能抑制劑 的英文怎麼說

中文拼音 [néngyìzhìjì]
能抑制劑 英文
nassa
  • 能 : 能名詞（姓氏） a surname
  • 抑 : Ⅰ動詞（向下按; 壓制） restrain; repress; curb Ⅱ連詞[書面語]1 （表示抉擇） or 2 （表示轉折） but3 ...
  • 制 : Ⅰ動詞1 （製造） make; manufacture 2 （擬訂; 規定） draw up; establish 3 （用強力約束; 限定; 管束...
  • 劑 : Ⅰ名詞1 （藥劑; 制劑） a pharmaceutical or other chemical preparation 2 （某些有化學作用的物品） a...
  • 抑制 : 1 （控制） restrain; control; check; hold up; curb; stop; repress; bridle; choke; prehension; sup...
  1. Clay coats can be particularly important as inhibitors of later quartz cementation.

    粘土包殼作為石英晚期膠結作用的抑制劑可能是特別重要的。
  2. After careful studying their relative importance to immune response and the possibility of the match, seventeen sequences of interest were selected for further experiment, including estss analogous to 11. 5kd antibacterial peptide, lysozyme, serine protease and its inhibitor, lectin, antifreeze protein, et al. primers designed according to the sequences were used to amplify the corresponding estss from both blood and cephalothorax cdna library

    在仔細分析了它們在免疫系統中的重要性和在對蝦中出現的可能性之後，從中選出了17條可能編碼抗菌肽，溶菌酶，凝集素、絲氨酸蛋白酶及其抑制劑，抗凍蛋白等蛋白質的序列，以此為依據設計引物，在中國對蝦的血液和頭胸部cdna文庫中擴增相應的序列。
  3. When the inhibitors existing, the ways that the electrons enter the electron transport chain coupling with the sulfide - stimulate atp production show significantly tissue - specific characters and corresponded with the tissues " physiological function

    當抑制劑存在時，其相關的電子傳遞方式具有顯著的組織特異性，並與其生理功能相對應。
  4. Using the mouse fetal ovary serum - free culture model, fetal ovaries from 14 day post coitus ( 14 dpc ) mouse were cultured, and treated by ay9944 - a - 7, nystatin and rs - 21745. the results showed that 0. 025, 0. 0625 and 0. 125 um ay9944 - a - 7 or 25, 50 and 75 iu / ml nystatin increased the total number of follicles per ovary significantly ; however, ay9944 - a - 7 and nystatin at the same doses could n ' t cause the same effect on the number of growing follicles and the average diameter of five largest follicles per ovary. 50 u. m rs - 21745 decreased the total number of follicles, the number of growing follicles and diameter of follicles per ovary significantly after 48 h

    首先利用小鼠胚胎卵巢的體外無血清培養模型，培養妊娠14天（ 14daypost - coitus ， 14dpc ）小鼠胚胎卵巢，分別添加能促進mas積累的ay9944 ，制黴菌素，和能抑制mas產生的rs - 21745進行處理，結果表明： 0 . 025 、 0 . 0625利0 . 125 m的ay9944 - a - 7與25 、 50和75iu ml的制黴菌素能顯著提高卵巢中形成卵泡的總數量，但是對生長卵泡數和卵泡直徑的作用不同；而mas合成抑制劑rs - 21745能夠顯著降低形成卵泡的總數量。
  5. In this thesis, the development of emulsion polymerization theory and related new technologies are comprehensively reviewed, and the synthetic technologies of acrylate latex modified by organosilicon both at home and abroad are also reviewed. based on the current development and research in this field, attentions of this study are focused on three ways for preparing novel acrylate latexes modified by organosilicons, that is, 1 ) the acrylate monomers are copolymerized with unsaturated silicons by emulsion copolymerization ; 2 ) a new latex with microphase separation morphology is synthesized, which shows a core - shell structure character ; 3 ) soap - free polymerization is explored for preparing a higher - performance latex using an unsaturated silicon monomer, different acrylates and a reactive emulsifier. by using techniques of delaying addition of organosilicon monomer and a hydrolysis inhibitor, the hydrolysis and condensation of 3 - ( trimethoxysilyl ) propyl methacrylate during polymerization can be effectively prevented, as a result, organosilicon content in the macromolecular chain is increased

    同時採用有機硅單體延遲滴加及添加水解抑制劑等技術，有效防止了-甲基丙烯酰氧基丙基三甲氧基硅烷在乳液聚合過程中的過渡水解及縮合反應，提高了聚合物大分子鏈中有機硅鏈節的含量；利用紅外光譜與差示掃描量熱儀對產物分子結構進行了表徵，並通過對共聚產物力學和吸水率的測試，證實了本研究所制備的有機硅改性丙烯酸酯共聚物具有比純丙烯酸酯聚合物更優良的力學及耐水性能；從分子設計角度出發，利用醇解反應合成出水解、縮合反應速率較慢的兩種新型不飽和有機硅單體： ?甲基丙烯酰氧基丙基三乙氧基硅烷和?甲基丙烯酰氧基丙基三異丙氧基硅烷；利用核磁共振對新型硅烷單體結構進行了證實；研究表明利用新型硅烷單體可以制備出高硅烷含量的有機硅改性丙烯酸酯乳液，且其聚合產物具有較高的力學及耐水性能。
  6. We showed here that axudl mrna expression was elevated by tgf - 1 treatment in a time and dose - dependent manner in hepg2 hepatoma cells and spc - a1 lung carcinomas cells, and also indicated that de novo protein synthesis was required for this response using the protein synthesis inhibitor cycloheximide, suggesting that axudl is a primary target of tgf - signalling

    在hepg2和spc - a1細胞中， tgf - 1能明顯誘導這兩種細胞中的axud1基因的表達，而且表現出時間和濃度的依賴效應。同時，利用第一軍醫大學博士學位論文蛋白質合成的特異抑制劑還發現， tgf一pl誘導的axudl基因的表達過程需要新的蛋白質的合成，提示axudl基因是tgf一p信號通路的一個主要靶分子。
  7. Inhibition by zn2 + and mn2 + additive, and almost 100 % of t he activity was inhibited under their physiologically significant concentrations. these results suggest that the protease is possibly regulated by divalent cations in vivo

    蛋白酶的活性受到某些二價金屬陽離于的抑制，比如zn訃、 mg卜、 hg熒光發射光譜結果顯示，在不同的抑制劑作用下，蛋白酶的高級構象可能發生了較大變化。
  8. They are pkc, pka, mek1 in erk pathway, mekk1 in sapk / jnk, p38 in p38 pathway, the three latter pathways all belong to the map kiiiase pathway. the inhibition of pkc decreases the proliferation after the il - 16 treatments, which hint its role in proliferation signal transduction

    結果表明，加入pkc的抑制劑，強烈抑制了所有濃度16處理下細胞的增殖，暗示pkc在u一16與cd4結合后，可能傳遞了增殖相關信號，它的存在是jllrk盯細胞的生長增殖必須的。
  9. The expansion agents can only make up the shrinkage to some extent, and the compensation effects would be reduced when the retardener and fly - ash are used. the expansion agents are not panaceas to avoid the shrinkage cracking as expansion can also reduce the concrete soundness. under bad curing condition, the polypropylene fibrillated film fiber can improve concrete ' s anti - crarking property, while the nominal steels have very unobvious effects. to reduce the concrete shrinkage thus avoid the cracking, the former factors must all be taken into account in concrete proportion design to develop sound concrete

    研究結果表明，水泥的品種和用量是影響混凝土收縮值的主要因素之一，當混凝土中水泥用量超過470kg / m ~ 3時，混凝土的收縮值超過400 10 ~ （ - 6 ） ，在約束狀態下存在高開裂風險；採用細砂使混凝土單位用水量顯著提高，收縮值也大幅增加；優質粉煤灰總體上能抑制混凝土的收縮，以超量方式摻入其抑制作用更加明顯，但粉煤灰混凝土早期的粘聚性較差，應注意養護，以免失水產生龜裂；早強減水劑和緩凝減水劑都會使混凝土收縮值增加；膨脹劑只能補償混凝土部分收縮，同時受緩凝劑和粉煤灰的抑制，而且膨脹使混凝土的體積安定性增加了不確定因素，膨脹劑不是解決混凝土收縮裂縫的良方。
  10. On the conventional whole cell patch clamp mode. howevef, under the perforated whole cell patch clamp mode, l00 ll m snp caused a efficient increase in ik (. ) by 20 ' 2 % t4. 5 % at 60mv 4 - ap l0 mm, a kind of selective inhibiter of delayed rectifier potassium current [ ik ( v ) ], can not inhibit the snp - induced increase of ik ( c. )

    應用相同的刺激模式，一在傳統全細胞模式下s pnovm 0卜m于m00vm對ik （ c一尤影啊… o仍）然而在穿孔模式下當細胞膜去極化至均0 v時， 1皿卜m p可明顯增加人0川達zo二士牛5 … 8廠選擇性延遲整流型鉀電流阻斷劑10mm個ap不能抑制snp對ik （ c 。
  11. Inhibitors of cyp51, such as azalanstat ( rs - 2i607 ) and rs - 2i745, could inhibit the synthesis of ff - mas to decrease the accumulation of ff - mas. inhibitor of a14 - reductase, such as ay9944 - a - 7, could inhibit the metabolism of ff - mas to increase the accumulation of ff - mas ; and some other reagents, such as nystatin, could combine with the downstream intermediate in the cholesterol biosynthesis pathway to accumulate mas. in this study, we investigated the role of mas by using these reagents to change the level of endogenous ff - mas

    抑制cyp51酶的抑制劑，如azalanstat （ rs - 21607 ）和rs - 21745等，均能抑制mas的合成，降低mas的積累；而抑制14 -還原酶的抑制劑，如ay9944 - a - 7等，能抑制ff - mas向t - mas的轉化而造成ff - mas的積累；還有一些物質，如制黴菌素，能阻止mas向下游的代謝而造成其積累，本文主要通過應用這些物質降低、或增加組織細胞中內源性mas的積累，來研究mas的作用。
  12. Inhibitors and promoters may affect the rate of oxidation.

    抑制劑和促進劑能影響氧化速率。
  13. 1 ) the synthesis and structural characterization of 5, 10, 15 - tris ( penta - fluorophenyl ) corrole and its corresponding [ 5, 10, 15 - tris ( pentafluorophenyl ) corrolato ] manganese ( iii ) ; 2 ) the synthesis and structural characterization of series of porphyrin and metalloporphyrins as follows : chloro [ 5, 10, 15, 20 - tetra ( p - methyl - phenyl ) - porphinato ] manganese ( iii ), chloro [ 5, 10, 15, 20 - tetra ( p - methyl - phenyl ) - porphinato ] iron ( iii ), [ 5, 10, 15, 20 - tetra ( p - methyl - phenyl ) - porphinato ] copper ( ) and - oxo - bis [ 5, 10, 15, 20 - tetra ( p - methyl - phenyl ) - porphinatomanganese ( iii ) ]. 2. in the third charpter, a highly selected silver electrode based on 5, 10, 15 - tris ( pentafluorophenyl ) corrole has been prepared, and its response was compared with that of metallo corrole counterpart and 5, 10, 15, 20 - tetra ( phenyl ) porphyrin

    3 、制備了以-氧-雙（ 5 ， 10 ， 15 ， 20 -四（對甲基苯基） ）錳卟啉載體的鉬酸根選擇性電極，並與5 ， 10 ， 15 ， 20 -四（對甲基苯基）鐵卟啉、 5 ， 10 ， 15 ， 20 -四（對甲基苯基）錳卟啉、 5 ， 10 ， 15 ， 20 -四（對甲基苯基）銅卟啉電極的響應性能進行了比較，對電極的膜組份進行了優化，並分別考查了電極的選擇性、 ph值影響、穩定性和壽命等，並將該電極應用於腐蝕抑制劑中鉬酸根的測定。
  14. Among antihypertensive measures, blockade of the raas by means of ace inhibitors or angiotensin ii receptor antagonists recently emerged as a potentially polyvalent approach, not only for treating hypertension and reducing cardiovascular events, but also to prevent or reduce albuminuria, counteract diabetic nephropathy and lower the occurrence of new type 2 diabetes in individuals at risk

    在抗高血壓藥物治療中，通過用ace抑制劑或血管緊張素受體拮抗劑可阻滯腎素-血管緊張素-醛固酮系統激活，最近其可作為一種潛在多能的治療方法，不僅可治療高血壓和減少心血管事件，也能夠預防或減少蛋白尿，阻止糖尿病性腎病變，並使新糖尿病患者發生風險性降得更低。
  15. Would you like to outlook the direct rennin inhibition in the future

    您能否展望這種腎素抑制劑的未來應用前景？
  16. Vanadate, a potent ptpase inhibitor, locks adipocyte differentiation at an early stage in the program and leds to the accumulation of p - c - crkii, a phosphotyrosyl protein that is a substrate for ptpase ha2

    研究發現一種強烈的磷酸酯酶抑制劑- -釩酸鈉能夠作用於脂肪細胞的分化早期過程從而抑制其分化，並使一種ptpha2的底物即酪氨酸磷酸化的蛋白質p - c - crkii累積。
  17. The combination of meja and fc did not show significant additive effect on enzyme activity. 3. phosphorylation and dephosphorlation of pm h ^ - atpase after treatments of meja and fc 1 ) in vitro, phosphatase inhibitors, okadaic acid and cantharidin, enhanced meja - induced increase of the enzyme activity to 60 % and 50 %, respectively

    Tllrase過程中可能發生的磷酸化和去磷酸化作用1 ）磷酸酶抑制劑斑螫素、崗田酸可以增強meja對酶的刺激作用，崗田酸的效應較強，而斑鰲素的作用略弱，增幅分別為60和50左右。
  18. H2o2 was cytochemically detected in the cells of epidermal hair and the cell wall of vascular parenchyma cell. cat and apx were the two major h2o2 - scavenging enzymes in plants. when seedlings of arabidopsis thaliana were treated by vd - toxin, the activity of cat and cat3 mrna level were decreased after sa treatment

    外源sa 、 no供體處理擬南芥幼苗均能誘導h _ 2o _ 2的積累， no供體的誘導作用最強； no合酶抑制劑處理則未表現出h _ 2o _ 2含量的增強： h _ 2o _ 2的積累部位主要在葉片的表皮毛和維管束組織。
  19. The patch clamp experiment : the cell - attached and inside - out configurations of the patch - clamp techniques were used to investigate single channel properties of nmd a receptors in the actuely dissociated neurons of the marginal division in the rat striatum, recording the current amplitude. long / short term opening / closing times indexes and the effects of incitants and agonists of the nmd a receptors on those parameters. we find that two types of conductance of 42ps and 20ps were recorded, the 42ps was the advantaged conductance

    本研究是在本實驗室以前研究的基礎上，通過膜片鉗（ pachclamp ）觀測sd （ sprague - dawley ， sd ）的mrd上nmda受體通道的電生理特性；繼而對青壯年sd大鼠的mrd 、海馬進行毀損並腹腔注射nmda受體阻滯劑ktm （ ketamine ， ktm ） ，觀察其對大鼠學習記憶能力的影響：對于學習記憶能力下降的老年鼠進一步做顱內定位注射nmda受體激動劑與抑制劑，觀察其在特定部位的作用；最後，應用fmri （ functionalmagneticresonanceimaging ; fmri ）對注射ktm的志願者做學習記憶與痛覺的對比觀察。
  20. Secondly, analysis of peroxidase isoenzyme with polyacrylamidedel electrophoresis for was performed in order to investigate the changes of gene expression under sound stimulation. it could be seen from electrophoresis gel that each group had 6 enzyme bands. new enzyme band in pod electrophoretogram was n ' t detected for stressed groups

    此外，在部分實驗組的培養基中加入不同濃度的蛋白質合成抑制劑環己亞胺酮（ chm ）后發現， pod和cat的活性有所降低，暗示著聲波處理使保護酶活性升高的原因可能是聲波處理促進了細胞內酶的合成。
分享友人
分享到 Line

分享到臉書