-
1
-
-
0024828987
-
Chronic myelomonocytic leukemia: Natural history and prognostic determinants
-
Tefferi A, Hoagland HC, Therneau TM, Pierre RV. Chronic myelomonocytic leukemia: natural history and prognostic determinants. Mayo Clin Proc. 1989; 64(10):1246-54.
-
(1989)
Mayo Clin Proc.
, vol.64
, Issue.10
, pp. 1246-1254
-
-
Tefferi, A.1
Hoagland, H.C.2
Therneau, T.M.3
Pierre, R.V.4
-
2
-
-
0036464647
-
Prognostic factors in chronic myelomonocytic leukemia: A retrospective analysis of 213 patients
-
Onida F. Prognostic factors in chronic myelomonocytic leukemia: a retrospective analysis of 213 patients. Blood 2002;99(3):840-9.
-
(2002)
Blood
, vol.99
, Issue.3
, pp. 840-849
-
-
Onida, F.1
-
3
-
-
70349256226
-
The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: Rationale and important changes
-
Vardiman JW, Thiele J, Arber DA, Brunning RD, Borowitz MJ, Porwit A, et al. The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood. 2009;114(5):937-51.
-
(2009)
Blood.
, vol.114
, Issue.5
, pp. 937-951
-
-
Vardiman, J.W.1
Thiele, J.2
Arber, D.A.3
Brunning, R.D.4
Borowitz, M.J.5
Porwit, A.6
-
4
-
-
0036789943
-
Chronic myelomonocytic leukemia requires granulocyte-macrophage colonystimulating factor for growth in vitro and in vivo
-
Ramshaw HS, Bardy PG, Lee MA, Lopez AF. Chronic myelomonocytic leukemia requires granulocyte-macrophage colonystimulating factor for growth in vitro and in vivo. Exp Hematol. 2002;30(10):1124-31.
-
(2002)
Exp Hematol.
, vol.30
, Issue.10
, pp. 1124-1131
-
-
Ramshaw, H.S.1
Bardy, P.G.2
Lee, M.A.3
Lopez, A.F.4
-
5
-
-
33646512610
-
Survivin expression, apoptosis and proliferation in chronic myelomonocytic leukemia
-
Invernizzi R, Travaglino E, Benatti C, Malcovati L, Della Porta M, Cazzola M, et al. Survivin expression, apoptosis and proliferation in chronic myelomonocytic leukemia. Eur J Haematol. 2006;76(6):494-501.
-
(2006)
Eur J Haematol.
, vol.76
, Issue.6
, pp. 494-501
-
-
Invernizzi, R.1
Travaglino, E.2
Benatti, C.3
Malcovati, L.4
della Porta, M.5
Cazzola, M.6
-
6
-
-
0028069002
-
The chronic myeloid leukaemias: Guidelines for distinguishing chronic granulocytic, atypical chronic myeloid, and chronic myelomonocytic leukaemia. Proposals by the French-American-British Cooperative Leukaemia Group
-
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DA, Gralnick H, et al. The chronic myeloid leukaemias: guidelines for distinguishing chronic granulocytic, atypical chronic myeloid, and chronic myelomonocytic leukaemia. Proposals by the French-American-British Cooperative Leukaemia Group. Br J Haematol. 1994; 87(4):746-54.
-
(1994)
Br J Haematol.
, vol.87
, Issue.4
, pp. 746-754
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
Flandrin, G.4
Galton, D.A.5
Gralnick, H.6
-
7
-
-
77958591628
-
ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia
-
Gelsi-Boyer V, Trouplin V, Roquain J, Adélaïde J, Carbuccia N, Esterni B, et al. ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia. Br J Haematol. 2010;151(4):365-75.
-
(2010)
Br J Haematol.
, vol.151
, Issue.4
, pp. 365-375
-
-
Gelsi-Boyer, V.1
Trouplin, V.2
Roquain, J.3
Adélaïde, J.4
Carbuccia, N.5
Esterni, B.6
-
8
-
-
77955081371
-
Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias
-
Rocquain J, Carbuccia N, Trouplin V, Raynaud S, Murati A, Nezri M, et al. Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias. BMC Cancer. 2010; 10:401-17.
-
(2010)
BMC Cancer.
, vol.10
, pp. 401-417
-
-
Rocquain, J.1
Carbuccia, N.2
Trouplin, V.3
Raynaud, S.4
Murati, A.5
Nezri, M.6
-
9
-
-
77955085750
-
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders
-
Ernst T, Chase AJ, Score J, Hidalgo-Curtis CE, Bryant C, Jones AV, et al. Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders. Nat Genet. 2010;42(8):722-6.
-
(2010)
Nat Genet.
, vol.42
, Issue.8
, pp. 722-726
-
-
Ernst, T.1
Chase, A.J.2
Score, J.3
Hidalgo-Curtis, C.E.4
Bryant, C.5
Jones, A.V.6
-
10
-
-
84861702964
-
Mutation analysis of ASXL1, CBL, DNMT3A, IDH1, IDH2, JAK2, MPL, NF1, SF3B1, SUZ12 and TET2 in myeloproliferative neoplasms
-
Brecqueville M, Rey J, Bertucci F, Coppin E, Finetti P, Carbuccia N, et al. Mutation analysis of ASXL1, CBL, DNMT3A, IDH1, IDH2, JAK2, MPL, NF1, SF3B1, SUZ12 and TET2 in myeloproliferative neoplasms. Genes Chromosome Cancer. 2012; 51(8):743-55.
-
(2012)
Genes Chromosome Cancer.
, vol.51
, Issue.8
, pp. 743-755
-
-
Brecqueville, M.1
Rey, J.2
Bertucci, F.3
Coppin, E.4
Finetti, P.5
Carbuccia, N.6
-
11
-
-
84859595800
-
Mutations affecting mRNA splicing define distinct clinical phenotypes and correlate with patient outcome in myelodysplastic syndromes
-
Damm F, Kosmider O, Gelsi-Boyer V, Renneville A, Carbuccia N, Hidalgo-Curtis C, et al. Mutations affecting mRNA splicing define distinct clinical phenotypes and correlate with patient outcome in myelodysplastic syndromes. Blood. 2012;119(14): 3211-8.
-
(2012)
Blood.
, vol.119
, Issue.14
, pp. 3211-3218
-
-
Damm, F.1
Kosmider, O.2
Gelsi-Boyer, V.3
Renneville, A.4
Carbuccia, N.5
Hidalgo-Curtis, C.6
-
12
-
-
33646390671
-
Gene expression profiling shows medullary breast cancer is a subgroup of basal breast cancers
-
Bertucci F, Finetti P, Cervera N, Charafe-Jauffret E, Mamessier E, Adélaïde J, et al. Gene expression profiling shows medullary breast cancer is a subgroup of basal breast cancers. Cancer Res. 2006;66(9):4636-44.
-
(2006)
Cancer Res.
, vol.66
, Issue.9
, pp. 4636-4644
-
-
Bertucci, F.1
Finetti, P.2
Cervera, N.3
Charafe-Jauffret, E.4
Mamessier, E.5
Adélaïde, J.6
-
13
-
-
0033569406
-
Molecular classification of cancer: Class discovery and class prediction by gene expression monitoring
-
Golub TR, Slonim DK, Tamayo P, Huard C, Gaasenbeek M, Mesirov JP, et al. Molecular classification of cancer: class discovery and class prediction by gene expression monitoring. Science. 1999;286(5439):531-7.
-
(1999)
Science.
, vol.286
, Issue.5439
, pp. 531-537
-
-
Golub, T.R.1
Slonim, D.K.2
Tamayo, P.3
Huard, C.4
Gaasenbeek, M.5
Mesirov, J.P.6
-
14
-
-
33745615399
-
Gene expression profiles of CD34+ cells in myelodysplastic syndromes: Involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype
-
Pellagatti A, Cazzola M, Giagounidis AA, Malcovati L, Porta MG, Killick S, et al. Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype. Blood. 2006;108(1):337-45.
-
(2006)
Blood.
, vol.108
, Issue.1
, pp. 337-345
-
-
Pellagatti, A.1
Cazzola, M.2
Giagounidis, A.A.3
Malcovati, L.4
Porta, M.G.5
Killick, S.6
-
15
-
-
70349249936
-
Microarray-based classifiers and prognosis models identify subgroups with distinct clinical outcomes and high risk of AML transformation of myelodysplastic syndrome
-
Mills KI, Kohlmann A, Williams PM, Wieczorek L, Liu WM, Li R, et al. Microarray-based classifiers and prognosis models identify subgroups with distinct clinical outcomes and high risk of AML transformation of myelodysplastic syndrome. Blood. 2009;114(5):1063-72.
-
(2009)
Blood.
, vol.114
, Issue.5
, pp. 1063-1072
-
-
Mills, K.I.1
Kohlmann, A.2
Williams, P.M.3
Wieczorek, L.4
Liu, W.M.5
Li, R.6
-
16
-
-
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(43):15545-50.
-
(2005)
Proc Natl Acad Sci USA.
, vol.102
, Issue.43
, pp. 15545-15550
-
-
Subramanian, A.1
Tamayo, P.2
Mootha, V.K.3
Mukherjee, S.4
Ebert, B.L.5
Gillette, M.A.6
-
17
-
-
77950943405
-
Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells
-
Pellagatti A, Cazzola M, Giagounidis A, Perry J, Malcovati L, Della Porta MG, et al. Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells. Leukemia. 2010;24(4):756-64.
-
(2010)
Leukemia.
, vol.24
, Issue.4
, pp. 756-764
-
-
Pellagatti, A.1
Cazzola, M.2
Giagounidis, A.3
Perry, J.4
Malcovati, L.5
della Porta, M.G.6
-
18
-
-
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(6):788-800.
-
(2009)
Br J Haematol.
, vol.145
, Issue.6
, pp. 788-800
-
-
Gelsi-Boyer, V.1
Trouplin, V.2
Adélaïde, J.3
Bonansea, J.4
Cervera, N.5
Carbuccia, N.6
-
19
-
-
73149114865
-
Molecular basis of myelodysplastic/ myeloproliferative neoplasms
-
Reiter A, Invernizzi R, Cross NC, Cazzola M. Molecular basis of myelodysplastic/ myeloproliferative neoplasms. Haematologica. 2009;94(12):1634-8.
-
(2009)
Haematologica.
, vol.94
, Issue.12
, pp. 1634-1638
-
-
Reiter, A.1
Invernizzi, R.2
Cross, N.C.3
Cazzola, M.4
-
20
-
-
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(26):2496-506.
-
(2011)
N Engl J Med.
, vol.364
, Issue.26
, pp. 2496-2506
-
-
Bejar, R.1
Stevenson, K.2
Abdel-Wahab, O.3
Galili, N.4
Nilsson, B.5
Garcia-Manero, G.6
-
21
-
-
84857633350
-
Mutations in epigenetic regulators in myelodysplastic syndromes
-
Nikoloski G, van der Reijden BA, Jansen JH. Mutations in epigenetic regulators in myelodysplastic syndromes. Int J Hematol. 2012;95(1):8-16.
-
(2012)
Int J Hematol.
, vol.95
, Issue.1
, pp. 8-16
-
-
Nikoloski, G.1
van der Reijden, B.A.2
Jansen, J.H.3
-
22
-
-
77956237515
-
Nextgeneration sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1
-
Kohlmann A, Grossmann V, Klein HU, Schindela S, Weiss T, Kazak B, et al. Nextgeneration sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1. J Clin Oncol. 2010;28(24):3858-65.
-
(2010)
J Clin Oncol.
, vol.28
, Issue.24
, pp. 3858-3865
-
-
Kohlmann, A.1
Grossmann, V.2
Klein, H.U.3
Schindela, S.4
Weiss, T.5
Kazak, B.6
-
23
-
-
83555174295
-
TET2 deletions are a recurrent but rare phenomenon in myeloid malignancies and are frequently accompanied by TET2 mutations on the remaining allele
-
Bacher U, Weissmann S, Kohlmann A, Schindela S, Alpermann T, Schnittger S, et al. TET2 deletions are a recurrent but rare phenomenon in myeloid malignancies and are frequently accompanied by TET2 mutations on the remaining allele. Br J Haematol. 2011;156(1):67-75.
-
(2011)
Br J Haematol.
, vol.156
, Issue.1
, pp. 67-75
-
-
Bacher, U.1
Weissmann, S.2
Kohlmann, A.3
Schindela, S.4
Alpermann, T.5
Schnittger, S.6
-
24
-
-
79952451556
-
A deep-sequencing study of chronic myeloid leukemia patients in blast crisis (BC-CML) detects mutations in 76.9% of cases
-
Grossmann V, Kohlmann A, Zenger M, Schindela S, Eder C, Weissmann S, et al. A deep-sequencing study of chronic myeloid leukemia patients in blast crisis (BC-CML) detects mutations in 76.9% of cases. Leukemia. 2011;25(3):557-60.
-
(2011)
Leukemia.
, vol.25
, Issue.3
, pp. 557-560
-
-
Grossmann, V.1
Kohlmann, A.2
Zenger, M.3
Schindela, S.4
Eder, C.5
Weissmann, S.6
-
25
-
-
80053135096
-
Mutational spectrum analysis of chronic myelomonocytic leukemia includes genes associated with epigenetic regulation: UTX, EZH2, and DNMT3A
-
Jankowska AM, Makishima H, Tiu RV, Szpurka H, Huang Y, Traina F, et al. Mutational spectrum analysis of chronic myelomonocytic leukemia includes genes associated with epigenetic regulation: UTX, EZH2, and DNMT3A. Blood. 2011; 118(4):3932-41.
-
(2011)
Blood.
, vol.118
, Issue.4
, pp. 3932-3941
-
-
Jankowska, A.M.1
Makishima, H.2
Tiu, R.V.3
Szpurka, H.4
Huang, Y.5
Traina, F.6
-
26
-
-
84856401799
-
Chronic myelomonocytic leukemia and atypical chronic myeloid leukemia: Novel pathogenetic lesions
-
Muramatsu H, Makishima H, Maciejewski JP. Chronic myelomonocytic leukemia and atypical chronic myeloid leukemia: novel pathogenetic lesions. Semin Oncol. 2012; 39(1):67-73.
-
(2012)
Semin Oncol.
, vol.39
, Issue.1
, pp. 67-73
-
-
Muramatsu, H.1
Makishima, H.2
McIejewski, J.P.3
-
27
-
-
77957987676
-
Novel homo-and hemizygous mutations in EZH2 in myeloid malignancies
-
Makishima H, Jankowska AM, Tiu RV, Szpurka H, Sugimoto Y, Hu Z, et al. Novel homo-and hemizygous mutations in EZH2 in myeloid malignancies. Leukemia. 2010; 24(10):1799-804.
-
(2010)
Leukemia.
, vol.24
, Issue.10
, pp. 1799-1804
-
-
Makishima, H.1
Jankowska, A.M.2
Tiu, R.V.3
Szpurka, H.4
Sugimoto, Y.5
Hu, Z.6
-
28
-
-
79960248721
-
DNMT3A mutational analysis in primary myelofibrosis, chronic myelomonocytic leukemia and advanced phases of myeloproliferative neoplasms
-
Abdel-Wahab O, Pardanani A, Rampal R, Lasho TL, Levine RL, Tefferi A. DNMT3A mutational analysis in primary myelofibrosis, chronic myelomonocytic leukemia and advanced phases of myeloproliferative neoplasms. Leukemia. 2011;25(7):1219-20.
-
(2011)
Leukemia.
, vol.25
, Issue.7
, pp. 1219-1220
-
-
Abdel-Wahab, O.1
Pardanani, A.2
Rampal, R.3
Lasho, T.L.4
Levine, R.L.5
Tefferi, A.6
-
29
-
-
79960227474
-
Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms
-
Abdel-Wahab O, Pardanani A, Patel J, Wadleigh M, Lasho T, Heguy A, et al. Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms. Leukemia. 2011;25(7):1200-2.
-
(2011)
Leukemia.
, vol.25
, Issue.7
, pp. 1200-1202
-
-
Abdel-Wahab, O.1
Pardanani, A.2
Patel, J.3
Wadleigh, M.4
Lasho, T.5
Heguy, A.6
-
30
-
-
79960255863
-
Recurrent DNMT3A mutations in patients with myelodysplastic syndromes
-
Walter MJ, Ding L, Shen D, Shao J, Grillot M, McLellan M, et al. Recurrent DNMT3A mutations in patients with myelodysplastic syndromes. Leukemia. 2011;25(7):1153-8.
-
(2011)
Leukemia.
, vol.25
, Issue.7
, pp. 1153-1158
-
-
Walter, M.J.1
Ding, L.2
Shen, D.3
Shao, J.4
Grillot, M.5
McLellan, M.6
-
31
-
-
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(7367):64-9.
-
(2011)
Nature.
, vol.478
, Issue.7367
, pp. 64-69
-
-
Yoshida, K.1
Sanada, M.2
Shiraishi, Y.3
Nowak, D.4
Nagata, Y.5
Yamamoto, R.6
-
32
-
-
84857994411
-
SF3B1, a splicing factor is frequently mutated in refractory anemia with ring sideroblasts
-
Visconte V, Makishima H, Jankowska A, Szpurka H, Traina F, Jerez A, et al. SF3B1, a splicing factor is frequently mutated in refractory anemia with ring sideroblasts. Leukemia 2012;26(3):542-5.
-
(2012)
Leukemia
, vol.26
, Issue.3
, pp. 542-545
-
-
Visconte, V.1
Makishima, H.2
Jankowska, A.3
Szpurka, H.4
Traina, F.5
Jerez, A.6
-
33
-
-
80054010617
-
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts
-
Papaemmanuil E, Cazzola M, Boultwood J, Malcovati L, Vyas P, Bowen D, et al. Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts. N Engl J Med. 2011; 365(15):1384-95.
-
(2011)
N Engl J Med.
, vol.365
, Issue.15
, pp. 1384-1395
-
-
Papaemmanuil, E.1
Cazzola, M.2
Boultwood, J.3
Malcovati, L.4
Vyas, P.5
Bowen, D.6
-
34
-
-
84872085802
-
Spliceosomal gene mutations are frequent in the diverse mutational spectrum of chronic myelomonocytic leukemia but largely absent in juvenile myelomonocytic leukemia
-
Abu Kar S, Jankowska AM, Makishima H, Visconte V, Jerez A, Sugimoto Y, et al. Spliceosomal gene mutations are frequent in the diverse mutational spectrum of chronic myelomonocytic leukemia but largely absent in juvenile myelomonocytic leukemia. Haematologica. 2013;98(1):107-13.
-
(2013)
Haematologica.
, vol.98
, Issue.1
, pp. 107-113
-
-
Abu Kar, S.1
Jankowska, A.M.2
Makishima, H.3
Visconte, V.4
Jerez, A.5
Sugimoto, Y.6
-
35
-
-
83455234787
-
Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myeloproliferative/myelodysplastic neoplasms
-
Malcovati L, Papaemmanuil E, Bowen DT, Boultwood J, Della Porta MG, Pascutto C, et al. Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myeloproliferative/myelodysplastic neoplasms. Blood. 2011;118(24):6239-46.
-
(2011)
Blood.
, vol.118
, Issue.24
, pp. 6239-6246
-
-
Malcovati, L.1
Papaemmanuil, E.2
Bowen, D.T.3
Boultwood, J.4
della Porta, M.G.5
Pascutto, C.6
-
36
-
-
84859856420
-
Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes
-
Thol F, Kade S, Schlarmann C, Loffeld P, Morgan M, Krauter J, et al. Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes. Blood. 2012; 119(15):3578-84.
-
(2012)
Blood.
, vol.119
, Issue.15
, pp. 3578-3584
-
-
Thol, F.1
Kade, S.2
Schlarmann, C.3
Loffeld, P.4
Morgan, M.5
Krauter, J.6
-
37
-
-
84871236747
-
Emerging roles of the spliceosomal machinery in myelodysplastic syndromes and other hematological disorders
-
Visconte V, Makishima H, Maciejewski JP, Tiu RV. Emerging roles of the spliceosomal machinery in myelodysplastic syndromes and other hematological disorders. Leukemia. 2012;26(12):2447-54.
-
(2012)
Leukemia.
, vol.26
, Issue.12
, pp. 2447-2454
-
-
Visconte, V.1
Makishima, H.2
McIejewski, J.P.3
Tiu, R.V.4
-
38
-
-
80054718383
-
Rare mutations in DNMT3A in myeloproliferative neoplasms and myelodysplastic syndromes
-
Brecqueville M, Cervera N, Gelsi-Boyer V, Murati A, Adélaïde J, Chaffanet M, et al. Rare mutations in DNMT3A in myeloproliferative neoplasms and myelodysplastic syndromes. Blood Cancer J. 2011;1(5):e18.
-
(2011)
Blood Cancer J.
, vol.1
, Issue.5
-
-
Brecqueville, M.1
Cervera, N.2
Gelsi-Boyer, V.3
Murati, A.4
Adélaïde, J.5
Chaffanet, M.6
-
39
-
-
44849143798
-
The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts
-
Boultwood J, Pellagatti A, Nikpour M, Pushkaran B, Fidler C, Cattan H, et al. The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts. PLoS One. 2008;3(4):e1970.
-
(2008)
PLoS One.
, vol.3
, Issue.4
-
-
Boultwood, J.1
Pellagatti, A.2
Nikpour, M.3
Pushkaran, B.4
Fidler, C.5
Cattan, H.6
-
40
-
-
84859597590
-
Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
-
Makishima H, Visconte V, Sakaguchi H, Jankowska AM, Abu Kar S, Jerez A, et al. Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis. Blood. 2012;119(14):3203-10.
-
(2012)
Blood.
, vol.119
, Issue.14
, pp. 3203-3210
-
-
Makishima, H.1
Visconte, V.2
Sakaguchi, H.3
Jankowska, A.M.4
Abu Kar, S.5
Jerez, A.6
-
41
-
-
80054810315
-
Transcriptome profiling and sequencing of differentiated human hematopoietic stem cells reveal lineage-specific expression and alternative splicing of genes
-
th, Munson PJ, Raghavachari N. Transcriptome profiling and sequencing of differentiated human hematopoietic stem cells reveal lineage-specific expression and alternative splicing of genes. Physiol Genomics. 2011;43(20):1117-34.
-
(2011)
Physiol Genomics.
, vol.43
, Issue.20
, pp. 1117-1134
-
-
Liu, P.1
Barb, J.2
Woodhouse, K.3
Taylor VI, J.G.4
Munson, P.J.5
Raghavachari, N.6
-
42
-
-
84868091622
-
SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes
-
Visconte V, Rogers HJ, Singh J, Barnard J, Bupathi M, Traina F, et al. SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes. Blood. 2012;120(16):3173-86.
-
(2012)
Blood.
, vol.120
, Issue.16
, pp. 3173-3186
-
-
Visconte, V.1
Rogers, H.J.2
Singh, J.3
Barnard, J.4
Bupathi, M.5
Traina, F.6
-
43
-
-
77954301966
-
TIF1LLcontrols erythroid cell fate by regulating transcription elongation
-
Bai X, Kim J, Yang Z, Jurynec MJ, Akie TE, Lee J, et al. TIF1LLcontrols erythroid cell fate by regulating transcription elongation. Cell. 2010;142(1):133-43.
-
(2010)
Cell.
, vol.142
, Issue.1
, pp. 133-143
-
-
Bai, X.1
Kim, J.2
Yang, Z.3
Jurynec, M.J.4
Akie, T.E.5
Lee, J.6
-
44
-
-
79952762446
-
The gata1/pu.1 lineage fate paradigm varies between blood populations and is modulated by tif1gamma
-
Monteiro R, Pouget C, Patient R. The gata1/pu.1 lineage fate paradigm varies between blood populations and is modulated by tif1gamma. EMBO J. 2011; 30(6):1093-103.
-
(2011)
EMBO J.
, vol.30
, Issue.6
, pp. 1093-1103
-
-
Monteiro, R.1
Pouget, C.2
Patient, R.3
-
45
-
-
79957917231
-
Transcription intermediary factor 1TTis a tumor suppressor in mouse and human chronic myelomonocytic leukemia
-
Aucagne R, Droin N, Paggetti J, Lagrange B, Largeot A, Hammann A, et al. Transcription intermediary factor 1TTis a tumor suppressor in mouse and human chronic myelomonocytic leukemia. J Clin Invest. 2011;21(6):2361-70.
-
(2011)
J Clin Invest.
, vol.21
, Issue.6
, pp. 2361-2370
-
-
Aucagne, R.1
Droin, N.2
Paggetti, J.3
Lagrange, B.4
Largeot, A.5
Hammann, A.6
-
46
-
-
84865161055
-
Myeloid malignancies: Mutations, models and management
-
Murati A, Brecqueville M, Devillier R, Mozziconacci MJ, Gelsi-Boyer V, Birnbaum D. Myeloid malignancies: mutations, models and management. BMC Cancer. 2012; 12(1):304.
-
(2012)
BMC Cancer.
, vol.12
, Issue.1
, pp. 304
-
-
Murati, A.1
Brecqueville, M.2
Devillier, R.3
Mozziconacci, M.J.4
Gelsi-Boyer, V.5
Birnbaum, D.6
-
47
-
-
84857683658
-
Evolution d'une cytopénie réfractaire avec dysplasie multilignage et sidéroblastes en couronne en leucémie myélomonocytaire chronique
-
Ben Salah N, Gouider E, Belakhal F, El Borgi W, Menif S, Ben Abid H, et al. [Evolution d'une cytopénie réfractaire avec dysplasie multilignage et sidéroblastes en couronne en leucémie myélomonocytaire chronique]. Tunis Med. 2011;89(10):806-7.
-
(2011)
Tunis Med.
, vol.89
, Issue.10
, pp. 806-807
-
-
Ben Salah, N.1
Gouider, E.2
Belakhal, F.3
El Borgi, W.4
Menif, S.5
Ben Abid, H.6
-
48
-
-
70449486011
-
Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis
-
Malcovati L, Della Porta MG, Pietra D, Boveri E, Pellagatti A, Gallì A, et al. Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis. Blood. 2009;114(17):3538-45.
-
(2009)
Blood.
, vol.114
, Issue.17
, pp. 3538-3545
-
-
Malcovati, L.1
Della Porta, M.G.2
Pietra, D.3
Boveri, E.4
Pellagatti, A.5
Gallì, A.6
|