A homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assembly-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assembly

Published:2020-07 Issue: Volume:141 Page:104880
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Di Nottia Michela,Marchese Maria,Verrigni Daniela,Mutti Christian Daniel,Torraco Alessandra,Oliva Romina,Fernandez-Vizarra Erika,Morani Federica,Trani Giulia,Rizza Teresa,Ghezzi Daniele^ORCID,Ardissone Anna,Nesti Claudia,Vasco Gessica,Zeviani Massimo,Minczuk Michal,Bertini Enrico,Santorelli Filippo Maria,Carrozzo Rosalba^ORCID

Funder

Italian Ministry of Health Ricerca Corrente

Italian Ministry of Health Ricerca Finalizzata

Regione Toscana

Telethon Foundation

MRC

ERC Advanced Grant

NRJ-Institut de France

Publisher

Elsevier BV

Subject

Neurology

Reference53 articles.

1. Ribosome. The structure of the human mitochondrial ribosome;Amunts;Science,2015

2. MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities;Baertling;Neurogenetics,2015

3. High-resolution structures of mitochondrial ribosomes and their functional implications;Bieri;Curr. Opin. Struct. Biol.,2018

4. Kinetics and mechanism of mammalian mitochondrial ribosome assembly;Bogenhagen;Cell Rep.,2018

5. The social life of ribosomal proteins;Brodersen;FEBS J.,2005

Cited by 31 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. Biallelic variants inDAP3result in reduced assembly of the mitoribosomal small subunit with altered intrinsic and extrinsic apoptosis and a Perrault syndrome-spectrum phenotype;2024-08-21

2. Targeting autophagy impairment improves the phenotype of a novel CLN8 zebrafish model;Neurobiology of Disease;2024-07

3. Supernumerary proteins of the human mitochondrial ribosomal small subunit are integral for assembly and translation;iScience;2024-07

4. Molecular pathways in mitochondrial disorders due to a defective mitochondrial protein synthesis;Frontiers in Cell and Developmental Biology;2024-05-24

5. Unveiling the role of Tdark genes in genetic diseases and phenotypes through bioinformatics-based functional enrichment and network analyses;2024-01-15

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