exon的例句大全

Conclusion: Exon 18 might be one of hot points of mutation in chinese WD gene.

结论：exon18是中国人WD基因突变热点之一，大多数WD患者为复合杂合子；

A study of WD gene exon ′ s mutation in Anhui Han ′ s

安徽汉族人肝豆状核变性基因突变的检测与分析

The polymorphism of INSR gene Exon 17 has unconcern with EH whether complicated by renal damage and with renal damage complicated by hypertension as well.

肾实质性高血压患者无论是否并发肾功能衰竭，均未发现INSR基因第17外显子多态性改变。

Two kinds of band type appeared in exon 8. A g/ t polymorphism was found 32 bp from the splice donor site of intron 8 in six tumors.

但外显子8表现出两种不同带型，该基因存在多态性，6例肿瘤在内含子8距拼接部32bp处存在两种不同碱基，基因型为g/t。

PTEN gene mutation test results: 86 cases of soft tissue sarcoma detected two cases of PTEN gene exon 8 mutation ( 2.3%), and the remaining cases the mutation was not detected.

结果：1.PTEN基因突变检测结果：86例软组织肉瘤中检测2例PTEN基因第8外显子的突变（2.3%），其余病例均未检测到突变。

Studies on Exon 8 Mutation of p53 Gene of Rats' Spermary Caused by ZEN by PCR-SSCP

利用PCR-SSCP检测ZEN对大鼠睾丸中p53基因第八外显子突变的研究

In AIDS group, finding some amino acid mutations at specific position of tat exon 1, position 58 T substitutes A. This variation appeared only in AIDS group.

AIDS患者体内病毒tat区第一外显子发生氨基酸突变，58位点出现T取代A，无症状感染者未发现此变异。

Mutations in Exon 7 of the Phenylalanine Hydroxylase ( PAH) Gene in Chinese Patients with Phenylketonuria

苯丙氨酸羟化酶（PAH）基因外显子7及其两侧内含子的突变研究

Objectives: To examine the frequency of exon 15 missense mutation ( D442G) and intron 14 splice defect ( I14A) in cholesteryl ester transfer protein gene in Chinese atherosclerotic subjects.

目的：检测中国人群动脉粥样硬化（AS）患者和正常人的胆固醇酯转运蛋白（CETP）基因15外显子D442G突变和14内含子I14A突变。

Objective To investigate the characteristics of gene mutations of connexin 32 exon 2 in Charcot Marie Tooth disease in Chinese patients.

目的了解中国人进行性腓骨肌萎缩症（Charcot-Marie-Tooth disease，CMT）连接蛋白32（connexin32，Cx32）基因外显子2的突变情况。

A splice mutation were identified in interface of exon 5 and intron 5 ( 1875+ G? A).

通过对ALD基因研究发现一例患者ALD基因外显子5内含子5交界处发生了1875+G→A。

Single Nucleotide Polymorphism Analysis in Chicken Leptin Receptor Exon 9

鸡瘦蛋白受体（OBR）基因外显子9单核苷酸多态性分析

Objective To investigate the association of the 48 bp variable number tandem repeat ( VNTR) polymorphism in the dopamine D4 receptor ( DRD4) gene exon III with schizophrenia in Chinese Han population.

目的在中国汉族人群中寻找散发精神分裂症与多巴胺D4受体（DRD4）基因第3外显子48bp片段可变数串联重复（VNTR）多态性的关系。

The research on the mutation feature of exon 13 of RET gene in Chinese Hirschsprung's disease

中国人先天性巨结肠RET基因突变及Bcl-2的表达

Study of RET Proto-oncogene Exon 13 DNA Polymorphism in Patients with Hirschsprung's Disease in Tianjin District

天津地区先天性巨结肠RET基因13号外显子基因多态性研究

Identification of exon 18 and exon 14 mutation of WD gene with PCR-SSCP

PCR-SSCP技术检测中国人肝豆状核变性基因第18、14外显子突变

Objective To study the characteristic of mutation and polymorphism in exon 4 of tuberous sclerosis complex gene ( TSC1) in Chinese.

目的探讨中国人结节性硬化症（Tuberous Sclerosis Complex，TSC）基因（TSC1）外显子4的基因突变特征及多态现象。

Determination of exon 7 mutation in PAH gene of 16 cases of phenylketonuria

16例苯丙酮尿症PAH基因Exon7突变的检测

Detection of exon 11 mutation in PAH gene of classical phenylketonuria in Inner Mongolia

内蒙古经典型苯丙酮尿症PAH基因外显子11突变的检测

Objective To obtain the mutation spectrum of exon 12 of the phenylalanine hydroxylase ( PAH) gene.

目的了解中国人苯丙酮尿症（phenylketonuria，PKU）患者的苯丙氨酸羟化酶（Phenylalanine hydroxylase，PAH）基因第12外显子点突变种类和频率。