Only a fraction of breast cancers result from an inherited gene mutation. 乳腺癌只有小部分是遗传自基因突变。
To study the relationships between the expression level of PTEN gene, gene mutation and occurrence and development of glioma. 目的:探讨PTEN基因表达水平及其基因突变与脑胶质瘤的发生及恶性进展的关联性。
Progress on the thyroid hormone receptor gene mutation and its downstream pathways associated with tumor 甲状腺激素受体(TR)基因突变及其下游通路与肿瘤相关研究进展
In2001 Fu and her colleagues discovered a different gene mutation that causes FASPS. 其实早在2001年,傅英惠和她的同事就发现了另外一种能够引起家族性睡眠状态提前综合征的基因突变。
The pathogenesis of pituitary adenomas is considered to be related with gene mutation, growth factors, cell receptors, transcription factors, and cellular signaling pathways. 目前认为垂体腺瘤的发生与基因突变、生长因子、细胞受体、转录因子和细胞信号通路等有关。
Single strand conformation polymorphism ( SSCP) essay and sequence analysis of the PCR product were used to ascertain the gene mutation. 方法应用PCR及单链构象多态性(SSCP)分析技术结合基因序列测定方法确定突变类型。
Objective To explore the disease-associated gene mutation of multiple exostoses by family analysis. 目的:经家系分析探索多发性外生性骨疣的相关基因变异。
The progress of relationship between K-ras gene mutation and pancreatic cancer K-ras基因突变与胰腺癌关系的研究进展
Detection of Gene Mutation Using DNA-gold Nanoparticle Probes and Gene Chips 应用DNA-纳米金探针和基因芯片检测基因突变的研究
Detection of parkin gene mutation in sporadic Parkinson disease 散发性帕金森病Parkin基因突变检测
Gene Mutation Analysis of Duchenne Muscular Dystrophy and Tuberous Sclerosis Complex 杜氏肌营养不良症和结节性硬化症的基因突变分析
The New Assay Exploration and Significance for Detection of EGFR Gene Mutation in Non-small-cell Lung Cancer 表皮生长因子受体基因突变检测新方法探讨及在非小细胞肺癌中的临床病理意义
Gene mutation analysis was performed for patients with BH4 deficiency and their parents. 对BH4缺乏症者及父母进行基因突变检测。
Effects of space flight on glycyrrhizic acid-related gene mutation in Glycyrrhiza uralensis 太空环境对甘草中甘草酸生物合成相关基因的诱变作用分析
Detection and Its Clinical Significance of EGFR Gene Mutation and Gene Amplification in 187 Patients with Non-small Cell Lung Cancer 187例非小细胞肺癌中EGFR基因突变和扩增的检测及其临床意义
F ⅷ Gene Mutation Spectrum in Chinese Hemophilia A Patients 中国血友病A患者基因突变谱的研究
The β_1 subunit expression and gene mutation analysis of voltage-gated sodium channel in spontaneously epileptic rat hippocampus 自发性癫痫大鼠海马电压门控性钠通道β1亚基表达与基因突变分析
The Relativity Study between Clinical and TTR Gene Mutation of Familial Vitreous Amyloidosis 家族性玻璃体淀粉样变性的临床及TTR基因突变的相关性研究
Detection of Beta-Catenin Protein Expression and Gene Mutation in Tumorigenesis of Endometrioid Adenocarcinoma 子宫内膜样腺癌发生过程中β-catenin蛋白异常表达和基因突变的检测
Conclusions PAX9 and MSX1 gene mutation can cause different phenotypes of tooth agenesis. 结论PAX9或MSX1基因突变导致的先天性缺牙表型有明显差异。
Clinical analysis and PACT gene mutation test in microtia patients 先天性小耳畸形临床分析和PACT基因检测
Objective To explore the tk gene mutation spectrum in spontaneous and induced WTK1 mutants. 目的探讨WTK1细胞tk位点自发和诱发突变体的突变谱和突变热点。
The researchers are not yet certain how the gene mutation works to shift people's sleep time. 但科学家们目前尚不能确定这种基因突变是如何改变人们睡眠时间的。
Objective To detect the type of gene mutation of thalassemia in Kunming city. 目的探讨昆明市珠蛋白生成障碍贫血(地贫)的基因突变类型。
In recent years, PCR-SSCP is used in many fields of Entomology: screening gene mutation, identifying insects, studying the diversity of the genes, and constructing the genetic linkage map. 尤其是近年来该技术在昆虫学研究中涉及了:基因突变位点的检测、昆虫分类鉴定、多样性分析及连锁图谱的构建等多个领域。
The frequency of two CETP gene mutation had no significant difference in patients and controls. 心梗、脑卒中患者两种CETP基因突变频率与健康人无差别。
Objective: To study the effects of propolis against gene mutation induced by powerful mutagens in mice. 目的:探讨蜂胶对环磷酰胺等强诱变剂诱发基因突变的抑制作用。