p cell 中文意思是什麼

p cell 解釋
起搏細胞
  • p :
  • cell : n 1 小室，單室；隔間，艙；〈詩〉茅舍；（單個的）蜂窩，蜂房。2 〈詩〉墓穴，墓。3 （大修道院附屬的...
  1. P. ussuriensis, p. davidiana and a. ginnala can adjust osmosis by improving the proportion of bound water, m. baccata adjust osmosis by decreasing the volume of cell and increasing content of solute

    山梨、山桃、茶條槭能通過提高束縛水比例來實現滲透調節，山荊子通過細胞體積減小和增加溶質含量來實現滲透調節。
  2. Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel

    結果如下：皮下包埋卜周者，無細胞真皮基質漸與周圍組織粘附，顏色由蒼白轉紅；皮下包埋3周者，無細胞真皮基質與周圍組織緊密枯附，盾晰葉辯；術后卜周，包埋的基質面積變化較包埋前無統計學差異o川0引，術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ） 。光鏡下術后卜周，宿主的淋巳組織細胞、成纖維細胞浸入生長，釉附在膠原纖維上，少量血管內皮細胞浸入基質；術后34周，無細胞真皮基質內較多的血管形成，故可認為無細胞真皮基質免疫原性低，能誘導宿主的成纖維細胞、巨噬細胞浸入生長，為一種新型的真皮替代物。第四部分無細胞真皮基質與自體斷層皮片復合移棺的研究， sd大鼠10隻，在其背部卜方造成全厚皮膚缺損的創面
  3. Effect 0f 2, 3, 7, 8 - tetrachloro - p - dibenzodioxin on the secretion of ovarian granulose cell in rats

    英對大鼠卵巢顆粒細胞分泌功能的影響
  4. 2. hemolymph immune reaction of p. americanna to the m. anisopliae injected cell immune is the main reaction of p. americanna to the injected m. anisopliae

    2蜚蠊血細胞對注射綠僵菌孢子的免疫反應蜚蠊對綠僵菌孢子的免疫反應主要由血細胞完成。
  5. N. veissid, p. nubile, a. f. beloto, a. m. andrade, 1990, “ the solar cell experiment of the first brazilian complete space mission satellite ”, ieee, pp. 1184 - 1187

    陳建富等， 1999 ， 「單相三線式光伏能量轉換系統之研究」 ，電力電子技術，第50期，頁93 - 101 。
  6. Mdr1 express product p - glycoprotein was detected by immunocytochemical method and flowcytometry. the cytotoxicity and multidrug resistance reversion effect of tea polyphenol was examined by mtt assay in mcf - 7 and mcf - 7 adr carcinoma cell lines, and compared with pgp inhibitor quinidine. the pgp expression of mcf - 7 adr was strongly positive, the positive rate was 15 % ; the pgp expression of mcf - 7 was negative, the positive rate was 1. 8 %. ic50 of tea polyphenol to mcf - 7 and mcf - 7 adr is 115. 2g ml and 207. 6g ml respectively. ic50 of quinidine to mcf - 7 and mcf - 7 adr is 129. 8mol l 42. 1g ml and 94. 1mol l 30. 5g ml respectively. tea polyphenol and quinidine changed little toxicity of adriamycin to mcf - 7, but tea polyphenol and quinidine improved the sensitivity of mcf - 7adr to adriamycin significantly. immunocytochemistry and flow cytometry can detect p - glycoprotein expression level qualitatively and quantitatively. tea polyphenol is not only an anti - tumor agent, but also a multidrug resistant modulator similar as quinidine. tea polyphenol is advantageous for its little toxicity in tumor treatment

    用免疫組化法和流式細胞儀對腫瘤細胞系mcf - 7和mcf - 7 adr的p -糖蛋白表達水平進行定性定量研究。用噻唑藍比色法mtt研究茶多酚的細胞毒性及其對耐藥性的逆轉作用，並與pgp抑制劑奎尼定進行了比較。免疫組化法檢測p -糖蛋白表達水平， mcf - 7 adr呈強陽性，而mcf - 7呈陰性流式細胞儀定量檢測結果mcf - 7 adr細胞系細胞陽性率為15 % ， mcf - 7細胞系細胞陽性率為1 . 8 % 。
  7. Stefanini p, carboni m, patrassi n, et al. beta - islet cell tumors of the pancreas : results of a study on 1 067 cases. surgery, 1974, 75 : 597 - 609

    陳元方.胰腺的內分泌腫瘤.見：呂新生，韓明，總主編鐘守先，主編.胰腺外科.長沙：湖南科學技術出版社， 1997 568 - 594
  8. 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。
  9. The burst size of the cyanophage was ca. 200 pfu ? cell " 1. the rate of adsorption to host was markedly higher under light condition than that under dark condition ( p = 0. 02 ), and light was necessary for infection

    此外，固體培養條件下，織線藻的生長速率與噬藻斑的擴大之間有明顯的同步性，即生長速度越大，噬藻斑的擴大就越明顯。
  10. Studies revealed that p - catenin dissociated from ccc and translocated into free catenin pool in cytosol after it has been phosphorylated at tyrosine or serine residues, and in this situation, the ccc has been disrupted and cell adhesion function disturbed. a large amount of the free p - catenins in the cytosol can be degraded by the tumor suppressor apc, and the remains translocate into nucleus and bind to transcriptional factor tcf / lef in the nucleus and then promote cell proliferation related gene or anti - apoptosis gene transcription

    當-連環蛋白酪氨酸或絲氨酸殘基磷酸化后，就與ajs發生解離而游離到細胞漿中，此時細胞的粘附功能也發生障礙，游離到胞漿中的-連環蛋白，一部分被抑癌因子apc降解，一部分則轉移到細胞核內，與核內的轉錄因子tcf lef結合，啟動與細胞增殖有關的基因轉錄。
  11. The expression efficiency difference between ped5 and pcdhfrl, a vector utilizing cmv enhancer / promoter ( pcmv - ie ) for foreign protein production, was analyzed using human interferon - p ( ifn - ) gene and human secreted alkaline phosphatase ( seap ) gene as reporters. when analyzed in transient expression, ped5 showed a little more protein produciton than pcdhfrl. however, in continuous expression, when serum concentration was lessened to slow down cell proliferation, ped5 expressed 3. 1 times more reporter proteins than pcdhfrl, which implied that pef - io was less affected by cell cycle status in contrast to pcmv - ie, making ped5 a good expression vector for foreign protein production

    應用人-干擾素（ ifn - ）和人分泌型堿性磷酸酶（ seap ）基因作為報告基因，對含有巨細胞病毒即早期啟動子（ p _ （ cmv - ie ） ）的表達載體pcdhfr1和ped5表達外源蛋白的能力進行了比較，發現對于瞬時表達， ped5略好於pcdhfr1 ；在穩定表達中，通過降低血清濃度，使細胞增殖緩慢，這時ped5表達外源蛋白的能力較pcdhfr1高3 . 1倍。
  12. The design of resonant p. a. cell is one of the most important parts, including p. a. cell structure, first resonance frequency, optical reflection sets, and couple between optical fiber and p. a

    諧振式光聲腔的設計是該系統的關鍵，包括光聲腔結構設計、第一諧振頻率及品質因子的確定、光學反射裝置、光纖和光聲腔的耦合等。
  13. In the paper we mainly researched space gainp2 / gaas / ge high efficiency tandem cells " making process by home - made low pressure mocvd technology and new solar concentrators. firstly, we presented reseached and development of solar cells in china and foreign countries ; secondly, on the basis of fundamental priciples and theories, we discussed some factors of influcing conversion efficiency of solar cells, and analysed the i - v output feature of two - junction tandem cells ; then the design concept of gainp2 / gaas / ge two - junction tandem cells was discussed, the detailed aspects of gainp2 / gaas / ge tandem cells epitaxy growth by low pressure mocvd was studied, and some questions on epitaxy growth ( such as crystal qualities, interface stress, element interdiffusion, n - and p - type doping et all ) were solved ; after that, the cell fabrication process was described ; finally, we reseached the hot pressing and mould process technology of an arched line - focus fresnel lens made by pmma, designed and fixed new solar concentrators

    本文致力於用自製的低壓mocvd裝置進行cainp _ 2 / gaas / ge空間用高效級聯太陽能電池製作的工藝以及聚光太陽能電池組件的研究。首先，介紹了國內外太陽能電池的研究現狀及應用情況；其次，運用太陽能電池基本原理討論影響電池轉換效率的因素，分析了級聯電池的伏安特性；隨后，討論了cainp _ 2 / gaas / ge雙結級聯電池的結構設計理念，研究了採用低壓mocvd技術生長cainp _ 2 / gaas / ge級聯太陽電池材料的工藝過程，解決了異質材料生長的結晶質量、界面應力、材料互擴散以及材料n 、 p型摻雜等一系列問題；然後總結了級聯電池的后工藝製作；最後，研究了以pmma為材料的菲涅耳線聚焦透鏡的熱壓成型工藝及其模具的加工工藝，設計並安裝完成新型聚光太陽能電池組件。
  14. In order to study the function of cycling2 in vitro culturing cell line, we used pires - g2 eukaryotic expression vector transfecting human gastric cell line sgc - 7901 and human embryo kidney hek - 293 cells by lipofectamine plus reagent, and studied the function of cycling2 expression on the cell proliferation in vitro, further investigated the regulation mechanism of cycling2. at the same time, we made a study on the expression level change of cycling2 in normal gastric tissue and different type and different stage of gastric carcinoma tissue. material and method 1 material : piresneo vector was purchased from clonetech, plasmid extraction and purification kit was purchased from qiagen company ; rpmi 1640, dmem fetal calf serum were obtained from gibco / brl ; lipofectamine plus and g418 were purchased from life technologies ; ultrasensitive ? s - p kit, mouse monoclonal antibody p21wafl ( in use ), dab staining kit were purchased from maixin company

    實驗材料與方法1 .實驗試劑高糖dmem 、 rpmll640和胎牛血清購自美國g山eo / brl公司; dmewf12 （ 1 : 1 ）混合培養液購自美國hyclone公司;胰蛋白酶購自美國si目叮a公司; hepes由美國amersco公司分裝;脂質體轉染試劑（ upofectalnineplusreageni ）和以18為美國玩vitrogen公司產品; piresneo載體購自美國cloneteeh公司;質粒提取及純化試劑盒購自德國qiagen公司; ultresensitive翎s一p免疫組織化學試劑盒;鼠單克隆抗體戶3 （ do一7 ）蛋白（即用型） ;鼠單克隆抗體p21waf ， （即用型） ; dab染色試劑盒均購自福建邁新公司;鼠單克隆抗體pziwa曰（濃縮型） ;辣根過氧化酶標記羊抗鼠二抗購自北京中山公司; ecl試劑盒購自美國santacruze公司; dcproteinassay試劑盒購自bi 。
  15. Anderson p, askgoard d, ljunggvist l, et al. t cell proliprative response to antigens secreted by mycobacterium [ j ]. tuberculosis infection and immunity, 1991, 59 : 1558

    陸學東，孫惠平，張銀輝.免疫印跡技術在臨床結核病血清學診斷中的應用[ j ] .中華結核和呼吸雜志， 1993 ， 16 : 357 359
  16. Methods serums containing whole wmt and its disassembled formulas, including the formula consisted of warming jing and boosting qi part wenjin yiqi, wy and that of promoting blood circulation part huoxue tongmai, ht, as well as the serum contained high concentration of lipids were prepared conventionally, respectively. the adhesion of monocytes cell strain thp1 to human umbilical vascular endothelial cells huvec was determined by rose bengal stain method, and elisa was used to detect expressions of intercellular adhesion molecule icam1, vascular cellular adhesion molecule vcam1 and p selectin on huvec surface

    方法常規制備溫脈通全方溫經益氣拆方活血通脈拆方含藥血清和高脂血清，採用虎紅染色法檢測藥物血清對高脂誘導的人臍靜脈內皮細胞huvec和單核細胞株thp1黏附的作用用細胞elisa法檢測huvec表面細胞間黏附分子1 icam1血管細胞黏附分子1 vcam1 p選擇素pselectin的表達。
  17. The sensor operation speed can be 64ms / frame ~ 2ms / frame. in the research of photoelectric cell, device physics structure of pixels have been optimized. deep junction depth photodiodes, such as p + / n - well / p - sub structure, have been used and the photo - response of the sensor has been greatly enhanced

    復位信號為sv時的單幀感光動態范圍為60db ，採用改變復位信號頻率的二次掃描方式可將傳感器的總的感光動態范圍擴大到84db ，可對0石10 ， 000lx光照強度的信號進行傳感。
  18. Much work has been done to prompt the rapid establishment of fuel cell technology in china. with the help of the visiting scholar, p. j. van den enden, the standard performance test of single mcfc has been done smoothly

    重建了荷蘭delft大學熔融碳酸鹽燃料電池單電池試驗系統，並以標準氣體、水煤氣、甲烷等氣體作為燃料氣體，獲得了單電池的性能。
  19. Normal bn rats were vaccinated intraperitoneally with lctcv, ltcv and rpmi1640 culture buffer ( blank control ) respectively. one - way mixed lymphocyte reaction ( mlr ), flow cytometric analysis of the apoptosis of peripheral t cell and the rate of cd4 / cd8 in peripheral blood were performed before and after vaccination. results mlr showed that the immune response capability of bn rat spleen cells in lctcv group were suppressed significantly after vaccination ( p < 0. 01 )

    于疫苗接種前和每次接種后第5天以被免疫bn大鼠的脾細胞作為反應細胞，以lou c大鼠的脾細胞作為刺激細胞（經絲裂黴素處理） ，進行單向混合淋巴細胞反應（ mlr ） ，同時對外周血t細胞凋亡和cd _ 4 ~ + 、 cd _ 8 ~ + t細胞亞群進行流式細胞分析。
  20. The system properties of single - loop system, such as velocity, torque, bifurcated power, transmission efficiency are researched deeply using theoretical analysis and numerical computing, and gives new methods for designing which according to the design parameter a and combine with the system diffluent coefficient q and the ratio of x, p cell transmission. so the theoretical expressions for designing this kind of transmission is established. the design parameter a is put forward as the ratio of confluent power and the input power of single - loop system

    通過對單環路系統的運動學和動力學特性、功率流特性、傳動效率特性等所進行的理論分析和數值計算，提出了以單環路系統主支路功率大小與輸入總功率的比值為關鍵設計參數的設計新方法，並結合系統的功率分流系數q和各組成單元的傳動比，得到了單環路系統的速度、力矩、功率流、傳動效率等計算公式，為該種傳動類型的設計提供了必要的理論依據。
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