名词解释 整码突变(in-frame mutation) 答案: 当插入或缺失连续排列的核苷酸数目是3的整数倍时,其结果仅导致密码子的插入或缺失突变,而不引起移码突变 手机看题 你可能感兴趣的试题 名词解释 拟表型(phenocopy) 答案: 是指由于环境因素的作用所产生的疾病或表型与某一特定基因突变所产生的表型相同或相似的现象。
网络释义 1. 整码突变 frame in的中文翻译,frame in中文是什么意思... ... 嵌墙樘子(嵌墙樘子) keyed-in frame 整码突变(整码突变) in-frame mutation ... www.nciku.cn|基于4个网页必应词典应用 准确权威无广告去官网了解更多 下载手机版必应词典 iOS Windows Phone Android 体验P C 版必应词典Win...
百度试题 题目整码突变(in-frame mutation) 相关知识点: 试题来源: 解析 当插入或缺失连续排列的核苷酸数目是3的整数倍时,其结果仅导致密码子的插入或缺失突变,而不引起移码突变 反馈 收藏
框内突变框内突变((inframeinframemutationmutation))::33个或是个或是33的的 倍数的倍数的碱基缺失或插入导致的突变碱基缺失或插入导致的突变,,使基因丢使基因丢 失或增加失或增加11个或几个氨基酸个或几个氨基酸。。 DNADNA大片段缺失或复制大片段缺失或复制((largelargedeletiondeletionoror duplication)duplicatio...
基因突变类型框内突变inframemutation 定位候选克隆 GDB或GenBank 已知的基因或EST 与疾病关系 确定致病基因 候选克隆 利用被定位的基因与在同一染色体上另一遗传座位相连锁的特点,将该基因定位在某一染色体或染色体某一区带上。 连锁分析 DNA STR SNP 常见遗传标记 PCR-STR连锁分析 CA CA CA Primer 1 Primer 2 ...
The results were shown in form of a heatmap with colors of cells showing log10(HR) and the frame meaning significance. Integrated analysis of tumor-infiltrating immune cells Pancancer-normalized mRNA expression dataset (n = 11,060) and curated clinical data (n = 12,591) were ...
A downside of PLA is that it requires fixation and has multiple incubation steps, meaning it cannot be used as HTS but would likely be useful in the validation of hits. Unlike PLA, split FP can easily be conducted on a large scale as it has limited sample or data processing, specialised...
(Fig.1a, upper panel). We found that the locusLOC_Os05g38550, encoding an E2 ubiquitin-conjugating enzyme OsUBC12, is localized to this region, and that although only a T/C synonymous mutation without changing the amino acid residue was detected in its ORFs between Koshihikari and IR64 (...
as well as a subset of those sequences that are only sampled from England (arguably more relevant to our sequences from the ONS-CIS). When doing this, we controlled for major lineage, meaning, for example, if a mutation occurred in a BA.1 persistent infection, we only considered the num...
A novel frame shift mutation in the GHRH receptor gene in familial isolated GH deficiency: Early occurrence of anterior pituitary hypoplasia (Journal of Clinical Endocrinology and Metabolism (2011) 96 (2982-2986)) 来自 国家科技图书文献中心 喜欢 0 阅读量: 13 作者:...