-
1
-
-
0019952276
-
Proposals for the classification of the myelodysplastic syndromes
-
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DA, Gralnick HR et al. Proposals for the classification of the myelodysplastic syndromes. Br J Haematol 1982; 51: 189-199.
-
(1982)
Br J Haematol
, vol.51
, pp. 189-199
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
Flandrin, G.4
Galton, D.A.5
Gralnick, H.R.6
-
2
-
-
0003477486
-
-
IARC Press: Lyon
-
Jaffe ES, Harris NL, Stein H, Vardiman JW. World Health Organization Classification of Tumors: Pathology & Genetics Tumors of Haematopoietic and lymphoid tissues. IARC Press: Lyon, 2001, pp 45-52.
-
(2001)
World Health Organization Classification of Tumors: Pathology & Genetics Tumors of Haematopoietic and lymphoid tissues
, pp. 45-52
-
-
Jaffe, E.S.1
Harris, N.L.2
Stein, H.3
Vardiman, J.W.4
-
3
-
-
17344371122
-
RAS, FMS and p53 mutations and poor clinical outcome in myelodysplasias: A 10-year follow-up
-
Padua RA, Guinn BA, Al-Sabah AI, Smith M, Taylor C, Pettersson T et al. RAS, FMS and p53 mutations and poor clinical outcome in myelodysplasias: A 10-year follow-up. Leukemia 1998; 12: 887-892.
-
(1998)
Leukemia
, vol.12
, pp. 887-892
-
-
Padua, R.A.1
Guinn, B.A.2
Al-Sabah, A.I.3
Smith, M.4
Taylor, C.5
Pettersson, T.6
-
4
-
-
0024998851
-
RAS mutations are rare events in Philadelphia chromosome-negative/bcr gene rearrangement-negative chronic myelogenous leukemia, but are prevalent in chronic myelomonocytic leukemia
-
Hirsch-Ginsberg C, LeMaistre AC, Kantarjian H, Talpaz M, Cork A, Freireich EJ et al. RAS mutations are rare events in Philadelphia chromosome-negative/bcr gene rearrangement-negative chronic myelogenous leukemia, but are prevalent in chronic myelomonocytic leukemia. Blood 1990; 76: 1214-1219.
-
(1990)
Blood
, vol.76
, pp. 1214-1219
-
-
Hirsch-Ginsberg, C.1
LeMaistre, A.C.2
Kantarjian, H.3
Talpaz, M.4
Cork, A.5
Freireich, E.J.6
-
5
-
-
0036045381
-
Tyrosine kinase fusion genes in chronic myeloproliferative diseases
-
Cross NC, Reiter A. Tyrosine kinase fusion genes in chronic myeloproliferative diseases. Leukemia 2002; 16: 1207-1212.
-
(2002)
Leukemia
, vol.16
, pp. 1207-1212
-
-
Cross, N.C.1
Reiter, A.2
-
6
-
-
1542503817
-
Acquisition of FLT3 or N-ras mutations is frequently associated with progression of myelodysplastic syndrome to acute myeloid leukemia
-
Shih LY, Huang CF, Wang PN, Wu JH, Lin TL, Dunn P et al. Acquisition of FLT3 or N-ras mutations is frequently associated with progression of myelodysplastic syndrome to acute myeloid leukemia. Leukemia 2004; 18: 466-475.
-
(2004)
Leukemia
, vol.18
, pp. 466-475
-
-
Shih, L.Y.1
Huang, C.F.2
Wang, P.N.3
Wu, J.H.4
Lin, T.L.5
Dunn, P.6
-
7
-
-
4143053704
-
Internal tandem duplication of fms-like tyrosine kinase 3 is associated with poor outcome in patients with myelodysplastic syndrome
-
Shih LY, Lin TL, Wang PN, Wu JH, Dunn P, Kuo MC et al. Internal tandem duplication of fms-like tyrosine kinase 3 is associated with poor outcome in patients with myelodysplastic syndrome. Cancer 2004; 101: 989-998.
-
(2004)
Cancer
, vol.101
, pp. 989-998
-
-
Shih, L.Y.1
Lin, T.L.2
Wang, P.N.3
Wu, J.H.4
Dunn, P.5
Kuo, M.C.6
-
8
-
-
16344370044
-
Heterogeneous patterns of CEBPα mutation status in the progression of myelodysplastic syndrome and chronic myelomonocytic leukemia to acute myeloid leukemia
-
Shih LY, Huang CF, Lin TL, Wu JH, Wang PN, Dunn P et al. Heterogeneous patterns of CEBPα mutation status in the progression of myelodysplastic syndrome and chronic myelomonocytic leukemia to acute myeloid leukemia. Clin Cancer Res 2005; 11: 1821-1826.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 1821-1826
-
-
Shih, L.Y.1
Huang, C.F.2
Lin, T.L.3
Wu, J.H.4
Wang, P.N.5
Dunn, P.6
-
9
-
-
0030061554
-
AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis
-
Okuda T, van Deursen J, Hiebert SW, Grosveld G, Downing JR. AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis. Cell 1996; 84 321-330.
-
(1996)
Cell
, vol.84
, pp. 321-330
-
-
Okuda, T.1
van Deursen, J.2
Hiebert, S.W.3
Grosveld, G.4
Downing, J.R.5
-
10
-
-
0029918597
-
Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis
-
Wang Q, Stacy T, Binder M, Marin-Padilla M, Sharpe AH, Speck NA. Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis. Proc Natl Acad Sci USA 1996; 93: 3444-3449.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 3444-3449
-
-
Wang, Q.1
Stacy, T.2
Binder, M.3
Marin-Padilla, M.4
Sharpe, A.H.5
Speck, N.A.6
-
11
-
-
0037321711
-
The role of a Runt domain transcription factor AML1/RUNX1 in leukemogenesis and its clinical implications
-
Asou N. The role of a Runt domain transcription factor AML1/RUNX1 in leukemogenesis and its clinical implications. Crit Rev Oncol Hematol 2003; 45: 129-150.
-
(2003)
Crit Rev Oncol Hematol
, vol.45
, pp. 129-150
-
-
Asou, N.1
-
12
-
-
0036636857
-
Core-binding factors in haematopoiesis and leukaemia
-
Speck NA, Gilliland DG. Core-binding factors in haematopoiesis and leukaemia. Nat Rev Cancer 2002; 2: 502-513.
-
(2002)
Nat Rev Cancer
, vol.2
, pp. 502-513
-
-
Speck, N.A.1
Gilliland, D.G.2
-
13
-
-
0033559746
-
Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias
-
Osato M, Asou N, Abdalla E, Hoshino K, Yamasaki H, Okubo T et al. Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias. Blood 1999; 93: 1817-1824.
-
(1999)
Blood
, vol.93
, pp. 1817-1824
-
-
Osato, M.1
Asou, N.2
Abdalla, E.3
Hoshino, K.4
Yamasaki, H.5
Okubo, T.6
-
14
-
-
0037441589
-
M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: A report of 59 cases by the Groupe Francais d'Hematologie Cellulaire (GFHC) and the Groupe Francais de Cytogenetique Hematologique (GFCH)
-
Roumier C, Eclache V, Imbert M, Davi F, MacIntyre E, Garand R et al M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: A report of 59 cases by the Groupe Francais d'Hematologie Cellulaire (GFHC) and the Groupe Francais de Cytogenetique Hematologique (GFCH). Blood 2003; 101: 1277-1283.
-
(2003)
Blood
, vol.101
, pp. 1277-1283
-
-
Roumier, C.1
Eclache, V.2
Imbert, M.3
Davi, F.4
MacIntyre, E.5
Garand, R.6
-
15
-
-
0037438508
-
Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia
-
Harada H, Harada Y, Tanaka H, Kimura A, Inaba T. Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia. Blood 2003; 101: 673-680.
-
(2003)
Blood
, vol.101
, pp. 673-680
-
-
Harada, H.1
Harada, Y.2
Tanaka, H.3
Kimura, A.4
Inaba, T.5
-
16
-
-
4444302228
-
Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation
-
Christiansen DH, Andersen MK, Pedersen-Bjergaard J. Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation. Blood 2004; 104: 1474-1481.
-
(2004)
Blood
, vol.104
, pp. 1474-1481
-
-
Christiansen, D.H.1
Andersen, M.K.2
Pedersen-Bjergaard, J.3
-
17
-
-
1542373639
-
High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia
-
Harada H, Harada Y, Niimi H, Kyo T, Kimura A, Inaba T. High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia. Blood 2004; 103: 2316-2324.
-
(2004)
Blood
, vol.103
, pp. 2316-2324
-
-
Harada, H.1
Harada, Y.2
Niimi, H.3
Kyo, T.4
Kimura, A.5
Inaba, T.6
-
18
-
-
12444314088
-
Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia
-
Steensma DP, Gibbons RJ, Mesa RA, Tefferi A, Higgs DR. Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia. Eur J Haematol 2005; 74: 47-53.
-
(2005)
Eur J Haematol
, vol.74
, pp. 47-53
-
-
Steensma, D.P.1
Gibbons, R.J.2
Mesa, R.A.3
Tefferi, A.4
Higgs, D.R.5
-
19
-
-
3042541853
-
Novel loss-of-function mutations of the haematopoiesis-related transcription factor, acute myeloid leukaemia 1/ runt-related transcription factor 1, detected in acute myeloblastic leukaemia and myelodysplastic syndrome
-
Nakao M, Horiike S, Fukushima-Nakase Y, Nishimura M, Fujita Y, Taniwaki M et al. Novel loss-of-function mutations of the haematopoiesis-related transcription factor, acute myeloid leukaemia 1/ runt-related transcription factor 1, detected in acute myeloblastic leukaemia and myelodysplastic syndrome. Br J Haematol 2004; 125 709-719.
-
(2004)
Br J Haematol
, vol.125
, pp. 709-719
-
-
Nakao, M.1
Horiike, S.2
Fukushima-Nakase, Y.3
Nishimura, M.4
Fujita, Y.5
Taniwaki, M.6
-
20
-
-
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
-
21
-
-
0030897009
-
International scoring system for evaluating prognosis in myelodysplastic syndromes
-
Greenberg P, Cox C, LeBeau MM, Fenaux P, Morel P, Sanz G et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 1997; 89: 2079-2088.
-
(1997)
Blood
, vol.89
, pp. 2079-2088
-
-
Greenberg, P.1
Cox, C.2
LeBeau, M.M.3
Fenaux, P.4
Morel, P.5
Sanz, G.6
-
22
-
-
0036786289
-
Internal tandem duplication of FLT3 in relapsed acute myeloid leukemia: A comparative analysis of bone marrow samples from 108 adult patients at diagnosis and relapse
-
Shih LY, Huang CF, Wu JH, Lin TL, Dunn P, Wang PN et al. Internal tandem duplication of FLT3 in relapsed acute myeloid leukemia: A comparative analysis of bone marrow samples from 108 adult patients at diagnosis and relapse. Blood 2002; 100: 2387-2392.
-
(2002)
Blood
, vol.100
, pp. 2387-2392
-
-
Shih, L.Y.1
Huang, C.F.2
Wu, J.H.3
Lin, T.L.4
Dunn, P.5
Wang, P.N.6
-
23
-
-
0033616725
-
Crystal structure of a thermostable type B DNA polymerase from Thermococcus gorgonarius
-
Hopfner KP, Eichinger A, Engh RA, Laue F, Ankenbauer W, Huber R et al Crystal structure of a thermostable type B DNA polymerase from Thermococcus gorgonarius. Proc Natl Acad Sci USA 1999; 96: 3600-3605.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 3600-3605
-
-
Hopfner, K.P.1
Eichinger, A.2
Engh, R.A.3
Laue, F.4
Ankenbauer, W.5
Huber, R.6
-
24
-
-
0032830638
-
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
-
Song WJ, 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
-
25
-
-
0034332068
-
Mutations of the AML1 gene in myelodysplastic syndrome and their functional implications in leukemogenesis
-
Imai Y, Kurokawa M, Izutsu K, Hangaishi A, Takeuchi K, Maki K et al Mutations of the AML1 gene in myelodysplastic syndrome and their functional implications in leukemogenesis. Blood 2000; 96: 3154-3160.
-
(2000)
Blood
, vol.96
, pp. 3154-3160
-
-
Imai, Y.1
Kurokawa, M.2
Izutsu, K.3
Hangaishi, A.4
Takeuchi, K.5
Maki, K.6
-
26
-
-
34548044732
-
Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia
-
Dicker F, Haferlach C, Kern W, Haferlach T, Schnittger S. Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia. Blood 2007; 110: 1308-1316.
-
(2007)
Blood
, vol.110
, pp. 1308-1316
-
-
Dicker, F.1
Haferlach, C.2
Kern, W.3
Haferlach, T.4
Schnittger, S.5
-
27
-
-
0036124315
-
Mutational analyses of the AML1 gene in patients with myelodysplastic syndrome
-
Imai O, Kurokawa M, Izutsu K, Hangaishi A, Maki K, Ogawa S et al. Mutational analyses of the AML1 gene in patients with myelodysplastic syndrome. Leuk Lymphoma 2002; 43: 617-621.
-
(2002)
Leuk Lymphoma
, vol.43
, pp. 617-621
-
-
Imai, O.1
Kurokawa, M.2
Izutsu, K.3
Hangaishi, A.4
Maki, K.5
Ogawa, S.6
-
28
-
-
0037082499
-
In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: Implications for mechanisms of pathogenesis
-
Michaud J, Wu F, Osato M, Cottles GM, Yanagida M, Asou N et al. In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: Implications for mechanisms of pathogenesis. Blood 2002; 99: 1364-1372.
-
(2002)
Blood
, vol.99
, pp. 1364-1372
-
-
Michaud, J.1
Wu, F.2
Osato, M.3
Cottles, G.M.4
Yanagida, M.5
Asou, N.6
-
29
-
-
33644881695
-
Point mutations in the AML1/RUNX1 gene associated with myelodysplastic syndrome
-
Harada H, Harada Y. Point mutations in the AML1/RUNX1 gene associated with myelodysplastic syndrome. Crit Rev Eukartyot Gene Expr 2005; 15: 183-196.
-
(2005)
Crit Rev Eukartyot Gene Expr
, vol.15
, pp. 183-196
-
-
Harada, H.1
Harada, Y.2
-
30
-
-
0031940065
-
Intrinsic transcriptional activation-inhibition domains of the polyomavirus enhancer binding protein 2/core binding factor alpha subunit revealed in the presence of the beta subunit
-
Kanno T, Kanno Y, Chen LF, Ogawa E, Kim WY, Ito Y. Intrinsic transcriptional activation-inhibition domains of the polyomavirus enhancer binding protein 2/core binding factor alpha subunit revealed in the presence of the beta subunit. Mol Cell Biol 1998; 18: 2444-2454.
-
(1998)
Mol Cell Biol
, vol.18
, pp. 2444-2454
-
-
Kanno, T.1
Kanno, Y.2
Chen, L.F.3
Ogawa, E.4
Kim, W.Y.5
Ito, Y.6
-
32
-
-
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, Grardel-Duflos N, Garand R, Lai JL 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
Grardel-Duflos, N.4
Garand, R.5
Lai, J.L.6
|