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- Coincidentally, the psoriasis paper mentioned a recent study that linked SLE to low copy number of complement C4 genes. 巧合的是，银屑病论文提到近期一项研究将SLE与补体蛋白C4基因拷贝数低联系起来。
- Dit is controlled only by nuclear gene. 芽鞘紫线受核基因控制，无细胞质效应；
- Objective To search responsible nuclear genes for matrilineal non-syndromic deafness. 目的探索与母系遗传性非综合征性耳聋相关的核基因。
- Conclusion: The method combined DOP-PCR with CGH can realize the cytogenetic analysis of the human genome from low copy number, and the analysis result is accurate and reliable. 结论：本研究所建立的单细胞全基因组扩增联合比较基因组杂交技术适用于单细胞等低拷贝样本的分析，分析结果准确、可靠。
- Nuclear genes phylogenetically related to mitochondrial homologs were discovered in Archezoa, including Giardia(4,5). 在种系发生上与线粒体同系物相关的核基因在源真核生物中也找得到，包括鞭毛虫（4，5）。
- Thus, codon usage bias of nuclear genes appeared to be affected by translational selection. 因此，核基因的密码子使用偏好性受到翻译选择的影响。
- The majority of mitochondrial proteins are encoded by nuclear genes, synthesized in the cytosol and subsequently imported into mitochondria. 摘要线粒体的大多数蛋白质是由核基因编码、细胞质合成，而最终运输到线粒体。
- The rate of low copy number of CATT repeat (less or equal to 6) was significantly higher in lung tuberculosis patients than in normal people(85.6% vs 66.6%),suggesting that MIF might play a reciprocity in the pathogenesis of tuberculosis. 对比分析提示;肺结核病人MIF基因启动子区CATT低拷贝数(低于或等于6个)出现的频率明显高于正常人(85.;6%25比66
- Because copies of nuclear genes are likely to be very rare in Neandertal bones, finding them is probably beyond the reach of present-day technology. 因为这些核基因的复本在尼安德塔人的骨头中似乎很少见，所以要在他们的身上发现这些，大概还不是今日科技所能达到。
- This explanation is compelling because nuclear genes do not show the same "evidence" that the mitochondrial gene does. 这种解释是牵强的，因为核心基因与线粒体基因不同，不会显示相同的“证据”。
- Seed dormancy were generally quantitative traits influenced by a large number of genes including nuclear gene and plasmagene. 影响休眠性状表达的基因既有核基因，又有质基因，休眠通常表现为一种受多基因控制的数量性状。
- Some pathogenicity was steadily inherited, which suggested that the virulence genes controlling the pathogenicity appeared to be homozygous nuclear gene. 控制大豆疫霉菌的致病基因分布在不同位点，有的遗传稳定，由纯合的核基因控制；
- Genetic analysis showed 291S might be a genic male sterile line, its sterility was controlled by a major recessive nuclear gene and was influenced by other minor genes. 遗传分析表明，291S可能为隐性核不育类型，其不育性由一对主效基因控制，还受到微效基因的修饰作用。
- A phylogeny of Bombina is reconstructed based on three mitochondrial and two nuclear gene fragments. 萨维奇环北极分布假说影响广泛，但一直没有被检验过。
- Phylogenetic analysis shows that GAPDH is a classical nuclear gene, a house-keeping gene and a function gene. 对于距现今较近的动物，用其作为近亲缘关系的属内种间的标记基因，可能产生偏差。
- The present study examined the utility of nuclear gene c-mos in higher level phylogeny among lizards, caenophidian snakes and amniotes. 鬣蜥科是避役科的姐妹群，盾蜥科与环尾蜥科紧密关联，鳄蜥与巨蜥相聚。
- Leaf varie- gation resulted from mutation of 8 Arabidopsis nuclear genes, IMMUTANS, VAR1, VAR2, CHM, CUE1, PAC, ATD2 and VAR3, has been reviewed. Proteins encoded by these genes and variegation mechanisms related to these genes were presented. 综述了拟南芥菜IM、VAR1、VAR2、CHM、CUE1、PAC、ATD2和VAR3等8个细胞核基因突变后引起的叶片花斑,主要包括这些基因所编码的蛋白质以及它们突变以后引起花斑的机制。
- From the studies in the variegated mutants (im, var2, var1 and chm), a kind of mutants deficient in plastid development, we know it is the mutations in nuclear genes that induce these phenotype. 在已报道的若干花斑突变体(imvar2、var1和chm)的研究中发现引起花斑的是一些核基因。
- The government is trying to keep a low profile on this issue. 政府力图在这个问题上保持低姿态。
- In this review, we focus on some of the common causes of syndromic hearing impairment due to nuclear gene abnormalities, oudining the current state of knowledge o... 本文将简要介绍综合征型和非综合征型听力损害的核基因定位克隆和突变的研究进展,以及遗传性损害基因突变检测的临床应用情况。
