酶缺乏 的英文怎麼說

中文拼音 [quēfá]
酶缺乏 英文
azymia
  • 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 ...
  • 乏 : Ⅰ動詞1. （缺少） lack Ⅱ形容詞1. （疲倦） tired 2. （貧困） poor 3. [方言] （沒力量; 不起作用） exhausted; useless
  • 缺乏 : be short of; lack; deficiency; insufficiency; be wanting in
  1. Scid with adenosine deaminase deficiency scid

    並線苷酸去胺酶缺乏
  2. E. coli is capable of metabolizing both hexose and pentose sugars, but it lacks pdc - adh ii system. however, zymomonas mobilis is able to produce ethanol efficiently by an overactive pdc - adh ii system, but its utilizable substrate range is restricted to glucose and fructose

    大腸桿菌含有同化戊糖和己糖的所有必需酶，但缺乏pdc - adh系統，只能生成非常少的酒精。相反，運動發酵單胞菌具有較強的pdc - adh系統，能很好地發酵生成酒精，但只能利用葡萄糖和果糖。
  3. A similar, less severe, metabolic disorder is congenital lactase deficiency

    類似的，病癥略輕為一點的代謝紊亂疾病是乳糖分解酶素缺乏癥。
  4. Many asian adults are lactose intolerant, as a result of a lack of the digestive enzyme lactase in the gut

    許多亞洲成年人有乳糖不耐受癥，因為他們消化道中缺乏消化乳糖的乳糖酶。
  5. Phenylketonuria is a condition in which phenylalanine to tyrosine conversion is diminished because the enzyme phenylalanine hydroxylaze is deficient.

    苯丙酮酸尿癥是一種由於苯丙氨酸羥化酶缺乏，苯丙氨酸轉變成酪氨酸的過程被削弱的病。
  6. Phenylketonuria ( pku ) is an inherited metabolic disease that results in mental retardation and other neurological problems when treatment is not started within the first few weeks of life. the disease arises from the deficiency of a single enzyme, phenylalanine hydroxylase, which converts the essential amino acid, phenylalanine, to another amino acid, tyrosine. failure of the conversion to take place results in a buildup of phenylalanine in the body that then damages the central nervous system

    苯丙酮尿癥（ pku ）是一種智力發育不全的先天性疾病，患者由於肝贓內苯丙氨酸羥化酶缺乏，苯丙氨酸不能正常代謝為酪氨酸，從而導致苯丙氨酸在肌體組織內積累，引起腦損傷和累進性精神障礙，臨床表現為智力低下，頭發顏色轉黃，尿有異臭味，重者似鼠臭。
  7. Many legume plants may produce the beneficial isoflavones, which are vital to the formation of nitrogen - fixing root - nodules and the disease resistance response of plants. white clover ( trifolium repens ), a high quality legume forage, however, has little isoflavones. to improve the isoflavone contents of such forage, an available strategy is to introduce gene ( s ) encoding the key enzyme ( s ) in the biosynthesis pathway of insoflavones

    許多豆科植物中都含有異黃酮類化合物，異黃酮對植物根瘤的形成和植物的防禦反應至關重要，但是在牧草白三葉中缺乏這種有益的化合物，因此通過轉基因實驗將異黃酮合成酶基因導入白三葉中，提高其異黃酮的含量，增加白三葉的營養價值。
  8. Study of newborn umbilical blood screening of g6pd deficiency

    磷酸脫氫酶缺乏的研究
  9. P - galactosidase of e. coli which is scarce in human blood plasma and has a variety of substrates, is one of the most frequently used enzyme labels. it is used both in heterogeneous and homogeneous enzyme immunoassay

    大腸桿菌的-半乳糖苷酶，因人血漿中缺乏此酶，並具有大量易得的底物，被用於均相及非均相免疫分析，是目前最常用的標記酶之一。
  10. Hypophosphatasia is a rare inherited metabolic disease characterized by rickets with reduced plasma and tissue alkaline phosphatase activity

    摘要先天性磷酸酶缺乏癥為一少見之代謝性疾病，其主要特徵為血清及組識之鹼性磷酸酶下降以及佝僂癥。
  11. But there are still no reports about the relationships of dnpi - like and gabaergic immunoreactive ( gad - li ) terminals with pag - like immunoreactive ( pag - li ) neurons in " zone - shaped area ". to answer these questions, we observed systemically the synaptic connections among the pv - like immunoreactive neurons, fibers and terminals and the connections between dnpi - like, gabaergic terminals and pag - li neurons using the methods of electron microscopic imrnunohistochemistry, triple - immunofluorescence histochemistry and retrograde tracing method combined with pre - embeded immunoelectron microscopic double - labeled technique

    但是目前對新發現的囊泡膜mu轉運體一dnn樣陽性終末與帶狀區內pag樣陽性神經元之間ej關系，以及谷氨酸脫發酶（ gad ，是gaba能神經元和終末的特異性標識物）是否參與其調控作用，尚缺乏系統的形態學資料。
  12. Z which involve in melanin, tyrosinase related protein 1 gene ( tyrpi ) and dermal melanin inhibitor gene ( id ). the genomic structure of tyrp1 was determined and its correlation between melanin accumulation and tyrp1 expression was studied. moreover, we constructed a bac contig near id locus which was on a region short of dna marker in chr. z

    利用構建的bac文庫對z染色體上黑色素相關基因酪氨酸酶相關蛋白1基因（ tyrp1 ）的基因結構以及該基因的表達與黑色素沉積的關系進行了研究，同時構建了位於z染色體上缺乏標記區段的表皮黑色素抑制因子基因（ id ）的bac重疊群。
  13. The enzyme lactate gastrointestinal lack of fresh milk to drink or diarrhea, may be diverted volunteers

    對于胃腸道缺乏乳酸酶或喝鮮牛奶容易腹瀉的人，可改喝酸奶。
  14. Effect of vitamin a deficiency on rat ' s sperms and enzymes activities of testis

    缺乏對大鼠生精能力及睪丸標志酶活性的影響
  15. ( 3 ) there was only ldh5 in the livers of al l groups of microtus fortis. the ldh4 and ldh5 were absent in the kidneys of the small voles from heilongjiang, but five kinds of ldh isozymes were all found in the kidneys of the other three groups

    （ 3 ）四類東方田鼠的肝臟中都只含ldh5 ；腎臟中，除黑龍江小體型東方田鼠缺乏ldh4和ldh5外，其餘三類東方田鼠都含五種ldh同工酶。
  16. Proofreading activity and low replication fidelity in vitro, distributive manner in dna synthesis, poor ability to discriminate nucleotides at the level of binding and also the possibility of its expanded roles in long patch ber, ner, dna replication and recombination at its excess state

    Lp表現出很低的dna復制保真度：它沒有3 』一5 』外切酶活性因而在a復制中缺乏校讀活性：對底物dn p鑒別能力低卜在長單鏈模權上催化dna復制時散布式的合成方式。
  17. These observations appear, in theory, to suggest that life - threatening cancer progression could be indefinitely avoided by the roughly decadal reseeding of all our stem cell pools with autologous ones that had been engineered ex vivo to lack the genes for telomerase or alt, but to have long telomeres

    在理論上，這些觀察顯然提示了，威脅生命的癌癥進展可以被無限期地避免，辦法是大約10年就用自身幹細胞來種植一次我們的全部幹細胞庫這些自身幹細胞已在體外經過加工，使其缺乏端粒酶基因或alt基因、但有很長的端粒。
  18. After the gst fusion proteins were processed by factor xa and were purified by gluta - thione - sepharose 4b affinity chromatography, the recombinant protein hbrp with high purification would be acquired. during the process of separation and purification, the every result which can show the location of the aim protein was monitored by 10 % sds - page. the gst fusion proteins acquired finally were examined and analyzed by the methods of western - blottin

    原核表達系統具有表達效率高，操作方便等特點，但缺乏翻譯? 3 ?后修飾，以pgex載體表達的gst hbrp融合蛋白，具有表達的蛋白穩定性好，在體外易於純化等優點，表達的gst融合蛋白可用gluthioneseph刪sc4b進一步純化一factorxa酶切與測分離，從而大量獲得hbrp重組蛋白，而且一次回收率大約在90以上。
  19. It is well documented that they jointly take part in gene transcription that led by rna polymerase ii. however, whether baf complex and nf1 / ctf are also involved in the formation of rna polymerase ii - mediated transcription initiation complex is still uncertain, and a number of the currently proposed models still lack the support of experimental data

    哺乳動物swi snf （ baf ）復合物和轉錄因子（ nf1 ctf ）都是轉錄活動的重要調控因子，許多實驗證實，它們共同參與了基因轉錄調控活動。 baf復合物與轉錄因子nf1 ctf是否一同參加了由rna聚合酶介導的基因轉錄起始復合物的形成，目前還沒有比較一致的認識，已有的模型仍缺乏實驗支持。
  20. Standard guide for detection of nucleic acid sequences of the human immunodeficiency virus hiv - 1 by the polymerase chain reaction technique

    用聚合酶鏈反應技術探測人體免疫缺乏病毒hiv - 1的核酸類的標準指南
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