-
1
-
-
0028330771
-
t(12:21): A new recurrent translocation in acute lymphoblastic leukemia
-
Romana, S. P., Le Coniat, M. and Berger, R. t(12:21): a new recurrent translocation in acute lymphoblastic leukemia. Genes Chromosom. Cancer, 9, 186-191 (1994).
-
(1994)
Genes Chromosom. Cancer
, vol.9
, pp. 186-191
-
-
Romana, S.P.1
Le Coniat, M.2
Berger, R.3
-
2
-
-
0029004541
-
Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia
-
Golub, T. R., Barker, G. F., Bohlander, S. K., Hiebert, S. W., Ward, D. C., Bray-Ward, P., Morgan, E., Raimondi, S. C., Rowley, J. D. and Gilliland, D. G. Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia. Proc. Natl. Acad. Sci. USA, 92, 4917-4921 (1995).
-
(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
Morgan, E.7
Raimondi, S.C.8
Rowley, J.D.9
Gilliland, D.G.10
-
3
-
-
0029045087
-
The t(12:21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion
-
Romana, S. P., Mauchauffe, M., Le Coniat, M., Chumakov, I., Le Paslier, D., Berger, R. and Bernard, O. A. The t(12:21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion. Blood, 85, 3662-3670 (1995).
-
(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
Bernard, O.A.7
-
4
-
-
0028805405
-
High frequency of t(12:21) in childhood B-lineage acute lymphoblastic leukemia
-
Romana, S. P., Poirel, H., Leconiat, M., Flexor, M. A., Mauchauffe, M., Jonveaux, P., Macintyre, E. A., Berger, R. and Bernard, O. A. High frequency of t(12:21) in childhood B-lineage acute lymphoblastic leukemia. Blood, 86, 4263-4269 (1995).
-
(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
Macintyre, E.A.7
Berger, R.8
Bernard, O.A.9
-
5
-
-
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, S. A., Buijs, A., Behm, F. G., Rubnitz, J. E., Raimondi, S. C., Hancock, M. L., Chan, G. C., Pui, C. H., Grosveld, G. and Downing, J. R. 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, 9, 1985-1989 (1995).
-
(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
Chan, G.C.7
Pui, C.H.8
Grosveld, G.9
Downing, J.R.10
-
6
-
-
0030250347
-
Hidden monosomy 7 in acute myeloid leukemia and myelodysplastic syndrome detected by interphase fluorescence in situ hybridization
-
Arif, M., Tanaka, K., Damodaran, C., Asou, H., Kyo, T., Dohy, H. and Kamada, N. Hidden monosomy 7 in acute myeloid leukemia and myelodysplastic syndrome detected by interphase fluorescence in situ hybridization. Leuk. Res., 20, 709-716 (1996).
-
(1996)
Leuk. Res.
, vol.20
, pp. 709-716
-
-
Arif, M.1
Tanaka, K.2
Damodaran, C.3
Asou, H.4
Kyo, T.5
Dohy, H.6
Kamada, N.7
-
7
-
-
0031016787
-
Frequent jumping translocations of chromosomal segments involving the ABL oncogene alone or in combination with CD3-MLL genes in secondary leukemias
-
Tanaka, K., Arif, M., Eguchi, M., Kyo, T., Dohy, H. and Kamada, N. Frequent jumping translocations of chromosomal segments involving the ABL oncogene alone or in combination with CD3-MLL genes in secondary leukemias. Blood, 89, 596-600 (1997).
-
(1997)
Blood
, vol.89
, pp. 596-600
-
-
Tanaka, K.1
Arif, M.2
Eguchi, M.3
Kyo, T.4
Dohy, H.5
Kamada, N.6
-
9
-
-
0030951918
-
Detection of residual host cells in sex-mismatched bone marrow transplantation in various hematological diseases by fluorescence in situ hybridization
-
Arif, M., Tanaka, K., Kumaravel, T. S., Eguchi, M., Iwato, K., Dohy, H. and Kamada, N. Detection of residual host cells in sex-mismatched bone marrow transplantation in various hematological diseases by fluorescence in situ hybridization. Jpn. J. Cancer Res., 88, 420-126 (1997).
-
(1997)
Jpn. J. Cancer Res.
, vol.88
, pp. 420-1126
-
-
Arif, M.1
Tanaka, K.2
Kumaravel, T.S.3
Eguchi, M.4
Iwato, K.5
Dohy, H.6
Kamada, N.7
-
10
-
-
0029653616
-
A second-generation YAC contig map of human chromosome 12
-
Krauter, K., Montgomery, K., Yoon, S. J., LeBlanc-Straceski, J., Renault, B., Marondel, I., Herdman, V., Cupelli, L., Banks, A., Lieman, J., Menninger, J., Bray-Ward, P., Nadkarni, P., Weissenbach, J., LePaslier, D., Rigault, P., Chumakov, I., Cohen, D., Miller, P., Ward, D. and Kucherlapati, R. A second-generation YAC contig map of human chromosome 12. Nature, 377, 321-333 (1995).
-
(1995)
Nature
, vol.377
, pp. 321-333
-
-
Krauter, K.1
Montgomery, K.2
Yoon, S.J.3
LeBlanc-Straceski, J.4
Renault, B.5
Marondel, I.6
Herdman, V.7
Cupelli, L.8
Banks, A.9
Lieman, J.10
Menninger, J.11
Bray-Ward, P.12
Nadkarni, P.13
Weissenbach, J.14
LePaslier, D.15
Rigault, P.16
Chumakov, I.17
Cohen, D.18
Miller, P.19
Ward, D.20
Kucherlapati, R.21
more..
-
11
-
-
0026738541
-
Continuum of overlapping clones spanning the entire human chromosome 21q
-
Chumakov, I., Rigault, P., Guillou, S., Ougen, P., Billaut, A., Guasconi, G., Gervy, P., LeGall, I., Soularue, P., Grinas, L., Bougueleret, L., Bellanné-Chantelot, C., Lacroix, B., Barillot, E., Gesnouin, P., Pook, S., Vaysseix, G., Frelat, G., Schmitz, A., Sambucy, J., Bosch, A., Estivill, X., Weissenbach, J., Vignal, A., Riethman, H., Cox, D., Patterson, D., Gardiner, K., Hattori, M., Sakaki, Y., Ichikawa, H., Ohki, M., LePaslier, D., Heilig, R., Antonarakis, S. and Cohen, D. Continuum of overlapping clones spanning the entire human chromosome 21q. Nature, 359, 380-387 (1992).
-
(1992)
Nature
, vol.359
, pp. 380-387
-
-
Chumakov, I.1
Rigault, P.2
Guillou, S.3
Ougen, P.4
Billaut, A.5
Guasconi, G.6
Gervy, P.7
LeGall, I.8
Soularue, P.9
Grinas, L.10
Bougueleret, L.11
Bellanné-Chantelot, C.12
Lacroix, B.13
Barillot, E.14
Gesnouin, P.15
Pook, S.16
Vaysseix, G.17
Frelat, G.18
Schmitz, A.19
Sambucy, J.20
Bosch, A.21
Estivill, X.22
Weissenbach, J.23
Vignal, A.24
Riethman, H.25
Cox, D.26
Patterson, D.27
Gardiner, K.28
Hattori, M.29
Sakaki, Y.30
Ichikawa, H.31
Ohki, M.32
LePaslier, D.33
Heilig, R.34
Antonarakis, S.35
Cohen, D.36
more..
-
12
-
-
0029889231
-
Genomic organization of TEL: The human ETS-variant gene 6
-
Baens, M., Peeters, P., Guo, C., Aerssens, J. and Marynen, P. Genomic organization of TEL: the human ETS-variant gene 6. Genome Res., 6, 404-413 (1996).
-
(1996)
Genome Res.
, vol.6
, pp. 404-413
-
-
Baens, M.1
Peeters, P.2
Guo, C.3
Aerssens, J.4
Marynen, P.5
-
13
-
-
0029100157
-
Alternative splicing and genomic structure of the AML1 gene involved in acute myeloid leukemia
-
Miyoshi, H., Ohira, M., Shimizu, K., Mitani, K., Hirai, H., Imai, T., Yokoyama, K., Soeda, E. and Ohki, M. Alternative splicing and genomic structure of the AML1 gene involved in acute myeloid leukemia. Nucleic Acids Res., 23, 2762-2769 (1995).
-
(1995)
Nucleic Acids Res.
, vol.23
, pp. 2762-2769
-
-
Miyoshi, H.1
Ohira, M.2
Shimizu, K.3
Mitani, K.4
Hirai, H.5
Imai, T.6
Yokoyama, K.7
Soeda, E.8
Ohki, M.9
-
14
-
-
0030984969
-
Minimal residual disease with TEL-AML1 fusion transcript in childhood acute lymphoblastic leukaemia with t(12:21)
-
Satake, N., Kobayashi, H., Tsunematsu, Y., Kawasaki, H., Horikoshi, Y., Koizumi, S. and Kaneko, Y. Minimal residual disease with TEL-AML1 fusion transcript in childhood acute lymphoblastic leukaemia with t(12:21). Br. J. Haematol., 97, 607-611 (1997).
-
(1997)
Br. J. Haematol.
, vol.97
, pp. 607-611
-
-
Satake, N.1
Kobayashi, H.2
Tsunematsu, Y.3
Kawasaki, H.4
Horikoshi, Y.5
Koizumi, S.6
Kaneko, Y.7
-
15
-
-
0030055379
-
The der(21)t(12;21) chromosome is always formed in a 12;21 translocation associated with childhood acute lymphoblastic leukaemia
-
Kobayashi, H., Satake, N., Maseki, N., Sakashita, A. and Kaneko, Y. The der(21)t(12;21) chromosome is always formed in a 12;21 translocation associated with childhood acute lymphoblastic leukaemia. Br. J. Haematol., 94, 105-111 (1996).
-
(1996)
Br. J. Haematol.
, vol.94
, pp. 105-111
-
-
Kobayashi, H.1
Satake, N.2
Maseki, N.3
Sakashita, A.4
Kaneko, Y.5
-
16
-
-
9544235164
-
Detection and quantification of TEL/AML1 fusion transcripts by polymerase chain reaction in childhood acute lymphoblastic leukemia
-
Nakao, M., Yokota, S., Horiike, S., Taniwaki, M., Kashima, K., Sonoda, Y., Koizumi, S., Takaue, Y., Matsushita, T., Fujimoto, T. and Misawa, S. Detection and quantification of TEL/AML1 fusion transcripts by polymerase chain reaction in childhood acute lymphoblastic leukemia. Leukemia, 10, 1463-1470 (1996).
-
(1996)
Leukemia
, vol.10
, pp. 1463-1470
-
-
Nakao, M.1
Yokota, S.2
Horiike, S.3
Taniwaki, M.4
Kashima, K.5
Sonoda, Y.6
Koizumi, S.7
Takaue, Y.8
Matsushita, T.9
Fujimoto, T.10
Misawa, S.11
-
17
-
-
84891583465
-
-
Wiley-Liss, Inc., New York
-
Heim, S. and Mitelman, F. "Cancer Cytogenetics," pp. 211-213 (1995). Wiley-Liss, Inc., New York.
-
(1995)
Cancer Cytogenetics
, pp. 211-213
-
-
Heim, S.1
Mitelman, F.2
-
18
-
-
0030056476
-
High incidence of TEL/AML1 fusion resulting from a cryptic t(12:21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan
-
Liang, D. C., Chou, T. B., Chen, J. S., Shurtleff, S. A., Rubnitz, J. E., Downing, J. R., Pui, C. H. and Shih, L. Y. High incidence of TEL/AML1 fusion resulting from a cryptic t(12:21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan. Leukemia, 10, 991-993 (1996).
-
(1996)
Leukemia
, vol.10
, pp. 991-993
-
-
Liang, D.C.1
Chou, T.B.2
Chen, J.S.3
Shurtleff, S.A.4
Rubnitz, J.E.5
Downing, J.R.6
Pui, C.H.7
Shih, L.Y.8
-
19
-
-
0029056756
-
Frequent loss of heterozygosity at the TEL gene locus in acute lymphoblastic leukemia of childhood
-
Stegmaier, K., Pendse, S., Barker, G. F., Bray-Ward, P., Ward, D. C., Montgomery, K. T., Krauter, K. S., Reynolds, C., Sklar, J., Donnelly, M., Bohlander, S. K., Rowley, J. D., Sallan, S. E., Gilliland, D. G. and Golub, T. R. Frequent loss of heterozygosity at the TEL gene locus in acute lymphoblastic leukemia of childhood. Blood, 86, 38-44 (1995).
-
(1995)
Blood
, vol.86
, pp. 38-44
-
-
Stegmaier, K.1
Pendse, S.2
Barker, G.F.3
Bray-Ward, P.4
Ward, D.C.5
Montgomery, K.T.6
Krauter, K.S.7
Reynolds, C.8
Sklar, J.9
Donnelly, M.10
Bohlander, S.K.11
Rowley, J.D.12
Sallan, S.E.13
Gilliland, D.G.14
Golub, T.R.15
-
20
-
-
0028875251
-
Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1
-
Cave, H., Gerard, B., Martin, E., Guidal, C., Devaux, I., Weissenbach, J., Elion, J., Vilmer, E. and Grandchamp, B. Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1. Blood, 86, 3869-3875 (1995).
-
(1995)
Blood
, vol.86
, pp. 3869-3875
-
-
Cave, H.1
Gerard, B.2
Martin, E.3
Guidal, C.4
Devaux, I.5
Weissenbach, J.6
Elion, J.7
Vilmer, E.8
Grandchamp, B.9
-
21
-
-
15844416307
-
Acute lymphoblastic leukemia of childhood: Identification of two distinct regions of deletion on the short arm of chromosome 12 in the region of TEL and KIP1
-
Takeuchi, S., Bartram, C. R., Miller, C. W., Reiter, A., Seriu, T., Zimmermann, M., Schrappe, M., Mori, N., Slater, J., Miyoshi, I. and Koeffler, H. P. Acute lymphoblastic leukemia of childhood: identification of two distinct regions of deletion on the short arm of chromosome 12 in the region of TEL and KIP1. Blood, 87, 3368-3374 (1996).
-
(1996)
Blood
, vol.87
, pp. 3368-3374
-
-
Takeuchi, S.1
Bartram, C.R.2
Miller, C.W.3
Reiter, A.4
Seriu, T.5
Zimmermann, M.6
Schrappe, M.7
Mori, N.8
Slater, J.9
Miyoshi, I.10
Koeffler, H.P.11
-
22
-
-
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., Guidal-Giroux, C., Guo, C., Vilmer, E., Marynen, P. and Grandchamp, B. The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia. Blood, 87, 2891-2899 (1996).
-
(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
Guidal-Giroux, C.7
Guo, C.8
Vilmer, E.9
Marynen, P.10
Grandchamp, B.11
-
23
-
-
0030070736
-
Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12:21)
-
Romana, S. P., Le Coniat, M., Poirel, H., Marynen, P., Bernard, O. A. and Berger, R. Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12:21). Leukemia, 10, 167-170 (1996).
-
(1996)
Leukemia
, vol.10
, pp. 167-170
-
-
Romana, S.P.1
Le Coniat, M.2
Poirel, H.3
Marynen, P.4
Bernard, O.A.5
Berger, R.6
|