細胞的自主性 的英文怎麼說

中文拼音 [xìbāodezìzhǔxìng]
細胞的自主性 英文
cellular autonomy
  • 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...
  • 的 : 4次方是 The fourth power of 2 is direction
  • 自 : Ⅰ代詞（自己） self; oneself; one s own Ⅱ副詞（自然;當然） certainly; of course; naturally; willin...
  • 性 : Ⅰ名詞1 （性格） nature; character; disposition 2 （性能; 性質） property; quality 3 （性別） sex ...
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  • 自主性 : autonomy自主性交易 autonomous transaction; 自主性專業組織 autonomous professional organization
  • 自主 : 1 （自己做主） act on one s own; be one s own master; decide for oneself; keep the initiative in ...
  1. It is an important that bacteria contaminated vaccine in the biologicals production. we collected 703 samples of cell culture, virus cultivation and harvest which were contaminated by bacteria during poliovaccine production within two years. we checked these samples by bacteriological method and antibiotics sensitivity tests were done. it shows that 1 ) the main contaminated bacteria come from staphylococci, bacilli and streptococci of environment in the poliovaccine production. 2 ） it is effect that antibiotics to contaminated bacteria are doxycycline, albiotic, prescription 2, cefotaxime na salt, gentamycin, neomycin, aureomycin and erythromycin

    在疫苗生產實踐中，細菌污染是影響疫苗質量和產量的關鍵性因素，筆者通過了兩年左右的時間，選取正常生產中零星細菌污染的細胞培養瓶、病毒培養瓶及收毒污染樣品等共703份，進行細菌學檢查，並對造成污染的主要細菌種類進行了各種抗菌藥物的耐藥性實驗，結果表明：我所脊灰疫苗生產中主要的污染威脅來自環境中的葡萄球菌，潛在威脅是桿菌和鏈球菌；強力黴素、林可黴素、配方2 、噻孢黴素鈉鹽、慶大黴素、新黴素、金黴素和紅黴素等抗生素對目前引起污染優勢細菌-葡萄球菌有明顯的抑菌效果，可作為疫苗生產后備抗菌手段參考
  2. Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel

    結果如下：皮下包埋卜周者，無細胞真皮基質漸與周圍組織粘附，顏色由蒼白轉紅；皮下包埋3周者，無細胞真皮基質與周圍組織緊密枯附，盾晰葉辯；術后卜周，包埋的基質面積變化較包埋前無統計學差異o川0引，術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ） 。光鏡下術后卜周，宿主的淋巳組織細胞、成纖維細胞浸入生長，釉附在膠原纖維上，少量血管內皮細胞浸入基質；術后34周，無細胞真皮基質內較多的血管形成，故可認為無細胞真皮基質免疫原性低，能誘導宿主的成纖維細胞、巨噬細胞浸入生長，為一種新型的真皮替代物。第四部分無細胞真皮基質與自體斷層皮片復合移棺的研究， sd大鼠10隻，在其背部卜方造成全厚皮膚缺損的創面
  3. 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
  4. The study on the relationship between iccs and the self - excited contraction of urinary muscle

    樣細胞與逼尿肌自主興奮收縮性的關系探討
  5. Myocardial bioelectric phenomena and their mechanism, the characters of excitation transmission in heart ; the periodicity changes and their characters of myocardial excitability, autorhythmicity and pacemaker of heart ; pumping function of heart and evaluation ; the concept, mechanism and influencing factors of arterial blood pressure ; carotid sinus and aortic arch baroreceptor reflex

    心肌細胞（工作細胞和自律細胞）的生物電現象及其形成的機制，心內興奮傳播的特點；心肌興奮性的周期性變化及其特點，自律性和心臟的起搏點；心臟的泵血功能及其評價；動脈血壓的概念、形成機制、影響因素；頸動脈竇和主動脈弓壓力感受性反射。
  6. The biological characteristics and toxicity of russula subnigricans hongo was studied for the first time from ecology and morphologic characteristics and histology, the orthogonal experiment of the optimum culture condition, the analysis of components, apoptosis of the cells from little white rat liver and kidney induced by extract of russula subnigricans hongo, to the histopathologic changes observation of little white rat liver and kidney through ecological observation, light microscopy and scanning electron microscopy, reversed - phase high performance liquid chromatography, agarose gel electrophoresis, transmission electron micioscopy. the result showed as below : based on ecological observation of russula subnigricans hongo, its ecological environment was investigated in order to simulate its ecological environment when they are cultivated

    利用菌種分離技術、光鏡技術、電鏡技術、高效液相色譜技術、毒理實驗技術、電泳方法等對亞稀褶黑菇（ russulasubnigricanshongo ）的生物學特性和毒性機理進行了研究，主要包括以下內容：亞稀褶黑菇的生態學和組織學研究、菌種分離培養、掃描電鏡觀察、成分分析、粗毒液誘導小自鼠肝腎細胞凋亡，小白鼠中毒后肝腎細胞透射電鏡觀察，研究結果如下： 1
  7. The improvement of culture condition of ivm is essential to achieve better outcome of ivm. during the development of follicles, granulosa cells proliferate and differentiate under fsh control. granulosa cells mediate fsh control on oocyte maturation and secrete several factors to maintain an appropriate rnicroenvironment for oocytes to mature

    卵泡是一個結構和功能單位，其中顆粒細胞是卵泡內主要的體細胞成分，它介導促性腺激素對卵母細胞的調節，同時通過自分泌或旁分泌作用，維持有利於卵母細胞成熟的微環境。
  8. It is also used in clinical trials for treatment of such autoimmune disorders as multiple sclerosis, rheumatoid arthritis, scleroderma, and graft - versus - host disease, a complication that can occur after stem cell transplants

    它也為如多發性硬化、類風濕性關節炎、硬皮病和移植物抗宿主反應的自身免疫的病變的治療被用於臨床實驗對-宿主疾病，在幹細胞移植之後能發生的復雜化。
  9. On the basis of traditional chinese medicine channels and collaterals study and bionics, the e - mini cpu underwear adopt the technology of the digital medical treatment to make especially, the magnetized wave of the e - mini cpu underwear can adjust the endocrine and ultimately stimulate the growth of the breast cell in the milk to make you have the beautiful breast without any side effect occurred by the operation. the magnetized wave repeatedly massage and stimulate on the breast, with promotion the blood circulation in the breast, and providing the sufficient nutrition to the breast to make the breast develop secondly

    E -美人微電腦納米美胸寶主機所產生的生物磁頻波能調節人體內分泌，產生胸部肌肉運動，加速乳房血液循環，刺激卵細胞的促乳素，進而乳素中脂肪細胞的生長和增大，她所產生的磁頻波頻率對乳房產生反復的調節和協助運動，充分調動您自身的生理潛能，促進乳房的血液循環，為乳房提供充足的營養，加強乳房的代謝，讓乳房健康成長刺激乳頭，促使體內產生高水平的荷爾蒙女性激素，激活休眠細胞，啟動乳房組織二次發育。
  10. Using a stringent objectie statistical algorithm to reduce false discoery rates below 5 %, we isolated a panel of 87 genes that represent major focal points of the autonomous response of cancer cells to the abrogation of microtubule dynamics

    用嚴格客觀的統計表格減少假陽性率至5 %以下，我們對一組87個基因（代表著腫瘤細胞自主反應的主要局部位點）進行分離到無微小管動力學存在的水平。
  11. [ note : in neurodegeneration the main aggregates tend to form in other parts of the cell than the lysosome, but there is good evidence that this is a compensatory measure when neurons ' lysosomes stop working properly as a result of the more modest accumulation of lysosomal toxins, so if we fix the lysosome then the non - lysosomal aggregates should disappear naturally

    [附註：在神經性退化中，主要的堆積物往往在細胞的其他部分形成、而不是在溶酶體形成，但有很好的證據表明，這是一種補償措施：當神經原的溶酶體因溶酶體毒素積累到一定程度就停止工作，所以，如果我們修理了溶酶體，那麼非溶酶體的堆積物就會自然消失。
  12. The upr pathway in mammals links with several branches, including the increased transcription of a series of genes that encode folding - related proteins, the ubiquitous down - regulation of protein translation, programmed cell death mediated by chop and degradation of er - related proteins, etc. though somewhat independent, these branches do have multiple connections

    哺乳動物細胞的upr通路涉及與折疊能力相關的一系列基因轉錄上調、蛋白質普啟蒙翻譯下降、 ghop介導的程序性死亡及內質網相關性蛋白降解等多個分支。這些分支雖有一定的自主性，但卻存在著千絲萬縷的聯系，因此其中某個支路上效應成分的改變，就可能會對整個upr通路產生影響，甚至影響細胞的命運。
  13. The basic theory of cellular automata, the ways how algorithms are designed based on cellular automata and the security of the algorithms have been discussed in this thesis

    本文主要對細胞自動機的基本理論、利用細胞自動機構造密碼的各種方式及其安全性進行了研究。
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