-
1
-
-
18344418672
-
Functional and phenotypic characterization of cord blood and bone marrow subsets expressing FLT3 (CD135) receptor tyrosine kinase
-
Rappold I, Ziegler BL, Kohler I, et al. Functional and phenotypic characterization of cord blood and bone marrow subsets expressing FLT3 (CD135) receptor tyrosine kinase. Blood. 1997;90:111-125.
-
(1997)
Blood
, vol.90
, pp. 111-125
-
-
Rappold, I.1
Ziegler, B.L.2
Kohler, I.3
-
2
-
-
0036720398
-
The roles of FLT3 in hematopoiesis and leukemia
-
Gilliland DG, Griffin JD. The roles of FLT3 in hematopoiesis and leukemia. Blood. 2002;100: 1532-1542.
-
(2002)
Blood
, vol.100
, pp. 1532-1542
-
-
Gilliland, D.G.1
Griffin, J.D.2
-
3
-
-
0001097136
-
Tandem duplication of the FLT3 gene is found in acute lymphoblastic leukaemia as well as acute myeloid leukaemia but not in myelodysplastic syndrome or juvenile chronic myelogenous leukaemia in children
-
Xu F, Taki T, Yang HW, et al. Tandem duplication of the FLT3 gene is found in acute lymphoblastic leukaemia as well as acute myeloid leukaemia but not in myelodysplastic syndrome or juvenile chronic myelogenous leukaemia in children. Br J Haematol. 1999;105:155-162.
-
(1999)
Br J Haematol
, vol.105
, pp. 155-162
-
-
Xu, F.1
Taki, T.2
Yang, H.W.3
-
4
-
-
0036850573
-
Alterations of the FLT3 gene in acute promyelocytic leukemia: Association with diagnostic characteristics and analysis of clinical outcome in patients treated with the Italian AIDA protocol
-
Noguera NI, Breccia M, Divona M, et al. Alterations of the FLT3 gene in acute promyelocytic leukemia: association with diagnostic characteristics and analysis of clinical outcome in patients treated with the Italian AIDA protocol. Leukemia. 2002;16:2185-2189.
-
(2002)
Leukemia
, vol.16
, pp. 2185-2189
-
-
Noguera, N.I.1
Breccia, M.2
Divona, M.3
-
5
-
-
0037097716
-
Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: Association with FAB subtypes and identification of subgroups with poor prognosis
-
Thiede C, Steudel C, Mohr B, et al. Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: association with FAB subtypes and identification of subgroups with poor prognosis. Blood. 2002;99:4326-4335.
-
(2002)
Blood
, vol.99
, pp. 4326-4335
-
-
Thiede, C.1
Steudel, C.2
Mohr, B.3
-
6
-
-
0035871889
-
Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies
-
Yamamoto Y, Kiyoi H, Nakano Y, et al. Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies. Blood. 2001;97:2434-2439.
-
(2001)
Blood
, vol.97
, pp. 2434-2439
-
-
Yamamoto, Y.1
Kiyoi, H.2
Nakano, Y.3
-
7
-
-
0041572472
-
Flt3D835/1836 point mutations in acute myeloid leukemia: Correlaiion to cytogenetics, cytomorphology, and prognosis in 1229 patients
-
Schnittger S, Boell I, Schoch C, et al. Flt3D835/ 1836 point mutations in acute myeloid leukemia: correlaiion to cytogenetics, cytomorphology, and prognosis in 1229 patients [abstract]. Blood. 2002;100:329a.
-
(2002)
Blood
, vol.100
-
-
Schnittger, S.1
Boell, I.2
Schoch, C.3
-
8
-
-
0035204051
-
Internal tandem duplications of the FLT3 and MLL genes are mainly observed in aiypical cases of therapy-related acute myeloid leukemia with a normal karyotype and are unrelated to type of previous therapy
-
Christiansen DH, Pedersen-Bjergaard J. Internal tandem duplications of the FLT3 and MLL genes are mainly observed in aiypical cases of therapy-related acute myeloid leukemia with a normal karyotype and are unrelated to type of previous therapy. Leukemia. 2001;15:1848-1851.
-
(2001)
Leukemia
, vol.15
, pp. 1848-1851
-
-
Christiansen, D.H.1
Pedersen-Bjergaard, J.2
-
9
-
-
0036785393
-
Studies of FLT3 mutations in paired presentation and relapse samples from patients with acute myeloid leukemia: Implications for the role of FLT3 mutations in leukemogenesis, minimal residual disease detection, and possible therapy with FLT3 inhibitors
-
Kottaridis PD, Gale RE, Langabeer SE, Frew ME, Bowen DT, Linch DC. Studies of FLT3 mutations in paired presentation and relapse samples from patients with acute myeloid leukemia: implications for the role of FLT3 mutations in leukemogenesis, minimal residual disease detection, and possible therapy with FLT3 inhibitors. Blood: 2002;100:2393-2398.
-
(2002)
Blood
, vol.100
, pp. 2393-2398
-
-
Kottaridis, P.D.1
Gale, R.E.2
Langabeer, S.E.3
Frew, M.E.4
Bowen, D.T.5
Linch, D.C.6
-
10
-
-
0034235115
-
Biological and therapeutic aspects of infant leukemia
-
Biondi A, Cimino G, Pieters R, Pui CH. Biological and therapeutic aspects of infant leukemia. Blood. 2000;96:24-33.
-
(2000)
Blood
, vol.96
, pp. 24-33
-
-
Biondi, A.1
Cimino, G.2
Pieters, R.3
Pui, C.H.4
-
11
-
-
13344284642
-
Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5
-
Poirel H, Rack K, Delabesse E, et al. Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5. Blood. 1996;87:2496-2505.
-
(1996)
Blood
, vol.87
, pp. 2496-2505
-
-
Poirel, H.1
Rack, K.2
Delabesse, E.3
-
12
-
-
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
-
13
-
-
0036169298
-
Clinical and biological implications of partial tandem duplication of the MLL gene in acute myeloid leukemia without chromosomal abnormalities at 11q23
-
Shiah HS, Kuo YY, Tang JL, et al. Clinical and biological implications of partial tandem duplication of the MLL gene in acute myeloid leukemia without chromosomal abnormalities at 11q23. Leukemia. 2002;16:196-202.
-
(2002)
Leukemia
, vol.16
, pp. 196-202
-
-
Shiah, H.S.1
Kuo, Y.Y.2
Tang, J.L.3
-
14
-
-
13344249756
-
Partial tandem duplication of ALL1 as a recurrent molecular defect in acute myeloid leukemia with trisomy 11
-
Caligiuri MA, Strout MP, Schichman SA, et al. Partial tandem duplication of ALL1 as a recurrent molecular defect in acute myeloid leukemia with trisomy 11. Cancer Res. 1996;56:1418-1425.
-
(1996)
Cancer Res
, vol.56
, pp. 1418-1425
-
-
Caligiuri, M.A.1
Strout, M.P.2
Schichman, S.A.3
-
15
-
-
0032170594
-
Partial tandem duplications of the MLL gene are detectable in peripheral blood and bone marrow of nearly all healthy donors
-
Schnittger S, Wormann B, Hiddemann W, Griesinger F. Partial tandem duplications of the MLL gene are detectable in peripheral blood and bone marrow of nearly all healthy donors. Blood. 1998;92:1728-1734.
-
(1998)
Blood
, vol.92
, pp. 1728-1734
-
-
Schnittger, S.1
Wormann, B.2
Hiddemann, W.3
Griesinger, F.4
-
16
-
-
0030012114
-
Site-specific DNA cleavage within the MLL breakpoint cluster region induced by topoisomerase II inhibitors
-
Aplan PD, Chervinsky DS, Stanulla M, Burhans WC. Site-specific DNA cleavage within the MLL breakpoint cluster region induced by topoisomerase II inhibitors. Blood. 1996;87:2649-2658.
-
(1996)
Blood
, vol.87
, pp. 2649-2658
-
-
Aplan, P.D.1
Chervinsky, D.S.2
Stanulla, M.3
Burhans, W.C.4
-
17
-
-
0030941555
-
MLL cleavage occurs in approximately 5% of de novo acute myeloid leukemia, including patients analyzed before treatment induction
-
Macintyre E, Bourquelot P, Leboeuf D, et al. MLL cleavage occurs in approximately 5% of de novo acute myeloid leukemia, including patients analyzed before treatment induction. Blood. 1997;89: 2224-2226.
-
(1997)
Blood
, vol.89
, pp. 2224-2226
-
-
Macintyre, E.1
Bourquelot, P.2
Leboeuf, D.3
-
18
-
-
0034712748
-
Dietary bioflavonoids induce cleavage in the MLL gene and may contribute to infant leukemia
-
Strick R, Strissel PL, Borgers S, Smith SL, Rowley JD. Dietary bioflavonoids induce cleavage in the MLL gene and may contribute to infant leukemia. Proc Natl Acad Sci U S A. 2000;97:4790-4795.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 4790-4795
-
-
Strick, R.1
Strissel, P.L.2
Borgers, S.3
Smith, S.L.4
Rowley, J.D.5
-
19
-
-
20244365471
-
Detection of the chromosome 16 CBF beta-MYH11 fusion transcript in myelomonocytic leukemias
-
Poirel H, Radford-Weiss I, Rack K, et al. Detection of the chromosome 16 CBF beta-MYH11 fusion transcript in myelomonocytic leukemias. Blood. 1995;85:1313-1322.
-
(1995)
Blood
, vol.85
, pp. 1313-1322
-
-
Poirel, H.1
Radford-Weiss, I.2
Rack, K.3
-
20
-
-
9244255318
-
Molecular detection of t(8;21)/AML1-ETO in AML M1/M2: Correlation with cytogenetics, morphology and immunophenotype
-
Andrieu V, Radford-Weiss I, Troussard X, et al. Molecular detection of t(8;21)/AML1-ETO in AML M1/M2: correlation with cytogenetics, morphology and immunophenotype. Br J Haematol. 1996;92: 855-865.
-
(1996)
Br J Haematol
, vol.92
, pp. 855-865
-
-
Andrieu, V.1
Radford-Weiss, I.2
Troussard, X.3
-
21
-
-
0034665892
-
The incidence of clonal T-cell receptor rearrangements in B-cell precursor acute lymphobrastic leukemia varies with age and genotype
-
Brumpt C, Delabesse E, Beldjord K, et al. The incidence of clonal T-cell receptor rearrangements in B-cell precursor acute lymphobrastic leukemia varies with age and genotype. Blood. 2000;96:2254-2261.
-
(2000)
Blood
, vol.96
, pp. 2254-2261
-
-
Brumpt, C.1
Delabesse, E.2
Beldjord, K.3
-
22
-
-
0033758958
-
FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group
-
Abu-Duhier FM, Goodeve AC, Wilson GA, et al. FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group. Br J Haematol. 2000;111:190-195.
-
(2000)
Br J Haematol
, vol.111
, pp. 190-195
-
-
Abu-Duhier, F.M.1
Goodeve, A.C.2
Wilson, G.A.3
-
23
-
-
0034936404
-
Identification of novel FLT-3 Asp835 mutations in adult acute myeloid leukaemia
-
Abu-Duhier FM, Goodeve AC, Wilson GA, Care RS, Peake IR, Reilly JT. Identification of novel FLT-3 Asp835 mutations in adult acute myeloid leukaemia. Br J Haematol. 2001;113:983-988.
-
(2001)
Br J Haematol
, vol.113
, pp. 983-988
-
-
Abu-Duhier, F.M.1
Goodeve, A.C.2
Wilson, G.A.3
Care, R.S.4
Peake, I.R.5
Reilly, J.T.6
-
24
-
-
85044551987
-
Evaluation of candidate control genes for diagnosis and residual disease detection in leukemic patients using "real-time" quantitative reverse-transcriptase polymerase chain reaction (RQPCR): A Europe Against Cancer Program
-
In press
-
Beillard E, Pallisgaard N, van der Velden VHJ, et al. Evaluation of candidate control genes for diagnosis and residual disease detection in leukemic patients using "real-time" quantitative reverse-transcriptase polymerase chain reaction (RQPCR): a Europe Against Cancer Program. Leukemia. In press.
-
Leukemia
-
-
Beillard, E.1
Pallisgaard, N.2
Van der Velden, V.H.J.3
-
25
-
-
0036659931
-
Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: Correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease
-
Schnittger S, Schoch C, Dugas M, et al. Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease. Blood. 2002;100:59-66.
-
(2002)
Blood
, vol.100
, pp. 59-66
-
-
Schnittger, S.1
Schoch, C.2
Dugas, M.3
-
26
-
-
85044554931
-
Acute myeloblastic leukemia (AML) with inv(16)(p13;q22) and the rare I type CBFbeta-MYH11 transcript: Report of two new cases
-
Grardel N, Roumier C, Soenen V, et al. Acute myeloblastic leukemia (AML) with inv(16)(p13;q22) and the rare I type CBFbeta-MYH11 transcript: report of two new cases. Leukemia. 2002;16:150-151.
-
(2002)
Leukemia
, vol.16
, pp. 150-151
-
-
Grardel, N.1
Roumier, C.2
Soenen, V.3
-
27
-
-
0031859607
-
Inversion of chromosome 16 and uncommon rearrangements of the CBFB and MYH 11 genes in therapy-related acute myeloid leukemia: Rare events related to DNA-topoisomerase II inhibitors?
-
Dissing M, Le Beau MM, Pedersen-Bjergaard J. Inversion of chromosome 16 and uncommon rearrangements of the CBFB and MYH 11 genes in therapy-related acute myeloid leukemia: rare events related to DNA-topoisomerase II inhibitors? J Clin Oncol. 1998;16:1890-1896.
-
(1998)
J Clin Oncol
, vol.16
, pp. 1890-1896
-
-
Dissing, M.1
Le Beau, M.M.2
Pedersen-Bjergaard, J.3
-
28
-
-
0028952036
-
Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia
-
Liu PP, Hajra A, Wijmenga C, Collins FS. Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia. Blood. 1995;85:2289-2302.
-
(1995)
Blood
, vol.85
, pp. 2289-2302
-
-
Liu, P.P.1
Hajra, A.2
Wijmenga, C.3
Collins, F.S.4
-
29
-
-
0013312329
-
Inhibition of FLT3 in MLL: Validation of a therapeutic target identified by gene expression based classification
-
Armstrong SA, Kung AL, Mabon ME, et al. Inhibition of FLT3 in MLL: validation of a therapeutic target identified by gene expression based classification. Cancer Cell. 2003;3:173-183.
-
(2003)
Cancer Cell
, vol.3
, pp. 173-183
-
-
Armstrong, S.A.1
Kung, A.L.2
Mabon, M.E.3
-
30
-
-
18544375333
-
MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia
-
Armstrong SA, Staunton JE, Silverman LB, et al. MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia. Nat Genet. 2002;30:41-47.
-
(2002)
Nat Genet
, vol.30
, pp. 41-47
-
-
Armstrong, S.A.1
Staunton, J.E.2
Silverman, L.B.3
-
31
-
-
4243988958
-
FIt3 mutations in the activating loop of tyrosine kinase domain are frequently found in infant ALL with MLL gene rearrangement
-
Taketani T, Taki T, Ishii E, et al. FIt3 mutations in the activating loop of tyrosine kinase domain are frequently found in infant ALL with MLL gene rearrangement [abstract]. Blood. 2002;100:740a.
-
(2002)
Blood
, vol.100
-
-
Taketani, T.1
Taki, T.2
Ishii, E.3
-
32
-
-
0035839840
-
DNA double strand break repair and chromosomal translocation: Lessons from animal models
-
Ferguson DO, Alt FW. DNA double strand break repair and chromosomal translocation: lessons from animal models. Oncogene. 2001;20:5572-5579.
-
(2001)
Oncogene
, vol.20
, pp. 5572-5579
-
-
Ferguson, D.O.1
Alt, F.W.2
-
33
-
-
0037093250
-
Myeloid leukemias have increased activity of the nonhomologous end-joining pathway and concomitant DNA misrepair that is dependent on the Ku70/86 heterodimer
-
Gaymes TJ, Mufti GJ, Rassool FV. Myeloid leukemias have increased activity of the nonhomologous end-joining pathway and concomitant DNA misrepair that is dependent on the Ku70/86 heterodimer. Cancer Res. 2002;62:2791-2797.
-
(2002)
Cancer Res
, vol.62
, pp. 2791-2797
-
-
Gaymes, T.J.1
Mufti, G.J.2
Rassool, F.V.3
-
34
-
-
0035866811
-
Transplacental chemical exposure and risk of infant leukemia with MLL gene fusion
-
Alexander FE, Patheal SL, Biondi A, et al. Transplacental chemical exposure and risk of infant leukemia with MLL gene fusion. Cancer Res. 2001;61:2542-2546.
-
(2001)
Cancer Res
, vol.61
, pp. 2542-2546
-
-
Alexander, F.E.1
Patheal, S.L.2
Biondi, A.3
-
35
-
-
0033564977
-
Prevalence of the inactivating 609C→T polymorphism in the NAD(P)H:quinone oxidoreductase (NQO1) gene in patients with primary and therapy-related myeloid leukemia
-
Larson RA, Wang Y, Banerjee M, et al. Prevalence of the inactivating 609C→T polymorphism in the NAD(P)H:quinone oxidoreductase (NQO1) gene in patients with primary and therapy-related myeloid leukemia. Blood. 1999;94:803-807.
-
(1999)
Blood
, vol.94
, pp. 803-807
-
-
Larson, R.A.1
Wang, Y.2
Banerjee, M.3
-
36
-
-
0032478140
-
The partial tandem duplication of ALL1 (MLL) is consistently generated by Alu-mediated homologous recombination in acute myeloid leukemia
-
Strout MP, Marcucci G, Bloomfield CD, Caligiuri MA. The partial tandem duplication of ALL1 (MLL) is consistently generated by Alu-mediated homologous recombination in acute myeloid leukemia. Proc Natl Acad Sci U S A. 1998;95:2390-2395.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 2390-2395
-
-
Strout, M.P.1
Marcucci, G.2
Bloomfield, C.D.3
Caligiuri, M.A.4
-
37
-
-
0031686409
-
Internal tandem duplication of the FLT3 gene is a novel modality of elongation mutation which causes constitutive activation of the product
-
Kiyoi H, Towatari M, Yokota S, et al. Internal tandem duplication of the FLT3 gene is a novel modality of elongation mutation which causes constitutive activation of the product. Leukemia. 1998;12:1333-1337.
-
(1998)
Leukemia
, vol.12
, pp. 1333-1337
-
-
Kiyoi, H.1
Towatari, M.2
Yokota, S.3
-
38
-
-
0034212650
-
The protein encoded by the proto-oncogene DEK changes the topology of chromatin and reduces the efficiency of DNA replication in a chromatin-specific manner
-
Alexiadis V, Waldmann T, Andersen J, Mann M, Knippers R, Gruss C. The protein encoded by the proto-oncogene DEK changes the topology of chromatin and reduces the efficiency of DNA replication in a chromatin-specific manner. Genes Dev. 2000;14:1308-1312.
-
(2000)
Genes Dev
, vol.14
, pp. 1308-1312
-
-
Alexiadis, V.1
Waldmann, T.2
Andersen, J.3
Mann, M.4
Knippers, R.5
Gruss, C.6
-
39
-
-
0032058483
-
Experience treating a patient with Bloom syndrome and acute myelogenous leukemia
-
Grasemann H, Kremens B, Passarge E. Experience treating a patient with Bloom syndrome and acute myelogenous leukemia. Med Pediatr Oncol. 1998;30:309-310.
-
(1998)
Med Pediatr Oncol
, vol.30
, pp. 309-310
-
-
Grasemann, H.1
Kremens, B.2
Passarge, E.3
-
40
-
-
0033598931
-
A role for PML and the nuclear body in genomic stability
-
Zhong S, Hu P, Ye TZ, Stan R, Ellis NA, Pandolfi PP. A role for PML and the nuclear body in genomic stability. Oncogene. 1999;18:7941-7947.
-
(1999)
Oncogene
, vol.18
, pp. 7941-7947
-
-
Zhong, S.1
Hu, P.2
Ye, T.Z.3
Stan, R.4
Ellis, N.A.5
Pandolfi, P.P.6
-
41
-
-
17144458786
-
Fusion proteins of the retinoic acid receptor-alpha recruit histone deacetylase in promyelocytic leukaemia
-
Grignani F, De Matteis S, Nervi C, et al. Fusion proteins of the retinoic acid receptor-alpha recruit histone deacetylase in promyelocytic leukaemia. Nature. 1998;391:815-818.
-
(1998)
Nature
, vol.391
, pp. 815-818
-
-
Grignani, F.1
De Matteis, S.2
Nervi, C.3
-
42
-
-
0034718552
-
Retrovirus-mediated gene transfer of MLL-ELL transforms primary myeloid progenitors and causes acute myeloid leukemias in mice
-
Lavau C, Luo RT, Du C, Thirman MJ. Retrovirus-mediated gene transfer of MLL-ELL transforms primary myeloid progenitors and causes acute myeloid leukemias in mice. Proc Natl Acad Sci U S A. 2000;97:10984-10989.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 10984-10989
-
-
Lavau, C.1
Luo, R.T.2
Du, C.3
Thirman, M.J.4
-
43
-
-
0034282527
-
Chromatin-related properties of CBP fused to MLL generate a myelodysplastic-like syndrome that evolves into myeloid leukemia
-
Lavau C, Du C, Thirman M, Zeleznik-Le N. Chromatin-related properties of CBP fused to MLL generate a myelodysplastic-like syndrome that evolves into myeloid leukemia. EMBO J. 2000;19: 4655-4664.
-
(2000)
EMBO J
, vol.19
, pp. 4655-4664
-
-
Lavau, C.1
Du, C.2
Thirman, M.3
Zeleznik-Le, N.4
-
44
-
-
0012571667
-
Networks of molecular mutations in acute myeloid leukemia and their correlations to cytogenetics and morphology
-
Schnittger S, Schoch C, Boell B, Dugas M, Haferlach T, Hiddemann W. Networks of molecular mutations in acute myeloid leukemia and their correlations to cytogenetics and morphology [abstract]. Blood. 2002;100:196a.
-
(2002)
Blood
, vol.100
-
-
Schnittger, S.1
Schoch, C.2
Boell, B.3
Dugas, M.4
Haferlach, T.5
Hiddemann, W.6
-
45
-
-
0028811336
-
Therapy-related acute promyelocytic leukemia with t(15; 17) (q22;q12) following chemotherapy with drugs targeting DNA topolsomerase II: A report of two cases and a review of the literature
-
Hoffmann L, Moller P, Pedersen-Bjergaard J, Waage A, Pedersen M, Hirsch FR. Therapy-related acute promyelocytic leukemia with t(15; 17) (q22;q12) following chemotherapy with drugs targeting DNA topolsomerase II: a report of two cases and a review of the literature. Ann Oncol. 1995;6:781-788.
-
(1995)
Ann Oncol
, vol.6
, pp. 781-788
-
-
Hoffmann, L.1
Moller, P.2
Pedersen-Bjergaard, J.3
Waage, A.4
Pedersen, M.5
Hirsch, F.R.6
-
46
-
-
0031877960
-
Etoposide-related acute promyelocytic leukemia
-
Kudo K, Yoshida H, Kiyoi H, Numata S, Horibe K, Naoe T. Etoposide-related acute promyelocytic leukemia. Leukemia. 1998;12:1171-1175.
-
(1998)
Leukemia
, vol.12
, pp. 1171-1175
-
-
Kudo, K.1
Yoshida, H.2
Kiyoi, H.3
Numata, S.4
Horibe, K.5
Naoe, T.6
-
47
-
-
0034667690
-
High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21
-
Preudhomme C, Warot-Loze D, Roumier C, et al. High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B 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
-
48
-
-
0035001987
-
Coduplication of the MLL and FLT3 genes in patients with acute myeloid leukemia
-
Jamal R, Taketani T, Taki T, et al. Coduplication of the MLL and FLT3 genes in patients with acute myeloid leukemia. Genes Chromosomes Cancer. 2001;31:187-190.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 187-190
-
-
Jamal, R.1
Taketani, T.2
Taki, T.3
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