-
1
-
-
84866467141
-
Loss of the tumor suppressor BAP1 causes myeloid transformation
-
Dey A, Seshasayee D, Noubade R, French DM, Liu J, Chaurushiya MS et al. Loss of the tumor suppressor BAP1 causes myeloid transformation. Science 2012; 337: 1541-1546.
-
(2012)
Science
, vol.337
, pp. 1541-1546
-
-
Dey, A.1
Seshasayee, D.2
Noubade, R.3
French, D.M.4
Liu, J.5
Chaurushiya, M.S.6
-
2
-
-
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
-
3
-
-
71749110779
-
The deubiquitinating enzyme BAP1 regulates cell growth via interaction with HCF-1
-
Machida YJ, Machida Y, Vashisht AA, Wohlschlegel JA, Dutta A. The deubiquitinating enzyme BAP1 regulates cell growth via interaction with HCF-1. J Biol Chem 2009; 284: 34179-34188.
-
(2009)
J Biol Chem
, vol.284
, pp. 34179-34188
-
-
Machida, Y.J.1
Machida, Y.2
Vashisht, A.A.3
Wohlschlegel, J.A.4
Dutta, A.5
-
4
-
-
67649634849
-
Defining the human deubiquitinating enzyme interaction landscape
-
Sowa ME, Bennett EJ, Gygi SP, Harper JW. Defining the human deubiquitinating enzyme interaction landscape. Cell 2009; 138: 389-403.
-
(2009)
Cell
, vol.138
, pp. 389-403
-
-
Sowa, M.E.1
Bennett, E.J.2
Gygi, S.P.3
Harper, J.W.4
-
5
-
-
0031946630
-
The additional sex combs gene of Drosophila encodes a chromatin protein that binds to shared and unique Polycomb group sites on polytene chromosomes
-
Sinclair DA, Milne TA, Hodgson JW, Shellard J, Salinas CA, Kyba M et al. The additional sex combs gene of Drosophila encodes a chromatin protein that binds to shared and unique Polycomb group sites on polytene chromosomes. Development 1998; 125: 1207-1216.
-
(1998)
Development
, vol.125
, pp. 1207-1216
-
-
Sinclair, D.A.1
Milne, T.A.2
Hodgson, J.W.3
Shellard, J.4
Salinas, C.A.5
Kyba, M.6
-
6
-
-
78651404455
-
Additional sex comb-like (ASXL) proteins 1 and 2 play opposite roles in adipogenesis via reciprocal regulation of peroxisome proliferator-activated receptor {gamma}
-
Park UH, Yoon SK, Park T, Kim EJ, Um SJ. Additional sex comb-like (ASXL) proteins 1 and 2 play opposite roles in adipogenesis via reciprocal regulation of peroxisome proliferator-activated receptor {gamma}. J Biol Chem 2011; 286: 1354-1363.
-
(2011)
J Biol Chem
, vol.286
, pp. 1354-1363
-
-
Park, U.H.1
Yoon, S.K.2
Park, T.3
Kim, E.J.4
Um, S.J.5
-
7
-
-
73649142039
-
ASXL1 represses retinoic acid receptor-mediated transcription through associating with HP1 and LSD1
-
Lee SW, Cho YS, Na JM, Park UH, Kang M, Kim EJ et al. ASXL1 represses retinoic acid receptor-mediated transcription through associating with HP1 and LSD1. J Biol Chem 2010; 285: 18-29.
-
(2010)
J Biol Chem
, vol.285
, pp. 18-29
-
-
Lee, S.W.1
Cho, Y.S.2
Na, J.M.3
Park, U.H.4
Kang, M.5
Kim, E.J.6
-
8
-
-
33745842538
-
Additional sex comb-like 1 (ASXL1), in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor
-
Cho YS, Kim EJ, Park UH, Sin HS, Um SJ. Additional sex comb-like 1 (ASXL1), in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor. J Biol Chem 2006; 281: 17588-17598.
-
(2006)
J Biol Chem
, vol.281
, pp. 17588-17598
-
-
Cho, Y.S.1
Kim, E.J.2
Park, U.H.3
Sin, H.S.4
Um, S.J.5
-
9
-
-
74949143986
-
Loss-offunction additional sex combs like 1 mutations disrupt hematopoiesis but do not cause severe myelodysplasia or leukemia
-
Fisher CL, Pineault N, Brookes C, Helgason CD, Ohta H, Bodner C et al. Loss-offunction additional sex combs like 1 mutations disrupt hematopoiesis but do not cause severe myelodysplasia or leukemia. Blood 2010; 115: 38-46.
-
(2010)
Blood
, vol.115
, pp. 38-46
-
-
Fisher, C.L.1
Pineault, N.2
Brookes, C.3
Helgason, C.D.4
Ohta, H.5
Bodner, C.6
-
10
-
-
84855695098
-
The HARE-HTH and associated domains: Novel modules in the coordination of epigenetic DNA and protein modifications
-
Aravind L, Iyer LM. The HARE-HTH and associated domains: novel modules in the coordination of epigenetic DNA and protein modifications. Cell Cycle 2012; 11: 119-131.
-
(2012)
Cell Cycle
, vol.11
, pp. 119-131
-
-
Aravind, L.1
Iyer, L.M.2
-
11
-
-
84255176496
-
ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN Favorable genetic category
-
Metzeler KH, Becker H, Maharry K, Radmacher MD, Kohlschmidt J, Mrozek K et al. ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN Favorable genetic category. Blood 2011; 118: 6920-6929.
-
(2011)
Blood
, vol.118
, pp. 6920-6929
-
-
Metzeler, K.H.1
Becker, H.2
Maharry, K.3
Radmacher, M.D.4
Kohlschmidt, J.5
Mrozek, K.6
-
12
-
-
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: 1200-1202.
-
(2011)
Leukemia
, vol.25
, pp. 1200-1202
-
-
Abdel-Wahab, O.1
Pardanani, A.2
Patel, J.3
Wadleigh, M.4
Lasho, T.5
Heguy, A.6
-
13
-
-
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
-
14
-
-
84863393263
-
Prognostic relevance of integrated genetic profiling in acute myeloid leukemia
-
Patel JP, Gonen M, Figueroa ME, Fernandez H, Sun Z, Racevskis J et al. Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. N Engl J Med 2012; 366: 1079-1089.
-
(2012)
N Engl J Med
, vol.366
, pp. 1079-1089
-
-
Patel, J.P.1
Gonen, M.2
Figueroa, M.E.3
Fernandez, H.4
Sun, Z.5
Racevskis, J.6
-
15
-
-
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
-
16
-
-
77952421834
-
Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia
-
Boultwood J, Perry J, Pellagatti A, Fernandez-Mercado M, Fernandez-Santamaria C, Calasanz MJ et al. Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia. Leukemia 2010; 24: 1062-1065.
-
(2010)
Leukemia
, vol.24
, pp. 1062-1065
-
-
Boultwood, J.1
Perry, J.2
Pellagatti, A.3
Fernandez-Mercado, M.4
Fernandez-Santamaria, C.5
Calasanz, M.J.6
-
17
-
-
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: 788-800.
-
(2009)
Br J Haematol
, vol.145
, pp. 788-800
-
-
Gelsi-Boyer, V.1
Trouplin, V.2
Adelaide, J.3
Bonansea, J.4
Cervera, N.5
Carbuccia, N.6
-
18
-
-
77952429798
-
Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB
-
Scheuermann JC, de Ayala Alonso AG, Oktaba K, Ly-Hartig N, McGinty RK, Fraterman S et al. Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB. Nature 2010; 465: 243-247.
-
(2010)
Nature
, vol.465
, pp. 243-247
-
-
Scheuermann, J.C.1
De Ayala Alonso, A.G.2
Oktaba, K.3
Ly-Hartig, N.4
McGinty, R.K.5
Fraterman, S.6
-
19
-
-
55949124844
-
EZH1 mediates methylation on histone H3 lysine 27 and complements EZH2 in maintaining stem cell identity and executing pluripotency
-
Shen X, Liu Y, Hsu YJ, Fujiwara Y, Kim J, Mao X et al. EZH1 mediates methylation on histone H3 lysine 27 and complements EZH2 in maintaining stem cell identity and executing pluripotency. Mol Cell 2008; 32: 491-502.
-
(2008)
Mol Cell
, vol.32
, pp. 491-502
-
-
Shen, X.1
Liu, Y.2
Hsu, Y.J.3
Fujiwara, Y.4
Kim, J.5
Mao, X.6
-
20
-
-
55949132133
-
Ezh1 and Ezh2 maintain repressive chromatin through different mechanisms
-
Margueron R, Li G, Sarma K, Blais A, Zavadil J, Woodcock CL et al. Ezh1 and Ezh2 maintain repressive chromatin through different mechanisms. Mol Cell 2008; 32: 503-518.
-
(2008)
Mol Cell
, vol.32
, pp. 503-518
-
-
Margueron, R.1
Li, G.2
Sarma, K.3
Blais, A.4
Zavadil, J.5
Woodcock, C.L.6
-
21
-
-
15144342687
-
BAP1: A novel ubiquitin hydrolase which binds to the BRCA1 RING finger and enhances BRCA1-mediated cell growth suppression
-
Jensen DE, Proctor M, Marquis ST, Gardner HP, Ha SI, Chodosh LA et al. BAP1: a novel ubiquitin hydrolase which binds to the BRCA1 RING finger and enhances BRCA1-mediated cell growth suppression. Oncogene 1998; 16: 1097-1112.
-
(1998)
Oncogene
, vol.16
, pp. 1097-1112
-
-
Jensen, D.E.1
Proctor, M.2
Marquis, S.T.3
Gardner, H.P.4
Ha, S.I.5
Chodosh, L.A.6
-
22
-
-
52049085265
-
BRCA1-associated protein-1 is a tumor suppressor that requires deubiquitinating activity and nuclear localization
-
Ventii KH, Devi NS, Friedrich KL, Chernova TA, Tighiouart M, Van Meir EG et al. BRCA1-associated protein-1 is a tumor suppressor that requires deubiquitinating activity and nuclear localization. Cancer Res 2008; 68: 6953-6962.
-
(2008)
Cancer Res
, vol.68
, pp. 6953-6962
-
-
Ventii, K.H.1
Devi, N.S.2
Friedrich, K.L.3
Chernova, T.A.4
Tighiouart, M.5
Van Meir, E.G.6
-
23
-
-
0011153988
-
Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma
-
Kovacs G, Erlandsson R, Boldog F, Ingvarsson S, Muller-Brechlin R, Klein G et al. Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma. Proc Natl Acad Sci USA 1988; 85: 1571-1575.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 1571-1575
-
-
Kovacs, G.1
Erlandsson, R.2
Boldog, F.3
Ingvarsson, S.4
Muller-Brechlin, R.5
Klein, G.6
-
24
-
-
78649700287
-
Frequent mutation of BAP1 in metastasizing uveal melanomas
-
Harbour JW, Onken MD, Roberson ED, Duan S, Cao L, Worley LA et al. Frequent mutation of BAP1 in metastasizing uveal melanomas. Science 2010; 330: 1410-1413.
-
(2010)
Science
, vol.330
, pp. 1410-1413
-
-
Harbour, J.W.1
Onken, M.D.2
Roberson, E.D.3
Duan, S.4
Cao, L.5
Worley, L.A.6
-
25
-
-
84856023369
-
Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers
-
Abdel-Rahman MH, Pilarski R, Cebulla CM, Massengill JB, Christopher BN, Boru G et al. Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers. J Med Genet 2011; 48: 856-859.
-
(2011)
J Med Genet
, vol.48
, pp. 856-859
-
-
Abdel-Rahman, M.H.1
Pilarski, R.2
Cebulla, C.M.3
Massengill, J.B.4
Christopher, B.N.5
Boru, G.6
-
26
-
-
79959694149
-
The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma
-
Bott M, Brevet M, Taylor BS, Shimizu S, Ito T, Wang L et al. The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma. Nat Genet 2011; 43: 668-672.
-
(2011)
Nat Genet
, vol.43
, pp. 668-672
-
-
Bott, M.1
Brevet, M.2
Taylor, B.S.3
Shimizu, S.4
Ito, T.5
Wang, L.6
-
27
-
-
80053385701
-
Germline BAP1 mutations predispose to malignant mesothelioma
-
Testa JR, Cheung M, Pei J, Below JE, Tan Y, Sementino E et al. Germline BAP1 mutations predispose to malignant mesothelioma. Nat Genet 2011; 43: 1022-1025.
-
(2011)
Nat Genet
, vol.43
, pp. 1022-1025
-
-
Testa, J.R.1
Cheung, M.2
Pei, J.3
Below, J.E.4
Tan, Y.5
Sementino, E.6
-
28
-
-
80053386896
-
Germline mutations in BAP1 predispose to melanocytic tumors
-
Wiesner T, Obenauf AC, Murali R, Fried I, Griewank KG, Ulz P et al. Germline mutations in BAP1 predispose to melanocytic tumors. Nat Genet 2011; 43: 1018-1021.
-
(2011)
Nat Genet
, vol.43
, pp. 1018-1021
-
-
Wiesner, T.1
Obenauf, A.C.2
Murali, R.3
Fried, I.4
Griewank, K.G.5
Ulz, P.6
-
29
-
-
84655176646
-
Frequent mutations of genes encoding ubiquitin-mediated proteolysis pathway components in clear cell renal cell carcinoma
-
Guo G, Gui Y, Gao S, Tang A, Hu X, Huang Y et al. Frequent mutations of genes encoding ubiquitin-mediated proteolysis pathway components in clear cell renal cell carcinoma. Nat Genet 2012; 44: 17-19.
-
(2012)
Nat Genet
, vol.44
, pp. 17-19
-
-
Guo, G.1
Gui, Y.2
Gao, S.3
Tang, A.4
Hu, X.5
Huang, Y.6
-
30
-
-
84862988411
-
BAP1 loss defines a new class of renal cell carcinoma
-
Pena-Llopis S, Vega-Rubin-de-Celis S, Liao A, Leng N, Pavia-Jimenez A, Wang S et al. BAP1 loss defines a new class of renal cell carcinoma. Nat Genet 2012; 44: 751-759.
-
(2012)
Nat Genet
, vol.44
, pp. 751-759
-
-
Pena-Llopis, S.1
Vega-Rubin-De-Celis, S.2
Liao, A.3
Leng, N.4
Pavia-Jimenez, A.5
Wang, S.6
-
31
-
-
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
-
32
-
-
77957853061
-
The ubiquitin carboxyl hydrolase BAP1 forms a ternary complex with YY1 and HCF-1 and is a critical regulator of gene expression
-
Yu H, Mashtalir N, Daou S, Hammond-Martel I, Ross J, Sui G et al. The ubiquitin carboxyl hydrolase BAP1 forms a ternary complex with YY1 and HCF-1 and is a critical regulator of gene expression. Mol Cell Biol 2010; 30: 5071-5085.
-
(2010)
Mol Cell Biol
, vol.30
, pp. 5071-5085
-
-
Yu, H.1
Mashtalir, N.2
Daou, S.3
Hammond-Martel, I.4
Ross, J.5
Sui, G.6
-
33
-
-
79960909421
-
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome
-
Hoischen A, van Bon BW, Rodriguez-Santiago B, Gilissen C, Vissers LE, de Vries P et al. De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome. Nat Genet 2011; 43: 729-731.
-
(2011)
Nat Genet
, vol.43
, pp. 729-731
-
-
Hoischen, A.1
Van Bon, B.W.2
Rodriguez-Santiago, B.3
Gilissen, C.4
Vissers, L.E.5
De Vries, P.6
-
34
-
-
84863723010
-
The mutational landscape of lethal castration-resistant prostate cancer
-
Grasso CS, Wu YM, Robinson DR, Cao X, Dhanasekaran SM, Khan AP et al. The mutational landscape of lethal castration-resistant prostate cancer. Nature 2012; 487: 239-243.
-
(2012)
Nature
, vol.487
, pp. 239-243
-
-
Grasso, C.S.1
Wu, Y.M.2
Robinson, D.R.3
Cao, X.4
Dhanasekaran, S.M.5
Khan, A.P.6
-
35
-
-
64649106796
-
Association of C-terminal ubiquitin hydrolase BRCA1-associated protein 1 with cell cycle regulator host cell factor 1
-
Misaghi S, Ottosen S, Izrael-Tomasevic A, Arnott D, Lamkanfi M, Lee J et al. Association of C-terminal ubiquitin hydrolase BRCA1-associated protein 1 with cell cycle regulator host cell factor 1. Mol Cell Biol 2009; 29: 2181-2192.
-
(2009)
Mol Cell Biol
, vol.29
, pp. 2181-2192
-
-
Misaghi, S.1
Ottosen, S.2
Izrael-Tomasevic, A.3
Arnott, D.4
Lamkanfi, M.5
Lee, J.6
-
36
-
-
79955934205
-
An emerging model for BAP1's role in regulating cell cycle progression
-
Eletr ZM, Wilkinson KD. An emerging model for BAP1's role in regulating cell cycle progression. Cell Biochem Biophys 2011; 60: 3-11.
-
(2011)
Cell Biochem Biophys
, vol.60
, pp. 3-11
-
-
Eletr, Z.M.1
Wilkinson, K.D.2
-
37
-
-
79551661274
-
O-GlcNAc transferase catalyzes site-specific proteolysis of HCF-1
-
Capotosti F, Guernier S, Lammers F, Waridel P, Cai Y, Jin J et al. O-GlcNAc transferase catalyzes site-specific proteolysis of HCF-1. Cell 2011; 144: 376-388.
-
(2011)
Cell
, vol.144
, pp. 376-388
-
-
Capotosti, F.1
Guernier, S.2
Lammers, F.3
Waridel, P.4
Cai, Y.5
Jin, J.6
-
38
-
-
33748190398
-
Host cell factor-1 and E2F4 interact via multiple determinants in each protein
-
Knez J, Piluso D, Bilan P, Capone JP. Host cell factor-1 and E2F4 interact via multiple determinants in each protein. Mol Cell Biochem 2006; 288: 79-90.
-
(2006)
Mol Cell Biochem
, vol.288
, pp. 79-90
-
-
Knez, J.1
Piluso, D.2
Bilan, P.3
Capone, J.P.4
-
39
-
-
34250823511
-
E2F activation of S phase promoters via association with HCF-1 and the MLL family of histone H3K4 methyltransferases
-
Tyagi S, Chabes AL, Wysocka J, Herr W. E2F activation of S phase promoters via association with HCF-1 and the MLL family of histone H3K4 methyltransferases. Mol Cell 2007; 27: 107-119.
-
(2007)
Mol Cell
, vol.27
, pp. 107-119
-
-
Tyagi, S.1
Chabes, A.L.2
Wysocka, J.3
Herr, W.4
-
40
-
-
84860184939
-
Bittersweet memories: Linking metabolism to epigenetics through O-GlcNAcylation
-
Hanover JA, Krause MW, Love DC. Bittersweet memories: linking metabolism to epigenetics through O-GlcNAcylation. Nat Rev Mol Cell Biol 2012; 13: 312-321.
-
(2012)
Nat Rev Mol Cell Biol
, vol.13
, pp. 312-321
-
-
Hanover, J.A.1
Krause, M.W.2
Love, D.C.3
-
41
-
-
62749165324
-
Functional conservation of Asxl2, a murine homolog for the Drosophila enhancer of trithorax and polycomb group gene Asx
-
Baskind HA, Na L, Ma Q, Patel MP, Geenen DL, Wang QT. Functional conservation of Asxl2, a murine homolog for the Drosophila enhancer of trithorax and polycomb group gene Asx. PLoS One 2009; 4: e4750.
-
(2009)
PLoS One
, vol.4
-
-
Baskind, H.A.1
Na, L.2
Ma, Q.3
Patel, M.P.4
Geenen, D.L.5
Wang, Q.T.6
-
42
-
-
70450239681
-
Mutations of ASXL1 gene in myeloproliferative neoplasms
-
Carbuccia N, Murati A, Trouplin V, Brecqueville M, Adelaide J, Rey J et al. Mutations of ASXL1 gene in myeloproliferative neoplasms. Leukemia 2009; 23: 2183-2186.
-
(2009)
Leukemia
, vol.23
, pp. 2183-2186
-
-
Carbuccia, N.1
Murati, A.2
Trouplin, V.3
Brecqueville, M.4
Adelaide, J.5
Rey, J.6
-
43
-
-
81055126771
-
EZH2 mutational status predicts poor survival in myelofibrosis
-
Guglielmelli P, Biamonte F, Score J, Hidalgo-Curtis C, Cervantes F, Maffioli M et al. EZH2 mutational status predicts poor survival in myelofibrosis. Blood 2011; 118: 5227-5234.
-
(2011)
Blood
, vol.118
, pp. 5227-5234
-
-
Guglielmelli, P.1
Biamonte, F.2
Score, J.3
Hidalgo-Curtis, C.4
Cervantes, F.5
Maffioli, M.6
-
44
-
-
76549109434
-
Genetic analysis of transforming events that convert chronic myeloproliferative neoplasms to leukemias
-
Abdel-Wahab O, Manshouri T, Patel J, Harris K, Yao J, Hedvat C et al. Genetic analysis of transforming events that convert chronic myeloproliferative neoplasms to leukemias. Cancer Res 2010; 70: 447-452.
-
(2010)
Cancer Res
, vol.70
, pp. 447-452
-
-
Abdel-Wahab, O.1
Manshouri, T.2
Patel, J.3
Harris, K.4
Yao, J.5
Hedvat, C.6
-
45
-
-
33749993417
-
The consensus coding sequences of human breast and colorectal cancers
-
Sjoblom T, Jones S, Wood LD, Parsons DW, Lin J, Barber TD et al. The consensus coding sequences of human breast and colorectal cancers. Science 2006; 314: 268-274.
-
(2006)
Science
, vol.314
, pp. 268-274
-
-
Sjoblom, T.1
Jones, S.2
Wood, L.D.3
Parsons, D.W.4
Lin, J.5
Barber, T.D.6
-
46
-
-
54549094903
-
Somatic mutations affect key pathways in lung adenocarcinoma
-
Ding L, Getz G, Wheeler DA, Mardis ER, McLellan MD, Cibulskis K et al. Somatic mutations affect key pathways in lung adenocarcinoma. Nature 2008; 455: 1069-1075.
-
(2008)
Nature
, vol.455
, pp. 1069-1075
-
-
Ding, L.1
Getz, G.2
Wheeler, D.A.3
Mardis, E.R.4
McLellan, M.D.5
Cibulskis, K.6
|