1) acceptor splice site 剪接受点2) splice acceptor 剪接受体3) splice site 剪接位点 1. Identification of splice sites based on feature mining and integration; 基于特征挖掘与融合的剪接位点识别 2. Splice Site Identification Based on Hidden Markov Support Vector Machines; 基于HM-SVM的剪接位点...
网络受体位点 网络释义 1. 受体位点 ...r splice site): GT 内含子3’端受体位点(acceptor splice site): AG 预测工具: GENSCAN,GENEMARK NetGene2, Splice Vie… wenku.baidu.com|基于4个网页
网络一致拼接受体 网络释义 1. 一致拼接受体 什么意思... ... splice-acceptor site 剪接受体位点consensus splice acceptor一致拼接受体Splice acceptor sites 体位点 ... dict.youdao.com|基于 1 个网页
This disease-causing mutation is a single base-pair change (G to A) in the splice-acceptor region of APC intron 3 that creates a mutant RNA without exon 4 of APC. The observation of the same APC mutation in five families from the same geographic area demonstrates a founder effect. ...
Congenital tooth agenesis is caused by mutations in the MSX1, PAX9, WNT10A, or AXIN2 genes. Here, we report a Japanese family with nonsyndromic tooth agenesis caused by a novel nucleotide substitution in the intronic region between exons 1 and 2 of the MSX1 gene. Because the mutation is ...
A splice acceptor site mutation inTaGW2-A1increases thousand grain weight in tetraploid and hexaploid wheat through wider and longer grains 2016. A splice acceptor site mutation in TaGW2-A1 increases thousand grain weight in tetraploid and hexaploid wheat through wider and longer grains. TAG... J...
OPEN Citation: Transl Psychiatry (2015) 5, e651; doi:10.1038/tp.2015.149 www.nature.com/tp ORIGINAL ARTICLE Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence DB Hancock1, GW Reginsson2, NC Gaddis3, X Chen4,5, NL Saccone6, ...
The normal 3′-splice acceptor site of intron 1 in one of the two chromosomes is abolished by the G→C substitution in position −1. Acknowledgements We thank the EPM1 patients and their families for their participation in these studies, the General Clinical Research Center of the University...
AnewVCAN/versicanspliceacceptorsitemutationinaFrenchWagnerfamilyassociatedwithvascularandinflammatoryocularfeaturesAntoineP.Brézin,1BrigitteNedelec,2AmandineBarjol,1Pierre-RaphaelRothschild,2MarcDelpech,2,3SophieValleix2,31UniversitéParis-Descartes,CentreCochinAmbulatoired’Ophtalmologie,AssistancePubliqueHôpitauxde...