-
1
-
-
1642512884
-
Synovial sarcomas in serous bursae and tendon sheaths
-
Berger L., Synovial sarcomas in serous bursae and tendon sheaths. Am J Cancer 1938; 34: 501-538.
-
(1938)
Am J Cancer
, vol.34
, pp. 501-538
-
-
Berger, L.1
-
2
-
-
84916726167
-
Synovioma of the hand. Report of a case
-
Black WC,. Synovioma of the hand. Report of a case. Am J Cancer 1936; 28: 481-484.
-
(1936)
Am J Cancer
, vol.28
, pp. 481-484
-
-
Black, W.C.1
-
3
-
-
0002050744
-
Sarcoma aponeuroticum
-
Laskowski J., Sarcoma aponeuroticum. Nowotwory 1961; 11: 61-67.
-
(1961)
Nowotwory
, vol.11
, pp. 61-67
-
-
Laskowski, J.1
-
4
-
-
0014882130
-
Epithelioid sarcoma. A sarcoma simulating a granuloma or a carcinoma
-
Enzinger FM,. Epithelioid sarcoma. A sarcoma simulating a granuloma or a carcinoma. Cancer 1970; 26: 1029-1041.
-
(1970)
Cancer
, vol.26
, pp. 1029-1041
-
-
Enzinger, F.M.1
-
6
-
-
0031059732
-
'Proximal-type' epithelioid sarcoma, a distinctive aggressive neoplasm showing rhabdoid features. Clinicopathologic, immunohistochemical, and ultrastructural study of a series
-
Guillou L, Wadden C, Coindre JM, et al., 'Proximal-type' epithelioid sarcoma, a distinctive aggressive neoplasm showing rhabdoid features. Clinicopathologic, immunohistochemical, and ultrastructural study of a series. Am J Surg Pathol 1997; 21: 130-146.
-
(1997)
Am J Surg Pathol
, vol.21
, pp. 130-146
-
-
Guillou, L.1
Wadden, C.2
Coindre, J.M.3
-
7
-
-
20144386270
-
SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas
-
Modena P, Lualdi E, Facchinetti F, et al., SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas. Cancer Res 2005; 65: 4012-4019.
-
(2005)
Cancer Res
, vol.65
, pp. 4012-4019
-
-
Modena, P.1
Lualdi, E.2
Facchinetti, F.3
-
8
-
-
63849343469
-
Loss of INI1 expression is characteristic of both conventional and proximal-type epithelioid sarcoma
-
Hornick JL, Dal Cin P, Fletcher CD,. Loss of INI1 expression is characteristic of both conventional and proximal-type epithelioid sarcoma. Am J Surg Pathol 2009; 33: 542-550.
-
(2009)
Am J Surg Pathol
, vol.33
, pp. 542-550
-
-
Hornick, J.L.1
Dal Cin, P.2
Fletcher, C.D.3
-
9
-
-
59049105526
-
Infrequent SMARCB1/INI1 gene alteration in epithelioid sarcoma: A useful tool in distinguishing epithelioid sarcoma from malignant rhabdoid tumor
-
Kohashi K, Izumi T, Oda Y, et al., Infrequent SMARCB1/INI1 gene alteration in epithelioid sarcoma: a useful tool in distinguishing epithelioid sarcoma from malignant rhabdoid tumor. Hum Pathol 2009; 40: 349-355.
-
(2009)
Hum Pathol
, vol.40
, pp. 349-355
-
-
Kohashi, K.1
Izumi, T.2
Oda, Y.3
-
10
-
-
84875216002
-
SMARCB1 protein and mRNA loss is not caused by promoter and histone hypermethylation in epithelioid sarcoma
-
Papp G, Changchien YC, Peterfia B, et al., SMARCB1 protein and mRNA loss is not caused by promoter and histone hypermethylation in epithelioid sarcoma. Mod Pathol 2013; 26: 393-403.
-
(2013)
Mod Pathol
, vol.26
, pp. 393-403
-
-
Papp, G.1
Changchien, Y.C.2
Peterfia, B.3
-
11
-
-
68349137634
-
Re: Infrequent SMARCB1/INI1 gene alteration in epithelioid sarcoma: A useful tool in distinguishing epithelioid sarcoma from malignant rhabdoid tumor: Direct evidence of mutational inactivation of SMARCB1/INI1 in epithelioid sarcoma
-
author reply 1362-1364
-
Flucke U, Slootweg PJ, Mentzel T, et al., Re: Infrequent SMARCB1/INI1 gene alteration in epithelioid sarcoma: a useful tool in distinguishing epithelioid sarcoma from malignant rhabdoid tumor: direct evidence of mutational inactivation of SMARCB1/INI1 in epithelioid sarcoma. Hum Pathol 2009; 40: 1361-1362; author reply 1362-1364.
-
(2009)
Hum Pathol
, vol.40
, pp. 1361-1362
-
-
Flucke, U.1
Slootweg, P.J.2
Mentzel, T.3
-
12
-
-
84875215214
-
Epithelioid sarcoma is associated with a high percentage of SMARCB1 deletions
-
Sullivan LM, Folpe AL, Pawel BR, et al., Epithelioid sarcoma is associated with a high percentage of SMARCB1 deletions. Mod Pathol 2013; 26: 385-392.
-
(2013)
Mod Pathol
, vol.26
, pp. 385-392
-
-
Sullivan, L.M.1
Folpe, A.L.2
Pawel, B.R.3
-
13
-
-
84897522563
-
Consistent SMARCB1 homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material
-
Le Loarer F, Zhang L, Fletcher CD, et al., Consistent SMARCB1 homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material. Genes Chromosomes Cancer 2014; 53: 475-486.
-
(2014)
Genes Chromosomes Cancer
, vol.53
, pp. 475-486
-
-
Le Loarer, F.1
Zhang, L.2
Fletcher, C.D.3
-
14
-
-
84890120594
-
SMARCB1 expression in epithelioid sarcoma is regulated by miR-206, miR-381, and miR-671-5p on both mRNA and protein levels
-
Papp G, Krausz T, Stricker TP, et al., SMARCB1 expression in epithelioid sarcoma is regulated by miR-206, miR-381, and miR-671-5p on both mRNA and protein levels. Genes Chromosomes Cancer 2014; 53: 168-176.
-
(2014)
Genes Chromosomes Cancer
, vol.53
, pp. 168-176
-
-
Papp, G.1
Krausz, T.2
Stricker, T.P.3
-
15
-
-
84901852715
-
Differential microRNA expression profiles between malignant rhabdoid tumor and epithelioid sarcoma: MiR193a-5p is suggested to downregulate SMARCB1 mRNA expression
-
Kohashi K, Yamamoto H, Kumagai R, et al., Differential microRNA expression profiles between malignant rhabdoid tumor and epithelioid sarcoma: miR193a-5p is suggested to downregulate SMARCB1 mRNA expression. Mod Pathol 2014; 27: 832-839.
-
(2014)
Mod Pathol
, vol.27
, pp. 832-839
-
-
Kohashi, K.1
Yamamoto, H.2
Kumagai, R.3
-
16
-
-
84914102658
-
The expanding family of SMARCB1 (INI1)-deficient neoplasia: Implications of phenotypic, biological, and molecular heterogeneity
-
Agaimy A., The expanding family of SMARCB1 (INI1)-deficient neoplasia: implications of phenotypic, biological, and molecular heterogeneity. Adv Anat Pathol 2014; 21: 394-410.
-
(2014)
Adv Anat Pathol
, vol.21
, pp. 394-410
-
-
Agaimy, A.1
-
17
-
-
84864746573
-
A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers
-
Lee RS, Stewart C, Carter SL, et al., A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers. J Clin Invest 2012; 122: 2983-2988.
-
(2012)
J Clin Invest
, vol.122
, pp. 2983-2988
-
-
Lee, R.S.1
Stewart, C.2
Carter, S.L.3
-
18
-
-
34248188610
-
Mutation of the INI1 gene in composite rhabdoid tumor of the endometrium
-
Donner LR, Wainwright LM, Zhang F, et al., Mutation of the INI1 gene in composite rhabdoid tumor of the endometrium. Hum Pathol 2007; 38: 935-939.
-
(2007)
Hum Pathol
, vol.38
, pp. 935-939
-
-
Donner, L.R.1
Wainwright, L.M.2
Zhang, F.3
-
19
-
-
81355138920
-
Atypical teratoid/rhabdoid tumor arising in a ganglioglioma: Genetic characterization
-
Kleinschmidt-DeMasters BK, Birks DK, Aisner DL, et al., Atypical teratoid/rhabdoid tumor arising in a ganglioglioma: genetic characterization. Am J Surg Pathol 2011; 35: 1894-1901.
-
(2011)
Am J Surg Pathol
, vol.35
, pp. 1894-1901
-
-
Kleinschmidt-DeMasters, B.K.1
Birks, D.K.2
Aisner, D.L.3
-
20
-
-
79955556660
-
Epithelioid sarcoma and unclassified sarcoma with epithelioid features: Clinicopathological variables, molecular markers, and a new experimental model
-
Sakharpe A, Lahat G, Gulamhusein T, et al., Epithelioid sarcoma and unclassified sarcoma with epithelioid features: clinicopathological variables, molecular markers, and a new experimental model. Oncologist 2011; 16: 512-522.
-
(2011)
Oncologist
, vol.16
, pp. 512-522
-
-
Sakharpe, A.1
Lahat, G.2
Gulamhusein, T.3
-
21
-
-
0031570878
-
Involvement of 8q, 22q, and monosomy 21 in an epithelioid sarcoma
-
Sonobe H, Ohtsuki Y, Sugimoto T, et al., Involvement of 8q, 22q, and monosomy 21 in an epithelioid sarcoma. Cancer Genet Cytogenet 1997; 96: 178-180.
-
(1997)
Cancer Genet Cytogenet
, vol.96
, pp. 178-180
-
-
Sonobe, H.1
Ohtsuki, Y.2
Sugimoto, T.3
-
22
-
-
33646894662
-
Prognostic significance of dysadherin expression in epithelioid sarcoma and its diagnostic utility in distinguishing epithelioid sarcoma from malignant rhabdoid tumor
-
Izumi T, Oda Y, Hasegawa T, et al., Prognostic significance of dysadherin expression in epithelioid sarcoma and its diagnostic utility in distinguishing epithelioid sarcoma from malignant rhabdoid tumor. Mod Pathol 2006; 19: 820-831.
-
(2006)
Mod Pathol
, vol.19
, pp. 820-831
-
-
Izumi, T.1
Oda, Y.2
Hasegawa, T.3
-
23
-
-
67649406102
-
Mutation of FOXL2 in granulosa-cell tumors of the ovary
-
Shah SP, Kobel M, Senz J, et al., Mutation of FOXL2 in granulosa-cell tumors of the ovary. N Engl J Med 2009; 360: 2719-2729.
-
(2009)
N Engl J Med
, vol.360
, pp. 2719-2729
-
-
Shah, S.P.1
Kobel, M.2
Senz, J.3
-
24
-
-
84867164956
-
Integrative analysis of genome-wide loss of heterozygosity and monoallelic expression at nucleotide resolution reveals disrupted pathways in triple-negative breast cancer
-
Ha G, Roth A, Lai D, et al., Integrative analysis of genome-wide loss of heterozygosity and monoallelic expression at nucleotide resolution reveals disrupted pathways in triple-negative breast cancer. Genome Res 2012; 22: 1995-2007.
-
(2012)
Genome Res
, vol.22
, pp. 1995-2007
-
-
Ha, G.1
Roth, A.2
Lai, D.3
-
25
-
-
84880799426
-
Distinguishing somatic and germline copy number events in cancer patient DNA hybridized to whole-genome SNP genotyping arrays
-
Ha G, Shah S,. Distinguishing somatic and germline copy number events in cancer patient DNA hybridized to whole-genome SNP genotyping arrays. Methods Mol Biol 2013; 973: 355-372.
-
(2013)
Methods Mol Biol
, vol.973
, pp. 355-372
-
-
Ha, G.1
Shah, S.2
-
26
-
-
79957829805
-
DeFuse: An algorithm for gene fusion discovery in tumor RNA-Seq data
-
McPherson A, Hormozdiari F, Zayed A, et al., deFuse: an algorithm for gene fusion discovery in tumor RNA-Seq data. PLoS Comput Biol 2011; 7: e1001138.
-
(2011)
PLoS Comput Biol
, vol.7
, pp. e1001138
-
-
McPherson, A.1
Hormozdiari, F.2
Zayed, A.3
-
27
-
-
84859249611
-
JointSNVMix: A probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing data
-
Roth A, Ding J, Morin R, et al., JointSNVMix: a probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing data. Bioinformatics 2012; 28: 907-913.
-
(2012)
Bioinformatics
, vol.28
, pp. 907-913
-
-
Roth, A.1
Ding, J.2
Morin, R.3
-
28
-
-
84880507665
-
Mutational heterogeneity in cancer and the search for new cancer-associated genes
-
Lawrence MS, Stojanov P, Polak P, et al., Mutational heterogeneity in cancer and the search for new cancer-associated genes. Nature 2013; 499: 214-218.
-
(2013)
Nature
, vol.499
, pp. 214-218
-
-
Lawrence, M.S.1
Stojanov, P.2
Polak, P.3
-
29
-
-
34548668191
-
Optimal primer design using the novel primer design program: MSPprimer provides accurate methylation analysis of the ATM promoter
-
Brandes JC, Carraway H, Herman JG,. Optimal primer design using the novel primer design program: MSPprimer provides accurate methylation analysis of the ATM promoter. Oncogene 2007; 26: 6229-6237.
-
(2007)
Oncogene
, vol.26
, pp. 6229-6237
-
-
Brandes, J.C.1
Carraway, H.2
Herman, J.G.3
-
30
-
-
84902358492
-
No small surprise - Small cell carcinoma of the ovary, hypercalcaemic type, is a malignant rhabdoid tumour
-
Foulkes WD, Clarke BA, Hasselblatt M, et al., No small surprise-small cell carcinoma of the ovary, hypercalcaemic type, is a malignant rhabdoid tumour. J Pathol 2014; 233: 209-214.
-
(2014)
J Pathol
, vol.233
, pp. 209-214
-
-
Foulkes, W.D.1
Clarke, B.A.2
Hasselblatt, M.3
-
31
-
-
84879295073
-
SMARCB1/INI1 genetic inactivation is responsible for tumorigenic properties of epithelioid sarcoma cell line VAESBJ
-
Brenca M, Rossi S, Lorenzetto E, et al., SMARCB1/INI1 genetic inactivation is responsible for tumorigenic properties of epithelioid sarcoma cell line VAESBJ. Mol Cancer Ther 2013; 12: 1060-1072.
-
(2013)
Mol Cancer Ther
, vol.12
, pp. 1060-1072
-
-
Brenca, M.1
Rossi, S.2
Lorenzetto, E.3
-
32
-
-
0942287188
-
INK4a is required for hSNF5 chromatin remodeler-induced cellular senescence in malignant rhabdoid tumor cells
-
INK4a is required for hSNF5 chromatin remodeler-induced cellular senescence in malignant rhabdoid tumor cells. J Biol Chem 2004; 279: 3807-3816.
-
(2004)
J Biol Chem
, vol.279
, pp. 3807-3816
-
-
Oruetxebarria, I.1
Venturini, F.2
Kekarainen, T.3
-
33
-
-
84924407460
-
A comprehensive transcriptional portrait of human cancer cell lines
-
Klijn C, Durinck S, Stawiski EW, et al., A comprehensive transcriptional portrait of human cancer cell lines. Nature Biotechnol 2015; 33: 306-312.
-
(2015)
Nature Biotechnol
, vol.33
, pp. 306-312
-
-
Klijn, C.1
Durinck, S.2
Stawiski, E.W.3
-
34
-
-
0028978202
-
VA-ES-BJ - An epithelioid sarcoma cell-line
-
Helson C, Melamed M, Braverman S, et al., VA-ES-BJ-an epithelioid sarcoma cell-line. Int J Oncol 1995; 7: 51-56.
-
(1995)
Int J Oncol
, vol.7
, pp. 51-56
-
-
Helson, C.1
Melamed, M.2
Braverman, S.3
-
35
-
-
84876823334
-
SNF5 is an essential executor of epigenetic regulation during differentiation
-
You JS, De Carvalho DD, Dai C, et al., SNF5 is an essential executor of epigenetic regulation during differentiation. PLoS Genet 2013; 9: e1003459.
-
(2013)
PLoS Genet
, vol.9
, pp. e1003459
-
-
You, J.S.1
De Carvalho, D.D.2
Dai, C.3
-
36
-
-
84896126029
-
ARID1B is a specific vulnerability in ARID1A-mutant cancers
-
Helming KC, Wang X, Wilson BG, et al., ARID1B is a specific vulnerability in ARID1A-mutant cancers. Nature Med 2014; 20: 251-254.
-
(2014)
Nature Med
, vol.20
, pp. 251-254
-
-
Helming, K.C.1
Wang, X.2
Wilson, B.G.3
-
37
-
-
33746300640
-
Epithelioid sarcoma: Still an only surgically curable disease
-
de Visscher SA, van Ginkel RJ, Wobbes T, et al., Epithelioid sarcoma: still an only surgically curable disease. Cancer 2006; 107: 606-612.
-
(2006)
Cancer
, vol.107
, pp. 606-612
-
-
De Visscher, S.A.1
Van Ginkel, R.J.2
Wobbes, T.3
-
38
-
-
49349114592
-
Epithelioid sarcoma: The University of Washington experience
-
Wolf PS, Flum DR, Tanas MR, et al., Epithelioid sarcoma: the University of Washington experience. Am J Surg 2008; 196: 407-412.
-
(2008)
Am J Surg
, vol.196
, pp. 407-412
-
-
Wolf, P.S.1
Flum, D.R.2
Tanas, M.R.3
-
39
-
-
84903872180
-
Gemcitabine and docetaxel for epithelioid sarcoma: Results from a retrospective, multi-institutional analysis
-
Pink D, Richter S, Gerdes S, et al., Gemcitabine and docetaxel for epithelioid sarcoma: results from a retrospective, multi-institutional analysis. Oncology 2014; 87: 95-103.
-
(2014)
Oncology
, vol.87
, pp. 95-103
-
-
Pink, D.1
Richter, S.2
Gerdes, S.3
-
40
-
-
84908109246
-
Combined targeting of mTOR and c-MET signaling pathways for effective management of epithelioid sarcoma
-
Imura Y, Yasui H, Outani H, et al., Combined targeting of mTOR and c-MET signaling pathways for effective management of epithelioid sarcoma. Mol Cancer 2014; 13: 185.
-
(2014)
Mol Cancer
, vol.13
, pp. 185
-
-
Imura, Y.1
Yasui, H.2
Outani, H.3
-
41
-
-
80052833534
-
Combining EGFR and mTOR blockade for the treatment of epithelioid sarcoma
-
Xie X, Ghadimi MP, Young ED, et al., Combining EGFR and mTOR blockade for the treatment of epithelioid sarcoma. Clin Cancer Res 2011; 17: 5901-5912.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 5901-5912
-
-
Xie, X.1
Ghadimi, M.P.2
Young, E.D.3
-
42
-
-
33748367886
-
Mammalian SWI/SNF complexes facilitate DNA double-strand break repair by promoting γ-H2AX induction
-
Park JH, Park EJ, Lee HS, et al., Mammalian SWI/SNF complexes facilitate DNA double-strand break repair by promoting γ-H2AX induction. EMBO J 2006; 25: 3986-3997.
-
(2006)
EMBO J
, vol.25
, pp. 3986-3997
-
-
Park, J.H.1
Park, E.J.2
Lee, H.S.3
-
43
-
-
23044479628
-
Distinct roles for the RSC and Swi/Snf ATP-dependent chromatin remodelers in DNA double-strand break repair
-
Chai B, Huang J, Cairns BR, et al., Distinct roles for the RSC and Swi/Snf ATP-dependent chromatin remodelers in DNA double-strand break repair. Genes Dev 2005; 19: 1656-1661.
-
(2005)
Genes Dev
, vol.19
, pp. 1656-1661
-
-
Chai, B.1
Huang, J.2
Cairns, B.R.3
-
44
-
-
84899635480
-
Recurrent SMARCA4 mutations in small cell carcinoma of the ovary
-
Jelinic P, Mueller JJ, Olvera N, et al., Recurrent SMARCA4 mutations in small cell carcinoma of the ovary. Nature Genet 2014; 46: 424-426.
-
(2014)
Nature Genet
, vol.46
, pp. 424-426
-
-
Jelinic, P.1
Mueller, J.J.2
Olvera, N.3
|