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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...

    m.wenda.so.com/q/1662428691214840

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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...

    cn.bing.com/dict/splicingmutation

  • 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...

    www.dict.cn/splicing mutation

  • 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

  • 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 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

    ORIGINALPAPERSplicingmutationinMVKisacauseofporokeratosisofMibelliKangZeng•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...

    www.do纪欢换我结好还片血c88.com/p-1136636267557.html

  • 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 mut还诉ation in FUS. (a) Agaro el electrophoresis of FUS cDNA amplified in one unrelated control, and two affected family members II:5, III:8), showing the wild-type allel..

    www.natu场迅社re.com/artic期跑讲台鲁易四留点换突les/jhg2...

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