early transcription 中文意思是什麼

early transcription 解釋
早期轉錄
  • early : n 厄利〈姓氏〉。adj 1 早；（果實等）早熟的。2 早日的，及早的。3 早期的，很久以前的，古代的；近日...
  • transcription : n 謄寫，抄寫；轉錄；抄本，繕本，副本；轉寫，翻譯；【音樂】樂曲改作；【無線電】錄音；錄音廣播；（...
  1. Subsequently by taking “ ancient - style poems ” as center, make an exploration into the acceptant condition of traditional poems collection to canons in the preceding dynasties at the time of “ canon ” being established, from a comprehensive view by editor ' s selection basis, arrangement of collection and readers ' acceptability : among which the “ ancient poems collection ” to the superficial succession and meaning transfer of tu ' s poems canon as well as to the polemic interpretation and conclusion of five - character and seven - character poems canon, and the acceptability and misreading of “ poems of transcription in modern style ” in the mid of ching dynasty to “ ancient poems collection ”, all of which are sufficient to verify the alternative of “ canon ” for traditional poems collection that most of them adopt measures of succeeding canon in early times first, then making an increase and reduction ; while the selection of canon takes “ direct variation of polemics ” as premise, followed by a consideration of degree of art values ; it can be the concrete index of trend to make comments on poems on the selection and interpretation of canon for masters of each school

    其後，再由綜觀編者評選基準、選集編排、讀者接受等多重角度，以王士禎《古詩選》為中心來探究常規詩選集在創建典律時，對前代典律的接受狀況：其中由《古詩選》對杜詩典律的表面繼承與意義轉移、對五古、七古詩典律的辨體詮釋與總結，以及清中葉《今體詩鈔》等選集對《古詩選》的接受與誤讀…等，皆足以驗證常規詩選集的典律交替，大多採取先繼承前代、再漸進轉換新典律的作法；且其典律的選立每先以辨體之正變為前提，再考量藝術價值的高低；而於各體名家典律的選擇與詮釋上，則通常可作為其論詩趨向的具體指針。
  2. The results of these early research work showed that rna polymerase transcription was localized in the nucleoli and rna polymerase and in the nucleoplasm

    當時的研究結果顯示： rna聚合酶的轉錄發生在核仁內， rna聚合酶和rna聚合酶的位於核質中。
  3. The results of these early research work showed that rna polymerase iii transcription was localized in the nucleoplasm. however, with the development and the application of new technologies since 1990s, the controversy arose on the transcription sites of rna polymerase iii. in recent years, more and more scientists presumed that rna polymerase iii transcription might not occur in the nucleoplasm but in the nucleoli

    自上個世紀八十年代初期，人們相繼運用細胞化學染色、電鏡放射自顯影等進行研究的結果表明： rna聚合酶的轉錄發生在核質中，但隨著新的研究技術的發展和應用，人們卻發現rna聚合酶的轉錄可能發生在核仁中，從而對早期的研究結果提出了質疑。
  4. Ie protein have multiple functions, such as conversion of the host cell into a metabolically activate states, activation of viral early genes in the early phase, repression of their own transcription. ie 180 proteins can stimulate transcription from both homologous such as the icp4 of hsv ( herpes simplex virus ) and heterologous viral and cellular promoter such as - globe protein

    經分析偽狂犬病病毒立即早期蛋白（ immediate - earlyprotein180 ， ie180 ）的蛋白質結構，發現ie180具有轉錄激活因子的結構特徵，能與類rna聚合酶結合， ie180基因缺失突變體對sv40及cmv啟動子調控作用的研究，是考察ie180能否作為轉錄激活因子應用的關鍵。
  5. The ie 180 mutant combined with two special protein binding - sites and inhibited the promoter transcription. accidentally in the approach showed that the plasimd pcdna3 show as activator to sv40 and cmv early promoter. the result is acquired by instantaneous transinfect

    這說明不同的ie180突變體，對于sv40啟動于這類在轉錄起始位置一側只有一個「 5 』 atcgt 3 』 」特徵蛋白質結合序列的11類基因啟動于，可分別表現出抑制活性與激活性。
  6. The krupple type zinc finger motif found in many transcription factors is thought to be important for nucleic acid binding and / or dimerization. here we have identified and characterized two novel zinc finger genes named znf323 and znf360 using degenerate primers from an early human embryo heart cdna library

    本文利用kr ppel型（ cys _ 2 his _ 2型）鋅指基因順序上的保守特徵，設計簡並引物從人類早期胚胎cdna文庫中初步篩選克隆出四個kr pple型鋅指蛋白新基因，經國際基因命名委員會批準命名為znf323 、 znf360 、 znf359和zfp28 。
  7. The aim of this study was to investigate the differential expression of mpges and cpges in mouse uterus during early pregnancy and its regulation under different conditions by in situ hybridization and immunohistochemistry. mpges expression in the preimplantation mouse embryos was also performed by reverse transcription pcr ( rt - pcr )

    本實驗首先利用原位雜交和免疫細胞化學的方法，檢測小鼠正常妊娠1 - 8天子宮中mpges和cpges的表達情況，並利用假孕、延遲著床和人工誘導蛻膜化等模型研究mpges和cpges的表達及其調節。
  8. In order to get some functional clues from their structures, the upstream regulation region of ndrgl gene and second structure of ndrg2 protein are performed bioinformatics analysis ; we found that there are several binding sequences of some diffirent transcription factors, their functions include regulating tissue - specific gene expression, regulating expression of genes related to growth and early development of cells, besides this, regulating expression of genes under some stimulated conditions, and so on. predict in protein fold classification shows that ndrg2 belongs to alpha / beta hydrolase fold family, and there are high similarity between ndrg2 and epoxide hydrolase from bacteria, this suggests that ndrg2 protein may has enzymatic functions associated with resisting the oxidative stress, maintaining the balance of cell redox potential, involving in the metabolism process of xenobiotics or intracellular toxic molecules

    研究發現呷基因的調控區存在多種轉錄因子結合位點，功能主要涉及組織特異性表達調控，細胞生長發育相關基因的表達調控，刺激反應基因的表達調控等； ndrgz蛋白在結構上屬于a小水解酶類折疊，折疊分類預測表明ndrg2與其中的的細菌環氧化物水解酶的二級結構極為相似，提示ndrgz蛋白具有一定酶活性，可能參與細胞抗氧化應激反應，維持細， an ） armtbffiofbfochmilsyn ） mdafblechmrbfobo4第四軍醫大學碩士學位論文胞內氧還電勢平衡，參與內外源有毒物質的代謝等。
  9. Rna polymerase i synthesizes the three largest rrnas. rna polymerase ii mainly produces mrna encoding proteins and most of sn rnas, and rna polymerase iii makes 5s rrna and trna, as well as a few small nuclear rnas. the transcription sites of the polymerases have been studied since early 1980s

    真核生物細胞核中有三種rna聚合酶，即rna聚合酶、和，它們分別轉錄產生不同的rna ，其中rna聚合酶（ pol ）轉錄合成45srrna前體；聚合酶（ pol ）轉錄合成mrna前體及大多數snrna ；聚合酶（ pol ）轉錄合成5srrna 、 trna和一些小分子rna 。
  10. Rna polymerase synthesizes the three largest rrnas, 5. 8s, 18s and 28s rrna. rna polymerase mainly produces mrna encoding proteins, and rna polymerase makes 5s rrna and trnas, as well as a few small nuclear rnas. the transcription sites of the polymerases have been studied since early 1980s

    在細胞中它們的功能各不相同： rna聚合酶負責催化合成5 . 8s 、 18s和28srrna ， rna聚合酶主要負責mrna的轉錄合成，而rna聚合酶則負責催化5srrna 、 trna 、多數的snrna以及某些病毒基因（如va基因）等的轉錄。
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