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mutation

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mutation GREGMAT雅思

英音:/mjuː'teɪʃ(ə)n/美音:/mju'teʃən/ 全球发音: 生词本: 添加笔记:
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| 划词
n. 变;变化;元音变化
gene mutation 基因
mutation breeding 诱变育种
mutation rate 变率;变异概率;变速率
point mutation
genetic mutation 基因
induced mutation 诱发
mutation frequency 变频率
mutation theory 变学说
missense mutation [遗传学]错义
bud mutation 芽变,芽条变异

Gene mutations are alterations in the DNA code.

基因是指DNA 密码的改变。

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微导致致癌倾向综合征着色性干皮病。

Technique of mutation breeding in gladiola was studied by meansof electron beam.

用电子束辐射唐菖蒲种球,研究唐菖蒲的诱变育种。

Technique of mutation breeding in gladiola was studied by means of electron beam.

摘 要: 用电子束辐射唐菖蒲种球,研究唐菖蒲的诱变育种。

We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病基因,实验动物模型是一个常好的方式。

Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.

目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因,为进一步开展基因诊断和基因治疗奠定基础。

Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶基因外显子6区13389G缺失,引起移码变。

CodonCode Aligner is a program for sequence assembly, contig editing, and mutation detection, available for Windows and Mac OS X.

DNA测序trace图编辑、分析、contig编辑、序列拼接软件。

Because ELN mutations cause vascular disease but not cognitive abnormalities, these data implicate LIMK1 hemizygosity in imparied visuospatial constructive cognition.

因为ELN引起血管的疾病,但没有认知的异常,这些示了激酶1半合性基因在视觉空间建构认知障碍中的作用。

At least some of the mutations responsible for this loss of vision differed between the 29 populations of cavefish known to exist.

目前现存的29种洞穴鱼,其眼盲亦与这些有关,但是其基因变的位置并不相同。

Cleidocranial dysostosis or Cleidocranial dysplasia is a hereditary congenital abnormality of humans due to haploinsufficiency caused by mutations in the CBFA1 gene.

什么是'锁骨颅骨发育不全-罕见的遗传性疾病导致矮身材'?

This indicats that gamma ray irradiation can increase the frequency of mutations and produces special types of flower in Godetia grandiflora breeding.

花色变异主要是颜色变浅,甚至变为白色。花瓣变异可由原来的单瓣变为重瓣花。

Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).

结果23个杂合子变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出变分别为22个(96%)、20个(87%)和23个(100%)。

Base pair substitution mutation and frame shift mutation were caused by folpet in Ames test.And DNA breakage in human PMNC might be induced by folpet.

灭菌丹可引起鼠伤寒沙门氏菌碱基置换和移码变,并可能损伤人外周血淋巴细胞DNA的完整性。

The mutation potential of ethephon was by investigated the micronucleus test of bone marrow polychromatophilic erythroblasts (PCE) cells and sperm shape abnormality test in mice.

摘要为测定乙烯利对人体健康的影响,采用小鼠骨髓细胞微核试验和小鼠精子畸形试验分别检测了乙烯利对小鼠体细胞和生殖细胞的致变性。

The streak-plate method was used to separate Chlorella colonies.The selected strain, induced by mutation using a laser, was cultured heterotrophically to obtain a high biomass.

用小球藻干粉培养草履虫和萼花臂尾轮虫,减低了水体中细菌的种类和数量,达到大量稳定培养轮虫的目的。

Allelotype analysis was done at five short tandem repeat markers (D17S855, D17S1322, D17S1323, D17S1326, and D17S1327) in or adjacent to BRCA1 on the recurrent mutation carriers.

对发现携带有相同的个体选取5个与BRCA1基因连锁的标记(D17S855、D17S1322、D17S1323、D17S1326和D17S1327)进行单倍型分析。

Recent studies indicate an increased frequency of mutations in the gene encoding glucocerebrosidase (GBA), a deficiency of which causes Gaucher's disease, among patients with Parkinson's disease.

最近的研究表明,在帕金森患者的脑苷脂(GBA)基因编码中频率增加。脑苷脂的缺乏可导致高歇氏病。

A mutant, TS-N-121 was obtained by mutation and plate screening from a parent strain Mycobacterium fortuitum MF2 , which could transform sterol into androstanedione as the main product.

从雄甾二酮的转化产生菌偶发分枝杆菌MF2出发,经紫外诱变结合平板筛选,获得一株主要转化生产睾酮的变株TS-N-121。

Liver function tests and hepatitis B virus (HBV) DNA (Versant 3.0) were assessed bimonthly, whereas adefovir-related mutations were searched by INNO-LiPA assay at baseline and at yearly intervals.

我们评估了阿德-拉米联合治疗能否克服这种风险。

声明:以上例句、词性分类均由互联网源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。

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相似单词


mutarotase, mutarotation, mutase, mutate, mutatest, mutation, mutationism, mutatis mutandis, mutative, mutatoxanthin,
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