-
1
-
-
84867744264
-
Evolution of the cancer genome
-
Yates LR, Campbell PJ, (2012) Evolution of the cancer genome. Nat Rev Genet 13: 795–806. doi: 10.1038/nrg3317 23044827
-
(2012)
Nat Rev Genet
, vol.13
, pp. 795-806
-
-
Yates, L.R.1
Campbell, P.J.2
-
2
-
-
84861550476
-
The life history of 21 breast cancers
-
Nik-Zainal S, Van Loo P, Wedge DC, Alexandrov LB, Greenman CD, et al. (2012) The life history of 21 breast cancers. Cell 149: 994–1007. doi: 10.1016/j.cell.2012.04.023 22608083
-
(2012)
Cell
, vol.149
, pp. 994-1007
-
-
Nik-Zainal, S.1
Van Loo, P.2
Wedge, D.C.3
Alexandrov, L.B.4
Greenman, C.D.5
-
3
-
-
84873441292
-
Half or more of the somatic mutations in cancers of self-renewing tissues originate prior to tumor initiation
-
Tomasetti C, Vogelstein B, Parmigiani G, (2013) Half or more of the somatic mutations in cancers of self-renewing tissues originate prior to tumor initiation. Proc Natl Acad Sci U S A 110: 1999–2004. doi: 10.1073/pnas.1221068110 23345422
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. 1999-2004
-
-
Tomasetti, C.1
Vogelstein, B.2
Parmigiani, G.3
-
5
-
-
79951494668
-
Initial genome sequencing and analysis of multiple myeloma
-
Chapman MA, Lawrence MS, Keats JJ, Cibulskis K, Sougnez C, et al. (2011) Initial genome sequencing and analysis of multiple myeloma. Nature 471: 467–472. doi: 10.1038/nature09837 21430775
-
(2011)
Nature
, vol.471
, pp. 467-472
-
-
Chapman, M.A.1
Lawrence, M.S.2
Keats, J.J.3
Cibulskis, K.4
Sougnez, C.5
-
6
-
-
77951139631
-
Genome remodelling in a basal-like breast cancer metastasis and xenograft
-
Ding L, Ellis MJ, Li S, Larson DE, Chen K, et al. (2010) Genome remodelling in a basal-like breast cancer metastasis and xenograft. Nature 464: 999–1005. doi: 10.1038/nature08989 20393555
-
(2010)
Nature
, vol.464
, pp. 999-1005
-
-
Ding, L.1
Ellis, M.J.2
Li, S.3
Larson, D.E.4
Chen, K.5
-
7
-
-
78649906060
-
DNMT3A mutations in acute myeloid leukemia
-
Ley TJ, Ding L, Walter MJ, McLellan MD, Lamprecht T, et al. (2010) DNMT3A mutations in acute myeloid leukemia. N Engl J Med 363: 2424–2433. doi: 10.1056/NEJMoa1005143 21067377
-
(2010)
N Engl J Med
, vol.363
, pp. 2424-2433
-
-
Ley, T.J.1
Ding, L.2
Walter, M.J.3
McLellan, M.D.4
Lamprecht, T.5
-
8
-
-
79960036578
-
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
-
Puente XS, Pinyol M, Quesada V, Conde L, Ordonez GR, et al. (2011) Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia. Nature 475: 101–105. doi: 10.1038/nature10113 21642962
-
(2011)
Nature
, vol.475
, pp. 101-105
-
-
Puente, X.S.1
Pinyol, M.2
Quesada, V.3
Conde, L.4
Ordonez, G.R.5
-
9
-
-
84862776906
-
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
-
Ding L, Ley TJ, Larson DE, Miller CA, Koboldt DC, et al. (2012) Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. Nature 481: 506–510. doi: 10.1038/nature10738 22237025
-
(2012)
Nature
, vol.481
, pp. 506-510
-
-
Ding, L.1
Ley, T.J.2
Larson, D.E.3
Miller, C.A.4
Koboldt, D.C.5
-
10
-
-
78049398107
-
Distant metastasis occurs late during the genetic evolution of pancreatic cancer
-
Yachida S, Jones S, Bozic I, Antal T, Leary R, et al. (2010) Distant metastasis occurs late during the genetic evolution of pancreatic cancer. Nature 467: 1114–1117. doi: 10.1038/nature09515 20981102
-
(2010)
Nature
, vol.467
, pp. 1114-1117
-
-
Yachida, S.1
Jones, S.2
Bozic, I.3
Antal, T.4
Leary, R.5
-
11
-
-
84874102335
-
Evolution and impact of subclonal mutations in chronic lymphocytic leukemia
-
Landau DA, Carter SL, Stojanov P, McKenna A, Stevenson K, et al. (2013) Evolution and impact of subclonal mutations in chronic lymphocytic leukemia. Cell 152: 714–726. doi: 10.1016/j.cell.2013.01.019 23415222
-
(2013)
Cell
, vol.152
, pp. 714-726
-
-
Landau, D.A.1
Carter, S.L.2
Stojanov, P.3
McKenna, A.4
Stevenson, K.5
-
12
-
-
44249124028
-
Karyotype evolution on fluorescent in situ hybridization analysis is associated with short survival in patients with chronic lymphocytic leukemia and is related to CD49d expression
-
Shanafelt TD, Hanson C, Dewald GW, Witzig TE, LaPlant B, et al. (2008) Karyotype evolution on fluorescent in situ hybridization analysis is associated with short survival in patients with chronic lymphocytic leukemia and is related to CD49d expression. J Clin Oncol 26: e5–6. doi: 10.1200/JCO.2008.16.7874 18467710
-
(2008)
J Clin Oncol
, vol.26
, pp. 5-6
-
-
Shanafelt, T.D.1
Hanson, C.2
Dewald, G.W.3
Witzig, T.E.4
LaPlant, B.5
-
13
-
-
84862526929
-
The clonal and mutational evolution spectrum of primary triple-negative breast cancers
-
Shah SP, Roth A, Goya R, Oloumi A, Ha G, et al. (2012) The clonal and mutational evolution spectrum of primary triple-negative breast cancers. Nature 486: 395–399. doi: 10.1038/nature10933 22495314
-
(2012)
Nature
, vol.486
, pp. 395-399
-
-
Shah, S.P.1
Roth, A.2
Goya, R.3
Oloumi, A.4
Ha, G.5
-
14
-
-
80055101101
-
Temporal Dissection of Tumorigenesis in Primary Cancers
-
Durinck S, Ho C, Wang NJ, Liao W, Jakkula LR, et al. (2011) Temporal Dissection of Tumorigenesis in Primary Cancers. Cancer Discovery 1: 137–143. doi: 10.1158/2159-8290.CD-11-0028 21984974
-
(2011)
Cancer Discovery
, vol.1
, pp. 137-143
-
-
Durinck, S.1
Ho, C.2
Wang, N.J.3
Liao, W.4
Jakkula, L.R.5
-
15
-
-
70149121277
-
Trends in childhood rhabdomyosarcoma incidence and survival in the United States, 1975–2005
-
Ognjanovic S, Linabery AM, Charbonneau B, Ross JA, (2009) Trends in childhood rhabdomyosarcoma incidence and survival in the United States, 1975–2005. Cancer 115: 4218–4226. doi: 10.1002/cncr.24465 19536876
-
(2009)
Cancer
, vol.115
, pp. 4218-4226
-
-
Ognjanovic, S.1
Linabery, A.M.2
Charbonneau, B.3
Ross, J.A.4
-
16
-
-
84861214958
-
Rhabdomyosarcoma: review of the Children's Oncology Group (COG) Soft-Tissue Sarcoma Committee experience and rationale for current COG studies
-
Malempati S, Hawkins DS, (2012) Rhabdomyosarcoma: review of the Children's Oncology Group (COG) Soft-Tissue Sarcoma Committee experience and rationale for current COG studies. Pediatr Blood Cancer 59: 5–10. doi: 10.1002/pbc.24118 22378628
-
(2012)
Pediatr Blood Cancer
, vol.59
, pp. 5-10
-
-
Malempati, S.1
Hawkins, D.S.2
-
17
-
-
18744413524
-
Prognostic factors and clinical outcomes in children and adolescents with metastatic rhabdomyosarcoma—a report from the Intergroup Rhabdomyosarcoma Study IV
-
Breneman JC, Lyden E, Pappo AS, Link MP, Anderson JR, et al. (2003) Prognostic factors and clinical outcomes in children and adolescents with metastatic rhabdomyosarcoma—a report from the Intergroup Rhabdomyosarcoma Study IV. J Clin Oncol 21: 78–84. 12506174
-
(2003)
J Clin Oncol
, vol.21
, pp. 78-84
-
-
Breneman, J.C.1
Lyden, E.2
Pappo, A.S.3
Link, M.P.4
Anderson, J.R.5
-
18
-
-
50649115948
-
PAX3-FOXO1 fusion gene in rhabdomyosarcoma
-
Linardic CM, (2008) PAX3-FOXO1 fusion gene in rhabdomyosarcoma. Cancer Lett 270: 10–18. doi: 10.1016/j.canlet.2008.03.035 18457914
-
(2008)
Cancer Lett
, vol.270
, pp. 10-18
-
-
Linardic, C.M.1
-
19
-
-
0009615132
-
A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting
-
Scrable H, Cavenee W, Ghavimi F, Lovell M, Morgan K, et al. (1989) A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting. Proc Natl Acad Sci U S A 86: 7480–7484. 2798419
-
(1989)
Proc Natl Acad Sci U S A
, vol.86
, pp. 7480-7484
-
-
Scrable, H.1
Cavenee, W.2
Ghavimi, F.3
Lovell, M.4
Morgan, K.5
-
20
-
-
0024388736
-
Detection of point mutations in N-ras and K-ras genes of human embryonal rhabdomyosarcomas using oligonucleotide probes and the polymerase chain reaction
-
Stratton MR, Fisher C, Gusterson BA, Cooper CS, (1989) Detection of point mutations in N-ras and K-ras genes of human embryonal rhabdomyosarcomas using oligonucleotide probes and the polymerase chain reaction. Cancer Research 49: 6324–6327. 2680062
-
(1989)
Cancer Research
, vol.49
, pp. 6324-6327
-
-
Stratton, M.R.1
Fisher, C.2
Gusterson, B.A.3
Cooper, C.S.4
-
21
-
-
84856555606
-
Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcoma and neuroblastoma with mutated genes in growth signaling pathways
-
Shukla N, Ameur N, Yilmaz I, Nafa K, Lau CY, et al. (2012) Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcoma and neuroblastoma with mutated genes in growth signaling pathways. Clin Cancer Res 18: 748–757. doi: 10.1158/1078-0432.CCR-11-2056 22142829
-
(2012)
Clin Cancer Res
, vol.18
, pp. 748-757
-
-
Shukla, N.1
Ameur, N.2
Yilmaz, I.3
Nafa, K.4
Lau, C.Y.5
-
22
-
-
70449450426
-
Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models
-
Taylor JGt, Cheuk AT, Tsang PS, Chung JY, Song YK, et al. (2009) Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models. J Clin Invest 119: 3395–3407. doi: 10.1172/JCI39703 19809159
-
(2009)
J Clin Invest
, vol.119
, pp. 3395-3407
-
-
Taylor, J.G.1
Cheuk, A.T.2
Tsang, P.S.3
Chung, J.Y.4
Song, Y.K.5
-
23
-
-
84896691170
-
Comprehensive genomic analysis of rhabdomyosarcoma reveals a landscape of alterations affecting a common genetic axis in fusion-positive and fusion-negative tumors
-
Shern JF, Chen L, Chmielecki J, Wei JS, Patidar R, et al. (2014) Comprehensive genomic analysis of rhabdomyosarcoma reveals a landscape of alterations affecting a common genetic axis in fusion-positive and fusion-negative tumors. Cancer Discov 4: 216–231. doi: 10.1158/2159-8290.CD-13-0639 24436047
-
(2014)
Cancer Discov
, vol.4
, pp. 216-231
-
-
Shern, J.F.1
Chen, L.2
Chmielecki, J.3
Wei, J.S.4
Patidar, R.5
-
24
-
-
84891953948
-
Targeting oxidative stress in embryonal rhabdomyosarcoma
-
Chen X, Stewart E, Shelat AA, Qu C, Bahrami A, et al. (2013) Targeting oxidative stress in embryonal rhabdomyosarcoma. Cancer Cell 24: 710–724. doi: 10.1016/j.ccr.2013.11.002 24332040
-
(2013)
Cancer Cell
, vol.24
, pp. 710-724
-
-
Chen, X.1
Stewart, E.2
Shelat, A.A.3
Qu, C.4
Bahrami, A.5
-
25
-
-
84874025843
-
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
-
Cibulskis K, Lawrence MS, Carter SL, Sivachenko A, Jaffe D, et al. (2013) Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat Biotechnol 31: 213–219. doi: 10.1038/nbt.2514 23396013
-
(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
-
26
-
-
63449141981
-
Human mutation rate associated with DNA replication timing
-
Stamatoyannopoulos JA, Adzhubei I, Thurman RE, Kryukov GV, Mirkin SM, et al. (2009) Human mutation rate associated with DNA replication timing. Nature Genetics 41: 393–395. doi: 10.1038/ng.363 19287383
-
(2009)
Nature Genetics
, vol.41
, pp. 393-395
-
-
Stamatoyannopoulos, J.A.1
Adzhubei, I.2
Thurman, R.E.3
Kryukov, G.V.4
Mirkin, S.M.5
-
27
-
-
77950661675
-
Impact of replication timing on non-CpG and CpG substitution rates in mammalian genomes
-
Chen CL, Rappailles A, Duquenne L, Huvet M, Guilbaud G, et al. (2010) Impact of replication timing on non-CpG and CpG substitution rates in mammalian genomes. Genome Research 20: 447–457. doi: 10.1101/gr.098947.109 20103589
-
(2010)
Genome Research
, vol.20
, pp. 447-457
-
-
Chen, C.L.1
Rappailles, A.2
Duquenne, L.3
Huvet, M.4
Guilbaud, G.5
-
29
-
-
0030059906
-
In vivo amplification of the PAX3-FKHR and PAX7-FKHR fusion genes in alveolar rhabdomyosarcoma
-
Barr FG, Nauta LE, Davis RJ, Schafer BW, Nycum LM, et al. (1996) In vivo amplification of the PAX3-FKHR and PAX7-FKHR fusion genes in alveolar rhabdomyosarcoma. Human Molecular Genetics 5: 15–21. 8789435
-
(1996)
Human Molecular Genetics
, vol.5
, pp. 15-21
-
-
Barr, F.G.1
Nauta, L.E.2
Davis, R.J.3
Schafer, B.W.4
Nycum, L.M.5
-
30
-
-
0037283966
-
The structure and function of PKN, a protein kinase having a catalytic domain homologous to that of PKC
-
Mukai H, (2003) The structure and function of PKN, a protein kinase having a catalytic domain homologous to that of PKC. Journal of Biochemistry 133: 17–27. 12761194
-
(2003)
Journal of Biochemistry
, vol.133
, pp. 17-27
-
-
Mukai, H.1
-
31
-
-
84889070659
-
Protein Kinase PKN1 Represses Wnt/beta-Catenin Signaling in Human Melanoma Cells
-
James RG, Bosch KA, Kulikauskas RM, Yang PTT, Robin NC, et al. (2013) Protein Kinase PKN1 Represses Wnt/beta-Catenin Signaling in Human Melanoma Cells. Journal of Biological Chemistry 288: 34658–34670. doi: 10.1074/jbc.M113.500314 24114839
-
(2013)
Journal of Biological Chemistry
, vol.288
, pp. 34658-34670
-
-
James, R.G.1
Bosch, K.A.2
Kulikauskas, R.M.3
Yang, P.T.T.4
Robin, N.C.5
-
32
-
-
0035281564
-
Regulation of gene expression by the small GTPase Rho through the ERK6 (p38 gamma) MAP kinase pathway
-
Marinissen MT, Chiariello M, Gutkind JS, (2001) Regulation of gene expression by the small GTPase Rho through the ERK6 (p38 gamma) MAP kinase pathway. Genes & Development 15: 535–553.
-
(2001)
Genes & Development
, vol.15
, pp. 535-553
-
-
Marinissen, M.T.1
Chiariello, M.2
Gutkind, J.S.3
-
33
-
-
84901687144
-
A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations
-
Kohsaka S, Shukla N, Ameur N, Ito T, Ng CKY, et al. (2014) A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations. Nature Genetics 46: 595–600. doi: 10.1038/ng.2969 24793135
-
(2014)
Nature Genetics
, vol.46
, pp. 595-600
-
-
Kohsaka, S.1
Shukla, N.2
Ameur, N.3
Ito, T.4
Ng, C.K.Y.5
-
34
-
-
0037228055
-
High frequency of BRAF mutations in nevi
-
Pollock PM, Harper UL, Hansen KS, Yudt LM, Stark M, et al. (2003) High frequency of BRAF mutations in nevi. Nature Genetics 33: 19–20. 12447372
-
(2003)
Nature Genetics
, vol.33
, pp. 19-20
-
-
Pollock, P.M.1
Harper, U.L.2
Hansen, K.S.3
Yudt, L.M.4
Stark, M.5
-
35
-
-
0042941629
-
BRAF and KRAS mutations in colorectal hyperplastic polyps and serrated adenomas
-
Chan TL, Zhao W, Leung SY, Yuen ST, Project CG, (2003) BRAF and KRAS mutations in colorectal hyperplastic polyps and serrated adenomas. Cancer Research 63: 4878–4881. 12941809
-
(2003)
Cancer Research
, vol.63
, pp. 4878-4881
-
-
Chan, T.L.1
Zhao, W.2
Leung, S.Y.3
Yuen, S.T.4
Project, C.G.5
-
36
-
-
57149118627
-
Genomic analysis of the clonal origins of relapsed acute lymphoblastic leukemia
-
Mullighan CG, Phillips LA, Su X, Ma J, Miller CB, et al. (2008) Genomic analysis of the clonal origins of relapsed acute lymphoblastic leukemia. Science 322: 1377–1380. doi: 10.1126/science.1164266 19039135
-
(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
-
37
-
-
0025738681
-
Uniparental Paternal Disomy in a Genetic Cancer-Predisposing Syndrome
-
Henry I, Bonaitipellie C, Chehensse V, Beldjord C, Schwartz C, et al. (1991) Uniparental Paternal Disomy in a Genetic Cancer-Predisposing Syndrome. Nature 351: 665–667. 1675767
-
(1991)
Nature
, vol.351
, pp. 665-667
-
-
Henry, I.1
Bonaitipellie, C.2
Chehensse, V.3
Beldjord, C.4
Schwartz, C.5
-
38
-
-
0021327569
-
Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour
-
KOUFOS A, HANSEN MF, LAMPKIN BC, WORKMAN ML, COPELAND NG, et al. (1984) Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour. Nature 309: 170–172. 6325936
-
(1984)
Nature
, vol.309
, pp. 170-172
-
-
Koufos, A.1
Hansen, M.F.2
Lampkin, B.C.3
Workman, M.L.4
Copeland, N.G.5
-
40
-
-
79955043471
-
Cancer in Noonan, Costello, Cardiofaciocutaneous and LEOPARD Syndromes
-
Kratz CP, Rapisuwon S, Reed H, Hasle H, Rosenberg PS, (2011) Cancer in Noonan, Costello, Cardiofaciocutaneous and LEOPARD Syndromes. American Journal of Medical Genetics Part C-Seminars in Medical Genetics 157C: 83–89. doi: 10.1002/ajmg.c.30300 21500339
-
(2011)
American Journal of Medical Genetics Part C-Seminars in Medical Genetics
, vol.157C
, pp. 83-89
-
-
Kratz, C.P.1
Rapisuwon, S.2
Reed, H.3
Hasle, H.4
Rosenberg, P.S.5
-
41
-
-
2342557132
-
Neurofibromatosis in children with rhabdomyosarcoma: A report from the intergroup Rhabdomyosarcoma Study IV
-
Sung L, Anderson JR, Arndt C, Raney B, Meyer WH, et al. (2004) Neurofibromatosis in children with rhabdomyosarcoma: A report from the intergroup Rhabdomyosarcoma Study IV. Journal of Pediatrics 144: 666–668. 15127010
-
(2004)
Journal of Pediatrics
, vol.144
, pp. 666-668
-
-
Sung, L.1
Anderson, J.R.2
Arndt, C.3
Raney, B.4
Meyer, W.H.5
-
42
-
-
0031940675
-
Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry
-
DeBaun MR, Tucker MA, (1998) Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry. Journal of Pediatrics 132: 398–400. 9544889
-
(1998)
Journal of Pediatrics
, vol.132
, pp. 398-400
-
-
DeBaun, M.R.1
Tucker, M.A.2
-
43
-
-
84889070659
-
Protein kinase PKN1 represses Wnt/beta-catenin signaling in human melanoma cells
-
James RG, Bosch KA, Kulikauskas RM, Yang PT, Robin NC, et al. (2013) Protein kinase PKN1 represses Wnt/beta-catenin signaling in human melanoma cells. J Biol Chem 288: 34658–34670. doi: 10.1074/jbc.M113.500314 24114839
-
(2013)
J Biol Chem
, vol.288
, pp. 34658-34670
-
-
James, R.G.1
Bosch, K.A.2
Kulikauskas, R.M.3
Yang, P.T.4
Robin, N.C.5
-
44
-
-
0034624990
-
Phosphorylation of protein kinase N by phosphoinositide-dependent protein kinase-1 mediates insulin signals to the actin cytoskeleton
-
Dong LQ, Landa LR, Wick MJ, Zhu L, Mukai H, et al. (2000) Phosphorylation of protein kinase N by phosphoinositide-dependent protein kinase-1 mediates insulin signals to the actin cytoskeleton. Proc Natl Acad Sci U S A 97: 5089–5094. 10792047
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 5089-5094
-
-
Dong, L.Q.1
Landa, L.R.2
Wick, M.J.3
Zhu, L.4
Mukai, H.5
-
45
-
-
38049147787
-
MEF2: a central regulator of diverse developmental programs
-
Potthoff MJ, Olson EN, (2007) MEF2: a central regulator of diverse developmental programs. Development 134: 4131–4140. 17959722
-
(2007)
Development
, vol.134
, pp. 4131-4140
-
-
Potthoff, M.J.1
Olson, E.N.2
-
46
-
-
81055140859
-
The Hippo Transducer TAZ Confers Cancer Stem Cell-Related Traits on Breast Cancer Cells
-
Cordenonsi M, Zanconato F, Azzolin L, Forcato M, Rosato A, et al. (2011) The Hippo Transducer TAZ Confers Cancer Stem Cell-Related Traits on Breast Cancer Cells. Cell 147: 759–772. doi: 10.1016/j.cell.2011.09.048 22078877
-
(2011)
Cell
, vol.147
, pp. 759-772
-
-
Cordenonsi, M.1
Zanconato, F.2
Azzolin, L.3
Forcato, M.4
Rosato, A.5
-
47
-
-
84905716960
-
The Hippo Transducer YAP1 Transforms Activated Satellite Cells and Is a Potent Effector of Embryonal Rhabdomyosarcoma Formation
-
Tremblay AM, Missiaglia E, Galli GG, Hettmer S, Urcia R, et al. (2014) The Hippo Transducer YAP1 Transforms Activated Satellite Cells and Is a Potent Effector of Embryonal Rhabdomyosarcoma Formation. Cancer Cell 26: 273–287. doi: 10.1016/j.ccr.2014.05.029 25087979
-
(2014)
Cancer Cell
, vol.26
, pp. 273-287
-
-
Tremblay, A.M.1
Missiaglia, E.2
Galli, G.G.3
Hettmer, S.4
Urcia, R.5
-
48
-
-
84904024982
-
KRAS and YAP1 Converge to Regulate EMT and Tumor Survival
-
Shao DD, Xue W, Krall EB, Bhutkar A, Piccioni F, et al. (2014) KRAS and YAP1 Converge to Regulate EMT and Tumor Survival. Cell 158: 171–184. doi: 10.1016/j.cell.2014.06.004 24954536
-
(2014)
Cell
, vol.158
, pp. 171-184
-
-
Shao, D.D.1
Xue, W.2
Krall, E.B.3
Bhutkar, A.4
Piccioni, F.5
-
49
-
-
84903984143
-
Yap1 Activation Enables Bypass of Oncogenic Kras Addiction in Pancreatic Cancer
-
Kapoor A, Yao WT, Ying HQ, Hua SJ, Liewen A, et al. (2014) Yap1 Activation Enables Bypass of Oncogenic Kras Addiction in Pancreatic Cancer. Cell 158: 185–197. doi: 10.1016/j.cell.2014.06.003 24954535
-
(2014)
Cell
, vol.158
, pp. 185-197
-
-
Kapoor, A.1
Yao, W.T.2
Ying, H.Q.3
Hua, S.J.4
Liewen, A.5
-
50
-
-
0031056441
-
Clinical relevance of DNA ploidy and proliferative activity in childhood rhabdomyosarcoma: a retrospective analysis of patients enrolled onto the Italian Cooperative Rhabdomyosarcoma Study RMS88
-
De Zen L, Sommaggio A, d'Amore ES, Masiero L, di Montezemolo LC, et al. (1997) Clinical relevance of DNA ploidy and proliferative activity in childhood rhabdomyosarcoma: a retrospective analysis of patients enrolled onto the Italian Cooperative Rhabdomyosarcoma Study RMS88. Journal of Clinical Oncology 15: 1198–1205. 9060564
-
(1997)
Journal of Clinical Oncology
, vol.15
, pp. 1198-1205
-
-
De Zen, L.1
Sommaggio, A.2
d'Amore, E.S.3
Masiero, L.4
di Montezemolo, L.C.5
-
51
-
-
0026747342
-
Cytogenetic studies in subgroups of rhabdomyosarcoma
-
Whang-Peng J, Knutsen T, Theil K, Horowitz ME, Triche T, (1992) Cytogenetic studies in subgroups of rhabdomyosarcoma. Genes Chromosomes Cancer 5: 299–310. 1283318
-
(1992)
Genes Chromosomes Cancer
, vol.5
, pp. 299-310
-
-
Whang-Peng, J.1
Knutsen, T.2
Theil, K.3
Horowitz, M.E.4
Triche, T.5
-
52
-
-
34047274772
-
Tetraploidy, aneuploidy and cancer
-
Ganem NJ, Storchova Z, Pellman D, (2007) Tetraploidy, aneuploidy and cancer. Current Opinion in Genetics & Development 17: 157–162.
-
(2007)
Current Opinion in Genetics & Development
, vol.17
, pp. 157-162
-
-
Ganem, N.J.1
Storchova, Z.2
Pellman, D.3
-
53
-
-
0342926898
-
17P (p53) allelic losses, 4N (G(2)/tetraploid) populations, and progression to aneuploidy in Barrett's esophagus
-
Galipeau PC, Cowan DS, Sanchez CA, Barrett MT, Emond MJ, et al. (1996) 17P (p53) allelic losses, 4N (G(2)/tetraploid) populations, and progression to aneuploidy in Barrett's esophagus. Gastroenterology 110: A515–A515.
-
(1996)
Gastroenterology
, vol.110
, pp. 515
-
-
Galipeau, P.C.1
Cowan, D.S.2
Sanchez, C.A.3
Barrett, M.T.4
Emond, M.J.5
-
54
-
-
27144507868
-
Cytokinesis failure generating tetraploids promotes tumorigenesis in p53-null cells
-
Fujiwara T, Bandi M, Nitta M, Ivanova EV, Bronson RT, et al. (2005) Cytokinesis failure generating tetraploids promotes tumorigenesis in p53-null cells. Nature 437: 1043–1047. 16222300
-
(2005)
Nature
, vol.437
, pp. 1043-1047
-
-
Fujiwara, T.1
Bandi, M.2
Nitta, M.3
Ivanova, E.V.4
Bronson, R.T.5
-
55
-
-
66149138870
-
Credentialing a Preclinical Mouse Model of Alveolar Rhabdomyosarcoma
-
Nishijo K, Chen QR, Zhang L, McCleish AT, Rodriguez A, et al. (2009) Credentialing a Preclinical Mouse Model of Alveolar Rhabdomyosarcoma. Cancer Research 69: 2902–2911. doi: 10.1158/0008-5472.CAN-08-3723 19339268
-
(2009)
Cancer Research
, vol.69
, pp. 2902-2911
-
-
Nishijo, K.1
Chen, Q.R.2
Zhang, L.3
McCleish, A.T.4
Rodriguez, A.5
-
56
-
-
57149093809
-
Defining the Cooperative Genetic Changes That Temporally Drive Alveolar RhabdomyosarcomaU
-
Naini S, Etheridge KT, Adam SJ, Qualman SJ, Bentley RC, et al. (2008) Defining the Cooperative Genetic Changes That Temporally Drive Alveolar RhabdomyosarcomaU. Cancer Research 68: 9583–9588. doi: 10.1158/0008-5472.CAN-07-6178 19047133
-
(2008)
Cancer Research
, vol.68
, pp. 9583-9588
-
-
Naini, S.1
Etheridge, K.T.2
Adam, S.J.3
Qualman, S.J.4
Bentley, R.C.5
-
57
-
-
0032722352
-
Survival after relapse in children and adolescents with rhabdomyosarcoma: A report from the intergroup rhabdomyosarcoma study group
-
Pappo AS, Anderson JR, Crist WM, Wharam MD, Breitfeld PP, et al. (1999) Survival after relapse in children and adolescents with rhabdomyosarcoma: A report from the intergroup rhabdomyosarcoma study group. Journal of Clinical Oncology 17: 3487–3493. 10550146
-
(1999)
Journal of Clinical Oncology
, vol.17
, pp. 3487-3493
-
-
Pappo, A.S.1
Anderson, J.R.2
Crist, W.M.3
Wharam, M.D.4
Breitfeld, P.P.5
-
58
-
-
65449136284
-
TopHat: discovering splice junctions with RNA-Seq
-
Trapnell C, Pachter L, Salzberg SL, (2009) TopHat: discovering splice junctions with RNA-Seq. Bioinformatics 25: 1105–1111. doi: 10.1093/bioinformatics/btp120 19289445
-
(2009)
Bioinformatics
, vol.25
, pp. 1105-1111
-
-
Trapnell, C.1
Pachter, L.2
Salzberg, S.L.3
-
59
-
-
77952123055
-
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation
-
Trapnell C, Williams BA, Pertea G, Mortazavi A, Kwan G, et al. (2010) Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. Nat Biotechnol 28: 511–515. doi: 10.1038/nbt.1621 20436464
-
(2010)
Nat Biotechnol
, vol.28
, pp. 511-515
-
-
Trapnell, C.1
Williams, B.A.2
Pertea, G.3
Mortazavi, A.4
Kwan, G.5
-
60
-
-
84855566198
-
Performance comparison of whole-genome sequencing platforms
-
Lam HY, Clark MJ, Chen R, Natsoulis G, O'Huallachain M, et al. (2012) Performance comparison of whole-genome sequencing platforms. Nat Biotechnol 30: 78–82. doi: 10.1038/nbt.2065 22178993
-
(2012)
Nat Biotechnol
, vol.30
, pp. 78-82
-
-
Lam, H.Y.1
Clark, M.J.2
Chen, R.3
Natsoulis, G.4
O'Huallachain, M.5
-
61
-
-
84859216598
-
Sequencing of neuroblastoma identifies chromothripsis and defects in neuritogenesis genes
-
Molenaar JJ, Koster J, Zwijnenburg DA, van Sluis P, Valentijn LJ, et al. (2012) Sequencing of neuroblastoma identifies chromothripsis and defects in neuritogenesis genes. Nature 483: 589–593. doi: 10.1038/nature10910 22367537
-
(2012)
Nature
, vol.483
, pp. 589-593
-
-
Molenaar, J.J.1
Koster, J.2
Zwijnenburg, D.A.3
van Sluis, P.4
Valentijn, L.J.5
-
62
-
-
85027946522
-
Exome sequencing identifies GRIN2A as frequently mutated in melanoma
-
Wei X, Walia V, Lin JC, Teer JK, Prickett TD, et al. (2011) Exome sequencing identifies GRIN2A as frequently mutated in melanoma. Nature Genetics 43: 442–446. doi: 10.1038/ng.810 21499247
-
(2011)
Nature Genetics
, vol.43
, pp. 442-446
-
-
Wei, X.1
Walia, V.2
Lin, J.C.3
Teer, J.K.4
Prickett, T.D.5
-
63
-
-
84863393606
-
Whole genome sequencing of matched primary and metastatic acral melanomas
-
Turajlic S, Furney SJ, Lambros MB, Mitsopoulos C, Kozarewa I, et al. (2012) Whole genome sequencing of matched primary and metastatic acral melanomas. Genome Res 22: 196–207. doi: 10.1101/gr.125591.111 22183965
-
(2012)
Genome Res
, vol.22
, pp. 196-207
-
-
Turajlic, S.1
Furney, S.J.2
Lambros, M.B.3
Mitsopoulos, C.4
Kozarewa, I.5
|