遺傳基因突變 的英文怎麼說

中文拼音 [yízhuànjīyīntūbiàn]
遺傳基因突變 英文
genetic gene mutation
  • 遺 : 遺動詞[書面語] （贈與） offer as a gift; make a present of sth : 遺之千金 present sb with a gener...
  • 傳 : 傳名詞1 （解釋經文的著作） commentaries on classics 2 （傳記） biography 3 （敘述歷史故事的作品）...
  • 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...
  • 突 : Ⅰ動詞1 （猛沖） dash forward; shoot out 2 （高於周圍） protrude; bulgeⅡ副詞（突然） abruptly; sud...
  • 遺傳 : [生物學] heredity; hereditary; inheritance; inherit
  • 突變 : 1 （突然急劇的變化） sudden change; change suddenly; transilience; accident; saltation; revulsion...
  1. This paper introduced the application of biotechnology in rice genetics and breeding, including tissue culture, cell mutants selection, protoplast fusion, apomixis, molecular mark assisted breeding and genic transformation

    簡要綜述了生物技術在水稻遺傳育種中的應用，主要包括組織培養、細胞突變體的篩選、原生質體融合、無融合生殖以及分子標記輔助育種和轉基因技術等方面。
  2. The geneticists next tried crossing normal - looking rams who were carriers of the mutation with completely normal ewes

    接著，遺傳學家試著將攜帶突變基因，但看起來正常的公羊，與完全正常的母羊交配。
  3. The callipyge phenotype in sheep is an inherited muscular hypertrophy that affects only heterozygous individuals who receive the clpg mutation from their father

    只有遺傳了來源於父本的clpg突變的雜合子個體才能表達這一表型，因此推測這一性狀受印記基因的控制。
  4. One missense mutation was found in 48 hypertriglyceridemic patients and identified to be pro207 - leu by sequencing, pedigree analysis of this proband has been carried out and showed that the pro band ' s father is also a carrier of this mutation

    徵得患者家屬的同意和支持，對其家族三代十人進行了完整的家系分析。家系分析顯示，先證者的突變來自其父親的遺傳。在外顯子6 、 7 、 8中未檢出基因突變。
  5. This article reviews the clinical manifestations, mutation feature, gene location and phenotype of different ischemic cerebrovascular disease caused by monogenic disorders, including coagulation disorders, erythrocytic disorders, inherited small vessel disease, metabolic disorders, connective tissue diseases, vasculopathies and disorders of unknown etiology

    本文主要闡述了單基因遺傳障礙引起的缺血性腦血管病，包括凝血障礙、血細胞病、遺傳性小血管病、代謝障礙、結締組織病、大動脈病及不明原因引起缺血性腦血管病的臨床特徵、突變特點、基因定位及表型等遺傳學研究進展。
  6. Although many genetic mutations have been suggested as causes or risk factors for parkinson ' s disease, the low penetrance of some mutations and the low disease concordance in relatives suggests that there must be interactions between multiple factors

    雖然許多遺傳突變已經被認為是帕金森氏病的危險因素，但是一些突變基因的外顯率低，家族相關的發病率也低，這說明一定有多因素的交互作用。
  7. The topics include : structure and function of genes, chromosomes and genomes, biological variation resulting from recombination, mutation, and selection, population genetics, use of genetic methods to analyze protein function, gene regulation and inherited disease

    主題包括：基因、染色體與基因組的結構和功能；來自於基因重組、突變和篩選的生物變異；族群遺傳學；運用遺傳學的方法分析蛋白質的功能，基因的調控和遺傳性疾病。
  8. The mutant lines were crossed with deficiency lines on chromosome 2 and 3 respectively, and the genetic sites of 11 stocks have been determined. of them four showed a different phenotype from the known genes that control the heart development

    分別將這些有心臟突變的品系與果蠅第二和第三染色體缺失系雜交，測定了11個品系的遺傳學位點，其中4個品系在遺傳學位點上有別于已經報道的心臟發育控制基因。
  9. Accordingly, ers2 - 1 is still able to confer ethylene insensitivity via a single receptor gene ers1 in the quadruple mutant, but at a highly reduced level compared to its function in the triple mutants. the major difference between the quadruple and triple mutants is the absence of a wild - type ers2 gene in the quadruple mutant, and we propose that the dominance conferred by ers2 - 1 can be mediated and amplified via the wild - type ers2 to the subfamily i receptor ers1

    三突變體的遺傳背景與四突變體相比，只是在三突變體中保留了ers2的野生型基因，而當這個野生型的ers2基因突變后，對乙烯不敏感的ers2 - 1基因的功能便減弱了，說明顯性基因ers2 - 1在etr1 - 7 ； err2 - 3 ； ein4 - 4三突變體中的功能可以經由活化ers2后再傳給ers1 ，而不僅僅是直接傳給ers1 。
  10. From 19 arabidopsis male sterile lines isolated from an ethyl methanesulphonate - induced ( ems - induced ) population, a total of four male sterile mutants were screened with each mutant controlled by a single recessive gene

    首先對19個經化學誘變劑ems處理得到的雄性不育突變體進行背景純化和遺傳分析，從中篩選到四個單個隱性基因控制的雄性不育突變體（ ec2 - 157 、 ec1 - 188 、 ec2 - 115和ec2 - 214 ） 。
  11. The discoery of the genetic mutation ' s role in contributing to atrial fibrillation may ultimately improe physicians ' ability to identify patients who hae a hereditary predisposition to atrial fibrillation, which is often complicated by increased risk for stroke and heart failure

    這個對房顫有影響的基因突變的發現將可能最終提高內科醫生辨別易患房顫的遺傳體質病人的能力，房顫常因不斷增加的中風和心衰風險而復雜化。
  12. According to antibody - antibody ab - ab affinity and antibody - antigen ab - ag affinity, the algorithm can allot adaptively the scales of memory unit and antibody population. it is proved theoretically that the csaim is convergent with probability 1

    由於遺傳和免疫細胞在增殖中的基因突變，形成了免疫細胞的多樣性，這些細胞的不斷增殖形成無性繁殖系，無性繁殖稱為克隆。
  13. In the first large - scale screen of genetic changes in cancer cells, researchers have found that a typical breast or colorectal tumor results from mutations in about 90 genes, with different sets of mutations producing the same type of cancer

    在首次癌細胞遺傳改變的大規模篩選中，研究者發現典型乳腺或者結直腸腫瘤源於約90種基因突變，不同的突變組合產生同種類型的癌癥。
  14. The department has established the differential patterns of mutations causative of eye diseases in chinese in more than 10 candidate genes. it has gained international recognition through output from its research work, having contributed 42 publications on genetic eye diseases in international journals and presented 105 papers in international conferences. for clinical genetic screening service, a number of genetic markers based on disease causing mutations using blood samples have been established

    眼科及視覺科學學系已確立了十多個引致華人患上遺傳性眼疾的基因突變和標志，部份可作遺傳眼疾檢驗服務之用；這些研究成果獲得國際贊譽，眼科及視覺科學學系先後在國際眼科或遺傳醫學的雜志上發表了42篇論文，並在多個國際學術會議上發表了105個報告。
  15. Inherited gene mutations, such as those that cause hemophilia or muscular dystrophy, would have to be corrected as well before using a patient ' s own cells to create es cells

    在使用帶有遺傳性基因突變（例如血友病或肌肉營養性萎縮癥）患者的細胞來製造胚胎幹細胞之前，也需要先矯正缺陷基因。
  16. Actually, it ' s males that carry the mutant gene and pass it on, so it ' s his fault

    實際上，是雄性遺傳攜帶突變基因，所以都是他的錯
  17. 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。
  18. The article related research achievenment on the molecular genetics of mental disease and spirits obstruction, expounds the molecular genetics basis and the mechanism of result in mental disease from chromosome aberration, gene mutation, dynamic mutation and genetic heterogeneity, etc

    文章綜述了當前對精神病和精神障礙的分子遺傳學研究成果，從染色體畸變、基因突變、遺傳的異質性等方面闡明精神病發生的復雜的遺傳背景和機制。
  19. Variants have been deemed to confer susceptibility to common diseases and response to drug therapy in modern medicine study. it advances a challenge for gene mapping using polymorphic markers

    現代醫學研究認為疾病的發生、易感性及對藥物的反應差異性等復雜性狀與基因突變或遺傳多態性密切相關。
  20. Biotechnology. vocabulary. transgenic plants and cell cultures

    生物工程.詞匯.遺傳基因突變植物和細胞培植
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