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PAX3-FKHR and PAX7-FKHR gene fusions are prognostic indicators in alveolar rhabdomyosarcoma: a report from the children's oncology group.PAX3 - FKHR和PAX7 - FKHR基因融合是肺泡横纹肌肉瘤的预后指标:来自儿童肿瘤学组的报告。
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Detection of the PAX3-FKHR fusion gene in paediatric rhabdomyosarcoma: a reproducible predictor of outcome?小儿横纹肌肉瘤中PAX3-FKHR融合基因的检测:一种可重复的预后预测指标?
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PAX3/7-FOXO1 fusion status in older rhabdomyosarcoma patient population by fluorescent in situ hybridization.荧光原位杂交检测老年横纹肌肉瘤患者中 PAX3/7-FOXO1 融合状态。
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Fusion gene-negative alveolar rhabdomyosarcoma is clinically and molecularly indistinguishable from embryonal rhabdomyosarcoma.融合基因阴性肺泡横纹肌肉瘤在临床和分子上与胚胎性横纹肌肉瘤无法区分。
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PAX5 expression in rhabdomyosarcoma.PAX5在横纹肌肉瘤中的表达。
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Efficacy of CDK4 inhibition against sarcomas depends on their levels of CDK4 and p16ink4 mRNA.CDK4抑制对肉瘤的疗效取决于其CDK4和p16ink4 mRNA的水平。
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Cytological diagnosis of metastatic alveolar rhabdomyosarcoma in the ascitic fluid: Report of a case highlighting the diagnostic difficulties.腹水转移性肺泡横纹肌肉瘤的细胞学诊断:1例报告强调诊断难点
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本文引用的文献

1
Treatment results for patients with localized, completely resected (Group I) alveolar rhabdomyosarcoma on Intergroup Rhabdomyosarcoma Study Group (IRSG) protocols III and IV, 1984-1997: a report from the Children's Oncology Group.1984 年至 1997 年,国际横纹肌肉瘤研究组(IRSG)方案 III 和 IV 中局部完全切除(I 组)的肺泡横纹肌肉瘤患者的治疗结果:来自儿童肿瘤学组的报告。
Pediatr Blood Cancer. 2010 Oct;55(4):612-6. doi: 10.1002/pbc.22520.
2
Fusion-negative alveolar rhabdomyosarcoma: modification of risk stratification is premature.融合阴性肺泡横纹肌肉瘤:风险分层的修改为时尚早。
J Clin Oncol. 2010 Oct 10;28(29):e587-8; author reply e589-90. doi: 10.1200/JCO.2010.30.5466. Epub 2010 Aug 9.
3
Fusion gene-negative alveolar rhabdomyosarcoma is clinically and molecularly indistinguishable from embryonal rhabdomyosarcoma.融合基因阴性肺泡横纹肌肉瘤在临床和分子上与胚胎性横纹肌肉瘤无法区分。
J Clin Oncol. 2010 May 1;28(13):2151-8. doi: 10.1200/JCO.2009.26.3814. Epub 2010 Mar 29.
4
Diagnosing alveolar rhabdomyosarcoma: morphology must be coupled with fusion confirmation.诊断肺泡横纹肌肉瘤:形态学必须与融合确认相结合。
J Clin Oncol. 2010 May 1;28(13):2126-8. doi: 10.1200/JCO.2009.27.5339. Epub 2010 Mar 29.
5
Recurrent t(2;2) and t(2;8) translocations in rhabdomyosarcoma without the canonical PAX-FOXO1 fuse PAX3 to members of the nuclear receptor transcriptional coactivator family.横纹肌肉瘤中重现的 t(2;2) 和 t(2;8) 易位,而没有典型的 PAX-FOXO1 融合,使 PAX3 与核受体转录共激活因子家族的成员结合。
Genes Chromosomes Cancer. 2010 Mar;49(3):224-36. doi: 10.1002/gcc.20731.
6
The utility of FOXO1 fluorescence in situ hybridization (FISH) in formalin-fixed paraffin-embedded specimens in the diagnosis of alveolar rhabdomyosarcoma.FOXO1荧光原位杂交(FISH)在福尔马林固定石蜡包埋标本中诊断肺泡横纹肌肉瘤的应用价值。
Diagn Mol Pathol. 2009 Sep;18(3):138-43. doi: 10.1097/PDM.0b013e31818c2ea4.
7
Trends in childhood rhabdomyosarcoma incidence and survival in the United States, 1975-2005.1975 - 2005年美国儿童横纹肌肉瘤的发病率及生存率趋势
Cancer. 2009 Sep 15;115(18):4218-26. doi: 10.1002/cncr.24465.
8
Genomic and clinical analyses of 2p24 and 12q13-q14 amplification in alveolar rhabdomyosarcoma: a report from the Children's Oncology Group.肺泡横纹肌肉瘤中2p24和12q13-q14扩增的基因组及临床分析:来自儿童肿瘤协作组的报告
Genes Chromosomes Cancer. 2009 Aug;48(8):661-72. doi: 10.1002/gcc.20673.
9
Molecular classification of rhabdomyosarcoma--genotypic and phenotypic determinants of diagnosis: a report from the Children's Oncology Group.横纹肌肉瘤的分子分类——诊断的基因型和表型决定因素:来自儿童肿瘤研究组的报告
Am J Pathol. 2009 Feb;174(2):550-64. doi: 10.2353/ajpath.2009.080631. Epub 2009 Jan 15.
10
Analysis of prognostic factors in patients with nonmetastatic rhabdomyosarcoma treated on intergroup rhabdomyosarcoma studies III and IV: the Children's Oncology Group.横纹肌肉瘤研究组III和IV中接受治疗的非转移性横纹肌肉瘤患者的预后因素分析:儿童肿瘤研究组
J Clin Oncol. 2006 Aug 20;24(24):3844-51. doi: 10.1200/JCO.2005.05.3801.

Clinical utility gene card for: Alveolar rhabdomyosarcoma.

作者信息

Yu Zhongxin, Kelsey Anna, Alaggio Rita, Parham David

机构信息

Department of Pathology, University of Oklahoma, Oklahoma City, OK, USA.

出版信息

Eur J Hum Genet. 2012 Jan;20(1). doi: 10.1038/ejhg.2011.147. Epub 2011 Aug 10.

DOI:10.1038/ejhg.2011.147
PMID:21829230
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3234515/
Abstract
摘要