读音:美英 synonymous mutation基本解释 同义突变;重组错误 分词解释 synonymous同义的,类义的 mutation变化 synonymous mutation是什么意思 synonymous mutation怎么读 synonymous mutation在线翻译 synonymous mutation中文意思 synonymous mutation的解释 synonymous mutation的发音 synonymous mutation意思是什么 synonymous mutation怎...
synonymous mutation:同义突变。是指没有改变氨基酸序列的密码子变化显然这是与密码子的简并性相关的。missense mutation:错义突变。是指碱基序列的改变引起了产物氨基酸序列的改变。 synonymous mutation:同义突变。是指没有改变氨基酸序列的密码子变化,显然这是与密码子的简并性相关的。
名词解释 Synonymousmutation同义突变 答案: 指突变造成的核苷酸改变并未是其所在密码子的氨基酸决定性发生改变的现象。 手机看题 你可能感兴趣的试题 名词解释 Riboswitch核糖开关 答案: 指原核生物转录产物上一段可通过对小分子物质浓度的变化进行应答从而调控基因表达的调控序列。 手机看题 名词解释 Translesionreplicatio...
Synonymousmutation同义突变 正确答案 指突变造成的核苷酸改变并未是其所在密码子的氨基酸决定性发生改变的现象。 答案解析 略 真诚赞赏,手留余香 小额打赏 169人已赞赏
synonymous mutation同义突变 582021-11 3 riboswitch核糖核酸开关 532021-11 4 translestion replication跨损伤复制 572021-11 5 transcriptome转录物组 672021-11 6 missense mutation错义突变 652021-11 7 reverse transcription PCR反转录PCR 562021-11 8 post-tramscriptional gene silencing转录后基因沉默 542021-11...
2) nonsense mutation 无义突变 1. The nonsense mutation is a specific type of gene mutation. 无义突变(nonsense mutation)是一类特定类型的基因突变。 2. Method 1 Targeted correction of nonsense mutation in LDLR in HepG2 cell 1. 方法1 HepG2细胞LDLR基因无义突变模型原位修复 1。 3. ...
Nonsynonymous mutations have a much greater effect on an individual than a synonymous mutation. In a nonsynonymous mutation, there is usually an insertion or deletion of a single nucleotide in the sequence during transcription when the messenger RNA is copying the DNA. This single missing or added...
The combined somatic mutation list was carefully curated to eliminate duplicates and annotation errors.23 We then conducted a stringent three-step screening process to select high-confidence m6A-DMs (Figure 1A; STAR Methods). With this Discussion In this study, we cataloged and characterized a ...
Must be happy, forever, forgets me.[translate] a具体来说 就是 Concrete is[translate] a在干嘛呢‘’吃饭了没有 Was doing `' to eat meal[translate] aI‘m Fail , BUT I LOVE YOU I `m出故障,但我爱你[translate] aSame-sense or synonymous mutation 同样感觉或同义变化[translate]...
Bioinformatics prediction suggested that the synonymous mutation Tyr486Tyr in APC (APC(486s)) was likely a disease-causing polymorphism and may have induced the exon skipping of APC. A hybrid mini-gene assay was performed, which confirmed that the synonymous single nucleotide polymorphism APC(486s...