Prognostic impact of chromosomal aberrations in Ewing tumours
暂无分享,去创建一个
S. Knuutila | P. Ambros | J. Squire | U. Pötschger | H. Gadner | D. Betts | C. Hattinger | P. Thorner | L. Kager | M. Tarkkanen | F. Niggli | S. Kiuru-Kuhlefelt | M. Zielenska | Sakari Knuutila | Jeremy A. Squire | Helmut Gadner | Peter F. Ambros | David R. Betts | Felix Niggli | Paul S. Thorner | Ulrike Pötschger | S. Kiuru-Kuhlefelt | Leo Kager
[1] O. Haas,et al. Felix Mitelman: Database of chromosome aberrations in cancer , 2002, Human Genetics.
[2] J. Squire,et al. Acquisition of secondary structural chromosomal changes in pediatric ewing sarcoma is a probable prognostic factor for tumor response and clinical outcome , 2001, Cancer.
[3] M. Gessler,et al. Gain of 1q is associated with adverse outcome in favorable histology Wilms' tumors. , 2001, The American journal of pathology.
[4] A. Sandberg,et al. Updates on cytogenetics and molecular genetics of bone and soft tissue tumors: Ewing sarcoma and peripheral primitive neuroectodermal tumors. , 2000, Cancer genetics and cytogenetics.
[5] P. Ambros,et al. Molecular Cytogenetics in Ewing Tumors: Diagnostic and Prognostic Information , 2000, Oncology Research and Treatment.
[6] A. Craft,et al. Prognostic factors in Ewing's tumor of bone: analysis of 975 patients from the European Intergroup Cooperative Ewing's Sarcoma Study Group. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[7] G. Wei,et al. Prognostic impact of INK4A deletion in Ewing sarcoma , 2000, Cancer.
[8] M. Ladanyi,et al. Prognostic impact of P53 status in Ewing sarcoma , 2000, Cancer.
[9] C. Blomqvist,et al. Five-year results in Ewing's sarcoma. The Scandinavian Sarcoma Group experience with the SSG IX protocol. , 2000, European journal of cancer.
[10] S. Knuutila,et al. Clinical correlations of genetic changes by comparative genomic hybridization in Ewing sarcoma and related tumors. , 1999, Cancer genetics and cytogenetics.
[11] P. Ambros,et al. Prognostic impact of deletions at 1p36 and numerical aberrations in Ewing tumors , 1999, Genes, chromosomes & cancer.
[12] W. Winkelmann,et al. Evaluation of prognostic factors in a tumor volume-adapted treatment strategy for localized Ewing sarcoma of bone: The CESS 86 experience , 1999 .
[13] F. Mertens,et al. Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome? , 1999, Medical and pediatric oncology.
[14] O. Myklebost,et al. Molecular characterization of a novel amplicon at 1q21-q22 frequently observed in human sarcomas. , 1998, British Journal of Cancer.
[15] S. Knuutila,et al. DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies. , 1998, The American journal of pathology.
[16] W. Gerald,et al. EWS-FLI1 fusion transcript structure is an independent determinant of prognosis in Ewing's sarcoma. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[17] J. Fletcher,et al. Frequency and implications of chromosome 8 and 12 gains in Ewing sarcoma. , 1998, Cancer genetics and cytogenetics.
[18] H. Kovar,et al. Among genes involved in the RB dependent cell cycle regulatory cascade, the p16 tumor suppressor gene is frequently lost in the Ewing family of tumors , 1997, Oncogene.
[19] S. Ferrari,et al. Chemotherapy-induced tumor necrosis as a prognostic factor in localized Ewing's sarcoma of the extremities. , 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[20] T. Lion,et al. Demonstration of the translocation der(16)t(1;16)(q12;q11.2) in interphase nuclei of ewing tumors , 1996, Genes, chromosomes & cancer.
[21] A. Llombart‐Bosch,et al. Small round blue cell tumors in bone: prognostic factors correlated to Ewing's sarcoma and neuroectodermal tumors. , 1996, Seminars in diagnostic pathology.
[22] O. Delattre,et al. Does expression of different EWS chimeric transcripts define clinically distinct risk groups of Ewing tumor patients? , 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[23] F. Mitelman. ISCN 1995 : an international system for human cytogenetic nomenclature (1995) : recommendations of the International Standing Committee on Human Cytogenetic Nomenclature : Memphis, Tennessee, USA, October 9-13, 1994 , 1995 .
[24] N. Dracopoli,et al. Current protocols in human genetics , 1994 .
[25] H. Kovar,et al. Variability of EWS chimaeric transcripts in Ewing tumours: a comparison of clinical and molecular data. , 1994, British Journal of Cancer.
[26] T. Triche,et al. The Ewing family of tumors--a subgroup of small-round-cell tumors defined by specific chimeric transcripts. , 1994, The New England journal of medicine.
[27] H. Jürgens,et al. Ewing's sarcoma and peripheral primitive neuroectodermal tumor. , 1994, Current opinion in oncology.
[28] G. Thomas,et al. Interphase molecular cytogenetics of Ewing's sarcoma and peripheral neuroepithelioma t(11;22) with flanking and overlapping cosmid probes. , 1994, Cancer genetics and cytogenetics.
[29] H. Jürgens,et al. Treatment of soft tissue sarcoma in childhood and adolescence: A report of the german cooperative soft tissue sarcoma study , 1992, Cancer.
[30] P. D. de Jong,et al. Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints , 1992, Genes, chromosomes & cancer.
[31] G. Thomas,et al. Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours , 1992, Nature.
[32] H Kovar,et al. MIC2 is a specific marker for ewing's sarcoma and peripheral primitive neuroectodermal tumors. Evidence for a common histogenesis of ewing's sarcoma and peripheral primitive neuroectodermal tumors from MIC2 expression and specific chromosome aberration , 1991, Cancer.
[33] A. Aurias,et al. Chromosomes in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16). , 1988, Cancer genetics and cytogenetics.
[34] E. Korn,et al. Effective sample sizes for confidence intervals for survival probabilities. , 1987, Statistics in medicine.
[35] T. Triche,et al. Ifosfamide with mesna uroprotection and etoposide: an effective regimen in the treatment of recurrent sarcomas and other tumors of children and young adults. , 1987, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[36] M. Israel,et al. Chromosome translocation in peripheral neuroepithelioma. , 1984, The New England journal of medicine.
[37] DavidM. O. Becroft,et al. CHROMOSOME TRANSLOCATION IN EXTRASKELETAL EWING'S TUMOUR , 1984, The Lancet.
[38] Meyerhoff Jo. Exacerbation of psoriasis with meclofenamate. , 1983 .
[39] E. Kaplan,et al. Nonparametric Estimation from Incomplete Observations , 1958 .
[40] I. Cohen,et al. Additional chromosome 1q aberrations and der(16)t(1;16), correlation to the phenotypic expression and clinical behavior of the Ewing family of tumors , 2004, Journal of Neuro-Oncology.
[41] C. Blomqvist,et al. Ifosfamide, vincristine, doxorubicin and dacarbazine in adult patients with advanced soft-tissue sarcoma , 2004, Cancer Chemotherapy and Pharmacology.
[42] S. Ferrari,et al. Prognostic factors in nonmetastatic Ewing's sarcoma of bone treated with adjuvant chemotherapy: analysis of 359 patients at the Istituto Ortopedico Rizzoli. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[43] W. Winkelmann,et al. Evaluation of prognostic factors in a tumor volume-adapted treatment strategy for localized Ewing sarcoma of bone: the CESS 86 experience. Cooperative Ewing Sarcoma Study. , 1999, Medical and pediatric oncology.
[44] A. Nakagawara,et al. 1q23 gain is associated with progressive neuroblastoma resistant to aggressive treatment. , 1999, Genes, chromosomes & cancer.
[45] O. Myklebost,et al. Recurrent gains of 1q, 8 and 12 in the Ewing family of tumours by comparative genomic hybridization. , 1997, British Journal of Cancer.
[46] H. Kovar,et al. Regression and progression in neuroblastoma. Does genetics predict tumour behaviour? , 1995, European journal of cancer.
[47] M. Valentine,et al. A second nonrandom translocation, der(16)t(1;16)(q21;q13), in Ewing sarcoma and peripheral neuroectodermal tumor. , 1990, Cytogenetics and cell genetics.
[48] W. Winkelmann,et al. Multidisciplinary treatment of primary Ewing's sarcoma of bone. A 6‐year experience of a European cooperative trial , 1988, Cancer.
[49] Chromosomal translocations in Ewing's sarcoma. , 1983, The New England journal of medicine.
[50] Iscn. International System for Human Cytogenetic Nomenclature , 1978 .
[51] David R. Cox,et al. Regression models and life tables (with discussion , 1972 .
[52] D. Cox. Regression Models and Life-Tables , 1972 .