查询词典 recessive

Paper 2:Mutation analysis of EDA gene in Chinese families with X-linked hypohidrotic ectodermal dysplasiaX-linked hypohidrotic ectodermal dysplasia(XLHED,MIM305100) is a recessive disease characterized by severe hypohidrosis,hypotrichosis and hypodontia.

论文二X连锁无汗/少汗型外胚层发育不良中EDA基因致病突变鉴定X连锁隐性无汗/少汗型外胚层发育不良(X-linked anhidrotic/hypohidroticectodermal dysplasia，XLHED；MIM305100)是无汗/少汗型外胚层发育不良(anhidrotic/hypohidrotic ectodermal dysplasia，EDA)中最常见的一种，约占95%。

The result indicates that there are one dominant and one recessive complementary gene that are effective against the Indian race 2E16. However, the monosomic analysis results indicated there was one resistant gene to the Indian race 2E16 and the gene was located on chromosome 3B. The current study shows that it is different from the known genes.

采用常规杂交分析方法，对铭贤169与阿夫杂交的F_1、F_2、BC_1代及其亲本进行抗性鉴定和统计分析，结果表明，阿夫对2E16菌系的抗性至少由1对显性抗条锈基因控制；通过单体分析将阿夫抗2E16菌系的1对显性基因定位在3B染色体上，等位性分析表明该基因不同于目前的已知基因。

So far transgenic knockout models of AQP1, AQP3, AQP4 and AQP5, and a knock-in model introducing a point mutation (T126M) that causes autosomal recessive nephrogenic diabetes insipidus in human have been successfully established. Significant progresses have been made in characterizing the physiological functions of these AQPs by systematic mouse phenotype studies.

目前AQP1、3、4、5基因敲除和AQP2基因点突变的基因敲入小鼠模型（模拟人类常染色体隐性遗传尿崩症）已成功建立并广泛用于表型研究，在AQP水通道蛋白生理功能方面获得许多重要进展。

These animals have a recessive trait that causes a mostly patternless underside.

这些导致主要patternless 下面的一个隐性特徵。

These animals have a recessive trait that causes a mostly patternless underside.

这些导致主要patternless 下面的一个隱性特徵。

To distinguish between the phenotypically identical AA and Aa, these can be backcrossed to the homozygous recessive parent aa.

为了鉴定表现型完全相同的 AA 与 Aa ，我们用纯合的隐性亲本 aa 来进行回交。

Background and Objective Pseudohypertrophic muscular dystrophy is a kind of lethal X-chain recessive inherited disease. The etiological factor is mainly due to gene mutation of Xp21 which induce the structural and functional abnormality of a kind of cell skeleton protein: dystrophin.

背景和目的假肥大型肌营养不良症(pseudohypertrophic muscular dystrophy，PMD)是一种常见的致死性X-连锁隐性遗传病，病因主要是由于X染色体短臂2区1带(Xp21)的基因突变而导致一种细胞骨架蛋白——抗肌萎缩蛋白的结构和功能异常所致。

Today, our film culture is still somehow recessive men-gaze culture. The feminism films of Yang Yazhou recessively illustrate the hard situation of women in this culture.

杨亚洲的女性影像创作，是男权话语隐性存在语境下对女性困境的隐性言说，是男权话语政治延续语境下对女性主体性的复归。

The Deregulation Reform of Natural Monopoly Industry in China;2. Researching the Deregulation and Reregulation of Chinese Government;3. The author first defines the recessive deregulation of the crude oil industry of China in 1998, then takes a positive te.

通过对我国原油开采业1998年的隐性放松规制进行界定，建立计量模型对这次放松规制的效果进行了实证分析，从理论和实践两方面证实了放松规制有利于我国原油开采业产业绩效的提升。

The segregational proportions differ from the Mendelian mode in which selfed progenies of recessive individuals do not segregate.

湖北光敏感雄性不育水稻从1973年发现l'}至今已有15年f，最高世代已进入20代以上，育性仍在分离之中。

As she looked at Warrington's manly face, and dark, melancholy eyes, she had settled in her mind that he must have been the victim of an unhappy attachment.

每逢看到沃林顿那刚毅的脸，那乌黑、忧郁的眼睛，她便会相信，他一定作过不幸的爱情的受害者。

Maybe they'll disappear into a pothole.

也许他们将在壶穴里消失