顯性遺傳病 的英文怎麼說

中文拼音 [xiǎnxìngyízhuànbìng]
顯性遺傳病 英文
dominant genetic disease
  • 顯 : Ⅰ形容詞1 （明顯） apparent; obvious; noticeable; evident 2 （有名聲有權勢的） illustrious and inf...
  • 性 : Ⅰ名詞1 （性格） nature; character; disposition 2 （性能; 性質） property; quality 3 （性別） sex ...
  • 遺 : 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 : 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）...
  • 病 : Ⅰ名詞1 （疾病; 失去健康的狀態） illness; sickness; disease; malum; nosema; malady; morbus; vitium...
  • 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. 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。
  3. As with familial adenomatous polyposis, the inheritance pattern is autosomal dominant

    家族性腺瘤息肉病的遺傳方式是常染色體顯性遺傳。
  4. 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，以頜骨多發性角化囊腫，皮膚痣樣基底細胞癌及多種骨骼異常為主要臨床表現。
  5. Other genetic disorders become apparent when the demands of an independent existence after birth reveal a disorder of function such as renal failure, increased susceptibility to infection, or mental deficiency

    當出生后小兒獨立生存的需求呈現功能紊亂（如腎功能衰竭對感染敏感性增高或智力缺陷）時，另一些遺傳病就變為明顯。
  6. Does dominance hereditary disease have those ? recessive have those again

    像紅綠色盲，白化病，血友病都是隱性遺傳病，六指就是顯性的
  7. Two strains of prrsv were isolated from the swine infected with prrsv in shangdong province and daqing area, in order to clarify the source and genetic background of porcine reproductive and respiratory syndrome virus ( prrsv ) from different parts of china, thus providing theoretic basis for the study of vaccine against it. the prrsv was cultured on mark - 145 cells for 5 ~ ~ 6 passages. when the cpe was obvious, the virus was harvested and purified

    為了弄清我國不同地區prrsv的來源以及其遺傳學背景，為疫苗學研究提供理論根據，本研究在ch - 1a株完整的基因組獲得以後，從流行於我國山東（ sd ）和黑龍江大慶（ dq ）地區疑似prrs的豬體內分離到prrsv ，在mark - 145細胞上盲傳5 6代，細胞出現明顯病變以後，收獲病毒液，然後提純，提取全病毒rna ，經過反轉錄、 pcr擴增獲得結構基因orf2 7的目的基因片斷，然後與pmd - t載體連接，轉化，得到陽性質粒后進行測序，並將其與ch - 1a株進行了比較分析，同時對這兩個毒株的結構基因組的理化性質進行分析。
  8. If the influence of the home enironmental risk factors depends on genotype, as suggested by these results, genotype - enironment explains the large heritability for asthma and related disorders

    象這些結果所顯示的一樣，如果家庭環境有害因素的影響依賴于遺傳型，那麼遺傳型環境就能解釋其對哮喘和相關病癥巨大遺傳可能性。
  9. New york ( reuters health ) aug 07 - findings from an icelandic study suggest that there is a common genetic background for inflammatory bowel disease ( ibd ) and ankylosing spondylitis ( as )

    紐約（路透社） 8月7日，一項來自冰島的研究顯示：炎癥性腸病（ ibd ）和強直性脊柱炎（ as ）具有共同的遺傳學背景。
  10. 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顯示肝實質多個較大包囊，與顯性遺傳性多囊腎病人的肝臟病變相一致。
  11. " it seems that physical activity had an even more pronounced effect among those with the susceptibility gene apoe4, the most important risk factor for alzheimer ' s disease and dementia, " kivipelto added

    報道說，這項發表在新一期柳葉刀：神經病學雜志上的研究結果顯示，那些對癡呆癥具有遺傳易感性的人受到的效果最為明顯。
  12. Abstract : as the medicine science develops and improves, some human acquired diseases have been controlled on the whole. but the incidence of genetic diseases and congenital malformation rises gradually and the importance of their treatments appears by degree. to improve population quality, it is necessary to begin with controlling and changing genetic factor. that is, we should understand the classification of the genetic diseases and their incidence mechanism before we use various new technologies to find out and propose the ways of treatment such as antenatal diagnosis and gene project. thus we can achieve our goal of taking precautions against and curing genetic diseases

    文摘:由於醫學科學的發展和進步，一些人類後天的疾病基本上得以控制，而遺傳病和先天畸形的發病率則逐漸提高，並逐漸顯示出其重要性，要想提高人口素質，就要從控制和改變遺傳因素的方面做起，了解遺傳病的種類，發病原理，再利用現代的各種高新技術，找到和提出治療的方法，如產前診斷、遺傳工程等，從而達到預防和治療遺傳病的目的。
  13. Primary carnitine deficiency is a genetic disease, which shows no apparent symptoms in either the parent or the infant. however, the affected child is threatened with the danger of sudden death before the age of one. cardiomyopathy may develop in their later childhood

    有這種遺傳病的家庭父母一般都沒有明顯病徵，而患病的兒童可能在嬰兒時期（一般在一歲前）出現急性病徵，包括不省人事、低血醣，嚴重者會導致猝死。
  14. Some genetic disorders are evident at birth ( i. e. are congenital ), particularly those resulting in abnormalities of physical development

    一些遺傳病在出生時已很明顯（即先天性的） ，特別是那些導致身體發育畸形的遺傳病。
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