• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island.

作者信息

Heitz D, Rousseau F, Devys D, Saccone S, Abderrahim H, Le Paslier D, Cohen D, Vincent A, Toniolo D, Della Valle G

机构信息

Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Institut de Chimie Biologique, Faculté de Médecine, Strasbourg, France.

出版信息

Science. 1991 Mar 8;251(4998):1236-9. doi: 10.1126/science.2006411.

DOI:10.1126/science.2006411
PMID:2006411
Abstract

Yeast artificial chromosomes (YACs) were obtained from a 550-kilobase region that contains three probes previously mapped as very close to the locus of the fragile X syndrome. These YACs spanned the fragile site in Xq27.3 as shown by fluorescent in situ hybridization. An internal 200-kilobase segment contained four chromosomal breakpoints generated by induction of fragile X expression. A single CpG island was identified in the cloned region between markers DXS463 and DXS465 that appears methylated in mentally retarded fragile X males, but not in nonexpressing male carriers of the mutation nor in normal males. This CpG island may indicate the presence of a gene involved in the clinical phenotype of the syndrome.

摘要

相似文献

1
Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island.
Science. 1991 Mar 8;251(4998):1236-9. doi: 10.1126/science.2006411.
2
Molecular cloning and analysis of the fragile X region in man.人类脆性X区域的分子克隆与分析
Nucleic Acids Res. 1991 May 25;19(10):2567-72. doi: 10.1093/nar/19.10.2567.
3
Isolation of a human DNA sequence which spans the fragile X.一段跨越脆性X染色体的人类DNA序列的分离。
Am J Hum Genet. 1991 Sep;49(3):656-61.
4
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.鉴定出一个含有CGG重复序列的基因(FMR-1),该基因与脆性X综合征中表现出长度变异的断点簇区域一致。
Cell. 1991 May 31;65(5):905-14. doi: 10.1016/0092-8674(91)90397-h.
5
A YAC contig across the fragile X site defines the region of fragility.跨越脆性X位点的酵母人工染色体连续克隆系确定了脆性区域。
Nucleic Acids Res. 1991 Jun 25;19(12):3283-8. doi: 10.1093/nar/19.12.3283.
6
Methylation analysis of CGG sites in the CpG island of the human FMR1 gene.人类FMR1基因CpG岛中CGG位点的甲基化分析
Hum Mol Genet. 1992 Nov;1(8):571-8. doi: 10.1093/hmg/1.8.571.
7
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.FRA16A结构对染色体脆性位点发生机制的影响。
Science. 1994 Jun 24;264(5167):1938-41. doi: 10.1126/science.8009225.
8
Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage.通过脆性X位点断裂在体细胞杂种中分离人类染色体带Xq28。
Proc Natl Acad Sci U S A. 1990 May;87(10):3856-60. doi: 10.1073/pnas.87.10.3856.
9
DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene.对236名智力迟钝受试者进行脆性X综合征的DNA诊断及FMR-1基因突变逆转的证据。
Am J Med Genet. 1994 Jul 15;51(4):482-5. doi: 10.1002/ajmg.1320510437.
10
PCR amplification and analysis of yeast artificial chromosomes.
Genomics. 1992 Aug;13(4):1303-6. doi: 10.1016/0888-7543(92)90051-s.

引用本文的文献

1
Overview: Research on the Genetic Architecture of the Developing Cerebral Cortex in Norms and Diseases.概述:正常和疾病情况下大脑皮层发育的遗传结构研究。
Methods Mol Biol. 2024;2794:1-12. doi: 10.1007/978-1-0716-3810-1_1.
2
Native functions of short tandem repeats.短串联重复序列的固有功能。
Elife. 2023 Mar 20;12:e84043. doi: 10.7554/eLife.84043.
3
A Double Jeopardy: Loss of FMRP Results in DSB and Down-regulated DNA Repair.一种双重危害:FMRP缺失导致双链断裂和DNA修复下调。
21 Century Pathol. 2022;2(5). Epub 2022 Oct 17.
4
Non-Mendelian inheritance patterns and extreme deviation rates of CGG repeats in autism.自闭症中 CGG 重复的非孟德尔遗传模式和极端偏离率。
Genome Res. 2022 Nov-Dec;32(11-12):1967-1980. doi: 10.1101/gr.277011.122. Epub 2022 Nov 9.
5
, , , , , , , and Genetic Variants in Patients with Premature Ovarian Insufficiency in a Mexican Cohort.,,,,,,, 和 在一个墨西哥队列中患有卵巢早衰的患者中的遗传变异。
Genes (Basel). 2022 Mar 29;13(4):611. doi: 10.3390/genes13040611.
6
Advancing genomic technologies and clinical awareness accelerates discovery of disease-associated tandem repeat sequences.基因组技术和临床意识的进步加速了与疾病相关串联重复序列的发现。
Genome Res. 2022 Jan;32(1):1-27. doi: 10.1101/gr.269530.120. Epub 2021 Dec 29.
7
Towards Mechanism-Based Treatments for Fragile X Syndrome.迈向基于机制的脆性X综合征治疗方法
Brain Sci. 2019 Aug 16;9(8):202. doi: 10.3390/brainsci9080202.
8
Significantly Elevated mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing.两名具有自闭症特征的兄弟因脆性 X 检测而就诊,其 mRNA 水平显著升高,且存在甲基化前突变和全突变等位基因的嵌合体。
Int J Mol Sci. 2019 Aug 11;20(16):3907. doi: 10.3390/ijms20163907.
9
Deregulation of RNA Metabolism in Microsatellite Expansion Diseases.微卫星扩增疾病中RNA代谢的失调
Adv Neurobiol. 2018;20:213-238. doi: 10.1007/978-3-319-89689-2_8.
10
Fragility Extraordinaire: Unsolved Mysteries of Chromosome Fragile Sites.脆性非凡:染色体脆性位点未解之谜。
Adv Exp Med Biol. 2017;1042:489-526. doi: 10.1007/978-981-10-6955-0_21.