骨原細胞 的英文怎麼說

中文拼音 [gǔyuánxìbāo]
骨原細胞 英文
osteogenic cells
  • 骨 : 骨名詞1 （骨頭） bone2 （物體內部的支架） framework; skeleton 3 （品質; 氣概） character; spirit ...
  • 原 : Ⅰ形容詞1 （最初的; 原來的） primary; original; former 2 （沒有加工的） unprocessed; raw Ⅱ動詞（原...
  • 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 most frequent mistreating is curettage for a malignant lesion based on a misdiagnosis, such as osteomyelitis, fibrodysplacia, gct, cyst, etc

    對惡性骨腫瘤給予刮除植骨.該類錯誤治療的原因多是誤診為骨髓炎、纖維結構不良、骨巨細胞瘤或囊腫等。
  3. The expression of viral antigens on the cell surface and disruption of the cytoskeleton can cause the cell - to - cell interactions and cellular appearance to change, making the cell a target for immune cytolysis

    病毒抗原在細胞表面表達，以及細胞骨架的破壞能引起細胞細胞相互作用，細胞的外形會改變，導致細胞成為免疫殺傷的靶位。
  4. Facs results showed that umbilical cord blood mscs did not express antigens cd34, cdlla and cdllb, and expressed cd29 and cd71, which was identical to that of human bone marrow - derived mscs

    用流式細胞儀檢測msc的表面標志結果顯示，臍帶血msc不表達cd34 、 cd11a和cd11b ，強表達cd29 ，弱表達cd71 ，與骨髓msc表面抗原特性一致。
  5. The quantity and quality of hematoblast in umbilical cord blood ( ucb ) can be compared with bone marrow. furthermore, it has other advantages : widely sourced, no contamination of pathogeny, weakly antigenicity, and no mature lymphocyte, et al

    臍血中造血細胞的數量和質量都與骨髓相近，而且，具有來源豐富、無病原體污染、抗原性弱、淋巴細胞不成熟等優點。
  6. The higher concentration of extracellular calcium could influent the stability of microtubules in protoplast. mts in the protoplasts would depolymerize when the extracellular calcium concentration was rising up to lommoi / l. the intercellular washing fluid ( iwf ) of wheat - leaf rust fungus interaction which contains elicitor were used as stimulator to interact with the protoplast of cv

    試驗結果表明，在小麥葉肉細胞原生質體中，微管骨架呈網路狀分佈於整個細胞質中；胞外較高的ca ~ （ 2 + ）濃度對微管骨架的穩定性有影響，在本試驗系統中當胞外ca ~ （ 2 + ）達到10mmol / l時，微管骨架即開始發生解聚。
  7. In the early neurula, cortactin staining signals were detected in the developing primodium of forebrain as early as 10. 5 hpf ( hours post fertilization ), at the same time the tailbud areas were highly stained too. later, the staining was concentrating in the developing neural rod while paraxial mesoderm derivatives were not stained

    在早期神經胚，神經系統中的前腦原基最先出現染色，並保持頭尾兩端處染色最強的圖式，隨后，染色集中分佈在發育中的神經龍骨中，但近軸中胚層細胞沒有染色。
  8. Nogo - 66 receptor, ngr, cloned in 2001, is a leucine - rich - repeat glycophosphatidylinositol - anchored membrane protein which mediates nogo - 66 inhibition of axonal outgrowth. both the long acidic amino - terminal domain and the nogo - 66 fragment have strong neurite growth inhibitory activity suggest that nogo - a has at least two inhibitory domains. northern blot, in situ hybridization, western blot and immunocytochemistry analyses show that in addition to oligodendrocytes, nogo - a mrna and nogo - a protein are also expressed in neurons in developing and adult brain and spinal cord, nogo - a is also found in peripheral organs such as heart and testis

    Northernblot 、原位雜交、 westernblot和免疫組化結果證明： nogo amrna和nogo蛋白除了在cns的寡突膠質細胞中表達，還表達于發育階段和成年的腦、脊髓和外周神經節的某些神經元中，在外周組織如睪丸和心臟也有表達； nogoe在cns和pns以及多種外周組織中有廣泛分佈； nogo （除表達于腦和心臟外，在骨骼肌中有較高表達。
  9. 2nd : the in - depth stimulates the cell the synthesis metabolism, accelerates the new cell formation, the ossein and the elastic fiberproduction

    2深層刺激細胞的合成代謝，加速新細胞形成，骨膠原及彈性纖維的產生。
  10. 2nd, the in - depth stimulates the cell the synthesis metabolism, accelerates the new cell formation, the ossein and the elastic fiberproduction

    2深層刺激細胞的合成代謝，加速新細胞形成，骨膠原及彈性纖維的產生。
  11. Bamboo salt contain abundant vitamin and 100 % natural ossein fiber, which can go into the pore to activate body ' s ferment cells and effectively restrain and decompose melanin so as to maintain skin white and shine

    竹鹽蘊藏豐富的維他命及100 %純天然骨膠原纖維，能深入毛孔激發體內酵素細胞有效的防止黑色素的生成，並對其分解代謝，從而令肌膚白皙透亮。
  12. The total protein content and cell activity test results showed high proliferation ability and cell activity of the chondrocyte in modified pdl - la scaffold

    軟骨細胞的蛋白質含量和細胞活性測試結果表明，軟骨細胞在原位自修飾的聚乳酸三維支架內有較強的分裂增殖能力和較高的細胞活性。
  13. It also showed good cell affinity to the modified pdl - la scaffold investigated by scanning electronic microscopy ( sem ) and confocal laser scanning microscopy ( clsm ), comparing with the unmodified pdl - la scaffold

    掃描電鏡和激光共聚焦顯微鏡的測試結果顯示了軟骨細胞在原浙江大學博士學位論文（ 2003 ）位自修飾的聚乳酸三維支架內部良好的粘附與生長情況。
  14. Such cells are being tested by a number of researchers for their ability to grow fat, cartilage and bone on special biomaterial - based scaffolding, with the goal of producing soft tissue for reconstruction or augmentation, or to shore up bones left fragile by age or disease

    種植于特定生物材料支架上的生骨細胞經過大量研究人員的測定具備生成脂肪、軟骨組織及骨的能力，利用上述組織工程方法目的在於使軟組織重建或擴增，或補充由於年齡和疾病原因引起的骨丟失。
  15. Human bone morphogenetic protein 3 is a member of tgf - b superfamily. lt can induce the differentiation of cartilage and bone tissue in mesenchymal cell. and is important to bone self - repairment and bone development during embryo morphogenesis. in addition, some other biological activities of hbmp - 3 have also been found. such as inducing development of embryo and stimulating differentiation of neural and blood cells. therefore, there is a great prospect in the use of hbmp - 3. there is trace content of hbmp - 3 in human body. it has been expressed in the expression system of eukaryotes and prokaryotes respectively, but its application is restricted because of defects in the process and modification after translation in prokaryotic cells and higher costs and lower yields existed in eukaryotic expression system

    人骨形成蛋白3 （ hbmp - 3 ）屬于tgf -超家族的一員，可以誘導間充質細胞分化為軟骨和骨，在胚胎時期骨骼發育和骨再生修復中起著重要的作用，而且對胚胎發育過程中中胚層的誘導和分化、造血組織的發育以及神經系統的發育和修復等都起著重要作用，因而hbmp - 3有廣闊的市場前景。它在人體內含量極微，盡管研究人員已經在原核細胞和真核細胞表達系統中分別進行了表達，但是由於原核表達系統缺乏翻譯后的加工修飾，真核表達系統存在成本高、產量低等特點，限制了其在臨床上的應用。
  16. 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。
  17. There was no difference in other biologic characteristic of mscs between the two separation method, such as cell anchorage ratio and clone formation ratio. ( 2 ) plga film presented uniformity frame with no protuberance and fissure under scanning electron microscopy ( sem ). big aperture with smooth wall and average 400 m i n size running - through each other was observed in porous plga substrate, around the big aperture there were many round micropores about 5 m size. all of the structure were equal and uniform, which satisfied the further research work. ( 3 ) mscs adhesion at earlier time was promoted by biotiegenrafter 3h, cell number was ( 1. 5 0. 18 ) 105 in the plga film coated with biotiegen group, which was significantly higher than that in plga film group ( p < 0. 01 ) and higher than that in coverslip group ( p < 0. 05 ), which cell number was ( 1. 04 0. 21 ) 105. after 6h and 12h biotiegen could not promote cell adhesion, and cell proliferation and alkaline phosphatase ( alp ) activity were not promoted dramatically during 9 days. ( 4 ) cell adhesion was promoted by fibronectin or collagen type i

    G ） i型膠原、纖維粘連蛋白促進細胞增殖，細胞接種后3 、 6 、 gd三個檢測時間點，實驗組細胞均明顯高於對照組。與1型膠原相比，纖維粘連蛋白刺激作用更強。 ） i型膠原、纖維粘連蛋白尚能誘導mscs細胞向成骨細胞分化，不僅表達成骨細胞標志物ocn 、 alp 、 opnmrna ，而且堿性磷酸酶活性明顯增高，堿性磷酸酶及鈣結節7第四軍醫大學博士學位論文一染色均強陽性， i型膠原組mscs細胞堿性磷酸酶活性較fn組更高，有顯著性差異；同時，兔疫組化染色表明，經纖維粘連蛋白作用的mscs1型膠原表達陽性。
  18. 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
  19. In this paper, wheat cultivars lovrin 10 ( resistant ) and 5389 ( susceptible ) were selected as materials in this system. the mesophyll protoplasts of wheats ( mpw ) were isolated using cellulase and pectolase digestion. by the indirect immune fluorescent labeling, microtubules ( mts ) pattern in mpw were showed clearly under the confocal laser scanning microscope ( clsm )

    本試驗以抗（洛夫林10 ） 、感（ 5389 ）不同的兩小麥（ triticumaestivuml . ）品種為材料，採用酶解法制備小麥葉肉原生質體，利用間接免疫熒光方法結合激光共聚焦掃描顯微技術對小麥葉肉細胞原生質體的微管骨架進行了清晰的標記，並探索了微管骨架標記的影響因素。
  20. Aiming at the characteristics of the marrow cell image, the paper adopts continuous wavelet transform to process image so that main edges can be detected from different angle in the meanwhile original image noise being eliminated

    摘要針對骨髓細胞圖像的特點，採用連續小波變換對圖像進行了處理，在消除原始圖像噪聲的同時，從不同的角度檢測出圖像的主要邊緣。
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