Understanding how cystic fibrosis mutations disrupt CFTR function: From single molecules to animal models-Reference-Cited by-同舟云学术

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Understanding how cystic fibrosis mutations disrupt CFTR function: From single molecules to animal models

Published:2014-07 Issue: Volume:52 Page:47-57
ISSN:1357-2725
Container-title:The International Journal of Biochemistry & Cell Biology
language:en
Short-container-title:The International Journal of Biochemistry & Cell Biology

Author:

Wang Yiting,Wrennall Joe A.,Cai Zhiwei,Li Hongyu,Sheppard David N.

Funder

Cystic Fibrosis Foundation

Cystic Fibrosis Trust

Engineering and Physical Sciences Research Council

Publisher

Elsevier BV

Subject

Cell Biology,Biochemistry

Reference120 articles.

1. Neonates with cystic fibrosis have a reduced nasal liquid pH: a small pilot study;Abou Alaiwa;J Cyst Fibros,2014

2. Pancreatic damage in fetal and newborn cystic fibrosis pigs involves the activation of inflammatory and remodeling pathways;Abu-El-Haija;Am J Pathol,2012

3. Amino acid residues lining the chloride channel of the cystic fibrosis transmembrane conductance regulator;Akabas;J Biol Chem,1994

4. The first nucleotide binding domain of cystic fibrosis transmembrane conductance regulator is a site of stable nucleotide interaction, whereas the second is a site of rapid turnover;Aleksandrov;J Biol Chem,2002

5. Regulatory insertion removal restores maturation, stability and function of ΔF508 CFTR;Aleksandrov;J Mol Biol,2010

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