突变的

MoRGF1 was highly identical in amino acids with its homologs from other filamentous ascomycete fungi. The gene eletion mutants displayed slower growth and obviously reduced conidiation, although with no change in pathogenicity when compared with their wild type strain.

结果表明Mgg_11178.6编码一个假定的Rho族小G蛋白鸟苷酸交换因子(MoRGF1)，与多种丝状子囊菌RhoGEF亲缘关系密切；基因敲除突变体表现为生长速度减慢，产孢量明显减少，但是致病力没有变化。

The internal cause includes polarity variation , inbred variation , instability of hybridization and gene mutation . The external cause includes unfitting culture conditions , strain ag ing , unsuitable preservation and infection virus of asexuality propagation .

内因主要包括极性发生变异，自交产生的变异，杂交种性不稳定和基因突变；外因主要包括培养条件不适宜，菌种老化，菌种保藏不当和菌株无性繁殖体感染病毒。

For example, plants can sometimes transmit somatic mutations to their descendants asexually or sexually where flower buds develop in somatically mutated parts of plants.

例如，植物有时将体细胞突变通过无性或有性过程传递给后代，而花芽可能由植物的体细胞变异部分发育。

So they looked for the mutations in their study group of Ashkenazi, or Eastern European, Jews.

因此，他们期待为突变在其研究组的德系，或东欧，犹太人。

This genetic mutation occurs most often in Jewish women of Ashkenazi descent .

这个基因突变最常发生于犹太妇女的德系血统。

A BRCA1 or BRCA2 mutation was identified in 131 of the 1,102 women who were of Ashkenazi Jewish ancestry.

北欧犹太教家系的1102名女性患者中131名检测出BRCA1 或 BRCA2基因突变。

Objective: To discuss the molecular mechanism of hereditary cerebellar ataxia in waddles mouse.

目的：探查引起Waddles小鼠遗传性小脑性共济失调的突变基因。

Objective To study the gene mutation of the spinocerebellar ataxia（SCA types 1～3 in the patients with primary dystonia.

目的 研究原发性肌张力障碍患者脊髓小脑性共济失调1～3型基因的突变。

A disease caused by the presence of two recessive mutant genes on an autosome.

由于常染色体上出现突变基因而导致的疾病。

A disease caused by a dominant mutant gene on an autosome.

由于常染色体突变基因导致的疾病。

But we don't care about Battlegrounds.

但我们并不在乎沙场中的显露。

Ah! don't mention it, the butcher's shop is a horror.

啊！不用提了。提到肉，真是糟透了。