mutation gene 中文意思是什麼
mutation gene
解釋
突變基因-
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 -
Study on association of mutation of the 3 - adrenergic - receptor gene with niddm
腎上腺素能受體基因與2型糖尿病關系的研究 -
Androgen receptor gene mutation in children with hypospadias
銀染色法檢測尿道下裂患兒雄激素受體基因突變 -
Because the phenotype of osdd2 mutant was segregated with the basta resistance, it suggested that the mutation was arose by disruption of the wrky gene
根據已有的共分離數據和初步分析結果表明osdd2突變體的發育遲緩性狀是有外源基因插入引起。 -
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 -
The fusion protein was bactericidal active against staphylococcus aureus. in present study, we will truncate the none channel - forming do main, then attach the agrd to the pore - forming region ( k544 - i626 ) to construct a new engineered multidqmain protein machine - compact engineered peptide targeting staphylococcus aureus. such engineered peptide was constructed by linking the gene of staphylococcal agrd pheromone with the gene of c - terminal ( 1626 ) of colicin la pore - forming region ( k544 - i626 ) with site - directed mutation
利用點突變方法將金黃色葡萄球菌信息素agrd （ i型， ystcdfim ）的基因引入到大腸菌素fa梭基端1626基因上，並將限制性內切酶sacl酶切位點基因分別引入到大腸菌素fa的p4和k544上，通過酶切、膠回收、連接獲得含大腸菌素ia水性孔道結構域和金黃色葡萄球菌信息素agrd基因的重組質粒。 -
The contents of this studies include : 1 ) according to the researches on the correlation between the function and structure of the cmiv from bombyx - moxi before by others, especially by lixinlal in naigin normal university of china, we have designed and sythesized the mutation i of the gene of cmiv that was different from the natural cmiv about 50 % in amino sequence, using the favorable condon of the ecoli. after cheked the result of synthesis by sequence, we have cloned the gene into 3 " of the gene of thioredoxin in the thio - fusion expression vector ( ptxfus ), and the fusion protein of thio - cmiv was highly expressed in soluble form
本研究的內容包括：一、在前人對抗菌肽cmiv研究的基礎上，對n端和c端進行氨基酸保守變換，設計和合成了該基因，充分使用大腸桿菌偏愛的密碼子，並將該基因5端與硫氧還蛋白基因3端融合，通過ptxfus表達載體獲得較高可溶性表達（在15 sds - page膠上可見明顯的表達蛋白帶） 。 -
Esterase gene amplification and mutation associated with insecticide resistance
酯酶基因擴增及突變與昆蟲抗藥性 -
3 ) foa ( fluoroorotic acid ) treatment with the dominant negative mutants showed that the dominant negative effects of mutants were caused by the presence of the gpi17 vector, not by another mutation located somewhere in the genome and in a gene involved in the natural resistance against copper
3 ） foa （ 5 -氟-乳清酸）處理突變體細胞表明，得到的顯性負性突變體不是細胞中銅抗性基因突變的產物，其確為gpi17突變引起。 -
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。 -
Performance of the chinese hamster ovary cell hypoxanthine guanine phosphoribosyl transferase gene mutation assay
中國倉鼠卵巢細胞次黃質鳥嘌呤轉磷酸核糖基酶基因變異鑒定的操作 -
Hhc results from a mutation involving the hemochromatosis gene ( hfe ) that leads to increased iron absorption from the gut
該病是由於血色素沉著癥基因（ hfe ）突變使得腸吸收鐵增加所致。 -
Mutation analysis of gjb2 gene in keratitis ichthyosis deafness syndrome
2基因突變的研究 -
All f1 seedlings showed wild - type salt - sensibility, and two of four mutants were detected that the proportion of the salt - tolerance seedlings to salt - sensibility seedlings was 1 : 3 in f2 progenys. the results of genetic analysis suggested that this mutants have a monogenic recessive mutation in a nuclear gene
F _ 1代白花授粉所得的f _ 2代中，兩個株系抗鹽植株與不抗鹽植株的比例為1 ： 3 ，表明該突變體是隱性單基因突變體。 -
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。 -
We did not detect any somatic mutation in ptch gene
追蹤四個月並無復發的跡象。 -
Mutation spectrum analysis oftransglutaminase gene in streptomyces fradiae after irradiation by n ion
氟氏鏈黴菌離子束注入突變譜的分析 -
Pcr method was used to identify candidate ms 188. sequence analysis indicated that a point mutation occurred in the second exon of the atmyb103 gene in male sterile mutant with caa ( gln ) replaced by a stop codon taa
利用pcr的方法從突變體中擴增atmyb103基因並進行序列分析，結果表明突變體中atmyb103基因第二個外顯子上發生了點突變，由原來編碼谷氨酰胺的caa密碼子突變為終止密碼子taa 。 -
Tubercle bacillus drug - fast gene mutation
結核菌耐藥基因突變 -
Apparently, a mutation in this gene ? or, more probably, in the control system that activates it ? gave rise to volvox
顯然這個基因的突變，或更可能是激活這個基因的控制機制的突變產生了團藻。
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