結織細胞 的英文怎麼說

中文拼音 [jiēzhīxìbāo]
結織細胞 英文
connective tissue cell
  • 結 : 結動詞（長出果實或種子） bear （fruit）; form （seed）
  • 織 : 動詞（編織） knit; weave
  • 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 sequence analysis revealed that the as1 gene encodes a myb protein, which is a candidate transcription factor. in as1 and as2 mutants, the polarity formation in leaves is defective. cell differentiation along abaxial - adaxial, proximal - distal and media - lateral axes all shows an insufficient fashion

    通過掃描電鏡、干涉相差顯微鏡、組織切片、過量表達等手段研究了as1和as2的功能，包括觀察觀察突變體的組織、細胞結構及早期發育狀況，同時採用gus表達、 rt - pcr 、原位雜交、 northern等手段分析基因的表達情況。
  2. Using cd, cu, zn and cr as experimental toxicants and crucian as experimental creature, we employed the environmental biotechniques ( flame atomic absorption spectrophotometry, the method of improved pyrogallol autoxidation and electron microscopy ) to study the acute toxicity and secure concentrations of heavy metals to crucian ; the accumulation and distribution of mixed heavy metals to fingling crucian ; the activities of superoxide dismutase ( sod ) of gill and liver tissues and the hispathological and ultrastructural change of superfine structure of liver and kidney of crucian after cadmium exposure. through which, we intended to fully and systemically study the toxic influence of heavy metals to fish, and preliminarily discuss the influence of heavy metals pollution to the diversified level of fish such as individual, organ, tissue, cell and molecule. thus we tried to provide scientific evidence to establish preventative management measures, avoid and relieve the harm of heavy metals pollution to aquicolous ecosystem in time

    隨后以這幾種重金屬作為實驗毒物，以鯽魚為實驗動物，應用環境生物技術、火焰原子吸收分光光度法、鄰苯三酚自氧化法、透射電鏡等技術研究了重金屬cu 、 zn 、 cd和cr對鯽魚的急性毒性及其安全濃度評價、混合重金屬在鯽魚幼體組織內的積累和分佈、 cd對鯽魚鰓和肝臟中sod活性的影響、 cd對鯽魚肝細胞和腎細胞超微結構的影響等，全面和系統地研究了水環境中重金屬暴露對魚類的毒性影響，初步探討了重金屬污染對魚類的個體? ?器官? ?組織? ?細胞? ?分子等各水平層次的影響，為制定漁業生產上預防性的管理措施提供科學依據，及時避免或減輕重金屬污染對水生生態系統造成的損害。
  3. Mps is stored in connective tissue cells, fibers, and the ground sub - stance of corium and subcutis, where, over longer periods of time, it reaches concentrations which must be considered biologically active

    Mps （多磺酸粘多糖）儲存於結締組織細胞、纖維組織以及真皮和皮下組織基質，並在經過更長一段時間后在該處達到具有生物活性的濃度。
  4. 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
  5. Thus, in order to investigate the developmental pathways not only involved in the regulation of growth and patterning, but also in the determination of cell lineages and differentiation, we utilized the fluorescent immunohistochemical methods, flow cytometry analysis sorting ( facs ) and molecular methods to investigate the developmental law of mammary gland at the different developmental stages, distribution of the stem cells in mammary gland, the methods of isolation, culture and evaluation for the stem cells, the multipotent abilities in vivo and in vitro, and the efficient cultural system for stem cells enriched in vitro. the results showed below : 1

    我們以小鼠為模型，運用組織化學、免疫熒光組織（細胞）化學、流式細胞儀分選方法（ facs ）以及分子生物學手段，研究了小鼠乳腺的發育規律：小鼠乳腺組織中類乳腺幹細胞：小鼠乳腺細胞的分離、培養以及類乳腺幹細胞的鑒定；小鼠類乳腺幹細胞分化的潛能；小鼠乳腺類腺體體外短期培養富集類乳腺幹細胞體系的優化等。研究結果表明： 1
  6. Part 1 : the culture and identification of es - d3 cells and the study of the efficiency of eb formation from es cells when grown on mef feeder layer in es culture medium or cultured in es culture medium supplemented with lif 1000u / ml, es - d3 cells being used in our experiments formed normal clones, expressed akp and kept their normal karyotype over many passages. the in vitro and in vivo differentiation experiments showed that es - d3 cells could differentiate into variety of cell types derived from three primary germ layers

    結果顯示： eso3細胞在小鼠胚胎成纖維細胞上和或含白血病抑制因於億f ）的es細胞培養液中形成典型的胚胎幹細胞克隆，堿性磷酸酶染色結果為強陽性，具有正常二倍體核型以及具有在體內外分化為三個胚層來源的組織細胞的潛能，而且具有形成種系嵌合動物的能力。
  7. Different from mammals, the early embryos of fish can not be preserved for the long period at the very low temperature ( - 196 ). therefore, three methods were usually applied to cryogenic preservation of the fine and rare species of fish : 1 ) perserving fish spermatozoon in cryogenic condition. researchers have had systematically studied on this technique for many years, and this technique has been utilized in application and made a lot of effects ; 2 ) combining with the techniques of cell engineering ( nuclear transplantation and electric fusion etc. ), and through the process of culturing histiocyte of fish, cryopreservation and re - culture after thawing, carrying out somatic cell breeding of fish. the past studies showed that the nucleolus of somatic cells of fish have totipotency

    多年來，國內外學者對各種魚類精液的冷凍保存進行了大量的系統研究，目前這項技術已達到實用水平，並日益發揮作用；二是對魚類培養的組織細胞冷凍保存，通過魚類細胞的培養、超低溫凍存、解凍后再培養過程，結合細胞工程技術（如核移植、電融合等）進行體細胞育種；大量的研究結果表明魚類體細胞核具有發育的全能性，隨著細胞培養技術、細胞工程技術日益發展成熟，完全具備實現魚類物種種質長期保存的理論基礎和技術條件。
  8. Leaf gap ( lacuna ) a region of parenchyma differentiated in the stem vascular cylinder immediately above a diverging leaf trace. lateral connections insure no break in the vascular system

    葉隙：葉跡從中柱分出的上方，初生維管柱上方出現的一些薄壁組織細胞，與莖的維管柱結構不同，它的側向連接保證了莖葉維管系統的連續。
  9. Based on the reseaching of lycoris leaf micro - morphology characters by sem scanning, light microscope viewing and using paraffin method in the article, we try to provide the proofs of experiment and the efffective characer indexes to discuss the system and evolution of the lycoris. we find these microscope characers through reseach are as follows : the arrangement type, density and the length of stoma ; the shape and length of the epidermal cells ; the ridge of epidermis ; the transverse shape of leaf ; the number of the vascular bundle ; the style of vessel arrangement of vascular bundle in the middle vein ; the layers of palisade tissue ; the ratio of the thicken of palisade tissue to that of spongy tissue ; the angle number of the middle leaf ; the type of ventilating cavity etc. these characters are different from those of species in lycoris, meanwhile these characters are similar to those of some species in lycoris. so these characters can be used as the character indexes for differentiating species and reseaching systematic evolution of lycoris ; we can divide lycoris into two subgenus by these characteristic indexes : the species of one subgenus are l. aurea ( l " her. ) herb, chinensis traub, l. caldweuii traub, l. anhuiensis y. hsu et q. j. fan, l. longituba y. hsu et q. j. fan ; the species of another subgenu s are l. houdyshelii traub, l. albiflora koidz.,

    研究結果表明：葉表皮的氣孔排列方式、長度、長寬比，脊的明顯與否，葉表皮上的顆粒紋飾的多少、大小，葉表皮細胞長度、長寬比、垂周壁形狀，上部葉柵欄組織細胞層數、葉的維管束數、葉中脈導管組成數目，氣腔類型，葉的脊部遠軸面的角數，葉緣的形狀等這些特徵在種間存在差異，同時，在有些種之間又有相似性；因此，這些特徵既可以作為區分種的證據，又是研究石蒜屬植物系統演化的性狀指標，根據這些性狀指標，可以將石蒜屬植物大致分為兩個亞屬：一是忽地笑、中國石蒜、短蕊石蒜、安徽石蒜、長筒石蒜，二是江蘇石蒜、乳白石蒜、石蒜、玫瑰石蒜、稻草石蒜；在兩個亞屬中其中有些種如忽地笑、長筒石蒜、中國石蒜的親緣關系則更近些。
  10. In this experiment, by methods of transmission electron microscopy, effects of low dosage of cd2 + ( 1. 87mg / l ) on the ultrastructure of muscular cells in male crabs at the different times were studied from september to november in 2001. in the experiment, male crabs were bought from aquatic product market in taiyuan and raised in laboratory for more a weed before treatment

    體外暴露鎘對長江華溪蟹肌肉組織細胞超微結構的影響應用透射電鏡技術，於2001年9 10月，研究了鎘處理后5d 、 15d 、 30d時對長江華溪蟹（ sinopotamonyangtsekiense ）肌肉細胞超微結構的影響。
  11. Successful treatment of recurrent histiocytic necrotic lymphnoditis

    復發性組織細胞性壞死性淋巴結炎治驗
  12. Labeling tunel method. the cell ultrastructural changes were similar to apoptosis in animal cells : the apical meristemetic cells underwent the programmed cell death. this was first detected in the apex cells of apical meristem, while peripheral cells differentiated gradually into different parts of a floral bud. but all the cells in the floral bud were subjected to the pcd process before it developed into a complete flower. 140bp dna fragment was found to deposit in apical bud during the plant development. the most important role of caspase - 8 was detected by western blot, and the expression of the procaspase - 8 was time - related with the dna frgmentation and the transformation from vegetative to the reproductive growth. these results suggested that pcd was an active process during the differentiation of apical meristem, and the senescence observed in the apical bud was due to the pcd process

    顯微超微結構研究表明，短日照條件下豌豆頂芽的衰老過程是從營養生長錐向花芽的轉化，而用dna原位末端標記tunel caspase - 8 western blot和140 bp dna片斷積累的試驗結果證明，轉化為花芽的整個生長錐細胞發生了編程性死亡pcd ，而且其最頂端部分細胞首先發生pcd ，而頂端周圍的分生組織細胞逐漸分化出花芽的各部分，但頂芽最後並沒有發育成為完整的花，所有細胞就都發生pcd ，從而頂芽衰老。
  13. The oviduct wall consists of a thin layer of connective tissue, basal lamina and a layer of columnar epithelial cells

    輸卵管壁由一層上皮細胞、基膜及結締組織細胞組成。
  14. The stimulating effect of mps on the rate of synthesis of connective tissue cells has been documented in various investigations

    許多調查研究記錄了mps能促進結締組織細胞的合成。
  15. Before laying eggs, a lot of secretions appear in oviduct ; epithelial cells show tightly each other ; near the basal lamina, epithelial cells show finger - like protuberances ; the layer of basal lamina is thin and there are another layer of connective tissue cells out of the basal lamina

    產卵前：輸卵管管腔中有大量分泌物；上皮細胞排列緊密，胞核較大，在基膜處細胞呈指狀突起。基膜層較薄，外側有一層結締組織細胞。
  16. Four different types of connective tissue cells are found out of the basal lamina, hi the first type of connective tissue cells, most of the nuclei are occupied by normal chromatins, but in other three types of connective tissue cells, abnormal chromatins are rich in nuclei

    4 、結締組織細胞與基膜相連，主要有4類。第1類細胞：細胞核中常染色質居多，而其它3類細胞核內異染色質較多。第2類細胞：細胞質內含有許多體積較小的電子緻密顆粒。
  17. Then using ecbp21 antibody and immunogold transmission electron microscopy method, we studied the subcellular localization of ecbp21. the results indicated that the gold particles were mainly localized in the cell wall in callus cells and rachis cells of angelica dahurica. these results indicated that ecbp21 mainly localized in cell wall, which provide a direct evidence of the extracellular existence of ecbp21. furthermore, using ecbp21 antibody and immunohistochemical method, we studied the organic specially distribution of ecbp21, the results indicated that ecbp21 distributed in all organize, but it distributed more in leave n flower rachis than in leafstalk and root

    首先，構建了ecbp21表達載體，誘導了重組蛋白的表達，並通過膠回收法獲得了大量純化重組ecbp21蛋白，制備了高效價、高特異性抗體；隨后，利用ecbp21抗體，結合免疫膠體金電鏡定位技術進行了ecbp21亞細胞定位研究，結果顯示：在白芷愈傷組織細胞和花序軸細胞中金顆粒主要分佈在細胞壁區域，而在細胞內未發現或僅有少量金顆粒分佈，表明ecbp21蛋白主要定位於細胞壁區域，這為細胞外cambp （ ecbp21 ）的胞外存在提供了直接證據：進一步，利用ecbp21抗體，通過免疫組織化學分析研究了ecbp21組織特異性分佈狀況，結果表明ecbp21在白芷各組織中均有分佈，但在葉、花、花序軸中分佈較多，而在葉柄、根中分佈較少。
  18. Results essential oil was not found in the promeristem of stem ; in the primary meristem of stem and the early stage of stem ' s primary structure, the essential oil was mainly distributed in glandular hairs ; in the primary structure of stem, the essential oil was mainly distributed in cortex parenchyma cells ; in the secondary structure of stem, the essential oil was mainly distributed in remaining cortex parenchyma cell

    結果在廣藿香莖的原分生組織中，未觀察到有揮發油分佈；在莖的初生、分生組織和初生結構形成早期，揮發油主要分佈在莖表皮上著生的腺毛中；在莖的初生結構中，揮發油主要分佈在皮層薄壁組織細胞中；在莖的次生結構中，揮發油則主要分佈在殘存的皮層薄壁組織細胞中。
  19. Conclusion the more production of matrices ， the better formation of tissue - engineered cartiolage ； the constructs of chondrocytes seeded onto pga coating with pla ， lec and plys can form tissue - engineerd cartilage in animals who have inherited immunity

    結論細胞支架復合物體外培養期間有基質產生，是組織工程化軟骨生成的前提條件；以卵磷脂、多聚賴氨酸及聚乳酸共同修飾的聚羥基乙酸支架與軟骨細胞復合培養后回植到有免疫力的動物體內可生成組織工程化軟骨。
  20. The location, the histopathologic and immunohistochemical appearance of the tumor, and the time elapsed since the initial treatment make it probable that this tumor is associated with prior radiation treatment

    由其腫瘤位置、組織病理及免疫組織化學表現、最初治療結束至發病時間間隔等特性分析，此惡性纖維組織細胞瘤可能與先前之放射治療有密切關系。
分享友人
分享到 Line

分享到臉書