骨膜增生 的英文怎麼說

中文拼音 [zēngshēng]
骨膜增生 英文
periosteal proliferation
  • : 骨名詞1 (骨頭) bone2 (物體內部的支架) framework; skeleton 3 (品質; 氣概) character; spirit ...
  • : 名詞1. [生物學] (像薄皮的組織) membrane 2. (像膜的薄皮) film; thin coating
  • : 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;...
  1. Roentgenograms of the long bones revealed a periosteal reaction

    其長之放射線檢查呈現骨膜增生現象。
  2. 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關節部位,而致關節腫脹疼痛,常累及脛、腓、尺、橈等及關節,指趾末端往往膨大呈杵狀指, x線攝片檢查可見骨膜增生
  3. 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,以及細胞長曲線的測定,分析研究了fha薄材料對成細胞長的影響以及材料的浸提液對細胞殖的影響,通過細胞相對殖活性的測定對fha薄進行毒性評級。
  4. 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,研究出了體外組織潛能再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復制所需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復制的組織學基礎.為了驗證組織潛能再細胞的再潛能,建立了皮膚器官原位再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細胞的作用,確定命研究再物質的重要性,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復制的實體圖片,展示了潛能再細胞復制的組織器官和大器官司實體;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體外再復制;毛囊組織器官的原位和體外再復制;神經組織器官的原位復制;胰腺組織器官的體外復制;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
  5. 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,觀察組織工程種子細胞mscs細胞的粘附、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細胞的物學特性影響。 ( 2 )檢測基因勝肽膠對mscs細胞粘附、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 )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、殖及向成細胞分化效應及能力。
  6. 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.成細胞在旋轉壁式中空纖維物反應器內的大規模擴.第二屆全國化學工程與物化工年會. 2005年10月,北京
  7. Radiographically, periosteal thickening and increases in pericortical 99tcm - mdp uptake in bone scans may be seen

    放射線的證據包括了骨膜增生和核醫掃瞄下
  8. 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 )

    在右側的支氣管軟和左側充滿粘液的支氣管腔之間,平滑肌,水腫,炎癥(主要是嗜酸性粒細胞)等因素使粘下層厚。
  9. Use : collagen is used in many fields including cosmetic, food, medical care products and drink products etc. ; collagen can promote bone formation, treat arthritis, inhibit blood pressure raise and protect alimentary tract mucosa, at the same time collagen has beautification function

    膠原蛋白用途非常廣泛,用於化妝品食品醫藥保健品飲料等多方面領域在理機能方面,促進成修復關節炎抑制血壓上升保護消化道粘強美容效果皮膚頭發指甲
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