染色体基因

Germ-line mutations in the genes hTERT and hTR, encoding telomerase reverse transcriptase and telomerase RNA, respectively, cause autosomal dominant dyskeratosis congenita, a rare hereditary disorder associated with premature death from aplastic anemia and pulmonary fibrosis.

分别编码端粒末端转移酶反转录酶和端粒酶RNA的hTERT和hTR基因的种系突变导致常染色体显性先天性角化不良，它是一种罕见的因为再生障碍性贫血和肺纤维化而早亡的遗传性疾病。

Some environmental factors could confer a predisposition to depression by affecting the genome epigenetically — for example, increased maternal care in rodents causes an epigenetic change in the promoter region of the glucocorticoid-receptor gene.

一些环境因子可能赠予抑郁易感性，累及后生染色体—例如，在啮齿动物的糖皮质激素受体基因启动子区增加母体的忧虑可引起后生变化。

Among them, 1 QTL showing main effect only and 7 QTL showing epistatic effect only, they could explain 5.0% and 34.8% of total phenotypic variation respectively.

在仅表现上位性效应QTL所处的区间中，有3个区间也与前人所报道的抗稻瘟病主基因或QTL 具有相似的染色体位置。

Nasopharyngeal carcinoma is an endemic cancer with particulargeographic and ethnic distribution within southern China, most frequently, withinGuangdong province. Etiologically, the disease involves multiple factors includinggenetic, Epstein-Barr viral, as well as other food and environmental factors.Cytogenetic studies have revealed that loss of heterozygosity on chromosome3p occurred in as many as 95 - 100％ of NPCs and 75％ of precancerous lesions,suggesting the presence of NPC associated tumor suppressor genes.

鼻咽癌(Nasopharyngeal carcinoma，NPC)是中国南部、尤其是广东省最为常见的恶性肿瘤，其发病与遗传因素、EB病毒感染、以及环境和饮食等多种因素有关。3号染色体短臂(3p)在高达95-100％的鼻咽癌和75％的癌前病变中发生杂合性丢失(Loss of heterozygosity，LOH)，提示3p缺失区域中存在与鼻咽癌发生密切相关的抑癌基因。

Careful analysis of this theory indicates that the X chromosomes may not contain sex-determining genes for femaleness.

对这种理论的仔细分析表明，X染色体上可能并不含有确定女性性别的基因。

Careful analysis of this theory indicates that the X chromosomes may not contain sex determining genes for femaleness .

染色体上可能并不含有确定女性性别的基因。

Chromosome walking techniques are commonly used for cloning the known flanking sequence.

染色体步行是一种常用的克隆已知基因旁侧序列的技术。

Objective To add DXS7133, GATA198A10, DXS9896 and DXS6797 to the panel of forensically validated X chromosome markers, and apply the multiplex amplification system to a population study and forensic analysis on the Hans of Chengdu.

目的建立X染色体短串联重复序列DXS7133、GATA198A10、DXS9896、DXS6797基因座的复合扩增系统，调查成都汉族人群的遗传多态性并探讨其法医学应用价值。

Genotypical synthetic chromosomes are recursively expanded to produce a population of phenotypical state models, bit strings or other forms of encoding that suitably represent a particular problem set.

基因型合成染色体被递归地扩展以产生表型状态模型、位串或其他形式的编码的种群，其适合于表示特定问题。

A small segment of rye chromosome at telomere in a pair of wheat chromosome in the line was found by means of GISH.

这一结果指出，含有抗白粉病基因的黑麦染色体6R小片段被引入了小麦。

She gently rebuff ed him, but agreed that they could be friends

她婉言拒绝了，但同意作为朋友相处。

If in the penal farm, you were sure to be criticized.

要是在劳改农场，你等着挨绳子吧！