組織增殖 的英文怎麼說
中文拼音 [zǔzhīzēngzhí]
組織增殖
英文
hyperblastosis-
Proteins associated with callus proliferation and adventitious bud differentiation of populus euphratica
胡楊愈傷組織繼代增殖和器官發生中蛋白分子標記的研究Crown galls are cancerous growths composed of disorganized and proliferating plant cells.
冠癭是無組織的正在不斷增殖的植物細胞所組成的癌狀物。The histopathological study revealed acanthosis, papillomatosis and large amounts of xanthoma cells in the papillary dermis
組織病理學檢查顯示表皮肥厚伴隨乳頭樣增殖,及真皮層有大量黃色瘤細胞浸潤。At the same time, growth factors have relation to genesis of tumor. fibroblast growth factor ( fgf ) can promote proliferation of tissues derived from mesoderm or neuroectoderm and many tissues and cells can secrete fgf
成纖維細胞生長因子( fgf )能夠誘導中胚層和神經外胚層來源細胞的增殖和分化,許多組織和細胞都可以分泌fgf , fgf可以促進多種細胞的生長和分化。Effect of induction and proliferation of pinellia ternate thunb. breit. callus
半夏愈傷組織的誘導及增殖效應Nano - matreials have a perfect perspective for their volume effects and surface effects, which could enhance biologic activity, adhesiveness and proliferation of cells
納米材料因具有一些獨特的效應,如體積效應和表面效應,有利於細胞黏附、增殖和功能表達,因而作為生物醫用材料特別是組織工程支架材料具有良好的應用前景。The variety of the activity of na + / k + - atpase, ca2 + - atpase and sod by increase calcium concentration in the water, and the effects of cd2 +, estradiol - 17 and ca2 + on the lymphocyte proliferation from blood and head kidney of ctenopharyngodon idellus were also investigated the significance of this paper is that to research the toxicity of cadmium to the fish and to search the mechanism of the cadmium toxicity to the fish. and the protection of calcium on cd2 + toxicity
本論文研究了鎘對草魚的毒性作用,比較了在不同鈣濃度條件下,其鰓、肝臟、腦等組織中sod 、 na ~ + k ~ + ? atp酶、 ca ~ ( 2 + ) ? atp酶的活性變化規律以及鎘和17 ?雌二醇對草魚血液及頭腎淋巴細胞增殖的影響,評價鎘對魚類的毒害作用,探索鎘的毒害機理。Methods : the expression of pcna and fibronectin in placenta of 30 patients with early abortion were detected by immunohistochemistry
方法:通過免疫組織化學方法觀察30例早期自然流產患者胎盤中增殖細胞核抗原、纖粘連蛋白的表達。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The present results indicated that the paraventricular nucleus of the hypothalamus and the supraoptic nucleus might have important roles in neuroimmunomodulation. 2. following lps or seb was administered intraperitoneally, the expression of pcna of splenic cells and il - 1 receptor type i in pvn and son were observed by using immunocytochemistry in the mice. double fluorescent labeling technique was used to determine the relationship of il - 1 receptor type i co - expressions with arginine vasopressin or oxytocin
二、小鼠腹腔內給予細菌內毒素lps或腸毒素seb ,用免疫組織化學方法觀察了脾臟核增殖抗體及下丘腦室旁核和視上核中1型il 1受體的表達,並採用雙標記技術觀察了1型il刁受體陽性神經元和加壓素及催產素表達的關系。Effects of different freezing methods on the proliferative competence of follicle cells in rabbit ovarian tissue
不同冷凍方案對家兔卵巢組織卵泡細胞增殖活性的影響$ mx # ( 2bo2 ) ffr $ $ htet # $ nq9i & kk $ 4n8 $ $ 4ta scf mana $ ismffs whether s1eep deprivation cou1d induce neuron pro1iferation has not got definite conclusion so far. in the present research, we performed small pedestal s1eep deprivation method to remove rapid eye movement s1eep ( rems ). we observed the neuron pro1iferation and differential in immunohistochemistry and doub1e 1abeling iariunohistochemistry staining, and the expression of stem ce11 factor mrna in situ hybridization technique after s1eep deprivation in rat hippocampus
本研究應用細胞增殖標記brdu cna免疫組織化學方法結合雙重標記兔疫組織化學技術,觀察睡眠剝奪對成熟大鼠腦內神經元增殖及分化的影響,應用原位雜交技術觀察了睡眠剝奪大鼠海馬神經細胞scf基因inrna表達的變化,對睡眠剝奪引起海馬神經細胞增殖的分子機製作了初步探討。A large number of proliferating macrocapillaries coursed among them
有大量的增殖性巨大微血管橫列在這些組織之間。In this study, we use immunohistochemistry, electron microscope, cell culture, image analysis, mtt method and radioimmunoassay to study the localization, varies of quantitation, and possible frictions of 5 - ht and subtype of 5 - htr in human placenta. the results were as follows : 1
本研究用免疫組織化學、免疫電鏡、細胞培養、圖象分析、 mtt法和放射免疫等技術對5 -羥色胺及其受體亞型在胎盤絨毛中的細胞定位及對滋養層細胞增殖和激素分泌的影響進行了初步的探討,其結果如下: 1Effect of five species of epimedium on growth of cartilage and proliferation of cartilage cell in vitro
5種淫羊藿對軟骨組織生長和軟骨細胞增殖影響的對比研究By the compounds of submandibular gland cells and collagen sponges. we investigate the optimal cell denisity of tissue engineered compound of submandibular gland cells and collagen sponges, the cellular compatibility of tissue engineered compound of submandibular gland cells on the collagen sponges with different porosity and the influence of epidermal growth factor on the adherence of submandibular gland cell to collagen sponge. our studies can primary provide theoretical ground work to form the model in vitro of tissue engineering smg
在本研究中,以初步探討體外頜下腺細胞與膠原海綿支架相互作用為目的,採用體外分離培養sd大鼠頜下腺細胞,然後接種于膠原海綿支架上體外復合培養的方法;從不同接種細胞濃度對細胞一支架復合物影響,同一接種細胞濃度在不同孔隙率的支架上黏附、增殖的情況及表皮生長因子( egf )對頜下腺細胞的促增殖作用,促細胞在支架上黏附等三方面入手,初步研究了頜下腺細胞與膠原海綿相互作用的影響因素,為進一步在體外及體內構建較為理想的組織工程化頜下腺提供理論參數和實驗依據。The high parathormone levels increase osteoclast activity and produce irregular bone resorbtion with microfractures and hemorrhage and macrophage proliferation and fibrous connective tissue proliferation
高甲狀旁腺激素水平提高了破骨細胞的活性並導致不規則的骨溶解吸收,伴隨微骨折、出血、巨噬細胞增殖及纖維性結締組織增生。In addition, a specific calli - related protein 43kd were found and its expression only occurred in the proliferation of calli. we also found a kind of nonembryonic protein 35kd that expressed in nonembryonic calli and regenerated plants and disappeared in embryonic calli and embryogenetic stage
此外,我們還發現,與愈傷組織增殖有關的43kd愈傷組織特異性蛋白;在胚性愈傷組織和胚狀體發生階段特異性缺失的35kd蛋白組分,它可能與胚狀體發生能力的喪失有關。The embryogenic calli induced from the mature embryos of forty - five genotypes of sweet corn varieties were treated as materials to analyze the relationship between plant regeneration and callus induction rate, callus proliferation and bud points
摘要以45種基因型甜玉米的成熟胚為外植體材料,分析出愈率、愈傷組織增殖量、芽點數與植株再生的關系。Callus induction rate correlated with plant regeneration more closely than the latter two factors according to the experimental results
結果表明,出愈率與再生能力有較大的相關性,愈傷組織增殖量、芽點數次之。分享友人