β-glucuronidase mRNA levels are correlated with gait and working memory in premutation females: understanding the role of FMR1 premutation alleles
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep29366.pdf
Reference43 articles.
1. Lozano, R., Martinez-Cerdeno, V. & Hagerman, R. J. Advances in the Understanding of the Gabaergic Neurobiology of FMR1 Expanded Alleles Leading to Targeted Treatments for Fragile X Spectrum Disorder. Curr Pharm Des 21, 4972–4979 (2015).
2. Jin, P. et al. RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila. Neuron 39, 739–747 (2003).
3. Pastori, C. et al. Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome. Hum Genet 133, 59–67, 10.1007/s00439-013-1356-6 (2014).
4. Loesch, D. Z. et al. Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism. Genet Med 13, 392–399, 10.1097/GIM.0b013e3182064362 (2011).
5. Hukema, R. K. et al. Induced expression of expanded CGG RNA causes mitochondrial dysfunction in vivo . Cell Cycle 13, 2600–2608, 10.4161/15384101.2014.943112 (2014).
Cited by 10 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. Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome;American Journal of Medical Genetics Part A;2022-11-08
2. Synthesis, Biological Evaluation, and In Silico Studies of Novel Coumarin-Based 4H,5H-pyrano[3,2-c]chromenes as Potent β-Glucuronidase and Carbonic Anhydrase Inhibitors;ACS Omega;2022-08-04
3. Paternal retraction of a fragile X allele to normal size, showing normal function over two generations;American Journal of Medical Genetics Part A;2021-09-21
4. DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome;International Journal of Molecular Sciences;2020-10-19
5. FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome;Scientific Reports;2020-07-16
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3