核苷酸多性 的英文怎麼說
中文拼音 [hésuānduōxìng]
核苷酸多性
英文
single nucleotide polymorphism-
Multi - locus dna fingerprint technique was used to check the chimerism of chimeric mouse generated by injecting es cells into blastocysts and to detect whether the chimeric mouse is a germ - line chimeras. the results indicated that : the multi - locus dna fingerprint with a new synthesized probe - jl - 02, has enough polymerism and good stability, and should be very useful to monitor the chimerism in different tissues of es cell chimeric mouse and to check whether an es cell line has the capacity to enter the germ line, especially when involving strains that can not be discerned with coat color or biochemical markers
嘗試應用多位點dna指紋技術,檢測經過胚胎幹細胞es細胞途徑所獲得的嵌合體小鼠中es細胞在各種臟器中的嵌合情況檢測es細胞在嵌合體小鼠中是否實現種系傳遞。結果表明:採用新型的人工合成的寡核苷酸多聚體探針jl - 02探針的多位點dna指紋圖譜,具有足夠的多態性和很好的穩定性。The research development of single nucleotide polymorphism
單核苷酸多態性研究進展The massive amount of high - throughput microarray, snps and other biological data bring a great challenge of developing advanced statistical and computational data mining tools
大量的高產能微陣列、單點核苷酸多型性及其他生物資料也對高級統計計算之資料探勘工具產生極大的挑戰。System for detecting single nucleotide polymorphisms based on hybridization probes
熒光雜交探針技術檢測單核苷酸多態性Inherited genetic variation has a critical but as yet largely uncharacterized role in human disease. here we report a public database of common variation in the human genome : more than one million single nucleotide polymorphisms snps for which accurate and complete genotypes have been obtained in 269 dna samples from four populations, including ten 500 - kilobase regions in which essentially all information about common dna variation has been extracted
我們現在發表一個人類基因組常見遺傳變異的公開資料庫:這是一個對來自四個群體269個樣品內的一百萬個單核苷酸多態性( snps )進行了完整並準確的分析的研究成果;另外也確認了十個dna片段(每個片段含有五十萬個堿基)的所有常見遺傳變異資訊。But such single - nucleotide polymorphism ( snp ) profiles can be deceptive, duster warns
但達斯特提出警告,這種單核苷酸多型性的剖析可能會有錯誤。Genetic association between polymorphism of claudin 5 transmembrane protein gene and schizophrenia
膜轉運蛋白基因單核苷酸多態性與精神分裂癥A study of the relationship between single nucleotide polymorphisms of xrcc1 and susceptibility to radiation injury
1單核苷酸多態與輻射損傷易感性相關性研究Snp and cn ariation correlated with altered actiity in almost 900 and 240 genes, respectiely
單核苷酸多態性與變異基因拷貝數分別與近900和240個基因的活性改變有關。Some associations were not found in all four populations, two - thirds ( cns or snps ) being found in only one population
一些關聯在四種人群中沒有被發現,有2 / 3的(單核苷酸多態性或變異基因拷貝數變異)僅在一個人群中被發現。Funded by the national heart, lung, and blood institute ( nhlbi ) of the national institutes of health, the study, known as sea ( snps and extent of atherosclerosis ), will build on research from two preiously funded nhlbi projects
這項研究由美國心肺血液研究所( nhlbi )資助,研究名稱為sea (動脈粥樣硬化程度與單核苷酸多態性研究) 。Nucleotide polymorphism analysis of growth hormone gene in zang pigs
藏豬生長激素基因核苷酸多態性分析Snps in fie noel independent loci exhibited strong and consistent eidence of association with breast cancer ( p < 10 ( - 7 ) )
在五種新的獨立的基因位點的單核苷酸多態性顯出強的一致的證據與乳腺癌相關。Recent snps analysis tools are transforming the traditional genotyping and resequencing in the same way as expression arrays
有關單點核苷酸多型性的新進分析工具,將傳統的基因型?定資料與微陣列基因表現資料做同樣的轉換。The study was a massie undertaking : it included hap map genotype data on 700, 000 snps located close to genes, as well as 25, 000 sites interrogated for potential structural ariation to examine copy - number differences, looking at the actiity of 14, 000 genes in 210 unrelated indiiduals
這項研究是一項宏偉的事業,包括有關700000份定位於這些基因附近的單核苷酸多態性的人類基因組單體型圖的基因型數據,也包括被鉆研的25000個因蛋白結構性變異從而檢測基因拷貝數變異的研究位點同時也觀注著210個無親緣關系個體的14000個基因的活性。Pharmacogenomics combines traditional pharmaceutical sciences such as biochemistry with annotated knowledge of genes, proteins, and single nucleotide polymorphisms
藥物基因組學結合了傳統藥學理論(如生物化學)和已經定義了的基因、蛋白質和單核苷酸多態性等各類學科的研究成果。Snps are dna sequences that differ by a single nucleotide, or code letter, between one part of a population and another
這種標志稱為單核苷酸多型性( snp ) ,指的是族群中部份成員與其他成員的dna序列上,只出現一個核苷酸(編碼字母)的差異。Relationship between single nucleotide polymorphisms in the 5 ' - promoter region of beta fibrinogen gene and coronary artery disease : a case - control study in chinese population
纖維蛋白原基因啟動子區域單核苷酸多態性與冠心病的關系The results showed : ( 1 ) in the d - loop of mtdna genome from 18 individuals, there were only transition and transversion, were not insertion and deletion, and the frequency of transition was higher than transversion ; ( 2 ) and nucleotide diversity was 0. 0011, the sequence divergence values among haplotypes was 0. 005
研究結果顯示: ( 1 ) 18隻大鴇的301bp - 330bpmtdna控制區序列的突變只有轉換和顛換,無插入和缺失,且轉換的頻率高於顛換; ( 2 )核苷酸多態性只有0 . 0011 ,不同單元型間的序列差異值為0 . 5 。Methods we genotyped 317, 503 single - nucleotide polymorphisms ( snps ) in a combined case ? control study of 1522 case subjects with rheumatoid arthritis and 1850 matched control subjects
我們結合1522例類風濕關節炎患者和1850配對對照受試者進行病例對照研究,進行了317503個單鏈核苷酸多態性的基因分型。分享友人