...都是使用一对隐藏在第四个外显子(exon 4)内的剪接提供(splice donor)与接受(acceptor)序列来移除一段378-bp的插入子(intron…etdncku.lib.ncku.edu.tw|基于2个网页 2. 剪接供体 分子生物学与生物工程词汇对... ... spliced leader 剪接前导序列[见于反式剪接] splice donor 剪接供体 splice junction ...
网络释义 1. 剪接提供讯号 ...的原因是染色体DNA上一个G→T的点突变,产生一个剪接提供讯号(splice donor site),使得位在突变点前的序列被接入了… 210.60.224.4|基于3个网页 2. 拼接供体位点 site-英汉词典-英中字典... ... specific site [医]特异位点splice donor site[医]拼接供体位点splice site [医...
1) Splice donor sites prediction 剪接供体位点识别 2) 5 splice sites identification 5'剪接位点识别 3) recognition of splice site 剪接位点识别 例句>> 4) Recognition of splicing site 剪切位点识别 5) ribosome recognition site 核糖体识别位点
11、layersplice顺层连接,层编接 12、splicepad 拼合衬垫 13、splicesite 剪接位点 14、pilesplice堆拼接 15、splicebolt 拼接螺栓 16、splicejunction 剪接点 17、splicedonor 剪接供体 18、splicevariant 剪接变体 19、splicebar 鱼尾板;鱼尾板型钢;制造连接板用的异形钢材;拼接板...
自问自答！很有可能是个致病突变。因为剪接位点移动一个或两个碱基，实际相当于移码突变了，这种剪接...
PTEN Splice Donor Site Mutation (c.165-2A>C) Reference StandardEnquiry Product Description Product databaseCBP10718 Gene PTEN Description PTEN, phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN, is a tumor suppressor with roles in the cell cycle, ...
A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndrome. J Med Genet. 2014; 51 :185–196.Esmailpour T, Riazifar H, Liu L, et al. A splice donor mutation in NAA10 results in the dysregulation of the ...
匿名女性捐献者 没有医疗和遗传病史 跟以前一样 Anonymous female donor. Clean medical and heredity. The usual. 没什么特别的 A dime a dozen. 比例单位是一比一百万 One in a million. 等离子体再结合 人类-动物杂交混合 36545 号♥ 失败 -没有成功 -你用的什么酶 - It's not working. - ...
The mutation c.9690 + 1G> A was a splicing-site mutation resulting in a G to A transition at the donor splice site of intron 59. Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
特点 BRCA2 Splice Donor Site Mutation (c.1909+2T>C) Reference Standard 详细内容 CBP10466 Format Genomic DNA Description N/A Technical Data DNA Change: BRCA2 c.1909+2T>C AA Change N/A Mutation type Substitution - Missense Zygosity Heterozygous Allelic Frequency 50% Type Splice_Site Tran...