Molecular mechanism of anion permeation through CFTR channel pore.

The proposed research in my lab has been focusing on the structure, function and molecular pharmacology of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel; and the interaction of CFTR chloride channels with other ion channels, receptors in submucosal gland cells. Chro...

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Main Author: Gong, Alex Xiandi.
Other Authors: School of Biological Sciences
Format: Research Report
Language:English
Published: 2008
Subjects:
Online Access:http://hdl.handle.net/10356/14221
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author Gong, Alex Xiandi.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Gong, Alex Xiandi.
author_sort Gong, Alex Xiandi.
collection NTU
description The proposed research in my lab has been focusing on the structure, function and molecular pharmacology of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel; and the interaction of CFTR chloride channels with other ion channels, receptors in submucosal gland cells. Chronic lung infection and deterioration of lung function are the major causes of morbidity and death in cystic fibrosis (CF), the most common inherited lethal disease in Caucasians. Although the genetic defect in CF was discovered in 1989-mutations in the gene encoding the CFTR, the mechanism by which CFTR mutations cause lung disease remain uncertain. We arc very interested in studying a number of mechanisms proposed to link the CF genotype to clinical disease, particularly in defective airway submucosal gland secretion, loss of CFTR regulation of other transporting proteins such as other chloride channels, potassium channels, aquaporins in a serous epithelial cells. Determination of the mechanism linking genotype to disease is of crilical importance in developing therapies to treat CF.
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spelling ntu-10356/142212023-02-28T17:58:23Z Molecular mechanism of anion permeation through CFTR channel pore. Gong, Alex Xiandi. School of Biological Sciences DRNTU::Science::Biological sciences::Biochemistry The proposed research in my lab has been focusing on the structure, function and molecular pharmacology of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel; and the interaction of CFTR chloride channels with other ion channels, receptors in submucosal gland cells. Chronic lung infection and deterioration of lung function are the major causes of morbidity and death in cystic fibrosis (CF), the most common inherited lethal disease in Caucasians. Although the genetic defect in CF was discovered in 1989-mutations in the gene encoding the CFTR, the mechanism by which CFTR mutations cause lung disease remain uncertain. We arc very interested in studying a number of mechanisms proposed to link the CF genotype to clinical disease, particularly in defective airway submucosal gland secretion, loss of CFTR regulation of other transporting proteins such as other chloride channels, potassium channels, aquaporins in a serous epithelial cells. Determination of the mechanism linking genotype to disease is of crilical importance in developing therapies to treat CF. 2008-11-06T03:36:35Z 2008-11-06T03:36:35Z 2007 2007 Research Report http://hdl.handle.net/10356/14221 en 5 p. application/pdf
spellingShingle DRNTU::Science::Biological sciences::Biochemistry
Gong, Alex Xiandi.
Molecular mechanism of anion permeation through CFTR channel pore.
title Molecular mechanism of anion permeation through CFTR channel pore.
title_full Molecular mechanism of anion permeation through CFTR channel pore.
title_fullStr Molecular mechanism of anion permeation through CFTR channel pore.
title_full_unstemmed Molecular mechanism of anion permeation through CFTR channel pore.
title_short Molecular mechanism of anion permeation through CFTR channel pore.
title_sort molecular mechanism of anion permeation through cftr channel pore
topic DRNTU::Science::Biological sciences::Biochemistry
url http://hdl.handle.net/10356/14221
work_keys_str_mv AT gongalexxiandi molecularmechanismofanionpermeationthroughcftrchannelpore