-
1
-
-
0038470905
-
Molecular mechanisms of myelodysplastic syndrome
-
DOI 10.1093/jjco/hyg037
-
Hirai H. Molecular mechanisms of myelodysplastic syndrome. Jpn J Clin Oncol 2003; 33: 153-160. (Pubitemid 43102857)
-
(2003)
Japanese Journal of Clinical Oncology
, vol.33
, Issue.4
, pp. 153-160
-
-
Hirai, H.1
-
2
-
-
0032523011
-
Methylation of the p15(INK4b) gene in myelodysplastic syndromes is frequent and acquired during disease progression
-
Quesnel B, Guillerm G, Vereecque R, Wattel E, Preudhomme C, Bauters F et al. Methylation of the p15(INK4b) gene in myelodysplastic syndromes is frequent and acquired during disease progression. Blood 1998; 91: 2985-2990. (Pubitemid 28227550)
-
(1998)
Blood
, vol.91
, Issue.8
, pp. 2985-2990
-
-
Quesnel, B.1
Guillerm, G.2
Vereecque, R.3
Wattel, E.4
Preudhomme, C.5
Bauters, F.6
Vanrumbeke, M.7
Fenaux, P.8
-
3
-
-
0027247412
-
Mutations of the p53 gene in myelodysplastic syndrome (MDS) and MDS- derived leukemia
-
Sugimoto K, Hirano N, Toyoshima H, Chiba S, Mano H, Takaku F et al. Mutations of the p53 gene in myelodysplastic syndrome (MDS) and MDS-derived leukemia. Blood 1993; 81: 3022-3026. (Pubitemid 23162121)
-
(1993)
Blood
, vol.81
, Issue.11
, pp. 3022-3026
-
-
Sugimoto, K.1
Hirano, N.2
Toyoshima, H.3
Chiba, S.4
Mano, H.5
Takaku, F.6
Yazaki, Y.7
Hirai, H.8
-
4
-
-
0028065441
-
Expression of EVI1 in myelodysplastic syndromes and other hematologic malignancies without 3q26 translocations
-
Russell M, List A, Greenberg P, Woodward S, Glinsmann B, Parganas E et al. Expression of EVI1 in myelodysplastic syndromes and other hematologic malignancies without 3q26 translocations. Blood 1994; 84: 1243-1248.
-
(1994)
Blood
, vol.84
, pp. 1243-1248
-
-
Russell, M.1
List, A.2
Greenberg, P.3
Woodward, S.4
Glinsmann, B.5
Parganas, E.6
-
5
-
-
65549139174
-
Molecular pathways mediating MDS/AML with focus on AML1/RUNX1 point mutations
-
Harada Y, Harada H. Molecular pathways mediating MDS/AML with focus on AML1/RUNX1 point mutations. J Cell Physiol 2009; 220: 16-20.
-
(2009)
J Cell Physiol
, vol.220
, pp. 16-20
-
-
Harada, Y.1
Harada, H.2
-
6
-
-
0030071926
-
The t(3;5)(q25.1;q34) of myelodysplastic syndrome and acute myeloid leukemia produces a novel fusion gene, NPM-MLF1
-
Yoneda-Kato N, Look AT, Kirstein MN, Valentine MB, Raimondi SC, Cohen KJ et al. The t(3;5)(q25.1;q34) of myelodysplastic syndrome and acute myeloid leukemia produces a novel fusion gene, NPM-MLF1. Oncogene 1996; 12: 265-275. (Pubitemid 26042564)
-
(1996)
Oncogene
, vol.12
, Issue.2
, pp. 265-275
-
-
Yoneda-Kato, N.1
Look, A.T.2
Kirstein, M.N.3
Valentine, M.B.4
Raimondi, S.C.5
Cohen, K.J.6
Carroll, A.J.7
Morris, S.W.8
-
7
-
-
66249137734
-
Mutation in TET2 in myeloid cancers
-
Delhommeau F, Dupont S, Della Valle V, James C, Trannoy S, Masse A et al. Mutation in TET2 in myeloid cancers. N Engl J Med 2009; 360: 2289-2301.
-
(2009)
N Engl J Med
, vol.360
, pp. 2289-2301
-
-
Delhommeau, F.1
Dupont, S.2
Della Valle, V.3
James, C.4
Trannoy, S.5
Masse, A.6
-
8
-
-
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. (Pubitemid 37328932)
-
(2002)
Nature Reviews Cancer
, vol.2
, Issue.7
, pp. 502-513
-
-
Speck, N.A.1
Gilliland, D.G.2
-
9
-
-
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, Liu CY, Chou WC, Tseng MH 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: 5352-5361.
-
(2009)
Blood
, vol.114
, pp. 5352-5361
-
-
Tang, J.L.1
Hou, H.A.2
Chen, C.Y.3
Liu, C.Y.4
Chou, W.C.5
Tseng, M.H.6
-
10
-
-
0032830638
-
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
-
DOI 10.1038/13793
-
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. (Pubitemid 29455388)
-
(1999)
Nature Genetics
, vol.23
, Issue.2
, pp. 166-175
-
-
Song, W.-J.1
Sullivan, M.G.2
Legare, R.D.3
Hutchings, S.4
Tan, X.5
Kufrin, D.6
Ratajczak, J.7
Resende, I.C.8
Haworth, C.9
Hock, R.10
Loh, M.11
Felix, C.12
Roy, R.-C.13
Busque, L.14
Kurnit, D.15
Willman, C.16
Gewirtz, A.M.17
Speck, N.A.18
Bushweller, J.H.19
Li, F.P.20
Gardiner, K.21
Poncz, M.22
Maris, J.M.23
Gilliland, D.G.24
more..
-
11
-
-
2342451948
-
AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not for maintenance of hematopoietic stem cells in adult hematopoiesis
-
DOI 10.1038/nm997
-
Ichikawa M, Asai T, Saito T, Seo S, Yamazaki I, Yamagata T et al. AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not for maintenance of hematopoietic stem cells in adult hematopoiesis. Nat Med 2004; 10: 299-304. (Pubitemid 38667622)
-
(2004)
Nature Medicine
, vol.10
, Issue.3
, pp. 299-304
-
-
Ichikawa, M.1
Asai, T.2
Saito, T.3
Yamamoto, G.4
Seo, S.5
Yamazaki, I.6
Yamagata, T.7
Mitani, K.8
Chiba, S.9
Hirai, H.10
Ogawa, S.11
Kurokawa, M.12
-
12
-
-
0036463950
-
Expression of a conditional AML1-ETO oncogene bypasses embryonic lethality and establishes a murine model of human t(8;21) acute myeloid leukemia
-
DOI 10.1016/S1535-6108(02)00016-8
-
Higuchi M, O'Brien D, Kumaravelu P, Lenny N, Yeoh EJ, Downing JR. Expression of a conditional AML1-ETO oncogene bypasses embryonic lethality and establishes a murine model of human t(8;21) acute myeloid leukemia. Cancer Cell 2002; 1: 63-74. (Pubitemid 41039177)
-
(2002)
Cancer Cell
, vol.1
, Issue.1
, pp. 63-74
-
-
Higuchi, M.1
O'Brien, D.2
Kumaravelu, P.3
Lenny, N.4
Yeoh, E.-J.5
Downing, J.R.6
-
13
-
-
70350504453
-
The DNA-damage response in human biology and disease
-
Jackson SP, Bartek J. The DNA-damage response in human biology and disease. Nature 2009; 461: 1071-1078.
-
(2009)
Nature
, vol.461
, pp. 1071-1078
-
-
Jackson, S.P.1
Bartek, J.2
-
15
-
-
0035902108
-
Genome maintenance mechanisms for preventing cancer
-
DOI 10.1038/35077232
-
Hoeijmakers JH. Genome maintenance mechanisms for preventing cancer. Nature 2001; 411: 366-374. (Pubitemid 32467046)
-
(2001)
Nature
, vol.411
, Issue.6835
, pp. 366-374
-
-
Hoeijmakers, J.H.J.1
-
16
-
-
27744505649
-
Runx1 deficiency predisposes mice to T-lymphoblastic lymphoma
-
DOI 10.1182/blood-2005-04-1447
-
Kundu M, Compton S, Garrett-Beal L, Stacy T, Starost MF, Eckhaus M et al. Runx1 deficiency predisposes mice to T-lymphoblastic lymphoma. Blood 2005; 106: 3621-3624. (Pubitemid 41609202)
-
(2005)
Blood
, vol.106
, Issue.10
, pp. 3621-3624
-
-
Kundu, M.1
Compton, S.2
Garrett-Beal, L.3
Stacy, T.4
Starost, M.F.5
Eckhaus, M.6
Speck, N.A.7
Liu, P.P.8
-
18
-
-
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. (Pubitemid 12073508)
-
(1982)
British Journal of Haematology
, vol.51
, Issue.2
, pp. 189-199
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
-
19
-
-
1542373639
-
High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia
-
DOI 10.1182/blood-2003-09-3074
-
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. (Pubitemid 38326252)
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2316-2324
-
-
Harada, H.1
Harada, Y.2
Niimi, H.3
Kyo, T.4
Kimura, A.5
Inaba, T.6
-
20
-
-
57649194907
-
AML1/RUNX1 works as a negative regulator of c-Mpl in hematopoietic stem cells
-
Satoh Y, Matsumura I, Tanaka H, Ezoe S, Fukushima K, Tokunaga M et al. AML1/RUNX1 works as a negative regulator of c-Mpl in hematopoietic stem cells. J Biol Chem 2008; 283: 30045-30056.
-
(2008)
J Biol Chem
, vol.283
, pp. 30045-30056
-
-
Satoh, Y.1
Matsumura, I.2
Tanaka, H.3
Ezoe, S.4
Fukushima, K.5
Tokunaga, M.6
-
21
-
-
0037438508
-
Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia
-
DOI 10.1182/blood-2002-04-1010
-
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. (Pubitemid 36077592)
-
(2003)
Blood
, vol.101
, Issue.2
, pp. 673-680
-
-
Harada, H.1
Harada, Y.2
Tanaka, H.3
Kimura, A.4
Inaba, T.5
-
22
-
-
0028837972
-
An acute myeloid leukemia gene, AML1, regulates hemopoietic myeloid cell differentiation and transcriptional activation antagonistically by two alternative spliced forms
-
Tanaka T, Tanaka K, Ogawa S, Kurokawa M, Mitani K, Nishida J et al. An acute myeloid leukemia gene, AML1, regulates hemopoietic myeloid cell differentiation and transcriptional activation antagonistically by two alternative spliced forms. EMBO J 1995; 14: 341-350.
-
(1995)
EMBO J
, vol.14
, pp. 341-350
-
-
Tanaka, T.1
Tanaka, K.2
Ogawa, S.3
Kurokawa, M.4
Mitani, K.5
Nishida, J.6
-
23
-
-
0032489520
-
DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139
-
DOI 10.1074/jbc.273.10.5858
-
Rogakou EP, Pilch DR, Orr AH, Ivanova VS, Bonner WM. DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139. J Biol Chem 1998; 273: 5858-5868. (Pubitemid 28124064)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.10
, pp. 5858-5868
-
-
Rogakou, E.P.1
Pilch, D.R.2
Orr, A.H.3
Ivanova, V.S.4
Bonner, W.M.5
-
24
-
-
77950961695
-
Karagiannis TC. gammaH2AX: A sensitive molecular marker of DNA damage and repair
-
Mah LJ, El-Osta A, Karagiannis TC. gammaH2AX: a sensitive molecular marker of DNA damage and repair. Leukemia 2010; 24: 679-686.
-
(2010)
Leukemia
, vol.24
, pp. 679-686
-
-
Mah, L.J.1
El-Osta, A.2
-
25
-
-
29244435019
-
Multiple repair pathways mediate tolerance to chemotherapeutic cross-linking agents in vertebrate cells
-
DOI 10.1158/0008-5472.CAN-05-1214
-
Nojima K, Hochegger H, Saberi A, Fukushima T, Kikuchi K, Yoshimura M et al. Multiple repair pathways mediate tolerance to chemotherapeutic cross-linking agents in vertebrate cells. Cancer Res 2005; 65: 11704-11711. (Pubitemid 41821731)
-
(2005)
Cancer Research
, vol.65
, Issue.24
, pp. 11704-11711
-
-
Nojima, K.1
Hochegger, H.2
Saberi, A.3
Fukushima, T.4
Kikuchi, K.5
Yoshimura, M.6
Orelli, B.J.7
Bishop, D.K.8
Hirano, S.9
Ohzeki, M.10
Ishiai, M.11
Yamamoto, K.12
Takata, M.13
Arakawa, H.14
Buerstedde, J.-M.15
Yamazoe, M.16
Kawamoto, T.17
Araki, K.18
Takahashi, J.A.19
Hashimoto, N.20
Takeda, S.21
Sonoda, E.22
more..
-
26
-
-
0026201399
-
Simultaneous establishment of monoclonal antibodies specific for either cyclobutane pyrimidine dimer or (6-4)photoproduct from the same mouse immunized with ultraviolet-irradiated DNA
-
Mori T, Nakane M, Hattori T, Matsunaga T, Ihara M, Nikaido O. Simultaneous establishment of monoclonal antibodies specific for either cyclobutane pyrimidine dimer or (6-4)photoproduct from the same mouse immunized with ultraviolet-irradiated DNA. Photochem Photobiol 1991; 54: 225-232.
-
(1991)
Photochem Photobiol
, Issue.54
, pp. 225-232
-
-
Mori, T.1
Nakane, M.2
Hattori, T.3
Matsunaga, T.4
Ihara, M.5
Nikaido, O.6
-
27
-
-
64849100952
-
Repression of Gadd45alpha by activated FLT3 and GM-CSF receptor mutants contributes to growth, survival and blocked differentiation
-
Perugini M, Kok CH, Brown AL, Wilkinson CR, Salerno DG, Young SM et al. Repression of Gadd45alpha by activated FLT3 and GM-CSF receptor mutants contributes to growth, survival and blocked differentiation. Leukemia 2009; 23: 729-738.
-
(2009)
Leukemia
, vol.23
, pp. 729-738
-
-
Perugini, M.1
Kok, C.H.2
Brown, A.L.3
Wilkinson, C.R.4
Salerno, D.G.5
Young, S.M.6
-
28
-
-
0027435261
-
Analysis of the mammalian gadd45 gene and its response to DNA damage
-
Hollander MC, Alamo I, Jackman J, Wang MG, McBride OW, Fornace Jr AJ. Analysis of the mammalian gadd45 gene and its response to DNA damage. J Biol Chem 1993; 268: 24385-24393. (Pubitemid 23335431)
-
(1993)
Journal of Biological Chemistry
, vol.268
, Issue.32
, pp. 24385-24393
-
-
Hollander, M.C.1
Alamo, I.2
Jackman, J.3
Wang, M.G.4
McBride, O.W.5
Fornace Jr., A.J.6
-
29
-
-
0026496885
-
A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia
-
Kastan MB, Zhan Q, el-Deiry WS, Carrier F, Jacks T, Walsh WV et al. A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia. Cell 1992; 71: 587-597.
-
(1992)
Cell
, vol.71
, pp. 587-597
-
-
Kastan, M.B.1
Zhan, Q.2
El-Deiry, W.S.3
Carrier, F.4
Jacks, T.5
Walsh, W.V.6
-
30
-
-
0344604528
-
Genomic instability in Gadd45a-deficient mice
-
DOI 10.1038/13802
-
Hollander MC, Sheikh MS, Bulavin DV, Lundgren K, Augeri-Henmueller L, Shehee R et al. Genomic instability in Gadd45a-deficient mice. Nat Genet 1999; 23: 176-184. (Pubitemid 29455389)
-
(1999)
Nature Genetics
, vol.23
, Issue.2
, pp. 176-184
-
-
Hollander, M.C.1
Sheikh, M.S.2
Bulavin, D.V.3
Lundgren, K.4
Augeri-Henmueller, L.5
Shehee, R.6
Molinaro, T.A.7
Kim, K.E.8
Tolosa, E.9
Ashwell, J.D.10
Rosenberg, M.P.11
Zhan, Q.12
Fernandez-Salguero, P.M.13
Morgan, W.F.14
Deng, C.-X.15
Fornace Jr., A.J.16
-
31
-
-
33644807219
-
Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice
-
DOI 10.1111/j.1365-2141.2005.05793.x
-
Yamashita N, Osato M, Huang L, Yanagida M, Kogan SC, Iwasaki M et al. Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice. Br J Haematol 2005; 131: 495-507. (Pubitemid 43899649)
-
(2005)
British Journal of Haematology
, vol.131
, Issue.4
, pp. 495-507
-
-
Yamashita, N.1
Osato, M.2
Huang, L.3
Yanagida, M.4
Kogan, S.C.5
Iwasaki, M.6
Nakamura, T.7
Shigesada, K.8
Asou, N.9
Ito, Y.10
-
32
-
-
41349122682
-
P53 signaling in response to increased DNA damage sensitizes AML1-ETO cells to stress-induced death
-
DOI 10.1182/blood-2007-06-093682
-
Krejci O, Wunderlich M, Geiger H, Chou FS, Schleimer D, Jansen M et al. p53 signaling in response to increased DNA damage sensitizes AML1-ETO cells to stress-induced death. Blood 2008; 111: 2190-2199. (Pubitemid 351451533)
-
(2008)
Blood
, vol.111
, Issue.4
, pp. 2190-2199
-
-
Krejci, O.1
Wunderlich, M.2
Geiger, H.3
Chou, F.-S.4
Schleimer, D.5
Jansen, M.6
Andreassen, P.R.7
Mulloy, J.C.8
-
33
-
-
0347951358
-
Acute myeloid leukemia fusion proteins deregulate genes involved in stem cell maintenance and DNA repair
-
DOI 10.1172/JCI200317595
-
Alcalay M, Meani N, Gelmetti V, Fantozzi A, Fagioli M, Orleth A et al. Acute myeloid leukemia fusion proteins deregulate genes involved in stem cell maintenance and DNA repair. J Clin Invest 2003; 112: 1751-1761. (Pubitemid 38063733)
-
(2003)
Journal of Clinical Investigation
, vol.112
, Issue.11
, pp. 1751-1761
-
-
Alcalay, M.1
Meani, N.2
Gelmetti, V.3
Fantozzi, A.4
Fagioli, M.5
Orleth, A.6
Riganelli, D.7
Sebastiani, C.8
Cappelli, E.9
Casciari, C.10
Sciurpi, M.T.11
Mariano, A.R.12
Minardi, S.P.13
Luzi, L.14
Muller, H.15
Di Fiore, P.P.16
Frosina, G.17
Pelicci, P.G.18
-
34
-
-
0036324977
-
GADD45b and GADD45g are cdc2/cyclinB1 kinase inhibitors with a role in S and G2/M cell cycle checkpoints induced by genotoxic stress
-
DOI 10.1002/jcp.10140
-
Vairapandi M, Balliet AG, Hoffman B, Liebermann DA. GADD45b and GADD45g are cdc2/cyclinB1 kinase inhibitors with a role in S and G2/M cell cycle checkpoints induced by genotoxic stress. J Cell Physiol 2002; 192: 327-338. (Pubitemid 34827609)
-
(2002)
Journal of Cellular Physiology
, vol.192
, Issue.3
, pp. 327-338
-
-
Vairapandi, M.1
Balliet, A.G.2
Hoffman, B.3
Liebermann, D.A.4
-
35
-
-
0028569767
-
Interaction of the p53-regulated protein Gadd45 with proliferating cell nuclear antigen
-
Smith ML, Chen IT, Zhan Q, Bae I, Chen CY, Gilmer TM et al. Interaction of the p53-regulated protein Gadd45 with proliferating cell nuclear antigen. Science 1994; 266: 1376-1380.
-
(1994)
Science
, vol.266
, pp. 1376-1380
-
-
Smith, M.L.1
Chen, I.T.2
Zhan, Q.3
Bae, I.4
Chen, C.Y.5
Gilmer, T.M.6
-
36
-
-
0034053780
-
P53-mediated DNA repair responses to UV radiation: Studies of mouse cells lacking p53, p21, and/or gadd45 genes
-
DOI 10.1128/MCB.20.10.3705-3714.2000
-
Smith ML, Ford JM, Hollander MC, Bortnick RA, Amundson SA, Seo YR et al. p53-mediated DNA repair responses to UV radiation: studies of mouse cells lacking p53, p21, and/or gadd45 genes. Mol Cell Biol 2000; 20: 3705-3714. (Pubitemid 30243916)
-
(2000)
Molecular and Cellular Biology
, vol.20
, Issue.10
, pp. 3705-3714
-
-
Smith, M.L.1
Ford, J.M.2
Hollander, M.C.3
Bortnick, R.A.4
Amundson, S.A.5
Seo, Y.R.6
Deng, C.-X.7
Hanawalt, P.C.8
Fornace Jr., A.J.9
-
37
-
-
27944502181
-
Hematopoietic cells from Gadd45a- and Gadd45b-deficient mice are sensitized to genotoxic-stress-induced apoptosis
-
DOI 10.1038/sj.onc.1208847, PII 1208847
-
Gupta M, Gupta SK, Balliet AG, Hollander MC, Fornace AJ, Hoffman B et al. Hematopoietic cells from Gadd45a-and Gadd45b-deficient mice are sensitized to genotoxic-stress-induced apoptosis. Oncogene 2005; 24: 7170-7179. (Pubitemid 41679279)
-
(2005)
Oncogene
, vol.24
, Issue.48
, pp. 7170-7179
-
-
Gupta, M.1
Gupta, S.K.2
Balliet, A.G.3
Hollander, M.C.4
Fornace Jr., A.J.5
Hoffman, B.6
Liebermann, D.A.7
-
38
-
-
12444314088
-
Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia
-
DOI 10.1111/j.1600-0609.2004.00363.x
-
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. (Pubitemid 40143686)
-
(2005)
European Journal of Haematology
, vol.74
, Issue.1
, pp. 47-53
-
-
Steensma, D.P.1
Gibbons, R.J.2
Mesa, R.A.3
Tefferi, A.4
Higgs, D.R.5
-
39
-
-
34848824979
-
RUNX1 gene mutation in primary myelodysplastic syndrome - The mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome
-
DOI 10.1111/j.1365-2141.2007.06811.x
-
Chen CY, Lin LI, Tang JL, Ko BS, Tsay W, Chou WC et al. RUNX1 gene mutation in primary myelodysplastic syndromeFthe mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome. Br J Haematol 2007; 139: 405-414. (Pubitemid 47512182)
-
(2007)
British Journal of Haematology
, vol.139
, Issue.3
, pp. 405-414
-
-
Chen, C.-Y.1
Lin, L.-I.2
Tang, J.-L.3
Ko, B.-S.4
Tsay, W.5
Chou, W.-C.6
Yao, M.7
Wu, S.-J.8
Tseng, M.-H.9
Tien, H.-F.10
|