Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis
Author:
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology
Reference24 articles.
1. Regulation by ATP and ADP of CFTR Chloride Channels That Contain Mutant Nucleotide-Binding Domains
2. Congenital Bilateral Absence of the Vas Deferens
3. Defective acidification of intracellular organelles in cystic fibrosis
4. The Metabolic Basis of Inherited Disease;Boat,1989
5. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis
Cited by 1295 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 Role of Ion-Transporting Proteins in Human Disease;International Journal of Molecular Sciences;2024-01-31
2. Benchmarking AlphaMissense pathogenicity predictions against cystic fibrosis variants;PLOS ONE;2024-01-25
3. Two rare variants that affect the same amino acid in CFTR have distinct responses to ivacaftor;The Journal of Physiology;2024-01
4. The Effect of Complex Alleles of the CFTR Gene on the Clinical Manifestations of Cystic Fibrosis and the Effectiveness of Targeted Therapy;International Journal of Molecular Sciences;2023-12-21
5. Die Goldenen Zwanziger der Mukoviszidose;CME;2023-12
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
"全球学者库"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,当前全球学者库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 © 2019-2023 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