Suppr超能文献

肌营养不良症,小鼠8号染色体上的一种新型肌病。

Myodystrophy, a new myopathy on chromosome 8 of the mouse.

作者信息

Lane P W, Beamer T C, Myers D D

出版信息

J Hered. 1976 May-Jun;67(3):135-8. doi: 10.1093/oxfordjournals.jhered.a108687.

Abstract

A new recessive mutation, myd, causing a diffuse and progressive myopathy in the mouse is described. Histopathological comparisons with normal littermates showed widely distributed focal lesions in all skeletal muscles of myd/myd. Body and organ weights of affected mice were considerably less than those of normal littermates and the mean lifespan of myodystrophic mice that survived weaning was 17 weeks with a range of 5 to 39 weeks. Myodystrophy is located on chromosome 8; it is linked to Os with about 6 percent and to Eso with about 37 percent recombination.

摘要

本文描述了一种新的隐性突变基因myd,该基因可导致小鼠出现弥漫性进行性肌病。与正常同窝小鼠的组织病理学比较显示,myd/myd小鼠的所有骨骼肌中均有广泛分布的局灶性病变。患病小鼠的体重和器官重量明显低于正常同窝小鼠,断奶后存活的肌营养不良小鼠的平均寿命为17周,范围为5至39周。肌营养不良基因位于8号染色体上;它与Os的连锁率约为6%,与Eso的重组率约为37%。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验