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通过荧光原位杂交和体细胞杂交分析将人类Ror1基因(NTRKR1)定位于染色体1p31 - p32。

Localization of the human Ror1 gene (NTRKR1) to chromosome 1p31-p32 by fluorescence in situ hybridization and somatic cell hybrid analysis.

作者信息

Reddy U R, Phatak S, Allen C, Nycum L M, Sulman E P, White P S, Biegel J A

机构信息

Division of Neurology Research, Children's Hospital of Philadelphia, Pennsylvania 19104, USA.

出版信息

Genomics. 1997 Apr 15;41(2):283-5. doi: 10.1006/geno.1997.4653.

Abstract

Ror1 is an orphan cell surface receptor with strong homology to the tyrosine kinase domain of growth factor receptors, in particular the Trk family. Southern blot analysis of genomic DNA from somatic cell hybrids revealed that Ror1 is located on chromosome 1. We have mapped the Ror1 gene to chromosome 1p12-p32 using PCR on a somatic cell hybrid panel that subdivides chromosome 1p. We have further localized the gene to chromosome 1p31-p32 by fluorescence in situ hybridization using a PAC clone that contains the Ror1 gene.

摘要

Ror1是一种孤儿细胞表面受体,与生长因子受体的酪氨酸激酶结构域具有高度同源性,尤其是Trk家族。对体细胞杂种的基因组DNA进行Southern印迹分析表明,Ror1位于1号染色体上。我们使用对1号染色体短臂进行细分的体细胞杂种板,通过PCR将Ror1基因定位到1号染色体短臂1p12 - p32区域。我们进一步通过使用包含Ror1基因的PAC克隆进行荧光原位杂交,将该基因定位到1号染色体短臂1p31 - p32区域。

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