-
1
-
-
21744462604
-
Cancer biology: summing up cancer stem cells
-
Huntly BJ, Gilliland DG, (2005) Cancer biology: summing up cancer stem cells. Nature 435: 1169-1170.
-
(2005)
Nature
, vol.435
, pp. 1169-1170
-
-
Huntly, B.J.1
Gilliland, D.G.2
-
4
-
-
53249123632
-
-
Lyon, France: IARC Press
-
Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, et al., eds. (2008) WHO classification of tumours of haematopoietic and lymphoid tissues. Lyon, France: IARC Press.
-
(2008)
WHO classification of tumours of haematopoietic and lymphoid tissues
-
-
Swerdlow, S.H.1
Campo, E.2
Harris, N.L.3
Jaffe, E.S.4
Pileri, S.A.5
-
5
-
-
0026026981
-
Biochemical characterization of U2 snRNP auxiliary factor: an essential pre-mRNA splicing factor with a novel intranuclear distribution
-
Zamore PD, Green MR, (1991) Biochemical characterization of U2 snRNP auxiliary factor: an essential pre-mRNA splicing factor with a novel intranuclear distribution. Embo J 10: 207-214.
-
(1991)
Embo J
, vol.10
, pp. 207-214
-
-
Zamore, P.D.1
Green, M.R.2
-
6
-
-
0013394889
-
Mechanisms of alternative pre-messenger RNA splicing
-
Black DL, (2003) Mechanisms of alternative pre-messenger RNA splicing. Annu Rev Biochem 72: 291-336.
-
(2003)
Annu Rev Biochem
, vol.72
, pp. 291-336
-
-
Black, D.L.1
-
7
-
-
26944453614
-
Splicing in action: assessing disease causing sequence changes
-
Baralle D, Baralle M, (2005) Splicing in action: assessing disease causing sequence changes. J Med Genet 42: 737-748.
-
(2005)
J Med Genet
, vol.42
, pp. 737-748
-
-
Baralle, D.1
Baralle, M.2
-
8
-
-
84555192302
-
Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes
-
Graubert TA, Shen D, Ding L, Okeyo-Owuor T, Lunn CL, et al. (2011) Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes. Nat Genet 44: 53-57.
-
(2011)
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
-
9
-
-
80053900941
-
Frequent pathway mutations of splicing machinery in myelodysplasia
-
Yoshida K, Sanada M, Shiraishi Y, Nowak D, Nagata Y, et al. (2011) Frequent pathway mutations of splicing machinery in myelodysplasia. Nature 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
-
10
-
-
0022135739
-
Proposed revised criteria for the classification of acute myeloid leukaemia. A report of the French-American-British Cooperative Group
-
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DA, et al. (1985) Proposed revised criteria for the classification of acute myeloid leukaemia. A report of the French-American-British Cooperative Group. Ann Intern Med 103: 620-625.
-
(1985)
Ann Intern Med
, vol.103
, pp. 620-625
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
Flandrin, G.4
Galton, D.A.5
-
11
-
-
0034672269
-
Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group Study
-
Slovak ML, Kopecky KJ, Cassileth PA, Harrington DH, Theil KS, et al. (2000) Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group Study. Blood 96: 4075-4083.
-
(2000)
Blood
, vol.96
, pp. 4075-4083
-
-
Slovak, M.L.1
Kopecky, K.J.2
Cassileth, P.A.3
Harrington, D.H.4
Theil, K.S.5
-
12
-
-
0030897009
-
International scoring system for evaluating prognosis in myelodysplastic syndromes
-
Greenberg P, Cox C, LeBeau MM, Fenaux P, Morel P, et al. (1997) International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 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
-
13
-
-
77957752388
-
Rapid detection of JAK2 V617F mutation using high-resolution melting analysis with LightScanner platform
-
Qian J, Lin J, Yao DM, Chen Q, Xiao GF, et al. (2010) Rapid detection of JAK2 V617F mutation using high-resolution melting analysis with LightScanner platform. Clin Chim Acta 410: 2097-2100.
-
(2010)
Clin Chim Acta
, vol.410
, pp. 2097-2100
-
-
Qian, J.1
Lin, J.2
Yao, D.M.3
Chen, Q.4
Xiao, G.F.5
-
14
-
-
80055118997
-
Recurrent DNMT3A R882 mutations in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome
-
Lin J, Yao DM, Qian J, Chen Q, Qian W, et al. (2011) Recurrent DNMT3A R882 mutations in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome. PLoS One 6: e26906.
-
(2011)
PLoS One
, vol.6
-
-
Lin, J.1
Yao, D.M.2
Qian, J.3
Chen, Q.4
Qian, W.5
-
15
-
-
0035885955
-
The presence of a FLT3 internal tandem duplication in patients with acute myeloid leukemia (AML) adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: analysis of 854 patients from the United Kingdom Medical Research Council AML 10 and 12 trials
-
Kottaridis PD, Gale RE, Frew ME, Harrison G, Langabeer SE, et al. (2001) The presence of a FLT3 internal tandem duplication in patients with acute myeloid leukemia (AML) adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: analysis of 854 patients from the United Kingdom Medical Research Council AML 10 and 12 trials. Blood 98: 1752-1759.
-
(2001)
Blood
, vol.98
, pp. 1752-1759
-
-
Kottaridis, P.D.1
Gale, R.E.2
Frew, M.E.3
Harrison, G.4
Langabeer, S.E.5
-
16
-
-
43749099253
-
A new DNA-based test for detection of nucleophosmin exon 12 mutations by capillary electropheresis
-
Szankasi P, Jama M, Bahler DW, (2008) A new DNA-based test for detection of nucleophosmin exon 12 mutations by capillary electropheresis. J Mol Diagn 10: 236-241.
-
(2008)
J Mol Diagn
, vol.10
, pp. 236-241
-
-
Szankasi, P.1
Jama, M.2
Bahler, D.W.3
-
17
-
-
80055118997
-
Recurrent DNMT3A R882 mutations in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome
-
Lin J, Yao DM, Qian J, Chen Q, Qian W, et al. (2011) Recurrent DNMT3A R882 mutations in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome. PLoS One 6: e26906.
-
(2011)
PLoS One
, vol.6
-
-
Lin, J.1
Yao, D.M.2
Qian, J.3
Chen, Q.4
Qian, W.5
-
18
-
-
84860791715
-
IDH1 and IDH2 mutation analysis in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome
-
Lin J, Yao DM, Qian J, Chen Q, Qian W, et al. (2012) IDH1 and IDH2 mutation analysis in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome. Ann Hematol 91: 519-525.
-
(2012)
Ann Hematol
, vol.91
, pp. 519-525
-
-
Lin, J.1
Yao, D.M.2
Qian, J.3
Chen, Q.4
Qian, W.5
-
19
-
-
84859597590
-
Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
-
Makishima H, Visconte V, Sakaguchi H, Jankowska AM, Abu Kar S, et al. (2012) Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis. Blood 119: 3203-3210.
-
(2012)
Blood
, vol.119
, pp. 3203-3210
-
-
Makishima, H.1
Visconte, V.2
Sakaguchi, H.3
Jankowska, A.M.4
Abu Kar, S.5
-
20
-
-
84859856420
-
Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes
-
Thol F, Kade S, Schlarmann C, Löffeld P, Morgan M, et al. (2012) Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes. Blood 119: 3578-3584.
-
(2012)
Blood
, vol.119
, pp. 3578-3584
-
-
Thol, F.1
Kade, S.2
Schlarmann, C.3
Löffeld, P.4
Morgan, M.5
-
21
-
-
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, et al. (2012) Mutations affecting mRNA splicing define distinct clinical phenotypes and correlate with patient outcome in myelodysplastic syndromes. Blood 119: 3211-3218.
-
(2012)
Blood
, vol.119
, pp. 3211-3218
-
-
Damm, F.1
Kosmider, O.2
Gelsi-Boyer, V.3
Renneville, A.4
Carbuccia, N.5
-
22
-
-
55549143293
-
The emerging role of splicing factors in cancer
-
Grosso AR, Martins S, Carmo-Fonseca M, (2008) The emerging role of splicing factors in cancer. EMBO Rep 9: 1087-1093.
-
(2008)
EMBO Rep
, vol.9
, pp. 1087-1093
-
-
Grosso, A.R.1
Martins, S.2
Carmo-Fonseca, M.3
-
23
-
-
78049416081
-
Alternative pre-mRNA splicing regulation in cancer: pathways and programs unhinged
-
David CJ, Manley JL, (2010) Alternative pre-mRNA splicing regulation in cancer: pathways and programs unhinged. Genes Dev 24: 2343-2364.
-
(2010)
Genes Dev
, vol.24
, pp. 2343-2364
-
-
David, C.J.1
Manley, J.L.2
-
24
-
-
33947541694
-
Alternative splicing: an emerging topic in molecular and clinical oncology
-
Pajares MJ, Ezponda T, Catena R, Calvo A, Pio R, et al. (2007) Alternative splicing: an emerging topic in molecular and clinical oncology. Lancet Oncol 8: 349-357.
-
(2007)
Lancet Oncol
, vol.8
, pp. 349-357
-
-
Pajares, M.J.1
Ezponda, T.2
Catena, R.3
Calvo, A.4
Pio, R.5
-
25
-
-
0036468922
-
A misspliced form of the cholecystokinin-B/gastrin receptor in pancreatic carcinoma: role of reduced sellular U2AF35 and a suboptimal 3′-splicing site leading to retention of the fourth intron
-
Ding WQ, Kuntz SM, Miller LJ, (2002) A misspliced form of the cholecystokinin-B/gastrin receptor in pancreatic carcinoma: role of reduced sellular U2AF35 and a suboptimal 3′-splicing site leading to retention of the fourth intron. Cancer Res 62: 947-952.
-
(2002)
Cancer Res
, vol.62
, pp. 947-952
-
-
Ding, W.Q.1
Kuntz, S.M.2
Miller, L.J.3
-
26
-
-
33749471110
-
RNA interference knockdown of hU2AF35 impairs cell cycle progression and modulates alternative splicing of Cdc25 transcripts
-
Pacheco TR, Moita LF, Gomes AQ, Hacohen N, Carmo-Fonseca M, (2006) RNA interference knockdown of hU2AF35 impairs cell cycle progression and modulates alternative splicing of Cdc25 transcripts. Mol Biol Cell 17: 4187-4199.
-
(2006)
Mol Biol Cell
, vol.17
, pp. 4187-4199
-
-
Pacheco, T.R.1
Moita, L.F.2
Gomes, A.Q.3
Hacohen, N.4
Carmo-Fonseca, M.5
|