轉移抑制基因 的英文怎麼說

中文拼音 [zhuǎnyíyìzhìjīyīn]
轉移抑制基因 英文
metastasis suppressor gene
  • 轉 : 轉構詞成分。
  • 移 : Ⅰ動詞1. （移動） move; remove; shift 2. （改變; 變動） change; alter Ⅱ名詞（姓氏） a surname
  • 抑 : Ⅰ動詞（向下按; 壓制） restrain; repress; curb Ⅱ連詞[書面語]1 （表示抉擇） or 2 （表示轉折） but3 ...
  • 制 : Ⅰ動詞1 （製造） make; manufacture 2 （擬訂; 規定） draw up; establish 3 （用強力約束; 限定; 管束...
  • 因 : Ⅰ動詞[書面語] （沿襲） follow; carry on Ⅱ介詞1 [書面語] （憑借; 根據） on the basis of; in accord...
  • 轉移 : 1 （改換位置） shift; transfer; divert 2 （改變） change; transform 3 [醫學] （擴散） metastasis;...
  • 抑制 : 1 （控制） restrain; control; check; hold up; curb; stop; repress; bridle; choke; prehension; sup...
  1. 2. rat orthotopic liver trarlsplantation was performed in the strong rejecter combination of bn ( rtl " ) to lew ( rtl l ). this al1ogenic rejection model was stable and the survival time without immunosuppression agents was less than three weeks ( the average survival time was l 6. 6 i 2. 5 days, n = 5 )

    建立了大鼠bn （ rt1 ~ n ） lew （ rt1 ~ l ）原位肝移植同種異體排斥模型，該模博士學位論義基因轉移hu la個ig誘導大鼠移植肝免疫耐受的實驗研究中文摘要型排斥反應時間較為恆定，在不應用免疫抑制劑的情況下，生存期3周（平均生存時問人66士2
  2. It is applicable to coinject two or three genes whose expression products have no antagonistic action. 4. coinjection is a simple gene transfer method which saves time and money

    非桔抗基因（轉移基因的表達產物互不抑制）的共轉移（顯微注射法）是一種既經濟、又有效的方法。
  3. Dong z, bonfil rd, chinni s, et al. matrix metglloproteinase activity and osteoclasts in experimental prostate cancer bone metastasis tissue [ j ]. am j pathol, 2005, 166 ( 4 ) : 1173

    王醫術，周洪瀾，李亞娟，等.基質金屬蛋白酶及其抑制因子在前列腺癌侵襲和轉移中的作用[ j ] .吉林大學學報， 2006 ， 32 （ 5 ） : 847
  4. Firstly, according to the characteristic that the doppler frequency shift signal can be approximated as a single sinusoid signal, the extended sinusoid signal retrieval ( pisarenko and esprit ) methods are presented and signal state and measurement formulations are developed, so the kalman filter recursive method is got. the brief introduction of low velocity moving target doppler frequency shift signal wigner - ville transformation and wavelet transformation expression are presented in this paper. secondly, because the clutter is gaussian distribution, cumement and high - order spectrum based methods are presented and the simulation results prove their good performance to suppress gaussian clutter in low velocity moving target doppler frequency shift signal processing

    一個方面是根據低速目標的多普勒信號可簡化為單一正弦波形式這一特點，得到了擴展的高斯色噪聲背景下的諧波恢復演算法，即高斯色噪聲中的pisarenko諧波恢復法和旋轉因子不變法（ esprit ） ；並推導了信號的狀態方程和觀測方程，進而得到基於卡爾曼濾波的遞推演算法對信號進行提取；本文還簡單的介紹了低速運動目標的多普勒頻移信號的wigner - ville變換與小波變換；另一個方面是針對雜波服從高斯分佈這一特點，提出了對接收信號求累積量和高階譜來對高斯雜波進行抑制。
  5. Using ex vivo gene transfer technique, exogenous gene was introduced to the liver graft during cold preservation and express locally in the graft. the effect of inhibition of rejection and inducing liver graft tolerance was observed. through this study, the possibility of achieving graft tolerance by gene transfer without routine immunosuppressive drugs was explored

    我們採用adeasy腺病毒載體系統，自行構建攜帶huctla4 - ig的重組腺病毒，通過先體外后體內（ exvivo ）基因轉移技術，于供肝冷保存時，將該治療基因導入大鼠移植肝，使其于移植肝局部表達，觀察其抑制排斥反應，誘導大鼠移植肝免疫耐受的作用。
  6. The mechanism is that the introduced complementary oligonucleotides can bind to the corresponding mrna or double - stranded dna in genome and form partial double - stranded molecules or triple - stranded nucleic acid molecules by sequence - specific and nonsequence - specific antisense action, thus the target gene will be orientationally blocked and expression of the target inhibited so that therapeutic effect could be attained. in this study, we designed a fragment of human c ii ta cdna in antisense orientation using mrna of c ii ta as template. the primers were designed based on 94 - 500 nucleotides segment in 5 " end of ciita gene so that the interested gene contained 407 base pairs which included two aug codons in 1 16 and 188 nucleotides as well as the splicing site between the first and the second exons

    本研究設計以c tamrna為模板的反義cdna片段，從c ta基因5 』端第94位到500位核苷酸段設計引物，目的片段407bp ，覆蓋第116和188位兩個aug密碼子，也包含了第一外顯子和第二外顯子間的剪接位點：用常規分子生物學方法構建了反義片段的腺病毒表達載體（ padeasy - 1系統） ；腺病毒載體經hek293細胞包裝產生含反義片段的重組腺病毒，用氯化銫密度梯度離心法獲得純化的高滴度腺病毒；進行體外基因轉移，分別用反義片段真核表達載體轉染p388d1細胞和用重組腺病毒感染hela細胞，觀察導入的c ta基因反義rna抑制細胞內組成型或誘導型c ta基因表達的作用，從而達到調控mhc -類分子表達的目的。
  7. Objective the aim of this article was to induce long term survival allografts by blocking cd40 - cd40l pathway with homemade anti - cd40l monoclonal antibody mr1, then purify cd4 + cd25 + regulatory t cells from recipients with long term survival allografts, and adoptively cotransfer such cells together with tcr transgenic allogenic antigen specific cd8 + t cells into immunodeffient mouse. finally study whether cd4 + cd25 + t cells can suppress allogenic antigen specific cd8 + t cell mediated rejection, thus clarified whether cd4 + cd25 + t cell mediated regulation is one of mechanisms of prolongation of allograft survival by cd40 - - cd40l pathway blockade

    從移植物長期存活的受體內分選出cd4 + cd25 + t細胞，與tcr轉基因cds + t細胞同時過繼輸注到免疫缺陷小鼠體內，觀察co4 + co25 + t細胞對同種異體反應性cos + t細胞介導排斥反應的作用，探討在阻斷cd40se一~ cd40l共刺激途徑延長移植物存活中， cd4 + cd25 +調節性丁細胞是否是抑制排斥反應的機制之一。
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