gene mutation中文,gene mutation的意思,gene mutation翻译及用法

2026-05-06 08:37 浏览次数 17

gene mutation

英[dʒi:n mju:ˈteɪʃən]美[dʒin mjuˈteʃən]

[遗] 基因突变

gene mutation 英语释义

英语释义

  • a mutation due to an intramolecular reorganization of a gene

gene mutation 片语

片语

HPRT gene locus mutationHPRT基因位点突变

transgenation基因突变

c gene promoter mutationc基因启动子基因变异

gene spot mutation基因点突变

katG gene S315 mutation异烟肼

MHTFR gene C677T mutation四氢叶酸还原酶基因的C677T突变

genetic mutation基因突变

gene site mutation基因点突变

gene deletion mutation基因缺失突变

MTHFR Gene C677T MutationMTHFR基因C677T突变

gene targeting mutation基因打靶技术

gene mutation 例句

英汉例句

  • most stand shorter than 4 feet because the gene mutation prevents their bodies from properly using growth hormone.

    基因突变使他们的身体无法正确使用生长激素,其中大多数人的身高不足4英尺。

  • all 15 women had partners without the cf gene mutation and, apart from failing to conceive, other indicators of fertility were normal.

    所有15名妇女她们的搭档没有囊性纤维瘤基因变异,她们除了没有成功受孕外,其余指标均正常。

  • although a recent study found that a single gene mutation heightened the risk of obesity by up to 67 percent, genetics cannot explain the skyrocketing obesity trend.

    尽管最近的研究发现单基因突变使肥胖的风险增加高达67%,但是遗传不能解释飞涨的肥胖趋势。

  • a partial tandem duplication is a type of gene mutation that occurs when a section of a gene is repeated, like a stutter in the gene「s dna.

    部分串联复制是基因突变的一个类型,当一个基因片断重复时发生,就像停顿基因。

  • scientists have discovered a group of people in ecuador with a rare gene mutation that could reveal ways to extend the human life span.

    科学家在一群厄瓜多尔人身上发现了一种罕见的基因突变,有望据此揭开长寿的谜底。

  • the canadian gene cure foundation says the discovery of a rare gene mutation might spare certain type 1 diabetic children painful insulin injections.

    加拿大基因治疗基金会日前表示,该国研究人员最近发现的一种罕见的基因变异可能会减轻某些ⅰ型糖尿病患儿注射胰岛素的痛苦。

  • the team thought this protection might come from the same gene mutation that made these people so small.

    科学家认为,就是这种让人长不高的基因变异保护他们免受这些疾病侵袭。

  • objective to study and compare the hprt gene mutation in rat soma cells induced by internal exposure to radionuclides using cloning method.

    目的克隆法研究放射性核素内照射诱发大鼠体细胞hprt基因突变,比较不同体细胞hprt基因突变频率。

  • they say they may be able to use drugs to trigger a similar gene mutation in people to encourage hair to grow on bald patches.

    科学家们说他们或许可以利用药物在人体触发一种类似的基因突变,促进脱发部位头发的生长。

  • the variegation of petals originates chiefly from gene mutation and viral infection.

    花瓣彩斑主要由基因突变或病毒入侵而形成。

  • the next step is to look for a compound that would mimic the effects of the gene mutation – in other words, a pill that boosts the ability to remember.

    下一步是寻找可以模仿这种基因突变作用的化合物――也就是说,一种可以提高记忆力的药片。

  • however, the team deliberately chose a compatible donor who has a naturally occurring gene mutation that confers resistance to hiv.

    然而,这个小组有意的从匹配的捐赌者中挑选了一位因突变而得到一种hiv抗体的作为他的捐赠者。

  • fragile x is caused by a gene mutation in the female x chromosome that affects the construction of synapses, vital connection points between nerve cells.

    脆性x染色体是由雌性x染色体基因突变引发的,这种突变影响到了连接神经细胞间的关键接点———染色体结合的构造。

  • in 2001 fu and her colleagues discovered a different gene mutation that causes fasps.

    其实早在2001年,傅英惠和她的同事就发现了另外一种能够引起家族性睡眠状态提前综合征的基因突变。

  • objective to study the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7 (sca7).

    目的研究遗传性脊髓小脑性共济失调7型(sca7)的基因突变和临床特征。

  • nowadays, bigh3 gene mutation related corneal dystrophy is the most common etiological factor leading to corneal dystrophy in genetics.

    bigh3基因突变有关的角膜营养不良现今已是角膜营养不良最常见的遗传学致病因素。

  • gene mutation analysis is the important tool for genetic counseling and prenatal diagnosis.

    基因突变分析是开展遗传咨询和产前诊断的重要工具。

  • objective to study the gene mutation and clinical characteristics of hereditary spinocerebellar ataxia type 7 (sca7).

    目的研究中国人遗传性脊髓小脑型共济失调(sca)7型(sca7)的基因突变和临床特征。

  • previous research has shown that gene mutation in shank3 is associated with delayed language abilities, learning disability, and asds.

    之前的研究表明,shank3的基因突变与语言能力发育迟缓、学习障碍和泛自闭障碍癥有关。

  • objective to discuss the cloning method for detecting the hprt gene mutation of rats.

    目的探讨克隆法检测大鼠体细胞hprt基因突变,为后续研究打下基础。

  • take the gene mutation that causes phenylketonuria, or pku. people with the disease can」t break down the amino acid phenylalanine, a problem that can lead to severe cognitive damage.

    提取能导致苯丙酮尿癥(pku)的基因突变.患这种病的人不能分解氨基酸苯丙氨酸,这会导致严重的认知损坏。

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