1.
Assess the Genetic Damage and Study Dose-effect Manner by Hprt Gene Mutation and Comet Assay in Cervical Cancer Patients Undergoing Radiotherapy;
HPRT基因位点突变及彗星试验对宫颈癌放疗的损伤评估及剂量-效应关系研究
2.
Cloning the HPRT Gene and POU5F1 Gene of Rabbits Followed by Constructing the Targeting Vectors;
兔HPRT基因和POU5F1基因的克隆及其打靶载体的构建
3.
Comparisons of Induced Mutations at TK and HPRT Loci, Using Two Human Lymphoblastoid Cell Lines, TK6 and TK6-E6, Respectively;
TK6和TK6-E6细胞TK、HPRT基因突变实验比较研究
4.
Preliminary Studies on the HPRT Gene Mutation Mechanism in Lymphocytes from 1, 3-butadiene-exposed Workers;
1，3-丁二烯职业暴露人群HPRT基因分子突变机理的初步研究
5.
Study on HPRT Gene Mutation Induced by Internal Radiation and γ-ray Radiation Using Cloning;
克隆法研究放射性核素内照射和γ射线外照射诱发HPRT基因突变
6.
Study on HPRT Gene Locus Mutation Induced by Radiation Using Brdurd Labeling;
放射性核素内照射和γ射线外照射诱发HPRT基因突变
7.
Comparative Study on Human Peripheral Blood Chromosome Aberration,Micronucleus and HPRT Gene Mutation Induced by Neutron Irradiation
中子辐射诱发人外周血染色体畸变、微核HPRT基因突变的比较研究
8.
a locus with four alleles
具有四个等位基因的位点;具有四个等位基因的位点
9.
Locus (pl.loci) The position of a gene on a chromosome. Alleles of the same gene occupy the equivalent locus on homologous chromosomes.
基因位点，基因座：基因在染色体上的位置。等位基因位于同源染色体相对应的位点上。
10.
The dark-hair genes are epistatic to the red hair locus.
黑发基因对于红发基因位点来说是上位遗传的。
11.
A locus is the 'location'of a gene along a chromosome.
位点是基因在染色体的位置。
12.
Interaction between Two Biallelic Loci;
两个双等位基因位点之间的交互作用
13.
Research on the targeted integration efficiency of gene targeting of multiple sites
多位点基因打靶的定点整合效率研究
14.
The Relationship between CTLA49 Polymophism and Type 2 Diabetes;
CTLA-4基因外显子1的49位点基因多态性与T2DM
15.
Study on RAB27A, the Candidate Gene of Dilute Coat Color in Goat;
山羊毛色稀释位点候选基因RAB27A基因研究
16.
Integration Loci Structure and Genetic Expression of Green Fluorescent Protein (gfp) Gene in Transgenic Barley (Horsdeum Vulgare L.);
转基因大麦的gfp基因遗传表达及整合位点结构
17.
Copy Number and Integration Site of Transgene in Transgenic Pig
转基因猪中外源基因拷贝数和整合位点的研究
18.
Nowadays the pathogenesis of CFEOM has been studied in clinical pathology and molecular genetics fields, and researchers have found that it is a kind of primary neuropathy with secondary myopathic changes and that it has 3 genetic loci and 1 disease gene.
并发现3个遗传位点和1个致病基因。