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Items: 1 to 20 of 1468

1.

Combined use of expression and CGH arrays pinpoints novel candidate genes in Ewing sarcoma family of tumors.

Savola S, Klami A, Tripathi A, Niini T, Serra M, Picci P, Kaski S, Zambelli D, Scotlandi K, Knuutila S.

BMC Cancer. 2009 Jan 14;9:17. doi: 10.1186/1471-2407-9-17.

2.

EWS-ERG fusion transcript produced by chromosomal insertion in a Ewing sarcoma.

Kaneko Y, Kobayashi H, Handa M, Satake N, Maseki N.

Genes Chromosomes Cancer. 1997 Mar;18(3):228-31.

PMID:
9071576
3.

Variability in gene expression patterns of Ewing tumor cell lines differing in EWS-FLI1 fusion type.

Aryee DN, Sommergruber W, Muehlbacher K, Dockhorn-Dworniczak B, Zoubek A, Kovar H.

Lab Invest. 2000 Dec;80(12):1833-44.

PMID:
11140696
4.

Genetic imbalances revealed by comparative genomic hybridization in Ewing tumors.

Ozaki T, Paulussen M, Poremba C, Brinkschmidt C, Rerin J, Ahrens S, Hoffmann C, Hillmann A, Wai D, Schaefer KL, Boecker W, Juergens H, Winkelmann W, Dockhorn-Dworniczak B.

Genes Chromosomes Cancer. 2001 Oct;32(2):164-71.

PMID:
11550284
5.

The NFATc2 gene is involved in a novel cloned translocation in a Ewing sarcoma variant that couples its function in immunology to oncology.

Szuhai K, Ijszenga M, de Jong D, Karseladze A, Tanke HJ, Hogendoorn PC.

Clin Cancer Res. 2009 Apr 1;15(7):2259-68. doi: 10.1158/1078-0432.CCR-08-2184. Epub 2009 Mar 24.

6.

DNA copy number changes in high-grade malignant peripheral nerve sheath tumors by array CGH.

Kresse SH, Skårn M, Ohnstad HO, Namløs HM, Bjerkehagen B, Myklebost O, Meza-Zepeda LA.

Mol Cancer. 2008 Jun 3;7:48. doi: 10.1186/1476-4598-7-48.

7.

Molecular characterization of the genomic breakpoint junction in a t(11;22) translocation in Ewing sarcoma.

Obata K, Hiraga H, Nojima T, Yoshida MC, Abe S.

Genes Chromosomes Cancer. 1999 May;25(1):6-15.

PMID:
10221334
8.

Multiple chromosomal mechanisms generate an EWS/FLI1 or an EWS/ERG fusion gene in Ewing tumors.

Desmaze C, Brizard F, Turc-Carel C, Melot T, Delattre O, Thomas G, Aurias A.

Cancer Genet Cytogenet. 1997 Aug;97(1):12-9.

PMID:
9242212
9.

Identification of various exon combinations of the ews/fli1 translocation: an optimized RT-PCR method for paraffin embedded tissue -- a report by the CWS-study group.

Stegmaier S, Leuschner I, Aakcha-Rudel E, Münch P, Kazanowska B, Bekassy A, Treuner J, Koscielniak E.

Klin Padiatr. 2004 Nov-Dec;216(6):315-22.

PMID:
15565546
10.

Localization of genetic elements of intact and derivative chromosome 11 and 22 territories in nuclei of Ewing sarcoma cells.

Taslerová R, Kozubek S, Bártová E, Gajdusková P, Kodet R, Kozubek M.

J Struct Biol. 2006 Sep;155(3):493-504. Epub 2006 Jun 2.

PMID:
16837212
11.

Clinical correlations of genetic changes by comparative genomic hybridization in Ewing sarcoma and related tumors.

Tarkkanen M, Kiuru-Kuhlefelt S, Blomqvist C, Armengol G, Böhling T, Ekfors T, Virolainen M, Lindholm P, Monge O, Picci P, Knuutila S, Elomaa I.

Cancer Genet Cytogenet. 1999 Oct 1;114(1):35-41.

PMID:
10526533
12.

Expression profiling of t(12;22) positive clear cell sarcoma of soft tissue cell lines reveals characteristic up-regulation of potential new marker genes including ERBB3.

Schaefer KL, Brachwitz K, Wai DH, Braun Y, Diallo R, Korsching E, Eisenacher M, Voss R, Van Valen F, Baer C, Selle B, Spahn L, Liao SK, Lee KA, Hogendoorn PC, Reifenberger G, Gabbert HE, Poremba C.

Cancer Res. 2004 May 15;64(10):3395-405.

13.

Ewing sarcoma family of tumors.

Khoury JD.

Adv Anat Pathol. 2005 Jul;12(4):212-20. Review.

PMID:
16096383
14.

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.

Kloth JN, Oosting J, van Wezel T, Szuhai K, Knijnenburg J, Gorter A, Kenter GG, Fleuren GJ, Jordanova ES.

BMC Genomics. 2007 Feb 20;8:53.

15.
16.

A novel t(4;22)(q31;q12) produces an EWSR1-SMARCA5 fusion in extraskeletal Ewing sarcoma/primitive neuroectodermal tumor.

Sumegi J, Nishio J, Nelson M, Frayer RW, Perry D, Bridge JA.

Mod Pathol. 2011 Mar;24(3):333-42. doi: 10.1038/modpathol.2010.201. Epub 2010 Nov 26.

17.

Does expression of different EWS chimeric transcripts define clinically distinct risk groups of Ewing tumor patients?

Zoubek A, Dockhorn-Dworniczak B, Delattre O, Christiansen H, Niggli F, Gatterer-Menz I, Smith TL, Jürgens H, Gadner H, Kovar H.

J Clin Oncol. 1996 Apr;14(4):1245-51.

PMID:
8648380
18.

Array CGH and gene-expression profiling reveals distinct genomic instability patterns associated with DNA repair and cell-cycle checkpoint pathways in Ewing's sarcoma.

Ferreira BI, Alonso J, Carrillo J, Acquadro F, Largo C, Suela J, Teixeira MR, Cerveira N, Molares A, Goméz-López G, Pestaña A, Sastre A, Garcia-Miguel P, Cigudosa JC.

Oncogene. 2008 Mar 27;27(14):2084-90. Epub 2007 Oct 22.

PMID:
17952124
19.

Arrangement of chromosome 11 and 22 territories, EWSR1 and FLI1 genes, and other genetic elements of these chromosomes in human lymphocytes and Ewing sarcoma cells.

Taslerová R, Kozubek S, Lukásová E, Jirsová P, Bártová E, Kozubek M.

Hum Genet. 2003 Feb;112(2):143-55. Epub 2002 Nov 16.

PMID:
12522555
20.

Complex rearrangement of chromosomes 1, 7, 21, 22 in Ewing sarcoma.

Jinawath N, Morsberger L, Norris-Kirby A, Williams LM, Yonescu R, Argani P, Griffin CA, Murphy KM.

Cancer Genet Cytogenet. 2010 Aug;201(1):42-7. doi: 10.1016/j.cancergencyto.2010.04.021.

PMID:
20633768
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