-
1
-
-
0031438731
-
The AML1 gene: A transcription factor involved in the pathogenesis of myeloid and lymphoid leukemias
-
Lo Coco F, Pisegna S, Diverio D. The AML1 gene: a transcription factor involved in the pathogenesis of myeloid and lymphoid leukemias. Haematologica 1997; 82:364-70.
-
(1997)
Haematologica
, vol.82
, pp. 364-370
-
-
Lo Coco, F.1
Pisegna, S.2
Diverio, D.3
-
2
-
-
0032898523
-
The role of TEL fusion genes in pediatric leukemias
-
Rubnitz JE, Pui CH, Downing JR. The role of TEL fusion genes in pediatric leukemias. Leukemia 1999; 13:6-13.
-
(1999)
Leukemia
, vol.13
, pp. 6-13
-
-
Rubnitz, J.E.1
Pui, C.H.2
Downing, J.R.3
-
3
-
-
0030742017
-
Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials
-
Associazione Italiana di Oncologia Pediatrica and the Berlin-Frankfurt-Munster Study Group
-
Borkhardt A, Cazzaniga G, Viehmann S, et al. Incidence and clinical relevance of TEL/AML1 fusion genes in children with acute lymphoblastic leukemia enrolled in the German and Italian multicenter therapy trials. Associazione Italiana di Oncologia Pediatrica and the Berlin-Frankfurt-Munster Study Group. Blood 1997; 90:571-7.
-
(1997)
Blood
, vol.90
, pp. 571-577
-
-
Borkhardt, A.1
Cazzaniga, G.2
Viehmann, S.3
-
4
-
-
0030056476
-
High incidence of TEL/AML1 fusion resulting from a cryptic t(12;21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan
-
Liang DC, Chou TB, Chen JS, et al. High incidence of TEL/AML1 fusion resulting from a cryptic t(12;21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan. Leukemia 1996; 10:991-3.
-
(1996)
Leukemia
, vol.10
, pp. 991-993
-
-
Liang, D.C.1
Chou, T.B.2
Chen, J.S.3
-
5
-
-
0028805405
-
High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia
-
Romana SP, Poirel H, Leconiat M, et al. High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. Blood 1995; 86:4263-9.
-
(1995)
Blood
, vol.86
, pp. 4263-4269
-
-
Romana, S.P.1
Poirel, H.2
Leconiat, M.3
-
6
-
-
13344282725
-
TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis
-
Shurtleff SA, Buijs A, Behm FG, et al. TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis. Leukemia 1995; 9:1985-9.
-
(1995)
Leukemia
, vol.9
, pp. 1985-1989
-
-
Shurtleff, S.A.1
Buijs, A.2
Behm, F.G.3
-
7
-
-
0028224348
-
Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation
-
Golub TR, Barker GF, Lovett M, Gilliland DG. Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 1994; 77:307-16.
-
(1994)
Cell
, vol.77
, pp. 307-316
-
-
Golub, T.R.1
Barker, G.F.2
Lovett, M.3
Gilliland, D.G.4
-
8
-
-
0029004541
-
Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia
-
Golub TR, Barker GF, Bohlander SK, et al. Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia. Proc Natl Acad Sci USA 1995; 92:4917-21.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 4917-4921
-
-
Golub, T.R.1
Barker, G.F.2
Bohlander, S.K.3
-
9
-
-
0029045087
-
The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion
-
Romana SP, Mauchauffe M, Le Coniat M, et al. The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion. Blood 1995; 85:3662-70.
-
(1995)
Blood
, vol.85
, pp. 3662-3670
-
-
Romana, S.P.1
Mauchauffe, M.2
Le Coniat, M.3
-
10
-
-
0033559746
-
Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2aB gene associated with myeloblastic leukemias
-
Osato M, Asou N, Abdalla E, et al. Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2aB gene associated with myeloblastic leukemias. Blood 1999; 93:1817-24.
-
(1999)
Blood
, vol.93
, pp. 1817-1824
-
-
Osato, M.1
Asou, N.2
Abdalla, E.3
-
11
-
-
0032830638
-
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
-
Song WJ, Sullivan MG, Legare RD, et al. Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. Nat Genet 1999; 23:166-75.
-
(1999)
Nat Genet
, vol.23
, pp. 166-175
-
-
Song, W.J.1
Sullivan, M.G.2
Legare, R.D.3
-
12
-
-
0031689134
-
Comparative genomic hybridization in childhood acute lymphoblastic leukemia
-
Larramendy ML, Huhta T, Vettenranta K, et al. Comparative genomic hybridization in childhood acute lymphoblastic leukemia. Leukemia 1998; 12:1638-44.
-
(1998)
Leukemia
, vol.12
, pp. 1638-1644
-
-
Larramendy, M.L.1
Huhta, T.2
Vettenranta, K.3
-
13
-
-
0031895154
-
DNA copy number amplifications in human neoplasms: Review of comparative genomic hybridization studies
-
Knuutila S, Björkqvist AM, Autio K, et al. DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies. Am J Pathol 1998; 152:1107-23.
-
(1998)
Am J Pathol
, vol.152
, pp. 1107-1123
-
-
Knuutila, S.1
Björkqvist, A.M.2
Autio, K.3
-
14
-
-
0019489123
-
Culture of bone marrow reveals more cells with chromosomal abnormalities than the direct method in patients with hematologic disorders
-
Knuutila S, Vuopio P, Elonen E, et al. Culture of bone marrow reveals more cells with chromosomal abnormalities than the direct method in patients with hematologic disorders. Blood 1981; 58:369-75.
-
(1981)
Blood
, vol.58
, pp. 369-375
-
-
Knuutila, S.1
Vuopio, P.2
Elonen, E.3
-
15
-
-
0031472566
-
Optimization of comparative genomic hybridization using fluorochrome conjugated to dCTP and dUTP nucleotides
-
El-Rifai W, Larramendy ML, Björkqvist AM, Hemmer S, Knuutila S. Optimization of comparative genomic hybridization using fluorochrome conjugated to dCTP and dUTP nucleotides. Lab Invest 1997; 77:699-700.
-
(1997)
Lab Invest
, vol.77
, pp. 699-700
-
-
El-Rifai, W.1
Larramendy, M.L.2
Björkqvist, A.M.3
Hemmer, S.4
Knuutila, S.5
-
16
-
-
0030901159
-
Acute lymphoblastic leukemia and chromosome 21
-
Berger R. Acute lymphoblastic leukemia and chromosome 21. Cancer Genet Cytogen 1997; 94:8-12.
-
(1997)
Cancer Genet Cytogen
, vol.94
, pp. 8-12
-
-
Berger, R.1
-
17
-
-
0030661972
-
12p abnormalities and the TEL gene (ETV6) in childhood acute lymphoblastic leukemia
-
Raimondi SC, Shurtleff SA, Downing JR, et al. 12p abnormalities and the TEL gene (ETV6) in childhood acute lymphoblastic leukemia. Blood 1997; 90:4559-66.
-
(1997)
Blood
, vol.90
, pp. 4559-4566
-
-
Raimondi, S.C.1
Shurtleff, S.A.2
Downing, J.R.3
-
18
-
-
16944363891
-
The common TEL/AML1 rearrangement does not represent a frequent event in acute lymphoblastic leukaemia occurring in children with Down syndrome
-
Lanza C, Volpe G, Basso G, et al. The common TEL/AML1 rearrangement does not represent a frequent event in acute lymphoblastic leukaemia occurring in children with Down syndrome. Leukemia 1997; 11:820-1.
-
(1997)
Leukemia
, vol.11
, pp. 820-821
-
-
Lanza, C.1
Volpe, G.2
Basso, G.3
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