in vitro model 中文意思是什麼
in vitro model
解釋
體外模型-
Setting up of the tumor angiogenesis model in vitro
體外腫瘤微血管生成模型的建立 -
Application of caco - 2cell model in drug in vitro research
2細胞生物膜模型研究進展 -
In summary, we should investigate the more efficient cultural system for mammary orgnoids in vitro for enriched more mammary epithelial stem cells, and to screen the expression profiles in mammary epithelial stem cells to discover the specific marker for mammary epithelial stem cells in order to utilize the model of mammary epithelial stem cells to regenerate transgenic mammary glands in cow or sheep for human health, to uncover the mechanism of organogenesis, and differentiation
在此之前，仍然只能以造血幹細胞的特異性表達抗原scal - 1作為一個標記，進行類乳腺幹細胞的分析和分選研究。進一步研究類乳腺幹細胞的特異性表達譜，以期能夠找到類乳腺幹細胞的特異性表達抗原，分離得到類乳腺幹細胞，作為發育生物學和再生生物學研究的模型。 -
Establishment and application of a non - isotope model in vitro for screening 5 - reductase inhibitor
還原酶抑制劑體外篩選模型的建立和應用 -
In the present study, the grass carp ( ctenopharyngodon idellus ) cell line zc - 7901 and the colossoma brachypomum cell line cbs were used as in vitro model systems to study the effects of cold stress on the cell membrane fluidity, the level of cacium ion, the contents of malondialdehyde ( mda ), the level of c > 2 and the system of antioxidative enzymes in the fish cells
本文以培養的草魚（ ctenopharyngodonidellus ）吻端細胞系zc - 7901和淡水白鯧（ colossomabrachypomum ）吻端細胞系cbs為模型，研究低溫脅迫對其細胞膜流動性、鈣離子水平、 atp酶、丙二醛（ mda ）含量、超氧化物陰離子（ o2 - ' ）水平以及抗氧化酶系統的影響，以期探討它們與細胞耐寒性的關系。 -
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 -
A three - dimension in vitro model for angiogenesis of hemangioma
一種三維血管瘤血管生成體外培養模型的建立 -
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。 -
Scattering and absorbing characteristics of human artery and vein in kubelka - munk model to 632. 8nm wavelength of he - ne laser in vitro
數字散斑時間序列相關三維面形測量中提高精度的方法 -
Methods in vitro hypoxia model was used to evaluate the effect of hypoxic insult on neuronal function in the present study
方法1利用海馬腦片體外存活技術，建立大鼠離體海馬腦片的急性低氧模型。 -
This new co - culture method might be a promising in vitro model for studies of interactions between endothelial and smooth muscle cells
此種ec和smc共培養模型模擬了在體時ec和smc之間的結構關系，可以用來研究兩種細胞間的相互影響。 -
Construction of a three - dimensional human angiogenesis model in vitro for antiangiogenic drug selection
體外三維抗血管生成藥物篩選模型的建立 -
Methods subacute senile mouse model was established by injection of d - galactose. the splenic cells were isolated from mice and cultured in vitro following cona stimulation. expression of cd 137 on splenic t cells in the model and normal control groups were compared with each other by flow cytometry method at various cultural times after cona stimulation
方法取5周齡balb c雄性小鼠，頸背部皮下注射d -半乳糖，分別于造模型后一到五個月取脾臟淋巴細胞，同時取自然衰老小鼠脾臟淋巴細胞，在培養的第0 、 24 、 48 、 72 、 96 、 120 、 144h收集細胞，用流式細胞儀分析脾臟t細胞cd137的表達陽性率。 -
Establishment of the animal model of pneumocystis carinii pneumonia and its cultivation in vitro
卡氏肺孢子蟲肺炎動物模型及蟲體體外培養研究 -
Objective to investigate the influence of cardiac motion on the measurement of doppler blood flow velocity through an in vitro model
目的通過體外模擬實驗，研究心臟運動對頻譜多普勒血流速度測定的影響。 -
Establishment of an apoptosis model of vascular smooth muscle cells induced by ultraviolet - c radiation in vitro
Uv - c照射誘導體外血管平滑肌細胞凋亡模型的建立 -
Using km mouse as a animal model for studies on the maternal age effec t, we compared quantity, quality and in vitro developmental competence of oocytes from different age groups of mice to elucidate the possible mechanism of the decline in ageing - associated fertility
本實驗以昆明白小鼠作為研究母體年齡效應的動物模型，比較了不同年齡段小鼠卵母細胞的數量、質量及體外發育能力等，以探討與衰老相關生育力下降的機制。 -
In vitro model system, they found that stable - transfected cell lines which are over - express wnt - 1 or n - cadherin gene could differentiate into neuron - like cells without ra induction
目前從事的主要研究工作有：小鼠巢蛋白基因表達調控的分子機制；胚胎性癌細胞 -
The originalities of this paper are : 1, development of a a flow cytometry - based assay for quantitative analysis of cellular proliferation and cytotoxicity in vitro ; 2, the soluble secretion of k. 562 cell lines reduce the number of pbmc, but promote the activity of pbmc in dose - dependent manner ; 3, soluble secretion of k562 cell lines can induce the no production by pbmc, but no only plays a part of the role of soluble secretion of k562 cell lines ; 4, establishing a in vitro model and giving some parameters for sreening and appraising anti - tumor medicine
本研究的創新點在於： l 、建立了用流式細胞術定量測定細胞增殖和細胞毒性的直接檢測技術； 2發現k562可溶性分泌物劑量依賴性地使pbmc細胞數量減少但活性增加； 3 、 k562可溶性分泌物能誘導pbmc產生no ，但是no的作用並不等同於腫瘤上清的全部作用。 4 、為抗腫瘤藥物篩選提供了一個體外模型，並明確了一些篩選指標。 -
5 in vitro specific killing experiments showed that spleen cells induced by pi, p3 and p4, which contained higher proportion of cdg + cells and generated better ctl activity, could be introduced to in vivo experiment against hcv 6 we successfully setup a hcv structural gene in vitro cell - transfection system sp2 / 0 - hcv, through which also setup a murine model with subcutaneous transplanting tumor of hcv
將誘導的5種v特異性c l ，在體外進了丁特異性殺傷實驗，證一實，出n 、 p3和p4三條多肽誘導的脾糾泡含較高比例的cd 。糾1巾d ，叫產上較好的ctl殺傷活性，可以用作t細胞疫苗進fi體內抗hcv實驗。
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