染色體接合 的英文怎麼說

中文拼音 [rǎnshǎitǐjiēgě]
染色體接合 英文
chromosome conjugation
  • 染 : Ⅰ動詞1 （用染料著色）dye 2 （感染） catch [contract] （a disease） 3 （沾染） acquire （a bad hab...
  • 色 : 色名詞[口語] （顏色） colour
  • 體 : 體構詞成分。
  • 接 : Ⅰ動詞1 （靠近;接觸） come into contact with; come close to 2 （連接; 使連接） connect; join; put ...
  • 合 : 合量詞（容量單位） ge, a unit of dry measure for grain （=1 decilitre）
  • 染色體 : [生物學] chromosome染色體疾病 chromosomal disorders; 染色體異常 chromosome abnormality
  • 染色 : dye; dyeing; colouration; tintage; tinging; dyschroia; colouring; colour; [半] decoration染色不足...
  • 接合 : joint; zygosis; juncture; articulation; concrescent; nexus; coaptation; syndesis; synapsis; meet;...
  1. Fos + / th + / gfap + and fos + / vp + / gfap + triple labeled n - asc could be found in the mvz, pvn and son respectively ; ( 2 ) under electronic microscope, the astrocytic processes connected closely with the dendrites or axons of the neurons, where the bilateral membranes became thick. we call transiently it electron - dense areas ( edas ). the number of edas increased remarkably following hyperosmotic stimulation ; ( 3 ) when trace retrogradely, wga - hrp was microinjected into the unilateral son, pvn or nucleus of solitary tract ( nts ) respectively using the stereotaxic method, the n - ascs formed by the neurons triple - labeled with hrp / fos / th ( or vp ) and astrocytes labeled with gfap could be found in the mvz, son and pvn respectively ; ( 4 ) after being treated with heperosmotic nacl solution, intracellular calcium concentration in cultured hypothamic neurons and astrocytes increased and then decreased

    腦內gfap陽性結構也明顯增多，其分佈與fos陽性細胞分佈基本一致，表現為胞體肥大、突起粗長； ast緊密包繞在神經元周圍形成神經元- ast復合體（ n - asc ） ；在mvz 、 pvn和son三重免疫組化染色切片上可見到fos + th + gfap +第四軍醫大學博士學位論文和fos vp gfap三重標記asc ； （ 2 ）免疫電鏡下son內星型膠質細胞突起與神經元樹突或軸突之間接觸部位出現增厚的膜結構一電于緻密區（ edas ） ，高滲刺激后數量明顯增多： （ 3 ）將們個mp注入大鼠一側n卜、卜卜或孤束核（ ws ） ，分別在延髓內臟帶（ mvz ） 、 so和pvn內出現fos hrp th 、 fos hrp八p三重標記神經元和gfap陽性標記ast形成的n asc ； （ 4 ）高滲刺激使培養神經元和ast內鈣水平先升高后降低，最後維持在比高滲刺激前稍高的靜息鈣水平上。
  2. A novel dynamic evolutionary clustering algorithm ( deca ) is proposed in this paper to overcome the shortcomings of fuzzy modeling method based on general clustering algorithms that fuzzy rule number should be determined beforehand. deca searches for the optimal cluster number by using the improved genetic techniques to optimize string lengths of chromosomes ; at the same time, the convergence of clustering center parameters is expedited with the help of fuzzy c - means ( fcm ) algorithm. moreover, by introducing memory function and vaccine inoculation mechanism of immune system, at the same time, deca can converge to the optimal solution rapidly and stably. the proper fuzzy rule number and exact premise parameters are obtained simultaneously when using this efficient deca to identify fuzzy models. the effectiveness of the proposed fuzzy modeling method based on deca is demonstrated by simulation examples, and the accurate non - linear fuzzy models can be obtained when the method is applied to the thermal processes

    針對模糊聚類演算法不適應復雜環境的問題，提出了一種新的動態進化聚類演算法，克服了傳統模糊聚類建模演算法須事先確定規則數的缺陷.通過改進的遺傳策略來優化染色體長度，實現對聚類個數進行全局尋優;利用fcm演算法加快聚類中心參數的收斂;並引入免疫系統的記憶功能和疫苗接種機理，使演算法能快速穩定地收斂到最優解.利用這種高效的動態聚類演算法辨識模糊模型，可同時得到合適的模糊規則數和準確的前提參數，將其應用於控制過程可獲得高精度的非線性模糊模型
  3. Primary culture of rat preadipocyte were prepared from the epididymal, inguinal and perirenal the fat pads of male normal, healthy, 15 - 20 days sprague - dawley rats. the preadipocyte grew better under the condition of 37, 95 % humidity, 5 % co2, ph 7. 0 - 7. 2, centrifuged at 1000r / min, m199medium, and 10 % fetal bo vine serum, seeded at a density of 4 l04, 5 l04, / cm2. oil red o staining was the special method to distinguish adipocyte from other cells, gimsa and he could determine the stage of the adiopcyte differentiation through the number of lipid drop, size and the position of the nucleolus of the staining fat cell

    經過多次實驗，確定本實驗室大鼠前體脂肪細胞的最佳培養條件是：溫度為37 ，濕度為95 ， co _ 2濃度為5 ， ph值為7 . 0 7 . 2 ，離心力為1000r / min ，培養基為m _ （ 199 ）培養基，胎牛血清濃度為10 ，合適細胞接種密度為4 10 ~ 4 、 5 10 ~ 4個/ cm ~ 2 ，染色結果表明：油紅o染色是鑒定脂肪細胞的特異方法， gimsa和he染色可根據不同區域染色程度、著色差別判斷細胞核的位置及脂滴大小、多少，觀察大鼠前體脂肪細胞分化過程中的形態變化，進而確定脂肪細胞的分化階段。
  4. The co - expression of l l6 - hsd1 and gr in the saxne chorionic trophoblast suggests possible intrcrine achons ofglucoconicoid generated by l l6 - hsdl within the cells. 2. ewe radiomctric conversion assay showed that trctrient of the cells with the synthetic glucocorticoid - - dexarnethasone ( l0 - ' m ) for 24h increased the conversion of conisone to cortisol, and thes increase was blocked by the gr antagonist ru486

    雙標免疫組織化學染色結果顯示11p hsdi和gr共存於同一個滋養層細胞，提示在體內無活性的gc代謝產物?一17羥d脫氫皮質酮經11p hsdi還原活化后可以直接與同一個細胞內的gr結合，即以內在分泌（ intracrine ）形式發揮作用
  5. We propose that genetic materials in rootstock being translocated and integrated into the genome of the germ cells and embryonic cells in scion are the main reasons why the majority of the hybrid seedlings have wild properties and the heredity of fruit trees violate mendel ' s laws of heredity

    砧木中的遺傳物質轉移並整合到接穗生殖細胞和胚胎細胞的染色體組中，是雜種後代出現大量野生植株和果樹遺傳不遵守孟德爾定律的主要原因。
  6. It was also proved that the biosynthestic genes of apramycin was linked to the apramycin resistant gene in s. tenebrarius

    Pcr實驗證明基因重組菌株中接合轉移質粒同源整合到黑暗鏈黴菌h6的染色體上。
  7. We are also studying how the linear chromosomes and plasmids are transferred during conjugation

    此外我們也在研究線狀的染色體與線狀質體在接合生殖過程中如何地傳送。
  8. As cyclin b is the mark protein representing the process of prophase, we infered that cytochalasin b destroyed the polymerization of the nuclear actin and directly affected the process of prophase. nuclear actin played an important role in the process of the chromosome construction

    因為cyclinb是有絲分裂前期進程的標志性蛋白，所以我們認為細胞鬆弛素b破壞細胞核內肌動蛋白聚合后，直接影響了有絲分裂前期的進程，進而悅明核內肌動蛋白在有絲分裂前期染色體構建過程中起著重要作用。
  9. To detect the patients and carriers of the fragile x syndrome, various analytic methods could be used. one is cytogenetic diagnosis to observe the expression of the fragile site fraxa located at xq27. 3

    對脆x綜合征的診斷，可以通過細胞遺傳學方法觀察分析x染色體相應脆性位點的表達情況，或是通過southern印跡雜交的方法直接分析cgg重復的擴增突變。
  10. And the two pah ' s of pcr primers that bind to the adapter and the sequence of f fragment close by tn5 respectively were also designed. the genomic dna of b8 was isolated, digested with bamh i, and ligated to the adapter. using the two pairs of the primers, two rounds of pcr were performed hi turn and a fragment of 239bp was amplified successfully. lt was proved by cloning and sequencing that 18bp of the fragment is the sequence opposite to f fragment on the left of tn5 insertion site in b8f, the other is part of the 728 bp of f fragment. this result makes it possible to continue to carry out chromosome walking, to clone and sequence the whole genes of b fragment and f fragment, and to reveal the antagonistic molecular mechanism of b8

    試驗研究設計併合成了由40和44個堿基的寡聚脫氧核苷酸組成的染色體爬行接頭，在接頭序列和測定的f片段近tn5的序列上，設計了2對染色體爬行用的pcr引物，從b8菌株中提取基因組dna ， bamhi酶切，與染色體爬行接頭連接，依次用2對引物進行pcr ，擴增出239bp產物，經克隆、測序，發現其中18bp為擴增的相應于f片段在b8f菌株tn5插入位點對面的序列，其餘則為f片段728bp序列的一部分，為進一步進行染色體爬行，克隆和測定整個b和f基因，揭示陽菌株的拮抗分子機制提供了技術資料貯備。
  11. So that combine the genetic algorithms and neural network to complete the production of the system model of high - speed bidding. based on the reasonable model - building, use software " matlab " to get the achievement at the beginning. and take a lot of figures from project experiment as the sample to practice on the net, at the same time lots of experiments have been done to test them

    然後將經過0 - 1數字化處理的訓練集樣本送入網路，利用bp演算法訓練網路得出m組權值；之後採用實數編碼，將神經網路的權重作為ga的染色體，生成基因群體，再使用遺傳演算法尋優，使解碼得到的參數組合充分接近最佳參數組合，在此基礎上再用bp演算法對它們進行細調，從而來實現遺傳演算法和神經網路的結合，完成對投標快速報價系統的建模。
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