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EWS-FLI1 fusion protein up-regulates critical genes in neural crest development and is responsible for the observed phenotype of Ewing’s family of tumors. Cancer Res

机译：EWS-FLI1融合蛋白上调神经rest发育中的关键基因，并负责观察Ewing肿瘤家族的表型。癌症研究

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Siwen Hu-lieskovan; Jingsong Zhang; Lingtao Wu; Et Al; Contact The Aacr; Hiroyuki Shimada; Deborah E. Schofield; Timothy J. Triche;
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1. Inhibition of the transcriptional function of p53 by EWS-Fli1 chimeric protein in Ewing Family Tumors. [J] . Li Y, Tanaka K, Fan X, Cancer letters . 2010,第1期

机译：EWS-Fli1嵌合蛋白在尤因家族肿瘤中对p53转录功能的抑制。
2. EWS-FLI1 and EWS-ERG gene fusions are associated with similar clinical phenotypes in Ewing's sarcoma. [J] . Ginsberg JP, de Alava-E, Ladanyi M, Journal of Clinical Oncology . 1999,第6期

机译：EWS-FLI1和EWS-ERG基因融合与尤因肉瘤的相似临床表型有关。
3. Periosteal ewing sarcoma family of tumors of the femur confirmed by molecular detection of EWS-FLI1 fusion gene transcripts: a case report and review of the literature. [J] . Hakozaki M, Hojo H, Tajino T, Journal of pediatric hematology/oncology: Official journal of the American Society of Pediatric Hematology/Oncology . 2007,第8期

机译：EWS-FLI1融合基因转录物的分子检测证实了股骨骨膜尤文氏肉瘤家族病例的报道和文献复习。
4. Mouse and human phenotypes indicate a critical conserved role for ERK2 signaling in neural crest development [O] . Jason Newbern, Jian Zhong, Rasika S. Wickramasinghe, 2008

机译：小鼠和人类的表型表明ERK2信号在神经c发育中的关键保守作用
5. DNA microarrays reveal relationship of Ewing family tumors to both endothelial and fetal neural crest-derived cells and define novel targets. Cancer Res [O] . Martin S. Staege, Christoph Hutter, Ingo Neumann, 2004

机译：DNa微阵列揭示了尤因家族肿瘤与内皮和胎儿神经嵴衍生细胞的关系，并定义了新的靶标。癌症研究

EWS-FLI1 fusion protein up-regulates critical genes in neural crest development and is responsible for the observed phenotype of Ewing’s family of tumors. Cancer Res

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