Conclusion GSTM1 gene deletion is not related to senile cataract formation.
结论GSTM 1基因缺失与老年性白内障的发生缺乏显著关系。
It is also improved M and NS genes by a site mutation and a gene deletion method.
通过点变异和基因删除方法对M和NS基因进行改进；
The PMP22 gene deletion detected by gene diagnosis is the golden criterion for the diagnosis of HNPP.
结论电生理检查对HNPP的诊断很重要，基因检测发现PMP22基因缺失是诊断HNPP的金标准。
Conclusion There is no difference in frequency of CYP2A6 gene deletion between lung cancer cases and controls.
结论CYP2A6突变基因在肺癌组及对照组中的频率分布没有差异。
Dual FISH technique provides specific, sensitive and direct evidence for molecular cytogenetic evaluation of gene deletion in tumors.
双色FISH技术为评估基因的缺失提供了特异、敏感、直观的分子细胞遗传学证据。
In the present study, we investigated whether gene deletion of AT2 receptor causes the compensatory chaos of renin-angiotensin system in mice.
依据上述论点，本研究利用AT2受体基因敲出小鼠，观察了AT2受体缺失后是否造成肾素-血管紧张素系统其它成分代偿性紊乱。
In all of the 24 bases of mutants, the base replacement occupies about 87.5% of the total mutants with only a small portion of gene deletion (12.5%).
在检测到的24个碱基突变中，主要是碱基的置换(87.5%)，碱基缺失的比例比较小(12.5%)。
they observed no instances in the subjects with bipolar illness of the chromosome 22 gene deletion implicated in schizophrenia and the velocardiofacial syndrome.
他们并未观察到22号染色体缺失的躁郁患者实例。这条染色体牵涉到精神分裂症、腭心面综合征。
Objective To investigate the relationship between the angiotensin converting enzyme (ACE) gene deletion polymorphism and cerebral infarction, hypertensive cerebral hemorrhage in Chinese.
目的探讨血管紧张素转化酶(ace)基因缺失多态性与中国人脑梗死、高血压性脑出血的关系。
The main methods used, or under investigation, for production of rumen gene engineering bacteria are:gene deletion technique, gene recombination technique and the application of promotor.
正在应用的或处于研究阶段的构建瘤胃基因工程菌的方式主要有基因缺失技术、基因复制性重组技术和启动子的应用技术。
This can occur through a mutation in the gene's DNA sequence or through deletion of the gene.
这种缺失可能起源于基因的突变或者通过基因序列的缺失而产生。
Objective: to detect allelic deletion and mutation of FHIT gene in gastric cancer, and to analyze the role of the abnormalities in the carcinogenesis of gastric cancer.
目的：检测脆性组氨酸三联体基因在胃癌组织中等位基因缺失和突变情况，分析该异常在胃癌发生中的作用。
The deletion mutation and missense mutation of COL7A1 gene result in the specific mutation in patients with clinical symptoms.
结论COL7A1基因的缺失突变和错义突变引起该患者临床症状的特异突变。
Microdeletion — a chromosomal deletion that is too small to be seen under the microscope. See also contiguous gene syndrome.
无法用显微镜观察到的较小的染色体缺失。参见邻接基因综合征。
TK gene represent philic-nerves and its deletion enhances the ability of anti-latent infection.
TK基因对病毒嗜神经性，缺失后有抗潜伏感染的特性。
Conclusion Inherited afibrinogenemia is caused by the compound heterozygous deletion in the fibrinogen FGA gene.
结论纤维蛋白原FGA基因复合杂合缺失是引起该家系先证者无纤维蛋白原血症的原因。
AIM: to construct the recombinant plasmids expressing full-length HCV core protein gene and 3 different deletion mutated hepatitis core protein genes and to express them in E. coli.
目的：构建丙型肝炎病毒(HCV)全长及3种不同缺失突变的核心蛋白基因的原核表达载体，并在大肠杆菌中表达。
OsLBD gene families are characterized by subclasses parallel evolution and deletion of duplicated genes from Arabidopsis.
自拟南芥以来，水稻LBD基因家族的进化经历了亚家族平行进化和重复基因的缺失这个过程。
This variability means that a small deletion on the CCR5 gene.
这种变异是指CCR5基因上一小段缺失。
Conclusions No functional FANCA protein was found in these 3 cases of FA-A, and intragenic deletion, frame shift and splice site mutation were the major pathogenic mutations found in FANCA gene.
结论3例FA-A型患者均无功能性FANCA蛋白表达；基因缺失、移码突变和剪切位点突变是FANCA基因的主要失活方式。
A girl with a deletion of SHANK 3 in the third family suffered from autism while her brother, who had an additional copy of the gene, had a mild form of autism called Asperger syndrome.
在第三个家庭中，一个患自闭症的女孩缺失了SHANK3基因，而她的兄弟却因多了一个被复制的基因而患上了被称为阿斯佩各综合征的轻度自闭症。
Conclusions: Deletion polymorphism of the ACE gene is associated with UA p, indicating that it might be one of important risk factors for UAP.
结论：ace基因的缺失多态性与UAP发生相关，表明其可能是UAP发病的重要危险因素之一。
FAP is a monogenetic disease and is caused by the mutation or deletion of the adenomatous polyposis coli (APC) gene which is found on chromosome 5.
FAP是一种单基因遗传病，是由APC基因的突变或缺失引起的(apc)基因是5号染色体上发现的。
CONCLUSIONS: the deletion of ATM gene may play a role in the development of ovarian cancer. ATM gene may be identified as a potential target in gene therapy.
结论：atm基因缺失可能与卵巢癌的发生机制有关，有可能成为卵巢癌治疗新的分子靶点。
Conclusion FHIT gene expressing deletion was common in lung squamous carcinoma and was apparent correlative with smoking.
结论FHIT表达缺失是肺鳞癌的常见事件，而且与吸烟明显相关。
CONCLUSION: the high amplification of Cyclin D1 and the high deletion of P16 gene is closely related to the high activity of proliferation of lung cancer.
结论：细胞周期素d1的扩增和P 16的缺失与肺癌细胞的高增殖活性密切相关。
The gene overlapping(ATGA) is widespread in streptomycetes, making it difficult to perform in-frame deletion or replacement for functional analysis of target genes.
链霉菌基因组中常见连续两个基因重叠的现象（如ATGA），这为基因的同框敲除或取代研究带来很大困扰。
The gene overlapping(ATGA) is widespread in streptomycetes, making it difficult to perform in-frame deletion or replacement for functional analysis of target genes.
链霉菌基因组中常见连续两个基因重叠的现象（如ATGA），这为基因的同框敲除或取代研究带来很大困扰。
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