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NZB小鼠对NZB×NZW杂交种肾脏疾病的遗传贡献。

The genetic contribution of the NZB mouse to the renal disease of the NZB x NZW hybrid.

作者信息

Knight J G, Adams D D, Purves H D

出版信息

Clin Exp Immunol. 1977 May;28(2):352-8.

Abstract

The occurrence of lupus nephritis in (NZB x NZW)F1 mice appears to depend on the action of at least two dominant or co-dominant genes (at least one gene from each parent) as neither of the inbred parental strains shows the disorder. Identifying affected animals by antemortem determinations of renal function, using improved methods of measuring proteinuria and renal clearance, we have studied the incidence of the renal disease in 230 (NZB x NZW)F1 x NZW backcross mice. The incidence was 49-6% which indicates that NZB strain contributes only one gene, or cluster of closely linked genes, to the renal disorder of the F1 hybrid. The gene(s) must be dominant or co-dominant, as it expresses its effect in the heterozygous state. Study of the H-2 status of the backcross mice showed a loose linkage of the NZB renal disease gene(s) to the D end of the H-2 complex, the crossover frequency being 32-6+/-3-1%.

摘要

(新西兰黑鼠×新西兰白鼠)F1代小鼠狼疮性肾炎的发生似乎取决于至少两个显性或共显性基因的作用(每个亲本至少有一个基因),因为两个近交亲本品系均未表现出这种病症。通过采用改进的蛋白尿和肾脏清除率测量方法,在生前测定肾功能来识别患病动物,我们研究了230只(新西兰黑鼠×新西兰白鼠)F1代×新西兰白鼠回交小鼠的肾病发病率。发病率为49.6%,这表明新西兰黑鼠品系仅为F1代杂种的肾脏疾病贡献了一个基因或紧密连锁的基因簇。该基因或基因簇必定是显性或共显性的,因为它在杂合状态下就能表达其效应。对回交小鼠H-2状态的研究表明,新西兰黑鼠肾病基因与H-2复合体的D端存在松散连锁,交叉频率为32.6±3.1%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a8/1540763/990d27eb4df9/clinexpimmunol00237-0159-a.jpg

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