tissue interaction 中文意思是什麼

tissue interaction 解釋
組織相互作用
  • tissue : n. 1. 薄絹，薄紗羅（等織物）。2. 薄紙，棉紙 （＝tissue-paper）。3. （編造的謊話等的）一套，一連串。4. 【攝影】碳素印像紙。5. 【生物學】組織。
  • interaction : n. 1. 相互作用，相互影響，互動。2. 【航空】干擾。
  1. The micromechanism of laser acupuncture and moxibustion are investigated, from photothermal and photopressure interaction. based on the thermal equilibrium and electromagnetic theory, the photo - tissue thermal interaction are discussed

    摘要給出激光照射對組織熱和機械作用微觀機制，利用熱平衡理論和電磁理論對激光熱作用進行定量分析和計算，在此基礎上探討激光針灸作用機理。
  2. The env protein deduced from env gene encodes the hydrophilic surface protein ( su ) and the hydrophobic transmembrane domain ( tm ) that determine the specific interaction between virus particles and cell surface receptors during retroviral entry. the su of retroviruses is a highly variable genetic element, containing receptor binding sites and major antigenic determinants. exjsrv - specific dna probes were derived. by using these dna probes in tissue hybridization. we successfully identified jsrv mrna expression and proviruses dna in sheep lung tissues infected with jsrv and control group has no postive signals, validating the use of exogenous virus - specific dna probes in the analysis of oncogenic proviral integration sites and identification of integrated exogenous proviral sequences

    用地高辛隨機引物法標記exjsrv特異的env片段，制備探針，原位雜交檢測spa肺組織中的rna及前病毒dna ，結果表明spa患羊肺組織內有jsrvenv基因mrna的表達，同時也檢測到了前病毒dna ，而相應的陰性對照卻無陽性信號，證實外源性病毒特異的dna探針在致瘤性前病毒的整合位點和整合的外源性前病毒的檢測中具有可信度。
  3. The essentially universal biophysical phenomenon of " electroporation " occurs if an appropriate pulse field is applied. electroporation is believed to be the rapid creation of aqueous pathways through lipid - containing barriers in cells and tissue. the driving force is the physical interaction of electric fields with different dielectric constants

    電穿孔效應是指在適當高壓脈沖電場作用下，細胞或組織間起相對隔離作用的「屏障」內快速形成液態通道的現象，是電場與具有不同介電常數而且易變形的物質相互作用的結果。
  4. Aim : to analyze the mechanism, thermadynamic theoretical basis, dynamic mechanism and influencing factors of thermally induced phase separation ( tips ) in order to completely grasp the factors affecting the size, distribution and form of pores, so that the adjusted range of pore can be widened and the preparation of porous membrane can be repeated and controlled. methods : considering from the structural characteristics of tissue engineered materials, the methods of preparing porous membrane using tips technique, the hermadynamic theoretical basis, dynamic mechanism and influencing factors were analyzed, the problems and investigative directions in the future were also analyzed. tips technique is a process of phase separation of polymer homogenous solution under quenching, and it is suitable for diameter and structural form of the micropore materials prepared using tips are closely correlated with the kind and dispensing proportion of polymer attrnuant, polymer concentration and polymer molecular mass, etc. conducted, including determination of polymer - solvent system phase diagram, study of form and appearance of porous membrane of different thickness, study of form and appearance of porous membrane prepared with systems of different x, which is the parameter of polymer - solvent interaction

    目的:分析熱致相分離成膜過程的機理、熱力學理論基礎、動力學機制以及影響因素，以便充分掌握影響孔度大小、分佈、形態的因素，使孔度調控范圍得以拓寬，使多孔膜的制備能重復可控.方法:從組織工程材料結構特點出發，分析熱致相分離聚合物多孔膜的制備方法及該法成膜的熱力學理論基礎、動力學機制以及影響因素.並分析實驗中存在的問題及今後的研究方向.結果:以熱致相分離法可制備聚合物多孔膜.熱致相分離法制備多孔膜是高聚物均相溶液在淬冷條件下發生相分離的過程，它適用於上臨界共溶溫度型聚合物一稀釋劑二元體系.熱致相分離法成膜的過程，可以認為是旋節線機理佔主導地位.熱致相分離法制備的微孔材料，其孔隙率、孔徑大小、結構形態與聚合物稀釋劑的種類、組成配比、聚合物濃度、聚合物分子量等因素密切相關.結論:可採用熱致相分離技術制備多孔膜，通過改變不同的成膜條件可獲得一系列不同孔徑尺寸和孔徑分佈的多孔膜材料.對熱致相分離成膜過程中聚合物-溶劑體系的相圖測定，不同厚度的多孔膜形貌研究，不同x （聚合物-溶劑相互作用參數）體系所制備的多孔膜形貌等需深人研究
  5. The theoretical analysis of thermal interaction between laser and bio - tissue

    生物組織熱作用的電磁理論分析
  6. The initial event in the life cycle of a virus is its interaction with receptors present on the surface of a susceptible host cell. the term " virus receptor " here is used to mean a host surface component ( usually proteins ) that participates in virus binding, facilitates viral infection, and also one determinant of virus host range and tissue tropism

    其吸附，入侵肝細胞，是感染肝細胞並引起病變的第一步，病毒對細胞的感染常以病毒分子吸附於宿主細胞表面為先導，即病毒的囊膜蛋白（或無包膜病毒的衣殼蛋白）與細胞表面相應的病毒受體分子結合。
  7. The safe concentrations of zn, cd and cr to crucian were far exceeded the standard. the short - term accumulation and distribution in young crucian tissue of mixed secure concentrations of heavy metals cu, zn, cr and cd pollution was studied. the results showed that associated interaction of the four heavy metals was synergistic effect of accumulated toxic

    研究了安全濃度的混合重金屬cu 、 zn 、 cr 、 cd污染在鯽魚幼體組織中短期的積累和分佈，實驗結果表明： cu 、 zn 、 cd和cr四種重金屬之間的聯合作用為毒性劇增的快同作用。
  8. But the standard mc has some shortcomings : firstly, the standard mc picks up isosurfaces by threshold, however, threshold segmentation is invalid for picking up tissues or organs from some medical images ; secondly, the standard mc pocesses cubes one by one, that is to say, all the cubes will be checked, and the algorithm spents 30 % - 70 % of time to check the null units, so we need a reasonable data structure to travel the space data and accelerate the checking or filting of null units ; thirdly, the standard mc has a large scale of triangles, normally, the tissue or organ reconstructed includes hundreds of thousands so much as millions of triangles, this means it hardly to execute real - time rendering or interaction ; lastly, the standard mc can not get the very smoothly surface mesh, and there will be some unexpected accidented cases, especially in the case of big errors in oringinal data

    但是標準mc演算法存在較大的問題:標準mc演算法實質上是通過閾值分割來提取等值面，閾值分割對某些醫學圖像的組織或器官的提取難以得到較好的效果;標準mc演算法是逐個移動立方體來進行處理，就是說對所有的立方體都要進行一次檢測，演算法執行中30 % ~ 70 %的時間用在對空單元的檢測上，因此需要有一種合理的數據結構對空間數據進行有效的遍歷，以加速對空單元的檢測和過濾;標準mc演算法產生了大量的三角面片，一般重建的組織或器官包含數十萬甚至上百萬的三角面片，難以實現實時的繪制和交互操作;標準mc演算法得到的表面網格並不光滑，會有一些不期望的凹凸，特別是在原始數據有較大誤差的情況下尤其突出。
  9. Proteome techniques have widely been applied to the fields of plant genetics, plant development, and plant physiology and ecology to investigate plant genetic diversity, plant development such as seed maturation and germination processes, differentiation of plant tissue and organ, separation and functional identification of novel component of various organells, mechanisms of plant adapted to abiotic or biotic stresses including high temperature, low temperature, high salt, drought, and pathogens and insects, and interaction of plant with microbe

    摘要蛋白質組技術已廣泛應用於植物遺傳、發育和生理生態等諸多生物學領域，主要研究植物的遺傳多樣性、植物發育（如種子成熟與發芽過程） 、組織器官的分化過程、不同亞細胞結構的新蛋白組分的發現及其功能鑒定、植物對非生物逆境（包括高溫、低溫、高鹽和乾旱等）和生物逆境（病蟲害）的適應機制和植物與微生物（根瘤共生體）相互作用機制。
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