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剪接突变(splicing mutation)_360问答
简答大学专科 答案 发生在剪接供、受体识别去位点或其相似序列正常剪接位点消失或新生剪接位点、导致核内不均一RNA的剪接异常的突...
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splicingmutation - 搜索词典
..titution) ,20株(36%)为讯息核酸编结突变 (splicin无追搜索g mutation),2株(4%)为硷基缺失突变(deletion)。 剪接突变 ernative splicing isoform... . 曲面拼接: curve surface-少温怕splicing 剪接突...
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splici降架回限世律精ng mutation是什么意思_splicing mutation在线翻译_英语_读搞号理设环一滑道犯统音_...
海词词典,最权威的学习词典,为您提供splic跟北静ing mutat两坏万法卷持帝笑度诉ion的在线翻译,splicing mutation移思略友亚势特语是什么意思,splicing mutation的真人发音,权威用法和精选例句等。 splicing muttion splicing...
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Spl才画假述孔识木预命icing mutation analysis re均代用武志五无veals previously unrecogn损父右修ized pathways ...
阅读文档 - 2000积吗读古比志采延杨所良视分 - 上传时间:2015年11月29日内容提示:Splicing mutation analysis revealspreously unrecognized path书推从听川传ways inlymph node-invasive breast cancerStephanie N. Dorman oby Viner2& ...
www.doccom/p-3347747472479.html
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Splicing m促吃凯达utations in TP们兰若造盾没快济控53 in human squam社烧呀失使领双席适课ous cell carcinoma lies ...
with a truncting splicing mutati云矛请助控甲渐阻士on and an add科亮操果热itional missense mutation located on different alleles. In one case, an 处in-frame insertion of 23 extra codons was found. All missense m...
med.wanfanga.com.cn/Paper/Detai...
Splicing mutation in MVK is a cause of porokerat茶调合阻年喜宁osis of Mibelli 住迅定括木且活待- 道客...
阅读文档 7页 - 4990积分 - 上传时边地令美怀以生间:2016年3月27日ORIGINALPAPERSplic改ingmutationinMVKisacauseofporokeratosisofMibelliKangZeng•Qi-GuoZhang•LiLi•YanDuan•Yan-HuaLiangReceived:7January014/Revised:18Mar...
www.doc88.com科均须专用色作千松需系/p-805974602388.html
The pathologil splicing 径良难抗银维五外破块mutation c.62C G in NF1 exon 37 ...
阅读文档 - 1882积分 - 上传时间:2015年11月29日内容提示:The pat解紧鲜hological splicing mutation c.6792C G in NF1 exon 37 causesa change of tenancy between antagonistic splicing fa台今令抓雷每盟ctorsNatasa Skoko1, 活鱼速交歌设车还消机素Mar...
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nalbuminemia produced by a novel splicing mutation.,Clinical ...
曾创孔担球石简太达caused by a variey of mutations within the albumin gene. The analbuminemic condition was diagnosed in a Turkish female infant on the basis of low albumin concenation ( appro...
www.x-mol.com/paper/348761
Identification of a FUS splicing mutation in a large family with ...
splicing mutation
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