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According to compound genotypic allelomorph construction,there are nine kinds of haplotype allelomorph.

根据复合基因型的等位基因构成,存在九种单倍型等位基因。

Suspectible and resistant allele of pear scab located in different linkage groups,and resistant gene of pear scab was homologous to apple scab.

梨黑星病抗性等位基因和敏感性等位基因定位于不同的连锁基因组上,梨黑星病抗性基因与苹果黑星病抗性基因具有同源性。

In 110 Xinjiang unrelated healthy Uygur subjects, 27 alleles were detected in HLA-B loci. Of them, B * 35 and B * 51 were the most common alleles with an allele frequency of 0.1136 and 0.1136, respectively; while B * 41, B * 56 and B * 78 were the rare alleles with a frequency of 0.0045, 0.0045 and 0.0091, respectively. Frequencies of "Caucasoid origin" HLA alleles such as B * 08, B * 35 and B * 50 in Xinjiang Uygurs were higher than other ethnic groups in China.

在维吾尔族样品中共检出27个等位基因,其中高频率的等位基因为B*35(0.1136)和B*51(0.1136),低频率的等位基因为B*41(0.0045)、B*56(0.0045)和B*78(0.0091),B*08、B*35、B*50等"高加索人"起源的HLA基因在新疆维吾尔族的分布频率高于国内其他民族,与高加索人种的数值相当。

ASCL2 gene escapes genomic imprinting in skeletal muscle,fat, heart,liver,spleen,lung,kidney,stomach,small intestine,uterus,ovary and pituitary.(2) Both of the transcripts of NNAT gene is paternally expressed in skeletal muscle,fat,heart, liver,spleen,lung,kidney,stomach,small intestine,uterus,ovary and pituitary.(3) DIRAS3 gene is paternally expressed in skeletal muscle,fat,heart,liver,spleen,lung, kidney,stomach,small intestine,uterus,ovary and pituitary.(4) DLX5 gene is maternally expressed in skeletal muscle,fat,spleen,lung,stomach,small intestine,but escapes imprinting in heart,liver,kidney,uterus,ovary,testicle and pituitary.

1ASCL2基因在肌肉、脂肪、心、肝、脾、肺、肾、胃、小肠、子宫、卵巢和垂体中均逃脱印记;(2)NNAT基因两个转录本在肌肉、脂肪、心、肝、脾、肺、肾、胃、小肠、子宫、卵巢和垂体中均为母系印记:(3)DIRAS3基因在肌肉、脂肪、心、肝、脾、肺、肾、胃、小肠、子宫、卵巢和垂体中母系印记:(4)DLX5基因在骨骼肌、脂肪、肺、脾、胃和小肠中表达母本来源的等位基因,即表现为父系印记;而在心、肝、肾、子宫、卵巢、睾丸和垂体中表达双亲来源的等位基因,即逃脱印记。3。

The frequencies of CCR5delta32,CCR2b-64I,SDF1-3′A alleles in Dai population were 0.0000,0.2130,0.2030,respectively;The frequencies of CCR5delta32,CCR2b-64I,SDF1-3′A alleles in Chingpaw population were 0.000,0.1637,0.1770,respectively.Distributions of the CCR2b-64I,SDF1-3′A alleles among the both populations were in accordance with Hardy-Weinberg equilibrium.No statistical difference was found in the allelic frequencies of both CCR2b-64I and SDF1-3′A between male and female individuals.

结果表明,中国傣族景颇族人群中未发现CCR5△32等位基因突变;傣族CCR2b-64I、SDF1-3′A基因突变频率分别为0.2130和0.2030,景颇族CCR2b-64I和SDF1-3′A基因突变频率分别为0.1637和0.1770;与中国汉族人群相比较,傣族和景颇族中SDF1-3′A突变频率较低(P值分别为0.0322和0.0021);两个民族的CCR2b-64I和SDF1-3′A等位基因群体分布符合Hardy-Weinberg平衡,在性别之间分布无显著差异。

Five of 7 ae loci showed Gaoyou alleles in Hangzhou and all the ae loci but one had Sollux alleles in two locations of Germany increasing plant height. The digenic epistatic main effect accounted for one third of total additive main effects.

7个 ae 基因座位中,5个&高油&等位基因在杭州种植环境下,除一例外所有在德国环境下的互作基因座中,&Sollux&等位基因起着增加株高的作用,加加上位性主效总和为加性主效总和的三分之一。

Results:(1) totally, the distributions of alleles o r genotypes of drd3 ser9gly polymorphism are not significantly different between the groups of paren ts, unaffected-siblings and affected-siblings, and between the sub-types of schi zophrenia.

结果: (1)总体而言,drd3基因的ser9gly等位基因频度和基因型频度在父母组、非患病同胞组和患病同胞组之间差异无显著性,在精神分裂症不同亚型之间基因型频度和等位基因频度的分布差异也没有统计学意义。

Results:(1) totally, the distributions of alleles o r genotypes of drd3 ser9gly polymorphism are not significantly different between the groups of paren ts, unaffected-siblings and affected-siblings, and between the sub-types of schi zophrenia.

对drd3基因的ser9gly多态性进行检测。结果:(1)总体而言,drd3基因的ser9gly等位基因频度和基因型频度在父母组、非患病同胞组和患病同胞组之间差异无显著性,在精神分裂症不同亚型之间基因型频度和等位基因频度的分布差异也没有统计学意义。

The allele E of ADL252 had a significantly positive correlation with EW,and the allele C of ADL252 had a significantly negative correlation with egg weight at first egg in Silkies.

标记G01672基因型为EE、AE所对应开产蛋重最小二乘均值与基因型为CE、CC的对应值间差异显著;等位基因E与开产蛋重有显著正相关,等位基因C与开产蛋重有显著负相关。

FHIT gene alterations preferentially occur in squamous cell carcinoma patients and smokers, and FHIT gene may be a candidate molecular target of carcinogenesis in tobacco smoker. Allelic deletion of FHIT gene might be an early molecular event in smoking-related lung cancer.

FHIT等位基因缺失主要发生在肺鳞癌和吸烟患者中,且FHIT基因可能为烟草致肺癌的靶基因,其等位基因缺失可能是肺癌的早期分子事件。

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