A deafness-associated mitochondrial DNA mutation altered the tRNASer(UCN) metabolism and mitochondrial function
Author:
Funder
National Basic Research Priorities Program of China
National Natural Science Foundation of China
MXG
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Molecular Medicine
Reference67 articles.
1. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA;Andrews;Nat. Genet.,1999
2. Assaying mitochondrial respiratory complex activity in mitochondria isolated from human cells and tissues;Birch-Machin;Methods Cell Biol.,2001
3. The defective expression of gtpbp3 related to tRNA modification alters the mitochondrial function and development of zebrafish;Chen;Int. J. Biochem. Cell Biol.,2016
4. The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes;Chomyn;J. Biol. Chem.,2000
5. Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNASer(UCN) gene;del Castillo;J. Med. Genet.,2002
Cited by 13 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. The Association Between Mitochondrial tRNAGlu Variants and Hearing Loss: A Case-Control Study;Pharmacogenomics and Personalized Medicine;2024-03
2. Conserved spatiotemporal expression landscape of dominant tRNA genes in human and mouse;Biochemical and Biophysical Research Communications;2023-11
3. Conserved spatiotemporal expression landscape of dominant tRNA genes in human and mouse;2023-08-15
4. Maternally inherited non-syndromic hearing loss is linked with a novel mitochondrial ND6 gene mutation;Irish Journal of Medical Science (1971 -);2023-08-10
5. Hereditary spastic paraplegia (SPG 48) with deafness and azoospermia: A case report;Frontiers in Neurology;2023-04-03
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