<a name="home"></a>Prevalence of the A1555G (12S rRNA) and tRNA Ser(UCN) mitochondrial mutations in hearing-impaired Brazilian patients-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Prevalence of the A1555G (12S rRNA) and tRNA Ser(UCN) mitochondrial mutations in hearing-impaired Brazilian patients

Published:2006-02 Issue:2 Volume:39 Page:219-226
ISSN:0100-879X
Container-title:Brazilian Journal of Medical and Biological Research
language:
Short-container-title:Braz J Med Biol Res

Author:

Abreu-Silva R.S.¹,Lezirovitz K.¹,Braga M.C.C.²,Spinelli M.³,Pirana S.³,Della-Rosa V.A.²,Otto P.A.¹,Mingroni-Netto R.C.¹

Affiliation:

1. Universidade de São Paulo, Brasil

2. Universidade Estadual de Maringá, Brasil

3. Pontifícia Universidade Católica de São Paulo, Brasil

Publisher

FapUNIFESP (SciELO)

Subject

Cell Biology,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Immunology,Physiology,Biochemistry,General Neuroscience,Biophysics

Link

http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdf

Reference29 articles.

1. Genetic epidemiological studies of early-onset deafness in the U: S;Marazita ML;school-age population. American Journal of Medical Genetics,1993

2. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness;Prezant TR;Nature Genetics,1993

3. A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity;Guan MX;Human Molecular Genetics,2000

4. Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness;Hamasaki K;Biochemistry,1997

5. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides;Estivill X;American Journal of Human Genetics,1998

Cited by 29 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. Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America;Genes;2024-01-29

2. Crucial Roles of the m.1555A>G Mutation on MT-RNR1 Gene in Hearing Loss;J BIOL REG HOMEOS AG;2022

3. Genetic etiology of non-syndromic hearing loss in Latin America;Human Genetics;2021-10-15

4. Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss;Human Genetics;2021-10-01

5. Pharmacogenetic screening of A1555G and C1494T mitochondrial mutations and the use of ototoxic drugs among Jordanians;EUR REV MED PHARMACO;2021

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