突變子 的英文怎麼說
中文拼音 [tūbiànzi]
突變子
英文
muton-
Detection of fibroblast growth factor receptor 3 gene mutation at nucleotide 1138 site in congenital achondroplasia patients
先天性軟骨發育不全成纖維細胞生長因子受體3基因1138位核苷酸點突變的檢測This paper introduced the application of biotechnology in rice genetics and breeding, including tissue culture, cell mutants selection, protoplast fusion, apomixis, molecular mark assisted breeding and genic transformation
簡要綜述了生物技術在水稻遺傳育種中的應用,主要包括組織培養、細胞突變體的篩選、原生質體融合、無融合生殖以及分子標記輔助育種和轉基因技術等方面。Correlation between the mutation of the dcc gene codon 201 and gastric cancer
基因201密碼子突變與胃癌相關性的研究Among the 17 isolates, 8 isolates display tcg - ttg mutation in codon 531, 5 isolates have cac - tac or aac or cgc mutation in condon 526, 3 isolates have gac - gtc mutation in codon 516, and the last one has caa - aaa mutation in codon 513
其中8株為531位密碼子tcg ttg的突變, 5株為526位密碼子cac tac或aac或cgc的突變, 3株為516位密碼子gac gtc的突變,另一株發生了513位密碼子caa aaa的突變。Because of the cleavage site of enterokinase and cnbr was designed in the middle of thioredoxin and cmiv, the expressed peptides of the mutation of cmiv could be cuted down from the fusion protein by enterokinase or cnbr
由於硫氧還蛋白和抗菌肽之間設計了腸激酶( enterokinase )切割位點和cnbr切割位點,通過對該表達的融合蛋白的切割,可得到目標抗菌肽cmiv突變體多肽分子。Methods : nine heterozygous mutation carriers and nine healthy controls were investigated
方法:調查9名雜合子突變攜帶者和9名健康對照者。The callipyge phenotype in sheep is an inherited muscular hypertrophy that affects only heterozygous individuals who receive the clpg mutation from their father
只有遺傳了來源於父本的clpg突變的雜合子個體才能表達這一表型,因此推測這一性狀受印記基因的控制。In 138 han samples, homozygous and heterozygous genotypes of codon 54 allele in mbl structural gene were 2. 17 % and 21. 01 % respectively, while in 120 uigurs samples, those were 0. 83 % and 18. 34 %
17 ,雜合子29例,佔zi刀1 ; 120份維吾爾族標本中,檢出突變純合子1例,佔0Using the young seedlings of wild type ( wt ) and four mutants ( phya, phyb, phyaphyb and hy4 ) of arabidopsis thaliana as plant materials, the effects of light quality and kinetin ( kt ) on some photomorphogenesis responses such as cotyledon enlargement, hypocotyl growth inhibition, accumulation of chlorophyll and anthocyanin were investigated in the present study. photoreceptor functions and interaction of light and kt in the responses was examined and discussed
本文以擬南芥( arabidopsisthaliana )野生型( wt )和四種光突變體phya 、 phyb 、 phyaphyb和砂hy4為材料研究不同光質與細胞分裂素( kt )對幼苗子葉擴大、下胚軸伸長、葉綠素和花色素苷積累的影響,分析光受體參與的反應以及探討光與kt在調節各種反應中的相互關系。One missense mutation was found in 48 hypertriglyceridemic patients and identified to be pro207 - leu by sequencing, pedigree analysis of this proband has been carried out and showed that the pro band ' s father is also a carrier of this mutation
徵得患者家屬的同意和支持,對其家族三代十人進行了完整的家系分析。家系分析顯示,先證者的突變來自其父親的遺傳。在外顯子6 、 7 、 8中未檢出基因突變。An osmotic mutant of neurospora was permeable to polymers of molecular weight 18500.
脈孢殼屬的滲透突變體能透過分子量為18500的聚合物。They went on to isolate a series of revertants from several secondary mutants.
它們進一步從幾個第二次突變型中分離出一系列的回復子。The detection of p53 exon5 8 mutations in cervical cancer and cervical intraepithelial neoplasia
8外顯子突變的檢測Progress in the research of mutation of genetic intron and retinitis pigmentosa
基因內含子突變與視網膜色素變性的研究進展As social practice continues, things that give rise to man ' s sense perceptions and impressions in the course of his practice are repeated many times ; then a sudden change ( leap ) takes place in the brain in the process of cognition, and concepts are formed
社會實踐的繼續,使人們在實踐中引起感覺和印象的東西反復了多次,於是在人們的腦子里生起了一個認識過程中的突變(即飛躍) ,產生了概念。With systeamine pretreatment decreased yields of dominant lethals were obtained in spermatocytes, spermatids and in spermatozoa.
用半胱氨預先處理,在精母細胞、精子細胞和精蟲內均可使顯性致死突變值下降。With cysteamine pre-treatment, decreased yields of dominant lethals were obtained in spermatocytes, spermatids and in spermatozoa.
用半脘氨預先處理,在精母細胞,精子細胞和精蟲內均可使顯性致死突變值下降。There was no character however unexpected, no change of scene, no stage effect, but was obliged to clamber up this ladder
隨意編派的角色,機關布景,劇情突變,沒有一樣不是安排從這梯子上場的。This system included method of solid medium plate enveloped with parafilm to form colony, conjugational gene transfer in a selective medium, screening the nonmagnetic mutants by magnet adsorption technique
此體系包括:以平板封膜培養技術獲得單菌落,在選擇性培養液中進行遺傳因子接合轉移,以液體培養和磁鐵吸附技術篩選突變子。3. overexpression of wide - type smads resulted in up - regulation of axudl mrna expression in hepg2 cells, whereas axudl mrna expression was compromised by dominant - negative smad3 ( d407e )
3 .野生型的smad3的過表達能上調h即g2細胞中axudl基因mrna的表達,而smad3蛋白的顯性失活突變子smad3 ( d4o7e )卻下調其表達。分享友人