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Of or relating to or resulting from mutation .

属于或关于突变的,或由突变产生的。

Objective To compare the effectiveness of heteroduplex, SSCP and heteroduplexSSCP analyses in mutational screening.

目的比较异源双链、单链构像多态、异源双链SSCP法筛查突变的效率,寻找简便有效的基因突变筛查方法。

The pathogenicity of the mutations was confirmed by expression studies.

突变表达研究证实了这些突变的致病性。

Results The Val383Ile mutation was found in the heterozygous state in two diabetic subjects and none in control subjects.

结果 病例组中发现2例为GLUT4基因Val383Ile突变的杂合携带者,对照组中未发现GLUT4基因Val383Ile突变。

Objective To study RB1 heterozygous mutations in patients with retinoblastoma.

目的 检测视网膜母细胞瘤病人体细胞中RB1基因突变,探讨RB1基因突变的分子生物学机制。

Overexpression of MDR1, GST-π, p53 mRNA and their corresponding proteins in epithelial ovarian cancer participated in the formation of multidrug resistance in ovarian cancer and P53 may play a indirected role through regulating the expression of MDR1、GST-π.

卵巢癌化疗耐药与耐药基因GST-π、MDR1过表达及细胞凋亡相关基因P53突变密切相关,突变的P53可能通过调控耐药基因GST-π、MDR1而间接发挥其耐药作用。

Coli Min27 strain with mitomycin C. Twenty-one E. coli strains with various serotypes were infected with FMin27, and plaque formation and lysogenic conversion of them were investigated.

用丝裂霉素对该突变菌株进行诱导,结合抗性标记和PCR方法筛选出一株突变的志贺毒素2型噬菌体,命名为FMin27。

The otological, audiological and neurological examinations of these patients were conducted, including otoscopy, pure-tone (Madsen 522) and immittance(GSI 33) audiometry. MtDNA A1555G mutation and GJB2 235delC mutation were detected with specific restriction enzyme digestion methods.

对 148 名非综合征型感音神经性耳聋患者分别进行线粒体 DNA 12SrRNA基因A1555G 点突变和 GJB2 基因235delC突变的限制性内切酶分析。

Some patients took beta blockers and some didn't.

这其中包括了突变和未突变的患者

Mutations in the BRCA1 and BRCA2 genes are known to lead to breast and oarian cancer. Howeer, the frequency of these mutations in the general population has not been well-characterized.

熟知BRCA1和BRCA2基因突变可引起乳癌和卵巢癌,不过在普通人群中突变的频率还没有很好地描述。

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The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

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这种做法不仅鼓励了更多的反应,而且减少跟风的可能性。

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