-
1
-
-
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 Ematologia 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 Ematologia 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
-
2
-
-
0007055492
-
TEL/AML-1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia
-
McLean TW, Ringold S, Neuberg D, et al. TEL/AML-1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia. Blood 1996;88:4252-8.
-
(1996)
Blood
, vol.88
, pp. 4252-4258
-
-
McLean, T.W.1
Ringold, S.2
Neuberg, D.3
-
3
-
-
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
-
4
-
-
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
-
5
-
-
0034054133
-
The United Kingdom Childhood Cancer study: Objectives, materials and methods
-
UK Childhood Cancer Study Investigators
-
The United Kingdom Childhood Cancer study: objectives, materials and methods. UK Childhood Cancer Study Investigators. Br J Cancer 2000;82:1073-102.
-
(2000)
Br J Cancer
, vol.82
, pp. 1073-1102
-
-
-
6
-
-
0032515971
-
Fetal origins of the TEL-AML1 fusion gene in identical twins with leukemia
-
Ford AM, Bennett CA, Price CM, Bruin MC, Van Wering ER, Greaves M. Fetal origins of the TEL-AML1 fusion gene in identical twins with leukemia. Proc Natl Acad Sci USA 1998;95:4584-8.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 4584-4588
-
-
Ford, A.M.1
Bennett, C.A.2
Price, C.M.3
Bruin, M.C.4
Van Wering, E.R.5
Greaves, M.6
-
7
-
-
0033178875
-
Protracted and variable latency of acute lymphoblastic leukemia after TEL-AML1 gene fusion in utero
-
Wiemels JL, Ford AM, Van Wering ER, Postma A, Greaves M. Protracted and variable latency of acute lymphoblastic leukemia after TEL-AML1 gene fusion in utero. Blood 1999;94:1057-62.
-
(1999)
Blood
, vol.94
, pp. 1057-1062
-
-
Wiemels, J.L.1
Ford, A.M.2
Van Wering, E.R.3
Postma, A.4
Greaves, M.5
-
8
-
-
0035880244
-
Molecular tracking of leukemogenesis in a triplet pregnancy
-
Maia AT, Ford AM, Jalali GR, et al. Molecular tracking of leukemogenesis in a triplet pregnancy. Blood 2001;98:478-82.
-
(2001)
Blood
, vol.98
, pp. 478-482
-
-
Maia, A.T.1
Ford, A.M.2
Jalali, G.R.3
-
9
-
-
18644369598
-
Presence of clone-specific markers at birth in children with acute lymphoblastic leukaemia
-
Hjalgrim LL, Madsen HO, Melbye M, et al. Presence of clone-specific markers at birth in children with acute lymphoblastic leukaemia. Br J Cancer 2002;87:994-9.
-
(2002)
Br J Cancer
, vol.87
, pp. 994-999
-
-
Hjalgrim, L.L.1
Madsen, H.O.2
Melbye, M.3
-
10
-
-
0344838398
-
Prenatal origin of TEL-AML1-positive acute lymphoblastic leukemia in children born in California
-
McHale CM, Wiemels JL, Zhang L, et al. Prenatal origin of TEL-AML1-positive acute lymphoblastic leukemia in children born in California. Genes Chromosomes Cancer 2003;37:36-43.
-
(2003)
Genes Chromosomes Cancer
, vol.37
, pp. 36-43
-
-
McHale, C.M.1
Wiemels, J.L.2
Zhang, L.3
-
11
-
-
0033619452
-
Prenatal origin of acute lymphoblastic leukaemia in children
-
Wiemels JL, Cazzaniga G, Daniotti M, et al. Prenatal origin of acute lymphoblastic leukaemia in children. Lancet 1999;354:1499-503.
-
(1999)
Lancet
, vol.354
, pp. 1499-1503
-
-
Wiemels, J.L.1
Cazzaniga, G.2
Daniotti, M.3
-
12
-
-
16944367034
-
ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia
-
Cave H, Cacheux V, Raynaud S, et al. ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia. Leukemia (Baltimore) 1997;11:1459-64.
-
(1997)
Leukemia (Baltimore)
, vol.11
, pp. 1459-1464
-
-
Cave, H.1
Cacheux, V.2
Raynaud, S.3
-
13
-
-
0033000862
-
An investigation of the t(12;21) rearrangement in children with B-precursor acute lymphoblastic leukaemia using cytogenetic and molecular methods
-
Kempski H, Chalker J, Chessells J, et al. An investigation of the t(12;21) rearrangement in children with B-precursor acute lymphoblastic leukaemia using cytogenetic and molecular methods. Br J Haematol 1999;105:684-9.
-
(1999)
Br J Haematol
, vol.105
, pp. 684-689
-
-
Kempski, H.1
Chalker, J.2
Chessells, J.3
-
14
-
-
9244221153
-
The 12;21 translocation involving TEL and deletion of the other TEL allele: Two frequently associated alterations found in childhood acute lymphoblastic leukemia
-
Raynaud S, Cave H, Baens M, et al. The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia. Blood 1996;87:2891-9.
-
(1996)
Blood
, vol.87
, pp. 2891-2899
-
-
Raynaud, S.1
Cave, H.2
Baens, M.3
-
15
-
-
0344641922
-
Fine physical and transcript mapping of a 1.8 Mb region spanning the locus for childhood acute lymphoblastic leukemia on chromosome 12p12. 3
-
Aissani B, Sinnett D. Fine physical and transcript mapping of a 1.8 Mb region spanning the locus for childhood acute lymphoblastic leukemia on chromosome 12p12. 3. Gene (Amst) 1999;240:297-305.
-
(1999)
Gene (Amst)
, vol.240
, pp. 297-305
-
-
Aissani, B.1
Sinnett, D.2
-
16
-
-
0033557787
-
A physical, transcript, and deletion map of chromosome region 12p12.3 flanked by ETV6 and CDKNIB: Hypermethylation of the LRP6 CpG island in two leukemia patients with hemizygous del(12p)
-
Baens M, Wlodarska I, Corveleyn A, Hoornaert I, Hagemeijer A, Marynen P. A physical, transcript, and deletion map of chromosome region 12p12.3 flanked by ETV6 and CDKNIB: hypermethylation of the LRP6 CpG island in two leukemia patients with hemizygous del(12p). Genomics 1999;56:40-50.
-
(1999)
Genomics
, vol.56
, pp. 40-50
-
-
Baens, M.1
Wlodarska, I.2
Corveleyn, A.3
Hoornaert, I.4
Hagemeijer, A.5
Marynen, P.6
-
17
-
-
0037062496
-
Chromosome translocations and covert leukemic clones are generated during normal fetal development
-
Mori H, Colman SM, Xiao Z, et al. Chromosome translocations and covert leukemic clones are generated during normal fetal development. Proc Natl Acad Sci USA 2002;99:8242-7.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 8242-8247
-
-
Mori, H.1
Colman, S.M.2
Xiao, Z.3
-
18
-
-
0036636857
-
Core-binding factors in haematopoiesis and leukaemia
-
Speck NA, Gilliland DG. Core-binding factors in haematopoiesis and leukaemia. Nat Rev Cancer 2002;2:502-13.
-
(2002)
Nat Rev Cancer
, vol.2
, pp. 502-513
-
-
Speck, N.A.1
Gilliland, D.G.2
-
19
-
-
0033372067
-
Molecular genetics, natural history and the demise of childhood leukaemia
-
Greaves, M. Molecular genetics, natural history and the demise of childhood leukaemia. Eur J Cancer 1999;35:1941-53.
-
(1999)
Eur J Cancer
, vol.35
, pp. 1941-1953
-
-
Greaves, M.1
-
20
-
-
0035399173
-
Relapse of TEL-AML1-positive acute lymphoblastic leukemia in childhood: A matched-pair analysis
-
Seeger K, Stackelberg AV, Taube T, et al. Relapse of TEL-AML1-positive acute lymphoblastic leukemia in childhood: a matched-pair analysis. J Clin Oncol 2001;19:3188-93.
-
(2001)
J Clin Oncol
, vol.19
, pp. 3188-3193
-
-
Seeger, K.1
Stackelberg, A.V.2
Taube, T.3
-
21
-
-
0035437159
-
Origins of "late" relapse in childhood acute lymphoblastic leukemia with TEL-AML1 fusion genes
-
Ford AM, Fasching K, Panzer-Grumayer ER, Koenig M, Haas OA, Greaves MF. Origins of "late" relapse in childhood acute lymphoblastic leukemia with TEL-AML1 fusion genes. Blood 2001;98:558-64.
-
(2001)
Blood
, vol.98
, pp. 558-564
-
-
Ford, A.M.1
Fasching, K.2
Panzer-Grumayer, E.R.3
Koenig, M.4
Haas, O.A.5
Greaves, M.F.6
-
22
-
-
0030730333
-
Frequent deletion of chromosome 12p12.3 in children with acute lymphoblastic leukaemia
-
Baccichet A, Sinnett D. Frequent deletion of chromosome 12p12.3 in children with acute lymphoblastic leukaemia. Br J Haematol 1997; 99:107-14.
-
(1997)
Br J Haematol
, vol.99
, pp. 107-114
-
-
Baccichet, A.1
Sinnett, D.2
-
23
-
-
0032919213
-
Primers and protocols for standardized detection of minimal residual disease in acute lymphoblastic leukemia using immunoglobulin and T cell receptor gene rearrangements and TAL1 deletions as PCR targets: Report of the BIOMED-1 CONCERTED ACTION: Investigation of minimal residual disease in acute leukemia
-
Pongers-Willemse MJ, Seriu T, Stolz F, et al. Primers and protocols for standardized detection of minimal residual disease in acute lymphoblastic leukemia using immunoglobulin and T cell receptor gene rearrangements and TAL1 deletions as PCR targets: report of the BIOMED-1 CONCERTED ACTION: investigation of minimal residual disease in acute leukemia. Leukemia (Baltimore) 1999;13:110-8.
-
(1999)
Leukemia (Baltimore)
, vol.13
, pp. 110-118
-
-
Pongers-Willemse, M.J.1
Seriu, T.2
Stolz, F.3
-
24
-
-
0034850655
-
Precursor-B-ALL with D(H)-J(H) gene rearrangements have an immature immunogenotype with a high frequency of oligoclonality and hyperdiploidy of chromosome 14
-
Szczepanski T, Willemse MJ, van Wering ER, van Weerden JF, Kamps WA, van Dongen JJ. Precursor-B-ALL with D(H)-J(H) gene rearrangements have an immature immunogenotype with a high frequency of oligoclonality and hyperdiploidy of chromosome 14. Leukemia (Baltimore) 2001;15:1415-23.
-
(2001)
Leukemia (Baltimore)
, vol.15
, pp. 1415-1423
-
-
Szczepanski, T.1
Willemse, M.J.2
Van Wering, E.R.3
Van Weerden, J.F.4
Kamps, W.A.5
Van Dongen, J.J.6
-
25
-
-
0031452746
-
Heteroduplex PCR analysis of rearranged T cell receptor genes for clonality assessment in suspect T cell proliferations
-
Langerak AW, Szczepanski T, van der Burg M, Wolvers-Tettero IL, van Dongen JJ. Heteroduplex PCR analysis of rearranged T cell receptor genes for clonality assessment in suspect T cell proliferations. Leukemia (Baltimore) 1997;11:2192-9.
-
(1997)
Leukemia (Baltimore)
, vol.11
, pp. 2192-2199
-
-
Langerak, A.W.1
Szczepanski, T.2
Van Der Burg, M.3
Wolvers-Tettero, I.L.4
Van Dongen, J.J.5
-
26
-
-
0033566892
-
Structure and possible mechanisms of TEL-AML1 gene fusions in childhood acute lymphoblastic leukemia
-
Wiemels JL, Greaves M. Structure and possible mechanisms of TEL-AML1 gene fusions in childhood acute lymphoblastic leukemia. Cancer Res 1999;59:4075-82.
-
(1999)
Cancer Res
, vol.59
, pp. 4075-4082
-
-
Wiemels, J.L.1
Greaves, M.2
-
27
-
-
0347357869
-
Clonal variation of the immunogenotype in relapsed ETV6/RUNX1-positive acute lymphoblastic leukemia indicates subclone formation during early stages of leukemia development
-
Peham M, Konrad M, Harbott J, Konig M, Haas OA, Panzer-Grumayer ER. Clonal variation of the immunogenotype in relapsed ETV6/RUNX1-positive acute lymphoblastic leukemia indicates subclone formation during early stages of leukemia development. Genes Chromosomes Cancer 2004;39:156-60.
-
(2004)
Genes Chromosomes Cancer
, vol.39
, pp. 156-160
-
-
Peham, M.1
Konrad, M.2
Harbott, J.3
Konig, M.4
Haas, O.A.5
Panzer-Grumayer, E.R.6
-
28
-
-
0037866469
-
Late relapses evolve from slow-responding subclones in t(12;21)-positive acute lymphoblastic leukemia: Evidence for the persistence of a preleukemic clone
-
Konrad M, Metzler M, Panzer S, et al. Late relapses evolve from slow-responding subclones in t(12;21)-positive acute lymphoblastic leukemia: evidence for the persistence of a preleukemic clone. Blood 2003;101:3635-40.
-
(2003)
Blood
, vol.101
, pp. 3635-3640
-
-
Konrad, M.1
Metzler, M.2
Panzer, S.3
-
29
-
-
0242406704
-
Allelotype analysis in relapsed childhood acute lymphoblastic leukemia
-
Takeuchi S, Seriu T, van Dongen JJ, et al. Allelotype analysis in relapsed childhood acute lymphoblastic leukemia. Oncogene 2003;22: 6970-6.
-
(2003)
Oncogene
, vol.22
, pp. 6970-6976
-
-
Takeuchi, S.1
Seriu, T.2
Van Dongen, J.J.3
-
30
-
-
0028302083
-
AML1/ETO fusion mRNA can be detected in remission blood samples of all patients with t(8;;21) acute myeloid leukemia after chemotherapy or autologous bone marrow transplantation
-
Kusec R, Laczika K, Knobl P, et al. AML1/ETO fusion mRNA can be detected in remission blood samples of all patients with t(8;;21) acute myeloid leukemia after chemotherapy or autologous bone marrow transplantation. Leukemia (Baltimore) 1994;8:735-9.
-
(1994)
Leukemia (Baltimore)
, vol.8
, pp. 735-739
-
-
Kusec, R.1
Laczika, K.2
Knobl, P.3
-
31
-
-
9344257318
-
Persistence of multipotent progenitors expressing AML1/ETO transcripts in long-term remission patients with t(8;21) acute myelogenous leukemia
-
Miyamoto T, Nagafuji K, Akashi K, et al. Persistence of multipotent progenitors expressing AML1/ETO transcripts in long-term remission patients with t(8;21) acute myelogenous leukemia. Blood 1996;87: 4789-96.
-
(1996)
Blood
, vol.87
, pp. 4789-4796
-
-
Miyamoto, T.1
Nagafuji, K.2
Akashi, K.3
-
32
-
-
0027317604
-
Persistence of the 8;21 translocation in patients with acute myeloid leukemia type M2 in long-term remission
-
Nucifora G, Larson RA, Rowley JD. Persistence of the 8;21 translocation in patients with acute myeloid leukemia type M2 in long-term remission. Blood 1993;82:712-5.
-
(1993)
Blood
, vol.82
, pp. 712-715
-
-
Nucifora, G.1
Larson, R.A.2
Rowley, J.D.3
-
33
-
-
0141634051
-
Origins of chromosome translocations in childhood leukaemia
-
Greaves MF, Wiemels J. Origins of chromosome translocations in childhood leukaemia. Nat Rev Cancer 2003;3:639-49.
-
(2003)
Nat Rev Cancer
, vol.3
, pp. 639-649
-
-
Greaves, M.F.1
Wiemels, J.2
|