酶缺陷 的英文怎麼說

中文拼音 [quēxiàn]
酶缺陷 英文
enzyme defect
  • 酶 : 名詞[生物化學] （生物體的細胞產生的有機膠狀物質） enzyme; ferment
  • 缺 : Ⅰ動詞1 （缺乏; 短少） be short of; lack 2 （殘缺） be missing; be incomplete 3 （該到而未到） be ...
  • 陷 : Ⅰ名詞1 （陷阱） pitfall; trap2 （缺點） defect; deficiency Ⅱ動詞1 （掉進） get stuck or bogged do...
  • 缺陷 : defect; fault; faultiness; vitium; lesion; flaw; disorder; imperfection; drawback; blemish
  1. This is due to genetic deficiency of the adrenocortical enzyme which normally converts that substrate to a nonandrogenic steroid in the biosynthesis of cortisol

    這是由於在皮質醇生物合成中將底質轉變為非產生男性特徵類固醇的腎上腺皮質酶遺傳缺陷所致。
  2. Knowledge of distribution and regulation of ugts remains limited. liver microsomes is a frequently used enzyme source in in vitro study of glucuronidation, but it has the following deficient respects : 1. liver microsome is a mixture of various enzymes, and therefore the results from microsome cannot represent the function of a individual isozyme

    關于ugts的組織分佈和調節這方面的知識還不多，過去常採用肝微粒體進行研究，但有以下缺陷： u ）肝微粒體是多種藥酶沮合的復雜體系，因而實驗結果難以區分是一種同工醇的作用
  3. Isolation and characterization of nitrate reductase - deficient mutants of dunaliella salina

    杜氏鹽藻硝酸鹽還原酶缺陷型突變株的篩選與鑒定
  4. Isolation and identification of nitrate reductase - deficient mutants of dunaliella salina

    杜氏鹽藻硝酸鹽還原酶缺陷型突變藻株的分離和初步鑒定
  5. Although this method gives high sensitivity, the radioactive labels present many problems such as a potential hazard to analyst and environment, which limited its application in dna diagnostic laboratories. in order to overcome these problems a serious of non - radioactive dna probes such as fluorescent, chemiluminescent and electrochemical probes have been developed. although these new methods display many advantages, they have not been used to take place completely the traditional method because of low sensitivity or complex equipment or other shortcomings

    自20世紀80年代以來，各種非同位素如酶、熒光素、生物素、地高辛標記的化學發光法和熒光分析法以及以電活性物質做標記的電化學方法相繼問世，這些方法雖然在一定程度上克服了同位素標記的缺陷，但由於存在靈敏度不夠高或檢測系統龐雜或儀器價格昂貴或標記物不穩定等缺陷，還不能完全取代傳統方法。
  6. Although the development of relatively non - toxic immunosuppressive or tolerance - inducing regimens will be required to justify clinical trials using pig organs, recent advances in our understanding of the biology of xenograft rejection and zoonotic infections, and the generation of alpha1, 3 - galactosyltransferase - deficient pigs have moved this approach closer to clinical application

    盡管用豬的器官進行臨床試驗尚有賴于相對無毒的免疫抑制劑或致耐方法的發展，但是我們在異種移植排斥反應及豬源人畜共患病等方面生物學知識的進步，以及1 ， 3半乳糖轉移酶缺陷豬的產生，已經使異種移植離臨床應用更近了一步。
  7. The predicted protein contained 441 amino acids. the activity of the epsp synthase encoded by these two subclones was shown by complementation of the aroa mutation in e. coli strain er2799, indicating two subclones possess a intact activity of the enzyme 5 - enolpyuvyl - 3 - phosphoshikimic acid synthase

    採用互補試驗驗證分離的與草甘膦耐受相關的dna片段的生物學功能，結果顯示r3h1和r7h1均能使大腸桿菌epsp缺陷型菌株er2799恢復在限制性培養基上的生長能力，證明這兩個亞克隆的插入片段具有完整的epsp合成酶功能。
  8. Such deficiencies cause lysosomal storage disorders, such as gaucher ' s disease, and replacement of the gene is an effective treatment

    這樣的缺陷引起溶酶體堆積病（例如，高歇病） ，基因置換是一種有效的療法。
  9. Although the deelopment of relatiely non - toxic immunosuppressie or tolerance - inducing regimens will be required to justify clinical trials using pig organs, recent adances in our understanding of the biology of xenograft rejection and zoonotic infections, and the generation of alpha1, 3 - galactosyltransferase - deficient pigs hae moed this approach closer to clinical application

    盡管用豬的器官去驗證臨床試驗需要相對無毒的免疫抑制劑或致耐的方法，但隨著近來我們對異種移植排斥生物學及動物傳染病感染的深入理解，以及1 ， 3半乳糖轉移酶缺陷豬的產生，異種移植更接近臨床應用。
  10. In other studies of mutant ( knockout ) mice that fail to express the neuronal isoform of nitric oxide synthase ( nos ), smaller infarcts develop and the mice have less severe neurologic deficits than normal mice ( 61 )

    其他一些研究變異（被擊昏的）老鼠的試驗沒有能夠表達一氧化氮合酶（ nos ）的神經元對碘氧基苯甲醚，但是出現的梗死梗小，而且與正常的老鼠相比，老鼠的神經學缺陷也不那麼嚴重（ 61 ） 。
  11. The concept is a logical extension of the replacement of a natural lysosomal enzyme in people who are congenitally deficient for it, something that is already being done

    這個理念是病人天生缺陷的天然溶酶體酶置換的邏輯延伸，在這方面已經做了一些事情。
  12. The genetic polymorphisms due to mutations in the methylene tetrahydrofolate reductase gene may increase the risk for ntds

    亞甲基四氫葉酸還原酶基因突變導致的遺傳多態現象可增加神經管缺陷（ ntd ）發生的危險性。
  13. In this thesis, the hplap gene was cloned into the ppiczaa plasmid and induced expressed in the protease - deficient strain p. pastoris smd1 168. the clone that could secrete hplap with enzyme activity was selected

    本研究將hplap基岡兌隆到spiczoa質粒中並在畢赤酵母屍pastorjs蛋白酶缺陷菌株smdi168中誘導表達，獲得了有活性的分泌型hplap 。
  14. The hair of single gene disease is the commonnest in disease of single gene of ill mechanism include : metabolization is enzymatic kind of blemish disease, haemoglobin structure is unusual with quantitative blemish disease, blemish of other albumen factor

    單基因病的發病機制單基因疾病中最常見的包括：代謝酶類缺陷疾病，血紅蛋白結構異常和數量缺陷疾病，其他蛋白因子缺陷。
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