突變等位基因 的英文怎麼說

中文拼音 [tūbiànděngwèijīyīn]
突變等位基因 英文
mutant allele
  • 突 : Ⅰ動詞1 （猛沖） dash forward; shoot out 2 （高於周圍） protrude; bulgeⅡ副詞（突然） abruptly; sud...
  • 等 : Ⅰ量詞1 （等級） class; grade; rank 2 （種; 類） kind; sort; type Ⅱ形容詞（程度或數量上相同） equa...
  • 位 : Ⅰ名詞1 （所在或所佔的地方） place; location 2 （職位; 地位） position; post; status 3 （特指皇帝...
  • 因 : Ⅰ動詞[書面語] （沿襲） follow; carry on Ⅱ介詞1 [書面語] （憑借; 根據） on the basis of; in accord...
  • 突變 : 1 （突然急劇的變化） sudden change; change suddenly; transilience; accident; saltation; revulsion...
  1. The sequence analysis revealed that the as1 gene encodes a myb protein, which is a candidate transcription factor. in as1 and as2 mutants, the polarity formation in leaves is defective. cell differentiation along abaxial - adaxial, proximal - distal and media - lateral axes all shows an insufficient fashion

    通過掃描電鏡、干涉相差顯微鏡、組織切片、過量表達等手段研究了as1和as2的功能，包括觀察觀察突變體的組織、細胞結構及早期發育狀況，同時採用gus表達、 rt - pcr 、原位雜交、 northern等手段分析基因的表達情況。
  2. 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。
  3. Dominant negative alleles of gpil7p were produced by random pcr mutagenesis of three conserved fragments of gpi17p : 1 ) having generated the plasmid library which contains 100000 plasmids harboring gpi17 mutants then screened from 8000 clones, we got 25 strong and 3 very strong dominant negative alleles

    對gpi17p可能的三個保守區進行了pcr隨機誘變，並最終獲得顯性負性等位基因： 1 ）組建了gpi17p突變體質粒庫，其所含質粒數約為100000 。
  4. Of the 21 patients conservatively treated between 1975 and 1997, 12 had diffuse disease ( homozygous mutant alleles ) and 9 had presumed focal disease ( paternal mutant allele only )

    1975年至1997年期間接受保守治療的21例患者中， 12例為彌漫性病變（等位基因突變純合子） ， 9例為局灶性病變（僅父系等位基因突變） 。
  5. The high - enzyme activity has 2 base changes, resulting in long amino acid sequence with native amylase. this inducing method resolved the problem of non - effective induction as in base analogue induction. and the method we used provide a new measure for this kind of work

    高酶活編碼區位點突變導致c -端序列變化和終止子的后移本誘變方法克服了用堿基類似物在體內誘變由於核酸復制酶等的校正作用而造成誘變無效的難題，為基因的誘變找到了一條新途經。
  6. 3 ) the 3rd group of mutant alleles included f66, f15 - 28, f126 and f107. these alleles showed wing and cuticle phenotypes related to wg signaling pathway. this group of mutant alleles turned out to be a new component of wg singaling pathway

    這組的突變體等位基因編碼一個wg信號傳導途徑組成成分干gg由其特點是在n端含有一個核定位信號mls ） ，而在c端則含有一個pho結構域（一種c4hc3鋅指結構） 。
  7. The nature of all the three mutant alleles of this group is nonsense mutation disrupting the coding region of oxt gene

    該組的三個突變體等位基因的突變都是無義突變，它們都破壞了。 xt基因的編碼區。
  8. The sequence result showed that the nature of pygo mutant alleles f66, f15 - 108 and f126 were nonsense mutation, which probably led to truncated pro

    測序結果表明其中h個突變體等位基因f66 ， f15 108和f126均是無義突變。
  9. 1 ) the first group of the mutant alleles included b158, b140 and b173

    1 、分離到的第一類突變體等位基因的有b158 ， b140和b173 。
  10. These alleles showed wing and cuticle phenotypes related to both wg and hh signaling pathways ( notch and vein defect et al. )

    具該類突變體等位基因的果蠅呈現出與wg和hh信號傳導途徑相關的翅和表皮形態。
  11. The clpg mutation is a a g substitution 32. 8 kb upstream of gtl2, which was later shown to be the only difference between the callipyge and wild - type chromosome in what is probably a long - range control element ( lrce )

    2002年， freking等人發現了一個位於gtl2基因上游32 . 8kb的a g的突變，這一突變位於一個新發現的轉錄本clpg1內部，它是callipyge羊和正常羊的唯一不同之處。
  12. Genetic analysis of progeny from cross cex1 - 1 xcexi - 2 showed that cex1 - 1 and cex ! - 2 were allelic at the cex1 locus

    對cexll和cexl 2的等位性研究發現， cexl 1和cexl 2是等位基因突變體。
  13. By analyzing the wing phenotype, cuticle phenotype of germline clone embryo, deficiency kit mapping, direct sequencing and searching the genome sequence database, three genes : sll, oxt and pygo were identified ( each gene corresponding to one group of mutant alleles )

    並通過綜合分析翅的形態，生殖系克隆胚胎的表皮形態，以及缺失作圖，直接測序和搜索基因組數據庫，鑒定出了三個基因，這三個基因分別對應于該三類突變體等位基因。
  14. It was surprised that the frequencies of mutation of the exon 1 of mbl allele reached to 0. 29 in all and were much more different in population of different races

    突變等位基因頻率在不同種族人群差異很大，但總體上高的令人驚奇，可達0 . 29 。
  15. To the guangxi hanzu, the most allele is hve32 in the patients with chd or aci. but it is hve34, hve36, hve38 in the controls. the relative frequency of big allele ( = ^ hve38 ) in controls is higher than in patients of two native populations, but they have n ' t significant difference between the zhuangzu controls and hanzu controls of guangxi in xbal, ecori and 3xvntr allele distribute frequency

    05人結論：廣西地區壯、漢兩族人群之間在xbal和ecdi位點及3 』端箍因分佈沒有顯著區別；廣西壯族人群冠心病、腦梗塞的發病與xbal 、 』 ecori和3 』端vntr等位基因的分佈沒有明顯的關聯；廣西漢族人群冠心病、腦梗塞的發病與ecori位點的基因突變和3vntr等位基因的分佈有一定的聯系，但與xbal位點的基因突變沒有顯著的關聯。
  16. We summed up and analyzed the polymorphisms of the fut2 gene of three groups in the world with references to other published data. further discussion was made for the hypotheses of origin and generation of special point mutations of fut2 gene. master candidate : zhang ying major : microbiology and immunology supervisor : prof

    綜合目前已發表文獻報道的其它地區人群fut2等位基因的分佈狀況，我們對世界三大人群fut2基因的多態性進行了整理分析，並對fut2基因特定點突變的可能的起源及形成進行了討論。
  17. This group of mutant alleles turned out to be a gene encoding a xylosyltransferase, which is an enzyme transfers the xylose from udp - xylose to the serine of the protein core

    這一組突變體等位基因編碼一種木糖轉移酶- oxt ，這種轉移酶能夠將udp -木糖中的木糖轉移到核。
  18. The products were used in rflp analysis. we found the g849a nonsense mutation that was responsible for the se enzyme inactivation in shandong han chinese and mongolian of inner mongolia individuals was in the same frequency, 0. 55 %

    結果在兩個人群中均發現了一個攜帶g849a點突變的個體，該點突變產生的無功能等位基因se ~ （ 849 ）在兩個人群中的頻率均是0 . 55 。
  19. Objective to establish a complex pcr method and to investigate the genetic polymorphism and population difference of three loci on y - chromosome, so as to provide a database for forensic medicine casework. methods edta - blood specimens were collected from 163 unrelated males in han population in taiyuan. different tissues of one corpse were analyzed including blood, muscle, liver and kidney

    方法（ 1 ）樣本採集：隨機抽取163名太原地區漢族無親緣關系的男性個體的靜脈血， edta抗凝，進行dys390 、 dys391和dys393基因座等位基因及單倍型頻率分佈調查；採集同一屍體血液、肌肉、肝臟、腎組織進行同一性檢測；採集20例兩代家系血進行突變觀察；取20例女性個體血進行男性特異性檢驗。
  20. This study focused on three groups of mutant alleles from mutant alleles of unknown genes. all these three groups of alleles related to either wingless ( wg ) signaling pathway or hedgehog ( hh ) signaling pathway ( each group composed of 3 - 4 mutant alleles )

    從該f1遺傳篩選中分離出了很多已知基因的突變體等位基因，其中包括了那些與wingless （ wg ）信號傳導途徑和hedgehog （ hh ）信號傳導途徑相關的突變體等位基因。
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