SLC26A4基因,SLC26A4 gene
1)SLC26A4 geneSLC26A4基因
1.Molecular analysis of SLC26A4 gene in aChinese deafness family;一个中国耳聋家系的SLC26A4基因分析(英文)
2.Methods One hundred and forty-two samples including 33 positive cases carrying IVS7-2 A>G mutation were tested by SLC26A4 gene IVS7-2A>G mutation testing kit combined with PAGE silver staining and the results were compared with that of direct sequencing.目的建立应用标准试剂盒和PAGE银染方法检测SLC26A4基因IVS7-2A>G突变的程序,探索大前庭水管综合症的快速筛查和诊断方法。
3.GJB2 and SLC26A4 gene were the two major causes for non-syndromic hearing impairment, GJB2 gene mutation accounts for 50% autosomal recessive NSHI.而SLC26A4基因突变情况在全国还没有类似GJB2基因的大规模的研究,对SLC26A4基因突变筛查与鉴定,无疑将给遗传咨询带来很大帮助。
英文短句/例句

1.Molecular Epidemiology Investigation of Enlarged Vestibular Aqueduct Associated with SLC26A4 Gene;前庭水管扩大与SLC26A4基因分子流行病学研究
2.Clinical Analysis and Genetic Detection in 4 Cases of Large Vesticular Aquedeuct Syndrome;大前庭水管综合征4例临床分析和SLC26A4基因检测
3.Study on the Hot Spot Mutation of SLC26A4 Gene and LVAS in Sensorineural Hearing Loss with Unknown Reason;不明原因感音神经性聋SLC26A4基因热点突变与LVAS的研究
4.SLC26A4 IVS7-2A>G gene mutation in hereditary hearing loss families遗传性耳聋家系的SLC26A4 IVS7-2A>G基因突变分析
5.extinguisher loci消失基因座,绝灭基因座
6.Of, relating to, produced by, or being genes or a gene.基因的基因的,与基因有关的,基因产生的
7.Genes are described as DOMINANT or RECESSIVE.基因分为显性基因和隐性基因。
8.hypomorphic allele次等位因素对偶基因
9.Studies on Polymorphism of Prolactin Receptor Gene and Follicle-Stimulating Hormone Beta Subunit Gene in Swine;猪PRLR基因和FSHβ亚基基因多态性研究
10.Research on Hte Microarray Based Gene Mining Algorithm;基于基因表达谱的基因挖掘算法研究
11.Human Genome Project,Post-genome Research and Gene Medicine --New Century of Diagnosis,Pharmaceutics and Therapy with Gene Technique;人类基因组计划、后基因组研究与基因医学——基因诊断、基因制药与基因治疗的新世纪
12.Genetic material produced by gene-splicing.重组基因材料基因分割而产生的基因材料
13.Gene distribution was out of balance. Dominant genes were more than recessive ones.基因的分布是不对称的,显性基因多于隐性基因。
14.Association of apoE Gene, A2M Gene and ACE Gene Polymorphism with Alzheimer s Disease;apoE基因、A2M基因、ACE基因与汉人Alzheimer病的相关性研究
15.Study on Inheritance of the Quality Transgenes Over-expressed in Transgenic Wheat;转基因小麦外源基因品质基因表达的遗传研究
16.Legal Research on Gene Science and Technology--Does Gene Belong to Invention or Discovery;基因科技的法律问题研究——“发明”基因?“发现”基因?
17.Mapping of Genetic Modifiers of Eyal~(bor/bor) Mice定位Eyal~(bor/bor)基因型小鼠Eyal基因的遗传修饰基因
18.Analyses of Genome-wide Disease Resistance Genes and Their Expansion in Medicago truncatula蒺藜苜蓿全基因组抗病基因和基因扩张分析
相关短句/例句

SLC26A4SLC26A4基因
1.An Investigation of GJB2,SLC26A4 Gene Mutations in Nonsyndromic Hearing Loss in the Northwest of China;西北地区非综合征型耳聋患者GJB2、SLC26A4基因突变的分子流行病学研究
2.In deafness genes cloned,GJB2, SLC26A4,DNA12SrRNA,TMC1 and POU3F4 have the high mutation frequency in population from different ethnic origns.目前研究显示,在众多已明确的耳聋基因中,在人群中有较高突变频率的耳聋基因有GJB2基因、SLC26A4基因、线粒体DNA12SrRNA基因、TMC1基因和POU3F4基因等。
3)SLC26A4(PDS)geneSLC26A4(PDS)基因
4)PDS (SLC26A4) genePDS(SLC26A4)基因
5)SLC26A4(or PDS)SLC26A4(或PDS)
6)gene[英][d?i:n][美][d?in]基因
1.Study of the Preparation and the Characteristics of pRc/CMV-BChE Gene-chitosan nanoparticles ①;丁酰胆碱酯酶基因-壳聚糖纳米粒初步研究
2.Correlation between traditional Chinese medicine syndromes in primary immunoglobulin A nephropathy and A267G in 5'-untranslated region within exonal of megsin gene;Megsin基因E1-5’UTR区A267G与免疫球蛋白A型肾病阴虚证的相关性
3.Study on gene chip of leiomyoma of uterus;子宫肌瘤基因芯片的研究
延伸阅读

26-O-beta-D-Glycopyranosyl-22-hydroxyfurost-5-ene-3beta,26-diol-3-O-beta-diglucorhamnoside分子式:C51H84O22分子量:1049.21CAS号:55056-80-9性质: