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Fusion nucleic acid resulting from translocation of the nucleic acid and corresponding to a gene of chromosome 22 that is involved in recurrent chromosomal translocation involved in the development of carcinoma

机译:由该核酸易位产生的融合核酸,其对应于22号染色体的基因,该基因与癌症发展中涉及的复发性染色体易位有关

摘要

PCT No. PCT/FR93/00494 Sec. 371 Date Jan. 18, 1995 Sec. 102(e) Date Jan. 18, 1995 PCT Filed May 19, 1993 PCT Pub. No. WO93/23549 PCT Pub. Date Nov. 25, 1993Translocations of chromosome 22 are associated with various cancers. Hybrid DNA sequences, having a portion of the Ews gene of chromosome 22 and a portion of either the Hum-Fli-1 gene of chromosome 11, the Erg gene of chromosome 21, or the Atf-1 gene of chromosome 12, are disclosed. Proteins encoded by these hybrid DNAs are disclosed. Diagnosis of specific cancers based on detection of the translocations is disclosed.
机译:PCT号PCT / FR93 / 00494第二部分371日期1995年1月18日102(e)日期1995年1月18日PCT申请1993年5月19日PCT公布PCT公开号WO93 / 23549。日期:1993年11月25日,第22号染色体易位与各种癌症有关。公开了具有部分染色体22的Ews基因和部分染色体11的Hum-Fli-1基因,部分染色体21的Erg基因或部分染色体12的Atf-1基因的杂合DNA序列。公开了由这些杂合DNA编码的蛋白质。公开了基于对易位的检测的特定癌症的诊断。

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