saglio, G.9
Levis, A.10
-
6
-
-
34249081692
-
Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome
-
Agerstam H., Lilljebjörn H., Lassen C., Swedin A., Richter J., Vandenberghe P., Johansson B., and Fioretos T. Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome. Genes Chromosomes Cancer 46 (2007) 635-643
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 635-643
-
-
Agerstam, H.1
Lilljebjörn, H.2
Lassen, C.3
Swedin, A.4
Richter, J.5
Vandenberghe, P.6
Johansson, B.7
Fioretos, T.8
-
7
-
-
0021069856
-
The predictive value of initial cytogenetic studies in 148 adults with acute nonlymphocytic leukemia: a 12-year study (1970-1982)
-
Larson R.A., Le Beau M.M., Vardiman J.W., Testa J.R., Golomb H.M., and Rowley J.D. The predictive value of initial cytogenetic studies in 148 adults with acute nonlymphocytic leukemia: a 12-year study (1970-1982). Cancer Genet Cytogenet 10 (1983) 219-236
-
(1983)
Cancer Genet Cytogenet
, vol.10
, pp. 219-236
-
-
Larson, R.A.1
Le Beau, M.M.2
Vardiman, J.W.3
Testa, J.R.4
Golomb, H.M.5
Rowley, J.D.6
-
8
-
-
84905515146
-
Identification of four new translocations involving FGFR1 in myeloid disorders
-
Sohal J., Chase A., Mould S., Corcoran M., Oscier D., Iqbal S., Parker S., Welborn J., Harris R.I., Martinelli G., Montefusco V., Sinclair P., Wilkins B.S., van den Berg H., Vanstraelen D., Goldman J.M., and Cross N.C. Identification of four new translocations involving FGFR1 in myeloid disorders. Genes Chromosomes Cancer 32 (2001) 155-163
-
(2001)
Genes Chromosomes Cancer
, vol.32
, pp. 155-163
-
-
Sohal, J.1
Chase, A.2
Mould, S.3
Corcoran, M.4
Oscier, D.5
Iqbal, S.6
Parker, S.7
Welborn, J.8
Harris, R.I.9
Martinelli, G.10
Montefusco, V.11
Sinclair, P.12
Wilkins, B.S.13
van den Berg, H.14
Vanstraelen, D.15
Goldman, J.M.16
Cross, N.C.17
-
9
-
-
33646484524
-
NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique
-
Romana S.P., Radford-Weiss I., Ben Abdelali R., Schluth C., Petit A., Dastugue N., Talmant P., Bilhou-Nabera C., Mugneret F., Lafage-Pochitaloff M., Mozziconacci M.J., Andrieu J., Lai J.L., Terre C., Rack K., Cornillet-Lefebvre P., Luquet I., Nadal N., Nguyen-Khac F., Perot C., Van den Akker J., Fert-Ferrer S., Cabrol C., Charrin C., Tigaud I., Poirel H., Vekemans M., Bernard O.A., and Berger R. NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique. Leukemia 20 (2006) 696-706
-
(2006)
Leukemia
, vol.20
, pp. 696-706
-
-
Romana, S.P.1
Radford-Weiss, I.2
Ben Abdelali, R.3
Schluth, C.4
Petit, A.5
Dastugue, N.6
Talmant, P.7
Bilhou-Nabera, C.8
Mugneret, F.9
Lafage-Pochitaloff, M.10
Mozziconacci, M.J.11
Andrieu, J.12
Lai, J.L.13
Terre, C.14
Rack, K.15
Cornillet-Lefebvre, P.16
Luquet, I.17
Nadal, N.18
Nguyen-Khac, F.19
Perot, C.20
Van den Akker, J.21
Fert-Ferrer, S.22
Cabrol, C.23
Charrin, C.24
Tigaud, I.25
Poirel, H.26
Vekemans, M.27
Bernard, O.A.28
Berger, R.29
more..
|