顯性遺傳 的英文怎麼說

中文拼音 [xiǎnxìngzhuàn]
顯性遺傳 英文
dominant heredity
  • : Ⅰ形容詞1 (明顯) apparent; obvious; noticeable; evident 2 (有名聲有權勢的) illustrious and inf...
  • : Ⅰ名詞1 (性格) nature; character; disposition 2 (性能; 性質) property; quality 3 (性別) sex ...
  • : 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)...
  • 顯性 : [生物學] dominance顯性性狀 dominant character; 顯性修飾因子 dominigene; 顯性遺傳 dominant inheritance
  • 遺傳 : [生物學] heredity; hereditary; inheritance; inherit
  1. Twenty cases of euchromosome viewy genetic ill were analyzed in five years

    20例常染色體顯性遺傳病5年隨訪結果分析
  2. Former and scarce, for euchromosome dominance heredity, begin to last all one ' s life from the baby

    前者少見,為常染色體顯性遺傳,從嬰兒開始持續終生。
  3. The prussian blue iron stain reveals extensive hepatic hemosiderin deposition microscopically in this case of hereditary hemochromatosis ( hh )

    普魯士藍鐵染色示,血色素沉著癥( hh )患者在鏡下可見廣泛的肝臟含鐵血黃素沉著。
  4. These are inherent and apparently permanent and can be propagated vegetatively.

    這些具有內在的和明,並可以無繁殖。
  5. This is tuberous sclerosis, an autosomal dominant condition characterized by mental retardation and seizures beginning early in life

    結節硬化癥,常染色體顯性遺傳,表現為智力低下、癲癇發作等。
  6. Twenty f1 combinations crossed among 5 varieties and strains different in fiber properties according to complete diallel crossing design were used to evaluate the heterosis and gene action of boll weight and lint percentage in high quality fiber property varieties in upland cotton in 1998 1999 for two year successively at nanjing. it was indicated that there existed small interactions with the environmental factors without maternal effects and the additive gene effect was in chief, attaining to 51. 2 % and 65. 4 % respectively for boll weight and lint percentage. the dominant effect was also in higher rate, 32. 6 % and 16. 8 % respectively. the population mean heterosis of boll weight and lint percentage over the mid - parental mean were relatively prominent 13. 3 % and 3. 5 % respectively in extreme significance. however, boll weight showed no significantly surpassing parental f1 heterosis over the better parent based on population mean ( 2. 0 % ) ; while the lint percentage expressed significant negative heterosis value ( - 2. 1 % ). the gene actions were in conformity with the heterosis expression. it was shown clearly that the f1 combinations crossed between parents with similar performances had relatively high dominant effects and significant positive f1 surpassing parental heterosis ( f1 heterosis over the better parent ) ; while no f1 combination crossed between the parents with prominent mutual difference surpassed the higher parent in yield components, which indicated that among those parents with less difference and close relationships, there still existed sufficient genetic variation or certain mechanism for creating variation and achieving greater advances in breeding. correlation analyses also indicated that there still existed severely undesirable negative correlation between yield and fiber properties as well as the difficulties for their simultaneous improvements

    利用5個具有不同纖維品質狀的品種(系)配製完全雙列雜交組合20個,通過親本和f1的2年隨機區組試驗發現產量狀的鈴重和衣分與環境的互作效應小,不存在母體效應,並以加效應為主,分別占表型方差的51 . 2 %和65 . 4 % ;顯性遺傳效應所佔的比率也較高,分別為32 . 6 %和16 . 8 % .鈴重和衣分的群體平均優勢較大,分別為13 . 3 %和3 . 5 % ,達到了極著;鈴重的超親優勢為2 . 0 % ,不著;衣分為著的負值( - 2 . 1 % ) .分析與雜種優勢結果一致.具體表現在產量狀上,親本相當配製的組合雜合較高,其超親優勢正向著,而極值親本(差異較大)所配組合沒有超過高親的.這表明親本差異小、親源關系較近的親本中仍然存在足夠的變異或某種機制以創造變異使育種取得更大的進展.相關分析表明了仍然存在嚴重的品質與產量的負相關,改良的難度較大
  7. Thus, la presents a certain genotoxicity

    示一定濃度的稀土元素鑭具有明
  8. There are 17 affected members among 35 persons in 3 generations

    三代35人有17人得病,是為體染色體顯性遺傳
  9. Autosomal dominant inheritance,

    常染色體顯性遺傳
  10. According to genetic analysis, this disease is caused by autosomal dominant inheritance

    經過分析,認為該畸形屬常染色體顯性遺傳
  11. As with familial adenomatous polyposis, the inheritance pattern is autosomal dominant

    家族腺瘤息肉病的方式是常染色體顯性遺傳
  12. An additive - dominance model with independence of the genes in action and in distribution is demonstrated by the excellent unit - slope linearity for all viscosity measurements

    由各黏度測定值良佳之?歸斜率線獲證:基因作用與分佈獨立之累加顯性遺傳模式適用於這些被評估之黏度測定值。
  13. Nevoid basal cell carcinoma syndrome, also known as gorlin syndrome, is an autosomal dominant inherited disorder which is characterized by the presence of multiple maxillary keratocysts, facial basal cell carcinomas and kinds of musculo - skeletal disturbances

    摘要痣樣基底細胞癌綜合征是一種罕見的常染色體顯性遺傳疾病,以頜骨多發角化囊腫,皮膚痣樣基底細胞癌及多種骨骼異常為主要臨床表現。
  14. The variant alleles are very frequent in populations, with the hightest frequence, 0. 29, found in africas. the ggc 54gac allele is common in chinese with gene frequency above 0. 1. hence, mbl deficiency is the most frequent immunodeficiency, but its pathological mechanisms remain elusive and await further investigation

    這些等位基因為常染色體共顯性遺傳,人群中其基因頻率高得令人驚奇,最高者竟達0 . 29 ,我國漢族ggc54gac頻率約0 . 1 。
  15. Does dominance hereditary disease have those ? recessive have those again

    像紅綠色盲,白化病,血友病都是隱病,六指就是
  16. Of the species, . characters of ecology, reproductive biology, genetic diversity, population genetic structure, endangering mechanisms, and sampling strategy have been studied in view of conservation biology. the results may be summarized as follows : by field investigation, we found that the localities recorded for four specimens of d. versipellis and d. pleiantha had disappeared, and most of the present populations are located in protected subforests. the distributional range of d. versipellis has also been reduced greatly, evidently, the number of present populations has decreased, the resources are reduced sharply, and the species are clearly endangered

    從保育生物學的角度,對八角蓮種群生態學和生物學特多樣水平和結構、瀕危機制及保育取樣策略進行了研究,結果如下:通過野外調查發現,原標本記載的一些八角蓮和六角蓮種群已難以找到,該類群目前多分佈於自然保護區外圍次生林地帶,分佈范圍明縮小,現存群體的規模也明減少,資源量貧乏,物種處于瀕危狀況。
  17. Microsatellite dna is among the most efficient class of molecular markers due to their hyper - variable and co - dominant nature with relatively high abundance and random distribution in the genome, and have been applied to a variety of fields including population differentiation, kinship analysis, linkage analysis, and evolutional and ecological studies

    摘要微衛星dna由於具有高度多態、共顯性遺傳、基因組中含量豐富且隨機分佈等特點,目前已成為最有效的分子標記之一,並應用於種群分化研究、血緣分析、基因連鎖分析、進化以及生態學研究等許多領域。
  18. This transverse ct scan of the liver demonstrates multiple large cysts in the parenchyma, consistent with polycystic change in the liver of a patient with dominant polycystic kidney disease

    Ct示肝實質多個較大包囊,與顯性遺傳多囊腎病人的肝臟病變相一致。
  19. Dominant inherited peripheral retinal neovascularization

    顯性遺傳周邊部視網膜新生血管形成
  20. Numerous cysts appear in this liver from a patient with dominant polycystic kidney disease ( dpkd )

    顯性遺傳多囊腎( dpkd )患者的肝臟中具有大量包囊。
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