Literature DB >> 15901244

Membrane water transport and aquaporins: looking back.

Peter Agre1.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2005        PMID： 15901244     DOI： 10.1042/BC20050027

Source DB:  PubMed          Journal:  Biol Cell        ISSN： 0248-4900            Impact factor:   4.458


× No keyword cloud information.
  4 in total

1.  Functional characterization of a human aquaporin 0 mutation that leads to a congenital dominant lens cataract.

Authors:  K Varadaraj; S S Kumari; R Patil; M B Wax; R T Mathias
Journal:  Exp Eye Res       Date:  2008-04-10       Impact factor: 3.467

2.  The Arg233Lys AQP0 mutation disturbs aquaporin0-calmodulin interaction causing polymorphic congenital cataract.

Authors:  Shanshan Hu; Binbin Wang; Yanhua Qi; Hui Lin
Journal:  PLoS One       Date:  2012-05-25       Impact factor: 3.240

3.  A novel donor splice-site mutation of major intrinsic protein gene associated with congenital cataract in a Chinese family.

Authors:  Lu Zeng; Wenqiang Liu; Wenguo Feng; Xing Wang; Hui Dang; Luna Gao; Jing Yao; Xianqin Zhang
Journal:  Mol Vis       Date:  2013-11-14       Impact factor: 2.367

4.  AQP5-1364A/C Polymorphism Affects AQP5 Promoter Methylation.

Authors:  Katharina Rump; Theresa Spellenberg; Alexander von Busch; Alexander Wolf; Dominik Ziehe; Patrick Thon; Tim Rahmel; Michael Adamzik; Björn Koos; Matthias Unterberg
Journal:  Int J Mol Sci       Date:  2022-10-05       Impact factor: 6.208
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.