-
1
-
-
0029018546
-
Molecular basis of 11q23 rearrangements in hematopoietic malignant proliferations
-
Bernard OA, Berger R. Molecular basis of 11q23 rearrangements in hematopoietic malignant proliferations. Genes Chromos Cancer 1995; 13: 75-85.
-
(1995)
Genes Chromos Cancer
, vol.13
, pp. 75-85
-
-
Bernard, O.A.1
Berger, R.2
-
2
-
-
0030456247
-
Leukaemia: The 11q23 paradigm
-
Young BD, Saha V. Leukaemia: the 11q23 paradigm. Cancer Sur 1996; 28: 225-245.
-
(1996)
Cancer Sur
, vol.28
, pp. 225-245
-
-
Young, B.D.1
Saha, V.2
-
3
-
-
0030941513
-
Disruption of a homolog of trithorax by 11q23 translocations leukemogenic and transcriptional implications
-
Rauscher FJ III, Vogt PK (eds). Springer: Berlin
-
Waring PM, Cleary ML. Disruption of a homolog of trithorax by 11q23 translocations Leukemogenic and transcriptional implications. In: Rauscher FJ III, Vogt PK (eds). Chromosomal Translocations and Oncogenic Transcription Factors. Springer: Berlin, 1997, pp 1-23.
-
(1997)
Chromosomal Translocations and Oncogenic Transcription Factors
-
-
Waring, P.M.1
Cleary, M.L.2
-
4
-
-
0030869789
-
AF6q21, a novel partner of the MLL gene in t(6;11)(q21;q23), defines a forkhead transcriptional factor subfamily
-
Hillion J, le Coniat M, Jonveaux P, Berger R, Bernard OA. AF6q21, a novel partner of the MLL gene in t(6;11)(q21;q23), defines a forkhead transcriptional factor subfamily. Blood 1997; 90: 3714-3719.
-
(1997)
Blood
, vol.90
, pp. 3714-3719
-
-
Hillion, J.1
Le Coniat, M.2
Jonveaux, P.3
Berger, R.4
Bernard, O.A.5
-
5
-
-
0342590945
-
Cloning of a translocation t(5;11)(q31;q23) identities a new MLL fusion partner and the potential myeloid tumor suppressor gene at 5q31
-
Borkhardt A, Bojesen S, Haas OA, Cazzaniga G, Harbott J, Biondi A, Loncarevic I, Jaeger U, Lampert F. Cloning of a translocation t(5;11)(q31;q23) identities a new MLL fusion partner and the potential myeloid tumor suppressor gene at 5q31. Blood 1997; 90 (Suppl. 1): 488a.
-
(1997)
Blood
, vol.90
, Issue.SUPPL. 1
-
-
Borkhardt, A.1
Bojesen, S.2
Haas, O.A.3
Cazzaniga, G.4
Harbott, J.5
Biondi, A.6
Loncarevic, I.7
Jaeger, U.8
Lampert, F.9
-
6
-
-
0031439397
-
Adenoviral EIA-associated protein p300 is involved in acute myeloid leukemia with t(11;22)(q23;q13)
-
Ida K, Kitabayashi I, Taki M, Noro K, Yamamaoto M, Ohki M, Hayashi Y. Adenoviral EIA-associated protein p300 is involved in acute myeloid leukemia with t(11;22)(q23;q13). Blood 1997; 90: 4699-4704.
-
(1997)
Blood
, vol.90
, pp. 4699-4704
-
-
Ida, K.1
Kitabayashi, I.2
Taki, M.3
Noro, K.4
Yamamaoto, M.5
Ohki, M.6
Hayashi, Y.7
-
7
-
-
4243515794
-
A novel partner gene IF-15 is fused to MLL in the t(11;15)(q23;q15)
-
Kuefer MU, Behm FG, Naeve CW, Rakestaw KM, Raimondi SC, Morris SW. A novel partner gene IF-15 is fused to MLL in the t(11;15)(q23;q15). Blood 1997; 90: (Suppl. 1): 318a.
-
(1997)
Blood
, vol.90
, Issue.SUPPL. 1
-
-
Kuefer, M.U.1
Behm, F.G.2
Naeve, C.W.3
Rakestaw, K.M.4
Raimondi, S.C.5
Morris, S.W.6
-
8
-
-
0000778884
-
EEN encodes for a member of a new family of proteins containing an Src homology 3 domain and is the third gene located on chromosome 19p13 that fuses to MLL in human leukemia
-
So CW, Caldas C, Liu M-M, Chen SJ, Huang QH, Sham MH, Wiedemann LM, Chan LC. EEN encodes for a member of a new family of proteins containing an Src homology 3 domain and is the third gene located on chromosome 19p13 that fuses to MLL in human leukemia. Proc Natl Acad Sci USA 1997; 94: 2563-2568.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 2563-2568
-
-
So, C.W.1
Caldas, C.2
Liu, M.-M.3
Chen, S.J.4
Huang, Q.H.5
Sham, M.H.6
Wiedemann, L.M.7
Chan, L.C.8
-
9
-
-
12644314103
-
MLL is fused to CBP, a histone acetyltransferase, in therapy-related acute myeloid leukemia with a t(11;16)(q23;p13.3)
-
Sobulo OM, Borrow J, Tomek R, Reshmi S, Harden A, Schlegelberger B, Housman D, Doggett NA, Rowley JD, Zeleznik-Le NJ. MLL is fused to CBP, a histone acetyltransferase, in therapy-related acute myeloid leukemia with a t(11;16)(q23;p13.3). Proc Natl Acad Sci USA 1997; 94: 8732-8737.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 8732-8737
-
-
Sobulo, O.M.1
Borrow, J.2
Tomek, R.3
Reshmi, S.4
Harden, A.5
Schlegelberger, B.6
Housman, D.7
Doggett, N.A.8
Rowley, J.D.9
Zeleznik-Le, N.J.10
-
10
-
-
0030967030
-
The t(11;16)(q23;p13) translocation in myelodysplastic syndrome fuses the MLL gene to the CBP gene
-
Taki T, Sako M, Tsuchida M, Hayashi Y. The t(11;16)(q23;p13) translocation in myelodysplastic syndrome fuses the MLL gene to the CBP gene. Blood 1997; 89: 3945-3950.
-
(1997)
Blood
, vol.89
, pp. 3945-3950
-
-
Taki, T.1
Sako, M.2
Tsuchida, M.3
Hayashi, Y.4
-
11
-
-
0030999555
-
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
-
Mitelman F, Mertens F, Johansson B. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat Genet 1997; 15: 417-473.
-
(1997)
Nat Genet
, vol.15
, pp. 417-473
-
-
Mitelman, F.1
Mertens, F.2
Johansson, B.3
-
12
-
-
0028942107
-
A novel gene, AF1q, fused to MLL in t(1;11)(q21;q23), is specifically expressed in leukemic and immature hematopoietic cells
-
Tse W, Zhu W, Chen HS, Cohen A. A novel gene, AF1q, fused to MLL in t(1;11)(q21;q23), is specifically expressed in leukemic and immature hematopoietic cells. Blood 1995; 85: 650-656.
-
(1995)
Blood
, vol.85
, pp. 650-656
-
-
Tse, W.1
Zhu, W.2
Chen, H.S.3
Cohen, A.4
-
13
-
-
0026454451
-
Involvement of a homolog of Drosophila trihorax by 11q23 chromosomal translocation in acute leukemias
-
Tkatchuk DC, Kohler S, Cleary ML. Involvement of a homolog of Drosophila trihorax by 11q23 chromosomal translocation in acute leukemias. Cell 1992; 71: 691-700.
-
(1992)
Cell
, vol.71
, pp. 691-700
-
-
Tkatchuk, D.C.1
Kohler, S.2
Cleary, M.L.3
-
14
-
-
0028135353
-
Cloning of ELL, a gene that fuses to MLL in a t(11;19)(q23;p13) in acute myeloid leukemia
-
Thirman MJ, Levitan MJ, Kobayashi H, Simon MC, Rowley JD. Cloning of ELL, a gene that fuses to MLL in a t(11;19)(q23;p13) in acute myeloid leukemia. Proc Natl Acad Sci USA 1994; 91: 12110-12114.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 12110-12114
-
-
Thirman, M.J.1
Levitan, M.J.2
Kobayashi, H.3
Simon, M.C.4
Rowley, J.D.5
-
15
-
-
0032520975
-
Molecular cloning of translocation t(1;14)(q21;q32) defines a novel gene (BCL9) at chromosome 1q21
-
Willis TG, Zalcberg IR, Coignet LJA, Wlodarska I, Stul M, Jadayel DM, Bastard C, Treleaven JG, Catovsky D, Silva MLM, Dyer MJS. Molecular cloning of translocation t(1;14)(q21;q32) defines a novel gene (BCL9) at chromosome 1q21. Blood 1998; 91: 1873-1881.
-
(1998)
Blood
, vol.91
, pp. 1873-1881
-
-
Willis, T.G.1
Zalcberg, I.R.2
Coignet, L.J.A.3
Wlodarska, I.4
Stul, M.5
Jadayel, D.M.6
Bastard, C.7
Treleaven, J.G.8
Catovsky, D.9
Silva, M.L.M.10
Dyer, M.J.S.11
-
16
-
-
0022522720
-
Localisation anormale du proto-oncogène c-ets dans une leucémie aigüe avec translocation t(1;11)(q21;q23)
-
Caubet J-F, Gegonne A, Stéhelin D, Berger R. Localisation anormale du proto-oncogène c-ets dans une leucémie aigüe avec translocation t(1;11)(q21;q23). CR Acad Sci Paris 1986; 302: 589-591.
-
(1986)
CR Acad Sci Paris
, vol.302
, pp. 589-591
-
-
Caubet, J.-F.1
Gegonne, A.2
Stéhelin, D.3
Berger, R.4
-
17
-
-
0023636659
-
Cytogenetic studies of 519 consecutive de novo acute nonlymphocytic leukemias
-
Berger R, Flandrin G, Bernheim A, Le Coniat M, Vecchione D, Pacot A, Derré J, Daniel M-T, Valensi F, Sigaux F, Ochoa-Noguera ME. Cytogenetic studies of 519 consecutive de novo acute nonlymphocytic leukemias. Cancer Genet Cytogenet 1987; 29: 9-21.
-
(1987)
Cancer Genet Cytogenet
, vol.29
, pp. 9-21
-
-
Berger, R.1
Flandrin, G.2
Bernheim, A.3
Le Coniat, M.4
Vecchione, D.5
Pacot, A.6
Derré, J.7
Daniel, M.-T.8
Valensi, F.9
Sigaux, F.10
Ochoa-Noguera, M.E.11
-
18
-
-
0023719562
-
Cytogenetic studies on acute nonlymphocytic leukemia in relapse
-
Berger R, Le Coniat M, Derré J, Vecchione D, Pacot A, Chen SJ, Baranger L, Bernheim A. Cytogenetic studies on acute nonlymphocytic leukemia in relapse. Cancer Genet Cytogenet 1988; 34: 11-18.
-
(1988)
Cancer Genet Cytogenet
, vol.34
, pp. 11-18
-
-
Berger, R.1
Le Coniat, M.2
Derré, J.3
Vecchione, D.4
Pacot, A.5
Chen, S.J.6
Baranger, L.7
Bernheim, A.8
-
20
-
-
0025683018
-
In situ hybridization ascertains the presence of a translocation t(6;11) in an acute monocytic leukemia
-
Derré J, Cherif D, Le Coniat M, Julier C, Berger R. In situ hybridization ascertains the presence of a translocation t(6;11) in an acute monocytic leukemia. Genes Chromos Cancer 1990; 2: 341-344.
-
(1990)
Genes Chromos Cancer
, vol.2
, pp. 341-344
-
-
Derré, J.1
Cherif, D.2
Le Coniat, M.3
Julier, C.4
Berger, R.5
-
21
-
-
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
-
Beverloo HB, Le Coniat M, Wijsman J, Lillington DM, Bernard O, de Klein A, van Wering E, Welborn J, Young BD, Hagemeijer A, Berger R. 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. 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
Van Wering, E.7
Welborn, J.8
Young, B.D.9
Hagemeijer, A.10
Berger, R.11
-
22
-
-
0020535793
-
(1983) complete or partial trisomy for the long arm of chromosome 1 in patients with various hematologic malignancies
-
Mamaeva SE, Mamaev NN, Jartseva NM, Belyaeva LV, Scherbakova EG. (1983) Complete or partial trisomy for the long arm of chromosome 1 in patients with various hematologic malignancies. Hum Genet 1983; 63: 107-112.
-
(1983)
Hum Genet
, vol.63
, pp. 107-112
-
-
Mamaeva, S.E.1
Mamaev, N.N.2
Jartseva, N.M.3
Belyaeva, L.V.4
Bakova, E.G.5
-
23
-
-
0025189629
-
Karyotypic patterns in acute mixed lineage leukemia
-
Hayhashi Y, Sugita K, Nakazawa S, Abe T, Kojima S, Inaba T, Hanada R, Yamamoto K. Karyotypic patterns in acute mixed lineage leukemia. Leukemia 1990; 4: 121-126.
-
(1990)
Leukemia
, vol.4
, pp. 121-126
-
-
Hayhashi, Y.1
Sugita, K.2
Nakazawa, S.3
Abe, T.4
Kojima, S.5
Inaba, T.6
Hanada, R.7
Yamamoto, K.8
-
24
-
-
0029894820
-
Comparison of fluorescence in situ hybridization, cytogenetic analysis, and DNA index analysis to detect chromosomes 4 and 10 aneuploidy in pediatric acute lymphoblastic leukemia: A pediatric oncolology group study
-
Martin PL, Look AT, Schnell S, Harris MB, Pullen J, Shuster JJ, Carroll AJ, Pettenati PJ, Rao PN. Comparison of fluorescence in situ hybridization, cytogenetic analysis, and DNA index analysis to detect chromosomes 4 and 10 aneuploidy in pediatric acute lymphoblastic leukemia: a Pediatric Oncolology Group Study. J Pediatr Hematol/Oncol 1996; 18: 113-121.
-
(1996)
J Pediatr Hematol/Oncol
, vol.18
, pp. 113-121
-
-
Martin, P.L.1
Look, A.T.2
Schnell, S.3
Harris, M.B.4
Pullen, J.5
Shuster, J.J.6
Carroll, A.J.7
Pettenati, P.J.8
Rao, P.N.9
-
25
-
-
0031944101
-
Ten novel 11q23 chromosomal partner sites
-
Harrison CJ, Cuneo A, Clark R, Johansson B, Lafage-Pochitaloff M, Mugneret F, Moorman AV, Seeker-Walker LM on behalf of the European 11q23 Workshop participants. 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
Moorman, A.V.7
Seeker-Walker, L.M.8
-
26
-
-
0023264810
-
A t(1;11) in acute non-lymphocytic leukemia FAB type M4
-
Jani Sait SN, Raza A, Sandberg. A t(1;11) in acute non-lymphocytic leukemia FAB type M4. Cancer Genet Cytogenet 1987; 24: 181-183.
-
(1987)
Cancer Genet Cytogenet
, vol.24
, pp. 181-183
-
-
Jani Sait, S.N.1
Raza, A.2
-
27
-
-
0024514810
-
Translocation t(1;11)(q21;q23), a new subgroup within M4 acute nonlymphocytic leukemia
-
Meloni-Balliet AM, Morgan R, Piatt J, Sandberg AA. Translocation t(1;11)(q21;q23), a new subgroup within M4 acute nonlymphocytic leukemia. Cancer Genet Cytogenet 1989; 37: 269-271.
-
(1989)
Cancer Genet Cytogenet
, vol.37
, pp. 269-271
-
-
Meloni-Balliet, A.M.1
Morgan, R.2
Piatt, J.3
Sandberg, A.A.4
-
28
-
-
0026847807
-
Abnormalities of chromosome 11q in three cases of acute myeloid leukemia
-
Ten SK, Khor MK, Khalid HP, Ng SC, Cheong SK, Yasmin A, Khuzaiah RR. Abnormalities of chromosome 11q in three cases of acute myeloid leukemia. Singapore Med J 1992; 33: 164-166.
-
(1992)
Singapore Med J
, vol.33
, pp. 164-166
-
-
Ten, S.K.1
Khor, M.K.2
Khalid, H.P.3
Ng, S.C.4
Cheong, S.K.5
Yasmin, A.6
Khuzaiah, R.R.7
-
29
-
-
9344249535
-
Frequency and significance of the MLL gene rearrangements in infant acute leukemia
-
Taki T, Ida K, Bessho F, Hanada R, Kikuchi A, Yamamoto K, Sako M, Tsuchida M, Seto M, Ueda R, Hayashi Y. Frequency and significance of the MLL gene rearrangements in infant acute leukemia. Leukemia 1996; 10: 1303-1307.
-
(1996)
Leukemia
, vol.10
, pp. 1303-1307
-
-
Taki, T.1
Ida, K.2
Bessho, F.3
Hanada, R.4
Kikuchi, A.5
Yamamoto, K.6
Sako, M.7
Tsuchida, M.8
Seto, M.9
Ueda, R.10
Hayashi, Y.11
-
30
-
-
0031983604
-
Clinical and biological of adult de novo and secondary acute myeloid leukemia with balanced 11q23 chromosomal anomaly or MLL gene rearrangement compared to cases with unbalanced 11q23 anomaly: Confirmation of the existence of different entities with 11q23 breakpoint
-
Archimbaud E, Charrin C, Magaud J-P, Campos L, Thomas X, Fière D, Rimokh R. Clinical and biological of adult de novo and secondary acute myeloid leukemia with balanced 11q23 chromosomal anomaly or MLL gene rearrangement compared to cases with unbalanced 11q23 anomaly: confirmation of the existence of different entities with 11q23 breakpoint. Leukemia 1998; 12: 25-33.
-
(1998)
Leukemia
, vol.12
, pp. 25-33
-
-
Archimbaud, E.1
Charrin, C.2
Magaud, J.-P.3
Campos, L.4
Thomas, X.5
Fière, D.6
Rimokh, R.7
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