細胞毒性反應 的英文怎麼說

中文拼音 [xìbāodúxìngfǎnyīng]
細胞毒性反應 英文
cell-cytotoxic reaction
  • 細 : 形容詞1 （條狀物橫剖面小） thin; slender 2 （顆粒小） in small particles; fine 3 （音量小） thin ...
  • 胞 : Ⅰ名詞1 （胞衣） afterbirth2 （同一個國家或民族的人） fellow countryman; compatriot Ⅱ形容詞（同胞...
  • 毒 : Ⅰ名詞1 （對生物體有害的性質或物質; 毒物） poison; toxin 2 （毒品） drug; narcotics 3 （姓氏） a s...
  • 性 : Ⅰ名詞1 （性格） nature; character; disposition 2 （性能; 性質） property; quality 3 （性別） sex ...
  • 反 : Ⅰ名詞1 （方向相背） reverse side 2 （造反） rebellion 3 （指反革命、反動派） counterrevolutionari...
  • 應 : 應動詞1 （回答） answer; respond to; echo 2 （滿足要求） comply with; grant 3 （順應; 適應） suit...
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  • 毒性 : [藥理學] toxicity; virulence; poisonousness毒性測定 toxicity test
  1. Newcastle disease virus ( ndv ) strain 695, a thermostable nature avirulent strain, were replicated in embryonated chicken eggsand its rna was extracted from allantoic fluid. referred to the reported sequence of f gene, a pair of primers were designed and synthesized. f gene of ndv b95 strain was amplified by rt - pcr, the pcr products were checked by agrose gel electrophoresis and purified by agrose gel fracion method

    利用從國外引進的新城疫熱穩定性天然弱毒b _ （ 95 ）株接種spf雞胚繁殖病毒，經處理后提取病毒的基因組rna ，參考國內外發表的ndv融合蛋白基因序列，設計一對特異性引物，經反轉錄聚合酶鏈式反應（ rt - pcr ）擴增出約1700bp大小的特異性片段，將此片段回收純化后，利用t - a克隆技術將其克隆到pgem - t - easy克隆載體中，再轉化大腸桿菌jm109感受態細胞，轉化后經分子量比較、 pcr鑒定和酶切分析篩選陽性克隆。
  2. In one word, the methods for producing acellulace matrix have not been standardized. in this study, we want to select the best way to produce acellular matrix. we also use immunohistochemical method for detecting the magor heterogenetic antigen a - galactosyl residues ( a - gal ) in acellular matrix

    並應用免疫組化的方法檢測脫細胞后基質的主要異種抗原，用種植實驗觀察異種機體對脫細胞生物基質的組織反應倩況，另在其上種植鼠成纖維細胞以觀察脫細胞生物基質的細胞毒性和細胞相容問題。
  3. Objective the present study was to investigate the effects of endotoxin on capacitation and acrosome reaction ( ar ) of mouse, golden hamster and human sperm, on the sperm - oocyte fusion in mouse, and on the development of 1 - cell, 2 - cell and zona - free 2 - cell mouse embryos in vitro. the purpose was to definite the committed step and the mechanism during in vitro fertilization ( ivf ) on which endotoxin affected, and to distinguish the sensitivities to endotoxin of three developmental systems of mouse embryos. all these data would provide the reference to clinical and laboratory quality control

    目的研究內毒素對小鼠、金黃地鼠及人精子的體外獲能和頂體反應、小鼠精卵結合及小鼠1 -細胞、 2 -細胞和去卵透明帶2 -細胞胚胎體外發育的影響，探討內毒素影響體外受精結局的環節及可能的機制，確定三個體外培養系統對內毒素的敏感性，以期為臨床和實驗室質量控制提供參考。
  4. No, a first gas information molecule discovered in human being, is a typical endothelial - derived relaxant and mediates endothelium - dependent relaxation of blood vessels. in the pathogesis of endotoxin shock vec is one of the major target cells of lps and lps - induced proinflammatory cytokine such as tumor necrosis factor and interlukin 1 and activated. in vec inducible nitric oxide synthase ( inos ) is induced and lead to an increase in production of no, the while endothelial nitric oxide synthase ( enos ) is inhibited and elicit decrease in no formation, both of which are demonstrated to induce the

    在內毒素休克過程中vec是lps及其誘導機體產生的多種促炎細胞因子如tnf 、 il - 1作用的主要靶細胞， vec誘導型一氧化氮合酶（ induciblenitricoxidesynthase ， inos ）激活、 no大量誘生而內皮型一氧化氮合酶（ endothelialnitricoxidesynthase ， enos ）活性被抑制、 no生成障礙，是血管反應性異常變化、血管調節機制紊亂的重要發病環節。
  5. Effect of shenfu injection on hematological toxic reactions induced by vinoreibine plus cisplatin in the treatment of non - small cell lung cancer

    參附註射液對長春瑞賓聯合順鉑方案治療非小細胞肺癌引起血液學毒性反應的影響
  6. Salmonella typhimuriwn, one of the invasive bacterial species, can be attenuated without loss of invasiveness and thus used for delivery of eukaryotic expression vectors into host cells in vivo. the recombinant plasmid containing the target gene is released inside the host cells and gain entry into the nucleus, resulting in expression of encoded antigens and subsequent induction of humoral and cellular immune responses

    沙門氏菌（ salmonellatyphimurium ）是一種較為常見的侵襲性胞內菌，通過基因工程方法減毒后對宿主致病性顯著降低，但仍保留良好的侵襲力，可直接將真核表達質粒攜帶進入動物細胞內表達相應的蛋白而誘導特異性的免疫應答反應。
  7. Because dna vaccine can not only induce protective humoral immunity but also induce strong t cell toxic response, its application on parasital diseases prevention is becoming more and more popular and studies on this area is gradually deepening. dna vaccine has been considered to be a potentially promising approach, which certainly throwed lights on t. s prevention

    它不但可以產生保護性體液免疫，並且可以誘發強烈的細胞毒性t細胞反應，因此普遍認為， dna疫苗極具發展潛力，它的問世將為免疫預防旋毛蟲病提供新的途徑。
  8. No trace of any newly expressed protein band was noticed in supernant as well as in the cells by sds - page, except the verification of the substitution of beta - galactosidase gene ( the lose of galactosidase protein band ), which is a selective marker of the wild - type virus. elisa test results suggested the expression of egf in cells, but not in culture supernant. the quantitative calculation suggested the expressed egf was about 6 - 7 u g ( as egf standard ) per flask ( 2 > < 106 cells ) in the cellular extract

    將重組病毒rbmbacph - egf以10moi感染bmn細胞， 72小時后收集培養細胞和上清；培養上清和經超聲波處理的細胞樣品elisa檢測發現胞內樣品中存在能與egf抗體免疫反應的產物，粗略估計表達量約6 7 g 2 10 ~ 6個細胞（相當于egf標準品） ；重組病毒rbmbacph - egf穿刺接種5齡家蠶幼蟲，每隔24h收集蠶血淋巴，經elisa檢測發現第4天表達量最高，根據egf標準曲線計算蠶血淋巴的表達量約32 g ml ； elisa定性實驗還發現正常蠶血也存在與egf抗體間交叉反應的物質。
  9. Conclusion cck contained in the treated chicken calamus easily undergoes hydrolysis to release mainly some peptides which do not induce obvious toxic effects, suggesting the safe potential applications of cck conduit as a tissue - engineering biometerial

    結論雞羽根角蛋白管可被水解，釋放一些肽類物質，其浸提液對皮膚無致敏作用，皮內刺激反應弱，不引起全身急性毒性癥狀，無細胞毒性。
  10. The security of cp i according to the experiments of mice accute toxicity was evaluated, guinea pig sensitization and cytotoxicity experiment in integer level and cell level. it showed that : the mice had no toxic reaction ; the guinea pig ' s points of injection had no erythema and dropsy ; the cytotoxicity was lower than i class. the results proved that cp i had no poison side effects

    通過小鼠急性毒性試驗、豚鼠致敏試驗、細胞毒性試驗對自製cp進行整體水平和細胞水平的生物安全性評價，觀察期內，小鼠未見異常毒性反應；豚鼠注射點無紅斑及水腫情況；細胞毒性小於級，結果證明本方法制備的cp無毒副作用。
  11. The interesting gene fragment with ecori and noti were amplified by overlapping pcr, which inserted into vector plasmid ppic9k after degisted by ecori and noti, and the recombinant plasmid was transformed into competent dh5cc. positive clones were screened by pcr from the lb plate with amp. digesting analysis resulte shows that the interesting gene were inserted into the vector ppic9k with correct direction

    目的基因經雙酶切后連接載體ppic9k ，然後導入大腸桿菌dh5中，在含氨卞青霉素（ amp ）的lb板上用pcr反應篩選出陽性菌落，雙酶切結果表明目的基因已插入載體中，且方向正確，測序結果進一步證明人巨細胞病毒重組基因表達質粒成功地克隆了目的基因片段。
  12. It is thought that extracellular gsh protects the cells from oxidants released by inflammatory cells whilst intracellular gsh neutralizes the ros produced as a result of normal cell metabolism, as well as detoxifying xenobiotics ( 4 )

    研究者認為細胞外的谷胱甘肽可保戶細胞免受發炎細胞所釋放氧化劑的攻擊，而細胞內的谷胱甘肽可中和正常細胞代謝作用以及共棲生物解毒作用所產生的具反應性氧核素。
  13. Different hosts " response suggested that tumv - sd1 could infect plants of 10 species in 3 families. tumv - sd1 formed pine - wheel inclusion bodies in plant cells. the coat protein of the tumv - sd1 contains 3 components whose estimated molecular weight are 45kd, 38kd and 14kd respectively

    寄主反應特性表明， tumv - sd1 6能侵染3科10種植物， tumv - sd1在寄主細胞內形成風輪狀內含體，外殼蛋白為3組分，分子量分別為45kd 、 38kd和14kd ；提純的病毒粒體為長線條狀。
  14. " high - dose immunosuppression and ahst were performed with acceptable toxicity in a small number of patients with newly diagnosed type 1 dm

    「對小樣本初診1型糖尿病患者進行大劑量免疫抑制和自體非清髓造血幹細胞移植，毒性反應是可容許的。
  15. 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。
  16. Because grow, factor is secrete by normal cell, do not have medicaments already kind noxiousness, also do not have immune reaction, because this is studying mechanism of its physiology action while, some already try out at clinical cure

    由於生長因子是由正常細胞分泌，既無藥物類毒性，也無免疫反應，因此在研究其生理作用機制的同時，有的已試用於臨床治療。
  17. Lee, ys ; yovn, sj. immune response induced by immunization with hepatitis virus core dna isolated from chronic active hepatitis patients j. immunollett. 2001 ， 78 ( 1 ) : 1320

    賈戰生，慢性乙型肝炎病毒攜帶者外周單個核細胞體外抗原誘導的抗體反應j .第四軍醫大學學報， 2000 ， 20 （ 7 ） ： 4547
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