染色體缺失 的英文怎麼說

中文拼音 [rǎnshǎitǐquēshī]
染色體缺失 英文
chromosomal defect
  • 染 : Ⅰ動詞1 （用染料著色）dye 2 （感染） catch [contract] （a disease） 3 （沾染） acquire （a bad hab...
  • 色 : 色名詞[口語] （顏色） colour
  • 體 : 體構詞成分。
  • 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 ...
  • 染色體 : [生物學] chromosome染色體疾病 chromosomal disorders; 染色體異常 chromosome abnormality
  • 染色 : dye; dyeing; colouration; tintage; tinging; dyschroia; colouring; colour; [半] decoration染色不足...
  • 缺失 : hiatus; deficiency; [遺傳學] deletion
  1. In addition to avermectins, s. avermitilis produces oligomycin, a strongly toxic compound. gene deletion vector pxl05 was used to disrupt oligomycin polyketide synthase ( pks ) encoding genes ( olma ) in streptomyces avermitilis cz8 - 73, the producer of anthelmintic avermectins b and the cell growth inhibitor oligomycin. olma gene cluster in the chromosome was displaced by deletion allele on the plasmid via double crossover

    本研究以產阿維菌素b和寡黴素的阿維鏈黴菌cz8 - 73為出發菌株，構建了基因缺失載體pxl05 ，並將其轉入cz8 - 73中，通過缺失載體和染色體之間的同源雙交換，對染色體上長達90kb的寡黴素聚酮合酶（ pks ）基因簇（ olma ）進行了缺失。
  2. A segment of the chromosome may become lost, resulting in a deletion.

    染色體的一個片段可能會丟失，結果產生染色體的缺失。
  3. Most deletions are likely to be the result of two breaks with loss of the chromosomal material between them.

    大多數的缺失可能是由於發生了兩個斷裂，而兩個斷裂之間的那部分染色體物質失去了。
  4. Aneuploidy the condition, resulting from nondisjunction of homologous chromosomes at meiosis, in which one or more chromosomes are missing from or added to the normal somatic chromosome number

    非整倍性：在減數分裂的過程中同源染色體不分離而造成的一條或多條染色體的缺失或增加。
  5. If both of a pair of homologous chromosomes are missing, nullisomy results

    如果一對同源染色體都缺失了，稱為缺體。
  6. It is due to the lack of homologous pairs of chromosomes, so chromosomes cannot pair in meiosis, and the resulting gametes may have extra or missing chromosomes

    這歸因於染色體同系對的缺乏，以至於在減數分裂中染色體不能配對，導致配子有可能有額外或缺失染色體。
  7. Monosomy and srisomy are the conditions in which one or three homologs occur respectively, instead of the normal two

    單染色體以及三染色體都是正常的染色體缺失或增加一條染色體造成的。
  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. Chromosome karyotyping, the classical method in the technology of chromosome genetic analysis, is one of the important means in genetic research and supplementary clinical diagnosis

    染色體核型分析，是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。
  10. 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。
  11. After obvious cytopathogenic effects developed, virus - contained supematants were harvested, and the progeny viruses were screened for lacz - expressing viruses by a plaque assay using x - gal. single blue plaques were picked, and a recombinant prv stably expressing lacz gene ( designated as rprv - lacz ) was obtained after ten cycles of plague purification and pcr identification. the results showed that the lacz gene expression cassette was stably expressed in the recombinant rprv - lacz derived from bartha - k61 strain

    該載體與具有高度感染性的bartha - k61株基因組dna通過脂質體加plus法共轉染vero細胞，採用甲基纖維素固定病變， x - gal染色，經過10代藍斑純化獲得了一株穩定表達lacz基因的ge tk基因缺失突變株，命名為rprv - lacz 。
  12. The two end - points were localized on a 4. 3kb bamhl - ecor1 fragment of a cosmid 16c3 and a 1. 2kb sail fragment of a cosmid 17g7 respectively. the deletion junction was localized on a 2. 8kb bamhi fragment of the zx1 chromosome

    兩個端點分別定位在野生型菌株基因組文庫粘粒16c3的4 . 3kb的bamh1 - ecor1片段上和17g7的1 . 2kb的sal片段上，缺失界點定位在zx1染色體上的一個2 . 8kbbamh片段上。
  13. Partial tetrasomy 9 syndrome

    號染色體短臂部分缺失綜合征
  14. The nature of the mutant alleles is either nonsense mutation or the mutation which disrupted the splicing of the primary transcripts. anti - en antibody staining and in situ hybridization on sll germline clone ( glc ) embryo using wg antisense probe showed defective en protein bands and defective wg transcripts bands

    通過對sll生殖系克隆胚胎進行的抗engrailed （ en ）抗體染色和wg反義探針的原位雜交結果表明，與野生型果蠅的胚胎相比較， en蛋白和wg轉錄物條帶出現了明顯的缺失。
  15. Anti - en antibody staining and in situ hybridization on oxt glc embryo using wg antisense probe showed defective en protein and defective wg transcripts bands. the embryonic analysis results indicated that the disruption of oxt gene would lead to the disruption of wg transcription and the expression of engrailed gene, as the wg transcription is dependant on the engrailed

    通過對oxt生殖系克隆胚胎進行的抗en抗體染色和wg反義探針a雜交結果表明，與野生型果蠅的胚胎相比， en蛋白和wg轉錄物條帶都出現了明顯的缺失。
  16. The diagnosis and clinical of y chromosome microdeletions in male infertility

    染色體微缺失的診斷及臨床意義
  17. P. densata resembles its parents by combining patterns characteristic of each parent as well as shows new features resulting possibly from recombination and genome reorganization

    其同源染色體之一18srdna位點的缺失，可能是染色體重組的痕跡。
  18. The deletion mutants were proved to be genetically stable, and thus might be promising strains in industrial production of avermectins b. although s. avermitilis produces eight related components of avermectins, only two components, bla and bib, are available for the medical, veterinary and agricultural fields

    該缺失突變是在染色體上通過同源雙交換完成的，不會發生進一步的重組，因此突變株性狀穩定，在工業生產上具有應用價值。阿維菌素的天然發酵產物共有八個組分，其中只有b1組分的殺蟲活性最高，被作為殺蟲劑在農業和畜牧業中使用。
  19. In 2001, wilson and his colleagues cloned another two members - human wnk1 gene and wnk4 gene which were located on chromosome 12 and 17, respectively. the two genes are disease - causing genes responsible for a mendelian hypertension. the disease - causing mutations are the large deletions in the first intron in wnk1 gene, causing increased expression in leukocytes

    2001年， wilson等克隆了此家族的另兩個成員? ?人的wnk1和wnk4基因，分別位於12號和17號染色體，這兩個基因是一種孟德爾遺傳型高血壓病的致病基因，致病突變分別是wnk1基因第一內含子的大片段缺失，導致患者白細胞的基因表達量提高5倍左右。
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