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一种导致小鼠阴道闭锁的隐性突变。

A recessive mutation causing imperforate vagina in mice.

作者信息

Eisen E J, Hauser M E, Pomp D, Anderson S G, Newbold R R, McCormick G Y

机构信息

Department of Animal Science, North Carolina State University, Raleigh.

出版信息

J Hered. 1989 Nov-Dec;80(6):478-82. doi: 10.1093/oxfordjournals.jhered.a110904.

Abstract

A recessive mutation (ipv) causing imperforate vagina was discovered in a line of mice selected for low lean tissue mass as a proportion of body weight. Two full sisters were found to have marked swelling of the perineum and complete closure of the vagina. Crosses of heterozygotes identified by progeny testing produced a female progeny ratio not different from the 3 normal: 1 affected (chi 2 = 0.695; p less than .3) expected on the basis of a recessive allele at a single autosomal locus. As a consequence of the imperforate vagina, the uterus and vagina were greatly distended by fluid. The uterus of affected females displayed a swollen uterine lumen and thin endometrial stroma and muscularis. Ovarian tissue of affected females was similar to that of normal mice, and affected females produced ova that were normal in appearance. The mutation causing an imperforate vagina may present a useful model for studying the basis of abnormal vaginal development in other species and increasing the understanding of normal vaginal development in the mouse.

摘要

在一组因低瘦体重占体重比例而被选择的小鼠品系中,发现了一种导致阴道闭锁的隐性突变(ipv)。发现两只同胞姐妹会阴明显肿胀且阴道完全闭合。通过后代测试鉴定出的杂合子杂交产生的雌性后代比例与基于单个常染色体位点的隐性等位基因预期的3只正常:1只患病(卡方 = 0.695;p小于0.3)没有差异。由于阴道闭锁,子宫和阴道被液体严重扩张。患病雌性的子宫显示子宫腔肿胀,子宫内膜基质和肌层变薄。患病雌性的卵巢组织与正常小鼠相似,患病雌性产生的卵子外观正常。导致阴道闭锁的突变可能为研究其他物种阴道发育异常的基础以及增进对小鼠正常阴道发育的理解提供一个有用的模型。

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