splice donor site基本解释 剪接供体位点;供体位点;拼接供体位点 分词解释 splice绞接 donor捐赠者,[医]供血者,输血者 site地点,位置,场所猜你喜欢 delivery site交货地点:指商家或物流公司将货物送达的地点。 similar sites类似网站:指与某个特定网站在内容、功能、设计等方面相似或相同的其他网站。 active site...
网络剪接提供讯号;拼接供体位点;剪接供体位点 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 splice-site mutation in CUL4B is likely cause of X-linked intellectual disability. Am J Med Genet A 2014; 164A: 2294-2299.Londin, E. R. , Adijanto, J. , Philp, N. , Novelli, A. , Vitale, E. , Perria, C. , Serra, G. , Alesi, V. , Surrey, S. & Fortina, P....
必应词典为您提供donor-splice-site的释义,网络释义: 供者剪切位点;供体位点;
BRCA2 Splice Donor Site Mutation (c.1909+2T>C) Reference Standard询价 产品描述 产品数据库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 ...
To characterize the effect on mRNA splicing of a yet undescribed mutation located in intron 13 splice-donor sequence (IVS13 + 3A --> C) in the Rab-Escort-protein 1 gene of a patient with choroideremia.The base substitution was firstly detected by the Single Strand conformation analysis from ...
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...
名称AI-Edigene® MET Splice Donor Site Mutation (c 型号CBP10492 报价 特点AI-Edigene MET Splice Donor Site Mutation (c.3082+1G>T) Reference Standard Plus 详细内容 CBP10492 FormatGenomic DNA DescriptionN/A Technical Data DNA Changec.3082+1G>T ...
We describe the characterization of an alpha+-thalassaemia determinant as a result of a transition of G-->A of the donor splice consensus site sequence of the first intron of the alpha1-globin gene (alpha1IVS I-1). The mutation was found in combination with the South-East Asian alpha0-...
Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin gene. N. (2009). Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin gene...