-
1
-
-
33751267902
-
Acute myeloid leukaemia
-
Estey E, Dohner H. Acute myeloid leukaemia. Lancet 2006 368 : 1894 907.
-
(2006)
Lancet
, vol.368
, pp. 1894-907
-
-
Estey, E.1
Dohner, H.2
-
2
-
-
0032784783
-
World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: Report of the Clinical Advisory Committee meeting-Airlie House, Virginia, November 1997
-
Harris NL, Jaffe ES, Diebold J, Flandrin G, Muller-Hermelink HK, Vardiman J, Lister TA, Bloomfield CD. World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: report of the Clinical Advisory Committee meeting-Airlie House, Virginia, November 1997. J Clin Oncol 1999 17 : 3835 49.
-
(1999)
J Clin Oncol
, vol.17
, pp. 3835-49
-
-
Harris, N.L.1
Jaffe, E.S.2
Diebold, J.3
Flandrin, G.4
Muller-Hermelink, H.K.5
Vardiman, J.6
Lister, T.A.7
Bloomfield, C.D.8
-
3
-
-
0036890819
-
Rapid screening of leukemia fusion transcripts in acute leukemia by real-time PCR
-
Osumi K, Fukui T, Kiyoi H, et al. Rapid screening of leukemia fusion transcripts in acute leukemia by real-time PCR. Leuk Lymphoma 2002 43 : 2291 9.
-
(2002)
Leuk Lymphoma
, vol.43
, pp. 2291-9
-
-
Osumi, K.1
Fukui, T.2
Kiyoi, H.3
-
4
-
-
27244452986
-
Genetics of myeloid malignancies: Pathogenetic and clinical implications
-
Frohling S, Scholl C, Gilliland DG, Levine RL. Genetics of myeloid malignancies: pathogenetic and clinical implications. J Clin Oncol 2005 23 : 6285 95.
-
(2005)
J Clin Oncol
, vol.23
, pp. 6285-95
-
-
Frohling, S.1
Scholl, C.2
Gilliland, D.G.3
Levine, R.L.4
-
5
-
-
33846230449
-
Clinical relevance of mutations and gene-expression changes in adult acute myeloid leukemia with normal cytogenetics: Are we ready for a prognostically prioritized molecular classification?
-
Mrozek K, Marcucci G, Paschka P, Whitman SP, Bloomfield CD. Clinical relevance of mutations and gene-expression changes in adult acute myeloid leukemia with normal cytogenetics: are we ready for a prognostically prioritized molecular classification? Blood 2007 109 : 431 48.
-
(2007)
Blood
, vol.109
, pp. 431-48
-
-
Mrozek, K.1
Marcucci, G.2
Paschka, P.3
Whitman, S.P.4
Bloomfield, C.D.5
-
6
-
-
53249123632
-
-
Lyon. WHO Press
-
Swerdlow S, Campo E, Harris N, Jaffe E, Pileri S, Stein H, Thiele J, Vardiman J. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th edn. Lyon : WHO Press, 2008.
-
(2008)
WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, 4th Edn.
-
-
Swerdlow, S.1
Campo, E.2
Harris, N.3
Jaffe, E.4
Pileri, S.5
Stein, H.6
Thiele, J.7
Vardiman, J.8
-
7
-
-
0036636857
-
Core-binding factors in haematopoiesis and leukaemia
-
Speck NA, Gilliland DG. Core-binding factors in haematopoiesis and leukaemia. Nat Rev Cancer 2002 2 : 502 13.
-
(2002)
Nat Rev Cancer
, vol.2
, pp. 502-13
-
-
Speck, N.A.1
Gilliland, D.G.2
-
8
-
-
44049086446
-
Cooperating gene mutations in acute myeloid leukemia: A review of the literature
-
Renneville A, Roumier C, Biggio V, Nibourel O, Boissel N, Fenaux P, Preudhomme C. Cooperating gene mutations in acute myeloid leukemia: a review of the literature. Leukemia 2008 22 : 915 31.
-
(2008)
Leukemia
, vol.22
, pp. 915-31
-
-
Renneville, A.1
Roumier, C.2
Biggio, V.3
Nibourel, O.4
Boissel, N.5
Fenaux, P.6
Preudhomme, C.7
-
9
-
-
0026096185
-
P53 gene mutations in acute myeloid leukemia with 17p monosomy
-
Fenaux P, Jonveaux P, Quiquandon I, Lai JL, Pignon JM, Loucheux-Lefebvre MH, Bauters F, Berger R, Kerckaert JP. P53 gene mutations in acute myeloid leukemia with 17p monosomy. Blood 1991 78 : 1652 7.
-
(1991)
Blood
, vol.78
, pp. 1652-7
-
-
Fenaux, P.1
Jonveaux, P.2
Quiquandon, I.3
Lai, J.L.4
Pignon, J.M.5
Loucheux-Lefebvre, M.H.6
Bauters, F.7
Berger, R.8
Kerckaert, J.P.9
-
10
-
-
0025804270
-
Mutation of the p53 gene in human acute myelogenous leukemia
-
Slingerland JM, Minden MD, Benchimol S. Mutation of the p53 gene in human acute myelogenous leukemia. Blood 1991 77 : 1500 7.
-
(1991)
Blood
, vol.77
, pp. 1500-7
-
-
Slingerland, J.M.1
Minden, M.D.2
Benchimol, S.3
-
11
-
-
0033934763
-
Prognostic value of p53 gene mutations and the product expression in de novo acute myeloid leukemia
-
DOI 10.1034/j.1600-0609.2000.90138.x
-
Nakano Y, Naoe T, Kiyoi H, et al. Prognostic value of p53 gene mutations and the product expression in de novo acute myeloid leukemia. Eur J Haematol 2000 65 : 23 31. (Pubitemid 30432017)
-
(2000)
European Journal of Haematology
, vol.65
, Issue.1
, pp. 23-31
-
-
Nakano, Y.1
Naoe, T.2
Kiyoi, H.3
Kitamura, K.4
Minami, S.5
Miyawaki, S.6
Asou, N.7
Kuriyama, K.8
Kusumoto, S.9
Shimazaki, C.10
Akiyama, H.11
Saito, K.12
Nishimura, M.13
Motoji, T.14
Shinagawa, K.15
Saito, H.16
Ohno, R.17
-
12
-
-
0035281739
-
Mutations with loss of heterozygosity of p53 are common in therapy-related 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. Mutations with loss of heterozygosity of p53 are common in therapy-related 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 2001 19 : 1405 13.
-
(2001)
J Clin Oncol
, vol.19
, pp. 1405-13
-
-
Christiansen, D.H.1
Andersen, M.K.2
Pedersen-Bjergaard, J.3
-
13
-
-
33750326207
-
Alternative genetic pathways and cooperating genetic abnormalities in the pathogenesis of therapy-related myelodysplasia and acute myeloid leukemia
-
Pedersen-Bjergaard J, Christiansen DH, Desta F, Andersen MK. Alternative genetic pathways and cooperating genetic abnormalities in the pathogenesis of therapy-related myelodysplasia and acute myeloid leukemia. Leukemia 2006 20 : 1943 9.
-
(2006)
Leukemia
, vol.20
, pp. 1943-9
-
-
Pedersen-Bjergaard, J.1
Christiansen, D.H.2
Desta, F.3
Andersen, M.K.4
-
14
-
-
0033173221
-
No beneficial effect from addition of etoposide to daunorubicin, cytarabine, and 6-mercaptopurine in individualized induction therapy of adult acute myeloid leukemia: The JALSG-AML92 study. Japan Adult Leukemia Study Group
-
Miyawaki S, Tanimoto M, Kobayashi T, et al. No beneficial effect from addition of etoposide to daunorubicin, cytarabine, and 6-mercaptopurine in individualized induction therapy of adult acute myeloid leukemia: the JALSG-AML92 study. Japan Adult Leukemia Study Group. Int J Hematol 1999 70 : 97 104.
-
(1999)
Int J Hematol
, vol.70
, pp. 97-104
-
-
Miyawaki, S.1
Tanimoto, M.2
Kobayashi, T.3
-
15
-
-
29144468876
-
A randomized, postremission comparison of four courses of standard-dose consolidation therapy without maintenance therapy versus three courses of standard-dose consolidation with maintenance therapy in adults with acute myeloid leukemia: The Japan Adult Leukemia Study Group AML 97 Study
-
Miyawaki S, Sakamaki H, Ohtake S, et al. A randomized, postremission comparison of four courses of standard-dose consolidation therapy without maintenance therapy versus three courses of standard-dose consolidation with maintenance therapy in adults with acute myeloid leukemia: the Japan Adult Leukemia Study Group AML 97 Study. Cancer 2005 104 : 2726 34.
-
(2005)
Cancer
, vol.104
, pp. 2726-34
-
-
Miyawaki, S.1
Sakamaki, H.2
Ohtake, S.3
-
16
-
-
0033134792
-
Prognostic implication of FLT3 and N-RAS gene mutations in acute myeloid leukemia
-
Kiyoi H, Naoe T, Nakano Y, et al. Prognostic implication of FLT3 and N-RAS gene mutations in acute myeloid leukemia. Blood 1999 93 : 3074 80.
-
(1999)
Blood
, vol.93
, pp. 3074-80
-
-
Kiyoi, H.1
Naoe, T.2
Nakano, Y.3
-
17
-
-
10744230464
-
Biologic and clinical significance of the FLT3 transcript level in acute myeloid leukemia
-
Ozeki K, Kiyoi H, Hirose Y, et al. Biologic and clinical significance of the FLT3 transcript level in acute myeloid leukemia. Blood 2004 103 : 1901 8.
-
(2004)
Blood
, vol.103
, pp. 1901-8
-
-
Ozeki, K.1
Kiyoi, H.2
Hirose, Y.3
-
18
-
-
24144494881
-
Clinical characteristics and prognostic implications of NPM1 mutations in acute myeloid leukemia
-
Suzuki T, Kiyoi H, Ozeki K, et al. Clinical characteristics and prognostic implications of NPM1 mutations in acute myeloid leukemia. Blood 2005 106 : 2854 61.
-
(2005)
Blood
, vol.106
, pp. 2854-61
-
-
Suzuki, T.1
Kiyoi, H.2
Ozeki, K.3
-
19
-
-
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 9.
-
(2001)
Blood
, vol.97
, pp. 2434-9
-
-
Yamamoto, Y.1
Kiyoi, H.2
Nakano, Y.3
-
20
-
-
33847202261
-
JAK3 mutations occur in acute megakaryoblastic leukemia both in Down syndrome children and non-Down syndrome adults
-
Kiyoi H, Yamaji S, Kojima S, Naoe T. JAK3 mutations occur in acute megakaryoblastic leukemia both in Down syndrome children and non-Down syndrome adults. Leukemia 2007 21 : 574 6.
-
(2007)
Leukemia
, vol.21
, pp. 574-6
-
-
Kiyoi, H.1
Yamaji, S.2
Kojima, S.3
Naoe, T.4
-
21
-
-
1442356729
-
CEBPA mutations in younger adults with acute myeloid leukemia and normal cytogenetics: Prognostic relevance and analysis of cooperating mutations
-
Frohling S, Schlenk RF, Stolze I, Bihlmayr J, Benner A, Kreitmeier S, Tobis K, Dohner H, Dohner K. CEBPA mutations in younger adults with acute myeloid leukemia and normal cytogenetics: prognostic relevance and analysis of cooperating mutations. J Clin Oncol 2004 22 : 624 33.
-
(2004)
J Clin Oncol
, vol.22
, pp. 624-33
-
-
Frohling, S.1
Schlenk, R.F.2
Stolze, I.3
Bihlmayr, J.4
Benner, A.5
Kreitmeier, S.6
Tobis, K.7
Dohner, H.8
Dohner, K.9
-
22
-
-
33748467435
-
Adverse prognostic significance of KIT mutations in adult acute myeloid leukemia with inv(16) and t(8;21): A Cancer and Leukemia Group B Study
-
Paschka P, Marcucci G, Ruppert AS, et al. Adverse prognostic significance of KIT mutations in adult acute myeloid leukemia with inv(16) and t(8;21): a Cancer and Leukemia Group B Study. J Clin Oncol 2006 24 : 3904 11.
-
(2006)
J Clin Oncol
, vol.24
, pp. 3904-11
-
-
Paschka, P.1
Marcucci, G.2
Ruppert, A.S.3
-
23
-
-
48749118242
-
Combinatorial patterns of somatic gene mutations in cancer
-
Yeang CH, McCormick F, Levine A. Combinatorial patterns of somatic gene mutations in cancer. FASEB J 2008 22 : 2605 22.
-
(2008)
FASEB J
, vol.22
, pp. 2605-22
-
-
Yeang, C.H.1
McCormick, F.2
Levine, A.3
-
24
-
-
0033043084
-
Molecular evolution of acute myeloid leukaemia in relapse: Unstable N-ras and FLT3 genes compared with p53 gene
-
Nakano Y, Kiyoi H, Miyawaki S, Asou N, Ohno R, Saito H, Naoe T. Molecular evolution of acute myeloid leukaemia in relapse: unstable N-ras and FLT3 genes compared with p53 gene. Br J Haematol 1999 104 : 659 64.
-
(1999)
Br J Haematol
, vol.104
, pp. 659-64
-
-
Nakano, Y.1
Kiyoi, H.2
Miyawaki, S.3
Asou, N.4
Ohno, R.5
Saito, H.6
Naoe, T.7
-
26
-
-
0034654412
-
Deletions of chromosome 5q13.3 and 17p loci cooperate in myeloid neoplasms
-
Castro PD, Liang JC, Nagarajan L. Deletions of chromosome 5q13.3 and 17p loci cooperate in myeloid neoplasms. Blood 2000 95 : 2138 43.
-
(2000)
Blood
, vol.95
, pp. 2138-43
-
-
Castro, P.D.1
Liang, J.C.2
Nagarajan, L.3
-
27
-
-
49349140725
-
Mutations of the TP53 gene in acute myeloid leukemia are strongly associated with a complex aberrant karyotype
-
Haferlach C, Dicker F, Herholz H, Schnittger S, Kern W, Haferlach T. Mutations of the TP53 gene in acute myeloid leukemia are strongly associated with a complex aberrant karyotype. Leukemia 2008 22 : 1539 41.
-
(2008)
Leukemia
, vol.22
, pp. 1539-41
-
-
Haferlach, C.1
Dicker, F.2
Herholz, H.3
Schnittger, S.4
Kern, W.5
Haferlach, T.6
-
28
-
-
0026336513
-
Mutations in the p53 gene in myelodysplastic syndromes
-
Jonveaux P, Fenaux P, Quiquandon I, Pignon JM, Lai JL, Loucheux-Lefebvre MH, Goossens M, Bauters F, Berger R. Mutations in the p53 gene in myelodysplastic syndromes. Oncogene 1991 6 : 2243 7.
-
(1991)
Oncogene
, vol.6
, pp. 2243-7
-
-
Jonveaux, P.1
Fenaux, P.2
Quiquandon, I.3
Pignon, J.M.4
Lai, J.L.5
Loucheux-Lefebvre, M.H.6
Goossens, M.7
Bauters, F.8
Berger, R.9
-
29
-
-
0029917702
-
Cytogenetics of myelodysplastic syndromes
-
Fenaux P, Morel P, Lai JL. Cytogenetics of myelodysplastic syndromes. Semin Hematol 1996 33 : 127 38.
-
(1996)
Semin Hematol
, vol.33
, pp. 127-38
-
-
Fenaux, P.1
Morel, P.2
Lai, J.L.3
-
30
-
-
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. 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 1986 4 : 325 45.
-
(1986)
J Clin Oncol
, vol.4
, pp. 325-45
-
-
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
-
31
-
-
0025949901
-
Balanced translocations involving chromosome bands 11q23 and 21q22 are highly characteristic of myelodysplasia and leukemia following therapy with cytostatic agents targeting at DNA-topoisomerase II
-
Pedersen-Bjergaard J, Philip P. Balanced translocations involving chromosome bands 11q23 and 21q22 are highly characteristic of myelodysplasia and leukemia following therapy with cytostatic agents targeting at DNA-topoisomerase II. Blood 1991 78 : 1147 8.
-
(1991)
Blood
, vol.78
, pp. 1147-8
-
-
Pedersen-Bjergaard, J.1
Philip, P.2
-
32
-
-
0032006824
-
17p Deletion in acute myeloid leukemia and myelodysplastic syndrome. Analysis of breakpoints and deleted segments by fluorescence in situ
-
Soenen V, Preudhomme C, Roumier C, Daudignon A, Lai JL, Fenaux P. 17p Deletion in acute myeloid leukemia and myelodysplastic syndrome. Analysis of breakpoints and deleted segments by fluorescence in situ. Blood 1998 91 : 1008 15.
-
(1998)
Blood
, vol.91
, pp. 1008-15
-
-
Soenen, V.1
Preudhomme, C.2
Roumier, C.3
Daudignon, A.4
Lai, J.L.5
Fenaux, P.6
-
33
-
-
0033002273
-
Therapy-related myelodysplastic syndrome and acute myeloid leukemia with 17p deletion. A report on 25 cases
-
Merlat A, Lai JL, Sterkers Y, Demory JL, Bauters F, Preudhomme C, Fenaux P. Therapy-related myelodysplastic syndrome and acute myeloid leukemia with 17p deletion. A report on 25 cases. Leukemia 1999 13 : 250 7.
-
(1999)
Leukemia
, vol.13
, pp. 250-7
-
-
Merlat, A.1
Lai, J.L.2
Sterkers, Y.3
Demory, J.L.4
Bauters, F.5
Preudhomme, C.6
Fenaux, P.7
-
34
-
-
0023137891
-
Correlation between acquired pseudo-Pelger-Huet anomaly and involvement of chromosome 17 in chronic myeloid leukemia
-
Sessarego M, Ajmar F. Correlation between acquired pseudo-Pelger-Huet anomaly and involvement of chromosome 17 in chronic myeloid leukemia. Cancer Genet Cytogenet 1987 25 : 265 70.
-
(1987)
Cancer Genet Cytogenet
, vol.25
, pp. 265-70
-
-
Sessarego, M.1
Ajmar, F.2
-
35
-
-
0026004478
-
The spectrum of molecular alterations in the evolution of chronic myelocytic leukemia
-
Ahuja H, Bar-Eli M, Arlin Z, Advani S, Allen SL, Goldman J, Snyder D, Foti A, Cline M. The spectrum of molecular alterations in the evolution of chronic myelocytic leukemia. J Clin Invest 1991 87 : 2042 7.
-
(1991)
J Clin Invest
, vol.87
, pp. 2042-7
-
-
Ahuja, H.1
Bar-Eli, M.2
Arlin, Z.3
Advani, S.4
Allen, S.L.5
Goldman, J.6
Snyder, D.7
Foti, A.8
Cline, M.9
-
36
-
-
0036786901
-
The World Health Organization (WHO) classification of the myeloid neoplasms
-
Vardiman JW, Harris NL, Brunning RD. The World Health Organization (WHO) classification of the myeloid neoplasms. Blood 2002 100 : 2292 302.
-
(2002)
Blood
, vol.100
, pp. 2292-302
-
-
Vardiman, J.W.1
Harris, N.L.2
Brunning, R.D.3
-
37
-
-
41349105936
-
MLD according to the WHO classification in AML has no correlation with age and no independent prognostic relevance as analyzed in 1766 patients
-
Wandt H, Schakel U, Kroschinsky F, Prange-Krex G, Mohr B, Thiede C, Pascheberg U, Soucek S, Schaich M, Ehninger G. MLD according to the WHO classification in AML has no correlation with age and no independent prognostic relevance as analyzed in 1766 patients. Blood 2008 111 : 1855 61.
-
(2008)
Blood
, vol.111
, pp. 1855-61
-
-
Wandt, H.1
Schakel, U.2
Kroschinsky, F.3
Prange-Krex, G.4
Mohr, B.5
Thiede, C.6
Pascheberg, U.7
Soucek, S.8
Schaich, M.9
Ehninger, G.10
|