after-regeneration 中文意思是什麼

after-regeneration 解釋
伐后更新法
  • after : adv 在後;繼后;后來。 follow after 跟著。 look before and after 瞻前顧后,前思後想。 soon after ...
  • regeneration : n. 1. 再生,新生。2. 悔悟。3. 改造,革新。4. 回收。5. 【化學】交流換熱(法);【物理學】正回授[反饋]放大。
  1. Contains nutrition factors which are extracted repeatedly from herbs ( rcf ), adopts american technology, it will promete metabolism to reactivate your skin sell. it will activize and nourish skin, stimulate their regeneration process, prevent skin from ageing leave supple, whiten, smooth and ever - young complexion, used this product after seven times, you will have perfect skin

    引進美國技術,生物分化提取珍貴細胞再生因子( rcf ) ,其獨特的活化細胞再生功能可加快皮膚的新陳代謝,充分的補足深層肌膚的營養及水份,深度美白肌膚,使皮膚水嫩透白,光滑,富有彈性,只需使用七次,即可重現動人光彩。
  2. The research status of the world diesel exhaust aftertreatment technology is summarized systemicallyo at the same time, the development status and problems about oxygenation catalysis converter and particulate filter are analyzed on the basis of mentioned informations, we bring up a diesel exhaust cleanse system, that adopts the technique course of catalysis conversion combining particulate collection and regeneration the system collects exhaust particulate by means of efficacious filtering material it can oxidize ho co and macromolecule solvable organic via catalyst and diesel oil additive enhanced temperature will partly oxidize collected particulate and ultimately achieve the aim of exhaust reduction, after processing system frame design and trial matching, it ' s detected that the system can surely cleanse gas exhaust and particulate in addition, gas - ejected combustion - supporting regeneration for diesel particulate filter is also researched, we have rudimentarily designed the software and hardware of the g as - ejected combustion - supporting system having processed a series of trials, we discover the rules of the system credibly working these rules demonstrate the right direction for researching gas - ejected combustion - supporting regeneration technology

    本文系統地介紹了國內外柴油機排氣后處理技術的研究現狀,分析了氧化催化轉化器和微粒捕集器的發展現狀及存在的問題,以此為基礎,提出了一種柴油機排氣凈化系統,該系統採用催化轉化與微粒捕集及再生相結合的技術路線,通過過濾材料的有效過濾,將排氣中的微粒進行收集,藉助于催化劑和柴油添加劑使排氣中hc 、 co及高分子可溶性有機物氧化,產生的高溫使得收集到的微粒部分氧化,從而達到降低排放的效果。通過系統結構設計和試驗匹配,實現了對氣體排放物和微粒的凈化。同時,論文中還進行了柴油機微粒捕集器噴氣助燃再生的研究,初步設計了噴氣助燃系統,進行了控制系統軟、硬體的開發,通過正交試驗,摸索出了噴氣助燃系統可靠工作的一般規律,為噴氣助燃再生技術的開發提供了方向。
  3. Morphological study on the nerve fiber regeneration after heterograft by hrp

    法對異種神經移植后再生纖維恢復的形態學研究
  4. Effect of functional neuromuscular stimulation on the recovery of larynx function after regeneration of recurrent laryngeal nerve in canine

    功能性神經肌肉刺激對犬神經再支配喉功能恢復的作用
  5. Nerve regeneration after spinal cord injury review

    脊髓損傷后神經修復的研究進展
  6. The animal experiment is carried out in the first hospital of shanghai through renovating the injured nerve of the rats. four projects are used in this experiment : the conduits coated with pgla, the conduits coated with chitosan, the conduits coated with chitosan adding bridge - yarn and self - nerve migration. after 12 weeks, we observe and analyze the thickness of marrow theca, the diameter of axone, the density of regeneration nerve and then do electromyography and statistics analyzing, finding out that the third conduits have the best recovering effects on the injured nerve, close to the self - nerve migration

    因此我們選用加筋結構神經導管進行動物實驗。本課題動物實驗在上海市第一人民醫院進行,分別通過加筋結構塗pgla導管、加筋結構塗甲殼胺導管、加筋結構塗甲殼胺並加載縫芯線導管和自體神經移植四種方案對大鼠進行損傷神經修復實驗。在術后12周對四種方案再生神經的髓鞘厚度、軸突直徑、數量密度進行觀察分析,並進行肌電圖檢測和統計學分析。
  7. Research development on disinhibition of the regeneration after cns injury

    中樞神經損傷再生修復去抑制作用的研究
  8. In this report, we mainly covered the following aspects of " tissue organ regeneration and replication in situ " : 1 ) procedures of tissue organd regeneration and replication and replication in clnical practice ; 2 ) the discover and existence of potentiald regenerative cell ( prc ) ; 3 ) the proliferation, differentiation and regeneration law of potential law of potential regenerative cells ; 4 ) study procedure on tissue organ regeneration and replication from prcs in vitro based on the model of full skin organ regeneration in situ after extensive in vitro, set up the method and technology of searching life regenerative substance required in tissue organ regeneration and replication in situ. in this study, first, the whole human body is divided into 206 function units, which are the " tissue organ " in regeneration study. then the histology foundation of tissue organ regeneration and replication in situ is set up. in ordre to prove the existence of the potential regenerative cells and their potential baility and function, we established clinical tracking rechnique of skin organ regeneration in situ ; meanwhile, several tissue organ regeneration and replication in vitro models which represent different kinds of runctions were sucessfully set up, with all these techniques and models, we confirmed : 1 ) the existence, function and ability of pptemtoa regenerative cells ; 2 ) the importance of life regenerative substance ; 3 ) the feasibility of tissue organ regeneration and replication in situ ; 4 ) the big value of tissue organ regeneration and replication in situ in life science and medicine progerss. we also showed the possible foreground of capture cancer with this method and technologh. in this report, nearly 200 photographs of several tissue organ regeneration and replication in situ or in vitro demonstrated the whole process of tissue organ and big organ entities regeneration and replication from cells. the results of tissue organ regeneration and replication in situ mainly include : 1 ) whole skin organ regeneration and replication in situ ; 2 ) gastrointestinal mucosa tissue organ regeneration in vitro ; 3 ) hair follicle tissue organ regeneration in situ or in vitro ; 4 ) never tissue organ regeneration in situ ; 5 ) pancreas tissue organ regeneration and replication in vitro ; 5 ) marrow tissue regeneration in vitro ; 6 ) renal glomerulus and tubule tissue organ tugeneraation in vitro ; 7 ) heart muscle regeneration in vitro, etcl. in order to let more and more people know and understand this technology of tissue organd regeneration and replication in situ, herein, for the first time, we publicize the key points of actualizing this technology. also, we publicized the technology procedures and the frame constitute of life substances. we bilieve this is a big contribution to human science

    本研究報告,重點報道了組織器官的原位再生復制的臨床程序,報道了組織潛能再生細胞的發現和存在,以及該細胞的增殖分化和形成組織器官的變化規律.以燒傷后皮膚組織器官的原位再生復制為模型,研究出了體外組織潛能再生細胞復制組織器官的培養方法;以體外組織器官的復制為模型,建立了尋找原位組織器官再生復制所需生命物質的方法和技術.本研究,首先按人體的器官功能,分解為206個功能單位,確立了所復制的人體器官中的組織功能單位為組織器官,從而建立了原位組織器官再生復制的組織學基礎.為了驗證組織潛能再生細胞的再生潛能,建立了皮膚器官原位再生的實體臨床跟蹤技術,同時又建立了能代表有關器官功能類別的代表組織器官的原位和體外復制模型,以多組織器官的成功復制確定潛能再生細胞的作用,確定生命研究再生物質的重要性,確定組織器官原位再生復制的可行性,確定了組織器官原位再生復制的生命科學研究和醫學進步的重大應用價值,同時展示了用此方法和技術攻克癌癥的前景.本研究報告,以近二百幅多個組織器官原位和體外再生復制的實體圖片,展示了潛能再生細胞復制的組織器官和大器官司實體;展示了細胞再生復制器官的全過程.真實的報告了組織器官原位再生復制的成果.所公布的主要成果為:皮膚器官的原位再生復制;胃腸黏膜組織器官的原位和體外再生復制;毛囊組織器官的原位和體外再生復制;神經組織器官的原位復制;胰腺組織器官的體外復制;骨髓組織的體外復制;腎小球小管組織器官的體外復制;心肌的體外復制等.為了讓更多的人學會和掌握組織器官原位再生復制技術,本報告首次公布實施技術的重要環節和技術流程;首次公布了生命再生物質的框架和組成.作者自費研究成果對人類生命科學的一大貢獻
  9. Pre - differentiation and proper partial desiccation of calli before transferred to regeneration medium was found to apparently improve the frequency and quality of plant differentiation. with our optimized culture condition and treatment style, induction frequency of pei ' ai64s and 9311 can be reached 62. 45 % and 85. 30 % respectively and after 3 months of subculture calli can remain high - quality embryogenic state, when high - quality embryogenic calli after two times of subculture were used as acceptor, callus differentiation frequency can arrive at 85. 5 % and 87. 7 % respectively

    採用我們優化后的培養條件與處理方式,培矮64s和9311愈傷組織的誘導頻率分別可達到62 . 45和85 . 30 ;繼代培養時間達三個月左右仍能保持較好的胚性生長狀態;對于繼代兩次胚性生長狀態良好的愈傷組織分化頻率分別可達到85 . 5和87 . 7 。
  10. Change in the concentration and tissue - localization of endogenous iaa during the regeneration after girdling in

    構樹剝皮再生中內源iaa的變化及其組織定位
  11. Change in the concentration and tissue - localization of endogenous iaa during the regeneration after girdling in broussonetia papyrifera vent

    構樹剝皮再生中內源iaa的變化及其組織定位
  12. Contain vitamin e and hydrolyzed pearl, instantly penetrate into deep tissue, powerfully replenish water, activate cells regeneration, fade dull tone with whitening and protecting functions, skin appears white, tender, bright and healthy after use ; pure nature, make skin white, ruddy and glossy

    蘊含維他命e的精華液、珍珠水解液,一經接觸肌膚即能深層滲透,全日強力補充肌膚所需水分,激發細胞再生,抑制膚色暗啞;具有增白和保護肌膚作用,由內向外調理,肌膚煥發白皙、細膩光彩,呈現健康膚色;純凈質感,剔透嬌顏,白里透紅,煥發動人光彩。
  13. The activity of urease is hard to recover entirely with regeneration solution after contacting inhibitors for many times. for this reason, a renewable urease biosensor is highly desired. in chapter 3, a renewable potentiometric urease inhibition biosensor based on self - assembled gold nanoparticles has been developed for the determination of mercury ions

    2 .重金屬離子對脲酶的抑制作用是不可逆的,因此基於對脲酶抑制來檢測汞離子的傳感器在多次與抑制劑接觸后,很難使用再生溶液將脲酶的活性完全恢復,有必要研究一種可更新的脲酶傳感器。
  14. First, after investigation of two original strains " biological characteristics, we studied the main influence factors on protoplasts formation and regeneration in s. mycarofaciens and s. erythreus, and determined the best protoplasts formation and regeneration conditions of two original strains. the former shake - cultured in s " medium at 28 ?, 220r. min ~ ( - 1 ) for 24h, lysised by 3mg / ml lysozyme, keeping warm at 32 ? for 50 ~ 60min, regenerated on r _ ( 5 " ) medium, 28 ? for 5 ~ 6d. the latter used two - step culture, then used img / ml lysozyme keeping warm at 37 ? for ih ; the protoplasts were plated on r5 " regeneration medium at 28 ? for 5d

    首先在對兩親株的生物學特性進行了鑒定后,考察了影響兩親株原生質體形成和再生的主要因素,確定了生米卡鏈黴菌和紅黴素鏈黴菌原生質體形成及再生的最佳條件:前者用s培養基,在28 、 220r . min ~ ( - 1 )培養24h后,用3mg ml的溶菌酶在32恆溫酶解50 60min ,得到的原生質體在乾燥的r5培養基上28倒置培養5 6天,可得到再生率在20左右的再生菌落;後者採用二級菌絲培養,用1mg ml的溶菌酶在37恆溫酶解1h左右,得到的原生質體也在乾燥的r5培養基上28倒置培養5天,即可得到再生率在20左右的再生菌。
  15. Effects of selenium enriched spirulina platensis on antioxidation and regeneration of rat hepatocytes after hepatectomy

    硒螺旋藻對大鼠肝葉切除術后肝細胞再生和抗氧化能力的影響
  16. This paper discussed the material of equipmen t which was used to prepare diethyl oxalate by co coupling - regeneration reactio n wi th the method of weight. the seven kinds of metal material, such as 306, 314l, 316l, zr, ti ( 2 ), ti ( 10 ), 1cr18ni9ti and one kind nonmetal material ( pe ) have been hung in the liquid compound in the regeneration reactor for 1500hours. the experiment ind icative that the corrosion rate of the 306 is the biggest, in the after is 316l, t i ( 10 ), 1cr18ni9ti, zincorium ( zr ), ti ( 2 ), that of pe is lest ; 1cr18ni9ti is the better material of equipment

    沙河市散裝水泥事業起於上世紀九十年代初,經過十多年艱苦曲折的發展,目前我市水泥散裝率達到20 %左右,這一水平還達不到河北省水泥平均散裝水平,與先進省市"發散"水平相比更是相差太遠.我們對發達國家和我國"發散"先進省市的考察和對比分析,可以看出除國家行政推動外,市場有效需求是拉動散裝水泥發展的重要因素
  17. Drug treatment for promoting nerve regeneration after spinal cord injury

    促進脊髓損傷后神經再生的藥物治療
  18. Effect of transforming growth factor beta - 1 on regeneration of nerve after transplantation of fresh nerve allograft

    1對新鮮同種異體神經移植后神經再生的影響
  19. After regeneration experiment, two cultivars, cut flower shanchengzhiguang and japanese xiaohuang, were selected as target materials for genetic transformation in this paper. sag - ipt prolong the senescence of leaves. armed with sag - ipt, transgenic cut flowers with storage resistant, longer shelf life and longer flower period may be obtained

    所選用的外源基因為抑制葉片衰老的sag - ipt基因,以期得到耐貯運、瓶插壽命長的切花菊山城之光和抗衰老、花期長的綠化小菊日本小黃。
  20. The initial activity of pt / tio2 was higher than that of tio2 because it restrained the recombination of electron and hole with supported pt, however the regenerated ability of the pt / tio2 was lower than that of tio2. after the regeneration, the activity could come back to some 60 % of the original activity and the reaction activity declined rapidly. the reason might be that after regeneration on the surface of pt / tio2 the incomplete oxidation of h2s to produce s was enhanced

    Pt tio _ 2催化劑的初活性比單一的tio _ 2催化劑的初活性高,這是因為擔載的貴金屬抑制了電子與空穴的復合,但其再生性能比tio _ 2差,再生后活性只能恢復到初活性的約60 ,且反應活性迅速降低,這可能由於在再生后的pt tio _ 2表面上, h _ 2s通過不完全氧化生成s ~ 0的反應增強所致。
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