| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/1097-0142(20010601)91:11<2156::AID-CNCR1244>3.0.CO;2-I |
| P698 | PubMed publication ID | 11391597 |
| P50 | author | Jeremy A. Squire | Q39802515 |
| P2093 | author name string | Maria Zielenska | |
| Jane Bayani | |||
| Mark Greenberg | |||
| Zong Mei Zhang | |||
| Paul Thorner | |||
| Paula Marrano | |||
| Poul Sorensen | |||
| Kwan Ng | |||
| Oswaldo C. Ramirez | |||
| P2860 | cites work | Multicolor Spectral Karyotyping of Human Chromosomes | Q22065566 |
| Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours | Q24298221 | ||
| Mutations of mitotic checkpoint genes in human cancers | Q24320018 | ||
| Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases of remarkable consistency of t(11;22)(q24;q12) | Q28291773 | ||
| Application of comparative genomic hybridization, spectral karyotyping, and microarray analysis in the identification of subtype-specific patterns of genomic changes in rhabdomyosarcoma | Q34786049 | ||
| Recurrent gains of 1q, 8 and 12 in the Ewing family of tumours by comparative genomic hybridization | Q36421638 | ||
| The cytogenetic scenario of chronic myeloid leukemia | Q40785898 | ||
| Prognostic impact of deletions at 1p36 and numerical aberrations in Ewing tumors | Q50756853 | ||
| Diffuse Leiomyomatosis of the Esophagus: Disorder of Cell-Matrix Interaction? | Q59619342 | ||
| Interphase cytogenetics of prostatic adenocarcinoma and precursor lesions: Analysis of 25 radical prostatectomies and 17 adjacent prostatic intraepithelial neoplasias | Q63966402 | ||
| Incidence of malignant tumors in U.S. children | Q66908554 | ||
| Heterogeneity of lineage involvement by trisomy 8 in myelodysplastic syndrome. A multiparameter analysis combining conventional cytogenetics, DNA in situ hybridization, and bone marrow culture studies | Q72033642 | ||
| Clinical correlations of genetic changes by comparative genomic hybridization in Ewing sarcoma and related tumors | Q73094960 | ||
| Additional chromosome 1q aberrations and der(16)t(1;16), correlation to the phenotypic expression and clinical behavior of the Ewing family of tumors | Q73109102 | ||
| Frequency and implications of chromosome 8 and 12 gains in Ewing sarcoma | Q74036740 | ||
| Ewing's family of tumors in adults: multivariate analysis of survival and long-term results of multimodality therapy in 182 patients | Q77669887 | ||
| Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome? | Q78018572 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cancer research | Q3421914 |
| P304 | page(s) | 2156-2164 | |
| P577 | publication date | 2001-01-01 | |
| 2001-06-01 | |||
| P1433 | published in | Cancer | Q326041 |
| P1476 | title | Acquisition of secondary structural chromosomal changes in pediatric ewing sarcoma is a probable prognostic factor for tumor response and clinical outcome | |
| P478 | volume | 91 |
| Q33841580 | A rare case of translocation (12;22) (p13;Q) in Ewing's sarcoma |
| Q53520709 | Array CGH and gene-expression profiling reveals distinct genomic instability patterns associated with DNA repair and cell-cycle checkpoint pathways in Ewing's sarcoma |
| Q80510573 | Biology and therapy of malignant solid tumors in childhood |
| Q36907188 | Biomarkers in Ewing Sarcoma: The Promise and Challenge of Personalized Medicine. A Report from the Children's Oncology Group. |
| Q40126904 | Chromosome 9p21 gene copy number and prognostic significance of p16 in ESFT. |
| Q37078506 | Combined use of expression and CGH arrays pinpoints novel candidate genes in Ewing sarcoma family of tumors |
| Q34700651 | Copy Number Alterations and Methylation in Ewing's Sarcoma |
| Q37397291 | Ewing sarcoma fusion protein EWSR1/FLI1 interacts with EWSR1 leading to mitotic defects in zebrafish embryos and human cell lines |
| Q35057457 | Ewing's sarcoma: diagnostic, prognostic, and therapeutic implications of molecular abnormalities |
| Q39931953 | Genetically defined EWS/FLI1 model system suggests mesenchymal origin of Ewing's family tumors |
| Q35958348 | Guidelines for histopathological specimen examination and diagnostic reporting of primary bone tumours |
| Q28244685 | In Ewing's sarcoma CCN3(NOV) inhibits proliferation while promoting migration and invasion of the same cell type |
| Q54758814 | Karyotypic divergence and convergence in two synchronous lung metastases of a clear cell sarcoma of tendons and aponeuroses with t(12;22)(q13;q12) and type 1 EWS/ATF1. |
| Q73147225 | Molecular cytogenetic parameters in Ewing sarcoma |
| Q37200438 | Molecular inversion probe analysis detects novel copy number alterations in Ewing sarcoma |
| Q52852427 | Ploidy and karyotype complexity are powerful prognostic indicators in the Ewing's sarcoma family of tumors: a study by the United Kingdom Cancer Cytogenetics and the Children's Cancer and Leukaemia Group |
| Q36644524 | Prognostic impact of chromosomal aberrations in Ewing tumours |
| Q35957979 | The clinical use of biomarkers as prognostic factors in Ewing sarcoma |
Search more.