生體膜重建 的英文怎麼說

中文拼音 [shēngzhòngjiàn]
生體膜重建 英文
reconstitution of biomembrane
  • : Ⅰ動詞1 (生育; 生殖) give birth to; bear 2 (出生) be born 3 (生長) grow 4 (生存; 活) live;...
  • : 體構詞成分。
  • : 名詞1. [生物學] (像薄皮的組織) membrane 2. (像膜的薄皮) film; thin coating
  • : 重Ⅰ名詞(重量; 分量) weight Ⅱ動詞(重視) lay [place put] stress on; place value upon; attach im...
  • : Ⅰ動詞1 (建築) build; construct; erect 2 (建立; 設立; 成立) establish; set up; found 3 (提出;...
  • 重建 : 1. rebuild; reconstruct; reestablish; rehabilitate 2. reestablishment; reconstruction
  1. Almost one - third of all proteases can be classified as serine proteases, including complement subcomponent clr / cls, mannose - associated serine proteases ( masps ), ovochymase, spermadhesin, type ii transmembrane serine proteases ( ttsps ) etc. these proteins are involved in diverse biological processes, including developmental processes such as complement activation, ovulation, fertilization, tissue remodeling, cellular migration, cancer invasion and metastasis, intestinal digestion, embryogenesis, or organogenesis

    絲氨酸蛋白酶( serineprotease )是機要的酶分子之一,約占機蛋白酶的三分之一,我們較熟知的絲氨酸蛋白酶就包括補組分c1r c1s 、甘露糖結合絲氨酸蛋白酶、 ovochymase 、 spermadhesin和型跨絲氨酸蛋白酶等,它們參與了補活化、排卵、授精、組織、細胞遷移、腫瘤浸潤和轉移、消化、胚胎發育、器官形成等多項理功能。
  2. According to the fact that the basic features of apalmprint, including principal lines, wrinkles and ridges, havedifferent resolutions, in this paper we analyze palmprints using amulti - resolution method and define a novel palmprint feature, whichcalled wavelet energy feature, based on the wavelet transform. wef can reflect the wavelet energy distribution of the principal lines, wrinkles and ridges in different directions at different resolutions scales, thus it can efficiently characterize palmprints. this paperalso analyses the discriminabilities of each level wef and, according to these discriminabilities, chooses a suitable weight for each levelto compute the weighted city block distance for recognition. theexperimental results show that the order of the discriminabilities ofeach level wef, from strong to weak, is the 4th, 3rd, 5th, 2nd and 1stlevel

    作為對現有人物特徵識別技術的要補充,掌紋識別有著其獨特的優點:掌紋比指紋含有更多的可區分信息掌紋採集設備的價格比虹採集設備的價格要低廉得多掌紋特徵比簽名特徵更為穩定掌紋識別可獲得比人臉識別更高的識別精度掌紋含有獨特的線特徵包括主線和皺褶,這些線特徵具有很強的區分能力,並可以在低解析度圖像中提取出來可以將手掌上的各種特徵融合在一起立一個高精度的物識別系統等。
  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,點報道了組織器官的原位再復制的臨床程序,報道了組織潛能再細胞的發現和存在,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復制為模型,研究出了外組織潛能再細胞復制組織器官的培養方法;以外組織器官的復制為模型,立了尋找原位組織器官再復制所需命物質的方法和技術.本研究,首先按人的器官功能,分解為206個功能單位,確立了所復制的人器官中的組織功能單位為組織器官,從而立了原位組織器官再復制的組織學基礎.為了驗證組織潛能再細胞的再潛能,立了皮膚器官原位再的實臨床跟蹤技術,同時又立了能代表有關器官功能類別的代表組織器官的原位和外復制模型,以多組織器官的成功復制確定潛能再細胞的作用,確定命研究再物質的要性,確定組織器官原位再復制的可行性,確定了組織器官原位再復制的命科學研究和醫學進步的大應用價值,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外再復制的實圖片,展示了潛能再細胞復制的組織器官和大器官司實;展示了細胞再復制器官的全過程.真實的報告了組織器官原位再復制的成果.所公布的主要成果為:皮膚器官的原位再復制;胃腸黏組織器官的原位和外再復制;毛囊組織器官的原位和外再復制;神經組織器官的原位復制;胰腺組織器官的外復制;骨髓組織的外復制;腎小球小管組織器官的外復制;心肌的外復制等.為了讓更多的人學會和掌握組織器官原位再復制技術,本報告首次公布實施技術的要環節和技術流程;首次公布了命再物質的框架和組成.作者自費研究成果對人類命科學的一大貢獻
  4. Tianwei wood industry company has competely adopted advanced equipment and machinery of china and estalished strict quality control and management systeml. the " rose " brand series products of birch board. veneer and construction laminated board produced by this company with its advancd and precise equipment and testing devices are excellent in quality and wide in application. along wide in application, along with its continuous development, the company has put larger investments in quality control and technologies of producion so that its all kinds of products have won huge potentials to occupy the markets an have been well received by all the customers

    天威木業公司全部採用國內先進的機器設備,立嚴格的質量管理系;應用精密的儀器檢測產的「玫瑰」牌系列楊、樺木,膠合板及高檔築覆板,質量上承,用途廣泛,隨著公司的不斷發展,對板材質量,科技加大了投入,為各類產品贏得市場,搶占商機創造了巨大的潛力,得到了廣大消費者的厚愛,產品原暢銷于廣州、慶、北京、上海、及全國個大城市,自2002年以來已經全部實現出口日本、韓國、中東及歐美等國家和地區,取得了世界各國廣泛的贊譽和認可。
  5. Abstract : plant responses to salt stress via a complex mechanism, including sensing and transducing the stress signal, activating the transcription factors and the corresponding metabolizing genes. since the whole mechanism is still unclear, this review emphasize the biochemical events during the plant adaptation to salt stress referring to an index of importance : the homeostasis in cytoplasm, the biosynthesis of osmolytes and the transport of water. most of these biochemical events were elucidated by study of halophyte and salt - sensitive mutations, also many important genes involved were cloned and used to generate stress - tolerance phenotypes in transgenic plants. on the other hand, about the molecular mechanism in signal transduction, the research of arabidopsis mutations and yeast functional complementation provided helpful traces but not full pathway

    摘要植物對鹽脅迫的耐受反應是個復雜的過程,在分子水平上它包括對外界鹽信號的感應和傳遞,特異轉錄因子的激活和下游控制化應答的效應基因的表達.在化應答中,本文著討論負責維持和離子平衡的轉運蛋白、滲調劑的物合成和功能及水分控制.這些化應答最終使得液泡中離子濃度升高和滲調劑在胞質中積累.近年來,通過對各種鹽植物或鹽敏感突變株的研究,闡明了許多鹽應答的離子轉運途徑、水通道和物種特異的滲調劑代謝途徑,克隆了其相關基因並能在轉基因淡水植物中產耐鹽表型;另一方面,在擬南芥突變及利用酵母鹽敏感突變株功能互補篩選得到一些編碼信號傳遞蛋白的基因,這些都有助於闡明植物鹽脅迫應答的分子機制。
  6. Mutated plasmid was transformed into e. coli tg1 cells to produce engineered peptide, then the peptide was purified by cm sepharose ion - exchange column. in vitro bactericidal assay and drug withdrawal were used to identify the bioactivity of the engineered peptide. the planar lipid bilayer membrane was used to assay the electrophysiology of the engineered peptide. toxicity studies on mammalian cells were used to assay the toxicity of the engineered peptide

    組質粒轉化入大腸桿菌tgi工程菌中,產構的工程多膚,離子交換純化后獲得工程多膚初步純化產物,外抗菌試驗、藥物撤離試驗檢測工程多膚的抗菌活性,在人工脂質上測定其形成離子通道的特性以初步研究抗菌機理, ?並觀察其對真核細胞的毒性作用。
  7. Using the microwave selective heating property for materials, by setup equivalent equation, and first time inducing the electromagnetic field perturbation theory to the design of heating materials for substrate in mpcvd, three temperature distribution modes were established, including temperature distribution comprehensive mode of inhomogeneous plasma, temperature distribution composite mode of composite substrate materials, temperature distribution perturbation mode of composite materials, which ii provided an whole new technology route to the design of substrate heating system in mpcvd and guided the preparation of heating materials for substrate. and then the heating materials for substrate were designed and optimized to obtain large area homogeneous temperature distribution even larger than substrate holder ' s diameter. as an important part, this thesis researched the nucleation and growth of diamond films in mpcvd, systematically researched the effects of substrate pretreatment, methane concentration, deposition pressure and substrate temperature etc experimental technologic parameters on diamond films " quality on ( 100 ) single crystal silicon substrate in the process of mpcvd, characterized the films qualities in laser raman spectra ( raman ), x - ray diffraction ( xrd ), scanning electron microscopy ( sem ), infrared transmission spectra ( ir ), atomic force microscopy ( afm ), determined the optimum parameters for mpcvd high quality diamond in the mpcvd - 4 mode system

    該系統可通過沉積參數的精確控制,以控制沉積過程,減少金剛石長過程中的缺陷,並採用光纖光譜儀檢測分析等離子的可見光光譜以監測微波等離化學氣相沉積過程;利用微波對材料的選擇加熱特性,通過構造等效方程,並首次將電磁場攝動理論引入到mpcvd的基片加熱材料的設計中,立了非均勻等離子溫度場綜合模型、復合介質基片材料的復合溫度場模型及復合介質材料溫度場攝動模型,為mpcvd的基片加熱系統設計提供了一條全新的技術路線以指導基片加熱材料的制備,並對基片加熱材料進行了設計和優選,以獲取大面積均勻的溫度場區,甚至獲得大於基片臺尺寸的均勻溫度區;作為研究點之一,開展了微波等離化學氣相沉積金剛石的成核與長研究,系統地研究了在( 100 )單晶硅基片上mpcvd沉積金剛石的實驗過程中,基片預處理、甲烷濃度、沉積氣壓、基溫度等不同實驗工藝參數對金剛石薄質量的影響,分別用raman光譜、 x射線衍射( xrd ) 、掃描電鏡( sem ) 、紅外透射光譜( ir ) 、原子力顯微鏡( afm )對薄進行了表徵,確立了該系統上mpcvd金剛石的最佳的實驗工藝參數。
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