遺傳學與疾病 的英文怎麼說

中文拼音 [yízhuànxuéyǔjíbìng]
遺傳學與疾病 英文
genetics and disease
  • 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）...
  • 學 : Ⅰ動詞1 （學習） study; learn 2 （模仿） imitate; mimic Ⅱ名詞1 （學問） learning; knowledge 2 （學...
  • 疾 : Ⅰ名詞1 （疾病） disease; sickness; illness 2 （痛苦） suffering; pain; difficulty 3 （姓氏） a su...
  • 病 : Ⅰ名詞1 （疾病; 失去健康的狀態） illness; sickness; disease; malum; nosema; malady; morbus; vitium...
  • 遺傳學 : genetics; hereditism遺傳學家 geneticist
  • 遺傳 : [生物學] heredity; hereditary; inheritance; inherit
  • 疾病 : disease; illness; sickness; pathema
  1. 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。
  2. The new cnv map ? compiled from 270 individual genomes of people with african, asian and european ancestry ? will change the way in which scientists search for genes involved in disease

    根據來自非洲、亞洲和歐洲的270個人的基因分析資料，科學家們繪制了新的「復制數量變異」圖，它將改變科學家們尋找與疾病相關的遺傳因子的方式。
  3. Chromosome karyotypintg. the classical method in the technology of chromosome genetic analysis, is one of the important means in genetic research and supplementary clinical diagnosis. and it is then key index to analyze chromosome translocation or deficiency, and diagnosis of a variety of genetic diseases. the goal of chromosome analysis is to relate deviations from normal structure to biological or clinical effects

    染色體核型分析，染色體遺傳分析技術的經典方法，是遺傳學科學研究和輔助臨床診斷的重要手段之一，是分析染色體易位，缺失，診斷各種遺傳病變的關鍵指標，染色體分析的目的就是要確定細胞或個體的染色體組成，尤其是要將其與正常結構間的偏差和生理的或臨床疾病關聯起來。
  4. First half focuses on human genetics and molecular biology, covering fundamentals of pedigree analysis, linkage analysis, molecular cloning, and gene analysis as well as ethical / legal issues, all in the context of an auditory disorder

    前半段會著重於人類遺傳學與分子生物學，涵蓋家族系譜分析、連鎖分析、分子選殖、基因分析與道德法律議題的基礎概述，並且皆以聽覺系統疾病為例來說明。
  5. Use of genetic methods to analyze protein function, gene regulation and inherited disease

    以及運用遺傳學的方法分析蛋白質的功能、基因的調控與遺傳性的疾病。
  6. Although previous genetic studies found a link between crohn ' s disease and mutations in a gene known as card15, those mutations alone are not considered to account for the entire genetic component of disease

    雖然以前的遺傳學研究發現克羅恩病可能與一個叫做card15基因的突變有關，但僅僅這個突變不足以用來解釋疾病的整個遺傳因素。
  7. 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。
  8. They also scanned the dna to search for copy number variations, which are submicroscopic insertions and deletions of genetic material that scientists believe may be linked to autism and other diseases

    他們也掃描dna來尋求復制數的變化趨勢，發現科學家提出的遺傳學材料的亞微觀的插入或是刪除，可能與孤獨或其他疾病有關系。
  9. Ukraine has the capacity to produce over 70 million discs annually, significantly more than the expected legitimate demand for all of central and eastern europe in all of the copyright industries. ukraine s pirate material is flooding other countries and disrupting the already vulnerable markets throughout all of europe. losses to the music industry alone have been over 200 million annually for the past several years

    因為對細胞與遺傳的過程有進一步的了解，科學家們已經找出令人興奮的新研究途徑，為影響數百上千萬美國人的重大疾病，如帕金森癥及阿耳滋海默氏病、糖尿病、心臟病、愛滋病及癌癥等，尋找治療法。
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