Cognitive deficits in mice lacking Nsun5, a cytosine-5 RNA methyltransferase, with impairment of oligodendrocyte precursor cells-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Cognitive deficits in mice lacking Nsun5, a cytosine-5 RNA methyltransferase, with impairment of oligodendrocyte precursor cells

Published:2018-11-28 Issue:4 Volume:67 Page:688-702
ISSN:0894-1491
Container-title:Glia
language:en
Short-container-title:Glia

Author:

Zhang Tingting¹²,Chen Peipei²,Li Wei¹,Sha Sha²,Wang Ya²,Yuan Zihao²,Shen Bin¹,Chen Ling¹²^ORCID

Affiliation:

1. State Key Lab of Reproductive Medicine; Nanjing Medical University; Nanjing China

2. Department of Physiology; Nanjing Medical University; Nanjing China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

National 973 Basic Research Program of China

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/glia.23565/fullpdf

Reference52 articles.

1. Mutations in NSUN2 cause autosomal-recessive intellectual disability;Abbasi-Moheb;American Journal of Human Genetics,2012

2. Glutamatergic synapses on oligodendrocyte precursor cells in the hippocampus;Bergles;Nature,2000

3. NG2 regulates directional migration of oligodendrocyte precursor cells via rho GTPases and polarity complex proteins;Biname;The Journal of neuroscience : the official journal of the Society for Neuroscience,2013

4. Stem cell function and stress response are controlled by protein synthesis;Blanco;Nature,2016

5. Aberrant methylation of tRNAs links cellular stress to neuro-developmental disorders;Blanco;The EMBO Journal,2014

Cited by 20 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. Mice with NOP2/sun RNA methyltransferase 5 deficiency die before reaching puberty due to fatal kidney damage;Renal Failure;2024-05-07

2. The mutation of NSUN5 R295C promotes preeclampsia by impairing decidualization through downregulating IL-11Rα;iScience;2024-02

3. Roles of ribosomal RNA in health and disease;Frontiers in RNA Research;2024-01-19

4. Advances in brain epitranscriptomics research and translational opportunities;Molecular Psychiatry;2023-12-20

5. Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorder;Genetics in Medicine;2023-09

同舟云学术

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