β-Cell Function in Individuals Carrying the Mitochondrial tRNA Leu (UUR) Mutation-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

β-Cell Function in Individuals Carrying the Mitochondrial tRNA Leu (UUR) Mutation

Published:2007-01 Issue:1 Volume:34 Page:133-137
ISSN:0885-3177
Container-title:Pancreas
language:en
Short-container-title:

Author:

Salles João Eduardo,Kasamatsu Teresa S.,Dib Sérgio A.,Moisés Regina S.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Endocrinology,Hepatology,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference22 articles.

1. Mutation in the mitochondrial tRNALEU(UUR) gene in a large pedigree with maternally transmitted type II diabetes and deafness.;Van den Ouweland;Nat Genet,1992

2. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA.;Reardon;Lancet,1993

3. A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.;Kadowaki;N Engl J Med,1994

4. -cell loss and glucose induced signaling defects in diabetes mellitus caused by mitochondrial tRNALeu (UUR) gene mutation.;Oka;Diabetic Med,1996

5. Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu (UUR) gene mutation.;Velho;Diabetes,1995

Cited by 16 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. Mitochondrial diabetes in mice expressing a dominant-negative allele of nuclear respiratory factor-1 (Nrf1) in pancreatic β-cells;Biochemical and Biophysical Research Communications;2024-12

2. Mitochondrial diabetes in mice expressing a dominant-negative allele of nuclear respiratory factor-1 (Nrf1) in pancreatic β-cells;2023-01-22

3. Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations;Annales d'Endocrinologie;2020-06

4. Diabetes Mellitus in Mitochondrial Disease;Diabetes Associated with Single Gene Defects;2017

5. Association study of mitochondrial DNA polymorphisms with type 2 diabetes in Tunisian population;Mitochondrial DNA;2013-10-09

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