遺傳染的 的英文怎麼說
中文拼音 [yízhuànrǎnde]
遺傳染的
英文
infectious-
The majority of aberrations are sporadic although on rare occasions a chromosomal disorder is directly inherited.
盡管偶爾可見一種染色體疾病是直接遺傳的,但是大量的染色體異常是散發的。However, only three species of the cephalochordate including b. lanceolatum, b. floridae, and b. belcheri, have so far been studied for their chromosome numbers, and the karyotypic analysis and banding study of amphioxus chromosomes remains largely untouched
Floridae 、 b belcheri三種文昌魚染色體數目。有關文昌魚染色體核型和帶型的研究尚未見任何報道,文昌魚染色體核型和帶型的研究將為比較基因組學和細胞遺傳學研究提供珍貴的背景資料。Crossing over the exchange of material between homologous chromatids by the formation of chiasmata
交換:同源染色單體之間形成交叉時遺傳物質的交換現象。The same phenomenon was observed in interspecific hybridization between chlamys farreri and chlamys nobilis. the karyotypes of adult hybrids and their parents were analyzed and compared. the chlamys nobilis ' s diploid chromosome number is 2n = 32, karyotype consists of 6m + 26t, nf = 38
對該雜交組合的親本華貴櫛孔扇貝的染色體核型分析表明,華貴櫛孔扇貝雜交扇貝的細胞遺傳學研究共有zn = 32條染色體,核型公式為2n = 32 = 6m + 26t ,染色體臂數nf = 38 。Complex vertebral malformation ( cvm ), a lethal autosomal recessive inherited defect in holstein breed, was newly reported in demark
摘要荷斯坦奶牛脊柱畸形綜合征是近年新發現的一種常染色體隱性遺傳病,該病對純合子胎兒是致死性的。Here is a fellow, who, infected by the most pestilent and blasphemous code of devilry that ever was known, abandoned his property to the vilest scum of the earth that ever did murder by wholesale, and you ask me why i am sorry that a man who instructs youth knows him
有這么一個人,因為受到了人世間最險惡最褻瀆的魔鬼信條的傳染,竟然把財產放棄給了世界上最壞的殺人如麻的流氓,而一個教育青年的人竟然會認識他。對此你卻要來回我為什麼感到遺憾,好吧,我來回答你。Some of our dna - based services, for example, clinical diagnostics, pre - natal parentage testing and dna profiling are offered through our wholly owned subsidiary dna - tech limited
為傳染病和基因測試提供最新的獸類及臨床診斷方法,包括親子鑒證產前遺傳病測試dna指紋鑒證及基因改造食品檢測等。Episome is an additional genetic element that can exist either as an autonomous entity or be inserted into the continuity of the chromosome of a host cell.
附加體是能插入寄生細胞連續的染色體之中,也能以自主實體而存在的一種附加遺傳因素。Consider as what recessive heredity causes euchromosome to high myopia
對于高度近視則認為是常染色體隱性遺傳引起的。Under the general term genetic system we include the mode of reproduction of the species, its chromosome cycle.
我們在總術語遺傳系統中包括種的繁殖方式,染色體周史。The prussian blue iron stain reveals extensive hepatic hemosiderin deposition microscopically in this case of hereditary hemochromatosis ( hh )
普魯士藍鐵染色顯示,遺傳性血色素沉著癥( hh )患者在鏡下可見廣泛的肝臟含鐵血黃素沉著。Hemochromatosis can be primary ( the cause is probably an autosomal recessive genetic disease ) or secondary ( excess iron intake or absorption, liver disease, or numerous transfusions )
血色素沉著癥或可以是原發的(病因大概為常染色體隱性遺傳病) ,也可以是繼發的(過多的鐵攝取或吸收、肝臟疾病、大量輸血) 。During this process, a series of modification appeared on the xi, which led to the formation of stable heterochromatin that can be inherited steadily in cell duplication
失活的染色體上面往往發生一系列的修飾,導致產生非常穩定的異染色質且能在細胞復制的過程中穩定遺傳。The karyotye analysis was made on the 5th passage, the number of the chromosomes ranged from 187 to 200, and no heteroploid cell was found
對第5代的傳代細胞進行了遺傳學分析,傳代4次之後,其染色體形態正常, 4n為187一200之間,未發現明顯的異倍化現象。Since the important roles of eo protein in the viral infection. immunity and virus - host interaction. the homology of 21 csfv strains was investigated by sequence analysis of eo genes in this study, which will provide some evidence for epidemiological study. in addition, the eo gene of hog cholera lapinized vaccine ( hclv ) strain was expressed in the prokaryotic and eucaryotic systems, and the recombinant proteins were preliminarily analyzed by immunological method
鑒于eo蛋白在病毒感染,誘導機體免疫及與宿主細胞相互關系中的作用,本研究克隆了2株豬瘟病毒eo基因並將其與其它毒株eo基因進行了序列分析,揭示了我國豬瘟病毒流行株之間的遺傳演化關系,為豬瘟病毒的流行病學研究提供依據。Our feet are vulnerable to repetitive mechanical stress and skin irritations due to tremendous daily usage. common foot problems common foot problems in elderly people include dry skin, calluses, corns, friction blisters, ingrown toenail, foot deformity, fungal infection and warts
足部問題的成因很多,局部的如皮膚感染和不合適的鞋襪,另外,如糖尿病並發的周邊血管毛病遺傳性的變形足等,都是重要的因素。Y chromosome is transmitted in the form of hap - loid, leading to extreme disequilibrium of y chromosome genetic markers distribution in different population. the prerequisite of str application in forensic medicine is establishment of a database of population y - str loci haplotype distribution. therefore we need to form haplotypes by using the known highly polymorphic str loci and detect more local population
由於y染色體呈單倍體遺傳,導致y染色體遺傳標記在不同人群中的分佈極不平衡,群體差異比常染色體str位點更加顯著,在法醫學應用的前提條件是:建立含有多個y - str位點的單倍型的群體分佈數據庫。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。This paper reviews known and suspected causes of stillbirth including genetic abnormalities, infection, fetal - maternal hemorrhage, and a variety of medical conditions in the mother
這篇文章回顧了已知的和懷疑的造成死胎的原因,包括遺傳學的異常,感染,胎兒-母親出血和母親的醫療條件不同。A hereditary disorder principally affecting the connective tissues of the body, manifested in varying degrees by excessive bone elongation and joint flexibility and by abnormalities of the eye and cardiovascular system
馬方氏綜合癥:一種遺傳性的失調癥,主要感染身體的結締組織,骨骼顯露出不同程度地過長和關節過于靈活,以及眼睛和心血管系統異常等癥狀。分享友人