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Chromosomal translocations in Ewing's sarcoma.

出版信息

N Engl J Med. 1983 Aug 25;309(8):496-8.

PMID:6877319
Abstract
摘要

相似文献

1
Chromosomal translocations in Ewing's sarcoma.尤因肉瘤中的染色体易位
N Engl J Med. 1983 Aug 25;309(8):496-8.
2
[Chromosomal translocation (11; 22) in cell lines of Ewing's sarcoma].[尤因肉瘤细胞系中的染色体易位(11;22)]
C R Seances Acad Sci III. 1983;296(23):1101-3.
3
[Translocation of chromosome 22 in Ewing's sarcoma].[尤因肉瘤中22号染色体易位]
C R Seances Acad Sci III. 1983;296(23):1105-7.
4
The c-sis oncogene is not activated in Ewing's sarcoma.c-sis癌基因在尤因肉瘤中未被激活。
N Engl J Med. 1984 Feb 9;310(6):393. doi: 10.1056/NEJM198402093100618.
5
t(11;22) and other chromosomal rearrangements in Ewing's sarcoma.尤因肉瘤中的t(11;22)及其他染色体重排
J Natl Cancer Inst. 1986 Dec;77(6):1211-5.
6
Adamantinoma-like Ewing's sarcoma and Ewing's-like adamantinoma. The t(11; 22), t(21; 22) status.成釉细胞瘤样尤因肉瘤和尤因样成釉细胞瘤。t(11; 22)、t(21; 22)状态。
J Pathol. 2001 Sep;195(2):218-21. doi: 10.1002/path.919.
7
Molecular abnormalities in Ewing's sarcoma.尤因肉瘤中的分子异常
Expert Rev Anticancer Ther. 2008 Oct;8(10):1675-87. doi: 10.1586/14737140.8.10.1675.
8
An aggressive Ewing sarcoma associated with a new variant translocation, t(4;11;22)(q25;q24;q12), hyperdiploid karyotype, and tetrasomy 8.一种侵袭性尤因肉瘤,伴有新的变异易位t(4;11;22)(q25;q24;q12)、超二倍体核型和8号染色体四体性。
Cancer Genet Cytogenet. 2005 Dec;163(2):186-8. doi: 10.1016/j.cancergencyto.2005.04.015.
9
Cytogenetic studies on fine-needle aspiration samples from osteosarcoma and Ewing's sarcoma.骨肉瘤和尤因肉瘤细针穿刺样本的细胞遗传学研究。
Diagn Cytopathol. 1996 Jul;15(1):17-22. doi: 10.1002/(SICI)1097-0339(199607)15:1<17::AID-DC5>3.0.CO;2-N.
10
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.EWS/Fli1易位各种外显子组合的鉴定:一种针对石蜡包埋组织的优化逆转录聚合酶链反应方法——CWS研究小组的报告
Klin Padiatr. 2004 Nov-Dec;216(6):315-22. doi: 10.1055/s-2004-832338.

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Ewing's Sarcoma of Maxillary Sinus.上颌窦尤因肉瘤
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Primary Ewing sarcoma of the liver: Diagnosis, management, and prognosis: A case report and literature review.肝脏原发性尤因肉瘤:诊断、治疗及预后:一例病例报告并文献复习
Clin Case Rep. 2022 Nov 10;10(11):e6508. doi: 10.1002/ccr3.6508. eCollection 2022 Nov.
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Ewing sarcoma and related FET family translocation-associated round cell tumors: A century of clinical and scientific progress.
尤因肉瘤和相关 FET 家族易位相关性小圆细胞肿瘤:一个世纪的临床和科学进展。
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-The Most Common Rearranged Gene in Soft Tissue Lesions, Which Also Occurs in Different Bone Lesions: An Updated Review.软组织病变中最常见的重排基因,其也见于不同的骨病变:最新综述
Diagnostics (Basel). 2021 Jun 15;11(6):1093. doi: 10.3390/diagnostics11061093.
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Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.常见种系易感性基因座附近低频变异与尤文肉瘤风险相关。
PLoS One. 2020 Sep 3;15(9):e0237792. doi: 10.1371/journal.pone.0237792. eCollection 2020.
6
Development of an Ewing sarcoma cell line with resistance to EWS‑FLI1 inhibitor YK‑4‑279.建立一株对 EWS-FLI1 抑制剂 YK-4-279 具有耐药性的尤文肉瘤细胞系。
Mol Med Rep. 2020 Mar;21(3):1667-1675. doi: 10.3892/mmr.2020.10948. Epub 2020 Jan 16.
7
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility.全基因组关联研究鉴定出多个与尤文肉瘤易感性相关的新位点。
Nat Commun. 2018 Aug 9;9(1):3184. doi: 10.1038/s41467-018-05537-2.
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EWSR1-NFATC2 gene fusion in a soft tissue tumor with epithelioid round cell morphology and abundant stroma: a case report and review of the literature.上皮样圆形细胞和丰富基质的软组织肿瘤中存在 EWSR1-NFATC2 基因融合:病例报告及文献复习。
Hum Pathol. 2018 Nov;81:281-290. doi: 10.1016/j.humpath.2018.03.020. Epub 2018 Apr 4.
9
Primary Subcutaneous Ewing Sarcoma Presented as Pseudo Aneurysmal Subcutaneous Tumor.表现为假性动脉瘤样皮下肿瘤的原发性皮下尤因肉瘤
World J Oncol. 2010 Feb;1(1):47-49. doi: 10.4021/wjon2010.01.1205. Epub 2010 Feb 1.
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Fusions in solid tumours: diagnostic strategies, targeted therapy, and acquired resistance.实体瘤中的融合基因:诊断策略、靶向治疗及获得性耐药
Nat Rev Clin Oncol. 2017 Dec;14(12):735-748. doi: 10.1038/nrclinonc.2017.127. Epub 2017 Aug 31.