-
1
-
-
78650655385
-
Characteristics and outcome of patients with acute myeloid leukemia refractory to 1 cycle of high-dose cytarabine-based induction chemotherapy
-
Ravandi F, Cortes J, Faderl S, et al. Characteristics and outcome of patients with acute myeloid leukemia refractory to 1 cycle of high-dose cytarabine-based induction chemotherapy. Blood. 2010;116(26):5818-5823.
-
(2010)
Blood
, vol.116
, Issue.26
, pp. 5818-5823
-
-
Ravandi, F.1
Cortes, J.2
Faderl, S.3
-
2
-
-
0028091194
-
A cell initiating human acute myeloid leukaemia after transplantation into SCID mice
-
DOI 10.1038/367645a0
-
Lapidot T, Sirard C, Vormoor J, et al. A cell initiating human acute myeloid leukaemia after transplantation into SCID mice. Nature. 1994;367(6464): 645-648. (Pubitemid 24067706)
-
(1994)
Nature
, vol.367
, Issue.6464
, pp. 645-648
-
-
Lapidot, T.1
Sirard, C.2
Vormoor, J.3
Murdoch, B.4
Hoang, T.5
Caceres-Cortes, J.6
Minden, M.7
Paterson, B.8
Caligiuri, M.A.9
Dick, J.E.10
-
3
-
-
3242754448
-
Acute myeloid leukemia originates from a hierarchy of leukemic stem cell classes that differ in self-renewal capacity
-
DOI 10.1038/ni1080
-
Hope KJ, Jin L, Dick JE. Acute myeloid leukemia originates from a hierarchy of leukemic stem cell classes that differ in self-renewal capacity. Nat Immunol. 2004;5(7):738-743. (Pubitemid 39023306)
-
(2004)
Nature Immunology
, vol.5
, Issue.7
, pp. 738-743
-
-
Hope, K.J.1
Jin, L.2
Dick, J.E.3
-
4
-
-
84859854912
-
A clinically relevant population of leukemic CD34+CD38- Cells in acute myeloid leukemia
-
Gerber JM, Smith BD, Ngwang B, et al. A clinically relevant population of leukemic CD34+CD38- cells in acute myeloid leukemia. Blood. 2012;119(15): 3571-3577.
-
(2012)
Blood
, vol.119
, Issue.15
, pp. 3571-3577
-
-
Gerber, J.M.1
Smith, B.D.2
Ngwang, B.3
-
5
-
-
78650950098
-
Human acute myelogenous leukemia stem cells are rare and heterogeneous when assayed in NOD/SCID/IL2 Rgammac-deficient mice
-
Sarry JE, Murphy K, Perry R, et al. Human acute myelogenous leukemia stem cells are rare and heterogeneous when assayed in NOD/SCID/IL2 Rgammac-deficient mice. J Clin Invest. 2011; 121(1):384-395.
-
(2011)
J Clin Invest
, vol.121
, Issue.1
, pp. 384-395
-
-
Sarry, J.E.1
Murphy, K.2
Perry, R.3
-
6
-
-
77950451485
-
Leukemia-initiating cells from some acute myeloid leukemia patients with mutated nucleophosmin reside in the CD34(-) fraction
-
Taussig DC, Vargaftig J, Miraki-Moud F, et al. Leukemia-initiating cells from some acute myeloid leukemia patients with mutated nucleophosmin reside in the CD34(-) fraction. Blood. 2010; 115(10):1976-1984.
-
(2010)
Blood
, vol.115
, Issue.10
, pp. 1976-1984
-
-
Taussig, D.C.1
Vargaftig, J.2
Miraki-Moud, F.3
-
7
-
-
19944427850
-
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype
-
DOI 10.1056/NEJMoa041974
-
Falini B, Mecucci C, Tiacci E, et al. Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype. N Engl J Med. 2005; 352(3):254-266. (Pubitemid 40110814)
-
(2005)
New England Journal of Medicine
, vol.352
, Issue.3
, pp. 254-266
-
-
Falini, B.1
Mecucci, C.2
Tiacci, E.3
Alcalay, M.4
Rosati, R.5
Pasqualucci, L.6
La, S.R.7
Diverio, D.8
Colombo, E.9
Santucci, A.10
Bigerna, B.11
Pacini, R.12
Pucciarini, A.13
Liso, A.14
Vignetti, M.15
Fazi, P.16
Meani, N.17
Pettirossi, V.18
Saglio, G.19
Mandelli, F.20
Lo-Coco, F.21
Pelicci, P.-G.22
Martelli, M.F.23
more..
-
8
-
-
79953176952
-
Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia
-
Yan XJ, Xu J, Gu ZH, et al. Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia. Nat Genet. 2011;43(4):309-315.
-
(2011)
Nat Genet
, vol.43
, Issue.4
, pp. 309-315
-
-
Yan, X.J.1
Xu, J.2
Gu, Z.H.3
-
9
-
-
79952134550
-
RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis
-
Schnittger S, Dicker F, Kern W, et al. RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis. Blood. 2011;117(8):2348-2357.
-
(2011)
Blood
, vol.117
, Issue.8
, pp. 2348-2357
-
-
Schnittger, S.1
Dicker, F.2
Kern, W.3
-
10
-
-
78649906060
-
DNMT3A mutations in acute myeloid leukemia
-
Ley TJ, Ding L, Walter MJ, et al. DNMT3A mutations in acute myeloid leukemia. N Engl J Med. 2010;363(25):2424-2433.
-
(2010)
N Engl J Med
, vol.363
, Issue.25
, pp. 2424-2433
-
-
Ley, T.J.1
Ding, L.2
Walter, M.J.3
-
11
-
-
82155183257
-
Somatic mutations in the transcriptional corepressor gene BCORL1 in adult acute myelogenous leukemia
-
Li M, Collins R, Jiao Y, et al. Somatic mutations in the transcriptional corepressor gene BCORL1 in adult acute myelogenous leukemia. Blood. 2011; 118(22):5914-5917.
-
(2011)
Blood
, vol.118
, Issue.22
, pp. 5914-5917
-
-
Li, M.1
Collins, R.2
Jiao, Y.3
-
12
-
-
70149093912
-
Recurring mutations found by sequencing an acute myeloid leukemia genome
-
Mardis ER, Ding L, Dooling DJ, et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med. 2009;361(11): 1058-1066.
-
(2009)
N Engl J Med
, vol.361
, Issue.11
, pp. 1058-1066
-
-
Mardis, E.R.1
Ding, L.2
Dooling, D.J.3
-
13
-
-
73949090504
-
AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: Prognostic implication and interaction with other gene alterations
-
Tang JL, Hou HA, Chen CY, et al. AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: prognostic implication and interaction with other gene alterations. Blood. 2009; 114(26):5352-5361.
-
(2009)
Blood
, vol.114
, Issue.26
, pp. 5352-5361
-
-
Tang, J.L.1
Hou, H.A.2
Chen, C.Y.3
-
14
-
-
0035093813
-
Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia
-
DOI 10.1038/85820
-
Pabst T, Mueller BU, Zhang P, et al. Dominant-negative mutations of CEBPA, encoding CCAAT/ enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia. Nat Genet. 2001;27(3): 263-270. (Pubitemid 32201846)
-
(2001)
Nature Genetics
, vol.27
, Issue.3
, pp. 263-270
-
-
Pabst, T.1
Mueller, B.U.2
Zhang, P.3
Radomska, H.S.4
Narravula, S.5
Schnittger, S.6
Behre, G.7
Hiddemann, W.8
Tenen, D.G.9
-
15
-
-
78751661556
-
Evolution of human BCR-ABL1 lymphoblastic leukaemia-initiating cells
-
Notta F, Mullighan CG, Wang JC, et al. Evolution of human BCR-ABL1 lymphoblastic leukaemia-initiating cells. Nature. 2011;469(7330):362-367.
-
(2011)
Nature
, vol.469
, Issue.7330
, pp. 362-367
-
-
Notta, F.1
Mullighan, C.G.2
Wang, J.C.3
-
16
-
-
78751644099
-
Genetic variegation of clonal architecture and propagating cells in leukaemia
-
Anderson K, Lutz C, van Delft FW, et al. Genetic variegation of clonal architecture and propagating cells in leukaemia. Nature. 2011;469(7330):356- 361.
-
(2011)
Nature
, vol.469
, Issue.7330
, pp. 356-361
-
-
Anderson, K.1
Lutz, C.2
Van Delft, F.W.3
-
17
-
-
78649753896
-
Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia
-
Parkin B, Erba H, Ouillette P, et al. Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia. Blood. 2010; 116(23):4958-4967.
-
(2010)
Blood
, vol.116
, Issue.23
, pp. 4958-4967
-
-
Parkin, B.1
Erba, H.2
Ouillette, P.3
-
18
-
-
76749153827
-
Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution singlenucleotide polymorphism analysis
-
Bullinger L, Kronke J, Schon C, et al. Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution singlenucleotide polymorphism analysis. Leukemia. 2010;24(2):438-449.
-
(2010)
Leukemia
, vol.24
, Issue.2
, pp. 438-449
-
-
Bullinger, L.1
Kronke, J.2
Schon, C.3
-
19
-
-
69149100639
-
Acquired copy number alterations in adult acute myeloid leukemia genomes
-
Walter MJ, Payton JE, Ries RE, et al. Acquired copy number alterations in adult acute myeloid leukemia genomes. Proc Natl Acad Sci U S A. 2009;106(31):12950-12955.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, Issue.31
, pp. 12950-12955
-
-
Walter, M.J.1
Payton, J.E.2
Ries, R.E.3
-
20
-
-
68049118980
-
Loss of mismatched HLA in leukemia after stem-cell transplantation
-
Vago L, Perna SK, Zanussi M, et al. Loss of mismatched HLA in leukemia after stem-cell transplantation. N Engl J Med. 2009;361(5):478-488.
-
(2009)
N Engl J Med
, vol.361
, Issue.5
, pp. 478-488
-
-
Vago, L.1
Perna, S.K.2
Zanussi, M.3
-
21
-
-
70449715477
-
New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia
-
Tiu RV, Gondek LP, O'Keefe CL, et al. New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia. J Clin Oncol. 2009;27(31):5219-5226.
-
(2009)
J Clin Oncol
, vol.27
, Issue.31
, pp. 5219-5226
-
-
Tiu, R.V.1
Gondek, L.P.2
O'Keefe, C.L.3
-
22
-
-
42949142189
-
Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia
-
DOI 10.1056/NEJMoa074306
-
Schlenk RF, Dohner K, Krauter J, et al. Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia. N Engl J Med. 2008; 358(18):1909-1918. (Pubitemid 351620111)
-
(2008)
New England Journal of Medicine
, vol.358
, Issue.18
, pp. 1909-1918
-
-
Schlenk, R.F.1
Dohner, K.2
Krauter, J.3
Frohling, S.4
Corbacioglu, A.5
Bullinger, L.6
Habdank, M.7
Spath, D.8
Morgan, M.9
Benner, A.10
Schlegelberger, B.11
Heil, G.12
Ganser, A.13
Dohner, H.14
-
23
-
-
0029066836
-
Change in karyotype between diagnosis and first relapse in acute myelogenous leukemia
-
Estey E, Keating MJ, Pierce S, Stass S. Change in karyotype between diagnosis and first relapse in acute myelogenous leukemia. Leukemia. 1995; 9(6):972-976.
-
(1995)
Leukemia
, vol.9
, Issue.6
, pp. 972-976
-
-
Estey, E.1
Keating, M.J.2
Pierce, S.3
Stass, S.4
-
24
-
-
0036798512
-
Karyotype instability between diagnosis and relapse in 117 patients with acute myeloid leukemia: Implications for resistance against therapy
-
DOI 10.1038/sj.leu.2402654
-
Kern W, Haferlach T, Schnittger S, Ludwig WD, Hiddemann W, Schoch C. Karyotype instability between diagnosis and relapse in 117 patients with acute myeloid leukemia: implications for resistance against therapy. Leukemia. 2002;16(10): 2084-2091. (Pubitemid 35203452)
-
(2002)
Leukemia
, vol.16
, Issue.10
, pp. 2084-2091
-
-
Kern, W.1
Haferlach, T.2
Schnittger, S.3
Ludwig, W.D.4
Hiddemann, W.5
Schoch, C.6
-
25
-
-
0024401553
-
Cytogenetic studies of 103 patients with acute myelogenous leukemia in relapse
-
DOI 10.1016/0165-4608(89)90024-1
-
Garson OM, Hagemeijer A, Sakurai M, et al. Cytogenetic studies of 103 patients with acute myelogenous leukemia in relapse. Cancer Genet Cytogenet. 1989;40(2):187-202. (Pubitemid 19235688)
-
(1989)
Cancer Genetics and Cytogenetics
, vol.40
, Issue.2
, pp. 187-202
-
-
Garson, O.M.1
Hagemeijer, A.2
Sakurai, M.3
Reeves, B.R.4
Swansbury, G.J.5
Williams, G.J.6
Alimena, G.7
Arthur, D.C.8
Berger, R.9
De La, C.A.10
Dewald, G.W.11
Mitelman, F.12
Van Den, B.H.13
Lawler, S.D.14
Rowley, J.D.15
-
26
-
-
50949113696
-
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia
-
Raghavan M, Smith LL, Lillington DM, et al. Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia. Blood. 2008;112(3):814-821.
-
(2008)
Blood
, vol.112
, Issue.3
, pp. 814-821
-
-
Raghavan, M.1
Smith, L.L.2
Lillington, D.M.3
-
27
-
-
84862776906
-
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
-
Ding L, Ley TJ, Larson DE, et al. Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. Nature. 2012;481 (7382):506-510.
-
(2012)
Nature
, vol.481
, Issue.7382
, pp. 506-510
-
-
Ding, L.1
Ley, T.J.2
Larson, D.E.3
-
28
-
-
57149118627
-
Genomic analysis of the clonal origins of relapsed acute lymphoblastic leukemia
-
DOI 10.1126/science.1164266
-
Mullighan CG, Phillips LA, Su X, et al. Genomic analysis of the clonal origins of relapsed acute lymphoblastic leukemia. Science. 2008; 322(5906):1377-1380. (Pubitemid 352775249)
-
(2008)
Science
, vol.322
, Issue.5906
, pp. 1377-1380
-
-
Mullighan, C.G.1
Phillips, L.A.2
Su, X.3
Ma, J.4
Miller, C.B.5
Shurtleff, S.A.6
Downing, J.R.7
-
29
-
-
0034672269
-
Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: A Southwest Oncology Group/Eastern Cooperative Oncology Group Study
-
Slovak ML, Kopecky KJ, Cassileth PA, et al. Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group Study. Blood. 2000;96(13):4075-4083.
-
(2000)
Blood
, vol.96
, Issue.13
, pp. 4075-4083
-
-
Slovak, M.L.1
Kopecky, K.J.2
Cassileth, P.A.3
-
30
-
-
77955907917
-
Multiple distinct molecular mechanisms influence sensitivity and resistance to MDM2 inhibitors in adult acute myelogenous leukemia
-
Long J, Parkin B, Ouillette P, et al. Multiple distinct molecular mechanisms influence sensitivity and resistance to MDM2 inhibitors in adult acute myelogenous leukemia. Blood. 2010; 116(1):71- 80.
-
(2010)
Blood
, vol.116
, Issue.1
, pp. 71-80
-
-
Long, J.1
Parkin, B.2
Ouillette, P.3
-
31
-
-
0027421006
-
Immunophenotyping of acute leukemia by flow cytometric analysis: Use of CD45 and right-angle light scatter to gate on leukemic blasts in three-color analysis
-
Borowitz MJ, Guenther KL, Shults KE, Stelzer GT. Immunophenotyping of acute leukemia by flow cytometric analysis. Use of CD45 and right-angle light scatter to gate on leukemic blasts in three-color analysis. Am J Clin Pathol. 1993;100(5):534-540. (Pubitemid 23346202)
-
(1993)
American Journal of Clinical Pathology
, vol.100
, Issue.5
, pp. 534-540
-
-
Borowitz, M.J.1
Guenther, K.L.2
Shults, K.E.3
Stelzer, G.T.4
-
32
-
-
2542548405
-
dChipSNP: Significance curve and clustering of SNP-array-based loss-of-heterozygosity data
-
DOI 10.1093/bioinformatics/bth069
-
Lin M, Wei LJ, Sellers WR, Lieberfarb M, Wong WH, Li C. dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data. Bioinformatics. 2004;20(8):1233-1240. (Pubitemid 38807579)
-
(2004)
Bioinformatics
, vol.20
, Issue.8
, pp. 1233-1240
-
-
Lin, M.1
Wie, L.-J.2
Sellers, W.R.3
Lieberfarb, M.4
Wong, W.H.5
Li, C.6
-
33
-
-
34548064529
-
Comprehensive analysis of copy number and allele status identifies multiple chromosome defects underlying follicular lymphoma pathogenesis
-
DOI 10.1158/1078-0432.CCR-07-0456
-
Ross CW, Ouillette PD, Saddler CM, Shedden KA, Malek SN. Comprehensive analysis of copy number and allele status identifies multiple chromosome defects underlying follicular lymphoma pathogenesis. Clin Cancer Res. 2007;13(16):4777-4785. (Pubitemid 47294784)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.16
, pp. 4777-4785
-
-
Ross, C.W.1
Ouillette, P.D.2
Saddler, C.M.3
Shedden, K.A.4
Malek, S.N.5
-
34
-
-
77950461601
-
Origins and functional impact of copy number variation in the human genome
-
Conrad DF, Pinto D, Redon R, et al. Origins and functional impact of copy number variation in the human genome. Nature. 2010;464(7289):704- 712.
-
(2010)
Nature
, vol.464
, Issue.7289
, pp. 704-712
-
-
Conrad, D.F.1
Pinto, D.2
Redon, R.3
-
35
-
-
77955737728
-
NF1 inactivation in adult acute myelogenous leukemia
-
Parkin B, Ouillette P, Wang Y, et al. NF1 inactivation in adult acute myelogenous leukemia. Clin Cancer Res. 2010;16(16):4135-4147.
-
(2010)
Clin Cancer Res
, vol.16
, Issue.16
, pp. 4135-4147
-
-
Parkin, B.1
Ouillette, P.2
Wang, Y.3
-
36
-
-
80052936981
-
Acquired genomic copy number aberrations and survival in chronic lymphocytic leukemia
-
Ouillette P, Collins R, Shakhan S, et al. Acquired genomic copy number aberrations and survival in chronic lymphocytic leukemia. Blood. 2011; 118(11):3051-3061.
-
(2011)
Blood
, vol.118
, Issue.11
, pp. 3051-3061
-
-
Ouillette, P.1
Collins, R.2
Shakhan, S.3
-
37
-
-
70350720044
-
MDS and secondary AML display unique patterns and abundance of aberrant DNA methylation
-
Figueroa ME, Skrabanek L, Li Y, et al. MDS and secondary AML display unique patterns and abundance of aberrant DNA methylation. Blood. 2009;114(16):3448-3458.
-
(2009)
Blood
, vol.114
, Issue.16
, pp. 3448-3458
-
-
Figueroa, M.E.1
Skrabanek, L.2
Li, Y.3
-
38
-
-
60849089645
-
Aberrant DNA methylation is a dominant mechanism in MDS progression to AML
-
Jiang Y, Dunbar A, Gondek LP, et al. Aberrant DNA methylation is a dominant mechanism in MDS progression to AML. Blood. 2009;113(6): 1315-1325.
-
(2009)
Blood
, vol.113
, Issue.6
, pp. 1315-1325
-
-
Jiang, Y.1
Dunbar, A.2
Gondek, L.P.3
-
39
-
-
51649122312
-
Aberrant CpG island methylation in acute myeloid leukemia is accentuated at relapse
-
Kroeger H, Jelinek J, Estecio MR, et al. Aberrant CpG island methylation in acute myeloid leukemia is accentuated at relapse. Blood. 2008; 112(4):1366-1373.
-
(2008)
Blood
, vol.112
, Issue.4
, pp. 1366-1373
-
-
Kroeger, H.1
Jelinek, J.2
Estecio, M.R.3
-
40
-
-
84862012956
-
The role of minor subpopulations within the leukemic blast compartment of AML patients at initial diagnosis in the development of relapse
-
Bachas C, Schuurhuis GJ, Assaraf YG, et al. The role of minor subpopulations within the leukemic blast compartment of AML patients at initial diagnosis in the development of relapse. Leukemia. 2012;26(6):1313-1320.
-
(2012)
Leukemia
, vol.26
, Issue.6
, pp. 1313-1320
-
-
Bachas, C.1
Schuurhuis, G.J.2
Assaraf, Y.G.3
-
41
-
-
77957810002
-
Highf-requency type I/II mutational shifts between diagnosis and relapse are associated with outcome in pediatric AML: Implications for personalized medicine
-
Bachas C, Schuurhuis GJ, Hollink IH, et al. Highf-requency type I/II mutational shifts between diagnosis and relapse are associated with outcome in pediatric AML: implications for personalized medicine. Blood. 2010;116(15):2752-2758.
-
(2010)
Blood
, vol.116
, Issue.15
, pp. 2752-2758
-
-
Bachas, C.1
Schuurhuis, G.J.2
Hollink, I.H.3
-
42
-
-
33745198953
-
Stability and prognostic influence of FLT3 mutations in paired initial and relapsed AML samples
-
DOI 10.1038/sj.leu.2404246, PII 2404246
-
Cloos J, Goemans BF, Hess CJ, et al. Stability and prognostic influence of FLT3 mutations in paired initial and relapsed AML samples. Leukemia. 2006;20(7):1217-1220. (Pubitemid 43905824)
-
(2006)
Leukemia
, vol.20
, Issue.7
, pp. 1217-1220
-
-
Cloos, J.1
Goemans, B.F.2
Hess, C.J.3
Van Oostveen, J.W.4
Waisfisz, Q.5
Corthals, S.6
De Lange, D.7
Boeckx, N.8
Hahlen, K.9
Reinhardt, D.10
Creutzig, U.11
Schuurhuis, G.J.12
Zwaan, C..M.13
Kaspers, G.J.L.14
-
43
-
-
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(7):2393-2398.
-
(2002)
Blood
, vol.100
, Issue.7
, 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
-
44
-
-
33645501151
-
Nucleophosmin mutations in de novo acute myeloid leukemia: The age-dependent incidences and the stability during disease evolution
-
Chou WC, Tang JL, Lin LI, et al. Nucleophosmin mutations in de novo acute myeloid leukemia: the age-dependent incidences and the stability during disease evolution. Cancer Res. 2006;66(6): 3310-3316.
-
(2006)
Cancer Res
, vol.66
, Issue.6
, pp. 3310-3316
-
-
Chou, W.C.1
Tang, J.L.2
Lin, L.I.3
-
45
-
-
77950968519
-
Distinct clinical and biologic characteristics in adult acute myeloid leukemia bearing the isocitrate dehydrogenase 1 mutation
-
Chou WC, Hou HA, Chen CY, et al. Distinct clinical and biologic characteristics in adult acute myeloid leukemia bearing the isocitrate dehydrogenase 1 mutation. Blood. 2010;115(14):2749- 2754.
-
(2010)
Blood
, vol.115
, Issue.14
, pp. 2749-2754
-
-
Chou, W.C.1
Hou, H.A.2
Chen, C.Y.3
-
46
-
-
84862909358
-
DNMT3A mutations in acute myeloid leukemia: Stability during disease evolution and clinical implications
-
Hou HA, Kuo YY, Liu CY, et al. DNMT3A mutations in acute myeloid leukemia: stability during disease evolution and clinical implications. Blood. 2012;119(2):559-568.
-
(2012)
Blood
, vol.119
, Issue.2
, pp. 559-568
-
-
Hou, H.A.1
Kuo, Y.Y.2
Liu, C.Y.3
|