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- We carried out a genomewide association analysis to identify additional genetic loci associated with an increased risk of rheumatoid arthritis. 我们采用染色体组关联分析确定附加遗传基因座与类风湿关节炎的风险增高有关。
- The genetic loci of unc-10, syd-2, hlb-1, dlk-1, mkk-4, scd-2, snb-1, ric-4, nrx-1, unc-13 , sbt-1 and unc-64 might be involved in the aging control. 遗传位点 unc-10,syd-2,hlb-1,dlk-1,mkk-4,scd-2,snb-1,ric-4,nrx-1,unc-13,sbt-1,unc-64 可能参与线虫衰老的调控。
- The identification and manipulation of genetic loci determining quantitative traits (quantitative trait loci (QTLs)) is important in plant and animal breeding. 在动植物繁育过程中，对人类具有重要的经济价值。
- Conclusions We identified seeral genetic loci that, indiidually and in aggregate, substantially affect the risk of deelopment of coronary artery disease. 结论：我们鉴定出几个基因座，这些基因座无论从独立的或是联合的角度，确实均能影响冠心病发病风险。
- Objective To study the relationship between the loss of heterozygosity (LOH) at APC and MCC genetic loci and the incidence and development of esophageal carcinoma. 目的研究APC/MCC基因杂合性缺失(LOH)与食管癌发生发展的关系。
- Methods: Polymorphic analysis of the genetic loci of YNZ22 and DCC containing a variable number of tandem repeat was performed in 46 surgically resected specimens of esophageal carcinoma with PCR. 方法：应用聚合酶链反应技术对46例食管癌YNZ22位点和DCC基因数目可变的串联重复序列（VNTR）区进行了分析。
- Methods LOH at APC and MCC genetic loci in 46 specimens resected from esophageal neoplasm was studied with polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP). 方法应用多聚酶链反应技术及限制性片段长度多态现象对46例食管癌APC和MCC基因的LOH进行了分析。
- In the meio-gynogenetic-2 group, not only the examined genetic loci of each individual were homozygous but also the genotypes of all the analyzed individuals of the group were the same. 连续两代人工诱导雌核发育草鱼群体中不仅所检测个体的基因位点已完全纯合，并且各个体的基因型也完全相同。
- Although all the examined genetic loci in the analyzed individuals were in homozygous state, the genotypes of different individuals of the group were not identical in the meio-gynogenetic-1 group. 连续两代人工诱导雌核发育草鱼群体中不仅所检测个体的基因位点已完全纯合，并且各个体的基因型也完全相同。
- 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。
- It is concluded that LOH at MCC,DCC and YNZ22 loci may be involved in carcinogenesis of gastric cancer and LOH at DCC genetic locus may be related to prognosis of patients with gastric cancer. 结果提示，MCC、DCC基因和YNZ22位点LOH参与了胃癌的发生与发展，DCC基因LOH可能与预后相关。
- The centromere is a specific genetic locus and remains relatively uncoiled during prophase, appearing as a primary constriction. 着丝粒是一个特化的遗传区域，在细胞分裂的早期始终保持解开的结构，所以也叫做主缢痕。
- Using high-density genomewide single nucleotide polymorphism (SNP) genotyping arrays, they identified a genetic locus associated with the disease. 他们使用高密度基因组单核苷酸多态性(SNP)基因序列方法，辨识与此病症有关的基因位置；
- Objective To approach the application of STR genetic locus detection in allogeneic hematopoietic stem cell transplantation. 目的探讨短串联重复序列(STR)基因位点检查在异基因造血干细胞移植中的应用。
- One further challenge will be to determine whether and how opposing activities within a protein complex on a given genetic locus are regulated. 还有一个需要解决的问题是：蛋白复合体对已知的基因座是否发挥反作用，以及如何发挥作用。
- Screening for genetic loci affecting the active zone formation in C. Elegans 线虫中影响活动区形成遗传位点的遗传筛选
- Loss of heterozygosity at APC and MCC genetic loci in esophageal carcinoma 食管癌APC/MCC基因杂合缺失的研究
- Genetic material produced by gene-splicing. 重组基因材料基因分割而产生的基因材料
- Loss of heterozygosity on the genetic loci of the short arm of chromosome 1 in sporadic colorectal carcinoma 散发性结直肠癌1号染色体短臂遗传位点杂合缺失
- Mapping genetic Loci that determine leukocyte telomere length in a large sample of unselected female sibling pairs 对未选择的女性双卵双胞胎大样本的遗传基因位点作图决定白细胞端粒的长度
