chromosome (human) 中文意思是什麼

chromosome (human) 解釋

  • chromosome : n. 【生物學】染色體。
  • human : adj 1 人的，人類的 （opp divine animal）。2 凡人皆有的，顯示人類特點的。3 有人性的，通人情的。n ...
  1. 8p22 of human chromosome is an region with abundant disease - related genes. it is said that it is susceptible loci of hypertension and schizophrenia. the region is also the loci of oncogene and tumor su - pressor gene

    人染色體8p22區是疾病基因富含區域，有報道說該區域是高血壓、精神分裂癥等疾病的易感位點，也是癌基因和抑癌基因的研究熱點。
  2. Human gnt - v contains 741 amino acids with six potential sites for n - glycosylation and bears high homology to gnt - v of rat. its gene is located on chromosome 2q21 containing 17 exons. gnt - v protein is encoded by exons 2 - 17 as open reading frame

    人類gnt - v由741個氨基酸組成，有6個潛在的n -糖基化位點，基因定位於染色體2q21 ，含有17個外顯子，其開放閱讀框架由外顯子2 - 17進行編碼。
  3. Studies of genes related to heart development in drosophila contribute to reveal the mechanisms of human heart development and the congenital heart diseases. to clone and identify new genes that control the heart development, by a way of chemical mutagen, ems, we have established 1, 200 balanced - lethal lines on chromosome 2 and 3. with the screening the 330 stocks with immunochemical method using heart - specific antibody, mab. no. 3, we detected 60 lethal lines showing heart mutant phynotype

    為了克隆和鑒定控制心臟發育的新基因，本研究利用化學誘變劑甲磺酸乙酯大規模地誘變果蠅，並且建立了1200個第二和第三染色體的平衡致死系，利用心臟組織特異抗體mab . no . 3對其中330個品系進行免疫化學方法篩選，觀察到有60個致死系表現出心臟突變表型， 20個品系的心臟突變表型有待進一步證實。
  4. It have been reported that the 210 kb yeast artificial chromosome ( yac ) including the human a - lactalbumin gene could direct the transgene to express in a position - independent manner, therefore is an excellent expression vector to produce transgenic animal bioreactors

    根據報道含完整人-乳白蛋白基因的yac載體能指導外源基因的乳腺特異性高效表達，是生產動物乳腺生物反應器的理想表達載體。
  5. Fish study of human oocytes failed to fertilize in vitro characterised with chromosome 21 aneuploidy

    技術研究人類體外未受精卵的21號染色體非整倍體
  6. The chromosome is the carrier of genetic material. there are genes on it. it decides human being s configuration and physiological function

    染色體是遺傳物質的載體，它上面帶有遺傳因子，決定人體的形態特徵和生理機能。
  7. Fluorescence in situ hybridization detection of chromosome translocations induced by 60co - rays in human lymphocytes dose - response curve and persistence

    射線誘發人外周血淋巴細胞染色體易位率劑量效應曲線及易位的持續性研究
  8. Progress in study of human chromosome technology

    人類染色體技術的研究進展
  9. Moreover, asp immediately preceding the active site ser is necessary for proper folding of the catalytic site. the human clsp cdna corresponded to unigene cluster hs. 415792 located on human chromosome 12pl3. 31. nucleotide sequence alignment of clsp and this sequence enabled us to demonstrate the genomic structure of the clsp gene with appropriate exon - intron boundaries, which contained 6 exons and 5 introns

    Clsp在造血細胞系的表達較為特殊，不表達于淋巴瘤細胞系，只表達于單核髓系白血病細胞系，如慢性髓系白血病k一562 、髓系單核白血病thp一1 、前髓系白血病hl一60和b4 ，以及急性髓系白血病kg一1細胞系，其中thp一1細胞系經lps刺激后clsp表達水平亦呈上升趨勢。
  10. Location of the hbrp gene in the chromosome according to stanford g3 rh panel, a pair of primers are designed in the 3 " - utr region of the gene which is to be localized and human genome dna is amplified in advance whose products are examined by electrophoresis. then g3 panel is amplified and this process is repeated twice. the pcr result is sent to stanford human genome center ( shgc ) http : / / www - shgc

    Hbrp基因的染色體定位使用stanfordg3rhkadiationhybrid ）嵌板，在所要定位基因的3 』非翻譯區（ untranslatedregion ， utr ）設計引物，預先擴增人基因組dna ，電泳檢測產物大小，繼之擴增g3rhpanel ，重復兩次，將pcr結果輸人斯坦福人類基因組中心（ shgc ）的主頁（ http ： 、 shgc
  11. In the laboratory experiment part, human peripheral blood, cultured cells and icr mice were study objects. the changes of mitotic chromosome numbers were measured by human metaphase chromosome counts and statistic analyzed used x2 - test. the changes of meiotic chromosome numbers were measured by mice one - cell zygote chromosome counts and statistic analyzed usedx2 - test. the effects of low dose ionizing radiation on the expression of topoisomerase ii were measured by immunocytochemistry, western blot and rt - pcr

    流行病學結果顯示長期小劑量輻射接觸與染色體不分離呈正相關，為進一步在細胞遺傳學和分子生物學方面研究小劑量電離輻射與染色體不分離關系及其機制，本課題第二部分以外周血、培養細胞、 icr小鼠為研究對象，用外周血染色體計數和單細胞受精卵染色體計數的方法研究小劑量輻射和拓撲異構酶復旦大學2000級博士生學位論文11a抑制劑及其二者的協同效應對有絲分裂和減數分裂染色體不分離的影響，用免疫細胞化學染色、 westernblot 、 rt pcr等方法研究了電離輻射引起拓撲異構酶a表達變化。
  12. 8p22 of human chromosome is an region rich in disease - related genes and is also the susceptible loci of oncogenes and tumor suppressor genes

    人染色體8p22區是一個富含疾病基因的區域，是癌基因和抑癌基因的研究熱點。
  13. Detemination of the tsp in da pu tunnel of shanghai and study on its chromosome aberration effect for human peripheral blood lymphocytes

    上海市打浦路隧道內空氣懸浮顆粒物的分析及其誘發的人體外周血淋巴細胞染色體畸變效應
  14. The first big breakthrough in solving this problem was when it was found that one virus, the adeno - associated virus ( aav ), preferentially inserts into a particular ( safe ) place on human chromosome 19

    解決這一問題的第一個大突破，是發現一種病毒，即腺病毒相關病毒（ aav ） ，會有選擇地插進人類第19號染色體的一個特殊（安全）位置。
  15. Genetic polymorphism of human y chromosome specific str and its application in

    基因座多態性及其法醫學應用
  16. In addition, he has made significant contributions to the mapping and annotation of human chromosome 7, and, identification of many other disease genes

    除此以外，在斷定人類第七組染色體以及許多其他疾病基因，作出了重大的突破。
  17. Professor tsui is a discoverer of the gene for cystic fibrosis and has made significant contributions to the mapping and annotation of human chromosome 7 and identification of many other disease genes

    徐教授斷定了囊狀纖維的缺陷基因。此外，在鑒定人類第七組染色體及許多其他疾病基因亦作出了重大的突破。
  18. The researchers described seen genetic risk factors ? dna sequences present in some people but not others ? bunched in a relatiely small region of one of the human chromosomes, chromosome 8, that reliably predicted one ' s probability of deeloping prostate cancer

    研究者們介紹了這七個遺傳風險因子一些人所含有的特殊的dna序列而另外的人卻沒有聚集在人類8號染色體上一個相對較小的區域，而且它們能夠可靠的預測一個人患前列腺癌的可能性。
  19. Study on chromosome aberration in human peripheral blood lymphocytes induced by 188reo - 4 in vitro

    誘發人離體外周血淋巴細胞染色體畸變的初步研究
  20. He reconstructed chromosome mutation on a human subject

    他們在人身上實驗基因突變
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