The advanced genomics research of neurofibromatosis type 1

Y. Ke, Hong Zhang
{"title":"The advanced genomics research of neurofibromatosis type 1","authors":"Y. Ke, Hong Zhang","doi":"10.3969/J.ISSN.1003-0808.2010.02.023","DOIUrl":null,"url":null,"abstract":"Neurofibromatosis type 1 is a term of Von Recklinghausenan.It is an autosomal dominant inherited disease which derived by neural crest cell.Prevalence of this disease is 1/3000 1/3500 and is a disease with the highest mutation rate.The pathogenesis of neurofibromatosis type 1 is associated with the deficiency of NF1 gene.Recently,the genetics and genomics research of neurofibromatosis make a great progress.With the development of gene linkage and position cloning technology,the gene sequence of neurofibromatosis type 1 has been found.Recent research of genetics and genomics of NF1 and the structure and function,abnormal expression,the relation of genotype and phenotype,the mutation sensitivity domain of NF1 gene were reviewed. \n \nKey words: \nneurofibromatosis type 1; neurofibromatosis gene; genetics; genomics; gene mutation","PeriodicalId":186994,"journal":{"name":"Chinese Ophthalmic Research","volume":"22 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2010-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Ophthalmic Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3969/J.ISSN.1003-0808.2010.02.023","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Neurofibromatosis type 1 is a term of Von Recklinghausenan.It is an autosomal dominant inherited disease which derived by neural crest cell.Prevalence of this disease is 1/3000 1/3500 and is a disease with the highest mutation rate.The pathogenesis of neurofibromatosis type 1 is associated with the deficiency of NF1 gene.Recently,the genetics and genomics research of neurofibromatosis make a great progress.With the development of gene linkage and position cloning technology,the gene sequence of neurofibromatosis type 1 has been found.Recent research of genetics and genomics of NF1 and the structure and function,abnormal expression,the relation of genotype and phenotype,the mutation sensitivity domain of NF1 gene were reviewed. Key words: neurofibromatosis type 1; neurofibromatosis gene; genetics; genomics; gene mutation
1型神经纤维瘤病基因组学研究进展
1型神经纤维瘤病是Von Recklinghausenan的一个术语。它是一种常染色体显性遗传病,起源于神经嵴细胞。此病患病率为1/3000 /3500,是突变率最高的疾病。1型神经纤维瘤病的发病机制与NF1基因缺失有关。近年来,神经纤维瘤病的遗传学和基因组学研究取得了很大进展。随着基因连锁和位置克隆技术的发展,已经发现了1型神经纤维瘤病的基因序列。综述了近年来NF1基因的遗传学和基因组学研究进展,以及NF1基因的结构与功能、异常表达、基因型与表型的关系、突变敏感域等方面的研究进展。关键词:1型神经纤维瘤病;神经纤维瘤病基因;遗传学;基因组学;基因突变
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信