exon

exon

美 ['eks?n]  英 ['eks?n]

  • n.〔遺〕外顯子;編碼順序;基因外區;外子
  • 網絡編碼順序(exonextron);表現序列;顯譯子

詞形變化

復數:exons  

英漢解釋

n.
1.
〔遺〕外顯子
2.
編碼順序
3.
基因外區
4.
外子

英英解釋

n.

例句

Then, the free end of the exon attacks the 3' splice site, displacing the intron and forming a new bond with the next exon.

之后自由末端發起3’剪接攻擊替代內含后面形成

The first exon codes for a signal sequence ( cleaved from the protein during membrane passage).

第一編碼信號序列過程切除)。

Exon Trapping is a powerful method developed recently for isolating transcribed sequences from genomic DNA.

捕獲近年發展起來一種基因組DNA分離表達序列有效方法

Several strains of meat-type and egg laying chickens were found to segregate for an HindIII RFLP located in the intron preceding exon 4.

發現隔離位于第4內含前面

Objective: To detect the mutation in exon 15 of cholesteryl ester transfer protein gene and its properties.

目的檢測膽固醇轉移蛋白第15基因突變及其性質

Objective: To investigate the relationship between the mutation of ABCB4 gene exon 12 and intrahepatic cholestasis of pregnancy(ICP).

目的探討ABCB4基因12突變妊娠膽汁淤積癥ICP發病關系

The intensity of the higher molecular weight band (which included exon 51) was correspondingly reduced.

較高分子強度包括51)相應減少

Mutations in exon 12 cause cytoplasmic NPM1 localization, and consequently contribute to tumour development.

第12突變導致NPM1胞漿從而發生腫瘤轉化

Conclusion Deletion of DAZ exon may result in azoospermia.

結論DAZ基因缺失導致無精子

Deletion of exon 7 in SMN1 gene was detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).

采用聚合酶反應-限制性片段長度多態性分析(PCR-RFLP)檢測SMN1基因7缺失

Exon 11 mutation is closely related to the biological behavior, prognosis, drug treatment of GIST.

11突變GIST生物學行為預后以及藥物治療效果密切相關

We further show that CTCF binding to CD45 exon 5 is inhibited by DNA methylation, leading to reciprocal effects on exon 5 inclusion.

進一步研究表明CD455CTCF結合受到DNA甲基抑制從而導致第5包含相互影響

AVI is also evaluating a drug candidate AVI-5038, designed to skip exon 50, which is in preclinical development.

AVI也是衡量一個候選藥物AVI-5038,旨在跳過50,臨床前開發

Detection of JAK2 exon 12 mutations is useful for clinical diagnosis of PV.

JAK212突變檢測PV患者診斷分類重要臨床意義

Mutations in carcinoma tissues were not found in exon 9 and 20 of PIK3CA gene.

宮頸組織發現存在PIK3CA基因第920突變

Most deletion of P16 gene was loss of exon 2.

P16基因轉錄缺失主要發生2。

Objective: To study the effect of mutation of neurofibromatosis 2(NF2) gene (exon 2) in schwannomas.

目的研究神經鞘中型發神經纖維瘤病基因(NF2)2突變及其意義

Study of structural polymorphism of bcl-6 gene non-coding exon and its protein expression in transitional cell carcinomas

bcl-6基因編碼結構多態性蛋白表達移行上皮關系研究

the second exon M2 did not has genetic polymorphism during group;

第二M2群體遺傳多態性

Exon rearrangement analysis of parkin gene in patients with isolated early-onset parkinsonism using semi-quantitative PCR

熒光定量PCR散發性帕金森綜合parkin基因突變分析應用

Detection of deletions of the DMD gene by reverse dot-blotting hybridization with the cloned exon probes

克隆探針反向斑點雜交檢測DMD基因缺失

Studies on Single Nucleotide Polymorphism of OBR-exon 20 and Its Associations with Fattiness Traits in Chicken

OBR基因第20多態性脂肪性狀相關研究

Polymorphism of exon 10 of prolactin receptor gene and its relationship with prolificacy of Jining Grey goats

催乳素受體基因10多態性及其濟寧青山繁殖關系研究

Study on the Relationship between the Clinical Data of Type 2 Diabetes Mellitus and the Variation of Leptin Receptor Gene Exon

2糖尿病臨床變量瘦素受體基因變異關系研究

Single Nucleotide Polymorphism in Exon Partial Sequence of Sow Kappa Opioid Receptor Gene

Kappa阿片受體基因部分序列核苷酸多態分析

Establishing the mutant of coding calcium binding fragment of the 13th exon of human thrombospondin-1 gene with polymerase chain reaction

應用聚合酶反應技術構建血小板反應1基因第13編碼結合突變

Variants of Exon 4 and Its Flanking Region of LPL Gene in Patients with Hyperlipidemia

患者脂蛋白基因4區域變異研究

Genetic variants of the 6th exon of lipoprotein lipase in mixed hyperlipidemia

混合患者脂蛋白基因第6突變研究

Exon 8 of progesterone receptor gene and the failure of mifepristone induced interruption of early pregnancy

終止失敗激素受體基因第8相關性研究

Effect of the variation of exon 20 of leptin receptor gene on lipid metabolism in children with obesity

瘦素受體基因20突變兒童脂質代謝影響臨床研究

The Study of the Sequence Peculiarity of Exon and Intron in C-elegans Genome

線蟲基因組內含序列特征研究

Difference study on sporadic Parkinson's disease and familial Parkinson's disease in exon 4 of Parkin gene

家族散發帕金森Parkin基因4突變差異研究

Polymorphism in insulin receptor gene exon 17 in women with polycystic ovary syndrome

卵巢綜合征患者胰島素受體基因17多態研究

The relationship between the exon 4 gene polymorphism of TIM-1 and rheumatoid arthritis

TIM-14基因多態性類風濕關節炎關系研究

Characteristics of exon 4 variation in leptin receptor gene of patients with obesity

肥胖癥患者瘦素受體基因4變異特征

Analysis of homozygous deletion and point mutation of FHIT gene exon 5 in gastric carcinoma

胃癌基因FHIT5純合缺失突變

Analysis of the sequence of the variant exon-8 of fibroblastic Fas gene in keloid

瘢痕疙瘩纖維細胞Fas基因8基因突變序列分析

Study on polymorphism of MICA exon 5 microsatellite in Shanghai Han population

上海漢族人群MICA基因第5衛星多態研究

Genetic analysis of RET exon 11 in sporadic medullary thyroid carcinomas

散發甲狀腺髓樣RET基因第11序列分析

Mutation and polymorphism in exon 4 of tuberous sclerosis complex gene

結節硬化基因4基因突變多態研究