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- zero point mutation 起点突变,零点突变
- Say zero point two five per cent above your base rate. 就比基本利率高零点二五个百分点吧。
- Zero point eight one two five per cent for one year. 年利率是0.;8125%25。
- To measure the overall IG unit thickness, align the zero point. 要量测全面的复层玻璃厚度;请校准好零点.
- To use this, simply align the zero point as described previously. 使用此仪器;就像之前叙述的一样简易地校准零点.
- The zero point is the Vernal Equinox, also called the point of Aries. 零点是春分点，也叫做白羊座点。
- You can, however, set the grid origin independently from the ruler zero point. 不过,您可以将网格起点设置为独立于标尺的零点。
- Remedy: Check zero point correction of the star and re-adjust if necessary. 检查零点位置是否正确,并且需要时,加以调整。
- No deletion or point mutation in acrAB gene were found in Mar and susceptible clinical Escherichia coli isolates. 多重耐药株以及敏感株acrAB基因扩增产物无点突变和缺失。
- Ground Zero is Zero Point consciousness. The program ends in a New York Minute! 地面零点就是零点意识。在纽约的计划终端显现出来！
- The positive rates of HBV site 1896 point mutation are relatively higher in CAH and ALH than that in HCC patients. CAH和 ALH患者检出率较高 ,而 HCC患者检出率较低 ,说明 HBV突变与HBV在人体持续感染及感染后病情恶化有关 ;
- Delve into the ways to determine the zero point of the continuous function. 探究在某区间上图象连续的函数存在零点的判定方法.
- The style of K-ras gene point mutation at codon 12 was GAT in human pancreatic cancer cell line. 人胰腺癌细胞株PANC-1存在K-ras基因的点突变,其突变方式为CAT。
- The coercivity of soft magnetic materials is generally near to zero point. 软磁材料的矫顽力一般分布于零点附近。
- Detection of keratin 5 gene point mutation in a family with Weber Cockayne EBS by PCR and direct DNA sequencing. PCR-DNA直接测序检测1例单纯型大疱性表皮松解症Weber-Cockayne亚型(WC-EBS)患者角蛋白K5基因点突变
- No point mutation of FHIT gene exon 5 and exon 8 was found in 30 cases of tumor tissues. 所有胃癌组织标本均未检测到外显子5,8的点突变。
- Conclusion:The point mutation in this area of mitochondrial DNA might not be related hereditary ataxia. 结论:遗传性共济失调的发生、发展可能与该区域点突变无关。
- A score of zero points in a game or zero games in a set. 在一局或一盘比赛中得零分。
- No ABCB4 gene exon 6 and exon 14 deletion and point mutation were detected by PCR and PCR-SSCP, respectively. 对所有外显子6及外显子14的PCR产物进行SSCP筛查，无异常发现。
- Besides, sequence analysis demonstrated a new point mutation of at codon 159 (L159R) in all affected family members. 此外，以基因定序分析研究发现所有家族病患均有一个新的点突变L159R。
