(Q43737971)

26 November 2017

Identification of a region of strong discrimination in the pore of CFTR. (English)

1 reference

26 November 2017

McCarty NA

1

1 reference

PubMed ID

11557589

26 November 2017

Zhang ZR

series ordinal

2

1 reference

26 November 2017

1 October 2001

1 reference

American Journal of Physiology - Lung Cellular and Molecular Physiology

26 November 2017

1 reference

26 November 2017

281

1 reference

26 November 2017

L852-67

1 reference

26 November 2017

4

1 reference

Chemical rescue of phosphoryl transfer in a cavity mutant: a cautionary tale for site-directed mutagenesis

26 November 2017

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Cystic fibrosis transmembrane conductance regulator. Structure and function of an epithelial chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Long-range structural effects in a second-site revertant of a mutant dihydrofolate reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Locating the anion-selectivity filter of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Tris+/Na+ permeability ratios of nicotinic acetylcholine receptors are reduced by mutations near the intracellular end of the M2 region

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Cystic fibrosis-associated mutations at arginine 347 alter the pore architecture of CFTR. Evidence for disruption of a salt bridge.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

CFTR: domains, structure, and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Structural analysis of cloned plasma membrane proteins by freeze-fracture electron microscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Anion and cation permeability of a chloride channel in rat hippocampal neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Anion permeation in an apical membrane chloride channel of a secretory epithelial cell

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Structure of the light-driven chloride pump halorhodopsin at 1.8 A resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Ion transport through pores: A rate-theory analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Molecular determinants of anion selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Adenosine triphosphate-dependent asymmetry of anion permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Multi-Ion mechanism for ion permeation and block in the cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Non-pore lining amino acid side chains influence anion selectivity of the human CFTR Cl- channel expressed in mammalian cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Merck Frosst Award Lecture 1998. Molecular dissection of the human multidrug resistance P-glycoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Cystic fibrosis transmembrane conductance regulator (CFTR) anion binding as a probe of the pore

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Novel pore-lining residues in CFTR that govern permeation and open-channel block

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Anion permeation in Ca(2+)-activated Cl(-) channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Structure of the multidrug resistance P-glycoprotein to 2.5 nm resolution determined by electron microscopy and image analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Structure and function of the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Cystic fibrosis transmembrane conductance regulator. Physical basis for lyotropic anion selectivity patterns

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Mapping the receptor site for hanatoxin, a gating modifier of voltage-dependent K+ channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Halide permeation in wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Structural and ionic determinants of 5-nitro-2-(3-phenylprophyl-amino)-benzoic acid block of the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

The two halves of CFTR form a dual-pore ion channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

A single conductance pore for chloride ions formed by two cystic fibrosis transmembrane conductance regulator molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Interaction between permeation and gating in a putative pore domain mutant in the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Direct comparison of NPPB and DPC as probes of CFTR expressed in Xenopus oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

Multi-ion pore behaviour in the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.4.L852

10.1152/AJPLUNG.2001.281.4.L852

21 January 2018

Identifiers

DOI

0 references

PubMed ID

11557589

1 reference

PubMed ID

11557589