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Localization of the human oncostatin M gene (OSM) to chromosome 22q12, distal to the Ewing's sarcoma breakpoint.

作者信息

Giovannini M, Selleri L, Hermanson G G, Evans G A

机构信息

Molecular Genetics Laboratory, Salk Institute for Biological Studies, San Diego, CA 92138-9216.

出版信息

Cytogenet Cell Genet. 1993;62(1):32-4. doi: 10.1159/000133439.

DOI:10.1159/000133439
PMID:8422753
Abstract

Using fluorescence in situ hybridization, a cosmid clone containing the gene for oncostatin M (OSM) was mapped to human chromosome 22q12, placing the OSM gene in the same chromosome band as the leukemia-inhibitory factor gene (LIF). The location of the OSM gene was determined relative to the t(11;22)(q24;q12) of Ewing's sarcoma and found to be distal to the translocation breakpoint on chromosome 22. Analysis of physical distances by pulsed-field gel electrophoresis demonstrated further that the two genes lie within 500 kb of each other.

摘要

相似文献

1
Localization of the human oncostatin M gene (OSM) to chromosome 22q12, distal to the Ewing's sarcoma breakpoint.
Cytogenet Cell Genet. 1993;62(1):32-4. doi: 10.1159/000133439.
2
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Tandem linkage of genes coding for leukemia inhibitory factor (LIF) and oncostatin M (OSM) on human chromosome 22.人类22号染色体上编码白血病抑制因子(LIF)和抑瘤素M(OSM)的基因串联连接。
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Molecular cytogenetic analysis of a complex t(10;22;11) translocation in Ewing's sarcoma.
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