- 更多网络例句与等位基因的相关的网络例句 [注：此内容来源于网络，仅供参考]
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The allele frequency of ALDH2*1 between alcoholic cardiomyopathy group and alcohol dependent group was significantly higher than that in controls and the allele frequency of ALDH2*2 between alcoholic cardiomyopathy group and alcohol dependent group was significantly lower than that in controls.
嗜酒组和酒精性心肌病组ALDH2*1等位基因的频率高於对照(P.01)，ALDH2*2等位基因的频率低於对照组(P.01)。
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The interactions between the alleles controlling the crossability of wheat with rye may exist.
小麦可杂交性基因间存在互作，表现为纯合隐性等位基因对其它显性等位基因的抑制作用，而纯合隐性等位基因间的效应具有可加性。
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In white participants, the 1919T allele was associated with increased risk of stroke and cardioascular mortality, and in black participants, homozygosity for the 790T allele was associated with a fourfold increased risk of MI compared with homozygosity for the 790A allele.
在白人参与者中，1919T等位基因与中风和心血管病死亡率的危险增加有关，而在黑人参与者中，790T等位基因的同合子性比790A等位基因的同合子性与心肌梗死危险的关系高四倍。
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The differentiation coefficient is 0.07 between three inbreed families respectively. The highest level of genetic homozygosity is in families Ⅱ at 18, but genetic variation is a little difference between inbreeding pig and mice. However, this study revealed the pattern of genetic variation at microsatellite loci in the 3 inbred families of WZSP with one of the most important findings to be the high level of unexpected heterozygosity at some loci, e.g. Sw874 and Sw936 that could be part of the unique genetics of three families. A hypothesis is that certain functional genes linked with such microsatellite loci may be involved in the maintenance of viability of these inbred families of WZSP remains for further investigation.
随近交代数的推进，每个星座上等位基因数越来越少，基因的纯合度越来越高，但WZSP近交系微卫星等位基因的纯合度有一定的限度，与近交鼠有所不同；在近交系3个家系各个世代中有少数几个基因座，如Sw874和Sw936等一直处于高度杂合状态，这可能与WZSP近交家系的种质特异性有关，推测与这些基因座处于同一连锁群的某些功能基因在维持极高近交水平下WZSP的基本生存能力中起着关键作用。3个近交群体间的分化系数在0.07以上，已各自成为独立家系；3个家系的近交程度不完全一致，基因的纯合度亦不同，Ⅱ系最高、14个微卫星座中7个纯合，其次为Ⅰ系和Ⅲ系。
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Bi-allelic or biparental expression of alleles may be present in some tissues and uniparental expression in other tissues.
某些组织中可能出现等位基因的双等位基因或双亲表达，其他组织中是单亲表达。
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Bi-allelic or biparental expression of alleles may be present in some tissues and uniparental expression in other tissues.
某些组织中可能出现等位基因的双等位基因或双亲表达，其他组织中是单亲表达。angelman综合征和prader-willi综合征都可因第15号染色体缺失而产生。
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Based on this information, offspring from 10 crosses where parents were known were genotyped by the 6 microsatellite loci and used for parentage analysis. The result showed that assignment success of the progeny to their 'true' mother and father was 88% and 78% respectively, which were lower than predicted by the Cervus simulations. This could be explained by the existence of null or mutant alleles and by Taq DNA Polymerase slippage in the microsatellite loci.
在家系混养的模拟实验中使用这6个高多态性的微卫星基因座从20个候选雌虾中找到真正母亲的概率为88%，从30个候选雄虾中找到真正父亲的概率为78%，低于理论预测值，分析可能与微卫星基因座中的无效等位基因，等位基因的突变以及PCR过程中 Taq 酶发生链滑移等因素有关。
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To inquire into association between susceptibility to AIDP, AMAN and frequencies of HLA alleles and possible differencies in distribution of HLA alleles betwen AIDP and AMAN by genomic typing for HLA-class Ⅰ, class Ⅱ alleles, and to try to found out the effects of self intrinsic fators of GBS patients on occurence of two subtype from immunogenetic angle.
通过对AIDP和AMAN两种GBS亚型的HLA-Ⅰ类和Ⅱ类等位基因的分型，探讨两种亚型的易感性与HLA等位基因分型的关系以及两种亚型在HLA等位基因分布上可能存在的差异，从免疫遗传学角度寻找自身内在因素在GBS不同亚型发病中的可能作用。
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Studies on relationship between population size and sampling proportion revealed that population size had evident impact on the sampling proportion and retainment of variations in core collection.
以36对SSR引物的37个位点和2708份核心种质材料进行取样比例的研究结果认为，随着压缩比例的增大压缩群体的基因多样性指数先升高再降低，等位基因的数量和等位基因覆盖率持续下降并且速率逐渐加大。
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The results showed that activities of the forward sequence of both genotypes were higher than that of reverse sequence. Promoter activity of the recombinants with A allele was about one third lower than that with C allele.
实验结果表明，2种基因型的正向序列启动子活性均高于相应的反向序列，含有A等位基因的启动子片段活性比含有C等位基因的片段低约1/3。
- 更多网络解释与等位基因的相关的网络解释 [注：此内容来源于网络，仅供参考]
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allele：等位基因
2)等位基因(Allele) 位于同源染色体的同一位置上的基因,是由基因突变而起源的. 4)等位基因(allele)在一对同源染色体的同一基因座上的2个不同形式的基因.
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dominant allele：显性等位基因
2.(在遗传学)个体携带一些有缺陷的等位基因(allele),可能 被正常的显性等位基因(dominant allele)遮蔽.所以这样的个体自身 不受缺陷基因的危害,但可以将缺陷基因传递给它们的子代.在人类中, 妇女可能是红绿色盲和血友病基因的携带者,
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Multiple allele：复等位基因
造成基因多态性的原因:1复等位基因(multiple allele)位于一对同源染色体上对应位置的一对基因称为等位基因(allele). 由于群体中的突变,同一座位的基因系列称为复等位基因. 某些复合体基因的每一座位都存在为数众多的复等位基因,
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mutant allele：突变等位基因:任何和野生型基因不同的基因
mutant 突变体:发生突变的细胞或个体. | mutant allele 突变等位基因:任何和野生型基因不同的基因. | mutation 突变:除重组外任何使遗传物质发生改变的过程.
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allelic：等位基因的
aromatase 芳香酶 | allelic 等位基因的 | elucidate 阐明,解释
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allelic：等位的,等位基因的
acid soil 酸性土壤 | allelic 等位的,等位基因的(6,236) | allowable depletion 允许损耗值(4,181)
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allelic exclusion：等位(基因)排斥[一个杂合子表现其任一异型性状的现象,有时特指成熟
allelic diversity 等位(基因)多样化 | allelic exclusion 等位(基因)排斥[一个杂合子表现其任一异型性状的现象,有时特指成熟 | allelic inactivation 等位(基因)失活
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alleles：等位基因
4.4.2.3 等位基因(Alleles)符号c. 隐性等位基因应用突变基因词首的小写字母表示,如非野鼠色(nonagouti)基因a,其它所有的等位基因包括显性的、共显性的或有显性关系的基因符号都应该用一个大写词首字母加小写字母表示,
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multiple alleles：复等位基因
HLA的多态性主要是由于复等位基因和共显性所致: (1)复等位基因(multiple alleles),位于一对同源染色体上对应位置的一对基因叫等位基因. 由于群体的突变,同一基因座的基因系列称为复等位基因,对某一个体来说一个基因座只有一对等位基因,
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multiple alleles：多等位基因,复等位基因
multinucleate 多核的 | multiple alleles 多等位基因,复等位基因 | multipolar neurone 多极神经元