-
1
-
-
0026528225
-
T-cell lymphoblastic lymphoma with eosinophilia associated with subsequent myeloid malignancy
-
Abruzzo LV, Jaffe ES, Cotelingam JD, et al. T-cell lymphoblastic lymphoma with eosinophilia associated with subsequent myeloid malignancy. Am J Surg Pathol. 1992;16:236-245.
-
(1992)
Am J Surg Pathol
, vol.16
, pp. 236-245
-
-
Abruzzo, L.V.1
Jaffe, E.S.2
Cotelingam, J.D.3
-
2
-
-
0030842882
-
Abnormalities of chromosome band 8p11 in leukemia: Two clinical syndromes can be distinguished on the basis of MOZ involvement
-
Aguiar RC, Chase A, Coulthard S, et al. Abnormalities of chromosome band 8p11 in leukemia: two clinical syndromes can be distinguished on the basis of MOZ involvement. Blood. 1997;90:3130-3135.
-
(1997)
Blood
, vol.90
, pp. 3130-3135
-
-
Aguiar, R.C.1
Chase, A.2
Coulthard, S.3
-
3
-
-
0027851828
-
T lymphoid/myeloid bilineal crisis in chronic myelogenous leukemia
-
Akashi K, Mizuno S, Harada M, et al. T lymphoid/myeloid bilineal crisis in chronic myelogenous leukemia. Exp Hematol. 1993;21:743-748.
-
(1993)
Exp Hematol
, vol.21
, pp. 743-748
-
-
Akashi, K.1
Mizuno, S.2
Harada, M.3
-
4
-
-
0032784934
-
Precise developmental regulation of Ets family transcription factors during specification and commitment to the T cell lineage
-
Anderson MK, Hernandez-Hoyos G, Diamond RA, et al. Precise developmental regulation of Ets family transcription factors during specification and commitment to the T cell lineage. Development. 1999;126:3131-3148.
-
(1999)
Development
, vol.126
, pp. 3131-3148
-
-
Anderson, M.K.1
Hernandez-Hoyos, G.2
Diamond, R.A.3
-
5
-
-
0036193609
-
Constitutive expression of PU.1 in fetal hematopoietic progenitors blocks T cell development at the pro-T cell stage
-
Anderson MK, Weiss AH, Hernandez-Hoyos G, et al. Constitutive expression of PU.1 in fetal hematopoietic progenitors blocks T cell development at the pro-T cell stage. Immunity. 2002;16:285-296.
-
(2002)
Immunity
, vol.16
, pp. 285-296
-
-
Anderson, M.K.1
Weiss, A.H.2
Hernandez-Hoyos, G.3
-
6
-
-
0029007041
-
Translocation t(8;13) in a patient with T cell lymphoma and features of a myeloproliferative syndrome
-
Behringer D, Schaefer HE, Kunzmann R, et al. Translocation t(8;13) in a patient with T cell lymphoma and features of a myeloproliferative syndrome. Leukemia. 1995;9:988-992.
-
(1995)
Leukemia
, vol.9
, pp. 988-992
-
-
Behringer, D.1
Schaefer, H.E.2
Kunzmann, R.3
-
7
-
-
19944432120
-
8p11 myeloproliferative syndrome with a novel t(7;8) translocation leading to fusion of the FGFR1 and TIF1 genes
-
Belloni E, Trubia M, Gasparini P, et al. 8p11 myeloproliferative syndrome with a novel t(7;8) translocation leading to fusion of the FGFR1 and TIF1 genes. Genes Chromosomes Cancer. 2005;42:320-325.
-
(2005)
Genes Chromosomes Cancer
, vol.42
, pp. 320-325
-
-
Belloni, E.1
Trubia, M.2
Gasparini, P.3
-
8
-
-
0028837561
-
Proposals for the immunological classification of acute leukemias. European Group for the Immunological Characterization of Leukemias (EGIL)
-
Bene MC, Castoldi G, Knapp W, et al. Proposals for the immunological classification of acute leukemias. European Group for the Immunological Characterization of Leukemias (EGIL). Leukemia. 1995;9:1783-1786.
-
(1995)
Leukemia
, vol.9
, pp. 1783-1786
-
-
Bene, M.C.1
Castoldi, G.2
Knapp, W.3
-
9
-
-
0012585576
-
Acute leukemias of ambiguous lineage
-
eds, Lyon: IARC Press;
-
Brunning RD, Matutes E, Borowitz M, et al. Acute leukemias of ambiguous lineage. In: Jaffe ES, Harris NL, Stein H, et al, eds. Tumours of Haematopoietic and Lymphoid Tissues. Lyon: IARC Press; 2001:106-107.
-
(2001)
Tumours of Haematopoietic and Lymphoid Tissues
, pp. 106-107
-
-
Brunning, R.D.1
Matutes, E.2
Borowitz, M.3
-
10
-
-
17344393858
-
Immunophenotypic patterns and cytogenetic anomalies in acute non-lymphoblastic leukemia subtypes: A prospective study of 432 patients
-
Casasnovas RO, Campos L, Mugneret F, et al. Immunophenotypic patterns and cytogenetic anomalies in acute non-lymphoblastic leukemia subtypes: a prospective study of 432 patients. Leukemia. 1998;12:34-43.
-
(1998)
Leukemia
, vol.12
, pp. 34-43
-
-
Casasnovas, R.O.1
Campos, L.2
Mugneret, F.3
-
11
-
-
14444277275
-
t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12
-
Chaffanet M, Popovici C, Leroux D, et al. t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12. Oncogene. 1998;16:945-949.
-
(1998)
Oncogene
, vol.16
, pp. 945-949
-
-
Chaffanet, M.1
Popovici, C.2
Leroux, D.3
-
12
-
-
0029001407
-
Neutrophils and monocytes express high levels of PU.1 (Spi-1) but not Spi-B
-
Chen HM, Zhang P, Voso MT, et al. Neutrophils and monocytes express high levels of PU.1 (Spi-1) but not Spi-B. Blood. 1995;85:2918-2928.
-
(1995)
Blood
, vol.85
, pp. 2918-2928
-
-
Chen, H.M.1
Zhang, P.2
Voso, M.T.3
-
13
-
-
0031940365
-
Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization
-
Chernova O, Still I, Kalaycio M, et al. Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization. Genes Chromosomes Cancer. 1998;21:160-165.
-
(1998)
Genes Chromosomes Cancer
, vol.21
, pp. 160-165
-
-
Chernova, O.1
Still, I.2
Kalaycio, M.3
-
14
-
-
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 EJ, Heath C, et al. The t(8;22) in chronic myeloid leukemia fuses BCR to FGFR1: transforming activity and specific inhibition of FGFR1 fusion proteins. Blood. 2001;98:3778-3783.
-
(2001)
Blood
, vol.98
, pp. 3778-3783
-
-
Demiroglu, A.1
Steer, E.J.2
Heath, C.3
-
15
-
-
0027463046
-
Translocation (8;13) and T-cell lymphoma. A case report
-
Fagan K, Hyde S, Harrison P. Translocation (8;13) and T-cell lymphoma. A case report. Cancer Genet Cytogenet. 1993;65:71-73.
-
(1993)
Cancer Genet Cytogenet
, vol.65
, pp. 71-73
-
-
Fagan, K.1
Hyde, S.2
Harrison, P.3
-
16
-
-
0020505735
-
Novel reciprocal translocation between chromosomes 8 and 9 found in a patient with myeloproliferative disorder
-
Friedhoff F, Rajendra B, Moody R, et al. Novel reciprocal translocation between chromosomes 8 and 9 found in a patient with myeloproliferative disorder. Cancer Genet Cytogenet. 1983;9:391-394.
-
(1983)
Cancer Genet Cytogenet
, vol.9
, pp. 391-394
-
-
Friedhoff, F.1
Rajendra, B.2
Moody, R.3
-
17
-
-
1942422114
-
Identification of a novel gene, FGFR1OP2, fused to FGFR1 in 8p11 myeloproliferative syndrome
-
Grand EK, Grand FH, Chase AJ, et al. Identification of a novel gene, FGFR1OP2, fused to FGFR1 in 8p11 myeloproliferative syndrome. Genes Chromosomes Cancer. 2004;40:78-83.
-
(2004)
Genes Chromosomes Cancer
, vol.40
, pp. 78-83
-
-
Grand, E.K.1
Grand, F.H.2
Chase, A.J.3
-
18
-
-
0034161335
-
FGFR1 is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33)
-
Guasch G, Mack GJ, Popovici C, et al. FGFR1 is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33). Blood. 2000;95:1788-1796.
-
(2000)
Blood
, vol.95
, pp. 1788-1796
-
-
Guasch, G.1
Mack, G.J.2
Popovici, C.3
-
19
-
-
0037216062
-
Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3)
-
Guasch G, Popovici C, Mugneret F, et al. Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3). Blood. 2003;101:286-288.
-
(2003)
Blood
, vol.101
, pp. 286-288
-
-
Guasch, G.1
Popovici, C.2
Mugneret, F.3
-
20
-
-
0028941132
-
A syndrome of lymphoblastic lymphoma, eosinophilia, and myeloid hyperplasia/malignancy associated with t(8;13)(p11;q11): Description of a distinctive clinicopathologic entity
-
Inhorn RC, Aster JC, Roach SA, et al. A syndrome of lymphoblastic lymphoma, eosinophilia, and myeloid hyperplasia/malignancy associated with t(8;13)(p11;q11): description of a distinctive clinicopathologic entity. Blood. 1995;85:1881-1887.
-
(1995)
Blood
, vol.85
, pp. 1881-1887
-
-
Inhorn, R.C.1
Aster, J.C.2
Roach, S.A.3
-
21
-
-
0036207157
-
A fourth case of 8p11 myeloproliferative disorder transforming to B-lineage acute lymphoblastic leukaemia. A case report
-
JabbarAl-Obaidi M, Rymes N, White P, et al. A fourth case of 8p11 myeloproliferative disorder transforming to B-lineage acute lymphoblastic leukaemia. A case report. Acta Haematol. 2002;107:98-100.
-
(2002)
Acta Haematol
, vol.107
, pp. 98-100
-
-
JabbarAl-Obaidi, M.1
Rymes, N.2
White, P.3
-
22
-
-
0026723553
-
t(8;9)(p11;q32) in atypical chronic myeloid leukaemia: A new cytogenetic-clinicopathologic association?
-
Jotterand Bellomo M, Muhlematter D, Wicht M, et al. t(8;9)(p11;q32) in atypical chronic myeloid leukaemia: a new cytogenetic-clinicopathologic association? Br J Haematol. 1992;81:307-308.
-
(1992)
Br J Haematol
, vol.81
, pp. 307-308
-
-
Jotterand Bellomo, M.1
Muhlematter, D.2
Wicht, M.3
-
23
-
-
0037007023
-
Lineage infidelity in myeloid cells with TCR gene rearrangement: A latent developmental potential of proT cells revealed by ectopic cytokine receptor signaling
-
King AG, Kondo M, Scherer DC, et al. Lineage infidelity in myeloid cells with TCR gene rearrangement: a latent developmental potential of proT cells revealed by ectopic cytokine receptor signaling. Proc Natl Acad Sci U S A. 2002;99:4508-4513.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 4508-4513
-
-
King, A.G.1
Kondo, M.2
Scherer, D.C.3
-
24
-
-
0028276041
-
t(8;13) (p11;q12) translocation in a myeloproliferative disorder associated with a T-cell non-Hodgkin lymphoma
-
Leslie J, Barker T, Glancy M, et al. t(8;13) (p11;q12) translocation in a myeloproliferative disorder associated with a T-cell non-Hodgkin lymphoma. Br J Haematol. 1994;86:876-878.
-
(1994)
Br J Haematol
, vol.86
, pp. 876-878
-
-
Leslie, J.1
Barker, T.2
Glancy, M.3
-
25
-
-
0021082978
-
Philadelphia chromosome-negative chronic myelogenous leukemia in a child with t(8;9)(p11 or 12;q34)
-
Lewis JP, Jenks H, Lazerson J. Philadelphia chromosome-negative chronic myelogenous leukemia in a child with t(8;9)(p11 or 12;q34). Am J Pediatr Hematol Oncol. 1983;5:265-269.
-
(1983)
Am J Pediatr Hematol Oncol
, vol.5
, pp. 265-269
-
-
Lewis, J.P.1
Jenks, H.2
Lazerson, J.3
-
26
-
-
0028357763
-
An atypical myeloproliferative disorder with t(8;13) (p11;q12): A third case
-
Macdonald D, Sheerin SM, Cross NC, et al. An atypical myeloproliferative disorder with t(8;13) (p11;q12): a third case. Br J Haematol. 1994;86:879-880.
-
(1994)
Br J Haematol
, vol.86
, pp. 879-880
-
-
Macdonald, D.1
Sheerin, S.M.2
Cross, N.C.3
-
27
-
-
0031860817
-
Cytogenetic response induced by interferon alpha in the myeloproliferative disorder with eosinophilia, T cell lymphoma and the chromosomal translocation t(8;13)(p11;q12)
-
Martinez-Climent JA, Vizcarra E, Benet I, et al. Cytogenetic response induced by interferon alpha in the myeloproliferative disorder with eosinophilia, T cell lymphoma and the chromosomal translocation t(8;13)(p11;q12). Leukemia. 1998;12:999-1000.
-
(1998)
Leukemia
, vol.12
, pp. 999-1000
-
-
Martinez-Climent, J.A.1
Vizcarra, E.2
Benet, I.3
-
28
-
-
0033251639
-
A chronic myelogenous leukemia-like myeloproliferative disorder accompanied by T-cell lymphoblastic lymphoma with chromosome translocation t(8;13) (p11;q12): A Japanese case
-
Matsumoto K, Morita K, Takada S, et al. A chronic myelogenous leukemia-like myeloproliferative disorder accompanied by T-cell lymphoblastic lymphoma with chromosome translocation t(8;13) (p11;q12): a Japanese case. Int J Hematol. 1999;70:278-282.
-
(1999)
Int J Hematol
, vol.70
, pp. 278-282
-
-
Matsumoto, K.1
Morita, K.2
Takada, S.3
-
29
-
-
0031466392
-
Definition of acute biphenotypic leukemia
-
Matutes E, Morilla R, Farahat N, et al. Definition of acute biphenotypic leukemia. Haematologica. 1997;82:64-66.
-
(1997)
Haematologica
, vol.82
, pp. 64-66
-
-
Matutes, E.1
Morilla, R.2
Farahat, N.3
-
30
-
-
0030020206
-
About the t(8;13)(p11;q12) clinico-pathologic entity
-
Michaux L, Mecucci C, Pereira Velloso ER, et al. About the t(8;13)(p11;q12) clinico-pathologic entity. Blood. 1996;87:1658-1659.
-
(1996)
Blood
, vol.87
, pp. 1658-1659
-
-
Michaux, L.1
Mecucci, C.2
Pereira Velloso, E.R.3
-
31
-
-
31144434920
-
Molecular and phenotypic analysis of Philadelphia chromosome-positive bilineage leukemia: Possibility of a lineage switch from T-lymphoid leukemic progenitor to myeloid cells
-
Monma F, Nishii K, Ezuki S, et al. Molecular and phenotypic analysis of Philadelphia chromosome-positive bilineage leukemia: possibility of a lineage switch from T-lymphoid leukemic progenitor to myeloid cells. Cancer Genet Cytogenet. 2006;164:118-121.
-
(2006)
Cancer Genet Cytogenet
, vol.164
, pp. 118-121
-
-
Monma, F.1
Nishii, K.2
Ezuki, S.3
-
32
-
-
0029913153
-
Chronic myelomonocytic leukaemia with t(8;9)(p11;q34) in childhood: An example of the 8p11 myeloproliferative disorder?
-
Nakayama H, Inamitsu T, Ohga S, et al. Chronic myelomonocytic leukaemia with t(8;9)(p11;q34) in childhood: an example of the 8p11 myeloproliferative disorder? Br J Haematol. 1996;92:692-695.
-
(1996)
Br J Haematol
, vol.92
, pp. 692-695
-
-
Nakayama, H.1
Inamitsu, T.2
Ohga, S.3
-
33
-
-
0032146794
-
1 induces myeloid lineage commitment in multipotent hematopoietic progenitors
-
Nerlov C, Graf T. PU.1 induces myeloid lineage commitment in multipotent hematopoietic progenitors. Genes Dev. 1998;12:2403-2412.
-
(1998)
Genes Dev
, vol.12
, pp. 2403-2412
-
-
Nerlov, C.1
Graf, T.P.2
-
35
-
-
0032510791
-
Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)
-
Popovici C, Adelaide J, Ollendorff V, et al. Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13). Proc Natl Acad Sci U S A. 1998;95:5712-5717.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 5712-5717
-
-
Popovici, C.1
Adelaide, J.2
Ollendorff, V.3
-
36
-
-
0027070656
-
Cytogenetic evidence for extramedullary blast crisis with t(8;13)(q11;p11) in chronic myelomonocytic leukemia
-
Rao PH, Cesarman G, Coleman M, et al. Cytogenetic evidence for extramedullary blast crisis with t(8;13)(q11;p11) in chronic myelomonocytic leukemia. Acta Haematol. 1992;88:201-203.
-
(1992)
Acta Haematol
, vol.88
, pp. 201-203
-
-
Rao, P.H.1
Cesarman, G.2
Coleman, M.3
-
37
-
-
0032170974
-
Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome
-
Reiter A, Sohal J, Kulkarni S, et al. Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome. Blood. 1998;92:1735-1742.
-
(1998)
Blood
, vol.92
, pp. 1735-1742
-
-
Reiter, A.1
Sohal, J.2
Kulkarni, S.3
-
38
-
-
0036210261
-
Sequential transformation of t(8;13)-related disease: A case report
-
Roy S, Szer J, Campbell LJ, et al. Sequential transformation of t(8;13)-related disease: a case report. Acta Haematol. 2002;107:95-97.
-
(2002)
Acta Haematol
, vol.107
, pp. 95-97
-
-
Roy, S.1
Szer, J.2
Campbell, L.J.3
-
39
-
-
0033206227
-
ANF198-FGFR1 transforms Ba/F3 cells to growth factor independence and results in high level tyrosine phosphorylation of STATS 1 and 5
-
Smedley D, Demiroglu A, Abdul-Rauf M, et al. ANF198-FGFR1 transforms Ba/F3 cells to growth factor independence and results in high level tyrosine phosphorylation of STATS 1 and 5. Neoplasia. 1999;1:349-355.
-
(1999)
Neoplasia
, vol.1
, pp. 349-355
-
-
Smedley, D.1
Demiroglu, A.2
Abdul-Rauf, M.3
-
40
-
-
84905515146
-
Identification of four new translocations involving FGFR1 in myeloid disorders
-
Sohal J, Chase A, Mould S, et al. Identification of four new translocations involving FGFR1 in myeloid disorders. Genes Chromosomes Cancer. 2001;32:155-163.
-
(2001)
Genes Chromosomes Cancer
, vol.32
, pp. 155-163
-
-
Sohal, J.1
Chase, A.2
Mould, S.3
-
41
-
-
0031012459
-
Coexistent T-cell lymphoblastic lymphoma and an atypical myeloproliferative disorder associated with t(8;13)(p21;q14)
-
Somers GR, Slater H, Rockman S, et al. Coexistent T-cell lymphoblastic lymphoma and an atypical myeloproliferative disorder associated with t(8;13)(p21;q14). Pediatr Pathol Lab Med. 1997;17:141-158.
-
(1997)
Pediatr Pathol Lab Med
, vol.17
, pp. 141-158
-
-
Somers, G.R.1
Slater, H.2
Rockman, S.3
-
42
-
-
0030797764
-
Molecular characterization of the t(8;13)(p11;q12) translocation associated with an atypical myeloproliferative disorder: Evidence for three discrete loci involved in myeloid leukemias on 8p11
-
Still IH, Chernova O, Hurd D, et al. Molecular characterization of the t(8;13)(p11;q12) translocation associated with an atypical myeloproliferative disorder: evidence for three discrete loci involved in myeloid leukemias on 8p11. Blood. 1997;90:3136-3141.
-
(1997)
Blood
, vol.90
, pp. 3136-3141
-
-
Still, I.H.1
Chernova, O.2
Hurd, D.3
-
43
-
-
0012997768
-
Long-term complete haematological and molecular remission after allogeneic bone marrow transplantation in a patient with a stem cell myeloproliferative disorder associated with t(8;13)(p12;q12)
-
Suzan F, Guasch G, Terre C, et al. Long-term complete haematological and molecular remission after allogeneic bone marrow transplantation in a patient with a stem cell myeloproliferative disorder associated with t(8;13)(p12;q12). Br J Haematol. 2003;121:312-314.
-
(2003)
Br J Haematol
, vol.121
, pp. 312-314
-
-
Suzan, F.1
Guasch, G.2
Terre, C.3
-
44
-
-
0027500227
-
T-cell lymphoblastic lymphoma with blood eosinophilia and associated myeloid malignancy
-
Tassies D, Cervantes F, Feliu E, et al. T-cell lymphoblastic lymphoma with blood eosinophilia and associated myeloid malignancy. Am J Surg Pathol. 1993;17:92-93.
-
(1993)
Am J Surg Pathol
, vol.17
, pp. 92-93
-
-
Tassies, D.1
Cervantes, F.2
Feliu, E.3
-
45
-
-
0030054857
-
A young child with acquired t(8;9)(p11;q34): Additional proof that 8p11 is involved in mixed myeloid/T lymphoid malignancies
-
van den Berg H, Kroes W, van der Schoot CE, et al. A young child with acquired t(8;9)(p11;q34): additional proof that 8p11 is involved in mixed myeloid/T lymphoid malignancies. Leukemia. 1996;10:1252-1253.
-
(1996)
Leukemia
, vol.10
, pp. 1252-1253
-
-
van den Berg, H.1
Kroes, W.2
van der Schoot, C.E.3
-
46
-
-
0037222293
-
The myeloid master regulator transcription factor PU.1 is inactivated by AML1-ETO in t(8;21) myeloid leukemia
-
Vangala RK, Heiss-Neumann MS, Rangatia JS, et al. The myeloid master regulator transcription factor PU.1 is inactivated by AML1-ETO in t(8;21) myeloid leukemia. Blood. 2003;101:270-277.
-
(2003)
Blood
, vol.101
, pp. 270-277
-
-
Vangala, R.K.1
Heiss-Neumann, M.S.2
Rangatia, J.S.3
-
47
-
-
0021184596
-
Simultaneous occurrence of a T-cell lymphoma and a chronic myelogenous leukemia with an unusual karyotype
-
Vannier JP, Bizet M, Bastard C, et al. Simultaneous occurrence of a T-cell lymphoma and a chronic myelogenous leukemia with an unusual karyotype. Leuk Res. 1984;8:647-657.
-
(1984)
Leuk Res
, vol.8
, pp. 647-657
-
-
Vannier, J.P.1
Bizet, M.2
Bastard, C.3
-
48
-
-
0036110314
-
The stromal composition of malignant lymphoid aggregates in bone marrow: Variations in architecture and phenotype in different B-cell tumours
-
Vega F, Medeiros LJ, Lang WH, et al. The stromal composition of malignant lymphoid aggregates in bone marrow: variations in architecture and phenotype in different B-cell tumours. Br J Haematol. 2002;117:569-576.
-
(2002)
Br J Haematol
, vol.117
, pp. 569-576
-
-
Vega, F.1
Medeiros, L.J.2
Lang, W.H.3
-
49
-
-
11044238012
-
Clinical variability of patients with the t(6;8)(q27;p12) and FGFR1OP-FGFR1 fusion: Two further cases
-
Vizmanos JL, Hernandez R, Vidal MJ, et al. Clinical variability of patients with the t(6;8)(q27;p12) and FGFR1OP-FGFR1 fusion: two further cases. Hematol J. 2004;5:534-537.
-
(2004)
Hematol J
, vol.5
, pp. 534-537
-
-
Vizmanos, J.L.1
Hernandez, R.2
Vidal, M.J.3
-
50
-
-
20844443647
-
The t(8;17)(p11;q23) in the 8p11 myeloproliferative syndrome fuses MYO18A to FGFR1
-
Walz C, Chase A, Schoch C, et al. The t(8;17)(p11;q23) in the 8p11 myeloproliferative syndrome fuses MYO18A to FGFR1. Leukemia. 2005;19:1005-1009.
-
(2005)
Leukemia
, vol.19
, pp. 1005-1009
-
-
Walz, C.1
Chase, A.2
Schoch, C.3
-
51
-
-
33645731202
-
Human thymus contains multipotent progenitors with T/B lymphoid, myeloid, and erythroid lineage potential
-
Weerkamp F, Baert MR, Brugman MH, et al. Human thymus contains multipotent progenitors with T/B lymphoid, myeloid, and erythroid lineage potential. Blood. 2006;107:3131-3137.
-
(2006)
Blood
, vol.107
, pp. 3131-3137
-
-
Weerkamp, F.1
Baert, M.R.2
Brugman, M.H.3
-
52
-
-
37549066806
-
Clonal evolution of 8p11 stem cell syndrome in a 14-year-old Chinese boy: A review of literature of t(8;13) associated myeloproliferative diseases
-
Epub ahead of print
-
Wong WS, Cheng KC, Lau KM, et al. Clonal evolution of 8p11 stem cell syndrome in a 14-year-old Chinese boy: A review of literature of t(8;13) associated myeloproliferative diseases. Leuk Res. 2006. [Epub ahead of print].
-
(2006)
Leuk Res
-
-
Wong, W.S.1
Cheng, K.C.2
Lau, K.M.3
-
53
-
-
17344373285
-
FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome
-
Xiao S, Nalabolu SR, Aster JC, et al. FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome. Nat Genet. 1998;18:84-87.
-
(1998)
Nat Genet
, vol.18
, pp. 84-87
-
-
Xiao, S.1
Nalabolu, S.R.2
Aster, J.C.3
-
54
-
-
33748357533
-
A biphenotypic transformation of 8p11 myeloproliferative syndrome with CEP1/FGFR1 fusion gene
-
Yamamoto K, Kawano H, Nishikawa S, et al. A biphenotypic transformation of 8p11 myeloproliferative syndrome with CEP1/FGFR1 fusion gene. Eur J Haematol. 2006;77:349-354.
-
(2006)
Eur J Haematol
, vol.77
, pp. 349-354
-
-
Yamamoto, K.1
Kawano, H.2
Nishikawa, S.3
-
55
-
-
20444486562
-
Distinguishing between proliferating nodal lymphoid blasts in chronic myelogenous leukemia and non-Hodgkin lymphoma: Report of three cases and detection of a bcr/abl fusion signal by single-cell analysis
-
Yashima-Abo A, Satoh T, Abo T, et al. Distinguishing between proliferating nodal lymphoid blasts in chronic myelogenous leukemia and non-Hodgkin lymphoma: report of three cases and detection of a bcr/abl fusion signal by single-cell analysis. Pathol Int. 2005;55:273-279.
-
(2005)
Pathol Int
, vol.55
, pp. 273-279
-
-
Yashima-Abo, A.1
Satoh, T.2
Abo, T.3
-
56
-
-
1442307974
-
Internal tandem duplication mutation of FLT3 blocks myeloid differentiation through suppression of C/EBPalpha expression
-
Zheng R, Friedman AD, Levis M, et al. Internal tandem duplication mutation of FLT3 blocks myeloid differentiation through suppression of C/EBPalpha expression. Blood. 2004;103:1883-1890.
-
(2004)
Blood
, vol.103
, pp. 1883-1890
-
-
Zheng, R.1
Friedman, A.D.2
Levis, M.3
|