骨膜細胞 的英文怎麼說

中文拼音 [gǔmóxìbāo]
骨膜細胞 英文
cells lining bone surfaces
  • 骨 : 骨名詞1 （骨頭） bone2 （物體內部的支架） framework; skeleton 3 （品質; 氣概） character; spirit ...
  • 膜 : 名詞1. [生物學] （像薄皮的組織） membrane 2. （像膜的薄皮） film; thin coating
  • 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...
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  1. The image was obtained by taking multiple exposures through bandpass optical filter sets appropriate for fluorescein, texas red dye and dapi using a 100x plan apochromat objective

    成纖維細胞分化為成軟骨細胞、成膠原細胞和成骨細胞，形成體內的纖維組織、肌腱、腱膜、各種支持組織和粘合組織。
  2. The radiosensitive cells in bone are endosteal cells and epithelial cells on the bone surfaces

    對輻射敏感的細胞是骨內膜細胞和骨表面上皮細胞。
  3. Bone mesenchymal stem cell derived endothelial cells for constructing tissue engineered heart valve and its anti - thrombotic effects

    骨髓間充質幹細胞來源的內皮細胞構建組織工程瓣膜及其抗血栓作用
  4. A complex cytoskeleton of f - actin filaments and microtubules is often present, and appears to control the structure of the cytoplasm, cell movements, and movements of the cytoplasm and conformation of the membranes

    微絲和微管構成的復雜的細胞骨架存在於細胞質中，細胞骨架維持著細胞質的結構，細胞運動，胞質流動以及細胞膜的構象。
  5. Osteopontin enhances migratory ability of cultured aortic adventitial fibroblasts from spontaneously hypertensive rats

    骨橋蛋白增強自發性高血壓大鼠血管外膜成纖維細胞的遷移活性
  6. Because lung cancer cells may have some special hormone ( heterologous hormone ), and antigen enzyme, the role of these substances in the operation of bone joints, a result of bone and joint swelling pain, often involving the tibia, recife, ulnar and radial and bone and joints, often terminal expansion toes were clubbed fingers, x - ray radiography examination showed periosteal proliferation

    由於肺癌細胞可產生某些特殊的內分泌激素（異源性激素） 、抗原和酶，這些物質運轉作用於骨關節部位，而致骨關節腫脹疼痛，常累及脛、腓、尺、橈等骨及關節，指趾末端往往膨大呈杵狀指， x線攝片檢查可見骨膜增生。
  7. Cell compatibility of films is researched firstly, which will make a significant contribution to the using fha films in practice from development. cell cycle, measured by flow cytometer and mtt method, and cell growth curve are used to analyze the impact of material and the immersed medium to the multiplication of osteoblast - cell

    通過mtt法，流式細胞儀測定細胞周期，以及細胞生長曲線的測定，分析研究了fha薄膜材料對成骨細胞增殖生長的影響以及材料的浸提液對細胞增殖的影響，通過細胞相對增殖活性的測定對fha薄膜進行毒性評級。
  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. Result the fresh and freeze - stored fascial chondrocytes were superior to free grafts of chondrocytes in potentiality of formation of new cartilaginous tissue, structure and metabolism of newly formed tissue. relatively good results were also obtained similarly by using fresh autografts of periosteum and cartilage

    結果新鮮和凍存的筋膜軟骨細胞移植在結構、形成新的軟骨組織能力、代謝活性方面均優于游離軟骨細胞移植；新鮮的自體骨膜和軟骨移植同樣可獲得較好的結果。
  10. Electrophysiological characteristics of calcium ion signaling pathways in the whole cell membrane of human mesenchymal stem cells

    人骨髓間充質幹細胞全細胞膜上鈣離子通道的電生理學特性
  11. In vitro culture of human periosteal cells

    人骨膜細胞體外培養的實驗
  12. In this case, mouse bone marrow stem cells grew into cells that produce the cornea protein keratocan

    在這種情況下，老鼠骨髓幹細胞長成能夠產生眼角膜蛋白質的細胞。
  13. Cell adhesion to surface of the substrate is essential to development of the anchorage - dependent cells. only after adhering to surface followed by spreading can cells develop and proliferate. most synthetic polymers used as orthopaedic matrix substitute present hydrophobicity, which may correlates to the low degree of cell attachment. modification with cell adhesion protein / peptides can be benificial to the cell adhesion on polymers and then affect the cell proliferation and differentiation. cell attachment to substrate is primarily mediated by integrins, a widely expressed family of heterodimeric surface receptors. most extrcellular matrix proteins such as fibronectin, osteopontin, collagen type i, bone sialoprotein and vitronectin contain an arg - gly - asp ( rgd ) sequence which is specific to the fixation of cell membrane receptors like integrin. the main aim of this research is to measure, assess adhesion, proliferation of rabbit marrow stromal cells ( mscs ) on the polymers coated by fibronectin, collagen type i or biotie gen, which includes : ( 1 ) biologic characteristics of rabbit mscs were observed by two types of separating method in primary culture. ( 2 ) adhesion, proliferation and differentiation of mscs cultured on polymers coated with biotiegen were assessed. ( 3 ) also, adhesion, proliferation and differentiation of mscs were assessed on plga film or porous plga substrates coated with fibronectin, or collagen type i respectively. ( 4 ) bone formation was observed on the porous plga substrates coated with collagen type i in vivo. this research aims to give new way to make novel synthetic bone with cell adhesion and high bone induction capabilities

    因此將這些蛋白包被、固定到材料表面，觀察骨組織工程種子細胞mscs細胞的粘附、生長特性是本研究的中心環節，並從以下方面進行探討： （ 1 ）採用不同原代細胞分離方法，研究其對mscs細胞的生物學特性影響。 （ 2 ）檢測基因勝肽膠對mscs細胞粘附、增殖及分化的影響。 （ 3 ）分別採用型膠原及纖維粘連蛋白（ fibronectin ， fn ）包被聚乙醇酸-乳酸共聚物（ poly （ 1actide - co - glycolide ） ， plga ）膜及多孔塊型plga材料，觀察細胞在單層或三維培養狀態下，型膠原及fn對mscs細胞粘附、增殖及向成骨細胞分化效應及能力。
  14. The effects of enamel matrix proteins and bone morphogenetic protein 2 on cell proliferation by cultured human periodontal ligament cells

    釉基質蛋白和骨形成蛋白對牙周膜成纖維細胞增殖活性的影響
  15. The effects of enamel matrix proteins and bone morphogenetic protein 2 on cell mineralogical property by cultured human periodontal ligament cells

    釉基質蛋白和骨形成蛋白對牙周膜成纖維細胞礦化能力的影響
  16. Yan - fang wang, tian - qing liu, ke - dong song, xiang - qin li, chun - yu bao, xue - hu ma, large - scale expansion of rabbit marrow - derived mesenchymal stem cells ( mscs ) in rotating wall vessel bioreactor ( rwvb ), the 8th tissue engineering society international annual meeting, 2005, oct. 22 - 25, p235, shanghai, china

    趙虎，劉天慶，宋克東，李香琴，孫相玉，馬學虎.成骨細胞在旋轉壁式中空纖維膜生物反應器內的大規模擴增.第二屆全國化學工程與生物化工年會. 2005年10月，北京
  17. Between the bronchial cartilage at the right and the bronchial lumen filled with mucus at the left is a submucosa widened by smooth muscle hypertrophy, edema, and inflammation ( mainly eosinophils )

    在右側的支氣管軟骨和左側充滿粘液的支氣管腔之間，平滑肌增生，水腫，炎癥（主要是嗜酸性粒細胞）等因素使粘膜下層增厚。
  18. The biomacromolecular layers on the plla membrane surfaces had good stability and good cytocompatibiliry. cells spread very well on the gelatin or collagen coated membranes and had obviously improved adhesion rate, proliferation rate and mtt activity

    軟骨細胞培養結果表明明膠塗層或膠原塗層可明顯提高細胞在plla膜表面的粘附率、增殖率、細胞活性和鋪展性能。
  19. Zo - 2 is localized in the cytoplasmic plaque domain of tight junction. zo - 2 interacts with the integral membrane proteins via its first pdz domain or guk. domain

    Zo 2位於緊密連接處的質膜內表面，一方面與構成緊密連接的跨膜蛋白相互作用，另一方面與細胞骨架發生聯系。
  20. These results are very important for us to further understand the genetic background, biological characteristics, evolutionary rule and the anti - schistosomajaponicum mechanism of microtus fortis at the molecular levels. the specific base changes of the dna fragme nt between the two subspecies are probably correlative with the animal immigration, survival conditions, and species evolution. the cdna library of microtus fortis bone marrow cells was transferred in situ to nylon membrane, which was divided into eight equals ( ga ~ - gh )

    利用已經建立的東方田鼠骨髓細胞質粒cdna文庫，將cdna文庫轉化菌落印跡至尼龍膜，將膜均分成8份（ ga gh ） ，制備基因池，分別培養、提取基因池質粒dna ，通過lipofect - 2000脂質體轉染技術，將基因池質粒dna導入hek293細胞， 48h后收集轉染細胞上清液，即條件培養基。
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