inherited disease 中文意思是什麼

inherited disease 解釋
遺傳病
  • inherited : 繼承的
  • disease : n. 1. 病，疾病；【植物；植物學】病害。2. （精神等的）病態，弊病。3. （酒等的）變質；（食物等的）腐敗。4. 〈廢語〉不安。
  1. Gaucher ( pronounced " go - shay " ) disease is an inherited illness caused by a gene mutation

    戈謝病是一種由基因突變引起的疾病。
  2. Familial mediterranean fever, an inherited disease among people of mediterranean ancestry, is characterized by repeated attacks of fever and inflammation, commonly in the abdomen or lungs

    家族性地中海熱，是一種在有地中海的祖先的家族中傳播的遺傳病，臨床表現為反復發作的發熱和炎癥，通常發生在腹部和肺部。
  3. This article reviews the clinical manifestations, mutation feature, gene location and phenotype of different ischemic cerebrovascular disease caused by monogenic disorders, including coagulation disorders, erythrocytic disorders, inherited small vessel disease, metabolic disorders, connective tissue diseases, vasculopathies and disorders of unknown etiology

    本文主要闡述了單基因遺傳障礙引起的缺血性腦血管病，包括凝血障礙、血細胞病、遺傳性小血管病、代謝障礙、結締組織病、大動脈病及不明原因引起缺血性腦血管病的臨床特徵、突變特點、基因定位及表型等遺傳學研究進展。
  4. Phenylketonuria ( pku ) is an inherited metabolic disease that results in mental retardation and other neurological problems when treatment is not started within the first few weeks of life. the disease arises from the deficiency of a single enzyme, phenylalanine hydroxylase, which converts the essential amino acid, phenylalanine, to another amino acid, tyrosine. failure of the conversion to take place results in a buildup of phenylalanine in the body that then damages the central nervous system

    苯丙酮尿癥（ pku ）是一種智力發育不全的先天性疾病，患者由於肝贓內苯丙氨酸羥化酶缺乏，苯丙氨酸不能正常代謝為酪氨酸，從而導致苯丙氨酸在肌體組織內積累，引起腦損傷和累進性精神障礙，臨床表現為智力低下，頭發顏色轉黃，尿有異臭味，重者似鼠臭。
  5. In one particular inherited disease, sickle cell anaemia, the red blood cells, instead of being flat discs, are sickle shaped.

    在一種特殊的遺傳疾病鐮形細胞貧血癥中，紅血球不是圓盤狀而是鐮刀狀。
  6. The topics include : structure and function of genes, chromosomes and genomes, biological variation resulting from recombination, mutation, and selection, population genetics, use of genetic methods to analyze protein function, gene regulation and inherited disease

    主題包括：基因、染色體與基因組的結構和功能；來自於基因重組、突變和篩選的生物變異；族群遺傳學；運用遺傳學的方法分析蛋白質的功能，基因的調控和遺傳性疾病。
  7. Research on genetic eye diseases helps to understand how a disease develops and is inherited, as well as to develop genetic markers that aid to diagnose a disease sometimes even before symptoms appear. " nowadays biotechnology plays an important role in medical research and clinical practice

    遺傳眼疾的研究不但有助了解眼疾的成因和遺傳的模式，而且有助找出相關眼疾的基因標志，有可能在病徵出現前作出診斷。
  8. Hypophosphatasia is a rare inherited metabolic disease characterized by rickets with reduced plasma and tissue alkaline phosphatase activity

    摘要先天性磷酸酶缺乏癥為一少見之代謝性疾病，其主要特徵為血清及組識之鹼性磷酸酶下降以及佝僂癥。
  9. Inherited genetic variation has a critical but as yet largely uncharacterized role in human disease. here we report a public database of common variation in the human genome : more than one million single nucleotide polymorphisms snps for which accurate and complete genotypes have been obtained in 269 dna samples from four populations, including ten 500 - kilobase regions in which essentially all information about common dna variation has been extracted

    我們現在發表一個人類基因組常見遺傳變異的公開資料庫：這是一個對來自四個群體269個樣品內的一百萬個單核苷酸多態性（ snps ）進行了完整並準確的分析的研究成果；另外也確認了十個dna片段（每個片段含有五十萬個堿基）的所有常見遺傳變異資訊。
  10. Only later did she begin to display the symptoms of huntington ' s disease, an inherited brain disorder that produces horrific delusions and uncontrolled movements

    之後她開始表現出亨廷頓舞蹈病的癥狀。這種病是一種遺傳性大腦紊亂，會使病人產生可怕的幻覺和無法控制自己的行為。
  11. Wilson " s disease is the consequence of toxic accumulation of copper initially in the liver and later in extrahepatic sites, this disorder is inherited in autosomal recessive manner and is present in 1 in 30000 individuals in all populations

    其中研究最多的是銅代謝異常所引起的wilson ' s病，這種病是常染色體隱性遺傳病，如果肝臟中銅濃度達到毒性水平，將引發急性肝炎，其發生率為三萬分之一。
  12. Inherited the academic thoughts from classics as neijin, nanjin, and so on, this of exogenous febrile diseases improved the thoughts and may he an overview of exogenous febrile disease

    認為《傷寒例》在繼承《內經》 、 《難經》 、 《陰陽大論》等古籍學術思想基礎上對外感熱病學術理論又有創新，是中醫外感熱病的總論。
  13. It can be concluded from the experiment results that hatchery seed has lower genetic variation and large - scale hatchery seed releasing affects the genetic diversity of the natural population. the shrimp distributed along china coast in bohai sea and yellow sea may consist of more than one populations. the viral disease resistant ability of f. chinensis is proved to be genetically inherited and can be improved by genetic selection

    一通過對實驗結果的進一步分析認為：中國對蝦人工育苗的過程使後代群體的遺傳多樣性下降，人工培育苗種的大規模放流影響了自然群體的遺傳多樣性； ，分佈於我國沿海的中國對蝦可能由多個自然群體構成，還存在未被發現的種質資源：中國對蝦抗wssv病毒感染是由遺傳決定的，選育可提高中國對蝦對wssv的抗性。
  14. Inheritance patterns and percentage of affected pups in litters indicate that tns is inherited in a recessive manner ( like cl ) with both parents having to be carriers of the disease to produce an affected pup

    遺傳模式及同窩幼犬中患病者的比率表明tns以隱性方式遺傳（與蠟樣質脂褐素沉積病一樣） ，即親代雙方均為疾病攜帶者的情況下才能產生患犬。
  15. Linkage analysis plays an important role in gene mapping. the foundation : the two gene locuses which locate on the same chromosomal ( eg. disease gene and marker gene ) happen to cross over and recombine. the farther the distance between two locuses is, the higher the probability happening to cross over is, the lower the probability that the two locuses are inherited to offspring together is, that is, the degree of linkage is not strong. so we can estimate the distance and the degree of linkage by the recombination fraction between the two locuses to locate gene

    連鎖分析是基因定位主要策略之一，其基本原理是位於同一染色體上兩個基因位點（例致病基因與標記基因）在減數分裂的過程中會發生交換與重組，染色體上的兩個位點間距離越遠，發生重組的概率就越大，兩個位點在一起傳給後代的機會就越少，即連鎖程度弱，這樣由標記位點與疾病位點間的重組率可估算出兩者間的距離以及連鎖程度，達到基因定位的目的。
  16. Use of genetic methods to analyze protein function, gene regulation and inherited disease

    以及運用遺傳學的方法分析蛋白質的功能、基因的調控與遺傳性的疾病。
  17. The functions of the non - polarity field energy without polarity are very special. it removes negative disease information and preserves inherited, healthy, and positive information, and so it returns the body to the most positive state. this explains why spiritual practice can heal all diseases

    無極能量的功能很特別，它可以消除否定疾病的信息，保留先天的健康的肯定的信息，所以它讓人體恢復到最肯定的狀態，所以說明了為什麼靈修可以治愈所有疾病。
  18. Among the definable underlying diseases, 31. 0 % were diagnosed as inherited metabolic disorders, including mitochondrial disorders ( n = 4 ), primary systemic carnitine deficiency ( n = 1 ), pompe disease ( n = 3 ) and mucopolysaccharidosis ( mps ) i ( n = 1 )

    此外在這個研究分析中發現，有很大部分的心肌病變兒童（ 50 % ）並未找到造成疾病的根本原因；並且這部分的兒童亦未曾接受過適當的遺傳與代謝疾病篩檢。
  19. Huntington ' s disease ( hd ) is an inherited disease causing the death of dopamine - producing cells in the brain. its effects are progressive, affecting both mind and body

    亨廷頓氏病（簡稱hd ）是一種可以導致大腦中產生多巴胺的細胞死亡的，可遺傳的疾病。病情會日益加重，同時影響大腦和身體。
  20. Chelsea midfielder and england international joe is supporting the charity because both a relative and a family friend lost their lives to cystic fibrosis ( cf ), the uk ' s most common life - threatening inherited disease

    切爾西中場和英格蘭超級球星喬科爾在家族的一個朋友由於英國最普通的遺傳病而失去生命后而支持這個慈善活動
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