-
1
-
-
84870221419
-
The genetic basis of phenotypic heterogeneity in myelodysplastic syndromes
-
Raza A, Galili N. The genetic basis of phenotypic heterogeneity in myelodysplastic syndromes. Nat Rev Cancer 2012; 12: 849-859.
-
(2012)
Nat Rev Cancer
, vol.12
, pp. 849-859
-
-
Raza, A.1
Galili, N.2
-
2
-
-
46749151451
-
Myelodysplastic syndromes
-
Nimer SD. Myelodysplastic syndromes. Blood 2008; 111: 4841-4851.
-
(2008)
Blood
, vol.111
, pp. 4841-4851
-
-
Nimer, S.D.1
-
3
-
-
84891301466
-
The genetic basis of myelodysplasia and its clinical relevance
-
Cazzola M, Della Porta MG, Malcovati L. The genetic basis of myelodysplasia and its clinical relevance. Blood 2013; 122: 4021-4034.
-
(2013)
Blood
, vol.122
, pp. 4021-4034
-
-
Cazzola, M.1
Della Porta, M.G.2
Malcovati, L.3
-
4
-
-
84888219405
-
Clinical and biological implications of driver mutations in myelodysplastic syndromes
-
Papaemmanuil E, Gerstung M, Malcovati L, Tauro S, Gundem G, Van Loo P et al. Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood 2013; 122: 3616-3627.
-
(2013)
Blood
, vol.122
, pp. 3616-3627
-
-
Papaemmanuil, E.1
Gerstung, M.2
Malcovati, L.3
Tauro, S.4
Gundem, G.5
Van Loo, P.6
-
5
-
-
79952164235
-
Unraveling the molecular pathophysiology of myelodysplastic syndromes
-
Bejar R, Levine R, Ebert BL. Unraveling the molecular pathophysiology of myelodysplastic syndromes. J Clin Oncol 2011; 29: 504-515.
-
(2011)
J Clin Oncol
, vol.29
, pp. 504-515
-
-
Bejar, R.1
Levine, R.2
Ebert, B.L.3
-
6
-
-
66249137734
-
Mutation in TET2 in myeloid cancers
-
Delhommeau F, Dupont S, Della Valle V, James C, Trannoy S, Massé 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
Massé, A.6
-
7
-
-
67649876132
-
Acquired mutations in TET2 are common in myelodysplastic syndromes
-
Langemeijer SM, Kuiper RP, Berends M, Knops R, Aslanyan MG, Massop M et al. Acquired mutations in TET2 are common in myelodysplastic syndromes. Nat Genet 2009; 41: 838-842.
-
(2009)
Nat Genet
, vol.41
, pp. 838-842
-
-
Langemeijer, S.M.1
Kuiper, R.P.2
Berends, M.3
Knops, R.4
Aslanyan, M.G.5
Massop, M.6
-
8
-
-
79959794787
-
Clinical effect of point mutations in myelodysplastic syndromes
-
Bejar R, Stevenson K, Abdel-Wahab O, Galili N, Nilsson B, Garcia-Manero G et al. Clinical effect of point mutations in myelodysplastic syndromes. N Engl J Med 2011; 364: 2496-2506.
-
(2011)
N Engl J Med
, vol.364
, pp. 2496-2506
-
-
Bejar, R.1
Stevenson, K.2
Abdel-Wahab, O.3
Galili, N.4
Nilsson, B.5
Garcia-Manero, G.6
-
9
-
-
84866749552
-
Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes
-
Bejar R, Stevenson KE, Caughey BA, Abdel-Wahab O, Steensma DP, Galili N et al. Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes. J Clin Oncol 2012; 30: 3376-3382.
-
(2012)
J Clin Oncol
, vol.30
, pp. 3376-3382
-
-
Bejar, R.1
Stevenson, K.E.2
Caughey, B.A.3
Abdel-Wahab, O.4
Steensma, D.P.5
Galili, N.6
-
10
-
-
80053900941
-
Frequent pathway mutations of splicing machinery in myelodysplasia
-
Yoshida K, Sanada M, Shiraishi Y, Nowak D, Nagata Y, Yamamoto R et al. Frequent pathway mutations of splicing machinery in myelodysplasia. Nature 2011; 478: 64-69.
-
(2011)
Nature
, vol.478
, pp. 64-69
-
-
Yoshida, K.1
Sanada, M.2
Shiraishi, Y.3
Nowak, D.4
Nagata, Y.5
Yamamoto, R.6
-
11
-
-
84555192302
-
Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes
-
Graubert TA, Shen D, Ding L, Okeyo-Owuor T, Lunn CL, Shao J et al. Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes. Nat Genet 2012; 44: 53-57.
-
(2012)
Nat Genet
, vol.44
, pp. 53-57
-
-
Graubert, T.A.1
Shen, D.2
Ding, L.3
Okeyo-Owuor, T.4
Lunn, C.L.5
Shao, J.6
-
12
-
-
84874626718
-
Smap1 deficiency perturbs receptor trafficking and predisposes mice to myelodysplasia
-
Kon S, Minegishi N, Tanabe K, Watanabe T, Funaki T, Wong WF et al. Smap1 deficiency perturbs receptor trafficking and predisposes mice to myelodysplasia. J Clin Invest 2013; 123: 1123-1137.
-
(2013)
J Clin Invest
, vol.123
, pp. 1123-1137
-
-
Kon, S.1
Minegishi, N.2
Tanabe, K.3
Watanabe, T.4
Funaki, T.5
Wong, W.F.6
-
13
-
-
84885834757
-
Epigenetic aspects of MDS and its molecular targeted therapy
-
Yamazaki J, Issa JP. Epigenetic aspects of MDS and its molecular targeted therapy. Int J Hematol 2013; 97: 175-182.
-
(2013)
Int J Hematol
, vol.97
, pp. 175-182
-
-
Yamazaki, J.1
Issa, J.P.2
-
14
-
-
84887462456
-
Myelodysplastic syndromes are induced by histone methylation-altering ASXL1 mutations
-
Inoue D, Kitaura J, Togami K, Nishimura K, Enomoto Y, Uchida T et al. Myelodysplastic syndromes are induced by histone methylation-altering ASXL1 mutations. J Clin Invest 2013; 123: 4627-4640.
-
(2013)
J Clin Invest
, vol.123
, pp. 4627-4640
-
-
Inoue, D.1
Kitaura, J.2
Togami, K.3
Nishimura, K.4
Enomoto, Y.5
Uchida, T.6
-
15
-
-
84888083126
-
Concurrent loss of Ezh2 and Tet2 cooperates in the pathogenesis of myelodysplastic disorders
-
Muto T, Sashida G, Oshima M, Wendt GR, Mochizuki-Kashio M, Nagata Y et al. Concurrent loss of Ezh2 and Tet2 cooperates in the pathogenesis of myelodysplastic disorders. J Exp Med 2013; 210: 2627-2639.
-
(2013)
J Exp Med
, vol.210
, pp. 2627-2639
-
-
Muto, T.1
Sashida, G.2
Oshima, M.3
Wendt, G.R.4
Mochizuki-Kashio, M.5
Nagata, Y.6
-
16
-
-
84865152223
-
ASXL1 mutations promote myeloid transformation through loss of PRC2-mediated gene repression
-
Abdel-Wahab O, Adli M, LaFave LM, Gao J, Hricik T, Shih AH et al. ASXL1 mutations promote myeloid transformation through loss of PRC2-mediated gene repression. Cancer Cell 2012; 22: 180-193.
-
(2012)
Cancer Cell
, vol.22
, pp. 180-193
-
-
Abdel-Wahab, O.1
Adli, M.2
Lafave, L.M.3
Gao, J.4
Hricik, T.5
Shih, A.H.6
-
17
-
-
84888116023
-
Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo
-
Abdel-Wahab O, Gao J, Adli M, Dey A, Trimarchi T, Chung YR et al. Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo. J Exp Med 2013; 210: 2641-2659.
-
(2013)
J Exp Med
, vol.210
, pp. 2641-2659
-
-
Abdel-Wahab, O.1
Gao, J.2
Adli, M.3
Dey, A.4
Trimarchi, T.5
Chung, Y.R.6
-
18
-
-
80052285127
-
Deletion of Tet2 in mice leads to dysregulated hematopoietic stem cells and subsequent development of myeloid malignancies
-
Li Z, Cai X, Cai CL, Wang J, Zhang W, Petersen BE et al. Deletion of Tet2 in mice leads to dysregulated hematopoietic stem cells and subsequent development of myeloid malignancies. Blood 2011; 118: 4509-4518.
-
(2011)
Blood
, vol.118
, pp. 4509-4518
-
-
Li, Z.1
Cai, X.2
Cai, C.L.3
Wang, J.4
Zhang, W.5
Petersen, B.E.6
-
19
-
-
79960064353
-
Tet2 loss leads to increased hematopoietic stem cell self-renewal and myeloid transformation
-
Moran-Crusio K, Reavie L, Shih A, Abdel-Wahab O, Ndiaye-Lobry D, Lobry C et al. Tet2 loss leads to increased hematopoietic stem cell self-renewal and myeloid transformation. Cancer Cell 2011; 20: 11-24.
-
(2011)
Cancer Cell
, vol.20
, pp. 11-24
-
-
Moran-Crusio, K.1
Reavie, L.2
Shih, A.3
Abdel-Wahab, O.4
Ndiaye-Lobry, D.5
Lobry, C.6
-
20
-
-
84897019526
-
Loss of Asxl1 leads to myelodysplastic syndrome-like disease in mice
-
Wang J, Li Z, He Y, Pan F, Chen S, Rhodes S et al. Loss of Asxl1 leads to myelodysplastic syndrome-like disease in mice. Blood 2014; 123: 541-553.
-
(2014)
Blood
, vol.123
, pp. 541-553
-
-
Wang, J.1
Li, Z.2
He, Y.3
Pan, F.4
Chen, S.5
Rhodes, S.6
-
21
-
-
84858600403
-
Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases
-
Gelsi-Boyer V, Brecqueville M, Devillier R, Murati A, Mozziconacci MJ, Birnbaum D. Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases. J Hematol Oncol 2012; 5: 12.
-
(2012)
J Hematol Oncol
, vol.5
, pp. 12
-
-
Gelsi-Boyer, V.1
Brecqueville, M.2
Devillier, R.3
Murati, A.4
Mozziconacci, M.J.5
Birnbaum, D.6
-
22
-
-
84904392234
-
Dynamics of ASXL1 mutation and other associated genetic alterations during disease progression in patients with primary myelodysplastic syndrome
-
Chen TC, Hou HA, Chou WC, Tang JL, Kuo YY, Chen CY et al. Dynamics of ASXL1 mutation and other associated genetic alterations during disease progression in patients with primary myelodysplastic syndrome. Blood Cancer J 2014; 4: E177.
-
(2014)
Blood Cancer J
, vol.4
, pp. e177
-
-
Chen, T.C.1
Hou, H.A.2
Chou, W.C.3
Tang, J.L.4
Kuo, Y.Y.5
Chen, C.Y.6
-
23
-
-
79959317767
-
Prognostic significance of ASXL1 mutations in patients with myelodysplastic syndromes
-
Thol F, Friesen I, Damm F, Yun H, Weissinger EM, Krauter J et al. Prognostic significance of ASXL1 mutations in patients with myelodysplastic syndromes. J Clin Oncol 2011; 29: 2499-2506.
-
(2011)
J Clin Oncol
, vol.29
, pp. 2499-2506
-
-
Thol, F.1
Friesen, I.2
Damm, F.3
Yun, H.4
Weissinger, E.M.5
Krauter, J.6
-
24
-
-
84883742761
-
SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML monosomy 7 isochromosome i(17)(q10), ASXL1 and CBL mutations
-
Meggendorfer M, Bacher U, Alpermann T, Haferlach C, Kern W, Gambacorti-Passerini C et al. SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations. Leukemia 2013; 27: 1852-1860.
-
(2013)
Leukemia
, vol.27
, pp. 1852-1860
-
-
Meggendorfer, M.1
Bacher, U.2
Alpermann, T.3
Haferlach, C.4
Kern, W.5
Gambacorti-Passerini, C.6
-
25
-
-
84880976662
-
Somatic SETBP1 mutations in myeloid malignancies
-
Makishima H, Yoshida K, Nguyen N, Przychodzen B, Sanada M, Okuno Y et al. Somatic SETBP1 mutations in myeloid malignancies. Nat Genet 2013; 45: 942-946.
-
(2013)
Nat Genet
, vol.45
, pp. 942-946
-
-
Makishima, H.1
Yoshida, K.2
Nguyen, N.3
Przychodzen, B.4
Sanada, M.5
Okuno, Y.6
-
26
-
-
84893950322
-
Clinical implications of the SETBP1 mutation in patients with primary myelodysplastic syndrome and its stability during disease progression
-
Hou HA, Kuo YY, Tang JL, Chou WC, Yao M, Lai YJ et al. Clinical implications of the SETBP1 mutation in patients with primary myelodysplastic syndrome and its stability during disease progression. Am J Hematol 2014; 89: 181-186.
-
(2014)
Am J Hematol
, vol.89
, pp. 181-186
-
-
Hou, H.A.1
Kuo, Y.Y.2
Tang, J.L.3
Chou, W.C.4
Yao, M.5
Lai, Y.J.6
-
27
-
-
84893772765
-
Landscape of genetic lesions in 944 patients with myelodysplastic syndromes
-
Haferlach T, Nagata Y, Grossmann V, Okuno Y, Bacher U, Nagae G et al. Landscape of genetic lesions in 944 patients with myelodysplastic syndromes. Leukemia 2014; 28: 241-247.
-
(2014)
Leukemia
, vol.28
, pp. 241-247
-
-
Haferlach, T.1
Nagata, Y.2
Grossmann, V.3
Okuno, Y.4
Bacher, U.5
Nagae, G.6
-
28
-
-
84885571172
-
SETBP1 mutation analysis in 944 patients with MDS and AML
-
Thol F, Suchanek KJ, Koenecke C, Stadler M, Platzbecker U, Thiede C et al. SETBP1 mutation analysis in 944 patients with MDS and AML. Leukemia 2013; 27: 2072-2075.
-
(2013)
Leukemia
, vol.27
, pp. 2072-2075
-
-
Thol, F.1
Suchanek, K.J.2
Koenecke, C.3
Stadler, M.4
Platzbecker, U.5
Thiede, C.6
-
29
-
-
84871988651
-
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
-
Piazza R, Valletta S, Winkelmann N, Redaelli S, Spinelli R, Pirola A et al. Recurrent SETBP1 mutations in atypical chronic myeloid leukemia. Nat Genet 2013; 45: 18-24.
-
(2013)
Nat Genet
, vol.45
, pp. 18-24
-
-
Piazza, R.1
Valletta, S.2
Winkelmann, N.3
Redaelli, S.4
Spinelli, R.5
Pirola, A.6
-
30
-
-
79954449794
-
PP2A impaired activity is a common event in acute myeloid leukemia and its activation by forskolin has a potent anti-leukemic effect
-
Cristóbal I, Garcia-Orti L, Cirauqui C, Alonso MM, Calasanz MJ, Odero MD. PP2A impaired activity is a common event in acute myeloid leukemia and its activation by forskolin has a potent anti-leukemic effect. Leukemia 2011; 25: 606-614.
-
(2011)
Leukemia
, vol.25
, pp. 606-614
-
-
Cristóbal, I.1
Garcia-Orti, L.2
Cirauqui, C.3
Alonso, M.M.4
Calasanz, M.J.5
Odero, M.D.6
-
31
-
-
77449131060
-
SETBP1 overexpression is a novel leukemogenic mechanism that predicts adverse outcome in elderly patients with acute myeloid leukemia
-
Cristóbal I, Blanco FJ, Garcia-Orti L, Marcotegui N, Vicente C, Rifon J et al. SETBP1 overexpression is a novel leukemogenic mechanism that predicts adverse outcome in elderly patients with acute myeloid leukemia. Blood 2010; 115: 615-625.
-
(2010)
Blood
, vol.115
, pp. 615-625
-
-
Cristóbal, I.1
Blanco, F.J.2
Garcia-Orti, L.3
Marcotegui, N.4
Vicente, C.5
Rifon, J.6
-
32
-
-
84862734488
-
Setbp1 promotes the self-renewal of murine myeloid progenitors via activation of Hoxa9 and Hoxa10
-
Oakley K, Han Y, Vishwakarma BA, Chu S, Bhatia R, Gudmundsson KO et al. Setbp1 promotes the self-renewal of murine myeloid progenitors via activation of Hoxa9 and Hoxa10. Blood 2012; 119: 6099-6108.
-
(2012)
Blood
, vol.119
, pp. 6099-6108
-
-
Oakley, K.1
Han, Y.2
Vishwakarma, B.A.3
Chu, S.4
Bhatia, R.5
Gudmundsson, K.O.6
-
33
-
-
66849124925
-
Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia
-
Gelsi-Boyer V, Trouplin V, Adélaïde J, Bonansea J, Cervera N, Carbuccia N et al. Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia. Br J Haematol 2009; 145: 788-800.
-
(2009)
Br J Haematol
, vol.145
, pp. 788-800
-
-
Gelsi-Boyer, V.1
Trouplin, V.2
Adélaïde, J.3
Bonansea, J.4
Cervera, N.5
Carbuccia, N.6
-
34
-
-
77950976493
-
Hes1 immortalizes committed progenitors and plays a role in blast crisis transition in chronic myelogenous leukemia
-
Nakahara F, Sakata-Yanagimoto M, Komeno Y, Kato N, Uchida T, Haraguchi K et al. Hes1 immortalizes committed progenitors and plays a role in blast crisis transition in chronic myelogenous leukemia. Blood 2010; 115: 2872-2881.
-
(2010)
Blood
, vol.115
, pp. 2872-2881
-
-
Nakahara, F.1
Sakata-Yanagimoto, M.2
Komeno, Y.3
Kato, N.4
Uchida, T.5
Haraguchi, K.6
-
35
-
-
0034624828
-
A clonogenic common myeloid progenitor that gives rise to all myeloid lineages
-
Akashi K, Traver D, Miyamoto T, Weissman IL. A clonogenic common myeloid progenitor that gives rise to all myeloid lineages. Nature 2000; 404: 193-197.
-
(2000)
Nature
, vol.404
, pp. 193-197
-
-
Akashi, K.1
Traver, D.2
Miyamoto, T.3
Weissman, I.L.4
-
36
-
-
43249103972
-
AML1 mutations induced MDS and MDS/AML in a mouse BMT model
-
Watanabe-Okochi N, Kitaura J, Ono R, Harada H, Harada Y, Komeno Y et al. AML1 mutations induced MDS and MDS/AML in a mouse BMT model. Blood 2008; 111: 4297-4308.
-
(2008)
Blood
, vol.111
, pp. 4297-4308
-
-
Watanabe-Okochi, N.1
Kitaura, J.2
Ono, R.3
Harada, H.4
Harada, Y.5
Komeno, Y.6
-
37
-
-
0142227052
-
Retrovirusmediated gene transfer and expression cloning: Powerful tools in functional genomics
-
Kitamura T, Koshino Y, Shibata F, Oki T, Nakajima H, Nosaka T et al. Retrovirusmediated gene transfer and expression cloning: Powerful tools in functional genomics. Exp Hematol 2003; 31: 1007-1014.
-
(2003)
Exp Hematol
, vol.31
, pp. 1007-1014
-
-
Kitamura, T.1
Koshino, Y.2
Shibata, F.3
Oki, T.4
Nakajima, H.5
Nosaka, T.6
-
38
-
-
78149252441
-
Characterization of leukocyte mono-immunoglobulin-like receptor 7 (LMIR7)/CLM-3 as an activating receptor: Its similarities to and differences from LMIR4/CLM-5
-
Enomoto Y, Yamanishi Y, Izawa K, Kaitani A, Takahashi M, Maehara A et al. Characterization of leukocyte mono-immunoglobulin-like receptor 7 (LMIR7)/CLM-3 as an activating receptor: Its similarities to and differences from LMIR4/CLM-5. J Biol Chem 2010; 285: 35274-35283.
-
(2010)
J Biol Chem
, vol.285
, pp. 35274-35283
-
-
Enomoto, Y.1
Yamanishi, Y.2
Izawa, K.3
Kaitani, A.4
Takahashi, M.5
Maehara, A.6
-
39
-
-
44449177123
-
The organization of histone H3 modifications as revealed by a panel of specific monoclonal antibodies
-
Kimura H, Hayashi-Takanaka Y, Goto Y, Takizawa N, Nozaki N. The organization of histone H3 modifications as revealed by a panel of specific monoclonal antibodies. Cell Struct Funct 2008; 33: 61-73.
-
(2008)
Cell Struct Funct
, vol.33
, pp. 61-73
-
-
Kimura, H.1
Hayashi-Takanaka, Y.2
Goto, Y.3
Takizawa, N.4
Nozaki, N.5
-
40
-
-
27644569730
-
The tumor suppressor PP2A is functionally inactivated in blast crisis CML through the inhibitory activity of the BCR/ABL-regulated SET protein
-
Neviani P, Santhanam R, Trotta R, Notari M, Blaser BW, Liu S et al. The tumor suppressor PP2A is functionally inactivated in blast crisis CML through the inhibitory activity of the BCR/ABL-regulated SET protein. Cancer Cell 2005; 8: 355-368.
-
(2005)
Cancer Cell
, vol.8
, pp. 355-368
-
-
Neviani, P.1
Santhanam, R.2
Trotta, R.3
Notari, M.4
Blaser, B.W.5
Liu, S.6
-
41
-
-
15844405224
-
Novel insights into the biology of myelodysplastic syndromes: Excessive apoptosis and the role of cytokines
-
Raza A, Mundle S, Shetty V, Alvi S, Chopra H, Span L et al. Novel insights into the biology of myelodysplastic syndromes: Excessive apoptosis and the role of cytokines. Int J Hematol 1996; 63: 265-278.
-
(1996)
Int J Hematol
, vol.63
, pp. 265-278
-
-
Raza, A.1
Mundle, S.2
Shetty, V.3
Alvi, S.4
Chopra, H.5
Span, L.6
-
42
-
-
0029020851
-
Apoptosis in bone marrow biopsy samples involving stromal and hematopoietic cells in 50 patients with myelodysplastic syndromes
-
Raza A, Gezer S, Mundle S, Gao XZ, Alvi S, Borok R et al. Apoptosis in bone marrow biopsy samples involving stromal and hematopoietic cells in 50 patients with myelodysplastic syndromes. Blood 1995; 86: 268-276.
-
(1995)
Blood
, vol.86
, pp. 268-276
-
-
Raza, A.1
Gezer, S.2
Mundle, S.3
Gao, X.Z.4
Alvi, S.5
Borok, R.6
-
43
-
-
0032437584
-
Low-risk myelodysplastic syndrome is associated with excessive apoptosis and an increased ratio of pro-versus anti-apoptotic bcl-2-related proteins
-
Parker J, Fishlock K, Mijovic A, Czepulkowski B, Pagliuca A, Mufti G. 'Low-risk' myelodysplastic syndrome is associated with excessive apoptosis and an increased ratio of pro-versus anti-apoptotic bcl-2-related proteins. Br J Haematol 1998; 103: 1075-1082.
-
(1998)
Br J Haematol
, vol.103
, pp. 1075-1082
-
-
Parker, J.1
Fishlock, K.2
Mijovic, A.3
Czepulkowski, B.4
Pagliuca, A.5
Mufti, G.6
-
44
-
-
0034641918
-
The biochemistry of apoptosis
-
Hengartner MO. The biochemistry of apoptosis. Nature 2000; 407: 770-776.
-
(2000)
Nature
, vol.407
, pp. 770-776
-
-
Hengartner, M.O.1
-
45
-
-
0034551738
-
The role of apoptosis, proliferation, and the Bcl-2-related proteins in the myelodysplastic syndromes and acute myeloid leukemia secondary to MDS
-
Parker J, Mufti G, Rasool F, Mijovic A, Devereux S, Pagliuca A. The role of apoptosis, proliferation, and the Bcl-2-related proteins in the myelodysplastic syndromes and acute myeloid leukemia secondary to MDS. Blood 2000; 96: 3932-3938.
-
(2000)
Blood
, vol.96
, pp. 3932-3938
-
-
Parker, J.1
Mufti, G.2
Rasool, F.3
Mijovic, A.4
Devereux, S.5
Pagliuca, A.6
-
46
-
-
0035725856
-
International prognostic scoring system and TP53 mutations are independent prognostic indicators for patients with myelodysplastic syndrome
-
Kita-Sasai Y, Horiike S, Misawa S, Kaneko H, Kobayashi M, Nakao M et al. International prognostic scoring system and TP53 mutations are independent prognostic indicators for patients with myelodysplastic syndrome. Br J Haematol 2001; 115: 309-312.
-
(2001)
Br J Haematol
, vol.115
, pp. 309-312
-
-
Kita-Sasai, Y.1
Horiike, S.2
Misawa, S.3
Kaneko, H.4
Kobayashi, M.5
Nakao, M.6
-
47
-
-
66549085133
-
The role of PP2A A subunits in tumor suppression
-
Sablina AA, Hahn WC. The role of PP2A A subunits in tumor suppression. Cell Adh Migr 2007; 1: 140-141.
-
(2007)
Cell Adh Migr
, vol.1
, pp. 140-141
-
-
Sablina, A.A.1
Hahn, W.C.2
-
48
-
-
43049121301
-
A tumor suppressor role for PP2A-B56alpha through negative regulation of c-Myc and other key oncoproteins
-
Arnold HK, Sears RC. A tumor suppressor role for PP2A-B56alpha through negative regulation of c-Myc and other key oncoproteins. Cancer Metast Rev 2008; 27: 147-158.
-
(2008)
Cancer Metast Rev
, vol.27
, pp. 147-158
-
-
Arnold, H.K.1
Sears, R.C.2
-
49
-
-
33746498580
-
Transformation from committed progenitor to leukaemia stem cell initiated by MLL-AF9
-
Krivtsov AV, Twomey D, Feng Z, Stubbs MC, Wang Y, Faber J et al. Transformation from committed progenitor to leukaemia stem cell initiated by MLL-AF9. Nature 2006; 442: 818-822.
-
(2006)
Nature
, vol.442
, pp. 818-822
-
-
Krivtsov, A.V.1
Twomey, D.2
Feng, Z.3
Stubbs, M.C.4
Wang, Y.5
Faber, J.6
-
50
-
-
0034000574
-
Hoxa9 immortalizes a granulocytemacrophage colony-stimulating factor-dependent promyelocyte capable of biphenotypic differentiation to neutrophils or macrophages, independent of enforced meis expression
-
Calvo KR, Sykes DB, Pasillas M, Kamps MP. Hoxa9 immortalizes a granulocytemacrophage colony-stimulating factor-dependent promyelocyte capable of biphenotypic differentiation to neutrophils or macrophages, independent of enforced meis expression. Mol Cell Biol 2000; 20: 3274-3285.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 3274-3285
-
-
Calvo, K.R.1
Sykes, D.B.2
Pasillas, M.3
Kamps, M.P.4
-
51
-
-
27344435774
-
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
-
Subramanian A, Tamayo P, Mootha VK, Mukherjee S, Ebert BL, Gillette MA et al. Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles. Proc Natl Acad Sci USA 2005; 102: 15545-15550.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 15545-15550
-
-
Subramanian, A.1
Tamayo, P.2
Mootha, V.K.3
Mukherjee, S.4
Ebert, B.L.5
Gillette, M.A.6
-
52
-
-
33745082823
-
Role of transforming growth factor-beta in hematologic malignancies
-
Dong M, Blobe GC. Role of transforming growth factor-beta in hematologic malignancies. Blood 2006; 107: 4589-4596.
-
(2006)
Blood
, vol.107
, pp. 4589-4596
-
-
Dong, M.1
Blobe, G.C.2
-
53
-
-
0034704128
-
Inhibition of the transforming growth factor beta 1 signaling pathway by the AML1/ETO leukemia-associated fusion protein
-
Jakubowiak A, Pouponnot C, Berguido F, Frank R, Mao S, Massague J et al. Inhibition of the transforming growth factor beta 1 signaling pathway by the AML1/ETO leukemia-associated fusion protein. J Biol Chem 2000; 275: 40282-40287.
-
(2000)
J Biol Chem
, vol.275
, pp. 40282-40287
-
-
Jakubowiak, A.1
Pouponnot, C.2
Berguido, F.3
Frank, R.4
Mao, S.5
Massague, J.6
-
54
-
-
4544256756
-
Cytoplasmic PML function in TGF-beta signalling
-
Lin HK, Bergmann S, Pandolfi PP. Cytoplasmic PML function in TGF-beta signalling. Nature 2004; 431: 205-211.
-
(2004)
Nature
, vol.431
, pp. 205-211
-
-
Lin, H.K.1
Bergmann, S.2
Pandolfi, P.P.3
-
55
-
-
0035804227
-
Mutations of the Smad4 gene in acute myelogeneous leukemia and their functional implications in leukemogenesis
-
Imai Y, Kurokawa M, Izutsu K, Hangaishi A, Maki K, Ogawa S et al. Mutations of the Smad4 gene in acute myelogeneous leukemia and their functional implications in leukemogenesis. Oncogene 2001; 20: 88-96.
-
(2001)
Oncogene
, vol.20
, pp. 88-96
-
-
Imai, Y.1
Kurokawa, M.2
Izutsu, K.3
Hangaishi, A.4
Maki, K.5
Ogawa, S.6
-
56
-
-
0037071398
-
The proto-oncogene c-myc in hematopoietic development and leukemogenesis
-
Hoffman B, Amanullah A, Shafarenko M, Liebermann DA. The proto-oncogene c-myc in hematopoietic development and leukemogenesis. Oncogene 2002; 21: 3414-3421.
-
(2002)
Oncogene
, vol.21
, pp. 3414-3421
-
-
Hoffman, B.1
Amanullah, A.2
Shafarenko, M.3
Liebermann, D.A.4
-
57
-
-
58149468095
-
Chromatin immunoprecipitation on microarray analysis of Smad2/3 binding sites reveals roles of ETS1 and TFAP2A in transforming growth factor beta signaling
-
Koinuma D, Tsutsumi S, Kamimura N, Taniguchi H, Miyazawa K, Sunamura M et al. Chromatin immunoprecipitation on microarray analysis of Smad2/3 binding sites reveals roles of ETS1 and TFAP2A in transforming growth factor beta signaling. Mol Cell Biol 2009; 29: 172-186.
-
(2009)
Mol Cell Biol
, vol.29
, pp. 172-186
-
-
Koinuma, D.1
Tsutsumi, S.2
Kamimura, N.3
Taniguchi, H.4
Miyazawa, K.5
Sunamura, M.6
-
58
-
-
1542314236
-
Transforming growth factor beta-mediated transcriptional repression of c-myc is dependent on direct binding of Smad3 to a novel repressive Smad binding element
-
Frederick JP, Liberati NT, Waddell DS, Shi Y, Wang XF. Transforming growth factor beta-mediated transcriptional repression of c-myc is dependent on direct binding of Smad3 to a novel repressive Smad binding element. Mol Cell Biol 2004; 24: 2546-2559.
-
(2004)
Mol Cell Biol
, vol.24
, pp. 2546-2559
-
-
Frederick, J.P.1
Liberati, N.T.2
Waddell, D.S.3
Shi, Y.4
Wang, X.F.5
-
59
-
-
54049149411
-
Inhibition of the TGF-beta receptor i kinase promotes hematopoiesis in MDS
-
Zhou L, Nguyen AN, Sohal D, Ying Ma J, Pahanish P, Gundabolu K et al. Inhibition of the TGF-beta receptor I kinase promotes hematopoiesis in MDS. Blood 2008; 112: 3434-3443.
-
(2008)
Blood
, vol.112
, pp. 3434-3443
-
-
Zhou, L.1
Nguyen, A.N.2
Sohal, D.3
Ying Ma, J.4
Pahanish, P.5
Gundabolu, K.6
|