-
1
-
-
79953074952
-
Recent advances in diagnosis, molecular pathology and therapy of chronic myelomonocytic leukaemia
-
Bacher U, Haferlach T, Schnittger S, Kreipe H, Kroger N. Recent advances in diagnosis, molecular pathology and therapy of chronic myelomonocytic leukaemia. Br J Haematol. 2011;153(2):149-67.
-
(2011)
Br J Haematol.
, vol.153
, Issue.2
, pp. 149-167
-
-
Bacher, U.1
Haferlach, T.2
Schnittger, S.3
Kreipe, H.4
Kroger, N.5
-
2
-
-
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(14):3932-41.
-
(2011)
Blood.
, vol.118
, Issue.14
, pp. 3932-3941
-
-
Jankowska, A.M.1
Makishima, H.2
Tiu, R.V.3
Szpurka, H.4
Huang, Y.5
Traina, F.6
-
3
-
-
77956237515
-
Nextgeneration sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia (CMML) by detecting frequent alterations in TET2, CBL, RAS and RUNX1
-
Kohlmann A, Grossmann V, Klein H-U, 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 (CMML) 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
-
4
-
-
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. 2011;26(3):542-5.
-
(2011)
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
-
5
-
-
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
-
6
-
-
84859597590
-
Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
-
Makishima H, Visconte V, Sakaguchi H, Abu Kar S, Jankowska AM, 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
Abu Kar, S.4
Jankowska, A.M.5
Jerez, A.6
-
7
-
-
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
-
8
-
-
84555171449
-
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
-
Quesada V, Conde L, Villamor N, Ordonez GR, Jares P, Bassaganyas L, et al. Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia. Nat Genet. 2012; 44(1):47-52.
-
(2012)
Nat Genet.
, vol.44
, Issue.1
, pp. 47-52
-
-
Quesada, V.1
Conde, L.2
Villamor, N.3
Ordonez, G.R.4
Jares, P.5
Bassaganyas, L.6
-
9
-
-
84255160977
-
Mutations of the SF3B1 splicing factor in chronic lymphocytic leukemia: Association with progression and fludarabine-refractoriness
-
Rossi D, Bruscaggin A, Spina V, Rasi S, Khiabanian H, Messina M, et al. Mutations of the SF3B1 splicing factor in chronic lymphocytic leukemia: association with progression and fludarabine-refractoriness. Blood. 2011;118(26):6904-8.
-
(2011)
Blood.
, vol.118
, Issue.26
, pp. 6904-6908
-
-
Rossi, D.1
Bruscaggin, A.2
Spina, V.3
Rasi, S.4
Khiabanian, H.5
Messina, M.6
-
10
-
-
84855370035
-
SF3B1 and other novel cancer genes in chronic lymphocytic leukemia
-
Wang L, Lawrence MS, Wan Y, Stojanov P, Sougnez C, Stevenson K, et al. SF3B1 and other novel cancer genes in chronic lymphocytic leukemia. N Engl J Med. 2011; 365(26):2497-506.
-
(2011)
N Engl J Med.
, vol.365
, Issue.26
, pp. 2497-2506
-
-
Wang, L.1
Lawrence, M.S.2
Wan, Y.3
Stojanov, P.4
Sougnez, C.5
Stevenson, K.6
-
11
-
-
0030612083
-
Targeting of U2AF65 to sites of active splicing in the nucleus
-
Gama-Carvalho M, Krauss RD, Chiang L, Valcarcel J, Green MR, Carmo-Fonseca M. Targeting of U2AF65 to sites of active splicing in the nucleus. J Cell Biol. 1997;137 (5):975-87.
-
(1997)
J Cell Biol.
, vol.137
, Issue.5
, pp. 975-987
-
-
Gama-Carvalho, M.1
Krauss, R.D.2
Chiang, L.3
Valcarcel, J.4
Green, M.R.5
Carmo-Fonseca, M.6
-
12
-
-
1242316952
-
Arginine-serine-rich domains bound at splicing enhancers contact the branchpoint to promote prespliceosome assembly
-
Shen H, Kan JL, Green MR. Arginine-serine-rich domains bound at splicing enhancers contact the branchpoint to promote prespliceosome assembly. Mol Cell. 2004;13(3):367-76.
-
(2004)
Mol Cell.
, vol.13
, Issue.3
, pp. 367-376
-
-
Shen, H.1
Kan, J.L.2
Green, M.R.3
-
13
-
-
79952231064
-
The anti-tumor drug E7107 reveals an essential role for SF3b in remodeling U2 snRNP to expose the branch point-binding region
-
Folco EG, Coil KE, Reed R. The anti-tumor drug E7107 reveals an essential role for SF3b in remodeling U2 snRNP to expose the branch point-binding region. Genes Dev. 2011;25(5):440-4.
-
(2011)
Genes Dev.
, vol.25
, Issue.5
, pp. 440-444
-
-
Folco, E.G.1
Coil, K.E.2
Reed, R.3
-
15
-
-
70349256226
-
The 2008 revision of the 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 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
-
16
-
-
0036464647
-
Prognostic factors and scoring systems in chronic myelomonocytic leukemia: A retrospective analysis of 213 patients
-
Onida F, Kantarjian HM, Smith TL, Ball G, Keating MJ, Estey EH, et al. Prognostic factors and scoring systems 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
Kantarjian, H.M.2
Smith, T.L.3
Ball, G.4
Keating, M.J.5
Estey, E.H.6
-
17
-
-
0030977399
-
Chronic myelomonocytic leukemia in childhood: A retrospective analysis of 110 cases. European Working Group on Myelodysplastic Syndromes in Childhood (EWOG-MDS)
-
Niemeyer CM, Arico M, Basso G, Biondi A, Cantu RA, Creutzig U, et al. Chronic myelomonocytic leukemia in childhood: a retrospective analysis of 110 cases. European Working Group on Myelodysplastic Syndromes in Childhood (EWOG-MDS). Blood. 1997;89(10):3534-43.
-
(1997)
Blood.
, vol.89
, Issue.10
, pp. 3534-3543
-
-
Niemeyer, C.M.1
Arico, M.2
Basso, G.3
Biondi, A.4
Cantu, R.A.5
Creutzig, U.6
-
18
-
-
38949123096
-
Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML
-
Gondek LP, Tiu R, O'Keefe CL, Sekeres MA, Theil KS, Maciejewski JP. Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML. Blood. 2008;111(3):1534-42.
-
(2008)
Blood.
, vol.111
, Issue.3
, pp. 1534-1542
-
-
Gondek, L.P.1
Tiu, R.2
O'Keefe, C.L.3
Sekeres, M.A.4
Theil, K.S.5
Maciejewski, J.P.6
-
19
-
-
70449715477
-
New lesions detected by SNP array-based chromosomal analysis have important clinical impact in AML
-
Tiu RV, Gondek LP, O'Keefe CL, Huh J, Sekeres MA, McDevitt M, et al. New lesions detected by SNP array-based chromosomal analysis have important clinical impact in AML. J Clin Oncol. 2009; 27(31):5219-26.
-
(2009)
J Clin Oncol.
, vol.27
, Issue.31
, pp. 5219-5226
-
-
Tiu, R.V.1
Gondek, L.P.2
O'Keefe, C.L.3
Huh, J.4
Sekeres, M.A.5
McDevitt, M.6
-
20
-
-
0034554786
-
Report of an international working group to standardize response criteria for myelodysplastic syndromes
-
Cheson BD, Bennett JM, Kantarjian H, Pinto A, Schiffer CA, Nimer SD, et al. Report of an international working group to standardize response criteria for myelodysplastic syndromes. Blood. 2000; 96(12):3671-4.
-
(2000)
Blood.
, vol.96
, Issue.12
, pp. 3671-3674
-
-
Cheson, B.D.1
Bennett, J.M.2
Kantarjian, H.3
Pinto, A.4
Schiffer, C.A.5
Nimer, S.D.6
-
21
-
-
84859590749
-
SRSF2 is mutated in 47.2% (77/163) of chronic myelomonocytic leukemia (CMML) and prognostically favorable in cases with concomitant RUNX1 mutations
-
Schnittger S, Meggendorfer M, Kohlmann A, Grossman V, Yoshida K, Ogawa S, et al. SRSF2 is mutated in 47.2% (77/163) of chronic myelomonocytic leukemia (CMML) and prognostically favorable in cases with concomitant RUNX1 mutations. Blood. 2011;118(21):274 [abstract].
-
(2011)
Blood.
, vol.118
, Issue.21
, pp. 274
-
-
Schnittger, S.1
Meggendorfer, M.2
Kohlmann, A.3
Grossman, V.4
Yoshida, K.5
Ogawa, S.6
-
22
-
-
84857238789
-
Impact of molecular mutations on treatment response to hypomethylating agents in MDS
-
Traina F, Jankowska AM, Visconte V, Sugimoto Y, Szpurka H, Makishima H, et al. Impact of molecular mutations on treatment response to hypomethylating agents in MDS. Blood. 2011;118(21):213 [abstract].
-
(2011)
Blood.
, vol.118
, Issue.21
, pp. 213
-
-
Traina, F.1
Jankowska, A.M.2
Visconte, V.3
Sugimoto, Y.4
Szpurka, H.5
Makishima, H.6
-
23
-
-
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. 2011;44(1):53-7.
-
(2011)
Nat Genet.
, vol.44
, Issue.1
, pp. 53-57
-
-
Graubert, T.A.1
Shen, D.2
Ding, L.3
Okeyo Owuor, T.4
Lunn, C.L.5
Shao, J.6
-
24
-
-
61949288688
-
Correlation of clinical features with the mutational status of GM-CSF signaling pathway-related genes in juvenile myelomonocytic leukemia
-
Yoshida N, Yagasaki H, Xu Y, Matsuda K, Yoshimi A, Takahashi Y, et al. Correlation of clinical features with the mutational status of GM-CSF signaling pathway-related genes in juvenile myelomonocytic leukemia. Pediatr Res. 2009;65(3):334-40.
-
(2009)
Pediatr Res.
, vol.65
, Issue.3
, pp. 334-340
-
-
Yoshida, N.1
Yagasaki, H.2
Xu, Y.3
Matsuda, K.4
Yoshimi, A.5
Takahashi, Y.6
-
25
-
-
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.
-
(2010)
BMC Cancer.
, vol.10
, pp. 401
-
-
Rocquain, J.1
Carbuccia, N.2
Trouplin, V.3
Raynaud, S.4
Murati, A.5
Nezri, M.6
-
26
-
-
83455234787
-
Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative 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 myelodysplastic/myeloproliferative 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
-
27
-
-
84898108242
-
SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value
-
Patnaik MM, Lasho TL, Hodnefield JM, Knudson RA, Ketterling RP, Al-Kali A, et al. SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value. Blood. 2011;118(21):213 [abstract].
-
(2011)
Blood.
, vol.118
, Issue.21
, pp. 213
-
-
Patnaik, M.M.1
Lasho, T.L.2
Hodnefield, J.M.3
Knudson, R.A.4
Ketterling, R.P.5
Al-Kali, A.6
-
28
-
-
73149094518
-
TET2 gene mutation is a frequent and adverse event in chronic myelomonocytic leukemia
-
Kosmider O, Gelsi-Boyer V, Ciudad M, Racoeur C, Jooste V, Vey N, et al. TET2 gene mutation is a frequent and adverse event in chronic myelomonocytic leukemia. Haematologica. 2009;94(12): 1676-81.
-
(2009)
Haematologica.
, vol.94
, Issue.12
, pp. 1676-1681
-
-
Kosmider, O.1
Gelsi-Boyer, V.2
Ciudad, M.3
Racoeur, C.4
Jooste, V.5
Vey, N.6
-
29
-
-
66849124925
-
Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia
-
Gelsi-Boyer V, Trouplin V, Adelaide 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
Adelaide, J.3
Bonansea, J.4
Cervera, N.5
Carbuccia, N.6
-
30
-
-
78649753896
-
Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia
-
Parkin B, Erba H, Ouillette P, Roulston D, Purkayastha A, Karp J, et al. Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia. Blood. 2010;116(23):4958-67.
-
(2010)
Blood.
, vol.116
, Issue.23
, pp. 4958-4967
-
-
Parkin, B.1
Erba, H.2
Ouillette, P.3
Roulston, D.4
Purkayastha, A.5
Karp, J.6
-
31
-
-
84857734093
-
TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome
-
Rucker FG, Schlenk RF, Bullinger L, Kayser S, Teleanu V, Kett H, et al. TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome. Blood. 2011;119(9): 2114-21.
-
(2011)
Blood.
, vol.119
, Issue.9
, pp. 2114-2121
-
-
Rucker, F.G.1
Schlenk, R.F.2
Bullinger, L.3
Kayser, S.4
Teleanu, V.5
Kett, H.6
-
32
-
-
79957503201
-
Updates in cytogenetics and molecular markers in MDS
-
Tiu RV, Visconte V, Traina F, Schwandt A, Maciejewski JP. Updates in cytogenetics and molecular markers in MDS. Curr Hematol Malig Rep 2011;6(2):126-35.
-
(2011)
Curr Hematol Malig Rep
, vol.6
, Issue.2
, pp. 126-135
-
-
Tiu, R.V.1
Visconte, V.2
Traina, F.3
Schwandt, A.4
Maciejewski, J.P.5
-
33
-
-
79955513100
-
Aberrations of EZH2 in cancer
-
Chase A, Cross NC. Aberrations of EZH2 in cancer. Clin Cancer Res. 2011;17(9): 2613-8.
-
(2011)
Clin Cancer Res.
, vol.17
, Issue.9
, pp. 2613-2618
-
-
Chase, A.1
Cross, N.C.2
-
34
-
-
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
-
35
-
-
74949108515
-
Mutations of E3 ubiquitin ligase Cbl family members constitue a novel common pathogenic lesion in myeloid malignancies
-
Makishima H, Cazzolli H, Dunbar A, Muramatsu H, O'Keefe CL, Hsi E, et al. Mutations of E3 ubiquitin ligase Cbl family members constitue a novel common pathogenic lesion in myeloid malignancies. J Clin Oncol. 2009;27(36):6109-16.
-
(2009)
J Clin Oncol.
, vol.27
, Issue.36
, pp. 6109-6116
-
-
Makishima, H.1
Cazzolli, H.2
Dunbar, A.3
Muramatsu, H.4
O'Keefe, C.L.5
Hsi, E.6
-
36
-
-
79956291339
-
TP53 mutations in low-risk myelodysplastic syndromes with del(5q) predict disease progression
-
Jadersten M, Saft L, Smith A, Kulasekararaj A, Pomplun S, Gohring G, et al. TP53 mutations in low-risk myelodysplastic syndromes with del(5q) predict disease progression. J Clin Oncol. 2011;29(15): 1971-9.
-
(2011)
J Clin Oncol.
, vol.29
, Issue.15
, pp. 1971-1979
-
-
Jadersten, M.1
Saft, L.2
Smith, A.3
Kulasekararaj, A.4
Pomplun, S.5
Gohring, G.6
-
37
-
-
62749098351
-
A global view of cancer-specific transcript variants by subtractive transcriptome-wide analysis
-
He C, Zhou F, Zuo Z, Cheng H, Zhou R. A global view of cancer-specific transcript variants by subtractive transcriptome-wide analysis. PLoS ONE. 2009;4(3):e4732.
-
(2009)
PLoS ONE.
, vol.4
, Issue.3
-
-
He, C.1
Zhou, F.2
Zuo, Z.3
Cheng, H.4
Zhou, R.5
-
38
-
-
33947541694
-
Alternative splicing: An emerging topic in molecular and clinical oncology
-
Pajares MJ, Ezponda T, Catena R, Calvo A, Pio R, Montuenga LM. Alternative splicing: an emerging topic in molecular and clinical oncology. Lancet Oncol 2007; 8(4):349-57.
-
(2007)
Lancet Oncol
, vol.8
, Issue.4
, pp. 349-357
-
-
Pajares, M.J.1
Ezponda, T.2
Catena, R.3
Calvo, A.4
Pio, R.5
Montuenga, L.M.6
-
39
-
-
33646682821
-
Disease mechanism and biomarkers of oral squamous cell carcinoma
-
Brinkman BM, Wong DT. Disease mechanism and biomarkers of oral squamous cell carcinoma. Curr Opin Oncol. 2006;18(3): 228-33.
-
(2006)
Curr Opin Oncol.
, vol.18
, Issue.3
, pp. 228-233
-
-
Brinkman, B.M.1
Wong, D.T.2
-
40
-
-
84858672060
-
Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML
-
Hirabayashi S, Flotho C, Moetter J, Heuser M, Hasle H, Gruhn B, et al. Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML. Blood. 2012;119(11):e96-e9.
-
(2012)
Blood.
, vol.119
, Issue.11
-
-
Hirabayashi, S.1
Flotho, C.2
Moetter, J.3
Heuser, M.4
Hasle, H.5
Gruhn, B.6
|