-
1
-
-
17344366773
-
Establishment and characterization of a megakaryoblast cell line with amplification of MLL
-
Allen RJ, Smith SD, Moldwin RL, Lu M-M, Giordano L, Vignon C, Suto Y, Harden A, Tomek R, Veldman T, Ried T, Larson RA, Le Beau MM, Rowley JD, Zeleznik-Le N. 1998. Establishment and characterization of a megakaryoblast cell line with amplification of MLL. Leukemia 12:1119-1127.
-
(1998)
Leukemia
, vol.12
, pp. 1119-1127
-
-
Allen, R.J.1
Smith, S.D.2
Moldwin, R.L.3
Lu, M.-M.4
Giordano, L.5
Vignon, C.6
Suto, Y.7
Harden, A.8
Tomek, R.9
Veldman, T.10
Ried, T.11
Larson, R.A.12
Le Beau, M.M.13
Rowley, J.D.14
Zeleznik-Le, N.15
-
2
-
-
0035057424
-
Duplication of amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents
-
Andersen MK, Christiansen DH, Kirchhoff M, Pedersen-Bjergaard J. 2001. Duplication of amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents. Genes Chromosomes Cancer 31:33-41.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 33-41
-
-
Andersen, M.K.1
Christiansen, D.H.2
Kirchhoff, M.3
Pedersen-Bjergaard, J.4
-
3
-
-
0027519370
-
Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: Retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome
-
Boultwood J, Fidler C, Lewis S, MacCarthy A, Sheridan H, Kelly S, Oscier D, Buckle VJ, Wainscoat JS. 1993. Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome. Blood 82:2611-2616.
-
(1993)
Blood
, vol.82
, pp. 2611-2616
-
-
Boultwood, J.1
Fidler, C.2
Lewis, S.3
MacCarthy, A.4
Sheridan, H.5
Kelly, S.6
Oscier, D.7
Buckle, V.J.8
Wainscoat, J.S.9
-
4
-
-
0033978155
-
Identification and molecular characterization of CALM/AF10 fusion products in T cell acute lymphoblastic leukemia and acute myeloid leukemia
-
Carlson KM, Vignon C, Bohlander S, Martinez-Climent JA, Le Beau MM, Rowley JD. 2000. Identification and molecular characterization of CALM/AF10 fusion products in T cell acute lymphoblastic leukemia and acute myeloid leukemia. Leukemia 14:100-104.
-
(2000)
Leukemia
, vol.14
, pp. 100-104
-
-
Carlson, K.M.1
Vignon, C.2
Bohlander, S.3
Martinez-Climent, J.A.4
Le Beau, M.M.5
Rowley, J.D.6
-
5
-
-
0034654412
-
Deletions of chromosome 5q13.3 and 17p loci cooperate in myeloid neoplasms
-
Castro PD, Liang JC, Nagarajan L. 2000. Deletions of chromosome 5q13.3 and 17p loci cooperate in myeloid neoplasms. Blood 95:2138-2143.
-
(2000)
Blood
, vol.95
, pp. 2138-2143
-
-
Castro, P.D.1
Liang, J.C.2
Nagarajan, L.3
-
6
-
-
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, Roberts IAG, Goldman JM, Cross NCP. 1999. Fusion of ETV6 to the caudal-related homeobox gene CDX2 in acute myeloid leukemia with the t(12;13)(p13;q12). Blood 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
Roberts, I.A.G.7
Goldman, J.M.8
Cross, N.C.P.9
-
7
-
-
0035281739
-
Mutations with loss of heterozygosity of p53 are common in therapyrelated myelodysplasia and acute myeloid leukemia after exposure to alkylating agents and significantly associated with deletion or loss of 5q, a complex karyotype, and a poor prognosis
-
Christiansen DH, Andersen MK, Pedersen-Bjergaard J. 2001. Mutations with loss of heterozygosity of p53 are common in therapyrelated myelodysplasia and acute myeloid leukemia after exposure to alkylating agents and significantly associated with deletion or loss of 5q, a complex karyotype, and a poor prognosis. J Clin Oncol 19:1405-1413.
-
(2001)
J Clin Oncol
, vol.19
, pp. 1405-1413
-
-
Christiansen, D.H.1
Andersen, M.K.2
Pedersen-Bjergaard, J.3
-
8
-
-
0033025604
-
Myeloid- and lymphoid-specific breakpoint cluster regions in chromosome band 13q14 in acute leukemia
-
Coignet LJA, Lima CSP, Min T, Streubel B, Swansbury J, Telford N, Swanton S, Bowen A, Nagai M, Catovsky D, Fonatsch C, Dyer MJS. 1999. Myeloid- and lymphoid-specific breakpoint cluster regions in chromosome band 13q14 in acute leukemia. Genes Chromosomes Cancer 25:222-229.
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 222-229
-
-
Coignet, L.J.A.1
Lima, C.S.P.2
Min, T.3
Streubel, B.4
Swansbury, J.5
Telford, N.6
Swanton, S.7
Bowen, A.8
Nagai, M.9
Catovsky, D.10
Fonatsch, C.11
Dyer, M.J.S.12
-
9
-
-
0027537408
-
Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization
-
du Manoir S, Speicher MR, Joos S, Schröck E, Popp S, Döhner H, Kovacs G, Robert-Nicoud M, Lichter P, Cremer T. 1993. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Hum Genet 90:590-610.
-
(1993)
Hum Genet
, vol.90
, pp. 590-610
-
-
Du Manoir, S.1
Speicher, M.R.2
Joos, S.3
Schröck, E.4
Popp, S.5
Döhner, H.6
Kovacs, G.7
Robert-Nicoud, M.8
Lichter, P.9
Cremer, T.10
-
10
-
-
0027219166
-
Common region of ALL-1 gene disrupted in epipodophyllotoxin-related secondary acute myeloid leukemia
-
Felix CA, Winick NJ, Negrini M, Bowman WP, Croce CM, Lange BJ. 1993. Common region of ALL-1 gene disrupted in epipodophyllotoxin-related secondary acute myeloid leukemia. Cancer Res 53:2954-2956.
-
(1993)
Cancer Res
, vol.53
, pp. 2954-2956
-
-
Felix, C.A.1
Winick, N.J.2
Negrini, M.3
Bowman, W.P.4
Croce, C.M.5
Lange, B.J.6
-
11
-
-
0031838720
-
Association of germline p53 mutation with MLL segmental jumping translocation in treatment-related leukemia
-
Felix CA, Megonigal MD, Chervinsky DS, Leonard DGB, Tsuchida N, Kakati S, Block AMW, Fisher J, Grossi M, Salhany KI, Jani-Sait N, Aplan PD. 1998. Association of germline p53 mutation with MLL segmental jumping translocation in treatment-related leukemia. Blood 91:4451-4456.
-
(1998)
Blood
, vol.91
, pp. 4451-4456
-
-
Felix, C.A.1
Megonigal, M.D.2
Chervinsky, D.S.3
Leonard, D.G.B.4
Tsuchida, N.5
Kakati, S.6
Block, A.M.W.7
Fisher, J.8
Grossi, M.9
Salhany, K.I.10
Jani-Sait, N.11
Aplan, P.D.12
-
12
-
-
0032733441
-
Lack of IRF-1 expression in acute promyelocytic leukemia and in a subset of acute myeloid leukemias with del(5)(q31)
-
Green WB, Slovak ML, Chen I-M, Pallavicini M, Hecht JL, Willman CL. 1999. Lack of IRF-1 expression in acute promyelocytic leukemia and in a subset of acute myeloid leukemias with del(5)(q31). Leukemia 13:1960-1971.
-
(1999)
Leukemia
, vol.13
, pp. 1960-1971
-
-
Green, W.B.1
Slovak, M.L.2
Chen, I.-M.3
Pallavicini, M.4
Hecht, J.L.5
Willman, C.L.6
-
13
-
-
0026321198
-
t(10;11)(p13-14;q14-21): A recurrent translocation in T-cell acute lymphoblastic leukemia
-
Groupe Français de Cytogénétique Hématologique (GFCH). 1991. t(10;11)(p13-14;q14-21): a recurrent translocation in T-cell acute lymphoblastic leukemia. Genes Chromosomes Cancer 3:411-415.
-
(1991)
Genes Chromosomes Cancer
, vol.3
, pp. 411-415
-
-
-
14
-
-
0031830862
-
Outcome of secondary myeloid malignancy in Hodgkin's disease: The BNLI experience
-
Harrison CN, Vaughan Hudson G, Devereux S, Linch DC. 1998. Outcome of secondary myeloid malignancy in Hodgkin's disease: the BNLI experience. Eur J Haematol 61:109-112.
-
(1998)
Eur J Haematol
, vol.61
, pp. 109-112
-
-
Harrison, C.N.1
Vaughan Hudson, G.2
Devereux, S.3
Linch, D.C.4
-
16
-
-
0024786988
-
Cytogenetic and clinical investigations in 76 cases with therapy-related leukemia and myelodysplastic syndrome
-
Iurlo A, Mecucci C, Van Orshoven A, Michaux J-L, Boogaerts M, Noens L, Bosly A, Louwagie A, Van Den Berghe H. 1989. Cytogenetic and clinical investigations in 76 cases with therapy-related leukemia and myelodysplastic syndrome. Cancer Genet Cytogenet 43:227-241.
-
(1989)
Cancer Genet Cytogenet
, vol.43
, pp. 227-241
-
-
Iurlo, A.1
Mecucci, C.2
Van Orshoven, A.3
Michaux, J.-L.4
Boogaerts, M.5
Noens, L.6
Bosly, A.7
Louwagie, A.8
Van Den Berghe, H.9
-
17
-
-
0025818349
-
Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL)
-
Johansson B, Mertens F, Heim S, Kristoffersson U, Mitelman F. 1991. Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL). Eur J Haematol 47:17-27.
-
(1991)
Eur J Haematol
, vol.47
, pp. 17-27
-
-
Johansson, B.1
Mertens, F.2
Heim, S.3
Kristoffersson, U.4
Mitelman, F.5
-
18
-
-
0027378164
-
Cytogenetic deletion maps of hematological neoplasms: Circumstantial evidence for tumor suppressor loci
-
Johansson B, Mertens F, Mitelman F. 1993. Cytogenetic deletion maps of hematological neoplasms: circumstantial evidence for tumor suppressor loci. Genes Chromosomes Cancer 8:205-218.
-
(1993)
Genes Chromosomes Cancer
, vol.8
, pp. 205-218
-
-
Johansson, B.1
Mertens, F.2
Mitelman, F.3
-
20
-
-
0022617302
-
Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: Further evidence for characteristic abnormalities of chromosomes no. 5 and 7
-
Le Beau MM, Albain KS, Larson RA, Vardiman JW, Davis EM, Blough RR, Golomb HM, Rowley JD. 1986. Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7. J Clin Oncol 4:325-345.
-
(1986)
J Clin Oncol
, vol.4
, pp. 325-345
-
-
Le Beau, M.M.1
Albain, K.S.2
Larson, R.A.3
Vardiman, J.W.4
Davis, E.M.5
Blough, R.R.6
Golomb, H.M.7
Rowley, J.D.8
-
21
-
-
0027315865
-
Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases
-
Le Beau MM, Espinosa R III, Neuman WL, Stock W, Roulston D, Larson RA, Keinanen M, Westbrook CA. 1993. Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases. Proc Natl Acad Sci USA 90:5484-5488.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 5484-5488
-
-
Le Beau, M.M.1
Espinosa R. III2
Neuman, W.L.3
Stock, W.4
Roulston, D.5
Larson, R.A.6
Keinanen, M.7
Westbrook, C.A.8
-
22
-
-
0026584519
-
Leukemias and myelodysplastic syndromes secondary to drug, radiation, and environmental exposure
-
Levine EG, Bloomfield CD. 1992. Leukemias and myelodysplastic syndromes secondary to drug, radiation, and environmental exposure. Semin Oncol 19:47-84.
-
(1992)
Semin Oncol
, vol.19
, pp. 47-84
-
-
Levine, E.G.1
Bloomfield, C.D.2
-
23
-
-
0030777778
-
Spectral karyotyping, a 24-colour FISH technique for the identification of chromosomal rearrangements
-
Macville M, Veldman T, Padilla-Nash H, Wangsa D, O'Brien P, Schröck E, Ried T. 1997. Spectral karyotyping, a 24-colour FISH technique for the identification of chromosomal rearrangements. Histochem Cell Biol 108:299-305.
-
(1997)
Histochem Cell Biol
, vol.108
, pp. 299-305
-
-
Macville, M.1
Veldman, T.2
Padilla-Nash, H.3
Wangsa, D.4
O'Brien, P.5
Schröck, E.6
Ried, T.7
-
24
-
-
0033002273
-
Therapy-related myelodysplastic syndrome and acute myeloid leukemia with 17p deletion. A report on 25 cases
-
Merlar A, Lai JL, Sterkers Y, Demory JL, Bauters F, Preudhomme C, Fenaux P. 1999. Therapy-related myelodysplastic syndrome and acute myeloid leukemia with 17p deletion. A report on 25 cases. Leukemia 13:250-257.
-
(1999)
Leukemia
, vol.13
, pp. 250-257
-
-
Merlar, A.1
Lai, J.L.2
Sterkers, Y.3
Demory, J.L.4
Bauters, F.5
Preudhomme, C.6
Fenaux, P.7
-
25
-
-
8544258049
-
Alterations of p53 and Rb genes in a novel human GMCSF-dependent myeloid cell line (OHN-GM) established from therapy-related leukaemia
-
Nagai M, Fujita M, Ikeda T, Ohmori M, Kuwabara H, Yamaoka G, Tanaka K, Kamada N, Taniwaki M, Inoue T, Irino S, Takahara J. 1997. Alterations of p53 and Rb genes in a novel human GMCSF-dependent myeloid cell line (OHN-GM) established from therapy-related leukaemia. Br J Haematol 98:392-398.
-
(1997)
Br J Haematol
, vol.98
, pp. 392-398
-
-
Nagai, M.1
Fujita, M.2
Ikeda, T.3
Ohmori, M.4
Kuwabara, H.5
Yamaoka, G.6
Tanaka, K.7
Kamada, N.8
Taniwaki, M.9
Inoue, T.10
Irino, S.11
Takahara, J.12
-
26
-
-
0029704680
-
Deletion of chromosome 5 (5q-) in leukemia: Current knowledge
-
Freireich EG, Kantarjian H, editors. Boston: Kluwer Academic
-
Nagarajan L. 1996. Deletion of chromosome 5 (5q-) in leukemia: current knowledge. In: Freireich EG, Kantarjian H, editors. Molecular genetics and therapy of leukemia. Boston: Kluwer Academic. p 19-29.
-
(1996)
Molecular Genetics and Therapy of Leukemia
, pp. 19-29
-
-
Nagarajan, L.1
-
27
-
-
0023607867
-
The 5q- abnormality
-
Nimer SD, Golde DW. 1987. The 5q- abnormality. Blood 70:1705-1712.
-
(1987)
Blood
, vol.70
, pp. 1705-1712
-
-
Nimer, S.D.1
Golde, D.W.2
-
28
-
-
0027714648
-
Rearrangements involving chromosome band 11q23 in acute leukaemia
-
Rowley JD. 1993. Rearrangements involving chromosome band 11q23 in acute leukaemia. Cancer Biol 4:377-385.
-
(1993)
Cancer Biol
, vol.4
, pp. 377-385
-
-
Rowley, J.D.1
-
29
-
-
0036022067
-
Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: A detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH
-
Schoch C, Haferlach T, Bursch S, Gerstner D, Schnittger S, Dugas M, Kern W, Löffler H, Hiddemann W. 2002. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH. Genes Chromosomes Cancer 35:20-29.
-
(2002)
Genes Chromosomes Cancer
, vol.35
, pp. 20-29
-
-
Schoch, C.1
Haferlach, T.2
Bursch, S.3
Gerstner, D.4
Schnittger, S.5
Dugas, M.6
Kern, W.7
Löffler, H.8
Hiddemann, W.9
-
30
-
-
0038214755
-
Multicolor spectral karyotyping of human chromosomes
-
Schröck E, du Manoir S, Veldman T, Schoell B, Wienberg J, Ferguson-Smith MA, Ning Y, Ledbetter DH, Bar-Am I, Soenksen D, Garini Y, Ried T. 1996. Multicolor spectral karyotyping of human chromosomes. Science 273:494-497.
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schröck, E.1
Du Manoir, S.2
Veldman, T.3
Schoell, B.4
Wienberg, J.5
Ferguson-Smith, M.A.6
Ning, Y.7
Ledbetter, D.H.8
Bar-Am, I.9
Soenksen, D.10
Garini, Y.11
Ried, T.12
-
31
-
-
0034049468
-
Amplification of the MLL gene on double minutes, a homogeneously staining region, and ring chromosomes in five patients with acute myeloid leukemia or myelodysplastic syndrome
-
Struebel B, Valent P, Jäger U, Edelhäuser M, Wandt H, Wagner T, Büchner T, Lechner K, Fonatsch C. 2000. Amplification of the MLL gene on double minutes, a homogeneously staining region, and ring chromosomes in five patients with acute myeloid leukemia or myelodysplastic syndrome. Genes Chromosomes Cancer 27:380-386.
-
(2000)
Genes Chromosomes Cancer
, vol.27
, pp. 380-386
-
-
Struebel, B.1
Valent, P.2
Jäger, U.3
Edelhäuser, M.4
Wandt, H.5
Wagner, T.6
Büchner, T.7
Lechner, K.8
Fonatsch, C.9
-
32
-
-
0027132061
-
Rearrangements of the MLL gene in therapy-related acute myeloid leukemia in patients previously treated with agents targeting DNA-topoisomerase II
-
Super HJG, McCabe NR, Thirman MJ, Larson RA, Le Beau MM, Pedersen-Bjergaard J, Philip P, Diaz MO, Rowley JD. 1993. Rearrangements of the MLL gene in therapy-related acute myeloid leukemia in patients previously treated with agents targeting DNA-topoisomerase II. Blood 82:3705-3711.
-
(1993)
Blood
, vol.82
, pp. 3705-3711
-
-
Super, H.J.G.1
McCabe, N.R.2
Thirman, M.J.3
Larson, R.A.4
Le Beau, M.M.5
Pedersen-Bjergaard, J.6
Philip, P.7
Diaz, M.O.8
Rowley, J.D.9
-
33
-
-
0027465728
-
Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia
-
Willman CL, Sever CE, Pallavicini MG, Harada H, Tanaka N, Slovak ML, Yamamoto H, Harada K, Meeker TC, List AF, Taniguchi T. 1993. Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia. Science 259:968-971.
-
(1993)
Science
, vol.259
, pp. 968-971
-
-
Willman, C.L.1
Sever, C.E.2
Pallavicini, M.G.3
Harada, H.4
Tanaka, N.5
Slovak, M.L.6
Yamamoto, H.7
Harada, K.8
Meeker, T.C.9
List, A.F.10
Taniguchi, T.11
|