We found a recessive cataract mutation arose spontaneously in a KUNMING outbred mouse strain.

研究遗传性白内障致病基，实验动物模型是个非常好的方式。

Evidence is accumulating that a defective gene may be responsible for this disease.

越越多的证据表明该疾病是由种有缺陷的基的。

There is also GMO zucchini, crookneck squash, papaya, and alfalfa.

也有转基南瓜、转基葫芦、转基木瓜和转基苜蓿。

Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.

目前的研究热点还包括：基-环境相互作用、遗传药理学、基咨询等。

Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).

而纤毛虫和蚊子的粘液素基所表现出的基整合则是些例外。

Siblings and dizygotic twins share only 50% of their segregating genes.

同卵双生双胞胎和双卵双生双胞胎分享仅50%的基。

Most of these genes have not been reported to relate to the haematogenesis in ontogeny.

这些基大多数在胚胎分化造血发育中的作用尚未见报道。

You have good genes from your parents, so you should live a long time.

你从父母那儿获得优良的基, 所以能够活得很长。

That genal genome may lead to better treatment and control of diseaesthe disease.

那些基组能较好的治疗和疾病的控制。

Researchers are gradually deciphering the genetic structure found in the cells of organisms.

研究者正渐渐破译存于有机体细胞内的基结构。

The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.

干细胞白血病(CL)是新发现的与白血病发生有关的癌基。

Without this, you are reducing your chances of concentrating the genes of the linebred ancestor.

没有这种选择，你就正在降低强调在血系内繁殖中祖先基的机会。

Histones are characterized by numerous posttranslational modifications that influence gene transcription.

组蛋白的特点是大量的翻译后修饰，这些修饰可以影响基转录。

Genes tabA， tabB，tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.

野火氨酸的合成有tabA，tabB，talA，dapB等基参与，受lemA基调控。

The sequencing of the PCR product was determined by using dideoxy-mediated chain-termination method.

采用双脱氧DNA链合成终止法进行PCR产物直接测序,确认基型的测定结果。

Is Photosensitive Epilepsy Less Common in Males Due to Variation in X Chromosome Photopigment Genes?

光敏感性癫痫在男性较少见是否由于X染色头感光色素基变异？

Some people extoll GM foods’tremendous potential for good.

有些人赞赏转基事物的极大潜力。

Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.

瘦素(leptin)是肥胖基(ob基)编码，脂肪细胞分泌的种内源性激素，主要调控体重和脂肪分布。

Gene mutations are alterations in the DNA code.

基突变是指DNA 密码的改变。

A cofactor bound loosely to the apoenzyme and readily separable from it is a coenzyme.

与脱辅基蛋白结合松弛、易于与之分离的辅基子称为辅。