孟德爾基因 的英文怎麼說

中文拼音 [mèngdéěrjīyīn]
孟德爾基因 英文
mendelian factor
  • 孟 : Ⅰ名詞1 （指農歷一季的第一個月） the first month （of a season） 2 （姓氏） a surname Ⅱ形容詞（舊...
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  1. Mendelian gene is not a real physical entity but an abstraction or symbol.

    孟德爾式的基因並不是真正的實體，而是抽象概念或者是說明性的符號。
  2. If the characteristic is governed by simple mendelian genes, the typical monohybrid and dihybrid ratios become apparent in the f2 generation

    如果其特徵取決于單一孟德爾基因，那麼典型的單基因雜種和和雙基因雜種的遺傳比率將在子二代呈現。
  3. Add to that the exceptions of half - bloods, muggle - borns and squibs and the temptation to analyze its hereditability in terms of mendelian genetics becomes almost unbearable ( for some of us anyway )

    除此之外還有混血，麻瓜出身和啞炮，這更使運用孟德爾基因學理論分析遺傳的努力變得幾乎讓人無法忍受（至少對於我們中間的某些人來說） 。
  4. The tl seeds are screening on the ms medium which contains 50ug / ml kan, and there are about 70 % of the transgenic lines showed the kan - resistance with a ratio of 3 : 1. however, the other lines did n ' t show the ratio consistent with the mendelism. it might prove that most of the transgenic plants only have one insert

    對收獲的轉基因番茄t _ 1代種子進行卡那黴素抗性篩選，結果發現， 70以上獨立轉化株系的t _ 1代種子出現了3 1的抗性分離，另一些獨立轉化株系的種子並未表現出符合孟德爾遺傳的分離比，說明大部分er - shsp基因是以單拷貝的方式插入植物基因組。
  5. The individuals of rhd - positive phenotype with intact exons carried generally insert fragments and boxl box2 and box3 and this proved that inserts or rh box could n ' t affect the express of rh d gene. in 2 of the 5 wei nationality pedigrees whose proband were rh d - negative, rhc / e phenotype of all the rh negative individuals was ccee. rhd exon 4nsert and rh box did not be found in all individuals

    在7個先證者為rhd陰性的漢族家系中，大部分成員均出現插入片段和rhbox ，且在遺傳上符合孟德爾遺傳定律， d外顯子完整且表型為rhd陽性的家系個體成員廣泛帶有插入片段和box1 、 box2或box3 ，插入片段或rhbox並未影響d基因的表達。
  6. Microsatellite marker has many advantages such as a great quantity, extensive dispersion around the genome, high polyomorphism, mendelian codominant inheritance, rapid and convenient detection

    摘要微衛星標記具有數量多、在基因組中分佈廣、多態性豐富、呈孟德爾共顯性遺性、檢測快速方便等特點。
  7. Omim morbid map - alphabetical listing of diseases and corresponding cytogenetic map locations, with links to omim entries. accessible from omim page ( see genes )

    在線人類孟德爾遺傳?經常更新的人類基因和遺傳失調的目錄，有鏈接到其它相關的文獻參考，序列記錄，和相關數據庫。
  8. Results showed that : ( 1 ) in general, the segregation ratios of target gene in some tl lines are conformed to 3 : 1, however, some are not possibly due to gene silence or missing in the self - pollinated progeny ; ( 2 ) two homozygous plants were identified from 10 putative transgenic plants

    主要結果如下： （ 1 ）我們對外源基因在番茄體內的遺傳規律研究表明，在大多數情況下，單拷貝插入外源基因將導致轉基因後代按孟德爾單顯性基因3 1規律分離，但是部分轉化系比例偏低，可能發生了基因丟失或者沉默。
  9. On the medium containing 3 mg / l of ppt as selective agent, about 65 % of t1 seeds germinated, while only 5 % for wild - type seeds. on selection pressure - free medium, about 73 % of tl seedlings were gus - positive and none for the control seedlings. this is coincided with the mendel ' s law of 3 : 1 segregation

    T _ 1代的種子在含ppt3 . 0mg l的萌發培養基上萌發率為65 ，在沒有篩選壓的培養基上生長的苗子的gus陽性率為72 . 82 ，符合孟德爾的3 ： 1的分離定律（去除本身不萌發的因素） 。
  10. Walter s. sutton proposed that chromosomes were the site of mendel ' s hereditary factors. the hardy - weinberg law established the mathematical basis for studying heredity in populations

    薩頓提出染色體就是孟德爾的遺傳因子所在地。哈代魏因貝格二氏定律建立了研究種群遺傳的數學基礎。
  11. Futheralong, the work of gregor mendel, an austrian monk, on garden peas established the quantitative discipline of genetics

    現在仍然是基因控制的一種途徑。隨后，奧地利僧侶格里格?孟德爾關于國栽豌豆的著述確立了遺傳學的定量規律。
  12. 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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