Closely linked cis ‐acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes-Reference-Cited by-同舟云学术

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Closely linked cis ‐acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes

Published:2007-08-02 Issue:12 Volume:28 Page:1216-1224
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Ennis S.¹,Murray A.²,Brightwell G.³,Morton N.E.¹,Jacobs P.A.⁴

Affiliation:

1. Genetic Epidemiology Group, Human Genetics (MP808), Southampton General Hospital, Southampton, United Kingdom

2. Peninsula Medical School, St. Lukes, Exeter, United Kingdom

3. AgResearch, Hamilton, New Zealand

4. Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire, United Kingdom

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.20600

Reference39 articles.

1. DNA Sequences Tightly Bound to Proteins in Mouse Chromatin: Identification of Murine MER Sequences

2. Instability of a (CGG)98 repeat in the Fmr1 promoter

3. A high-density SNP map for the FRAX region of the X chromosome

4. Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation

5. Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Effects of genetic variation on the structure of RNA and protein;PROTEOMICS;2024-01-10

2. Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?;International Journal of Molecular Sciences;2022-05-12

3. Mystery of Expansion: DNA Metabolism and Unstable Repeats;Advances in Experimental Medicine and Biology;2020

4. The role of AGG interruptions in theFMR1gene stability: A survey in ethnic groups with low and high rate of consanguinity;Molecular Genetics & Genomic Medicine;2019-08-27

5. A Pipeline to Assess Disease-Associated Haplotypes in Repeat Expansion Disorders: The Example of MJD/SCA3 Locus;Frontiers in Genetics;2019-02-05

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