There is also GMO zucchini, crookneck squash, papaya, and alfalfa.
也有转基因南瓜、转基因葫芦、转基因木瓜和转基因苜蓿。
Genes tabA, tabB,tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.
野火氨酸的合成有tabA,tabB,talA,dapB等基因参与,受lemA基因调控。
Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).
而纤毛虫和蚊子的粘液素基因所表现出的基因整合则是。
Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.
目前的研究热点还包括:基因-环境相互作用、遗传药理学、基因咨询等。
Some people extoll GM foods’tremendous potential for good.
有人赞赏转基因事物的极大潜力。
Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.
瘦素(leptin)是肥胖基因(ob基因)编码,脂肪胞分泌的种内源性激素,主要调控体重和脂肪分布。
Gene mutations are alterations in the DNA code.
基因突变是指DNA 密码的改变。
That genal genome may lead to better treatment and control of diseaesthe disease.
那基因组能带来比较好的治疗和疾病的控制。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴疹样营养不良型大疱性表皮松解症家系的基因突变,为进步开展基因诊断和基因治疗奠基础。
You have good genes from your parents, so you should live a long time.
你从父母那儿获得优良的基因, 所以能够活得很长。
Researchers are gradually deciphering the genetic structure found in the cells of organisms.
研究者正渐渐破译存于有机体胞内的基因结构。
All the C3 allotype was C3S.The gene frequency was 1.
而且所有的第三补体异型均为C3S,而此基因频率为1。
Most of these genes have not been reported to relate to the haematogenesis in ontogeny.
这基因大多数在胚胎分化造血发育中的作用尚未见报道。
The ear diametre was inherited in a superdominant fashion with the additive gene as the dominant gene.
穗粗的遗传为超显性遗传,且显性基因为增效基因。
But, there were extremely low efficiency of integration, unstable hereditation and expression in transgenic animals by the technique.
但是,这种方法存在基因整合效率低、源基因不能在转基因动物体内稳遗传及表达的问题。
A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.
与脱辅基蛋白结合松弛、易于与之分离的辅基因子称为辅。
Evidence is accumulating that a defective gene may be responsible for this disease.
越来越多的证据表明该疾病是由种有缺陷的基因引起的。
Histones are characterized by numerous posttranslational modifications that influence gene transcription.
组蛋白的特点是大量的翻译后修饰,这修饰可以影响基因转录。
Siblings and dizygotic twins share only 50% of their segregating genes.
同卵双生双胞胎和双卵双生双胞胎分享仅50%的基因。
The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.
而且,位于目的基因下游的胭脂碱合成酶基因有表达。
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What genetic weaknesses run in your family?
你们家族还有什么因缺陷?
So basically—things like repair genes, immunity genes, and stress response genes.
本上是修复因、免疫因和应激反应因等。
But they may have different alleles, which are alternatives of the same genes.
但是他们可能有不同的等位因,这些等位因是相同因的替代品。
With genetic modification becoming commonplace, modified crops will be grown indoors.
随着因改造的推行,转因作物将在室内种植。
They've got the drinking genes or whatever.
比如有人有酿酒的因 或别的不好的因。
The team also could date when particular genes entered the mix.
研究团队也可以推定特定因进混合因组的时间。
The kat7 gene, Qu said, was most involved in the aging of cells.
表示,kat7因是最显著的促进细胞衰老因。
Consequently, Scott's body quieted some genes while amplifying others.
因此,斯科特的身体关闭了一些因,同时放大了其他因。
Some of us are genetically blessed.
我们中一些人的因是幸运的。
Oncogenes help cells grow and proliferate, while tumor suppressor genes slow down cell growth and proliferation.
致癌因加速细胞生长增殖,而抑癌因使细胞生长增殖变慢。
Native American genes were introduced into the typical African-American genome in the early 1600's.
17世纪初,美国本土因进了典型的非裔美国人的因组。
Now do we have to wait for an altruistic gene to be in the human race?
我们还要等人类因中出现利他因吗?
Of the human genome's 20,000 or so genes, almost a thousand code for olfactory receptors.
在人类因组中大约有20000个因,几乎有1000个嗅觉受体编码。
We can precisely edit genes with CRISPR.
我们能使用 CRISPR 技术精确编辑因。
These include the ARX, or Aristaless-related homeobox gene, and STXBP1, or syntaxin-binding protein 1, gene.
这些因包括ARX,即无芒相关同源框因以及STXBP1,即突触融合蛋白结合蛋白-1因。
The trait was passed on to almost 100 percent of the offspring of treated mosquitoes.
几乎100%的转因后代都携带了该因。
The genetic changes that cause cancer usually happen in three types of genes.
导致癌症的因改变通常发生在三种类型的因中。
A gene drive is a term for genetic engineering that alters the probability of genes passed to offspring.
因驱动是因工程的一个术语,它改变因传递给后代的可能性。
As such, they retain their own genes.
如此便保留住了因。
Now we're going to take a little sample here for genetics.
现在我们要取一些因样本。
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