結腸轉位 的英文怎麼說

中文拼音 [jiēchángzhuǎnwèi]
結腸轉位 英文
displacement of colon
  • 結 : 結動詞（長出果實或種子） bear （fruit）; form （seed）
  • 腸 : 名詞1. （消化器官的一部分, 通稱腸子） intestines 2. （用腸衣塞肉、魚等製成的食品） sausage 3. （感情; 情緒; 情感） heart
  • 轉 : 轉構詞成分。
  • 位 : Ⅰ名詞1 （所在或所佔的地方） place; location 2 （職位; 地位） position; post; status 3 （特指皇帝...
  • 結腸 : [生理學] colon; large intesting; col ; coli ; colo 結腸穿刺術 colocentesis; colipuncture; 結腸腹...
  1. The result showed that the homology rate of pila gene among the 5 avian pathogenic e. coli strains tested and one human e. coli were from 89. 8 % to 91. 1 %, and the homology rate of amino acid were from 88. 5 % to 91. 8 %. the homology rate of pila gene sequence among 5 avian pathogenic e. coli strains tested and avian pathogenic e. coli reported ( serotype o1, o2, o78 ) were from 87. 8 % to 90. 2 %, and the homology rate of amino acid were from 84. 6 % to 91. 2 %. there had homology in avian pathogenic e. coli. there had some common antigen side in type 1 pili of avian pathogenic e. coli

    結果表明：運用msha法檢測1型菌毛的檢出率為80 （ 36 45 ） ， pcr法的檢出率為95 . 5 （ 43 45 ） ， pcr方法用於1型菌毛的檢測比msha更加敏感、快速、特異性強；選擇5株優勢血清型雞源致病性大腸桿菌代表株（ o _ （ 89 ） ， o _ （ 119 ） ， o _ （ 141 ） ， o _ （ 127 ） ）的1型菌毛pila基因的pcr擴增片段經純化后，分別定向克隆到puc18質粒的多克隆位點，構建了含有目的基因片段的克隆質粒，並轉化到dh5株大腸桿菌載體菌中，篩選獲得陽性克隆菌株。
  2. Objective : to investigate the effect of pumpless portosystemic bypass in clinical piggyback liver transplantation. methods : after catheterized inferior mesenteric vein, the silastic catheter ( filled with heparin saline ) was connected with the catheterized tube of internal jugular vein or subclavian vein in four piggyback liver transplantation patients. the channel was opened after the portal vein was occluded. the portal vein blood poured into the superior vena cava through the pumpless channel. the changes of mesenteric congestion, portal vein pressure, blood pressure and pulse were observed. results : during the occlusion of portal vein, the portal vein pressure was increased greatly, the intestine was congested and swelled obviously and the blood pressure and pulse fluctuated gently. after the pumpless bypass opened, intestinal congestion and swell were abated markedly, the portal pressure, blood pressure and pulse gradually returned to normal range. conclusions : pumpless portosystemic bypass shows a great effect on clinical piggyback liver transplantation. it is a feasible and economical method

    目的探討背駝式原位肝移植術中採用體外門-體靜脈無泵轉流的臨床效果.方法4例行背駝式原位肝移植患者，腸系膜下靜脈屬支插管經體外硅膠管（充滿肝素鹽水）與頸內靜脈或鎖骨下靜脈插管相接，在阻斷門靜脈后開通腸系膜下靜脈插管，門靜脈血從體外無泵轉流管流入上腔靜脈，觀察轉流前後腸道瘀血、門靜脈壓、血壓、脈搏等變化情況.結果門靜脈阻斷后腸道明顯瘀血、腫脹，門靜脈壓力明顯升高，血壓、脈搏有不同程度的波動，無泵門靜脈轉流開放后，腸道瘀血、腫脹明顯好轉，門靜脈壓力逐漸恢復正常水平，血壓、脈搏恢復正常.結論背駝式原位肝移植術中體外門-體靜脈無泵流具有方便、經濟、實用等優點，具有良好的臨床效果
  3. In this study, we designed a pair of primers based on the sequence of the upstream and downstream of chicken il - 2 gene. about 600 bp chicken il - 2 cdna fragment was cloned from cona - stimulated chicken splenocytes by reverse transcription - polymerase chain reaction ( rt - pcr ) and was subcloned into puc18 vector. recombinant clone was demonstrated by restriction enzyme digestion and dna sequencing. next, we construct recombinant plasmid pproex ? t - il - 2. the cdna of chicken il - 2 gene was subcloned into bamh i / hind iii sites of vector. the recombinant plasmid pproex ? t - il - 2 was transformed into e. coli dh5a and the bacteria was induced with iptg. it was demonstrated by sds - page and western blot that a 18kda protein which was equal to chicken il - 2 protein in molecular weight was expressed in e. coli dh5a. the expression level was up to 30 % of the total bacterial proteins. the purified protein was used to prepare the antibody against chicken il - 2 protein

    經酶切鑒定及dna序列測定，該基因為雞il - 2基因，其序列與sundick等報道的完全一致。在此基礎上，我們把雞il - 2基因亞克隆到大腸桿菌原核表達載體pproex ~ （ tm ） ht中，構建重組表達質粒並進行確證性序列測定，重組質粒測序結果表明將編碼雞il - 2成熟蛋白的基因正確地插入到原核表達載體pproex ~ （ tm ） ht的目的位點。重組質粒轉化受體菌dh5後用iptg於37進行誘導培養， sds - page和westernblot分析顯示，表達的雞il - 2融合蛋白分子量約為18kda ，表達的融合蛋白經薄層掃描發現目的蛋白表達量約占菌體蛋白的30 。
  4. Reverse malignant phenotypes of colonic carcinoma cells transfected with antisense gene to htrt

    反義人端粒酶催化亞單位基因轉染對人結腸癌細胞惡性表型的逆轉作用
  5. In countries where hepatitis is not endemic, most malignant cancers in the liver are not primary liver cancer but metastasis ( spread ) of cancer from elsewhere in the body, e. g. the colon

    在肝炎不太流行的國家，最多見的肝臟惡性腫瘤不是原發性肝癌而是體內其他部位，如結腸癌癥轉移（擴散）所致。
  6. Here are liver metastases from an adenocarcinoma primary in the colon, one of the most common primary sites for metastatic adenocarcinoma to the liver

    結腸腺癌的肝臟轉移癌。結腸是肝臟轉移性腺癌的最主要原發部位。
  7. A new e. coli promoter - probe vector phn1005 was constructed by using a red - shift enhanced gfpmut3 as reporter gene and showed the following characters : 1, bamhi at the 5 " end of gfpmut3 structure gene could be used to clone promoter - active fragment and the strength of promoter could be quantitatively assayed. 2, a rrnbtlt2 terminator from rrna gene at the 3 " end of gfpmut3 could permit clone strong promoter. 3, another rrnbt1t2 terminator was inserted upstream bamhi to prevent reading through of promoters from puc19

    進一步以紅移且熒光強度提高21倍的gfpmut3為報告基因，構建了大腸桿菌啟動子探針載體phn1005 ，該載體上gfpmut3結構基因5 』端的bamhi位點可用來克隆具有啟動子活性的dna片段並定量分析插入的啟動子強度；其3 』端含rrnat1t2終止子，可允許克隆強啟動子；在bamhi上游同樣插入rrnat1t2終止子以防止載體puc19上的啟動子的轉錄通讀； gfpmut3結構基因上游還插入一段內含子序列使正反六種讀碼框的翻譯均可被終止，可保證gfpmut3以正確的讀碼框翻譯。
  8. A 1. 7kb fragment encoding ge of prv fa strain was obtained by pcr from plasmid ppge templated using a pair of the designed primers containing ecori and bamhi ' sites. the ge gene fragment cutted with ecori and bamhi was inserted into the expression plasmid pbv220 including these two endonuclease sites for constructing the recombinant plasmid pbvge. strain dh5a of e. coli contain pbvge was induced at 42 for 4 - 6hr after incubation with vigorous shaking at 30 for 3hr or so

    以質粒ppgedna為模板， pcr擴增出1 . 7kb的ge基因完整片段，將擴增產物以ecori和bamhi雙酶切后，插入原核表達載體pbv220的p _ rp _ l啟動子下游的ecori和bamhi位點間，得到重組表達質粒pbvge ，轉化了pbvge的大腸桿菌dh5a經溫敏誘導表達后，用sds - page和western - blot ，以及瓊脂雙擴散來檢測，結果表明prvfa株ge基因在原核載體上得到高效表達，表達產物約占總蛋白的17 。
  9. To construct eukaryotic expression vector of mbl gene with codon 54 point mutation, the target sequence in pgem - mbld plasmid, which conains mbl cdna with codon 54 mutant allele, was amplified by pcr. after the cdna fragement and plasmids pci - neo were prepared by digestion with sma i and sal i, the fragment was inserted into sma i and sal i site in pci - neo eukaryotic expression vector, and the recombinant vector, named pci - mbl54, was obtained. the pci - mbl54, digested with restriction enzymes, was found to contain the point mutation mbl cdna by agarose gel electrophoresis analysis

    本實驗以ggc54gacmbl突變為研究對象，選用真核表達質粒pci - neo ，根據已構建好的含54位密碼子突變型mbl基因t載體的結構，設計合成新的引物， pcr擴增54位密碼突變型mbl基因，凝膠回收，雙酶切pcr產物和pci - neo質粒， t4連接酶連接，將前者克隆至後者的sma和sal位點，轉化大腸桿菌xl - 1blue ，氨芐選擇培養。
  10. Sequences flanking tn5 - 1063a can be recovered from the genome of mutant by excision, self - ligation and transfer to e. coli. the total dna of mutant was excised with ecori, which cut the genome frequently but not cut the transposon. after sequencing the self - ligated transpon, dna fragment flanking tn5 was obtained. the result showed 042bm - x1 contains a tn5 insertion in the gene smc00190, which function was unknown and was demonstrated to be related to salt tolerance by this study, and the gene was named as rst - 0x1

    通過ecori酶切突變株基因組，得到完整的tn5 （含有在大腸桿菌中起始復制的oriv ）及其側翼的序列片段，該片段自連后轉化大腸桿菌，以tn5兩端已知的序列設計引物進行測序。 blast的分析測序結果表明， 042bm - x1和042bm - x2中tn5分別定位在苜蓿中華根瘤菌1021染色體上smc02682和smc00419基因內部，本實驗證明它們和042bm耐鹽相關，命名為rst - 0x1和rst - 0x2基因。
  11. Paraduodenal fossae originate as congenital peritoneal anomalies owing to failure of mesenteric fusion with the parietal peritoneum and an associated abnormal rotation during imprisonment of the small intestine beneath the developing colon ( 1 ? 3, 22, 27 ? 33 )

    十二指腸旁隱窩的產生是由於先天性的腹膜異常，即腸系膜與壁層腹膜融合失敗，同時小腸在局限於整條結腸中間位置的發育過程中旋轉異常。
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