-
1
-
-
0032717039
-
The role of chromosome translocations in leukemogenesis
-
Rowley JD. The role of chromosome translocations in leukemogenesis. Semin Hematol 1999; 36: 59-72.
-
(1999)
Semin. Hematol.
, vol.36
, pp. 59-72
-
-
Rowley, J.D.1
-
2
-
-
0030658039
-
Oncogenic transcription factors in the human acute leukemias
-
Look AT. Oncogenic transcription factors in the human acute leukemias. Science 1997; 278: 1059-1064.
-
(1997)
Science
, vol.278
, pp. 1059-1064
-
-
Look, A.T.1
-
3
-
-
0027970838
-
Chromosomal translocations in human cancer
-
Rabbitts TH. Chromosomal translocations in human cancer. Nature 1994; 372: 143-149.
-
(1994)
Nature
, vol.372
, pp. 143-149
-
-
Rabbitts, T.H.1
-
4
-
-
0034970067
-
An atlas of chromosomes in hematological malignancies. Example: 11q23 and MLL partners
-
Huret JL, Dessen P, Bernheim A. An atlas of chromosomes in hematological malignancies. Example: 11q23 and MLL partners. Leukemia 2001; 15: 987-989.
-
(2001)
Leukemia
, vol.15
, pp. 987-989
-
-
Huret, J.L.1
Dessen, P.2
Bernheim, A.3
-
5
-
-
0026765020
-
Disruption of the SCL gene by a t(1;3) translocation in a patient with T cell acute lymphoblastic leukemia
-
Aplan PD, Raimondi SC, Kirsch IR. Disruption of the SCL gene by a t(1;3) translocation in a patient with T cell acute lymphoblastic leukemia. J Exp Med 1992; 176: 1303-1310.
-
(1992)
J. Exp. Med.
, vol.176
, pp. 1303-1310
-
-
Aplan, P.D.1
Raimondi, S.C.2
Kirsch, I.R.3
-
6
-
-
0025040167
-
The t(1;14)(p34;q11) is nonrandom and restricted to T-cell acute lymphoblastic leukemia: A Pediatric Oncology Group study
-
Carroll AJ, Crist WM, Link MP, Amylon MD, Pullen DJ, Ragab AH, Buchanan GR, Wimmer RS, Vietti TJ. The t(1;14)(p34;q11) is nonrandom and restricted to T-cell acute lymphoblastic leukemia: a Pediatric Oncology Group study. Blood 1990; 76: 1220-1224.
-
(1990)
Blood
, vol.76
, pp. 1220-1224
-
-
Carroll, A.J.1
Crist, W.M.2
Link, M.P.3
Amylon, M.D.4
Pullen, D.J.5
Ragab, A.H.6
Buchanan, G.R.7
Wimmer, R.S.8
Vietti, T.J.9
-
7
-
-
0025889062
-
c-tal, a helix-loop-helix protein, is juxtaposed to the T-cell receptor-beta chain gene by a reciprocal chromosomal translocation: t(1;7)(p321-q35)
-
Fitzgerald TJ, Neale GA, Raimondi SC, Goorha RM. c-tal, a helix-loop-helix protein, is juxtaposed to the T-cell receptor-beta chain gene by a reciprocal chromosomal translocation: t(1;7)(p321-q35). Blood 1991; 78: 2686-2695.
-
(1991)
Blood
, vol.78
, pp. 2686-2695
-
-
Fitzgerald, T.J.1
Neale, G.A.2
Raimondi, S.C.3
Goorha, R.M.4
-
8
-
-
0344333431
-
Deregulated expression of the TAL1 gene by t(1;5)(p32;q31) in patient with T-cell acute lymphoblastic leukemia
-
Francois S, Delabesse E, Baranger L, Dautel M, Foussard C, Boasson M et al. Deregulated expression of the TAL1 gene by t(1;5)(p32;q31) in patient with T-cell acute lymphoblastic leukemia. Genes Chromosomes Cancer 1998; 23: 36-43.
-
(1998)
Genes Chromosomes Cancer
, vol.23
, pp. 36-43
-
-
Francois, S.1
Delabesse, E.2
Baranger, L.3
Dautel, M.4
Foussard, C.5
Boasson, M.6
-
9
-
-
0027447707
-
Site-specific deletions involving the tal-1 and sil genes are restricted to cells of the T cell receptor alpha/beta lineage: T cell receptor delta gene deletion mechanism affects multiple genes
-
Breit TM, Mol EJ, Wolvers-Tettero IL, Ludwig WD, van Wering ER, van Dongen JJ. Site-specific deletions involving the tal-1 and sil genes are restricted to cells of the T cell receptor alpha/beta lineage: T cell receptor delta gene deletion mechanism affects multiple genes. J Exp Med 1993; 177: 965-977.
-
(1993)
J. Exp. Med.
, vol.177
, pp. 965-977
-
-
Breit, T.M.1
Mol, E.J.2
Wolvers-Tettero, I.L.3
Ludwig, W.D.4
van Wering, E.R.5
van Dongen, J.J.6
-
10
-
-
0034781537
-
A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia
-
Bernard OA, Busson-LeConiat M, Ballerini P, Mauchauffe M, Della Valle V, Monni R et al. A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia. Leukemia 2001; 15: 1495-1504.
-
(2001)
Leukemia
, vol.15
, pp. 1495-1504
-
-
Bernard, O.A.1
Busson-LeConiat, M.2
Ballerini, P.3
Mauchauffe, M.4
Della Valle, V.5
Monni, R.6
-
11
-
-
85009836740
-
Translocation t(5;14)(q35;q32) in three cases of childhood T cell acute lymphoblastic leukemia: A new recurring and cryptic abnormality
-
Helias C, Leymarie V, Entz-Werle N, Falkenrodt A, Eyer D, Costa JA et al. Translocation t(5;14)(q35;q32) in three cases of childhood T cell acute lymphoblastic leukemia: a new recurring and cryptic abnormality. Leukemia 2002; 16: 7-12.
-
(2002)
Leukemia
, vol.16
, pp. 7-12
-
-
Helias, C.1
Leymarie, V.2
Entz-Werle, N.3
Falkenrodt, A.4
Eyer, D.5
Costa, J.A.6
-
12
-
-
0037097572
-
Recurrent involvement of the MLL gene in adult T-lineage acute lymphoblastic leukemia
-
Hayette S, Tigaud I, Maguer-Satta V, Bartholin L, Thomas X, Charrin C et al. Recurrent involvement of the MLL gene in adult T-lineage acute lymphoblastic leukemia. Blood 2002; 99: 4647-4649.
-
(2002)
Blood
, vol.99
, pp. 4647-4649
-
-
Hayette, S.1
Tigaud, I.2
Maguer-Satta, V.3
Bartholin, L.4
Thomas, X.5
Charrin, C.6
-
13
-
-
0037105455
-
Involvement of the MLL gene in T-lineage acute lymphoblastic leukemia
-
Moorman AV, Richards S, Harrison CJ. Involvement of the MLL gene in T-lineage acute lymphoblastic leukemia. Blood 2002; 100: 2273-2274.
-
(2002)
Blood
, vol.100
, pp. 2273-2274
-
-
Moorman, A.V.1
Richards, S.2
Harrison, C.J.3
-
14
-
-
0025328804
-
Poor prognosis of children with pre-B acute lymphoblastic leukemia is associated with the t(1;19)(q23;p13): A Pediatric Oncology Group study
-
Crist WM, Carroll AJ, Shuster JJ, Behm FG, Whitehead M, Vietti TJ et al. Poor prognosis of children with pre-B acute lymphoblastic leukemia is associated with the t(1;19)(q23;p13): a Pediatric Oncology Group study. Blood 1990; 76: 117-122.
-
(1990)
Blood
, vol.76
, pp. 117-122
-
-
Crist, W.M.1
Carroll, A.J.2
Shuster, J.J.3
Behm, F.G.4
Whitehead, M.5
Vietti, T.J.6
-
15
-
-
0031918423
-
Clinical significance of translocation t(1;19) in childhood acute lymphoblastic leukemia in the context of contemporary therapies: A report from the Children's Cancer Group
-
Uckun FM, Sensel MG, Sather HN, Gaynon PS, Arthur DC, Lange BJ et al. Clinical significance of translocation t(1;19) in childhood acute lymphoblastic leukemia in the context of contemporary therapies: a report from the Children's Cancer Group. J Clin Oncol 1998; 16: 527-535.
-
(1998)
J. Clin. Oncol.
, vol.16
, pp. 527-535
-
-
Uckun, F.M.1
Sensel, M.G.2
Sather, H.N.3
Gaynon, P.S.4
Arthur, D.C.5
Lange, B.J.6
-
16
-
-
0037329249
-
E2APBX1 fusion in adult acute lymphoblastic leukaemia: Biological and clinical features
-
Foa R, Vitale A, Mancini M. Cuneo A, Mecucci C. Elia L et al. E2APBX1 fusion in adult acute lymphoblastic leukaemia: biological and clinical features. Br J Haematol 2003; 120: 484-487.
-
(2003)
Br. J. Haematol.
, vol.120
, pp. 484-487
-
-
Foa, R.1
Vitale, A.2
Mancini, M.3
Cuneo, A.4
Mecucci, C.5
Elia, L.6
-
17
-
-
0027479344
-
Clinical features and outcome of T-cell acute lymphoblastic leukemia in childhood with respect to alterations at the TAL1 locus: A Pediatric Oncology Group study
-
Bash RO, Crist WM, Shuster JJ, Link MP, Amylon M, Pullen J et al. Clinical features and outcome of T-cell acute lymphoblastic leukemia in childhood with respect to alterations at the TAL1 locus: a Pediatric Oncology Group study. Blood 1993; 81: 2110-2117.
-
(1993)
Blood
, vol.81
, pp. 2110-2117
-
-
Bash, R.O.1
Crist, W.M.2
Shuster, J.J.3
Link, M.P.4
Amylon, M.5
Pullen, J.6
-
18
-
-
0027182991
-
Clinical significance of TAL1 gene alteration in childhood T-cell acute lymphoblastic leukemia and lymphoma
-
Kikuchi A, Hayashi Y, Kobayashi S, Hanada R, Moriwaki K, Yamamoto K et al. Clinical significance of TAL1 gene alteration in childhood T-cell acute lymphoblastic leukemia and lymphoma. Leukemia 1993; 7: 933-938.
-
(1993)
Leukemia
, vol.7
, pp. 933-938
-
-
Kikuchi, A.1
Hayashi, Y.2
Kobayashi, S.3
Hanada, R.4
Moriwaki, K.5
Yamamoto, K.6
-
19
-
-
17144474314
-
Gene expression signatures define novel oncogenic pathways in T cell acute lymphoblastic leukemia
-
Ferrando AA, Neuberg DS, Staunton J, Loh ML, Huard C, Raimondi SC et al. Gene expression signatures define novel oncogenic pathways in T cell acute lymphoblastic leukemia. Cancer Cell 2002; 1: 75-87.
-
(2002)
Cancer Cell
, vol.1
, pp. 75-87
-
-
Ferrando, A.A.1
Neuberg, D.S.2
Staunton, J.3
Loh, M.L.4
Huard, C.5
Raimondi, S.C.6
-
20
-
-
0036682493
-
HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis
-
Ballerini P, Blaise A, Busson-Le Coniat M, So XY; Zucman-Rossi J et al. HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis. Blood 2002; 100: 991-997.
-
(2002)
Blood
, vol.100
, pp. 991-997
-
-
Ballerini, P.1
Blaise, A.2
Busson-Le Coniat, M.3
So, X.Y.4
Zucman-Rossi, J.5
-
21
-
-
0033965477
-
The management of patients with leukaemia: The role of cytogenetics in this molecular era
-
Harrison CJ. The management of patients with leukaemia: the role of cytogenetics in this molecular era. Br J Haematol 2000; 108: 19-30.
-
(2000)
Br. J. Haematol.
, vol.108
, pp. 19-30
-
-
Harrison, C.J.1
-
22
-
-
0027205347
-
Southern blot analysis of ALL-1 rearrangements at chromosome 11q23 in acute leukemia
-
Lo Coco F, Mandelli F, Breccia M, Annino L, Guglielmi C, Petti MC et al. Southern blot analysis of ALL-1 rearrangements at chromosome 11q23 in acute leukemia. Cancer Res 1993; 53: 3800-3803.
-
(1993)
Cancer Res.
, vol.53
, pp. 3800-3803
-
-
Lo Coco, F.1
Mandelli, F.2
Breccia, M.3
Annino, L.4
Guglielmi, C.5
Petti, M.C.6
-
23
-
-
0032697175
-
Comparison of cytogenetics, Southern blotting, and fluorescence in situ hybridization as methods for detecting MLL gene rearrangements in children with acute leukemia and with 11q23 abnormalities
-
Mathew S, Behm F, Dalton J, Raimondi S. Comparison of cytogenetics, Southern blotting, and fluorescence in situ hybridization as methods for detecting MLL gene rearrangements in children with acute leukemia and with 11q23 abnormalities. Leukemia 1999; 13: 1713-1720.
-
(1999)
Leukemia
, vol.13
, pp. 1713-1720
-
-
Mathew, S.1
Behm, F.2
Dalton, J.3
Raimondi, S.4
-
24
-
-
0031059356
-
TEL gene rearrangement in acute lymphoblastic leukemia: A new genetic marker with prognostic significance
-
Rubnitz JE, Downing JR, Pui CH, Shurtleff SA, Raimondi SC, Evans WE et al. TEL gene rearrangement in acute lymphoblastic leukemia: a new genetic marker with prognostic significance. J Clin Oncol 1997; 15: 1150-1157.
-
(1997)
J. Clin. Oncol.
, vol.15
, pp. 1150-1157
-
-
Rubnitz, J.E.1
Downing, J.R.2
Pui, C.H.3
Shurtleff, S.A.4
Raimondi, S.C.5
Evans, W.E.6
-
25
-
-
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, d'Aniello E, Gameiro P, Pisa P 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 1999; 13: 110-118.
-
(1999)
Leukemia
, vol.13
, pp. 110-118
-
-
Pongers-Willemse, M.J.1
Seriu, T.2
Stolz, F.3
d'Aniello, E.4
Gameiro, P.5
Pisa, P.6
-
26
-
-
0027723122
-
Tal-1 deletions in T-cell acute lymphoblastic leukemia as PCR target for detection of minimal residual disease
-
Breit TM, Beishuizen A, Ludwig WD, Mol EJ, Adriaansen HJ, van Wering ER et al. tal-1 deletions in T-cell acute lymphoblastic leukemia as PCR target for detection of minimal residual disease. Leukemia 1993; 7: 2004-2011.
-
(1993)
Leukemia
, vol.7
, pp. 2004-2011
-
-
Breit, T.M.1
Beishuizen, A.2
Ludwig, W.D.3
Mol, E.J.4
Adriaansen, H.J.5
van Wering, E.R.6
-
27
-
-
18744372705
-
Site-specific translocation and evidence of postnatal origin of the t(1;19) E2A-PBX1 fusion in childhood acute lymphoblastic leukemia
-
Wiemels JL, Leonard BC, Wang Y, Segal MR, Hunger SP, Smith MT et al. Site-specific translocation and evidence of postnatal origin of the t(1;19) E2A-PBX1 fusion in childhood acute lymphoblastic leukemia. Proc Natl Acad Sci USA 2002; 99: 15101-15106.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 15101-15106
-
-
Wiemels, J.L.1
Leonard, B.C.2
Wang, Y.3
Segal, M.R.4
Hunger, S.P.5
Smith, M.T.6
-
28
-
-
0033795284
-
Microclustering of TEL-AML1 translocation break-points in childhood acute lymphoblastic leukemia
-
Wiemels JL, Alexander FE, Cazzaniga G, Biondi A, Mayer SP, Greaves M. Microclustering of TEL-AML1 translocation break-points in childhood acute lymphoblastic leukemia. Genes Chromosomes Cancer 2000; 29: 219-228.
-
(2000)
Genes Chromosomes Cancer
, vol.29
, pp. 219-228
-
-
Wiemels, J.L.1
Alexander, F.E.2
Cazzaniga, G.3
Biondi, A.4
Mayer, S.P.5
Greaves, M.6
-
29
-
-
9144265458
-
Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: Report of the BIOMED-2 Concerted Action BMH4-CT983936
-
van Dongen JJM, Langerak AW, Bruggemann M, Evans PA, Hummel M, Lavender FL et al. Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 Concerted Action BMH4-CT983936. Leukemia 2003; 17: 2257-2317.
-
(2003)
Leukemia
, vol.17
, pp. 2257-2317
-
-
van Dongen, J.J.M.1
Langerak, A.W.2
Bruggemann, M.3
Evans, P.A.4
Hummel, M.5
Lavender, F.L.6
-
30
-
-
0032757710
-
Standardized RT-PCR analysis of fusion gene transcripts from chromosome aberrations in acute leukemia for detection of minimal residual disease. Report of the BIOMED-1 Concerted Action: Investigation of minimal residual disease in acute leukemia
-
van Dongen JJM, Macintyre EA, Gabert JA, Delabesse E, Rossi V, Saglio C et al. Standardized RT-PCR analysis of fusion gene transcripts from chromosome aberrations in acute leukemia for detection of minimal residual disease. Report of the BIOMED-1 Concerted Action: investigation of minimal residual disease in acute leukemia. Leukemia 1999; 13: 1901-1928.
-
(1999)
Leukemia
, vol.13
, pp. 1901-1928
-
-
van Dongen, J.J.M.1
Macintyre, E.A.2
Gabert, J.A.3
Delabesse, E.4
Rossi, V.5
Saglio, C.6
-
31
-
-
0035411192
-
Minimal residual disease in leukaemia patients
-
Szczepanski T, Orfao A, van der Velden VH, San Miguel JF, van Dongen JJ. Minimal residual disease in leukaemia patients. Lancet Oncol 2001; 2: 409-417.
-
(2001)
Lancet Oncol.
, vol.2
, pp. 409-417
-
-
Szczepanski, T.1
Orfao, A.2
van der Velden, V.H.3
San Miguel, J.F.4
van Dongen, J.J.5
-
32
-
-
9144222001
-
Standardization and quality control studies of 'real-time' quantitative reverse transcriptase polymerase chain reaction of fusion gene transcripts for residual disease detection in leukemia - A Europe Against Cancer Program
-
Gabert J, Beillard F, Van Der Velden VH, Bi W, Grimwade D, Pallisgaard N et al. Standardization and quality control studies of 'real-time' quantitative reverse transcriptase polymerase chain reaction of fusion gene transcripts for residual disease detection in leukemia - A Europe Against Cancer Program. Leukemia 2003; 17: 2318-2357.
-
(2003)
Leukemia
, vol.17
, pp. 2318-2357
-
-
Gabert, J.1
Beillard, F.2
Van Der Velden, V.H.3
Bi, W.4
Grimwade, D.5
Pallisgaard, N.6
-
33
-
-
0033068058
-
The impact of the new FISH technologies on the cytogenetics of haematological malignancies
-
Kearney L. The impact of the new FISH technologies on the cytogenetics of haematological malignancies. Br J Haematol 1999; 104: 648-658.
-
(1999)
Br. J. Haematol.
, vol.104
, pp. 648-658
-
-
Kearney, L.1
-
34
-
-
85014169026
-
A single split-signal FISH probe set allows detection of TAL1 translocations as well as SIL-TAL1 fusion genes in a single test
-
van der Burg M, Smit B, Brinkhof B, Barendregt BH, Verschuren MCM, Dib M et al. A single split-signal FISH probe set allows detection of TAL1 translocations as well as SIL-TAL1 fusion genes in a single test. Leukemia 2002; 16: 755-761.
-
(2002)
Leukemia
, vol.16
, pp. 755-761
-
-
van der Burg, M.1
Smit, B.2
Brinkhof, B.3
Barendregt, B.H.4
Verschuren, M.C.M.5
Dib, M.6
-
35
-
-
0032715401
-
Rapid and sensitive detection of all types of MLL gene translocations with a single FISH probe set
-
van der Burg M, Beverloo HB, Langerak AW, Wijsman J, van Drunen E, Slater R et al. Rapid and sensitive detection of all types of MLL gene translocations with a single FISH probe set. Leukemia 1999; 13: 2107-2113.
-
(1999)
Leukemia
, vol.13
, pp. 2107-2113
-
-
van der Burg, M.1
Beverloo, H.B.2
Langerak, A.W.3
Wijsman, J.4
van Drunen, E.5
Slater, R.6
-
36
-
-
2642552975
-
Molecular detection of chromosome aberrations (Split-signal FISH probe tehnology)
-
International Patent PCT/NL98/00270
-
van Dongen JJM, Langerak AW. Molecular detection of chromosome aberrations (Split-signal FISH probe tehnology). International Patent 1998, PCT/NL98/00270.
-
(1998)
-
-
van Dongen, J.J.M.1
Langerak, A.W.2
-
37
-
-
0030772421
-
Panhandle PCR strategy to amplify MLL genomic breakpoints in treatment-related leukemias
-
Megonigal MD, Rappaport EF, Jones DH, Kim CS, Nowell PC, Lange Ell et al. Panhandle PCR strategy to amplify MLL genomic breakpoints in treatment-related leukemias. Proc Natl Acad Sci USA 1997; 94: 11583-11588.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 11583-11588
-
-
Megonigal, M.D.1
Rappaport, E.F.2
Jones, D.H.3
Kim, C.S.4
Nowell, P.C.5
Lange, B.J.6
-
38
-
-
0031833830
-
Panhandle PCR: A technical advance to amplify MLL genomic translocation breakpoints
-
Felix CA, Jones DH. Panhandle PCR: a technical advance to amplify MLL genomic translocation breakpoints. Leukemia 1998; 12: 976-981.
-
(1998)
Leukemia
, vol.12
, pp. 976-981
-
-
Felix, C.A.1
Jones, D.H.2
-
39
-
-
0014407722
-
Repeated sequences in DNA. Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms
-
Britten RJ, Kohne DE. Repeated sequences in DNA. Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms. Science 1968; 161: 529-540.
-
(1968)
Science
, vol.161
, pp. 529-540
-
-
Britten, R.J.1
Kohne, D.E.2
-
40
-
-
0025864962
-
Retroposons-seeds of evolution
-
Brosius L. Retroposons-seeds of evolution. Science 1991; 251: 753.
-
(1991)
Science
, vol.251
, pp. 753
-
-
Brosius, L.1
-
42
-
-
0020044638
-
SINEs and LINEs: Highly repeated short and long interspersed sequences in mammalian genomes
-
Singer MF. SINEs and LINEs: highly repeated short and long interspersed sequences in mammalian genomes. Cell 1982; 28: 433-434.
-
(1982)
Cell
, vol.28
, pp. 433-434
-
-
Singer, M.F.1
-
43
-
-
0023946286
-
Human genome organization: Alu, lines, and the molecular structure of metaphase chromosome bands
-
Korenberg JR, Rykowski MC. Human genome organization: Alu, lines, and the molecular structure of metaphase chromosome bands. Cell 1988; 53: 391-400.
-
(1988)
Cell
, vol.53
, pp. 391-400
-
-
Korenberg, J.R.1
Rykowski, M.C.2
-
44
-
-
0023576805
-
Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridization
-
Landegent JE, Jansen in de Wal N, Dirks RW, Baao F, van der Ploeg M. Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridization. Hum Genet 1987; 77: 366-370.
-
(1987)
Hum. Genet.
, vol.77
, pp. 366-370
-
-
Landegent, J.E.1
Jansen in de Wal, N.2
Dirks, R.W.3
Baao, F.4
van der Ploeg, M.5
-
45
-
-
0026341239
-
Sequence-selective recognition of DNA by strand displacement with a thymine-substituted polyamide
-
Nielsen PE, Egholm M, Berg RH, Buchardt O. Sequence-selective recognition of DNA by strand displacement with a thymine-substituted polyamide. Science 1991; 254: 1497-1500.
-
(1991)
Science
, vol.254
, pp. 1497-1500
-
-
Nielsen, P.E.1
Egholm, M.2
Berg, R.H.3
Buchardt, O.4
-
46
-
-
0027364174
-
PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen-bonding rules
-
Egholm M, Buchardt O, Christensen L, Behrens C, Freier SM, Driver DA et al. PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen-bonding rules. Nature 1993; 365: 566-568.
-
(1993)
Nature
, vol.365
, pp. 566-568
-
-
Egholm, M.1
Buchardt, O.2
Christensen, L.3
Behrens, C.4
Freier, S.M.5
Driver, D.A.6
-
47
-
-
2642531798
-
Combined use of PHA and DNA for fluorescence in situ hybridization (FISH)
-
Nielsen PE (ed). 2nd edn. Wymondham: Horizon Scientific Press
-
Nielsen KV, Müller S, Poulsen TS, Gabs S, Schonau A. Combined use of PHA and DNA for fluorescence in situ hybridization (FISH). In: Nielsen PE (ed). Peptide Nuclei Acid, Protocols and Applications, 2nd edn. Wymondham: Horizon Scientific Press, 2003, pp 227-260.
-
(2003)
Peptide Nuclei Acid, Protocols and Applications
, pp. 227-260
-
-
Nielsen, K.V.1
Müller, S.2
Poulsen, T.S.3
Gabs, S.4
Schonau, A.5
-
48
-
-
2642576532
-
Method and probes for the detection of chromosome aberrations (FISH probe/PNA based technology)
-
International Patent PCT/DK99/00245
-
van Dongen JJM, Vang Nielsen K, Pluzek KJ, Adelhorst K. Method and probes for the detection of chromosome aberrations (FISH probe/PNA based technology). International Patent 1999, PCT/DK99/00245.
-
(1999)
-
-
van Dongen, J.J.M.1
Vang Nielsen, K.2
Pluzek, K.J.3
Adelhorst, K.4
-
49
-
-
0024554495
-
A new DNA binding and dimerization motif in immunoglobulin enhancer binding, daughterless, MyoD, and myc proteins
-
Murre C, McCaw PS, Baltimore D. A new DNA binding and dimerization motif in immunoglobulin enhancer binding, daughterless, MyoD, and myc proteins. Cell 1989; 56: 777-783.
-
(1989)
Cell
, vol.56
, pp. 777-783
-
-
Murre, C.1
McCaw, P.S.2
Baltimore, D.3
-
50
-
-
0023029814
-
Balanced and unbalanced 1;19 translocation-associated acute lymphoblastic leukemias
-
Shikano T, Kaneko Y, Takazawa M, Ueno N, Ohkawa M, Fujimoto T. Balanced and unbalanced 1;19 translocation-associated acute lymphoblastic leukemias. Cancer 1986; 58: 2239-2243.
-
(1986)
Cancer
, vol.58
, pp. 2239-2243
-
-
Shikano, T.1
Kaneko, Y.2
Takazawa, M.3
Ueno, N.4
Ohkawa, M.5
Fujimoto, T.6
-
51
-
-
0027961005
-
Immunologic, cytogenetic, and clinical characterization of childhood acute lymphoblastic leukemia with the t(1;19) (q23; p13) or its derivative
-
Pui CH, Raimondi SC, Hancock ML, Rivera GK, Ribeiro RC, Mahmoud HH et al. Immunologic, cytogenetic, and clinical characterization of childhood acute lymphoblastic leukemia with the t(1;19) (q23; p13) or its derivative. J Clin Oncol 1994; 12: 2601-2606.
-
(1994)
J. Clin. Oncol.
, vol.12
, pp. 2601-2606
-
-
Pui, C.H.1
Raimondi, S.C.2
Hancock, M.L.3
Rivera, G.K.4
Ribeiro, R.C.5
Mahmoud, H.H.6
-
52
-
-
0026716252
-
Prognostic significance of the balanced t(1;19) and unbalanced der(19)t(1;19) translocations in acute lymphoblastic leukemia
-
Secker-Walker LM, Berger R, Fenaux P, Lai JL, Nelken B, Garson M et al. Prognostic significance of the balanced t(1;19) and unbalanced der(19)t(1;19) translocations in acute lymphoblastic leukemia. Leukemia 1992; 6: 363-369.
-
(1992)
Leukemia
, vol.6
, pp. 363-369
-
-
Secker-Walker, L.M.1
Berger, R.2
Fenaux, P.3
Lai, J.L.4
Nelken, B.5
Garson, M.6
-
53
-
-
0024465836
-
The gene for enhancer binding proteins E12/E47 lies at the t(1;19) breakpoint in acute leukemias
-
Mellentin JD, Murre C, Donlon TA, McCaw PS, Smith SD, Carroll AJ et al. The gene for enhancer binding proteins E12/E47 lies at the t(1;19) breakpoint in acute leukemias. Science 1989; 246: 379-382.
-
(1989)
Science
, vol.246
, pp. 379-382
-
-
Mellentin, J.D.1
Murre, C.2
Donlon, T.A.3
McCaw, P.S.4
Smith, S.D.5
Carroll, A.J.6
-
54
-
-
0025185904
-
Molecular analysis of the t(1;19) breakpoint cluster region in pre-B cell acute lymphoblastic leukemias
-
Mellentin JD, Nourse J, Hunger SP, Smith SD, Cleary ML. Molecular analysis of the t(1;19) breakpoint cluster region in pre-B cell acute lymphoblastic leukemias. Genes Chromosomes Cancer 1990; 2: 239-247.
-
(1990)
Genes Chromosomes Cancer
, vol.2
, pp. 239-247
-
-
Mellentin, J.D.1
Nourse, J.2
Hunger, S.P.3
Smith, S.D.4
Cleary, M.L.5
-
55
-
-
0025064238
-
Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor
-
Nourse J, Mellentin JD, Galili N, Wilkinson J, Stanbridge E, Smith SD et al. Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor. Cell 1990; 60: 535-545.
-
(1990)
Cell
, vol.60
, pp. 535-545
-
-
Nourse, J.1
Mellentin, J.D.2
Galili, N.3
Wilkinson, J.4
Stanbridge, E.5
Smith, S.D.6
-
56
-
-
0035129012
-
Detection of E2A translocations in leukemias via fluorescence in situ hybridization
-
Boomer T, Varella-Garcia M, McGavran L, Meltesen L, Olsen AS, Hunger SP. Detection of E2A translocations in leukemias via fluorescence in situ hybridization. Leukemia 2001; 15: 95-102.
-
(2001)
Leukemia
, vol.15
, pp. 95-102
-
-
Boomer, T.1
Varella-Garcia, M.2
McGavran, L.3
Meltesen, L.4
Olsen, A.S.5
Hunger, S.P.6
-
57
-
-
0035839891
-
The role of E2A-PBX1 in leukemogenesis
-
Aspland SE, Bendall HH, Murre C. The role of E2A-PBX1 in leukemogenesis. Oncogene 2001; 20: 5708-5717.
-
(2001)
Oncogene
, vol.20
, pp. 5708-5717
-
-
Aspland, S.E.1
Bendall, H.H.2
Murre, C.3
-
58
-
-
0036142364
-
Gradient of E2A activity in B-cell development
-
Herblot S, Aplan PD, Hoang T. Gradient of E2A activity in B-cell development. Mol Cell Biol 2002; 22: 886-900.
-
(2002)
Mol. Cell Biol.
, vol.22
, pp. 886-900
-
-
Herblot, S.1
Aplan, P.D.2
Hoang, T.3
-
59
-
-
0026761786
-
Hlf, a novel hepatic bZIP protein, shows altered DNA-binding properties following fusion to E2A in t(17;19) acute lymphoblastic leukemia
-
Hunger SP, Ohyashiki K, Toyama K, Cleary ML. Hlf, a novel hepatic bZIP protein, shows altered DNA-binding properties following fusion to E2A in t(17;19) acute lymphoblastic leukemia. Genes Dev 1992; 6: 1608-1620.
-
(1992)
Genes Dev.
, vol.6
, pp. 1608-1620
-
-
Hunger, S.P.1
Ohyashiki, K.2
Toyama, K.3
Cleary, M.L.4
-
60
-
-
0026744416
-
Fusion of the leucine zipper gene HLF to the E2A gene in human acute B-lineage leukemia
-
Inaba T, Roberts WM, Shapiro LH, Jolly KW, Raimondi SC, Smith SD et al. Fusion of the leucine zipper gene HLF to the E2A gene in human acute B-lineage leukemia. Science 1992; 257: 531-534.
-
(1992)
Science
, vol.257
, pp. 531-534
-
-
Inaba, T.1
Roberts, W.M.2
Shapiro, L.H.3
Jolly, K.W.4
Raimondi, S.C.5
Smith, S.D.6
-
61
-
-
0035839880
-
E2A-HLF usurps control of evolutionarily conserved survival pathways
-
Seidel MG, Look AT. E2A-HLF usurps control of evolutionarily conserved survival pathways. Oncogene 2001; 20: 5718-5725.
-
(2001)
Oncogene
, vol.20
, pp. 5718-5725
-
-
Seidel, M.G.1
Look, A.T.2
-
62
-
-
0033045755
-
Identification of a novel molecular partner of the E2A gene in childhood leukemia
-
Brambillasca F, Mosna G, Colombo M, Rivolta A, Caslini C, Minuzzo M et al. Identification of a novel molecular partner of the E2A gene in childhood leukemia. Leukemia 1999; 13: 369-375.
-
(1999)
Leukemia
, vol.13
, pp. 369-375
-
-
Brambillasca, F.1
Mosna, G.2
Colombo, M.3
Rivolta, A.4
Caslini, C.5
Minuzzo, M.6
-
63
-
-
0025137176
-
A new homeohox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B ALL
-
Kamps MP, Murre C, Sun XH, Baltimore D. A new homeohox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B ALL. Cell 1990; 60: 547-555.
-
(1990)
Cell
, vol.60
, pp. 547-555
-
-
Kamps, M.P.1
Murre, C.2
Sun, X.H.3
Baltimore, D.4
-
64
-
-
0029004562
-
Biology and treatment of infant leukemias
-
Pui CH, Kane JR, Crist WM. Biology and treatment of infant leukemias. Leukemia 1995; 9: 762-769.
-
(1995)
Leukemia
, vol.9
, pp. 762-769
-
-
Pui, C.H.1
Kane, J.R.2
Crist, W.M.3
-
65
-
-
0025833975
-
Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias
-
Ziemin-van der Poel S, McCabe NR, Gill HJ, Espinosa III R, Patel Y, Harden A et al. Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias. Proc Natl Acad Sci USA 1991; 88: 10735-10739.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 10735-10739
-
-
Ziemin-van der Poel, S.1
McCabe, N.R.2
Gill, H.J.3
Espinosa III, R.4
Patel, Y.5
Harden, A.6
-
66
-
-
0032530350
-
Immunophenotypic and genotypic features, clinical characteristics, and treatment outcome of adult pro-B acute lymphoblastic leukemia: Results of the German multicenter trials GMALL 03/87 and 04/89
-
Ludwig WD, Rieder H, Bartram CR, Heinze B, Schwartz S, Gassmann W et al. Immunophenotypic and genotypic features, clinical characteristics, and treatment outcome of adult pro-B acute lymphoblastic leukemia: results of the German multicenter trials GMALL 03/87 and 04/89. Blood 1998; 92: 1898-1909.
-
(1998)
Blood
, vol.92
, pp. 1898-1909
-
-
Ludwig, W.D.1
Rieder, H.2
Bartram, C.R.3
Heinze, B.4
Schwartz, S.5
Gassmann, W.6
-
67
-
-
0242500374
-
Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements
-
Pui CH, Chessells JM, Camitta B, Baruchel A, Biondi A, Boyett JM et al. Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements. Leukemia 2003; 17: 700-706.
-
(2003)
Leukemia
, vol.17
, pp. 700-706
-
-
Pui, C.H.1
Chessells, J.M.2
Camitta, B.3
Baruchel, A.4
Biondi, A.5
Boyett, J.M.6
-
68
-
-
0027132061
-
Rearrangements of the MLL gene in therapy-related acute myeloid leukemia in patients previously treated with agents targeting DNA- topoisomerase II
-
Super HJ, McCabe NR, Thirman MJ, Larson RA, Le Beau MM, Pedersen-Bjergaard J et al. Rearrangements of the MLL gene in therapy-related acute myeloid leukemia in patients previously treated with agents targeting DNA- topoisomerase II. Blood 1993; 82: 3705-3711.
-
(1993)
Blood
, vol.82
, pp. 3705-3711
-
-
Super, H.J.1
McCabe, N.R.2
Thirman, M.J.3
Larson, R.A.4
Le Beau, M.M.5
Pedersen-Bjergaard, J.6
-
69
-
-
0034791454
-
Therapy-related acute lymphoblastic leukaemia with MLL rearrangements following DNA topoisomerase II inhibitors, an increasing problem: Report on two new cases and review of the literature since 1992
-
Andersen MK, Christiansen DH, Jensen BA, Ernst P, Hauge G, Pedersen-Bjergaard J. Therapy-related acute lymphoblastic leukaemia with MLL rearrangements following DNA topoisomerase II inhibitors, an increasing problem: report on two new cases and review of the literature since 1992. Br J Haematol 2001; 114: 539-543.
-
(2001)
Br. J. Haematol.
, vol.114
, pp. 539-543
-
-
Andersen, M.K.1
Christiansen, D.H.2
Jensen, B.A.3
Ernst, P.4
Hauge, G.5
Pedersen-Bjergaard, J.6
-
70
-
-
0031944101
-
Ten novel 11q23 chromosomal partner sites
-
Harrison CJ, Cuneo A, Clark R, Johansson B, Lafage-Pochitaloff M, Mugneret F et al. Ten novel 11q23 chromosomal partner sites. Leukemia 1998; 12: 811-822.
-
(1998)
Leukemia
, vol.12
, pp. 811-822
-
-
Harrison, C.J.1
Cuneo, A.2
Clark, R.3
Johansson, B.4
Lafage-Pochitaloff, M.5
Mugneret, F.6
-
71
-
-
0031895675
-
Hematologic malignancies with t(4;11)(q21;q23) - A cytogenetic, morphologic, immunophenotypic and clinical study of 183 cases. European 11q23 Workshop participants
-
Johansson B, Moorman AV, Haas OA, Watmore AE, Cheung KL, Swanton S et al. Hematologic malignancies with t(4;11)(q21;q23) - a cytogenetic, morphologic, immunophenotypic and clinical study of 183 cases. European 11q23 Workshop participants. Leukemia 1998; 12: 779-787.
-
(1998)
Leukemia
, vol.12
, pp. 779-787
-
-
Johansson, B.1
Moorman, A.V.2
Haas, O.A.3
Watmore, A.E.4
Cheung, K.L.5
Swanton, S.6
-
72
-
-
0026496887
-
The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 gene
-
Gu Y, Nakamura T, Alder H, Prasad R, Canaani O, Cimino G et al. The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 gene. Cell 1992; 71: 701-708.
-
(1992)
Cell
, vol.71
, pp. 701-708
-
-
Gu, Y.1
Nakamura, T.2
Alder, H.3
Prasad, R.4
Canaani, O.5
Cimino, G.6
-
73
-
-
0031898443
-
The translocations, t(11;19)(q23;p13.1) and t(11;19)(q23;p13.3): A cytogenetic and clinical profile of 53 patients. European 11q23 Workshop participants
-
Moorman AV, Hagemeijer A, Charrin C, Rieder H, Secker Walker LM. The translocations, t(11;19)(q23;p13.1) and t(11;19)(q23;p13.3): a cytogenetic and clinical profile of 53 patients. European 11q23 Workshop participants. Leukemia 1998; 12: 805-810.
-
(1998)
Leukemia
, vol.12
, pp. 805-810
-
-
Moorman, A.V.1
Hagemeijer, A.2
Charrin, C.3
Rieder, H.4
Secker Walker, L.M.5
-
74
-
-
0031953952
-
Hematological malignancies with t(9;11)(p21-22;q23) - A laboratory and clinical study of 125 cases. European 11q23 Workshop participants
-
Swansbury GJ, Slater R, Bain BJ, Moorman AV, Secker-Walker LM. Hematological malignancies with t(9;11)(p21-22;q23) - a laboratory and clinical study of 125 cases. European 11q23 Workshop participants. Leukemia 1998; 12: 792-800.
-
(1998)
Leukemia
, vol.12
, pp. 792-800
-
-
Swansbury, G.J.1
Slater, R.2
Bain, B.J.3
Moorman, A.V.4
Secker-Walker, L.M.5
-
75
-
-
0031896465
-
The t(10;11)(p12;q23) translocation in acute leukaemia: A cytogenetic and clinical study of 20 patients. European 11q23 Workshop participants
-
Lillington DM, Young BD, Berger R, Martineau M, Moorman AV, Secker-Walker LM. The t(10;11)(p12;q23) translocation in acute leukaemia: a cytogenetic and clinical study of 20 patients. European 11q23 Workshop participants. Leukemia 1998; 12: 801-804.
-
(1998)
Leukemia
, vol.12
, pp. 801-804
-
-
Lillington, D.M.1
Young, B.D.2
Berger, R.3
Martineau, M.4
Moorman, A.V.5
Secker-Walker, L.M.6
-
76
-
-
0031919885
-
The t(6;11)(q27;q23) translocation in acute leukemia: A laboratory and clinical study of 30 cases. EU Concerted Action 11q23 Workshop participants
-
Martineau M, Berger R, Lillington DM, Moorman AV, Secker-Walker LM. The t(6;11)(q27;q23) translocation in acute leukemia: a laboratory and clinical study of 30 cases. EU Concerted Action 11q23 Workshop participants. Leukemia 1998; 12: 788-791.
-
(1998)
Leukemia
, vol.12
, pp. 788-791
-
-
Martineau, M.1
Berger, R.2
Lillington, D.M.3
Moorman, A.V.4
Secker-Walker, L.M.5
-
77
-
-
0026454451
-
Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias
-
Tkachuk DC, Kohler S, Cleary ML. Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias. Cell 1992; 71: 691-700.
-
(1992)
Cell
, vol.71
, pp. 691-700
-
-
Tkachuk, D.C.1
Kohler, S.2
Cleary, M.L.3
-
78
-
-
0028091804
-
11q23 translocations split the 'AT-hook' cruciform DNA-binding region and the transcriptional repression domain from the activation domain of the mixed-lineage leukemia (MLL) gene
-
Zeleznik-Le NJ, Harden AM, Rowley JD. 11q23 translocations split the 'AT-hook' cruciform DNA-binding region and the transcriptional repression domain from the activation domain of the mixed-lineage leukemia (MLL) gene. Proc Natl Acad Sci USA 1994; 91: 10610-10614.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 10610-10614
-
-
Zeleznik-Le, N.J.1
Harden, A.M.2
Rowley, J.D.3
-
79
-
-
0029990102
-
Double knockout of the ALL-1 gene blocks hematopoietic differentiation in vitro
-
Fidanza V, Melotti P, Yano T, Nakamura T, Bradley A, Canaani E et al. Double knockout of the ALL-1 gene blocks hematopoietic differentiation in vitro. Cancer Res 1996; 56: 1179-1183.
-
(1996)
Cancer Res.
, vol.56
, pp. 1179-1183
-
-
Fidanza, V.1
Melotti, P.2
Yano, T.3
Nakamura, T.4
Bradley, A.5
Canaani, E.6
-
80
-
-
0027283999
-
Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridisation
-
Kobayashi H, Espinosa R, Thirman MJ, Gill HJ, Fernaold AA, Diaz MO et al. Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridisation. Blood 1993; 82: 547-551.
-
(1993)
Blood
, vol.82
, pp. 547-551
-
-
Kobayashi, H.1
Espinosa, R.2
Thirman, M.J.3
Gill, H.J.4
Fernaold, A.A.5
Diaz, M.O.6
-
81
-
-
0031921715
-
Derivative chromosomes of 11q23 translocations in hematologic malignancies
-
Johansson B, Moorman AV, Secker-Walker LM. Derivative chromosomes of 11q23 translocations in hematologic malignancies. Leukemia 1998; 12: 828-833.
-
(1998)
Leukemia
, vol.12
, pp. 828-833
-
-
Johansson, B.1
Moorman, A.V.2
Secker-Walker, L.M.3
-
82
-
-
0035839952
-
Molecular mechanisms of leukemogenesis mediated by MLL fusion proteins
-
Ayton PM, Cleary ML. Molecular mechanisms of leukemogenesis mediated by MLL fusion proteins. Oncogene 2001; 20: 5695-5707.
-
(2001)
Oncogene
, vol.20
, pp. 5695-5707
-
-
Ayton, P.M.1
Cleary, M.L.2
-
83
-
-
0029890796
-
Exon/intron structure of the human ALL-1 (MLL) gene involved in translocations to chromosomal region 11q23 and acute leukaemias
-
Nilson I, Lochner K, Siegler G, Greil J, Beck JD, Fey GH et al. Exon/intron structure of the human ALL-1 (MLL) gene involved in translocations to chromosomal region 11q23 and acute leukaemias. Br J Haematol 1996; 93: 966-972.
-
(1996)
Br. J. Haematol.
, vol.93
, pp. 966-972
-
-
Nilson, I.1
Lochner, K.2
Siegler, G.3
Greil, J.4
Beck, J.D.5
Fey, G.H.6
-
84
-
-
6744221199
-
A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias
-
von Bergh A, Emanuel B, van Zelderen-Bhola S, Smetsers T, van Soest R, Stul M et al. A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias. Genes Chromosomes Cancer 2000; 28: 14-22.
-
(2000)
Genes Chromosomes Cancer
, vol.28
, pp. 14-22
-
-
von Bergh, A.1
Emanuel, B.2
van Zelderen-Bhola, S.3
Smetsers, T.4
van Soest, R.5
Stul, M.6
-
85
-
-
0029068727
-
Breakpoint heterogeneity in t(10;11) translocation in AML-M4/M5 resulting in fusion of AF10 and MLL is resolved by fluorescent in situ hybridization analysis
-
Beverloo HB, Le Coniat M, Wijsman J, Lillington DM, Bernard O, de Klein A et al. Breakpoint heterogeneity in t(10;11) translocation in AML-M4/M5 resulting in fusion of AF10 and MLL is resolved by fluorescent in situ hybridization analysis. Cancer Res 1995; 55: 4220-4224.
-
(1995)
Cancer Res.
, vol.55
, pp. 4220-4224
-
-
Beverloo, H.B.1
Le Coniat, M.2
Wijsman, J.3
Lillington, D.M.4
Bernard, O.5
de Klein, A.6
-
86
-
-
0030575543
-
The TEL gene and human leukemia
-
Golub TR, McLean T, Stegmaier K, Carroll M, Tomasson M, Gilliland DG. The TEL gene and human leukemia. Biochim Biophys Acta 1996; 1288: M7-M10.
-
(1996)
Biochim. Biophys. Acta
, vol.1288
-
-
Golub, T.R.1
McLean, T.2
Stegmaier, K.3
Carroll, M.4
Tomasson, M.5
Gilliland, D.G.6
-
87
-
-
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
-
88
-
-
0029889231
-
Genomic organization of TEL: The human ETS-variant gene 6
-
Baens M, Peeters P, Guo C, Aerssens J, Marynen P. Genomic organization of TEL: the human ETS-variant gene 6. Genome Res 1996; 6: 404-413.
-
(1996)
Genome Res.
, vol.6
, pp. 404-413
-
-
Baens, M.1
Peeters, P.2
Guo, C.3
Aerssens, J.4
Marynen, P.5
-
89
-
-
0032520176
-
Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignancies
-
Wlodarska I, La Starza R, Baens M, Dierlamm J, Uyttebroeck A, Selleslag D et al. Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignancies. Blood 1998; 91: 1399-1406.
-
(1998)
Blood
, vol.91
, pp. 1399-1406
-
-
Wlodarska, I.1
La Starza, R.2
Baens, M.3
Dierlamm, J.4
Uyttebroeck, A.5
Selleslag, D.6
-
90
-
-
0035399173
-
Relapse of TEL-AML1-positive acute lymphoblastic leukemia in childhood: A matched-pair analysis
-
Seeger K, von Stackelberg A, Taube T, Buchwald D, Korner G, Suttorp M et al. Relapse of TEL-AML1-positive acute lymphoblastic leukemia in childhood: a matched-pair analysis. J Clin Oncol 2001; 19: 3188-3193.
-
(2001)
J. Clin. Oncol.
, vol.19
, pp. 3188-3193
-
-
Seeger, K.1
von Stackelberg, A.2
Taube, T.3
Buchwald, D.4
Korner, G.5
Suttorp, M.6
-
91
-
-
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, Rubnitz JE, Raimondi SC, Hancock ML 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: 1985-1989.
-
(1995)
Leukemia
, vol.9
, pp. 1985-1989
-
-
Shurtleff, S.A.1
Buijs, A.2
Behm, F.G.3
Rubnitz, J.E.4
Raimondi, S.C.5
Hancock, M.L.6
-
92
-
-
0028805405
-
High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia
-
Romana SP, Poirel H, Leconiat M, Flexor MA, Mauchauffe M, Jonveaux P et al. High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. Blood 1995; 86: 4263-4269.
-
(1995)
Blood
, vol.86
, pp. 4263-4269
-
-
Romana, S.P.1
Poirel, H.2
Leconiat, M.3
Flexor, M.A.4
Mauchauffe, M.5
Jonveaux, P.6
-
93
-
-
0032841521
-
Cytogenetic abnormalities associated with the t(12;21): A collaborative study of 169 children with t(12;21)-positive acute lymphoblastic leukemia
-
Raynaud SD, Dastugue N, Zoccola D, Shurtleff SA, Mathew S, Raimondi SC. Cytogenetic abnormalities associated with the t(12;21): a collaborative study of 169 children with t(12;21)-positive acute lymphoblastic leukemia. Leukemia 1999; 13: 1325-1330.
-
(1999)
Leukemia
, vol.13
, pp. 1325-1330
-
-
Raynaud, S.D.1
Dastugue, N.2
Zoccola, D.3
Shurtleff, S.A.4
Mathew, S.5
Raimondi, S.C.6
-
94
-
-
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, Bastard C, Cacheux V, Grosgeorge J 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: 2891-2899.
-
(1996)
Blood
, vol.87
, pp. 2891-2899
-
-
Raynaud, S.1
Cave, H.2
Baens, M.3
Bastard, C.4
Cacheux, V.5
Grosgeorge, J.6
-
95
-
-
16944367034
-
ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia
-
Cave H, Cacheux V, Raynaud S, Brunie G, Bakkus M, Cochaux P et al. ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia. Leukemia 1997; 11: 1459-1564.
-
(1997)
Leukemia
, vol.11
, pp. 1459-1564
-
-
Cave, H.1
Cacheux, V.2
Raynaud, S.3
Brunie, G.4
Bakkus, M.5
Cochaux, P.6
-
96
-
-
0037669552
-
Expression profile of wild-type ETV6 in childhood acute leukaemia
-
Patel N, Goff LK, Clark T, Ford AM, Foot N, Lillington D et al. Expression profile of wild-type ETV6 in childhood acute leukaemia. Br J Haematol 2003; 122: 94-98.
-
(2003)
Br. J. Haematol.
, vol.122
, pp. 94-98
-
-
Patel, N.1
Goff, L.K.2
Clark, T.3
Ford, A.M.4
Foot, N.5
Lillington, D.6
-
97
-
-
0033565561
-
The biology of chronic myeloid leukemia
-
Faderl S, Talpaz M, Estrov Z, O'Brien S, Kurzrock R, Kantarjian HM. The biology of chronic myeloid leukemia. N Engl J Med 1999; 341: 164-172.
-
(1999)
N. Engl. J. Med.
, vol.341
, pp. 164-172
-
-
Faderl, S.1
Talpaz, M.2
Estrov, Z.3
O'Brien, S.4
Kurzrock, R.5
Kantarjian, H.M.6
-
98
-
-
0037108177
-
Characteristics and outcome of patients with Philadelphia chromosome negative, bcr/abl negative chronic myelogenous leukemia
-
Onida F, Ball G, Kantarjian HM, Smith TL, Glassman A, Albitar M et al. Characteristics and outcome of patients with Philadelphia chromosome negative, bcr/abl negative chronic myelogenous leukemia. Cancer 2002; 95: 1673-1684.
-
(2002)
Cancer
, vol.95
, pp. 1673-1684
-
-
Onida, F.1
Ball, G.2
Kantarjian, H.M.3
Smith, T.L.4
Glassman, A.5
Albitar, M.6
-
99
-
-
0035839842
-
Modeling Philadelphia chromosome positive leukemias
-
Wong S, Witte ON. Modeling Philadelphia chromosome positive leukemias. Oncogene 2001; 20: 5644-5659.
-
(2001)
Oncogene
, vol.20
, pp. 5644-5659
-
-
Wong, S.1
Witte, O.N.2
-
100
-
-
0034611661
-
Outcome of treatment in children with Philadelphia chromosome-positive acute lymphoblastic leukemia
-
Arico M, Valsecchi MC, Camitta B, Schrappe M, Chessells J, Baruchel A et al. Outcome of treatment in children with Philadelphia chromosome-positive acute lymphoblastic leukemia. N Engl J Med 2000; 342: 998-1006.
-
(2000)
N. Engl. J. Med.
, vol.342
, pp. 998-1006
-
-
Arico, M.1
Valsecchi, M.C.2
Camitta, B.3
Schrappe, M.4
Chessells, J.5
Baruchel, A.6
-
101
-
-
0025873083
-
Bcr encodes a GTPase-activating protein for p21rac
-
Diekmann D, Brill S, Garrett MD, Totty N, Hsuan J, Monfries C et al. Bcr encodes a GTPase-activating protein for p21rac. Nature 1991; 351: 400-402.
-
(1991)
Nature
, vol.351
, pp. 400-402
-
-
Diekmann, D.1
Brill, S.2
Garrett, M.D.3
Totty, N.4
Hsuan, J.5
Monfries, C.6
-
102
-
-
0029005995
-
Sequence and analysis of the human ABL gene, the BCR gene, and regions involved in the Philadelphia chromosomal translocation
-
Chissoe SL, Bodenteich A, Wang YF, Wang YP, Burian D, Clifton SW et al. Sequence and analysis of the human ABL gene, the BCR gene, and regions involved in the Philadelphia chromosomal translocation. Genomics 1995; 27: 67-82.
-
(1995)
Genomics
, vol.27
, pp. 67-82
-
-
Chissoe, S.L.1
Bodenteich, A.2
Wang, Y.F.3
Wang, Y.P.4
Burian, D.5
Clifton, S.W.6
-
103
-
-
0021346853
-
Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22
-
Groffen J, Stephenson JR, Heisterkamp N, de Klein A, Bartram CR, Grosveld G. Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22. Cell 1984; 36: 93-99.
-
(1984)
Cell
, vol.36
, pp. 93-99
-
-
Groffen, J.1
Stephenson, J.R.2
Heisterkamp, N.3
de Klein, A.4
Bartram, C.R.5
Grosveld, G.6
-
104
-
-
0021802841
-
Fused transcript of abl and bcr genes in chronic myelogenous leukaemia
-
Shtivelman E, Lifshitz B, Gale RP, Canaani E. Fused transcript of abl and bcr genes in chronic myelogenous leukaemia. Nature 1985; 315: 550-554.
-
(1985)
Nature
, vol.315
, pp. 550-554
-
-
Shtivelman, E.1
Lifshitz, B.2
Gale, R.P.3
Canaani, E.4
-
105
-
-
0023903502
-
Expression of a distinctive BCR-ABL oncogene in Ph1-positive acute lymphocytic leukemia (ALL)
-
Clark SS, McLaughlin J, Timmons M, Pendergast AM, Ben-Neriah Y, Dow LW et al. Expression of a distinctive BCR-ABL oncogene in Ph1-positive acute lymphocytic leukemia (ALL). Science 1988; 239: 775-777.
-
(1988)
Science
, vol.239
, pp. 775-777
-
-
Clark, S.S.1
McLaughlin, J.2
Timmons, M.3
Pendergast, A.M.4
Ben-Neriah, Y.5
Dow, L.W.6
-
106
-
-
0023133732
-
Unique forms of the abl tyrosine kinase distinguish Ph1-positive CML from Ph1-positive ALL
-
Clark SS, McLaughlin J, Crist WM, Champlin R, Witte ON. Unique forms of the abl tyrosine kinase distinguish Ph1-positive CML from Ph1-positive ALL. Science 1987; 235: 85-88.
-
(1987)
Science
, vol.235
, pp. 85-88
-
-
Clark, S.S.1
McLaughlin, J.2
Crist, W.M.3
Champlin, R.4
Witte, O.N.5
-
107
-
-
0025254224
-
Chronic myeloid leukemia may be associated with several bcr-abl transcripts including the acute lymphoid leukemia-type 7 kb transcript
-
Selleri L, von Lindern M, Hermans A, Meijer D, Torelli G, Grosveld G. Chronic myeloid leukemia may be associated with several bcr-abl transcripts including the acute lymphoid leukemia-type 7 kb transcript. Blood 1990; 75: 1146-1153.
-
(1990)
Blood
, vol.75
, pp. 1146-1153
-
-
Selleri, L.1
von Lindern, M.2
Hermans, A.3
Meijer, D.4
Torelli, G.5
Grosveld, G.6
-
108
-
-
0028181636
-
P190BCR-ABL chronic myeloid leukaemia: The missing link with chronic myelomonocytic leukaemia?
-
Melo JV, Myint H, Galton DA, Goldman JM. P190BCR-ABL chronic myeloid leukaemia: the missing link with chronic myelomonocytic leukaemia? Leukemia 1994; 8: 208-211.
-
(1994)
Leukemia
, vol.8
, pp. 208-211
-
-
Melo, J.V.1
Myint, H.2
Galton, D.A.3
Goldman, J.M.4
-
109
-
-
10144254429
-
Neutrophilic-chronic myeloid leukemia: A distinct disease with a specific molecular marker (BCR/ABL with C3/A2 junction)
-
Pane F, Frigeri F, Sindona M, Luciano L, Ferrara F, Cimino R et al. Neutrophilic-chronic myeloid leukemia: a distinct disease with a specific molecular marker (BCR/ABL with C3/A2 junction). Blood 1996; 88: 2410-2414.
-
(1996)
Blood
, vol.88
, pp. 2410-2414
-
-
Pane, F.1
Frigeri, F.2
Sindona, M.3
Luciano, L.4
Ferrara, F.5
Cimino, R.6
-
110
-
-
12944295358
-
Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia
-
Sinclair PB, Nacheva EP, Leversha M, Telford N, Chang J, Reid A et al. Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia. Blood 2000; 95: 738-743.
-
(2000)
Blood
, vol.95
, pp. 738-743
-
-
Sinclair, P.B.1
Nacheva, E.P.2
Leversha, M.3
Telford, N.4
Chang, J.5
Reid, A.6
-
111
-
-
0035525738
-
ABL-BCR expression does not correlate with deletions on the derivative chromosome 9 or survival in chronic myeloid leukemia
-
de la Fuente J, Merx K, Steer EJ, Muller M, Szydlo RM, Maywald O, Berger U, Hehlmann R, Goldman JM, Cross NC, Melo JV, Hochlaus A. ABL-BCR expression does not correlate with deletions on the derivative chromosome 9 or survival in chronic myeloid leukemia. Blood 2001; 98: 2879-2880.
-
(2001)
Blood
, vol.98
, pp. 2879-2880
-
-
de la Fuente, J.1
Merx, K.2
Steer, E.J.3
Muller, M.4
Szydlo, R.M.5
Maywald, O.6
Berger, U.7
Hehlmann, R.8
Goldman, J.M.9
Cross, N.C.10
Melo, J.V.11
Hochlaus, A.12
-
112
-
-
0042638382
-
Imatinib improves but may not fully reverse the poor prognosis of patients with CML with derivative chromosome 9 deletions
-
Huntly BJ, Guilhot F, Reid AG, Vassiliou G, Hennig E, Franke C et al. Imatinib improves but may not fully reverse the poor prognosis of patients with CML with derivative chromosome 9 deletions. Blood 2003; 102: 2205-2212.
-
(2003)
Blood
, vol.102
, pp. 2205-2212
-
-
Huntly, B.J.1
Guilhot, F.2
Reid, A.G.3
Vassiliou, G.4
Hennig, E.5
Franke, C.6
-
113
-
-
7344231641
-
TAL1 expression does not occur in the majority of T-ALL blasts
-
Delabesse E, Bernard M, Meyer V, Smit L, Pulford K, Cayuela JM et al. TAL1 expression does not occur in the majority of T-ALL blasts. Br J Haematol 1998; 102: 449-457.
-
(1998)
Br. J. Haematol.
, vol.102
, pp. 449-457
-
-
Delabesse, E.1
Bernard, M.2
Meyer, V.3
Smit, L.4
Pulford, K.5
Cayuela, J.M.6
-
114
-
-
0029073944
-
Does activation of the TAL1 gene occur in a majority of patients with T-cell acute lymphoblastic leukemia? A pediatric oncology group study
-
Bash RO, Hall S, Timmons CF, Crist WM, Amylon M, Smith RG et al. Does activation of the TAL1 gene occur in a majority of patients with T-cell acute lymphoblastic leukemia? A pediatric oncology group study. Blood 1995; 86: 666-676.
-
(1995)
Blood
, vol.86
, pp. 666-676
-
-
Bash, R.O.1
Hall, S.2
Timmons, C.F.3
Crist, W.M.4
Amylon, M.5
Smith, R.G.6
-
115
-
-
0028858855
-
Absence of blood formation in mice lacking the T-cell leukaemia oncoprotein tal-1/SCL
-
Shivdasani RA, Mayer EL, Orkin SH. Absence of blood formation in mice lacking the T-cell leukaemia oncoprotein tal-1/SCL. Nature 1995; 373: 432-434.
-
(1995)
Nature
, vol.373
, pp. 432-434
-
-
Shivdasani, R.A.1
Mayer, E.L.2
Orkin, S.H.3
-
116
-
-
0030581174
-
The T cell leukemia oncoprotein SCL/tal-1 is essential for development of all hematopoietic lineages
-
Porcher C, Swat W, Rockwell K, Fujiwara Y, Alt FW, Orkin SH. The T cell leukemia oncoprotein SCL/tal-1 is essential for development of all hematopoietic lineages. Cell 1996; 86: 47-57.
-
(1996)
Cell
, vol.86
, pp. 47-57
-
-
Porcher, C.1
Swat, W.2
Rockwell, K.3
Fujiwara, Y.4
Alt, F.W.5
Orkin, S.H.6
-
117
-
-
0029781248
-
The scl gene product is required for the generation of all hematopoietic lineages in the adult mouse
-
Robb L, Elwood NJ, Elefanty AG, Kontgen F, Li R, Barnett LD et al. The scl gene product is required for the generation of all hematopoietic lineages in the adult mouse. EMBO J 1996; 15: 4123-4129.
-
(1996)
EMBO J.
, vol.15
, pp. 4123-4129
-
-
Robb, L.1
Elwood, N.J.2
Elefanty, A.G.3
Kontgen, F.4
Li, R.5
Barnett, L.D.6
-
118
-
-
0027759976
-
TAL1, TAL2 and LYL1: A family of basic helix-loop-helix proteins implicated in T cell acute leukaemia
-
Baer R. TAL1, TAL2 and LYL1: a family of basic helix-loop-helix proteins implicated in T cell acute leukaemia. Semin Cancer Biol 1993; 4: 341-347.
-
(1993)
Semin. Cancer Biol.
, vol.4
, pp. 341-347
-
-
Baer, R.1
-
119
-
-
0025642707
-
Disruption of the human SCL locus by 'illegitimate' V-(D)-J recombinase activity
-
Aplan PD, Lombardi DP, Ginsberg AM, Cossman J, Bertness VL, Kirsch IR. Disruption of the human SCL locus by 'illegitimate' V-(D)-J recombinase activity. Science 1990; 250: 1426-1429.
-
(1990)
Science
, vol.250
, pp. 1426-1429
-
-
Aplan, P.D.1
Lombardi, D.P.2
Ginsberg, A.M.3
Cossman, J.4
Bertness, V.L.5
Kirsch, I.R.6
-
120
-
-
0025851073
-
Two site-specific deletions and t(1;14) translocation restricted to human T-cell acute leukemias disrupt the 5′ part of the tal-1 gene
-
Bernard O, Lecointe N, Jonveaux P, Souyri M, Mauchauffe M, Berger R et al. Two site-specific deletions and t(1;14) translocation restricted to human T-cell acute leukemias disrupt the 5′ part of the tal-1 gene. Oncogene 1991; 6: 1477-1488.
-
(1991)
Oncogene
, vol.6
, pp. 1477-1488
-
-
Bernard, O.1
Lecointe, N.2
Jonveaux, P.3
Souyri, M.4
Mauchauffe, M.5
Berger, R.6
-
121
-
-
0031456951
-
Simultaneous SIL-TAL1 RT-PCR detection of all tal(D) deletions and identification of novel tal(d) variants
-
Delabesse F, Bernard M, Landman-Parker J, Davi F, Leboeuf D, Varet B et al. Simultaneous SIL-TAL1 RT-PCR detection of all tal(D) deletions and identification of novel tal(d) variants. Br J Haematol 1997; 99: 901-907.
-
(1997)
Br. J. Haematol.
, vol.99
, pp. 901-907
-
-
Delabesse, F.1
Bernard, M.2
Landman-Parker, J.3
Davi, F.4
Leboeuf, D.5
Varet, B.6
-
122
-
-
17344367455
-
Immunoglobulin and T cell receptor gene rearrangement patterns in acute lymphoblastic leukemia are less mature in adults than in children: Implications for selection of PCR targets for detection of minimal residual disease
-
Szczepanski T, Langerak AW, Wolvers-Tettero IL, Ossenkoppele GJ, Verhoef G, Stul M et al. Immunoglobulin and T cell receptor gene rearrangement patterns in acute lymphoblastic leukemia are less mature in adults than in children: implications for selection of PCR targets for detection of minimal residual disease. Leukemia 1998; 12: 1081-1088.
-
(1998)
Leukemia
, vol.12
, pp. 1081-1088
-
-
Szczepanski, T.1
Langerak, A.W.2
Wolvers-Tettero, I.L.3
Ossenkoppele, G.J.4
Verhoef, G.5
Stul, M.6
-
123
-
-
0026042011
-
Structural characterization of SIL, a gene frequently disrupted in T-cell acute lymphoblastic leukemia
-
Aplan PD, Lombardi DP, Kirsch IR. Structural characterization of SIL, a gene frequently disrupted in T-cell acute lymphoblastic leukemia. Mol Cell Biol 1991; 11: 5462-5469.
-
(1991)
Mol. Cell Biol.
, vol.11
, pp. 5462-5469
-
-
Aplan, P.D.1
Lombardi, D.P.2
Kirsch, I.R.3
-
124
-
-
0026581804
-
Involvement of the putative hematopoietic transcription factor SCL in T-cell acute lymphoblastic leukemia
-
Aplan PD, Lombardi DP, Reaman GH, Sather HN, Hammond GD, Kirsch IR. Involvement of the putative hematopoietic transcription factor SCL in T-cell acute lymphoblastic leukemia. Blood 1992; 79: 1327-1333.
-
(1992)
Blood
, vol.79
, pp. 1327-1333
-
-
Aplan, P.D.1
Lombardi, D.P.2
Reaman, G.H.3
Sather, H.N.4
Hammond, G.D.5
Kirsch, I.R.6
-
125
-
-
0025151168
-
Site-specific recombination of the tal-1 gene is a common occurrence in human T cell leukemia
-
Brown L, Cheng JT, Chen Q, Siciliano MJ, Crist W, Buchanan G et al. Site-specific recombination of the tal-1 gene is a common occurrence in human T cell leukemia. EMBO J 1990; 9: 3343-3351.
-
(1990)
EMBO J.
, vol.9
, pp. 3343-3351
-
-
Brown, L.1
Cheng, J.T.2
Chen, Q.3
Siciliano, M.J.4
Crist, W.5
Buchanan, G.6
-
126
-
-
0025357145
-
Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemias
-
Bernard O, Guglielmi P, Jonveaux P, Cherif D, Gisselbrecht S, Mauchauffe M et al. Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemias. Genes Chromosomes Cancer 1990; 1: 194-208.
-
(1990)
Genes Chromosomes Cancer
, vol.1
, pp. 194-208
-
-
Bernard, O.1
Guglielmi, P.2
Jonveaux, P.3
Cherif, D.4
Gisselbrecht, S.5
Mauchauffe, M.6
-
127
-
-
0028968174
-
Cloning and characterization of TCTA, a gene located at the site of a t(1;3) translocation
-
Aplan PD, Johnson BE, Russell E, Chervinsky DS, Kirsch IR. Cloning and characterization of TCTA, a gene located at the site of a t(1;3) translocation. Cancer Res 1995; 55: 1917-1921.
-
(1995)
Cancer Res.
, vol.55
, pp. 1917-1921
-
-
Aplan, P.D.1
Johnson, B.E.2
Russell, E.3
Chervinsky, D.S.4
Kirsch, I.R.5
-
128
-
-
2642525992
-
Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: Results of EORTC studies 58881 and 58951
-
Cave H, Suciu S, Preudhomme C, Poppe B, Robert A, Uyttebroeck A et al. Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951. Blood 2003; 22: 22.
-
(2003)
Blood
, vol.22
, pp. 22
-
-
Cave, H.1
Suciu, S.2
Preudhomme, C.3
Poppe, B.4
Robert, A.5
Uyttebroeck, A.6
-
129
-
-
0035154384
-
Long-range comparison of human and mouse SCL loci: Localized regions of sensitivity to restriction endonucleases correspond precisely with peaks of conserved noncoding sequences
-
Gottgens B, Gilbert JG, Barton LM, Grafham D, Rogers J, Bentley DR et al. Long-range comparison of human and mouse SCL loci: localized regions of sensitivity to restriction endonucleases correspond precisely with peaks of conserved noncoding sequences. Genome Res 2001; 11: 87-97.
-
(2001)
Genome Res.
, vol.11
, pp. 87-97
-
-
Gottgens, B.1
Gilbert, J.G.2
Barton, L.M.3
Grafham, D.4
Rogers, J.5
Bentley, D.R.6
-
130
-
-
0036932841
-
High incidence of Hox11L2 expression in children with T-ALL
-
Mauvieux L, Leymarie V, Helias C, Perrusson N, Falkenrodt A, Lioure B et al. High incidence of Hox11L2 expression in children with T-ALL. Leukemia 2002; 16: 2417-2422.
-
(2002)
Leukemia
, vol.16
, pp. 2417-2422
-
-
Mauvieux, L.1
Leymarie, V.2
Helias, C.3
Perrusson, N.4
Falkenrodt, A.5
Lioure, B.6
-
131
-
-
0027174566
-
The HOX11 gene encodes a DNA-binding nuclear transcription factor belonging to a distinct family of homeobox genes
-
Dear TN, Sanchez-Garcia I, Rabbitts TH. The HOX11 gene encodes a DNA-binding nuclear transcription factor belonging to a distinct family of homeobox genes. Proc Natl Acad Sci USA 1993; 90: 4431-4435.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 4431-4435
-
-
Dear, T.N.1
Sanchez-Garcia, I.2
Rabbitts, T.H.3
-
132
-
-
0036849635
-
Disruption of the RanBP17/Hox11L2 region by recombination with the TCRdelta locus in acute lymphoblastic leukemias with t(5;14)(q34;q11)
-
Hansen-Hagge TE, Schafer M, Kiyoi H, Morris SW, Whitlock JA, Koch P et al. Disruption of the RanBP17/Hox11L2 region by recombination with the TCRdelta locus in acute lymphoblastic leukemias with t(5;14)(q34;q11). Leukemia 2002; 16: 2205-2212.
-
(2002)
Leukemia
, vol.16
, pp. 2205-2212
-
-
Hansen-Hagge, T.E.1
Schafer, M.2
Kiyoi, H.3
Morris, S.W.4
Whitlock, J.A.5
Koch, P.6
-
133
-
-
0034638621
-
Identification of a novel putative Ran-binding protein and its close homologue
-
Koch P, Bohlmann I, Schafer M, Hansen-Hagge TE, Kiyoi H, Wilda M et al. Identification of a novel putative Ran-binding protein and its close homologue. Biochem Biophys Res Commun 2000; 278: 241-249.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.278
, pp. 241-249
-
-
Koch, P.1
Bohlmann, I.2
Schafer, M.3
Hansen-Hagge, T.E.4
Kiyoi, H.5
Wilda, M.6
-
134
-
-
0034932866
-
Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome hands 11A4-A5 by in situ hybridization
-
Cinti R, Fava M, Sancandi M, Matera I, Ravazzolo R, Ceccherini I. Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome hands 11A4-A5 by in situ hybridization. Cytogenet Cell Genet 2001; 92: 354-355.
-
(2001)
Cytogenet. Cell Genet.
, vol.92
, pp. 354-355
-
-
Cinti, R.1
Fava, M.2
Sancandi, M.3
Matera, I.4
Ravazzolo, R.5
Ceccherini, I.6
-
135
-
-
0030667493
-
Visualization of mono-allelic chromosomal aberrations 3′ and 5′ of the cyclin D1 gene in mantle cell lymphoma using DNA fiber fluorescence in situ hybridization
-
de Boer CJ, Vaandrager JW, van Krieken JH, Holmes Z, Kluin PM, Schuuring E. Visualization of mono-allelic chromosomal aberrations 3′ and 5′ of the cyclin D1 gene in mantle cell lymphoma using DNA fiber fluorescence in situ hybridization. Oncogene 1997; 15: 1599-1603.
-
(1997)
Oncogene
, vol.15
, pp. 1599-1603
-
-
de Boer, C.J.1
Vaandrager, J.W.2
van Krieken, J.H.3
Holmes, Z.4
Kluin, P.M.5
Schuuring, E.6
-
136
-
-
0034283763
-
V(D)J recombinase-mediated transposition of the BCL2 gene to the IGH locus in follicular lymphoma
-
Vaandrager JW, Schuuring E, Philippo K, Kluin PM. V(D)J recombinase-mediated transposition of the BCL2 gene to the IGH locus in follicular lymphoma. Blood 2000; 96: 1947-1952.
-
(2000)
Blood
, vol.96
, pp. 1947-1952
-
-
Vaandrager, J.W.1
Schuuring, E.2
Philippo, K.3
Kluin, P.M.4
-
137
-
-
0034787189
-
Detection of illegitimate rearrangement within the immunoglobulin locus on 14q32.3 in B-cell malignancies using end-sequenced probes
-
Poulsen TS, Silahtaroglu AN, Gisselo CG, Gaarsdal E, Rasmussen T, Tommerup N et al. Detection of illegitimate rearrangement within the immunoglobulin locus on 14q32.3 in B-cell malignancies using end-sequenced probes. Genes Chromosomes Cancer 2001; 32: 265-274.
-
(2001)
Genes Chromosomes Cancer
, vol.32
, pp. 265-274
-
-
Poulsen, T.S.1
Silahtaroglu, A.N.2
Gisselo, C.G.3
Gaarsdal, E.4
Rasmussen, T.5
Tommerup, N.6
-
138
-
-
0036796972
-
Detection of illegitimate rearrangements within the immunoglobulin light chain loci in B cell malignancies using end sequenced probes Detection of illegitimate rearrangement within the immunoglobulin locus on 14q32.3 in B-cell malignancies using end-sequenced probes
-
Poulsen TS, Silahtaroglu AN, Gisselo CG, Tommerup N, Johnsen HE, Gaarsdal E et al. Detection of illegitimate rearrangements within the immunoglobulin light chain loci in B cell malignancies using end sequenced probes Detection of illegitimate rearrangement within the immunoglobulin locus on 14q32.3 in B-cell malignancies using end-sequenced probes. Leukemia 2002; 16: 2148-2155.
-
(2002)
Leukemia
, vol.16
, pp. 2148-2155
-
-
Poulsen, T.S.1
Silahtaroglu, A.N.2
Gisselo, C.G.3
Tommerup, N.4
Johnsen, H.E.5
Gaarsdal, E.6
-
139
-
-
0242417049
-
Molecular cytogenetic detection of chromosomal breakpoints in T-cell receptor gene loci
-
Gesk S, Martin-Subero JI, Harder L, Luhmann B, Schlegelberger B, Calasanz MJ et al. Molecular cytogenetic detection of chromosomal breakpoints in T-cell receptor gene loci. Leukemia 2003; 17: 738-745.
-
(2003)
Leukemia
, vol.17
, pp. 738-745
-
-
Gesk, S.1
Martin-Subero, J.I.2
Harder, L.3
Luhmann, B.4
Schlegelberger, B.5
Calasanz, M.J.6
-
140
-
-
26344475855
-
Immunobiological diversity in infant acute lymphoblastic leukemia
-
Jansen MJWC, Van der Velden VHJ, Den Boer ML, Pieters R, Van Dongen JJM. Immunobiological diversity in infant acute lymphoblastic leukemia. Blood 2003; 102: 21a.
-
(2003)
Blood
, vol.102
-
-
Jansen, M.J.W.C.1
Van der Velden, V.H.J.2
Den Boer, M.L.3
Pieters, R.4
Van Dongen, J.J.M.5
-
141
-
-
0032831130
-
MII rearrangements in haematological malignancies: Lessons from clinical and biological studies
-
Dimartino JF, Cleary ML. MII rearrangements in haematological malignancies: lessons from clinical and biological studies. Br J Haematol 1999; 106: 614-626.
-
(1999)
Br. J. Haematol.
, vol.106
, pp. 614-626
-
-
Dimartino, J.F.1
Cleary, M.L.2
-
142
-
-
0141816710
-
AML with 11q23/MLL abnormalities as defined by the WHO classification: Incidence, partner chromosomes, FAB subtype, age distribution, and prognostic impact in an unselected series of 1897 cytogenetically analyzed AML cases
-
Schoch C, Schnittger S, Klaus M, Kern W, Hiddemann W, Haferlach T. AML with 11q23/MLL abnormalities as defined by the WHO classification: incidence, partner chromosomes, FAB subtype, age distribution, and prognostic impact in an unselected series of 1897 cytogenetically analyzed AML cases. Blood 2003; 102: 2395-2402.
-
(2003)
Blood
, vol.102
, pp. 2395-2402
-
-
Schoch, C.1
Schnittger, S.2
Klaus, M.3
Kern, W.4
Hiddemann, W.5
Haferlach, T.6
-
143
-
-
2642563528
-
11q23 rearrangements in leukaemia
-
Huret JL. 11q23 rearrangements in leukaemia. Atlas Genet Cytogenet Oncol Haematol 2003. http://www.infobiogen.fr/services/chromcancer/Anomalies/11q23ID1030.html.
-
(2003)
Atlas Genet. Cytogenet. Oncol. Haematol.
-
-
Huret, J.L.1
-
144
-
-
0029004541
-
Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia
-
Golub TR, Barker GF, Bohlander SK, Hiebert SW, Ward DC, Bray-Ward P 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: 4917-4921.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 4917-4921
-
-
Golub, T.R.1
Barker, G.F.2
Bohlander, S.K.3
Hiebert, S.W.4
Ward, D.C.5
Bray-Ward, P.6
-
145
-
-
0029045087
-
The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion
-
Romana SP, Mauchauffe M, Le Coniat M, Chumakov I, Le Paslier D, Berger R et al. The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion. Blood 1995; 85: 3662-3670.
-
(1995)
Blood
, vol.85
, pp. 3662-3670
-
-
Romana, S.P.1
Mauchauffe, M.2
Le Coniat, M.3
Chumakov, I.4
Le Paslier, D.5
Berger, R.6
-
146
-
-
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: 307-316.
-
(1994)
Cell
, vol.77
, pp. 307-316
-
-
Golub, T.R.1
Barker, G.F.2
Lovett, M.3
Gilliland, D.G.4
-
147
-
-
0028936278
-
The novel activation of ABL by fusion to an ets-related gene, TEL
-
Papadopoulos P, Ridge SA, Boucher CA, Stocking C, Wiedemann LM et al. The novel activation of ABL by fusion to an ets-related gene, TEL. Cancer Res 1995; 55: 34-38.
-
(1995)
Cancer Res.
, vol.55
, pp. 34-38
-
-
Papadopoulos, P.1
Ridge, S.A.2
Boucher, C.A.3
Stocking, C.4
Wiedemann, L.M.5
-
148
-
-
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 et al. 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 1997; 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
-
149
-
-
0029061177
-
Translocation (12;22) (p13;q11) in myeloproliferative disorders results in fusion of the ETS-like TEL gene on 12p13 to the MN1 gene on 22q11
-
Buijs A, Sherr S, van Baal S, van Bezouw S, van der Plas D, Geurts van Kessel A et al. Translocation (12;22) (p13;q11) in myeloproliferative disorders results in fusion of the ETS-like TEL gene on 12p13 to the MN1 gene on 22q11. Oncogene 1995; 10: 1511-1519.
-
(1995)
Oncogene
, vol.10
, pp. 1511-1519
-
-
Buijs, A.1
Sherr, S.2
van Baal, S.3
van Bezouw, S.4
van der Plas, D.5
Geurts van Kessel, A.6
-
150
-
-
8944246791
-
Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): A recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes
-
Raynaud SD, Baens M, Grosgeorge J, Rodgers K, Reid CD, Dainton M et al. Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes. Blood 1996; 88: 682-689.
-
(1996)
Blood
, vol.88
, pp. 682-689
-
-
Raynaud, S.D.1
Baens, M.2
Grosgeorge, J.3
Rodgers, K.4
Reid, C.D.5
Dainton, M.6
-
151
-
-
0037308166
-
Acute myelogenous leukemia with the t(3;12)(q26;p13) translocation: Case report and review of the literature
-
Voutsadakis IA, Maillard N. Acute myelogenous leukemia with the t(3;12)(q26;p13) translocation: case report and review of the
-
(2003)
Am. J. Hematol.
, vol.72
, pp. 135-137
-
-
Voutsadakis, I.A.1
Maillard, N.2
-
152
-
-
0033199749
-
Fusion of a novel gene, BTL, to ETV6 in acute myeloid leukemias with a t(4;12)(q11-q12;p13)
-
Cools J, Bilhou-Nabera C, Wlodarska I, Cabrol C, Talmant P, Bernard P et al. Fusion of a novel gene, BTL, to ETV6 in acute myeloid leukemias with a t(4;12)(q11-q12;p13). Blood 1999; 94: 1820-1824.
-
(1999)
Blood
, vol.94
, pp. 1820-1824
-
-
Cools, J.1
Bilhou-Nabera, C.2
Wlodarska, I.3
Cabrol, C.4
Talmant, P.5
Bernard, P.6
-
153
-
-
0032778537
-
The tyrosine kinase abl-related gene ARG is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): Molecular cloning of both reciprocal transcripts
-
Cazzaniga G, Tosi S, Aloisi A, Giudici G, Daniotti M, Pioltelli P et al. The tyrosine kinase abl-related gene ARG is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): molecular cloning of both reciprocal transcripts. Blood 1999; 94: 4370-4373.
-
(1999)
Blood
, vol.94
, pp. 4370-4373
-
-
Cazzaniga, G.1
Tosi, S.2
Aloisi, A.3
Giudici, G.4
Daniotti, M.5
Pioltelli, P.6
-
154
-
-
0033557864
-
Fusion of ETV6 to neurotrophin-3 receptor TRKC in acute myeloid leukemia with t(12;15)(p13;q25)
-
Eguchi M, Eguchi-Ishimae M, Tojo A, Morishita K, Suzuki K, Sato Y et al. Fusion of ETV6 to neurotrophin-3 receptor TRKC in acute myeloid leukemia with t(12;15)(p13;q25). Blood 1999; 93: 1355-1363.
-
(1999)
Blood
, vol.93
, pp. 1355-1363
-
-
Eguchi, M.1
Eguchi-Ishimae, M.2
Tojo, A.3
Morishita, K.4
Suzuki, K.5
Sato, Y.6
-
155
-
-
0032904241
-
Fusion of ETV6 to the caudal-related homeobox gene CDX2 in acute myeloid leukemia with the t(12;13)(p13;q12)
-
Chase A, Reiter A, Burci L, Cazzaniga G, Biondi A, Pickard J et al. Fusion of ETV6 to the caudal-related homeobox gene CDX2 in acute myeloid leukemia with the t(12;13)(p13;q12). Blood 1999; 93: 1025-1031.
-
(1999)
Blood
, vol.93
, pp. 1025-1031
-
-
Chase, A.1
Reiter, A.2
Burci, L.3
Cazzaniga, G.4
Biondi, A.5
Pickard, J.6
-
156
-
-
0038717120
-
Identification of a novel fusion gene, TTL, fused to ETV6 in acute lymphoblastic leukemia with t(12;13)(p13;q14), and its implication in leukemogenesis
-
Qiao Y, Ogawa S, Hangaishi A, Yuji K, Izutsu K, Kunisato A et al. Identification of a novel fusion gene, TTL, fused to ETV6 in acute lymphoblastic leukemia with t(12;13)(p13;q14), and its implication in leukemogenesis. Leukemia 2003; 17: 1112-1120.
-
(2003)
Leukemia
, vol.17
, pp. 1112-1120
-
-
Qiao, Y.1
Ogawa, S.2
Hangaishi, A.3
Yuji, K.4
Izutsu, K.5
Kunisato, A.6
-
157
-
-
0035865603
-
Constitutive kinase activation of the TEL-Syk fusion gene in myelodysplastic syndrome with t(9;12)(q22;p12)
-
Kuno Y, Abe A, Emi N, Iida M, Yokozawa T, Towatari M et al. Constitutive kinase activation of the TEL-Syk fusion gene in myelodysplastic syndrome with t(9;12)(q22;p12). Blood 2001; 97: 1050-1055.
-
(2001)
Blood
, vol.97
, pp. 1050-1055
-
-
Kuno, Y.1
Abe, A.2
Emi, N.3
Iida, M.4
Yokozawa, T.5
Towatari, M.6
-
158
-
-
0035875036
-
The paired box domain gene PAX5 is fused to ETV6/TEL in an acute lymphoblastic leukemia case
-
Cazzaniga G, Daniotti M, Tosi S, Giudici G, Aloisi A, Pogliani E et al. The paired box domain gene PAX5 is fused to ETV6/TEL in an acute lymphoblastic leukemia case. Cancer Res 2001; 61: 4666-4670.
-
(2001)
Cancer Res.
, vol.61
, pp. 4666-4670
-
-
Cazzaniga, G.1
Daniotti, M.2
Tosi, S.3
Giudici, G.4
Aloisi, A.5
Pogliani, E.6
-
159
-
-
0037702860
-
PAX5/ETV6 fusion defines cytogenetic entity dic(9;12)(p13;p13)
-
Strehl S, Konig M, Dworzak MN, Kalwak K, Haas OA et al. PAX5/ETV6 fusion defines cytogenetic entity dic(9;12)(p13;p13). Leukemia 2003; 17: 1121-1123.
-
(2003)
Leukemia
, vol.17
, pp. 1121-1123
-
-
Strehl, S.1
Konig, M.2
Dworzak, M.N.3
Kalwak, K.4
Haas, O.A.5
-
160
-
-
0345269754
-
A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene
-
Penas EM, Cools J, Algenstaedt P, Hinz K, Seeger D, Schafhausen P et al. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene. Genes Chromosomes Cancer 2003; 37: 79-83.
-
(2003)
Genes Chromosomes Cancer
, vol.37
, pp. 79-83
-
-
Penas, E.M.1
Cools, J.2
Algenstaedt, P.3
Hinz, K.4
Seeger, D.5
Schafhausen, P.6
-
161
-
-
0034612278
-
The t(1;12)(q21;p13) translocation of human acute myeloblastic leukemia results in a TEL-ARNT fusion
-
Salomon-Nguyen F, Della-Valle V, Mauchauffe M, Busson-Le Coniat M, Ghysdael J, Berger R et al. The t(1;12)(q21;p13) translocation of human acute myeloblastic leukemia results in a TEL-ARNT fusion. Proc Natl Acad Sci USA 2000; 97: 6757-6762.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 6757-6762
-
-
Salomon-Nguyen, F.1
Della-Valle, V.2
Mauchauffe, M.3
Busson-Le Coniat, M.4
Ghysdael, J.5
Berger, R.6
-
162
-
-
0029895899
-
p190 BCR-ABL mRNA is expressed at low levels in p210-positive chronic myeloid and acute lymphoblastic leukemias
-
van Rhee F, Hochhaus A, Lin F, Melo JV, Goldman JM, Cross NC. p190 BCR-ABL mRNA is expressed at low levels in p210-positive chronic myeloid and acute lymphoblastic leukemias. Blood 1996; 87: 5213-5217.
-
(1996)
Blood
, vol.87
, pp. 5213-5217
-
-
van Rhee, F.1
Hochhaus, A.2
Lin, F.3
Melo, J.V.4
Goldman, J.M.5
Cross, N.C.6
|