等位染色體的 的英文怎麼說

中文拼音 [děngwèirǎnshǎitǐde]
等位染色體的 英文
allelosomal
  • 等 : Ⅰ量詞1 （等級） class; grade; rank 2 （種; 類） kind; sort; type Ⅱ形容詞（程度或數量上相同） equa...
  • 位 : Ⅰ名詞1 （所在或所佔的地方） place; location 2 （職位; 地位） position; post; status 3 （特指皇帝...
  • 染 : Ⅰ動詞1 （用染料著色）dye 2 （感染） catch [contract] （a disease） 3 （沾染） acquire （a bad hab...
  • 色 : 色名詞[口語] （顏色） colour
  • 體 : 體構詞成分。
  • 的 : 4次方是 The fourth power of 2 is direction
  • 染色體 : [生物學] chromosome染色體疾病 chromosomal disorders; 染色體異常 chromosome abnormality
  • 染色 : dye; dyeing; colouration; tintage; tinging; dyschroia; colouring; colour; [半] decoration染色不足...
  1. In this experiment, seedlings of arabidopsis thaliana ( col ) were observed after being treated by verlicillium dahliae ( vd - toxin ), exogenous salicylic acid ( sa ), nitric oxide donor ( snp ) and nitric oxide synthase inhibitor ( nna ), then we investigated the changes of endogenous h2o2 content, the activity of the antioxidant enzymes catalase ( cat, ec : 1. 11. 1. 6 ) and ascorbate peroxidase ( apx, ec : 1. 11. 1. 11 ) and mrna levels of cat3 in different stress conditions, we also identified the localizations of h2o2 and no accumulated in the leaves of arabidopsis

    本實驗研究了棉花黃萎病菌?大麗輪枝菌毒素（ vd - toxin ）與擬南芥幼苗互作反應中外源sa 、 no供體snp 、 no合酶抑制劑nna等不同處理對擬南芥幼苗h _ 2o _ 2含量、 cat和apx活性及cat基因mrna表達量的影響，並對no 、 h _ 2o _ 2的積累部位進行染色檢測。
  2. Various types of techniques have been applied to study the main principle problem. these techniques involve petrography, x - ray diffraction ( xrd ), scanning electron microscope ( sem ), carbon isotope, cathodoluminescence ( cl ), fluid inclusion, and epoxy - resin casts

    論文中所用的分析原理與技術方法包括：層序地層學分析、 x -衍射、掃描電鏡、穩定同位素、陰極發光、流體包裹體與染色鑄體薄片等。
  3. 8p22 of human chromosome is an region with abundant disease - related genes. it is said that it is susceptible loci of hypertension and schizophrenia. the region is also the loci of oncogene and tumor su - pressor gene

    人染色體8p22區是疾病基因富含區域，有報道說該區域是高血壓、精神分裂癥等疾病的易感位點，也是癌基因和抑癌基因的研究熱點。
  4. The purpose of this subject deals with the biological characters of megalobrama skolkovii dybowsky according to the results of convey of nature resource in heilongjiang waters, capture and transportation of brood fish, outer appearance, study of countable and measurable characters and all inner system, analysis of muscle composition, study of chromosome, and discuss the classification status, and also carried out the artificial fertilization

    本課題通過對黑龍江魴進行資源調查、親魚采捕和運輸、外部形態、外部可數及可量性狀和內部各系統的研究、肌肉成分的分析、染色體的研究等實驗，重點研究黑龍江魴的生物學特性，並對黑龍江魴的分類地位進行了探討，同時對黑龍江魴進行了人工繁殖。
  5. The localization and expression of prolactin receptor from inner mongolia alpas cashmere goat were studied by sacpic staining, in situ hybridization and western blotting. samples of skin were taken at interval three months from birth, three months old, six months old, nine months old, ten months old or twelve months old, which correspond to summer, autumn, winter and spring. paraffin sections of hair follicles were stained with sacpic staining and in situ hybridization. the protein of prolatin receptor is abstracted from samples of skin in order to study on expression of prolactin receptor. there are prolactin receptors in outer root sheath, dermal papilla and inner root sheath. the growth of primary follicle is continuous

    本實驗從絨山羊出生后每隔三個月采一次皮樣，共分為4個月齡（ 3 、 6 、 9 、 10或12 ）段，通過製作石蠟切片，原位雜交、染色，並提取皮樣蛋白做westernblotting等實驗研究方法，研究了催乳素受體mrna催乳素受體在不同生長季節的內蒙古阿爾巴斯白絨山羊皮膚毛囊中的定位與表達，染色結果發現阿爾巴斯白絨山羊初級毛囊全年持續生長，次級毛囊的生長情況隨季節而變化，秋冬季生長旺盛，夏季生長緩慢與絨毛生成規律呈正相關。
  6. In chapter 2, the process and fundament of simple ga are introduced. the basic terms are presented firstly, which include the relationships of chromosome, gene, alleles, locus, genetype, phenotype between the biology and ga

    首先介紹遺傳演算法的基本術語，即生物界中染色體、基因、等位基因、基因座、基因型和表現型與遺傳演算法中的對應關系。
  7. Locus ( pl. loci ) the position of a gene on a chromosome. alleles of the same gene occupy the equivalent locus on homologous chromosomes

    基因位點，基因座：基因在染色體上的位置。等位基因位於同源染色體相對應的位點上。
  8. Pseudoallele a mutation in a gene that produces an effect similar to another mutation at a different site in the same gene locus

    擬等位基因：指表型效應上相似，功能密切相關，在染色體上緊密鄰接的基因。
  9. The scc has the following advantages : remarkably reducing the noisy pollution and the worker s labor intensity in construction, deducing the rough surface or segregation because of missing - vibration or excessive - vibration in conventional construction, resolving the quality - defect problems resulting from lacking - vibration in the section of complex shapes and densely - packed reinforcement area. at the same time, large of industrial solid waste such as fly ash and blast furnace slag is utilized in the proportioning of scc. it is helpful in comprehensive utilization of resource and environment protection, so the scc belongs to " green concrete ", it is a branch of hpc which will be developed in the future

    這種混凝土可以顯著降低混凝土施工中的噪音污染；大幅度減輕工人的勞動強度；減少傳統混凝土施工中因漏振或過振造成的麻面或離析；解決了配筋密集、結構復雜部位因振搗不足而造成的質量缺陷問題；同時，由於自密實混凝土在配製中，大量利用粉煤灰、高爐礦渣等工業固體廢棄物，有利於資源的綜合利用和生態環境的保護；從而被譽為「綠色混凝土」 ，是未來混凝土向高性能發展的方向之一。
  10. Thirdly, the new method and nearest - neighbor method, single linear interpolation, bilinear interpolation were coded by vc + +, and a mfc application, bmpinterpolation, was achieved. many kinds of examples were tested using bmpinterpolation, including single color images and true color images ( 24bits ), photos and images after 3d rendering by 3dmax. the comparison between new method and the others indicates that the new method can not only get higher quality of images but also match the requirement of procedure speed

    用該程序可以實現了對單幅位圖文件的讀取和插值放大，通過單色和彩色圖像、照片圖像、三維渲染圖像等放大處理算例的檢驗，說明了本文的方法和程序是成功有效的，新演算法明顯優于幾種簡單插值放大方法的輪廓清晰度，且具有很好的快速性，兼顧了自動立體鏡三維顯示的快速性和清晰度要求。
  11. In the laboratory experiment part, human peripheral blood, cultured cells and icr mice were study objects. the changes of mitotic chromosome numbers were measured by human metaphase chromosome counts and statistic analyzed used x2 - test. the changes of meiotic chromosome numbers were measured by mice one - cell zygote chromosome counts and statistic analyzed usedx2 - test. the effects of low dose ionizing radiation on the expression of topoisomerase ii were measured by immunocytochemistry, western blot and rt - pcr

    流行病學結果顯示長期小劑量輻射接觸與染色體不分離呈正相關，為進一步在細胞遺傳學和分子生物學方面研究小劑量電離輻射與染色體不分離關系及其機制，本課題第二部分以外周血、培養細胞、 icr小鼠為研究對象，用外周血染色體計數和單細胞受精卵染色體計數的方法研究小劑量輻射和拓撲異構酶復旦大學2000級博士生學位論文11a抑制劑及其二者的協同效應對有絲分裂和減數分裂染色體不分離的影響，用免疫細胞化學染色、 westernblot 、 rt pcr等方法研究了電離輻射引起拓撲異構酶a表達變化。
  12. Although the above example shows a simple relationship between two alleles located at one gene locus, coat color in dogs is ultimately quite complicated and not fully understood

    盡管上述例子顯示了在（染色體上）同一個基因位置的等位基因的簡單關系，但最終決定狗的被毛顏色（的因素）是很復雜的，尚不能（為我們所）完全理解。
  13. In the second trial, this modified discontinuous percoll gradient centrifugation method was introduced to isolate spermatids from the semen of fifteen male infertile patients. then the effect was identified by wright - giemsa stain, flow cytometry analysis, immunocytochemistry and fluorescence in situ hybridization ( fish ). similary, the 22 % percoll fraction contained mostly haploid cells [ ( 91. 85 ? 5. 18 ) % ] ( p < 0. 005 ) and the mean density in this fraction was ( 1. 010 ? 0. 786 ) x 105 / ml

    C法，對15例各種類型不育患者的精液細胞進行分離，並利用瑞姬染色法、流式細胞術、免疫細胞化學和熒光原位雜交oisffi等方法，從細胞形態特徵、 dna倍體、細胞表面標i己與分化抗原，以及原位雜交信號的數目和位置結合細胞核特有的形態等方面加以鑒定。
  14. Genomic imprinting refers to parent - of - origin - dependent gene expression. the presence of imprinted gene can cause cells with a full parental complement of functional autosomal genes to specifically express one allele but not the other, resulting in monoalielic expression of imprinted loci

    基因組印記是指一種依賴于親本的基因表達形式，它導致常染色體上的功能基因單一表達一個等位基因而不表達另一個等位基因，造成印記位點的單等位基因表達。
  15. My period is in all the time ahead of schedule. 3 day 5 days sometimes fast half month such shifting to an earlier date

    引起月經顏色發黑的原因很多，子宮位置異常、子宮內膜感染、體內激素水平紊亂等，建議到醫院婦科進行相關檢查，明確診斷，對癥治療正常的月經多為暗紅色。
  16. In 2001, wilson and his colleagues cloned another two members - human wnk1 gene and wnk4 gene which were located on chromosome 12 and 17, respectively. the two genes are disease - causing genes responsible for a mendelian hypertension. the disease - causing mutations are the large deletions in the first intron in wnk1 gene, causing increased expression in leukocytes

    2001年， wilson等克隆了此家族的另兩個成員? ?人的wnk1和wnk4基因，分別位於12號和17號染色體，這兩個基因是一種孟德爾遺傳型高血壓病的致病基因，致病突變分別是wnk1基因第一內含子的大片段缺失，導致患者白細胞的基因表達量提高5倍左右。
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