Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.
瘦素(leptin)肥胖基因(ob基因)编码,脂肪细胞分泌
一种内源性激素,主要调控体重和脂肪分布。
Leptin is one endogenous excitatory autacoid, encoded by obese gene and secreted by adipose cells.
瘦素(leptin)肥胖基因(ob基因)编码,脂肪细胞分泌
一种内源性激素,主要调控体重和脂肪分布。
All the C3 allotype was C3S.The gene frequency was 1.
而且所有第三补体异型均为C3S,而此基因频率为1。
Gene mutations are alterations in the DNA code.
基因突变指DNA 密码
改变。
The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis.
干细胞白血病(CL)因现
与白血病
生有关
癌基因。
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因机会。
Through similar and supplementary action , polygenes can have important effects on total variability.
通过相同和添加
作用,多基因可以对总
变异起重大
影响。
That genal genome may lead to better treatment and control of diseaesthe disease.
那些基因组能带来比较好治疗和疾病
控制。
Most of these genes have not been reported to relate to the haematogenesis in ontogeny.
这些基因大多数在胚胎分化造血育中
作用尚未见报道。
You have good genes from your parents, so you should live a long time.
你从父母那儿获基因, 所以能够活
很长。
Genes tabA, tabB,tblA and dapB participate biosynthesis of tabtoxinine, which is regulated by lemA gene.
野火氨酸合成有tabA,tabB,talA,dapB等基因参与,受lemA基因调控。
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、易于与之分离辅基因子称为辅。
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因,实验动物模型一个非常好
方式。
Some exceptions are gene unscrambling in ciliates (4) and the bursicon gene in mosquitoes (5).
而纤毛虫和蚊子粘液素基因所表现出
基因整合则
一些例外。
Current areas of interest and inestigation—including gene–enironment interaction, pharmacogenetics, and genetic counseling—are also discussed.
目前研究热点还包括:基因-环境相互作用、遗传药理学、基因咨询等。
There is also GMO zucchini, crookneck squash, papaya, and alfalfa.
也有转基因南瓜、转基因葫芦、转基因木瓜和转基因苜蓿。
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基因结构。
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,确认基因型测定结果。
Evidence is accumulating that a defective gene may be responsible for this disease.
越来越多证据表明该疾病
由一种有缺陷
基因引起
。
Some people extoll GM foods’tremendous potential for good.
有些人赞赏转基因事物极大潜力。
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否由于X染色头感光色素基因变异?
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