外显子      exon 2(282) exons 2(18) extron 2(4) (exon 2(0)   exon 2      The differences in exon 2 of MTNR1A gene between Jining grey goats and Liaoning cashmere goats consisted of eleven nucleotide changes(A52G,T232C,T253C,A256G,T358G,T410A,A414T,C424T,A554G,T559C and C589A),and the homology of nucleotide sequence between them was 98.7%.      济宁青山羊与辽宁绒山羊MTNR1A基因外显子2的差异由11个核苷酸变化(A52G、T232C、T253C、A256G、T358G、T410A、A414T、C424T、A554G、T559C和C589A)组成,核苷酸同源性为98.7%。 短句来源      The SNPs Analysis of Exon2 and Exon3 in Chicken MHC-B-F      鸡MHC-B-F基因外显子2、3的SNPs分析 短句来源      The differences in exon 2 of MTNR1A gene between Small Tail Han sheep and Dorset sheep consisted of five nucleotide changes (C329T, G355T, C566T, C580A and A675G), and homology of nucleotide sequence was 99.4%.      小尾寒羊与多赛特羊MTNR1A基因外显子2的差异由5个变化的核苷酸(分别为C329T、G355T、C566T、C580A和A675G)组成,核苷酸同源性为99.4%。 短句来源      Polymorphisms of Exon 2 of MHC-DRB_3 Gene in Mongolian and Kazakh Sheep      蒙古绵羊和哈萨克绵羊MHC-DRB_3基因外显子2的多态性 短句来源      Polymorphism Analysis of the Exon 2 of SLA-DQA Gene of Tibet Pig by PCR- RFLP      藏猪SLA-DQA基因外显子2的PCR-RFLP多态性分析 短句来源 更多          exons 2      Methods:PCR SSP was used to amplify RhD gene exons 2,3,4,5,6,7,9,10 and intron 4 as well as RhCE gene intron 4 in 80 RhD negative blood donors which were determined by routine serological method.      方法 :采用PCR SSP法对 80名常规血清学RhD(- )本省供血者RhD基因外显子 2、3、4、5、6、7、9、10和内含子 4及RhCE基因内含子 4的特异性片段进行扩增。 短句来源      Analysis on polymorphism in exons 2,3 and 4 of the MICA gene in three different Chinese populations      三个群体MICA基因外显子2、3和4的多态性研究 短句来源      These PCR methods amplified RHD gene at exons 2、3、4、5、6、7、9、10 and at introm 4 and RHCE gene at intron 4.Results:RhD negative phenotypes consisted of 4 CCee,15 Ccee,14 ccee and 1 ccEe.      主要扩增RHD基因外显子2、3、4、5、6、7、9、10和内含子4以及RHCE基因内含子4。 结果：34名RhD（－）中国供血者的RhCcEe表型为4例CCee，15例Ccee和14例ccee及1例ccEe。 短句来源      Three pairs of primers were designed according to known DNA sequences tyrosinase in human and cattle, and exons 2, 3 and 4 were amplified of DNA sequences of tyrosinase in pig, which were 210, 135 and 182 bp in length.      实验根据人、牛的酪氨酸酶(TYR,tyrosinase)基因序列设计了3对引物,扩增出猪的酪氨酸酶基因外显子2,3,4序列,其长度分别为210,135,182bp。 短句来源      The exons 2 and 8 of the GUCY2D gene were analyzed using PCR heteroduplex SSCP method.      应用 PCR-异源双链- SSCP法分析 GUCY2 D基因外显子 2和 8,寻找可能的变异。 短句来源 更多          extron 2      PCR-SSCP Analysis on Extron 2 of Heart Fatty Acid Binding Protein Gene in Chicken      鸡H-FABP基因外显子2的PCR-SSCP分析 短句来源      Methods:Four parts of ODC gene which were extron2,extron3,extron6-10,extron11-12 were amplified from hepatic cancer cell by RT-PCR and then reversely subcloned into pcDNA3.1 vector.      方法采用RT PCR的方法从肝癌细胞中扩增出鸟氨酸脱羧酶(ODC),外显子2、外显子3、外显子610、外显子11124段基因片段。 短句来源      Conclusion:extron2,extron3 and extron6-10 were found to be the best antisense sites of inhibition.      结论ODC外显子2、外显子3、外显子610是较好的反义抑制敏感位点。 短句来源      p16INK4a gene extron 1 and extron 2 inactivation was detected by PCR for gene deletion, PCR-SSCP for gene mutation, and PCR-restriction enzyme assay for gene methylation respectively.      应用聚合酶链反应(PCR)、PCR-单链构象多态性以及PCR-限制性内切酶分析方法分别检测p16INK4a基因外显子1和外显子2的缺失、突变和甲基化。 短句来源   “外显子2”译为未确定词的双语例句      NDK/Nm23-H2interacted with FMRP exon1-12,as well as FMRP isoforms without exon12,and exons14-17.NDK/Nm23-H2couldn' t interact with FMRP exon1-6and exon2-7fragments.      (3)NDK/Nm23-H2与缺少外显子12、14-17的FMRP异构体,以及含FMRP外显子1-12的克隆相互作用,而与FMRP外显子1-6、外显子2-7不能直接结合。 短句来源      Three plant binary expression vectors pNAR501,pNAR502 and pNAR503 were constructed which carried exon 2-exon 3,5′partial deletion exon 1 and 5′partial deletion exon 1-exon 2-exon 3 of Pib gene driven by 35S separately.      将Pib结构基因克隆到双元载体,构建了3个植物表达载体pNAR501、pNAR502和pNAR503,这3个载体分别携带由35S驱动Pib结构基因的外显子2外显子3、5′端部分缺失外显子1和5′端部分缺失的外显子1外显子2外显子3的不同片段。 短句来源      Objective: To investigate the relationship between glucocorticoid receptor gene 2/1 codon 23 polymorphism and glucocorticoid-sensitive asthma.      目的：检测糖皮质激素受体（Glucocorticoid Receptor, GR）基因外显子2/1密码子23多态性，从而探讨糖皮质激素受体基因外显子2/1密码子23与激素敏感型支气管哮喘的相关性。 短句来源      case 2 carrying compound heterozygous point mutations of 527A→T and 1714G→C which caused heterozygous amino acid changes of D176V and V572L,respectively.      例2在外显子2出现527A→T杂合突变和外显子9出现1714G→C杂合突变,上述突变分别造成GNE出现H509Y的纯合突变以及D176V和V572L的复合杂合突变。 短句来源      2 cases were found in exon 5-6,5 in exon 7-8,1 in exon 9, the mutation rates were 5.71 % (2/ 35), 14. 29 (5/35) and 2. 86 (1/35) respectively.      其中,5-6外显子2例,变异率为5.71％(2/35); 7-8外显子5例,变异率为14.29％(5/35),是变异率最高的基因片段; 短句来源 更多        查询“外显子2”译词为用户自定义的双语例句     我想查看译文中含有：的双语例句 为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法，我们为您准备了出自英文原文的大量英语例句，供您参考。   exon 2 The variation of the exon 2 of the major histo-compatibility complex (MHC) class II gene DRB locus in three feline species were examined on clouded leopard (Neofelis nebulosa), leopard (Panthera pardus) and Amur tiger (Panthera tigris altaica). 例句来源       A pair of degenerated primers was used to amplify DRB locus covering almost the whole exon 2. 例句来源       Exon 2 encodes the β1 domain which is the most variable fragments of the MHC class II molecule. 例句来源       Totally eight distinct haplotypes of exon 2 were obtained in four individuals. 例句来源       The ratio of nonsynonymous substitutions (dN) was much higher than that of synonymous substitutions (dS), which indicated that balancing selection probably maintain the variation of exon 2. 例句来源       更多             exons 2 Exons 2 to 5 of mlc1 and mlc3 are highly conserved and have similar splicing sites. 例句来源       The molecular analysis of G6PD gene exons 2-13 was performed by a PCR-DHPLC-Sequencing or PCR-Sequencing. 例句来源       We describe a family with a large duplication of exons 2-16 of the dystrophin gene. 例句来源       Frequent polymorphisms within the flanking intronic sequences of both exons 2 and 4 were seen but at similar frequencies in controls. 例句来源       Variants lacking exons 2, 4, 5, and 7 are detected in the breast epithelial compartment of the normal human breast. 例句来源       更多             (exon 2 The variation of the exon 2 of the major histo-compatibility complex (MHC) class II gene DRB locus in three feline species were examined on clouded leopard (Neofelis nebulosa), leopard (Panthera pardus) and Amur tiger (Panthera tigris altaica). 例句来源       A pair of degenerated primers was used to amplify DRB locus covering almost the whole exon 2. 例句来源       Exon 2 encodes the β1 domain which is the most variable fragments of the MHC class II molecule. 例句来源       Totally eight distinct haplotypes of exon 2 were obtained in four individuals. 例句来源       The ratio of nonsynonymous substitutions (dN) was much higher than that of synonymous substitutions (dS), which indicated that balancing selection probably maintain the variation of exon 2. 例句来源       更多                    Exon 3 termination mutation of phenylalanine hydroxylase (PAH) gene, the only identified one causing classical phenylketonuria (PKU) in Chinese, was detected in fourteen PKU children from Xi'an. The genomic DNA from these patients was amplified by polymerase chain reaction(PCR) and dot hybridied with specific oligonucleotide probes. This mutation is not present in any of these affected children, which indicates that phenylketonuria in Chinese may be caused by other mutations in phenylalanine hydroxylase loc...             本文应用PCR和核酸杂交技术,在西安地区14例PKU患儿中检测了目前中国人中唯一确定引起PKU的PAH基因外显子3终止突变,结果发现这些患者的PAH基因均无终止突变,提示在我国有可能因PAH基因其它部位突变导致PKU的发生。我们体会DNA体外PCR扩增结合寡核苷酸探针点杂交方法可用于PKU的产前诊断和携带者检出。 文摘来源          Applying recombinant DNA techni- ques,the structures of red pigment gene(RPG)and green pigment gene(GPG)were analyzed for 43 pa- tients with protan or deutan(including 3 females),4 normal reladves and 3 carriers out of 3 families,as well as 11 normal controls.Abnormality of RPG was detected in all 19 protan and that of GPG was found in 14 out of 24 deutan.In about 80%(32/40) of protan and deutan the changing of exon 5 for RPG or GPG was discovered.In protan the normal RPG was replaced by a 5' red —3' green ...             应用分子杂交技术对43例先天性红与绿色觉异常患者(包括3例女性患者)、3个色觉异常家系的4名正常亲属及3名携带者、11例正常人的色觉基因进行了分析,发现100%(19/19)的红色觉异常、58%(14/24)的绿色觉异常可以发现红或绿色觉基因的异。80%(32/40)的患者可检测到红或绿色觉基因第5个外显子部分的改变。红色觉异常主要是正常红色觉基因被5′红—3′绿杂种基因替代所致;绿色觉异常主要是绿色觉基因完全缺失或形成5′绿—3′红杂种基因所致。另外,应用聚合酶链反应法可以较容易地检测出色觉基因第5个外显子的改变。 文摘来源          In this paper,we analyse Xba I/FⅧ_(E22)RFLP in the population of Suzhou usinga intragenic factor Ⅷ cDNA probe FⅧ_(E22).The results show 9.6/4.8 K b poly-morphism,and their frequency are 0.36/0.64 respectively.The value of PIC is 0.46Based on this polymorphism,carrier detection of hemophilia A was performed.             用FⅧ基因内第22外显子FⅧ_(E22)为探针,分析苏州地区正常人XbaI/FⅧ_(E22)RFLP,显示出9.6/4.8Kb 的多态性,频率为0.36/0.64.PIC 值为0.46。并以此为基础对1例甲型血友病携带者进行检测。 文摘来源   << 更多相关文摘         相关查询: 2外显子 第2外显子 基因外显子2 （2 2］ [ 2 [ 2 ] ～2 （2） 2（2 2’ —2）  对查询结果不满意

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