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HLA-DRB1 allele polymorphisms in genetic susceptibility to esophageal carcinoma 被引量:8
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作者 JunLin Chang-ShengDeng +5 位作者 JieSun Xian-GongZheng XingHuang yanzhou PingXiong Ya-PingWang 《World Journal of Gastroenterology》 SCIE CAS CSCD 2003年第3期412-416,共5页
AIM: To probe into the genetic susceptibility of HLA-DRB1 alleles to esophageal carcinoma in Han Chinese in Hubei Province.METHODS: HLA-DRB1 allele polymorphisms were typed by polymerase chain reaction with sequence-s... AIM: To probe into the genetic susceptibility of HLA-DRB1 alleles to esophageal carcinoma in Han Chinese in Hubei Province.METHODS: HLA-DRB1 allele polymorphisms were typed by polymerase chain reaction with sequence-specific primers (PCR-SSP) in 42 unrelated patients with esophageal cancer and 136 unrelated normal control subjects and the associated HLA-DRB1 allele was measured by nucleotide sequence analysis with PCR.SAS software was used in statistics.RESULTS: Allele frequency (AF) of HLA-DRB1·0901 was significantly higher in esophageal carcinoma patients than that in the normal controls (0.2500 vs0.1397, P=0.028, the odds ratio 2.053, etiologic fraction 0.1282). After analyzed the allele nucleotide sequence of HLA-DRB1·0901 which approachs to the corresponded exon 2 sequence of the allele in genebank. There was no association between patients and controls in the rested HLA-DRB1 alleles.CONCLUSION: HLA-DRB1·0901 allele is more common in the patients with esophageal carcinoma than in the healthy controls, which is positively associated with the patients of Hubei Han Chinese. Individuals carrying HLA-DRB1·0901may be susceptible to esophageal carcinoma. 展开更多
关键词 HLA-DRB1 等位基因 T细胞 食道癌 基因多态性 遗传易感性 PCR-SSP
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Gene Identification and Expression Analysis of 86,136 Expressed Sequence Tags(EST)from the Rice Genome 被引量:4
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作者 yanzhou JiabinTang +20 位作者 MichaelG.Walker XiuqingZhang JunWang SongnianHu HuayongXu SigiLiu HuanmingYang JunYu JianWang YajunDeng JianhaiDong LinYe LiLin JunLi XuegangWang HaoHu YibinPan WeiLin WeiTian JingLiu LipingWei 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2003年第1期26-42,共17页
Expressed Sequence Tag(EST)analysis has pioneered genome-wide gene discovery and expression profiling.In order to establish a gene expression index in the rice cultivar indica,we sequenced and analyzed 86,136 ESTs fro... Expressed Sequence Tag(EST)analysis has pioneered genome-wide gene discovery and expression profiling.In order to establish a gene expression index in the rice cultivar indica,we sequenced and analyzed 86,136 ESTs from nine rice cDNA libraries from the super hybrid cultivar LYP9 and its parental cultivars.We assembled these ESTs into 13,232 contigs and leave 8,976 singletons.Overall,7,497 sequences were found similar to the existing sequences in GenBank and 14,711 are novel.These sequences are classified by molecular function,biological process and pathways according to the Gene Ontology.We compared our sequenced ESTs with the publicly available 95,000 ESTs from japonica,and found little sequence variation,despite the large difference between genome sequences,We then assembled the combined 173,000 rice ESTs for further analysis.Using the pooled ESTs,we compared gene expression in metabolism pathway between rice and Arabidopsis according to KEGG.We further profiled gene expression patterns in different tissues,developmental stages,and in a conditional sterile mutant,after checking the libraries are comparable by means of sequence coverage.We also identified some possible library specific genes and a number of enzymes and transcription factors that contribute to rice development. 展开更多
关键词 EST 水稻 基因表达 基因分离 序列分析
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Identification and Expression Analysis of EST-based Genes in the Bud of Lycoris longituba 被引量:1
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作者 YonglanCui XinyeZhang +7 位作者 yanzhou HongYu LinTao LuZhang JianZhou QiangZhuge YoumingCai MinrenHuang 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2004年第1期43-46,共4页
To obtain a primary overview of gene diversity and expression pattern in Lycoris longituba, 4,992 ESTs (Expressed Sequence Tags) from L. Longituba bud were sequenced and 4,687 cleaned ESTs were used for gene expressio... To obtain a primary overview of gene diversity and expression pattern in Lycoris longituba, 4,992 ESTs (Expressed Sequence Tags) from L. Longituba bud were sequenced and 4,687 cleaned ESTs were used for gene expression analysis. Clustered by the PHRAP program, 967 contigs and 1,343 singlets were obtained. Blast search showed that 179 contigs and 227 singlets (totally 1,066 ESTs) had homologues in GenBank and 3,621 ESTs were novel. 展开更多
关键词 表达序列标签 EST 基因 草本植物 序列分析
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Structure Prediction of Membrane Proteins 被引量:1
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作者 ChunlongZhou YaoZheng yanzhou 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2004年第1期1-5,共5页
There is a large gap between the number of membrane protein (MP) sequences and that of their decoded 3D structures, especially high-resolution structures, due to difficulties in crystal preparation of MPs. However, de... There is a large gap between the number of membrane protein (MP) sequences and that of their decoded 3D structures, especially high-resolution structures, due to difficulties in crystal preparation of MPs. However, detailed knowledge of the 3D structure is required for the fundamental understanding of the function of an MP and the interactions between the protein and its inhibitors or activators. In this paper, some computational approaches that have been used to predict MP structures are discussed and compared. 展开更多
关键词 膜蛋白 结构预测 晶体 活化剂 抑制因子
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