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应用于囊性纤维化的疾病基因定位方法。

Approaches to localizing disease genes as applied to cystic fibrosis.

作者信息

Dean M, Drumm M L, Stewart C, Gerrard B, Perry A, Hidaka N, Cole J L, Collins F S, Iannuzzi M C

机构信息

Biological Carcinogenesis and Development Program, NCl-Frederick Cancer Research Facility, MD 21701.

出版信息

Nucleic Acids Res. 1990 Jan 25;18(2):345-50. doi: 10.1093/nar/18.2.345.

Abstract

Using chromosome jumping and walking and restriction fragment length polymorphism (RFLP) analysis, we have defined the region which must contain the cystic fibrosis gene. DNA segments spanning approximately 250 kb in the direction of the gene were isolated and used to identify several new polymorphisms informative in cystic fibrosis families. These RFLPs include a highly polymorphic, CA/GT repeat, and a 10 bp insertion uncovered using the polymerase chain reaction. By analyzing a family with a recombination near the gene, we can exclude this region as containing the mutation. Data on the extent of linkage disequilibrium of these markers provides additional information on where the gene is located.

摘要

利用染色体跳跃、步移和限制性片段长度多态性(RFLP)分析,我们确定了必须包含囊性纤维化基因的区域。分离出了在基因方向上跨度约250 kb的DNA片段,并用于鉴定囊性纤维化家族中几个新的多态性信息。这些RFLP包括一个高度多态的CA/GT重复序列,以及通过聚合酶链反应发现的一个10 bp的插入序列。通过分析一个在基因附近发生重组的家系,我们可以排除该区域包含突变。这些标记的连锁不平衡程度数据提供了关于该基因位置的额外信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57ff/330273/dcdff0520eba/nar00186-0124-a.jpg

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