遺傳染的 的英文怎麼說

中文拼音 [zhuànrǎnde]
遺傳染的 英文
infectious
  • : 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)...
  • : Ⅰ動詞1 (用染料著色)dye 2 (感染) catch [contract] (a disease) 3 (沾染) acquire (a bad hab...
  • : 4次方是 The fourth power of 2 is direction
  1. The majority of aberrations are sporadic although on rare occasions a chromosomal disorder is directly inherited.

    盡管偶爾可見一種色體疾病是直接,但是大量色體異常是散發
  2. However, only three species of the cephalochordate including b. lanceolatum, b. floridae, and b. belcheri, have so far been studied for their chromosome numbers, and the karyotypic analysis and banding study of amphioxus chromosomes remains largely untouched

    Floridae 、 b belcheri三種文昌魚色體數目。有關文昌魚色體核型和帶型研究尚未見任何報道,文昌魚色體核型和帶型研究將為比較基因組學和細胞學研究提供珍貴背景資料。
  3. Crossing over the exchange of material between homologous chromatids by the formation of chiasmata

    交換:同源色單體之間形成交叉時物質交換現象。
  4. The same phenomenon was observed in interspecific hybridization between chlamys farreri and chlamys nobilis. the karyotypes of adult hybrids and their parents were analyzed and compared. the chlamys nobilis ' s diploid chromosome number is 2n = 32, karyotype consists of 6m + 26t, nf = 38

    對該雜交組合親本華貴櫛孔扇貝色體核型分析表明,華貴櫛孔扇貝雜交扇貝細胞學研究共有zn = 32條色體,核型公式為2n = 32 = 6m + 26t ,色體臂數nf = 38 。
  5. Complex vertebral malformation ( cvm ), a lethal autosomal recessive inherited defect in holstein breed, was newly reported in demark

    摘要荷斯坦奶牛脊柱畸形綜合征是近年新發現一種常色體隱性病,該病對純合子胎兒是致死性
  6. Here is a fellow, who, infected by the most pestilent and blasphemous code of devilry that ever was known, abandoned his property to the vilest scum of the earth that ever did murder by wholesale, and you ask me why i am sorry that a man who instructs youth knows him

    有這么一個人,因為受到了人世間最險惡最褻瀆魔鬼信條,竟然把財產放棄給了世界上最壞殺人如麻流氓,而一個教育青年人竟然會認識他。對此你卻要來回我為什麼感到憾,好吧,我來回答你。
  7. Some of our dna - based services, for example, clinical diagnostics, pre - natal parentage testing and dna profiling are offered through our wholly owned subsidiary dna - tech limited

    病和基因測試提供最新獸類及臨床診斷方法,包括親子鑒證產前病測試dna指紋鑒證及基因改造食品檢測等。
  8. Episome is an additional genetic element that can exist either as an autonomous entity or be inserted into the continuity of the chromosome of a host cell.

    附加體是能插入寄生細胞連續色體之中,也能以自主實體而存在一種附加因素。
  9. Consider as what recessive heredity causes euchromosome to high myopia

    對于高度近視則認為是常色體隱性引起
  10. Under the general term genetic system we include the mode of reproduction of the species, its chromosome cycle.

    我們在總術語系統中包括種繁殖方式,色體周史。
  11. The prussian blue iron stain reveals extensive hepatic hemosiderin deposition microscopically in this case of hereditary hemochromatosis ( hh )

    普魯士藍鐵色顯示,性血色素沉著癥( hh )患者在鏡下可見廣泛肝臟含鐵血黃素沉著。
  12. Hemochromatosis can be primary ( the cause is probably an autosomal recessive genetic disease ) or secondary ( excess iron intake or absorption, liver disease, or numerous transfusions )

    血色素沉著癥或可以是原發(病因大概為常色體隱性病) ,也可以是繼發(過多鐵攝取或吸收、肝臟疾病、大量輸血) 。
  13. During this process, a series of modification appeared on the xi, which led to the formation of stable heterochromatin that can be inherited steadily in cell duplication

    失活色體上面往往發生一系列修飾,導致產生非常穩定色質且能在細胞復制過程中穩定
  14. The karyotye analysis was made on the 5th passage, the number of the chromosomes ranged from 187 to 200, and no heteroploid cell was found

    對第5代代細胞進行了學分析,代4次之後,其色體形態正常, 4n為187一200之間,未發現明顯異倍化現象。
  15. Since the important roles of eo protein in the viral infection. immunity and virus - host interaction. the homology of 21 csfv strains was investigated by sequence analysis of eo genes in this study, which will provide some evidence for epidemiological study. in addition, the eo gene of hog cholera lapinized vaccine ( hclv ) strain was expressed in the prokaryotic and eucaryotic systems, and the recombinant proteins were preliminarily analyzed by immunological method

    鑒于eo蛋白在病毒感,誘導機體免疫及與宿主細胞相互關系中作用,本研究克隆了2株豬瘟病毒eo基因並將其與其它毒株eo基因進行了序列分析,揭示了我國豬瘟病毒流行株之間演化關系,為豬瘟病毒流行病學研究提供依據。
  16. Our feet are vulnerable to repetitive mechanical stress and skin irritations due to tremendous daily usage. common foot problems common foot problems in elderly people include dry skin, calluses, corns, friction blisters, ingrown toenail, foot deformity, fungal infection and warts

    足部問題成因很多,局部如皮膚感和不合適鞋襪,另外,如糖尿病並發周邊血管毛病變形足等,都是重要因素。
  17. Y chromosome is transmitted in the form of hap - loid, leading to extreme disequilibrium of y chromosome genetic markers distribution in different population. the prerequisite of str application in forensic medicine is establishment of a database of population y - str loci haplotype distribution. therefore we need to form haplotypes by using the known highly polymorphic str loci and detect more local population

    由於y色體呈單倍體,導致y色體標記在不同人群中分佈極不平衡,群體差異比常色體str位點更加顯著,在法醫學應用前提條件是:建立含有多個y - str位點單倍型群體分佈數據庫。
  18. 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、色體與基因組結構和功能;來自於基因重組、突變和篩選生物變異;族群學;運用方法分析蛋白質功能,基因調控和性疾病。
  19. This paper reviews known and suspected causes of stillbirth including genetic abnormalities, infection, fetal - maternal hemorrhage, and a variety of medical conditions in the mother

    這篇文章回顧了已知和懷疑造成死胎原因,包括異常,感,胎兒-母親出血和母親醫療條件不同。
  20. A hereditary disorder principally affecting the connective tissues of the body, manifested in varying degrees by excessive bone elongation and joint flexibility and by abnormalities of the eye and cardiovascular system

    馬方氏綜合癥:一種失調癥,主要感身體結締組織,骨骼顯露出不同程度地過長和關節過于靈活,以及眼睛和心血管系統異常等癥狀。
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