SLC4A11 Three-Dimensional Homology Model Rationalizes Corneal Dystrophy-Causing Mutations-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

SLC4A11 Three-Dimensional Homology Model Rationalizes Corneal Dystrophy-Causing Mutations

Published:2016-12-27 Issue:3 Volume:38 Page:279-288
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Badior Katherine E.¹,Alka Kumari¹,Casey Joseph R.¹

Affiliation:

1. Department of Biochemistry; Membrane Protein Disease Research Group; University of Alberta; Edmonton Alberta Canada

Funder

Canadian Institutes of Health Research

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference77 articles.

1. Mutational spectrum of SLC4A11 in autosomal recessive CHED in Saudi Arabia;Aldahmesh;Invest Ophthalmol Vis Sci,2009

2. Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11;Aldave;Cornea,2007

3. Structure of eukaryotic purine/H(+) symporter UapA suggests a role for homodimerization in transport activity;Alguel;Nat Commun,2016

4. Crystal structure of the anion exchanger domain of human erythrocyte band 3;Arakawa;Science,2015

5. The SWISS-MODEL workspace: A web-based environment for protein structure homology modelling;Arnold;Bioinformatics,2006

Cited by 17 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. SLC4A11 mediates ammonia import and promotes cancer stemness in hepatocellular carcinoma;2024-08-08

2. Potential Theranostic Roles of SLC4 Molecules in Human Diseases;International Journal of Molecular Sciences;2023-10-13

3. Structural insights into the conformational changes of BTR1/SLC4A11 in complex with PIP2;Nature Communications;2023-10-03

4. Systematic review of SLC4A11, ZEB1, LOXHD1, and AGBL1 variants in the development of Fuchs’ endothelial corneal dystrophy;Frontiers in Medicine;2023-06-27

5. Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma;Genes;2023-01-25

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