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- Conclusion: The reproductive health situation in unmarried non-resident young women was serious, especially on sex violence, RTIs/STIs and higher rate of repeat induced abortion. 結論流動(dòng)人口未婚人工流產(chǎn)女青年存在較嚴重的生殖健康問(wèn)題，應關(guān)注流動(dòng)人口的生殖健康保健。
- No deletion or point mutation in acrAB gene were found in Mar and susceptible clinical Escherichia coli isolates. 多重耐藥株以及敏感株acrAB基因擴增產(chǎn)物無(wú)點(diǎn)突變和缺失。
- The positive rates of HBV site 1896 point mutation are relatively higher in CAH and ALH than that in HCC patients. CAH和 ALH患者檢出率較高 ,而 HCC患者檢出率較低 ,說(shuō)明 HBV突變與HBV在人體持續感染及感染后病情惡化有關(guān) ;
- The style of K-ras gene point mutation at codon 12 was GAT in human pancreatic cancer cell line. 人胰腺癌細胞株P(guān)ANC-1存在K-ras基因的點(diǎn)突變,其突變方式為CAT。
- Detection of keratin 5 gene point mutation in a family with Weber Cockayne EBS by PCR and direct DNA sequencing. PCR-DNA直接測序檢測1例單純型大皰性表皮松解癥Weber-Cockayne亞型(WC-EBS)患者角蛋白K5基因點(diǎn)突變
- No point mutation of FHIT gene exon 5 and exon 8 was found in 30 cases of tumor tissues. 所有胃癌組織標本均未檢測到外顯子5,8的點(diǎn)突變。
- Conclusion:The point mutation in this area of mitochondrial DNA might not be related hereditary ataxia. 結論:遺傳性共濟失調的發(fā)生、發(fā)展可能與該區域點(diǎn)突變無(wú)關(guān)。
- No ABCB4 gene exon 6 and exon 14 deletion and point mutation were detected by PCR and PCR-SSCP, respectively. 對所有外顯子6及外顯子14的PCR產(chǎn)物進(jìn)行SSCP篩查，無(wú)異常發(fā)現。
- Besides, sequence analysis demonstrated a new point mutation of at codon 159 (L159R) in all affected family members. 此外，以基因定序分析研究發(fā)現所有家族病患均有一個(gè)新的點(diǎn)突變L159R。
- He wrote, "we are likely to have been reached before, I have been talking about a point mutation. 他寫(xiě)道，“我們現在很可能已經(jīng)到達了我之前一直在談?wù)摰淖儺慄c(diǎn)。
- Here, we report a three-generation Chinese family with a point mutation in the MITF gene causing WS2. 先證者表現為先天性重度感音神經(jīng)性聾、虹膜異色、面部雀斑;
- Objective To detect the expression and point mutation of PTEN gene in bladder cancer. 目的檢測抑癌基因PTEN在膀胱癌組織中的表達和突變情況。
- K ras gene point mutation at codon 12 was found in human pancreatic carcinoma cell line PC 2, and the mutation style was CGT. 人胰腺癌細胞株P(guān)C 2存在K ras基因點(diǎn)突變 ,突變方式為CGT。
- A point mutation of ATG(Met) to ACG(Thr) at codon 918 in exon 16 of RET protooncogene was detected in this patient,but no such mutation in the parents. 檢測到患者RET原癌基因第 16外顯子 918密碼子存在A(yíng)TG(Met) /ACG(Thr)點(diǎn)突變 ,而在患者父母中未檢測到該突變。
- Objective To screen the point mutation at the codon 54(GGC54GAC) in the first exon of the mannan binding lectin (MBL) gene in Hans from Guangdong. 目的對廣東地區漢族人群的甘露聚糖結合凝集素結構基因第一外顯子第54位密碼點(diǎn)突變(GGC54GAC)進(jìn)行初步篩查。
- The PCR products of suspected cases with the point mutation were further DNA sequenced so as to determine its mutation characters. 對疑有點(diǎn)突變的病例，進(jìn)行DNA序列測定，以明確其具體的突變性質(zhì)。
- In BCR-ABL fusion gene negative myeloproliferative diseases,the discovery of JAK2V617F point mutation is an important landmark. 在BCR-ABL陰性的骨髓增殖性疾病的發(fā)病機制中,JAK2V617F點(diǎn)突變的發(fā)現是一個(gè)重大的突破。
- He made a resolution never to repeat the act. 他決心不再采取那種行動(dòng)。
- A rapid and simple point mutation genotyping method is developed based on polymerase specific extension and duplex inseting dye. 摘要利用聚合酶延伸技術(shù)及雙鏈特異性嵌入染料的特性，建立了一種快速簡(jiǎn)便的基因點(diǎn)東突變的檢測方法。
- Or you can say history repeat itself. 或者說(shuō)也可以說(shuō)，歷史經(jīng)常重演。
