-
1
-
-
0035750347
-
Chromosome translocations: Dangerous liaisons revisited
-
Rowley JD. Chromosome translocations: Dangerous liaisons revisited. Nat Rev Cancer 2001; 1: 245-250.
-
(2001)
Nat Rev Cancer
, vol.1
, pp. 245-250
-
-
Rowley, J.D.1
-
2
-
-
0029902171
-
Primary vs. secondary neoplasia-associated chromosomal abnormalities - Balanced rearrangements vs. genomic imbalances?
-
Johansson B, Mertens F, Mitelman F. Primary vs. secondary neoplasia-associated chromosomal abnormalities - balanced rearrangements vs. genomic imbalances? Genes Chromosomes Cancer 1996; 16: 155-163.
-
(1996)
Genes Chromosomes Cancer
, vol.16
, pp. 155-163
-
-
Johansson, B.1
Mertens, F.2
Mitelman, F.3
-
3
-
-
8544247921
-
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia
-
Johansson B, Mertens F, Mitelman F. Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia. Ann Med 2004; 36: 492-503.
-
(2004)
Ann Med
, vol.36
, pp. 492-503
-
-
Johansson, B.1
Mertens, F.2
Mitelman, F.3
-
4
-
-
1842474941
-
The FIP1L1-PDGFRα fusion tyrosine kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia: Implications for diagnosis, classification, and management
-
Gotlib J, Cools J, Malone III JM, Schrier SL, Gilliland DG, Coutré SE. The FIP1L1-PDGFRα fusion tyrosine kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia: Implications for diagnosis, classification, and management. Blood 2004; 103: 2879-2891.
-
(2004)
Blood
, vol.103
, pp. 2879-2891
-
-
Gotlib, J.1
Cools, J.2
Malone III, J.M.3
Schrier, S.L.4
Gilliland, D.G.5
Coutré, S.E.6
-
5
-
-
0025746321
-
t(8;21) breakpoints on chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene, AML1
-
Miyoshi H, Shimizu K, Kozu T, Maseki N, Kaneko Y, Ohki M. t(8;21) breakpoints on chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene, AML1. Proc Natl Acad Sci USA 1991; 88: 10431-10434.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 10431-10434
-
-
Miyoshi, H.1
Shimizu, K.2
Kozu, T.3
Maseki, N.4
Kaneko, Y.5
Ohki, M.6
-
6
-
-
0032830638
-
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
-
Song W-J, Sullivan MG, Legare RD, Hutchings S, Tan X, Kufrin D et al. Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. Nat Genet 1999; 23: 166-175.
-
(1999)
Nat Genet
, vol.23
, pp. 166-175
-
-
Song, W.-J.1
Sullivan, M.G.2
Legare, R.D.3
Hutchings, S.4
Tan, X.5
Kufrin, D.6
-
7
-
-
2942667930
-
Point mutations in the RUNX1/AML1 gene: Another actor in RUNX leukemia
-
Osato M. Point mutations in the RUNX1/AML1 gene: Another actor in RUNX leukemia. Oncogene 2004; 23: 4284-4296.
-
(2004)
Oncogene
, vol.23
, pp. 4284-4296
-
-
Osato, M.1
-
8
-
-
0242693950
-
Role of AML1/Runx1 in the pathogenesis of hematological malignancies
-
Kurokawa M, Hirai H. Role of AML1/Runx1 in the pathogenesis of hematological malignancies. Cancer Sci 2003; 94: 841-846.
-
(2003)
Cancer Sci
, vol.94
, pp. 841-846
-
-
Kurokawa, M.1
Hirai, H.2
-
9
-
-
0027373893
-
Fusion between transcription factor CBFβ/PEBP2β and a myosin heavy chain in acute myeloid leukemia
-
Liu P, Tarlé SA, Hajra A, Claxton DF, Marlton P, Freedman M et al. Fusion between transcription factor CBFβ/PEBP2β and a myosin heavy chain in acute myeloid leukemia. Science 1993; 261: 1041-1044.
-
(1993)
Science
, vol.261
, pp. 1041-1044
-
-
Liu, P.1
Tarlé, S.A.2
Hajra, A.3
Claxton, D.F.4
Marlton, P.5
Freedman, M.6
-
10
-
-
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
-
11
-
-
0347357871
-
A novel gene, FGA7, is fused to RUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T-cell acute lymphoblastic leukemia
-
Mikhail FM, Coignet L, Hatem N, Mourad ZI, Farawela HM, El Kaffash DM et al. A novel gene, FGA7, is fused to RUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T-cell acute lymphoblastic leukemia. Genes Chromosomes Cancer 2004; 39: 110-118.
-
(2004)
Genes Chromosomes Cancer
, vol.39
, pp. 110-118
-
-
Mikhail, F.M.1
Coignet, L.2
Hatem, N.3
Mourad, Z.I.4
Farawela, H.M.5
El Kaffash, D.M.6
-
12
-
-
0027218725
-
The t(8;21) translocation in acute myeloid leukemia results in production of an AML1-MTG8 fusion transcript
-
Miyoshi H, Kozu T, Shimizu K, Enomoto K, Maseki N, Kaneko Y et al. The t(8;21) translocation in acute myeloid leukemia results in production of an AML1-MTG8 fusion transcript. EMBO J 1993; 12: 2715-2721.
-
(1993)
EMBO J
, vol.12
, pp. 2715-2721
-
-
Miyoshi, H.1
Kozu, T.2
Shimizu, K.3
Enomoto, K.4
Maseki, N.5
Kaneko, Y.6
-
13
-
-
0028270494
-
Consistent intergenic splicing and production of multiple transcripts between AML1 at 21q22 and unrelated genes at 3q26 in (3;21)(q26;q22) translocations
-
Nucifora G, Begy CR, Kobayashi H, Roulston D, Claxton D, Pedersen-Bjergaard J et al. Consistent intergenic splicing and production of multiple transcripts between AML1 at 21q22 and unrelated genes at 3q26 in (3;21)(q26;q22) translocations. Proc Natl Acad Sci USA 1994; 91: 4004-4008.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 4004-4008
-
-
Nucifora, G.1
Begy, C.R.2
Kobayashi, H.3
Roulston, D.4
Claxton, D.5
Pedersen-Bjergaard, J.6
-
14
-
-
0032101547
-
The partner gene of AML1 in t(16;21) myeloid malignancies is a novel member of the MTG8 (ETO) family
-
Gamou T, Kitamura E, Hosoda F, Shimizu K, Shinohara K, Hayashi Y et al. The partner gene of AML1 in t(16;21) myeloid malignancies is a novel member of the MTG8 (ETO) family. Blood 1998; 91: 4028-4037.
-
(1998)
Blood
, vol.91
, pp. 4028-4037
-
-
Gamou, T.1
Kitamura, E.2
Hosoda, F.3
Shimizu, K.4
Shinohara, K.5
Hayashi, Y.6
-
15
-
-
3142741615
-
PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22)
-
Zhang Y, Emmanuel N, Kamboj G, Chen J, Shurafa M, Van Dyke DL et al. PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22). Genes Chromosomes Cancer 2004; 40: 365-370.
-
(2004)
Genes Chromosomes Cancer
, vol.40
, pp. 365-370
-
-
Zhang, Y.1
Emmanuel, N.2
Kamboj, G.3
Chen, J.4
Shurafa, M.5
Van Dyke, D.L.6
-
16
-
-
21144437550
-
AML1-FOG2 fusion protein in myelodysplasia
-
Chan EM, Comer EM, Brown FC, Richkind KE, Holmes ML, Chong BH et al. AML1-FOG2 fusion protein in myelodysplasia. Blood 2005; 105: 4523-4526.
-
(2005)
Blood
, vol.105
, pp. 4523-4526
-
-
Chan, E.M.1
Comer, E.M.2
Brown, F.C.3
Richkind, K.E.4
Holmes, M.L.5
Chong, B.H.6
-
17
-
-
0347356249
-
Cloning and enzymatic analysis of 22 novel human ubiquitin-specific proteases
-
Quesada V, Díaz-Perales A, Gutiérrez-Fernández A, Garabaya C, Cal S, López-Otín C. Cloning and enzymatic analysis of 22 novel human ubiquitin-specific proteases. Biochem Biophys Res Commun 2004; 314: 54-62.
-
(2004)
Biochem Biophys Res Commun
, vol.314
, pp. 54-62
-
-
Quesada, V.1
Díaz-Perales, A.2
Gutiérrez-Fernández, A.3
Garabaya, C.4
Cal, S.5
López-Otín, C.6
-
18
-
-
0038487005
-
Treatment stratification based on initial in vivo response in acute myeloid leukaemia in children without Down's syndrome: Results of NOPHO-AML trials
-
Lie SO, Abrahamsson J, Clausen N, Forestier E, Hasle H, Hovi L et al. Treatment stratification based on initial in vivo response in acute myeloid leukaemia in children without Down's syndrome: Results of NOPHO-AML trials. Br J Haematol 2003; 122: 217-225.
-
(2003)
Br J Haematol
, vol.122
, pp. 217-225
-
-
Lie, S.O.1
Abrahamsson, J.2
Clausen, N.3
Forestier, E.4
Hasle, H.5
Hovi, L.6
-
19
-
-
0032899273
-
New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling
-
Tanke HJ, Wiegant J, van Gijlswijk RPM, Bezrookove V, Pattenier H, Heetebrij RJ et al. New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling. Eur J Hum Genet 1999; 7: 2-11.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 2-11
-
-
Tanke, H.J.1
Wiegant, J.2
van Gijlswijk, R.P.M.3
Bezrookove, V.4
Pattenier, H.5
Heetebrij, R.J.6
-
20
-
-
5444224123
-
Human chromosome 7 circa 2004: A model for structural and functional studies of the human genome
-
Scherer SW, Green ED. Human chromosome 7 circa 2004: A model for structural and functional studies of the human genome. Hum Mol Genet 2004; 13: R303-R313.
-
(2004)
Hum Mol Genet
, vol.13
-
-
Scherer, S.W.1
Green, E.D.2
-
21
-
-
0034993604
-
t(7;12)(q36;p13) and t(7;12)(q32;p13) - Translocations involving ETV6 in children 18 months of age or younger with myeloid disorders
-
Slater RM, v Drunen E, Kroes WG, Weghuis DO, van den Berg E, Smit EM et al. t(7;12)(q36;p13) and t(7;12)(q32;p13) - translocations involving ETV6 in children 18 months of age or younger with myeloid disorders. Leukemia 2001; 15: 915-920.
-
(2001)
Leukemia
, vol.15
, pp. 915-920
-
-
Slater, R.M.1
v Drunen, E.2
Kroes, W.G.3
Weghuis, D.O.4
van den Berg, E.5
Smit, E.M.6
-
22
-
-
0035383839
-
Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis
-
Kolomietz E, Al-Maghrabi J, Brennan S, Karaskova J, Minkin S, Lipton J et al. Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis. Blood 2001; 97: 3581-3588.
-
(2001)
Blood
, vol.97
, pp. 3581-3588
-
-
Kolomietz, E.1
Al-Maghrabi, J.2
Brennan, S.3
Karaskova, J.4
Minkin, S.5
Lipton, J.6
-
23
-
-
0037162516
-
A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: Possible involvement in the genesis of the Philadelphia chromosome translocation
-
Saglio G, Storlazzi CT, Giugliano E, Surace C, Anelli L, Rege-Cambrin G et al. A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: Possible involvement in the genesis of the Philadelphia chromosome translocation. Proc Natl Acad Sci USA 2002; 99: 9882-9887.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 9882-9887
-
-
Saglio, G.1
Storlazzi, C.T.2
Giugliano, E.3
Surace, C.4
Anelli, L.5
Rege-Cambrin, G.6
-
24
-
-
12144286902
-
The isopeptidase USP2a regulates the stability of fatty acid synthase in prostate cancer
-
Graner E, Tang D, Rossi S, Baron A, Migita T, Weinstein LJ et al. The isopeptidase USP2a regulates the stability of fatty acid synthase in prostate cancer. Cancer Cell 2004; 5: 253-261.
-
(2004)
Cancer Cell
, vol.5
, pp. 253-261
-
-
Graner, E.1
Tang, D.2
Rossi, S.3
Baron, A.4
Migita, T.5
Weinstein, L.J.6
-
25
-
-
0032934989
-
A novel ubiquitin-specific protease, UBP43, cloned from leukemia fusion protein AML1-ETO-expressing mice, functions in hematopoietic cell differentiation
-
Liu L-Q, Ilaria R, Kingsley PD, Iwama A, van Etten RA, Palis J et al. A novel ubiquitin-specific protease, UBP43, cloned from leukemia fusion protein AML1-ETO-expressing mice, functions in hematopoietic cell differentiation. Mol Cell Biol 1999; 19: 3029-3038.
-
(1999)
Mol Cell Biol
, vol.19
, pp. 3029-3038
-
-
Liu, L.-Q.1
Ilaria, R.2
Kingsley, P.D.3
Iwama, A.4
van Etten, R.A.5
Palis, J.6
-
26
-
-
22544438745
-
A leukemia-enriched cDNA microarray platform identifies new transcripts with relevance to the biology of pediatric acute lymphoblastic leukemia
-
De Pittá C, Tombolan L, Campo Dell'Orto M, Accordi B, te Kronnie G, Romualdi C et al. A leukemia-enriched cDNA microarray platform identifies new transcripts with relevance to the biology of pediatric acute lymphoblastic leukemia. Haematologica 2005; 90: 890-898.
-
(2005)
Haematologica
, vol.90
, pp. 890-898
-
-
De Pittá, C.1
Tombolan, L.2
Campo Dell'Orto, M.3
Accordi, B.4
te Kronnie, G.5
Romualdi, C.6
-
27
-
-
19944423795
-
Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes
-
Oliveira AM, Perez-Atayde AR, Dal Cin P, Gebhardt MC, Chen C-J, Neff JR et al. Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes. Oncogene 2005; 24: 3419-3426.
-
(2005)
Oncogene
, vol.24
, pp. 3419-3426
-
-
Oliveira, A.M.1
Perez-Atayde, A.R.2
Dal Cin, P.3
Gebhardt, M.C.4
Chen, C.-J.5
Neff, J.R.6
-
28
-
-
0032532643
-
CBFA2(AML1) translocations with novel partner chromosomes in myeloid leukemias: Association with prior therapy
-
Roulston D, Espinosa III R, Nucifora G, Larson RA, Le Beau MM, Rowley JD. CBFA2(AML1) translocations with novel partner chromosomes in myeloid leukemias: Association with prior therapy. Blood 1998; 92: 2879-2885.
-
(1998)
Blood
, vol.92
, pp. 2879-2885
-
-
Roulston, D.1
Espinosa III, R.2
Nucifora, G.3
Larson, R.A.4
Le Beau, M.M.5
Rowley, J.D.6
-
29
-
-
0034667690
-
High incidence of biallelic point mutations in the Runt domain of the AML1/PEBPαB gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21
-
Preudhomme C, Warot-Loze D, Roumier C, Grardel-Duflos N, Garand R, Lai JL et al. High incidence of biallelic point mutations in the Runt domain of the AML1/PEBPαB gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21. Blood 2000; 96: 2862-2869.
-
(2000)
Blood
, vol.96
, pp. 2862-2869
-
-
Preudhomme, C.1
Warot-Loze, D.2
Roumier, C.3
Grardel-Duflos, N.4
Garand, R.5
Lai, J.L.6
-
30
-
-
0035865459
-
Dimerization with PEBP2β protects RUNX1/AML1 from ubiquitin-proteasome-mediated degradation
-
Huang G, Shigesada K, Ito K, Wee H-J, Yokomizo T, Ito Y. Dimerization with PEBP2β protects RUNX1/AML1 from ubiquitin-proteasome-mediated degradation. EMBO J 2001; 20: 723-733.
-
(2001)
EMBO J
, vol.20
, pp. 723-733
-
-
Huang, G.1
Shigesada, K.2
Ito, K.3
Wee, H.-J.4
Yokomizo, T.5
Ito, Y.6
-
31
-
-
12944262403
-
Identification of a gene at 11q23 encoding a guanine nucleotide exchange factor: Evidence for its fusion with MLL in acute myeloid leukemia
-
Kourlas PJ, Strout MP, Becknell B, Veronese ML, Croce CM, Theil KS et al. Identification of a gene at 11q23 encoding a guanine nucleotide exchange factor: Evidence for its fusion with MLL in acute myeloid leukemia. Proc Natl Acad Sci USA 2000; 97: 2145-2150.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 2145-2150
-
-
Kourlas, P.J.1
Strout, M.P.2
Becknell, B.3
Veronese, M.L.4
Croce, C.M.5
Theil, K.S.6
-
32
-
-
0037732866
-
Identification of CBL, a proto-oncogene at 11q23.3, as a novel MLL fusion partner in a patient with de novo acute myeloid leukemia
-
Fu J-F, Hsu J-J, Tang T-C, Shih L-Y. Identification of CBL, a proto-oncogene at 11q23.3, as a novel MLL fusion partner in a patient with de novo acute myeloid leukemia. Genes Chromosomes Cancer 2003; 37: 214-219.
-
(2003)
Genes Chromosomes Cancer
, vol.37
, pp. 214-219
-
-
Fu, J.-F.1
Hsu, J.-J.2
Tang, T.-C.3
Shih, L.-Y.4
-
33
-
-
0035883090
-
A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia
-
Jaju RJ, Fidler C, Haas OA, Strickson AJ, Watkins F, Clark K et al. A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia. Blood 2001; 98: 1264-1267.
-
(2001)
Blood
, vol.98
, pp. 1264-1267
-
-
Jaju, R.J.1
Fidler, C.2
Haas, O.A.3
Strickson, A.J.4
Watkins, F.5
Clark, K.6
-
34
-
-
16544369516
-
Use of gene-expression profiling to identify prognostic subclasses in adult acute myeloid leukemia
-
Bullinger L, Döhner K, Bair E, Fröhling S, Schlenk RF, Tibshirani R et al. Use of gene-expression profiling to identify prognostic subclasses in adult acute myeloid leukemia. N Engl J Med 2004; 350: 1605-1616.
-
(2004)
N Engl J Med
, vol.350
, pp. 1605-1616
-
-
Bullinger, L.1
Döhner, K.2
Bair, E.3
Fröhling, S.4
Schlenk, R.F.5
Tibshirani, R.6
|