-
2
-
-
77952305440
-
Prognostic effect of chromosomal abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: Results from the UK Medical Research Council ALL97/99 randomised trial
-
Moorman AV, Ensor HM, Richards SM, Chilton L, Schwab C, Kinsey SE et al. Prognostic effect of chromosomal abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: results from the UK Medical Research Council ALL97/99 randomised trial. Lancet Oncol 2010; 11: 429-438.
-
(2010)
Lancet Oncol
, vol.11
, pp. 429-438
-
-
Moorman, A.V.1
Ensor, H.M.2
Richards, S.M.3
Chilton, L.4
Schwab, C.5
Kinsey, S.E.6
-
3
-
-
77951441599
-
Molecular response to treatment redefines all prognostic factors in children and adolescents with B-cell precursor acute lymphoblastic leukemia: Results in 3184 patients of the AIEOP-BFM ALL 2000 study
-
Conter V, Bartram CR, Valsecchi MG, Schrauder A, Panzer-Grumayer R, Moricke A et al. Molecular response to treatment redefines all prognostic factors in children and adolescents with B-cell precursor acute lymphoblastic leukemia: results in 3184 patients of the AIEOP-BFM ALL 2000 study. Blood 2010; 115: 3206-3214.
-
(2010)
Blood
, vol.115
, pp. 3206-3214
-
-
Conter, V.1
Bartram, C.R.2
Valsecchi, M.G.3
Schrauder, A.4
Panzer-Grumayer, R.5
Moricke, A.6
-
4
-
-
77952483774
-
Long-term outcome in children with relapsed acute lymphoblastic leukemia after time-point and site-of-relapse stratification and intensified short-course multidrug chemotherapy: Results of trial ALL-REZ BFM 90
-
Tallen G, Ratei R, Mann G, Kaspers G, Niggli F, Karachunsky A et al. Long-term outcome in children with relapsed acute lymphoblastic leukemia after time-point and site-of-relapse stratification and intensified short-course multidrug chemotherapy: results of trial ALL-REZ BFM 90. J Clin Oncol 2010; 28: 2339-2347.
-
(2010)
J Clin Oncol
, vol.28
, pp. 2339-2347
-
-
Tallen, G.1
Ratei, R.2
Mann, G.3
Kaspers, G.4
Niggli, F.5
Karachunsky, A.6
-
5
-
-
67650421868
-
High hyperdiploid childhood acute lymphoblastic leukemia
-
Paulsson K, Johansson B. High hyperdiploid childhood acute lymphoblastic leukemia. Genes Chromosomes Cancer 2009; 48: 637-660.
-
(2009)
Genes Chromosomes Cancer
, vol.48
, pp. 637-660
-
-
Paulsson, K.1
Johansson, B.2
-
6
-
-
0141634051
-
Origins of chromosome translocations in childhood leukaemia
-
Greaves MF, Wiemels J. Origins of chromosome translocations in childhood leukaemia. Nat Rev Cancer 2003; 3: 639-649.
-
(2003)
Nat Rev Cancer
, vol.3
, pp. 639-649
-
-
Greaves, M.F.1
Wiemels, J.2
-
7
-
-
0036659908
-
Nondisjunction of chromosomes leading to hyperdiploid childhood B-cell precursor acute lymphoblastic leukemia is an early event during leukemogenesis
-
Panzer-Grumayer ER, Fasching K, Panzer S, Hettinger K, Schmitt K, Stockler-Ipsiroglu S et al. Nondisjunction of chromosomes leading to hyperdiploid childhood B-cell precursor acute lymphoblastic leukemia is an early event during leukemogenesis. Blood 2002; 100: 347-349.
-
(2002)
Blood
, vol.100
, pp. 347-349
-
-
Panzer-Grumayer, E.R.1
Fasching, K.2
Panzer, S.3
Hettinger, K.4
Schmitt, K.5
Stockler-Ipsiroglu, S.6
-
8
-
-
0242475207
-
Prenatal origin of hyperdiploid acute lymphoblastic leukemia in identical twins
-
Maia AT, van der Velden VH, Harrison CJ, Szczepanski T, Williams MD, Griffiths MJ et al. Prenatal origin of hyperdiploid acute lymphoblastic leukemia in identical twins. Leukemia 2003; 17: 2202-2206.
-
(2003)
Leukemia
, vol.17
, pp. 2202-2206
-
-
Maia, A.T.1
Van Der Velden, V.H.2
Harrison, C.J.3
Szczepanski, T.4
Williams, M.D.5
Griffiths, M.J.6
-
9
-
-
78650745577
-
Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia
-
Paulsson K, Forestier E, Lilljebjorn H, Heldrup J, Behrendtz M, Young BD et al. Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia. Proc Natl Acad Sci USA 2010; 107: 21719-21724.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 21719-21724
-
-
Paulsson, K.1
Forestier, E.2
Lilljebjorn, H.3
Heldrup, J.4
Behrendtz, M.5
Young, B.D.6
-
10
-
-
34147224008
-
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
-
Mullighan CG, Goorha S, Radtke I, Miller CB, Coustan-Smith E, Dalton JD et al. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature 2007; 446: 758-764.
-
(2007)
Nature
, vol.446
, pp. 758-764
-
-
Mullighan, C.G.1
Goorha, S.2
Radtke, I.3
Miller, C.B.4
Coustan-Smith, E.5
Dalton, J.D.6
-
11
-
-
38349177862
-
Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray
-
Kawamata N, Ogawa S, Zimmermann M, Kato M, Sanada M, Hemminki K et al. Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray. Blood 2008; 111: 776-784.
-
(2008)
Blood
, vol.111
, pp. 776-784
-
-
Kawamata, N.1
Ogawa, S.2
Zimmermann, M.3
Kato, M.4
Sanada, M.5
Hemminki, K.6
-
13
-
-
33947594129
-
Hyperactive Ras in developmental disorders and cancer
-
Schubbert S, Shannon K, Bollag G. Hyperactive Ras in developmental disorders and cancer. Nat Rev Cancer 2007; 7: 295-308.
-
(2007)
Nat Rev Cancer
, vol.7
, pp. 295-308
-
-
Schubbert, S.1
Shannon, K.2
Bollag, G.3
-
14
-
-
57149118627
-
Genomic analysis of the clonal origins of relapsed acute lymphoblastic leukemia
-
Mullighan CG, Phillips LA, Su X, Ma J, Miller CB, Shurtleff SA et al. Genomic analysis of the clonal origins of relapsed acute lymphoblastic leukemia. Science 2008; 322: 1377-1380.
-
(2008)
Science
, vol.322
, pp. 1377-1380
-
-
Mullighan, C.G.1
Phillips, L.A.2
Su, X.3
Ma, J.4
Miller, C.B.5
Shurtleff, S.A.6
-
15
-
-
79953090054
-
ETV6/RUNX1-positive relapses evolve from an ancestral clone and frequently acquire deletions of genes implicated in glucocorticoid signaling
-
Kuster L, Grausenburger R, Fuka G, Kaindl U, Krapf G, Inthal A et al. ETV6/RUNX1-positive relapses evolve from an ancestral clone and frequently acquire deletions of genes implicated in glucocorticoid signaling. Blood 2011; 117: 2658-2667.
-
(2011)
Blood
, vol.117
, pp. 2658-2667
-
-
Kuster, L.1
Grausenburger, R.2
Fuka, G.3
Kaindl, U.4
Krapf, G.5
Inthal, A.6
-
16
-
-
77952485949
-
Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: Presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations
-
Davidsson J, Paulsson K, Lindgren D, Lilljebjorn H, Chaplin T, Forestier E et al. Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations. Leukemia 2010; 24: 924-931.
-
(2010)
Leukemia
, vol.24
, pp. 924-931
-
-
Davidsson, J.1
Paulsson, K.2
Lindgren, D.3
Lilljebjorn, H.4
Chaplin, T.5
Forestier, E.6
-
17
-
-
84864865832
-
CREBBP HAT domain mutations prevail in relapse cases of high hyperdiploid childhood acute lymphoblastic leukemia
-
Inthal A, Zeitlhofer P, Zeginigg M, Morak M, Grausenburger R, Fronkova E et al. CREBBP HAT domain mutations prevail in relapse cases of high hyperdiploid childhood acute lymphoblastic leukemia. Leukemia 2012; 26: 1797-1803.
-
(2012)
Leukemia
, vol.26
, pp. 1797-1803
-
-
Inthal, A.1
Zeitlhofer, P.2
Zeginigg, M.3
Morak, M.4
Grausenburger, R.5
Fronkova, E.6
-
18
-
-
0029022770
-
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
-
Petrij F, Giles RH, Dauwerse HG, Saris JJ, Hennekam RC, Masuno M et al. Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP. Nature 1995; 376: 348-351.
-
(1995)
Nature
, vol.376
, pp. 348-351
-
-
Petrij, F.1
Giles, R.H.2
Dauwerse, H.G.3
Saris, J.J.4
Hennekam, R.C.5
Masuno, M.6
-
19
-
-
79952381408
-
CREBBP mutations in relapsed acute lymphoblastic leukaemia
-
Mullighan CG, Zhang J, Kasper LH, Lerach S, Payne-Turner D, Phillips LA et al. CREBBP mutations in relapsed acute lymphoblastic leukaemia. Nature 2011; 471: 235-239.
-
(2011)
Nature
, vol.471
, pp. 235-239
-
-
Mullighan, C.G.1
Zhang, J.2
Kasper, L.H.3
Lerach, S.4
Payne-Turner, D.5
Phillips, L.A.6
-
20
-
-
79952430906
-
Inactivating mutations of acetyltransferase genes in B-cell lymphoma
-
Pasqualucci L, Dominguez-Sola D, Chiarenza A, Fabbri G, Grunn A, Trifonov V et al. Inactivating mutations of acetyltransferase genes in B-cell lymphoma. Nature 2011; 471: 189-195.
-
(2011)
Nature
, vol.471
, pp. 189-195
-
-
Pasqualucci, L.1
Dominguez-Sola, D.2
Chiarenza, A.3
Fabbri, G.4
Grunn, A.5
Trifonov, V.6
-
21
-
-
80052922387
-
Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: A report from the Children's Oncology Group
-
Zhang J, Mullighan CG, Harvey RC, Wu G, Chen X, Edmonson M et al. Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group. Blood 2011; 118: 3080-3087.
-
(2011)
Blood
, vol.118
, pp. 3080-3087
-
-
Zhang, J.1
Mullighan, C.G.2
Harvey, R.C.3
Wu, G.4
Chen, X.5
Edmonson, M.6
-
22
-
-
84893452297
-
Use of allogeneic hematopoietic stem-cell transplantation based on minimal residual disease response improves outcomes for children with relapsed acute lymphoblastic leukemia in the intermediate-risk group
-
Eckert C, Henze G, Seeger K, Hagedorn N, Mann G, Panzer-Grumayer R et al. Use of allogeneic hematopoietic stem-cell transplantation based on minimal residual disease response improves outcomes for children with relapsed acute lymphoblastic leukemia in the intermediate-risk group. J Clin Oncol 2013; 31: 2736-2742.
-
(2013)
J Clin Oncol
, vol.31
, pp. 2736-2742
-
-
Eckert, C.1
Henze, G.2
Seeger, K.3
Hagedorn, N.4
Mann, G.5
Panzer-Grumayer, R.6
-
23
-
-
84871171498
-
Doxorubicin or daunorubicin given upfront in a therapeutic window are equally effective in children with newly diagnosed acute lymphoblastic leukemia. A randomized comparison in trial CoALL 07-03
-
Escherich G, Zimmermann M, Janka-Schaub G. Co ALLsg. Doxorubicin or daunorubicin given upfront in a therapeutic window are equally effective in children with newly diagnosed acute lymphoblastic leukemia. A randomized comparison in trial CoALL 07-03. Pediatr Blood Cancer 2013; 60: 254-257.
-
(2013)
Pediatr Blood Cancer
, vol.60
, pp. 254-257
-
-
Escherich, G.1
Zimmermann, M.2
Janka-Schaub, G.3
-
24
-
-
47149100125
-
Risk-adjusted therapy of acute lymphoblastic leukemia can decrease treatment burden and improve survival: Treatment results of 2169 unselected pediatric and adolescent patients enrolled in the trial ALL-BFM 95
-
Moricke A, Reiter A, Zimmermann M, Gadner H, Stanulla M, Dordelmann M et al. Risk-adjusted therapy of acute lymphoblastic leukemia can decrease treatment burden and improve survival: treatment results of 2169 unselected pediatric and adolescent patients enrolled in the trial ALL-BFM 95. Blood 2008; 111: 4477-4489.
-
(2008)
Blood
, vol.111
, pp. 4477-4489
-
-
Moricke, A.1
Reiter, A.2
Zimmermann, M.3
Gadner, H.4
Stanulla, M.5
Dordelmann, M.6
-
25
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 2009; 25: 1754-1760.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
26
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data
-
DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 2011; 43: 491-498.
-
(2011)
Nat Genet
, vol.43
, pp. 491-498
-
-
DePristo, M.A.1
Banks, E.2
Poplin, R.3
Garimella, K.V.4
Maguire, J.R.5
Hartl, C.6
-
27
-
-
84874025843
-
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
-
Cibulskis K, Lawrence MS, Carter SL, Sivachenko A, Jaffe D, Sougnez C et al. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat Biotechnol 2013; 31: 213-219.
-
(2013)
Nat Biotechnol
, vol.31
, pp. 213-219
-
-
Cibulskis, K.1
Lawrence, M.S.2
Carter, S.L.3
Sivachenko, A.4
Jaffe, D.5
Sougnez, C.6
-
28
-
-
84876030710
-
Using Dro-sophila melanogaster as a Model for Genotoxic Chemical Mutational Studies with a New Program, SnpSift
-
Cingolani P, Patel VM, Coon M, Nguyen T, Land SJ, Ruden DM et al. Using Dro-sophila melanogaster as a Model for Genotoxic Chemical Mutational Studies with a New Program, SnpSift. Front Genet 2012; 3: 35.
-
(2012)
Front Genet
, vol.3
, pp. 35
-
-
Cingolani, P.1
Patel, V.M.2
Coon, M.3
Nguyen, T.4
Land, S.J.5
Ruden, D.M.6
-
29
-
-
84863229597
-
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
-
Koboldt DC, Zhang Q, Larson DE, Shen D, McLellan MD, Lin L et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Res 2012; 22: 568-576.
-
(2012)
Genome Res
, vol.22
, pp. 568-576
-
-
Koboldt, D.C.1
Zhang, Q.2
Larson, D.E.3
Shen, D.4
McLellan, M.D.5
Lin, L.6
-
30
-
-
79958127503
-
PathScan: A tool for discerning mutational significance in groups of putative cancer genes
-
Wendl MC, Wallis JW, Lin L, Kandoth C, Mardis ER, Wilson RK et al. PathScan: a tool for discerning mutational significance in groups of putative cancer genes. Bioin-formatics 2011; 27: 1595-1602.
-
(2011)
Bioin-formatics
, vol.27
, pp. 1595-1602
-
-
Wendl, M.C.1
Wallis, J.W.2
Lin, L.3
Kandoth, C.4
Mardis, E.R.5
Wilson, R.K.6
-
31
-
-
84864598664
-
MuSiC: Identifying mutational significance in cancer genomes
-
Dees ND, Zhang Q, Kandoth C, Wendl MC, Schierding W, Koboldt DC et al. MuSiC: identifying mutational significance in cancer genomes. Genome Res 2012; 22: 1589-1598.
-
(2012)
Genome Res
, vol.22
, pp. 1589-1598
-
-
Dees, N.D.1
Zhang, Q.2
Kandoth, C.3
Wendl, M.C.4
Schierding, W.5
Koboldt, D.C.6
-
32
-
-
33845382806
-
Nonparametric estimation from incomplete observations
-
Kaplan EL MP. Nonparametric estimation from incomplete observations. J Am Stat Assoc 1958; 53: 4.
-
(1958)
J am Stat Assoc
, vol.53
, pp. 4
-
-
Kaplan, E.L.M.P.1
-
33
-
-
0000120995
-
A class of K-sample tests for comparing the cumulative incidence of a competing risk
-
Gray R. A class of K-sample tests for comparing the cumulative incidence of a competing risk. Ann Stat 1988; 16: 1141-1154.
-
(1988)
Ann Stat
, vol.16
, pp. 1141-1154
-
-
Gray, R.1
-
34
-
-
36549062445
-
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia
-
Paulsson K, Horvat A, Strombeck B, Nilsson F, Heldrup J, Behrendtz M et al. Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia. Genes Chromosomes Cancer 2008; 47: 26-33.
-
(2008)
Genes Chromosomes Cancer
, vol.47
, pp. 26-33
-
-
Paulsson, K.1
Horvat, A.2
Strombeck, B.3
Nilsson, F.4
Heldrup, J.5
Behrendtz, M.6
-
35
-
-
20144374673
-
RAS mutation is associated with hyperdiploidy and parental characteristics in pediatric acute lymphoblastic leukemia
-
Wiemels JL, Zhang Y, Chang J, Zheng S, Metayer C, Zhang L et al. RAS mutation is associated with hyperdiploidy and parental characteristics in pediatric acute lymphoblastic leukemia. Leukemia 2005; 19: 415-419.
-
(2005)
Leukemia
, vol.19
, pp. 415-419
-
-
Wiemels, J.L.1
Zhang, Y.2
Chang, J.3
Zheng, S.4
Metayer, C.5
Zhang, L.6
-
36
-
-
84892529734
-
Whole exome sequencing identifies novel recurrently mutated genes in patients with splenic marginal zone lymphoma
-
Parry M, Rose-Zerilli MJ, Gibson J, Ennis S, Walewska R, Forster J et al. Whole exome sequencing identifies novel recurrently mutated genes in patients with splenic marginal zone lymphoma. PLoS One 2013; 8: e83244.
-
(2013)
PLoS One
, vol.8
, pp. e83244
-
-
Parry, M.1
Rose-Zerilli, M.J.2
Gibson, J.3
Ennis, S.4
Walewska, R.5
Forster, J.6
-
37
-
-
84861541343
-
Mutational processes molding the genomes of 21 breast cancers
-
Nik-Zainal S, Alexandrov LB, Wedge DC, Van Loo P, Greenman CD, Raine K et al. Mutational processes molding the genomes of 21 breast cancers. Cell 2012; 149: 979-993.
-
(2012)
Cell
, vol.149
, pp. 979-993
-
-
Nik-Zainal, S.1
Alexandrov, L.B.2
Wedge, D.C.3
Van Loo, P.4
Greenman, C.D.5
Raine, K.6
-
38
-
-
84875721185
-
Minimal residual disease after induction is the strongest predictor of prognosis in intermediate risk relapsed acute lymphoblastic leukaemia-long-term results of trial ALL-REZ BFM P95/96
-
Eckert C, von Stackelberg A, Seeger K, Groeneveld TW, Peters C, Klingebiel T et al. Minimal residual disease after induction is the strongest predictor of prognosis in intermediate risk relapsed acute lymphoblastic leukaemia-long-term results of trial ALL-REZ BFM P95/96. Eur J Cancer 2013; 49: 1346-1355.
-
(2013)
Eur J Cancer
, vol.49
, pp. 1346-1355
-
-
Eckert, C.1
Von Stackelberg, A.2
Seeger, K.3
Groeneveld, T.W.4
Peters, C.5
Klingebiel, T.6
-
39
-
-
84856013431
-
Clonal evolution in cancer
-
Greaves M, Maley CC. Clonal evolution in cancer. Nature 2012; 481: 306-313.
-
(2012)
Nature
, vol.481
, pp. 306-313
-
-
Greaves, M.1
Maley, C.C.2
-
40
-
-
84871481072
-
Small sizes and indolent evolutionary dynamics challenge the potential role of P2RY8-CRLF2-harboring clones as main relapse-driving force in childhood ALL
-
Morak M, Attarbaschi A, Fischer S, Nassimbeni C, Grausenburger R, Bastelberger S et al. Small sizes and indolent evolutionary dynamics challenge the potential role of P2RY8-CRLF2-harboring clones as main relapse-driving force in childhood ALL. Blood 2012; 120: 5134-5142.
-
(2012)
Blood
, vol.120
, pp. 5134-5142
-
-
Morak, M.1
Attarbaschi, A.2
Fischer, S.3
Nassimbeni, C.4
Grausenburger, R.5
Bastelberger, S.6
-
41
-
-
84859193076
-
The origin and nature of tightly clustered BTG1 deletions in precursor B-cell acute lymphoblastic leukemia support a model of multiclonal evolution
-
Waanders E, Scheijen B, van der Meer LT, van Reijmersdal SV, van Emst L, Kroeze Y et al. The origin and nature of tightly clustered BTG1 deletions in precursor B-cell acute lymphoblastic leukemia support a model of multiclonal evolution. PLoS Genet 2012; 8: e1002533.
-
(2012)
PLoS Genet
, vol.8
, pp. e1002533
-
-
Waanders, E.1
Scheijen, B.2
Van Der Meer, L.T.3
Van Reijmersdal, S.V.4
Van Emst, L.5
Kroeze, Y.6
-
42
-
-
84874647204
-
The genomic landscape of hypodiploid acute lymphoblastic leukemia
-
Holmfeldt L, Wei L, Diaz-Flores E, Walsh M, Zhang J, Ding L et al. The genomic landscape of hypodiploid acute lymphoblastic leukemia. Nat Genet 2013; 45: 242-252.
-
(2013)
Nat Genet
, vol.45
, pp. 242-252
-
-
Holmfeldt, L.1
Wei, L.2
Diaz-Flores, E.3
Walsh, M.4
Zhang, J.5
Ding, L.6
-
43
-
-
84863187331
-
Is histone acetylation the most important physiological function for CBP and p300?
-
Bedford DC, Brindle PK. Is histone acetylation the most important physiological function for CBP and p300? Aging 2012; 4: 247-255.
-
(2012)
Aging
, vol.4
, pp. 247-255
-
-
Bedford, D.C.1
Brindle, P.K.2
-
44
-
-
84859174608
-
Histone-modifying enzymes: Regulators of developmental decisions and drivers of human disease
-
Butler JS, Koutelou E, Schibler AC, Dent SY. Histone-modifying enzymes: regulators of developmental decisions and drivers of human disease. Epigenomics 2012; 4: 163-177.
-
(2012)
Epigenomics
, vol.4
, pp. 163-177
-
-
Butler, J.S.1
Koutelou, E.2
Schibler, A.C.3
Dent, S.Y.4
-
45
-
-
84868569000
-
Targeting oncogenic Ras signaling in hemato-logic malignancies
-
Ward AF, Braun BS, Shannon KM. Targeting oncogenic Ras signaling in hemato-logic malignancies. Blood 2012; 120: 3397-3406.
-
(2012)
Blood
, vol.120
, pp. 3397-3406
-
-
Ward, A.F.1
Braun, B.S.2
Shannon, K.M.3
-
46
-
-
35648971073
-
Ras proteins: Paradigms for compartmentalised and isoform-specific signalling
-
Omerovic J, Laude AJ, Prior IA. Ras proteins: paradigms for compartmentalised and isoform-specific signalling. Cell Mol Life Sci 2007; 64: 2575-2589.
-
(2007)
Cell Mol Life Sci
, vol.64
, pp. 2575-2589
-
-
Omerovic, J.1
Laude, A.J.2
Prior, I.A.3
-
47
-
-
77953395033
-
Ras signaling requires dynamic properties of Ets1 for phosphorylation-enhanced binding to coactivator CBP
-
Nelson ML, Kang HS, Lee GM, Blaszczak AG, Lau DK, McIntosh LP et al. Ras signaling requires dynamic properties of Ets1 for phosphorylation-enhanced binding to coactivator CBP. Proc Natl Acad Sci USA 2010; 107: 10026-10031.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 10026-10031
-
-
Nelson, M.L.1
Kang, H.S.2
Lee, G.M.3
Blaszczak, A.G.4
Lau, D.K.5
McIntosh, L.P.6
-
48
-
-
84914106704
-
Ras pathway mutations are highly prevalent in relapsed childhood acute lymphoblastic leukaemia, may act as relapse-drivers and confer sensitivity to MEK inhibition
-
Irving J, Matheson E, Minto L, Blair H, Case M, Halsey C et al. Ras pathway mutations are highly prevalent in relapsed childhood acute lymphoblastic leukaemia, may act as relapse-drivers and confer sensitivity to MEK inhibition. Blood 2014; 124: 3420-3430.
-
(2014)
Blood
, vol.124
, pp. 3420-3430
-
-
Irving, J.1
Matheson, E.2
Minto, L.3
Blair, H.4
Case, M.5
Halsey, C.6
|