网络释义专业释义英英释义
...指DNA分子中碱基对的取代，使得mRNA的某一密码子发生变化，由他所编码的氨基酸就变成另一种不同的氨基酸，使得多肽链中氨基酸的顺序也相应地发生改变。无义突变(nonsense mutation)指由于碱基取代使原来可翻译某种氨基酸的密码子变成了终止密码子。
基于3065个网页-相关网页
...蛋白质合成的终止密码子，导致多肽链在成熟之前终止合成的改变 基于88个网页 - 无意义突变 (2) 无意义突变 ( nonsense mutation ):此种突变是由于某一碱基被替代之后,使原来编码某一氨基酸的密码子突变成为终止密码子,造成珠蛋白链合成时提早终止翻译,生成无功...
基于293个网页-相关网页
-
无义突变 - 引用次数：20
Other mutations in nucleotide are nonsense mutation.
其它位点的核普酸突变均为无义突变。
参考来源 - HLA -
无意义突变无义突变
·2,447,543篇论文数据，部分数据来源于NoteExpress
Nonsense mutation
- abstract: In genetics, a nonsense mutation is a point mutation in a sequence of DNA that results in a premature stop codon, or a nonsense codon in the transcribed mRNA, and in a truncated, incomplete, and usually nonfunctional protein product. It differs from a missense mutation, which is a point mutation where a single nucleotide is changed to cause substitution of a different amino acid.
以上来源于: WordNet
双语例句权威例句
-
Conclusions Novel compound heterozygous nonsense mutation of KCNQ1 can cause JLNS.
结论JLNS可由KCNQ1基因上复合的杂合突变所引起。
-
Conclusion R492X nonsense mutation of PINK1 gene was rare in Chinese sporadic patients with PD.
结论PINK1基因R 492x无义突变不大可能是中国散发性帕金森病患者的突变热点。
-
In most genetic conditions, between 5-15 per cent of cases are caused by a defect called a "nonsense mutation".
在多数基因情况下，约5 - 15%的病例都是由一种叫做“无意义突变”的缺陷引起。
应用推荐