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mutation

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英汉-汉英词典中发现10个解释错误,并通过审核,将获赠《欧路词典》授权一个

mutation 雅思GRE

英音:/mjuː'teɪʃ(ə)n/美音:/mju'teʃən/ 全球发音: 生词本: 添加笔记:
有奖纠错
| 划词
n. 化;元音
gene mutation 基因
mutation breeding 育种
mutation rate 率;异概率;速率
point mutation
genetic mutation 基因
induced mutation 诱发
mutation frequency 频率
mutation theory 理论;学说
missense mutation [遗传学]错义
bud mutation ,芽条

Gene mutations are alterations in the DNA code.

基因DNA 密码

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,实验动物模型一个非常好方式。

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

鉴定一痒疹样营养不良型大疱性表皮松解症家系基因,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

The research shows that the mutated IGRP gene blocks the action of a sensor called glucokinase.

该研究显示IGRP基因阻断了葡萄糖激酶作为感受器活性。

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引起血管疾病,但没有认知异常,这些资料暗示了激酶1半合性基因在视觉空间建构认知障碍中作用。

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29种洞穴鱼,其眼盲亦与这些有关,但其基因位置并不相同。

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

花色异主要颜色浅,甚至为白色。花瓣异可由原来单瓣为重瓣花。

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

什么'锁骨颅骨发育不全-罕见遗传性疾病导致矮身材'?

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

An antibiotic-resistant strain of staph bacteria began its globetrotting adventures in Europe and can mutate quickly as it spreads, a new study suggests.

一项最新研究表明,一种具有抗生素抗性葡萄球菌从欧洲开始了它环球冒险,并在传播过程中迅速

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,并可能损伤人外周血淋巴细胞DNA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,减低了水体中细菌种类和数量,达到大量稳定培养轮虫

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.

最近研究表明,在帕金森患者脑苷脂(GBA)基因编码中频率增加。脑苷脂缺乏可导致高歇氏病。

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.

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

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descending colon, descension, descensional, descensive, descensus, descent, descents, deschool, deschooler, deschooling,

相似单词


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