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   隐性上位作用 的翻译结果: 查询用时:0.185秒
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隐性上位作用
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  “隐性上位作用”译为未确定词的双语例句
     3.The genetic segregation is comprehensive when bi and Bt gene were in the same genetic background.
     3.当bi、Bt均在遗传背景中出现,遗传分离比例较复杂,bi对Bt存在隐性上位作用
短句来源
     The chp is recessive epistatic on ch-2.
     谈赤蚁(Ch~D)对第二隐性赤蚁(ch-2)有隐性上位作用.
短句来源
     For example, the additive effect is appeared in early-maturing and middle season variety (1: 6: 9), the independent segregation in late maturing variety (1: 3: 3: 9) and the recessive epistasis in NK 58 itself (4: 3: 9).
     这两对基因在不同类型的粳稻品种中其互作方式表现差异,即在早、中稻品种中表现积加作用(1:6:9),在晚稻品种中为独立分离(1:3:3:9),在农垦58品种本身的背景中表现隐性上位作用(4:3:9);
短句来源
     The linkage major genes had complementary, recessive-epistatic and additive-epistatic effect.
     主穗总粒数和千粒重2个性状受两对主基因+多基因控制,主基因作用方式分别为等加性和隐性上位作用
短句来源
     is controlled by two pairs of recessive major genes and the interaction of the genesis performed differently in parental varieties. For example, there appeared additiveeffect in early and middle rice, independent segregation in late rice and recessiveepistasis in Nongken 58 itself.
     结果表明,农垦58S光敏雄性不育性由2对隐性主基因控制:这2对基因在不同类型的梗稻品种中其互作方式表现差异,即在早、中稻品种中表现积加作用,在晚稻品种中为独立分高,在农垦58品种本身的背景中表现隐性上位作用,这种相互作用方式差异与分离世代植株的出穗期限有一定关系;
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  相似匹配句对
     ヽompared with the red egg gene,the mutant gene showed recessive epistasis.
     ③对红卵基因(re)表现隐性上位作用
     The Role by Covert Knowledge in Market-oriented Economy
     隐性知识在市场经济中的作用
短句来源
     Dominant Function and Recessive Function of Archives
     档案的显性作用隐性作用
短句来源
     The chp is recessive epistatic on ch-2.
     谈赤蚁(Ch~D)对第二隐性赤蚁(ch-2)有隐性上位作用.
短句来源
     w-3bt is epistatic to re.
     w -3bt对re表现上位作用
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A spontncous mutant or the chocolate parple has been discovered from white-5 egg system. Its morphological characters and hereditary mode arc different from Ia, sch, cm, ch and ch-2 apparently. The gene is marked with ch which is the allclc of+ch and ch. The relationship among three alleles is: +ch > ch> chp. The chp is recessive epistatic on ch-2.

自第5白卵系中发现新的自然突变——淡赤蚁.其形态和遗传方式与Ia、sch、cm、ch、ch-2判然各异,孵化时蚁体谈赤褐色.定名为谈赤蚁(chocolate purple).基因记号 ch~D.谈赤蚁为黑蚁和普通赤蚁(ch)的等位基因,三者显隐关系为+ch>ch>Ch~D.谈赤蚁(Ch~D)对第二隐性赤蚁(ch-2)有隐性上位作用.

Observation and analysis of the heading date and fertility of F_1,F_2 and BCF_1 descended from combinations (Nongken 58 S/nine japonica varie-ties)by using an indicator of bagged seed setting rate indicate that the photoperiodsensitive genie male-sterility (PSGM) of Nongken 58 S (Oryza sativa L.)is controlled by two pairs of recessive major genes and the interaction of the genesis performed differently in parental varieties. For example, there appeared additiveeffect in early and middle rice, independent segregation...

Observation and analysis of the heading date and fertility of F_1,F_2 and BCF_1 descended from combinations (Nongken 58 S/nine japonica varie-ties)by using an indicator of bagged seed setting rate indicate that the photoperiodsensitive genie male-sterility (PSGM) of Nongken 58 S (Oryza sativa L.)is controlled by two pairs of recessive major genes and the interaction of the genesis performed differently in parental varieties. For example, there appeared additiveeffect in early and middle rice, independent segregation in late rice and recessiveepistasis in Nongken 58 itself. The difference in interacting patterns is somewhatrelated to the heading date of F_1 F_2 and BCF_1, The PSGM of Nongken 58 S, whichmight be modified by two set of minor genes called Photoperiod and thermoperiodcontrol genes, is expressed in various genetic background. To explain the geneticmechanism of such phenomena, a hypothesis of "parallel mutation of the duplica-tion gene loci" has been advanced and genetic classification and selection of doublefunction line of PSGM slight response to photoperiod and thermoperiod arediscussed.

以套袋自交结实率为主要指标,观察分析了农垦58S与不同生态型的9个粳稻品种杂交的F_1,F_2,BCF_1代的抽穗期与育性。结果表明,农垦58S光敏雄性不育性由2对隐性主基因控制:这2对基因在不同类型的梗稻品种中其互作方式表现差异,即在早、中稻品种中表现积加作用,在晚稻品种中为独立分高,在农垦58品种本身的背景中表现隐性上位作用,这种相互作用方式差异与分离世代植株的出穗期限有一定关系;农垦58S光敏不育性在不同的遗传背景中都能表达,但受到光、温2组微效基因修饰。“重复基因位点平行突变假说”,可以较完满地解释农垦58S的遗传机制。本文还就光敏感雄性不育系的遗传分类和选育温光弱感型光敏雄性不育两用系进行了讨论。

It has been demonstrated from the experimental observation and analysis on the heading date and fertility of F_1, F_2 and BF_1 descended from combinations Nong ken 58S (NK58S) / nine japonica varieties by using an indicator of bagged seed setting rate that the photoperiod sensitive genic male-sterility of Nongken58S (PSGM NK58S) is controlled by two pairs of recessive major genes and the interaction of those genes is performed differently from parental varieties. For example, the additive effect is appeared...

It has been demonstrated from the experimental observation and analysis on the heading date and fertility of F_1, F_2 and BF_1 descended from combinations Nong ken 58S (NK58S) / nine japonica varieties by using an indicator of bagged seed setting rate that the photoperiod sensitive genic male-sterility of Nongken58S (PSGM NK58S) is controlled by two pairs of recessive major genes and the interaction of those genes is performed differently from parental varieties. For example, the additive effect is appeared in early-maturing and middle season variety (1: 6: 9), the independent segregation in late maturing variety (1: 3: 3: 9) and the recessive epistasis in NK 58 itself (4: 3: 9). The difference in the interacting pat- terns is somewhat related to the heading date of F_1, F_2 and BF_1 The PSGM NK58S, which might be modified by two set of minor genes called photoperiod and thermoperiod control genes, is expressed in va- rious genetic background. To explain the genetic mechanism of such phenomena, a hypothesis of paralled mutation on the duplicate gene loci was advanced and genetic classification and selection of double-func- tioned line of PSGM slightly response to photoperiod and thermoperiod were discussed.

以套袋自交结实率为主要指标,观察分析了农垦58S与不同生态型的9个粳稻品种杂交的F_1 、F_2、BF_1代的育性,同时记载抽穗期。结果表明,农垦58S光敏雄性不育性由两对隐性主基因控制;这两对基因在不同类型的粳稻品种中其互作方式表现差异,即在早、中稻品种中表现积加作用(1:6:9),在晚稻品种中为独立分离(1:3:3:9),在农垦58品种本身的背景中表现隐性上位作用(4:3:9); 这种相互作用方式差异与分离世代植株的抽穗期有一定关系。农垦58S光敏不育性在不同的遗传背景中都能表达,但受到光、温两组微效基因修饰。本文提出“重复基因位点平行突变假说”,可以较完满地解释农垦58S的遗传机制;同时就光敏感雄性不育系的遗传分类和选育温光弱感型光敏雄性不育两用系,提出了讨论。

 
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