α-COP binding to the survival motor neuron protein SMN is required for neuronal process outgrowth-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

α-COP binding to the survival motor neuron protein SMN is required for neuronal process outgrowth

Published:2015-10-13 Issue:25 Volume:24 Page:7295-7307
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Li Hongxia,Custer Sara K.,Gilson Timra,Hao Le Thi,Beattie Christine E.,Androphy Elliot J.

Funder

National Institute of Neurologic Disease/National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/24/25/7295/7148542/ddv428.pdf

Reference68 articles.

1. Molecular Functions of the SMN Complex

2. The SMN Complex: An Assembly Machine for RNPs

3. Ribonucleoprotein Assembly Defects Correlate with Spinal Muscular Atrophy Severity and Preferentially Affect a Subset of Spliceosomal snRNPs

4. An SMN-Dependent U12 Splicing Event Essential for Motor Circuit Function

5. Splicing changes in SMA mouse motoneurons and SMN-depleted neuroblastoma cells: Evidence for involvement of splicing regulatory proteins

Cited by 32 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. Early signs of neurodegenerative diseases: Possible mechanisms and targets for Golgi stress;Biomedicine & Pharmacotherapy;2024-06

2. Hepatocyte-intrinsic SMN deficiency drives metabolic dysfunction and liver steatosis in spinal muscular atrophy;Journal of Clinical Investigation;2024-05-09

3. COPI coatomer subunit α-COP interacts with the RNA binding protein Nucleolin via a C-terminal dilysine motif;Human Molecular Genetics;2023-09-02

4. Challenges and future perspective of antisense therapy for spinal muscular atrophy: A review;European Journal of Cell Biology;2023-06

5. Spinal Muscular Atrophy Patient iPSC-Derived Motor Neurons Display Altered Proteomes at Early Stages of Differentiation;ACS Omega;2021-12-15

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