全部

1·No pathogenic mutation was detected in the exon and franking regions of MYH9 gene except a synonymous mutation.

除同义突变外，在 MYH9 基因的外显子和弗兰克区域未检测到致病突变。

2·Results the DHPLC find the exon 7, 9 polymorphism.

结果：变性高效液相色谱检测出7、9号外显子多态性。

3·The effect of skipping just one exon can be dramatic for an organism.

仅仅略过一段表现子，就可能对生物体造成显著的影响。

4·The codon 778 of exon 8 in WD gene was one of mutation hotspots in Chinese.

结论WD基因第8外显子778位密码子系中国人的突变热点之一。

5·Conclusion JAK2 exon 12 mutations could exist in JAK2V617F-negative PV patients.

结论JAK2V 617 F点突变阴性的PV患者中存在JAK2外显子12突变。

6·Association studies revealed no association betweenG352A in exon 15 of DAT1 and ADHD.

家系和病例对照研究表明，DAT1第15外显子G352A 基因和ADHD 之间不存在关联。

7·Exon 11 mutation is closely related to the biological behavior, prognosis, drug treatment of GIST.

外显子11突变与GIST的生物学行为、预后以及药物治疗效果密切相关。

8·Conclusion Mutation of Exon a in ar gene plays an important part in infertile men with oligospermia.

结论雄性激素受体基因外显子A即基因转录激活区的突变是造成少精不育的重要原因。

9·Objective: To detect the mutation in exon 15 of cholesteryl ester transfer protein gene and its properties.

目的：检测胆固醇酯转移蛋白第15外显子基因突变及其性质。

10·Conclusion: No correlation was found between glucocorticoid receptor gene in exon 2/1 codons 23 and asthma.

结论：江西籍汉族人种中糖皮质激素受体基因外显子2/1密码子23基因未发现多态性的存在。

外显子

1·Median survival time for patients with an EGFR exon 19 deletion in serum was also substantially higher than in those with L858R mutations (32 months vs 14 months).

血浆中egfr外显子19删除患者的中位生存期要明显好于那些存在L 858r变异患者(32个月相对14个月)。

2·AIM: to observe the correlation of the 17 exon gene polymorphism of insulin receptor gene and the Chinese cerebral infarction and primary hypertension.

目的：观察胰岛素受体基因第17外显子基因多态性与中国人脑梗死和原发性高血压的相关性。

3·Objective: To detect the mutation in exon 15 of cholesteryl ester transfer protein gene and its properties.

目的：检测胆固醇酯转移蛋白第15外显子基因突变及其性质。

4·These gene mutation distributing in all over the whole coding section of ATM gene. Every Exon exist the gene mutated site and no obvious hot mutated site be discovered.

这些突变分布于atm基因整个编码区，每个外显子都存在基因变异位点，没有发现明显的突变热点。

5·AIM: To establish the mutant of coding calcium binding fragment of the 13th exon of human thrombospondin-1 (TSP-1) gene with polymerase chain reaction (PCR) site directed mutagenesis technology.

目的：利用聚合酶链反应定点突变技术构建人血小板反应素1基因第13外显子编码钙结合域突变体。