孟德爾遺傳 的英文怎麼說

中文拼音 [mèngdéěryízhuàn]
孟德爾遺傳 英文
mendelian inheritance
  • 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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  • 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）...
  • 遺傳 : [生物學] heredity; hereditary; inheritance; inherit
  1. Thomas in brno ? once in austria - hungary, today part of the czech republic ? mendel revealed the laws of inheritance by experimenting with pea hybrids in the walled monastic garden

    孟德爾在修道院圍墻內的花園進行豌豆雜交的實驗，因而發現了遺傳的定律。
  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. Characters controlled by the dna of extranuclear organelles are not inherited according to mendelian laws and are transmitted only through the female line, since only the female gametes have an appreciable amount of cytoplasm

    由於細胞質大多來自母體所產生的配子，所以由細胞核外的細胞器的dna所控制的遺傳性狀一般只隨母系而遺傳，也不符合孟德爾定律。
  4. 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） 。
  5. Mendel ' s law of inheritance

    孟德爾遺傳定律
  6. This information is valuable both as a prelude to linkage analysis, which generally assumes mendelian transmission

    因為性狀存在孟德爾遺傳是連鎖分析的潛在條件。
  7. Mendelian genetics, genetic mapping techniques, and statistical analysis of large populations and their application to particular studies in behavioral genetics

    孟德爾遺傳學，遺傳定位技術，和大母群的統計分析及其在行為遺傳學中特定研究之應用。
  8. Today the subject has four main subdivisions mendelian genetics ( classical genetics ), population genetics, cytogenetics, and molecular or biochemical genetics

    現在，該學科主要包括四大部分?孟德爾遺傳學（古典遺傳學） ，種群遺傳學，細胞遺傳學以及分子或生化遺傳學。
  9. He was blacklisted in the former soviet union and its satellites as the founder of a “ reactionary ” discipline, and mendelian genetics was declared a pseudoscience

    由於他是某個反動學說的創始者，因此前蘇聯及附庸國都將他列在黑名單上，孟德爾遺傳學也被打成偽科學。
  10. Ninety - four segregating markers were identified, among which 74 ( 78. 7 % ) were in agreement with 1 : 1 mendelian ratio, and 20 ( 21. 3 % ) were distorted markers

    有94條片段在父本或母本中分離。卡方檢驗顯示74 （ 78 . 7 % ）個分離標記符合孟德爾1 : 1遺傳比例， 20個為偏分離標記。
  11. 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。
  12. 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。
  13. 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。
  14. 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。
  15. Mendel also correctly stated that two copies of every factor exist and that one factor of inheritance could be dominant over another

    孟德爾還正確地說出，每個因子存在兩個復製品，一個遺傳因子可以較另一個為顯性。
  16. 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。
  17. The researches acquired suggest that manipulating ferritin expression and other soluble components of seed iron in soybeans and possibly other seeds, using mendelian genetic technique and biotechnological approaches, could contribute to a sustainable solution to the global problem of iron deficiency

    已有的研究表明，使用孟德爾遺傳方法和生物技術途徑提高大豆和其它穀物類種子中鐵蛋白的表達和其它可溶性鐵成分，將有助於全球性缺鐵問題的有效解決。
  18. We propose that genetic materials in rootstock being translocated and integrated into the genome of the germ cells and embryonic cells in scion are the main reasons why the majority of the hybrid seedlings have wild properties and the heredity of fruit trees violate mendel ' s laws of heredity

    砧木中的遺傳物質轉移並整合到接穗生殖細胞和胚胎細胞的染色體組中，是雜種後代出現大量野生植株和果樹遺傳不遵守孟德爾定律的主要原因。
  19. 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。
  20. 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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