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Paul Linsdell
Observed names:
Linsdell, Paul,
P Linsdell,
P. Linsdell
Institution:
Dalhousie University
Observed institutions:
Dalhousie University,
Mayo Clinic,
University of Leicester,
University of Washington,
Hospital for Sick Children,
Mayo Clinic in Arizona,
McGill University
show all 7
ORCID:
0000-0001-6257-6273
Observed ORCID:
0000-0001-6257-6273
OpenAlex ID:
A5033237248
Glutathione permeability of CFTR
1998
·
Paul Linsdell
, John W. Hanrahan
·
American Journal of Physiology-Cell Physiology
·
283
Permeability of Wild-Type and Mutant Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channels to Polyatomic Anions
1997
·
Paul Linsdell
, Joseph A. Tabcharani
, et al.
·
The Journal of General Physiology
·
226
Adenosine Triphosphate–dependent Asymmetry of Anion Permeation in the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel
1998
·
Paul Linsdell
, John W. Hanrahan
·
The Journal of General Physiology
·
152
PDF
Disulphonic stilbene block of cystic fibrosis transmembrane conductance regulator Cl‐ channels expressed in a mammalian cell line and its regulation by a critical pore residue.
1996
·
P Linsdell
, J W Hanrahan
·
The Journal of Physiology
·
129
Disease-associated Mutations in the Fourth Cytoplasmic Loop of Cystic Fibrosis Transmembrane Conductance Regulator Compromise Biosynthetic Processing and Chloride Channel Activity
1996
·
Fabian S. Seibert
, Paul Linsdell
, et al.
·
Journal of Biological Chemistry
·
124
Mechanism of chloride permeation in the cystic fibrosis transmembrane conductance regulator chloride channel
2005
·
Paul Linsdell
·
Experimental Physiology
·
114
Halide Permeation in Wild-Type and Mutant Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channels
1997
·
Joseph A. Tabcharani
, Paul Linsdell
, et al.
·
The Journal of General Physiology
·
114
Mechanism of direct bicarbonate transport by the CFTR anion channel
2008
·
Lin Tang
, Mohammad Fatehi
, et al.
·
Journal of Cystic Fibrosis
·
107
PDF
Cytoplasmic Loop Three of Cystic Fibrosis Transmembrane Conductance Regulator Contributes to Regulation of Chloride Channel Activity
1996
·
Fabian S. Seibert
, Paul Linsdell
, et al.
·
Journal of Biological Chemistry
·
104
PDF
Molecular Determinants of Anion Selectivity in the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore
2000
·
Paul Linsdell
, Alexandra Evagelidis
, et al.
·
Biophysical Journal
·
103
PDF
Characterization of basolateral K+ channels underlying anion secretion in the human airway cell line Calu‐3
2002
·
Elizabeth A. Cowley
, Paul Linsdell
·
The Journal of Physiology
·
93
Multi-Ion Mechanism for Ion Permeation and Block in the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel
1997
·
Paul Linsdell
, Joseph A. Tabcharani
, et al.
·
The Journal of General Physiology
·
86
Relationship between anion binding and anion permeability revealed by mutagenesis within the cystic fibrosis transmembrane conductance regulator chloride channel pore
2001
·
Paul Linsdell
·
The Journal of Physiology
·
79
Location of a Common Inhibitor Binding Site in the Cytoplasmic Vestibule of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore
2005
·
Paul Linsdell
·
Journal of Biological Chemistry
·
77
Positive Charges at the Intracellular Mouth of the Pore Regulate Anion Conduction in the CFTR Chloride Channel
2006
·
Chantal N. St. Aubin
, Paul Linsdell
·
The Journal of General Physiology
·
76
Flickery block of single CFTR chloride channels by intracellular anions and osmolytes
1996
·
P. Linsdell
, J. W. Hanrahan
·
American Journal of Physiology-Cell Physiology
·
74
Non‐pore lining amino acid side chains influence anion selectivity of the human CFTR Cl− channel expressed in mammalian cell lines
1998
·
Paul Linsdell
, Shu‐Xian Zheng
, et al.
·
The Journal of Physiology
·
72
Direct Comparison of the Functional Roles Played by Different Transmembrane Regions in the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore
2004
·
Ning Ge
, Chantal N. Muise
, et al.
·
Journal of Biological Chemistry
·
71
Molecular determinants of Au(CN)2− binding and permeability within the cystic fibrosis transmembrane conductance regulator Cl− channel pore
2002
·
Xiandi Gong
, Susan M. Burbridge
, et al.
·
The Journal of Physiology
·
71
Regulation of conductance by the number of fixed positive charges in the intracellular vestibule of the CFTR chloride channel pore
2010
·
Jing-Jun Zhou
, Man-Song Li
, et al.
·
The Journal of General Physiology
·
66
Oxidant stress stimulates anion secretion from the human airway epithelial cell line calu‐3: implications for cystic fibrosis lung disease
2002
·
Elizabeth A. Cowley
, Paul Linsdell
·
The Journal of Physiology
·
62
Changes in Accessibility of Cytoplasmic Substances to the Pore Associated with Activation of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel
2010
·
Yassine El Hiani
, Paul Linsdell
·
Journal of Biological Chemistry
·
57
PDF
Alignment of transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore
2011
·
Wuyang Wang
, Yassine El Hiani
, et al.
·
The Journal of General Physiology
·
56
Functional architecture of the CFTR chloride channel
2013
·
Paul Linsdell
·
Molecular Membrane Biology
·
55
PDF
Na+ channel mis‐expression accelerates K+ channel development in embryonic Xenopus laevis skeletal muscle.
1994
·
P Linsdell
, W J Moody
·
The Journal of Physiology
·
53
PDF
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Works count:
119
Citation count:
4,316
H-index:
38
I10-index:
86
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