1、

The test would evaluate DNA from esophageal-tissue biopsies, but significantly fewer tissue samples would need to be collected as compared to current endoscopic-surveillance methods.

试验将对食管活检组织的DNA进行评价。但值得注意的是组织样本少,需要通过目前的内窥镜检查监视方法比照收集。

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2、

A Comparison of DNA Ploidy in Stage Al and Stage D1 Prostatic Carcinoma

前列腺癌A1期和D1期DNA倍体的比较

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3、

Study on aberrant DNA methylation of dopamine D4 receptor gene in acute myeloid leukemia

白血病细胞多巴胺受体基因甲基化研究

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4、

RT-PCR for Diagnosis of Rubella and Analysis on E1 Region DNA Sequencing

RT-PCR诊断风疹及E1膜蛋白基因序列分析

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5、

Size of foreign DNA and deleted fragment of E3 is the key factor to construct recombinant adenovirus.

插入E3区外源DNA大小与E3区缺失大小是能否获得重组病毒的关键因素。

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6、

The sub G1 peak was found in DNA histogram by FCM.

DNA直方图出现亚G1峰。

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7、

The results indicated that the interaction between 1,4-DHP derivatives and CT-DNA was in the intercalative mode.

1, 4-DHP 衍生物4-取代基空间位阻越小,嵌入到CT -DNA 的程度越大.

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8、

Detection of DNA site damage in k-ras gene induced by BaP

苯并[a]芘致人k-ras基因DNA损伤位点检测

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9、

Methods Treated with different TAH concentrations for different times, HeLa cells were tested by flow cytometry, DNA agarose electrophoresis, light microscopy and transmissional electron microscopy.

方法将TAH以不同剂量和作用时间处理体外培养的人宫颈癌HeLa细胞,用流式细胞仪、电子显微镜、DNA琼脂糖电泳检测TAH诱发HeLa细胞凋亡情况。

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10、

The results showed that DNA fingerprinting map of the strains of S. warneri isolated from the nasal cavity of infected infants was identical to that from the medical staff.

结果:患儿与医务人员鼻腔的华纳葡萄球菌菌株的DNA指纹图谱完全一致。

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11、

Methods Growth curve, DNA content and change in cell cycle were determinated by Cytometry and FCM.

方法用细胞计数法和流式细胞仪(FCM) 测定细胞生长曲线 、 DNA含量及细胞周期的变化.

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12、

The results show that the distribution of DSB fragments is non-random, but concerned with DNA sequence.

结果发现DSB片段 是非 随机分布的, 而且这种分布与DNA序列有关.

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13、

Cells were harvested at 3,10 or 14 days with measurement of DNA , protein and DPM.

细胞收获点分别为3 、 10、14天.

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14、

Methods: We investigated chromosomal DNA copy number changes in 3 ESCC cell lines by comparative genomic hybridization ( CGH ).

方法: 采用比较基因组杂交法 ( CGH ) 分析3种ESCC细胞系的染色体DNA拷贝数改变情况.

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15、

The Nucleic Acid Analysis by DNA Chip Technique Based on Nuclease S1 Protection

基于核酸保护原理的DNA芯片检测技术

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16、

Analysis on the results of pre S1 antigen, HBV DNA detection

乙肝前S1抗原、E抗原及HBV-DNA检测结果分析

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17、

The result of DNA sequence analysis suggests that the Guangdong DEN2 local strains isolated in1998 were similar to those from Thailand.

基因序列分析提示:1998年广东省南海市分离的登革病毒2型可能来源于泰国。

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18、

The other is the signal amplification, including Branched DNA ( bDNA) and Invader et al.

另一类是信号放大扩增,如支链DNA、侵染探针等。

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19、

Conclusions PNA can be delivered into tumor cells in form of PNA-DNA hybrids by cationic liposome. Properly designed antisense PNA can inhibit MDR related P-gp expression of SK-N-SH cells efficien-tly and specifically.

结论PNA-DNA杂交阳离子脂质体转染法可有效增加细胞对PNA的摄取,特异序列的反义PNA可在一定程度上阻断神经母细胞瘤MDR相关蛋白P-gp的表达。

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20、

Primer synthesis and DNA sequencing were completed by Takara.

引物合成和DNA序列测定由Takara公司完成。

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