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对(新西兰黑鼠×新西兰白鼠)F1代小鼠中新西兰黑鼠对狼疮样自身免疫性疾病影响的基因分析。

Genetic analysis of the NZB contribution to lupus-like autoimmune disease in (NZB x NZW)F1 mice.

作者信息

Drake C G, Babcock S K, Palmer E, Kotzin B L

机构信息

Department of Pediatrics, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.

出版信息

Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):4062-6. doi: 10.1073/pnas.91.9.4062.

Abstract

Lupus-like autoimmunity in (NZB x NZW)F1 mice is frequently marked by the development of a severe and fatal renal disease. Genes from both NZB and NZW parents are required for the full expression of disease. We applied a mapping technique based on polymorphism in simple sequence repeats to the analysis of (NZB x NZW)F1 x NZW backcross mice to determine the NZB genetic contribution to disease. The results show that a single NZB locus or tightly linked group of loci on the distal part of chromosome 4 provides the strongest association with renal disease and death. This locus, designated here as nba-1 (New Zealand Black autoimmunity), lies distal to the locus elp-1, 60-70 centimorgans from the centromere. It is of interest that a gene encoding a receptor for tumor necrosis factor maps to the vicinity of this disease-associated gene.

摘要

(新西兰黑鼠×新西兰白鼠)F1代小鼠中的狼疮样自身免疫常常表现为严重且致命的肾脏疾病。NZB和NZW双亲的基因对于疾病的完全表达都是必需的。我们应用基于简单序列重复多态性的定位技术,对(新西兰黑鼠×新西兰白鼠)F1代与新西兰白鼠回交小鼠进行分析,以确定NZB基因对疾病的影响。结果显示,位于4号染色体远端的单个NZB位点或紧密连锁的位点群与肾脏疾病和死亡的关联性最强。这个位点在此处被命名为nba-1(新西兰黑鼠自身免疫),位于elp-1位点的远端,距离着丝粒60 - 70厘摩。有趣的是,一个编码肿瘤坏死因子受体的基因定位于这个与疾病相关的基因附近。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fae/43723/0e13bde7d66c/pnas01131-0595-a.jpg

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