Macromolecular interactions and ion transport in cystic fibrosis (Q35901540)

11 August 2017

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title

Macromolecular interactions and ion transport in cystic fibrosis (English)

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11 August 2017

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William B Guggino

1

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PubMed ID

15447951

11 August 2017

Susan P Banks-Schlegel

series ordinal

2

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PubMed ID

15447951

11 August 2017

language of work or name

English

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publication date

1 October 2004

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American Journal of Respiratory and Critical Care Medicine

11 August 2017

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11 August 2017

170

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11 August 2017

7

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11 August 2017

815-820

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Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

11 August 2017

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

CFTR: domains, structure, and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Syntaxin 1A inhibits CFTR chloride channels by means of domain-specific protein-protein interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

A Golgi-associated PDZ domain protein modulates cystic fibrosis transmembrane regulator plasma membrane expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Characterization of a protein cofactor that mediates protein kinase A regulation of the renal brush border membrane Na(+)-H+ exchanger

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Molecular studies of CFTR interacting proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Mu 2 binding directs the cystic fibrosis transmembrane conductance regulator to the clathrin-mediated endocytic pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Physiological modulation of CFTR activity by AMP-activated protein kinase in polarized T84 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Cysteine string protein interacts with and modulates the maturation of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Genotype-phenotype relationships in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Emerging drug treatments for cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Novel CFTR chloride channel activators identified by screening of combinatorial libraries based on flavone and benzoquinolizinium lead compounds

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Repeated adeno-associated virus serotype 2 aerosol-mediated cystic fibrosis transmembrane regulator gene transfer to the lungs of patients with cystic fibrosis: a multicenter, double-blind, placebo-controlled trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Structure of nucleotide-binding domain 1 of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Traffic pattern of cystic fibrosis transmembrane regulator through the early exocytic pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Traffic-independent function of the Sar1p/COPII machinery in proteasomal sorting of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Non-conventional trafficking of the cystic fibrosis transmembrane conductance regulator through the early secretory pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Modulation of mature cystic fibrosis transmembrane regulator protein by the PDZ domain protein CAL

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Regulation of plasma membrane recycling by CFTR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

A macromolecular complex of beta 2 adrenergic receptor, CFTR, and ezrin/radixin/moesin-binding phosphoprotein 50 is regulated by PKA

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Regulation of channel gating by AMP-activated protein kinase modulates cystic fibrosis transmembrane conductance regulator activity in lung submucosal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

CFTR is a monomer: biochemical and functional evidence

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Imaging CFTR: a tail to tail dimer with a central pore.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Foxj1 is required for apical localization of ezrin in airway epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Modifier genes and variation in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manif

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Use of protein repair therapy in the treatment of cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

THERAPIES DIRECTED AT THE BASIC DEFECT IN CYSTIC FIBROSIS

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200403-381WS

10.1164/RCCM.200403-381WS

21 January 2018

Identifiers

DOI

1 reference

11 August 2017

1 reference

PubMed ID

15447951