(Q34355404)

1 August 2017

1 reference

title

The cystic fibrosis transmembrane conductance regulator: an intriguing protein with pleiotropic functions (English)

1 reference

1 August 2017

transmembrane protein

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0 references

1 reference

Jean-Jacques Cassiman

series ordinal

3

object named as

Jean-Jacques Cassiman

0 references

Anne Vankeerberghen

series ordinal

1

object named as

Anne Vankeerberghen

0 references

author name string

Harry Cuppens

series ordinal

2

1 reference

1 August 2017

1 March 2002

1 reference

Journal of Cystic Fibrosis

1 August 2017

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1 August 2017

1

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1 August 2017

13-29

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1 August 2017

1

1 reference

CYSTIC FIBROSIS OF THE PANCREAS AND ITS RELATION TO CELIAC DISEASE

1 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Celiac syndrome; genetics of cystic fibrosis of the pancreas, with a consideration of etiology

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Identification of the cystic fibrosis gene: genetic analysis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

CFTR expression and organ damage in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Secondary genetic factors in cystic fibrosis lung disease

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Contribution of genetic factors other than CFTR to disease severity in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Alpha1-antitrypsin deficiency alleles and the Taq-I G-->A allele in cystic fibrosis lung disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Association of alpha(1)-antichymotrypsin deficiency with milder lung disease in patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

TGF-beta(1) genotype and accelerated decline in lung function of patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

HLA class II polymorphism in cystic fibrosis. A possible modifier of pulmonary phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Anti-neutrophil cytoplasmic antibodies (ANCA) against bactericidal/permeability-increasing protein (BPI) and cystic fibrosis lung disease

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Clinical spectrum in homozygotes and compound heterozygotes inheriting cystic fibrosis mutation 3849 + 10kbC > T: significance for geneticists

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Characterization of 19 disease-associated missense mutations in the regulatory domain of the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Chloride channels and cystic fibrosis of the pancreas

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Relative ion permeability of normal and cystic fibrosis nasal epithelium

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Abnormal Ion Permeation Through Cystic Fibrosis Respiratory Epithelium

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Normal bronchial epithelial cells constitutively produce the anti-inflammatory cytokine interleukin-10, which is downregulated in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Degradation of annexin I in bronchoalveolar lavage fluid from patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cystic fibrosis epithelial cells have a receptor for pathogenic bacteria on their apical surface

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Human beta-defensin-1 is a salt-sensitive antibiotic in lung that is inactivated in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cystic fibrosis transmembrane conductance regulator is an epithelial cell receptor for clearance of Pseudomonas aeruginosa from the lung.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Salmonella typhi uses CFTR to enter intestinal epithelial cells.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Tissue-specific in vivo transcription start sites of the human and murine cystic fibrosis genes

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

CFTR chloride channels in human and simian heart

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Increased proportion of exon 9 alternatively spliced CFTR transcripts in vas deferens compared with nasal epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Higher proportion of intact exon 9 CFTR mRNA in nasal epithelium compared with vas deferens.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Alternative splicing in the first nucleotide binding fold of CFTR

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cellular and viral splicing factors can modify the splicing pattern of CFTR transcripts carrying splicing mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

The biogenesis, traffic, and function of the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

A3 adenosine receptors regulate Cl- channels of nonpigmented ciliary epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Efficient endocytosis of the cystic fibrosis transmembrane conductance regulator requires a tyrosine-based signal

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

The carboxyl terminus of the cystic fibrosis transmembrane conductance regulator binds to AP-2 clathrin adaptors.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Intracellular distribution of proteasomes

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

The Hsc70 co-chaperone CHIP targets immature CFTR for proteasomal degradation

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

The mechanism underlying cystic fibrosis transmembrane conductance regulator transport from the endoplasmic reticulum to the proteasome includes Sec61beta and a cytosolic, deglycosylated intermediary

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Pyrophosphate stimulates wild-type and mutant cystic fibrosis transmembrane conductance regulator Cl- channels

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Protein phosphatase 2C dephosphorylates and inactivates cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Differential regulation of single CFTR channels by PP2C, PP2A, and other phosphatases.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

A novel model for the first nucleotide binding domain of the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Control of CFTR channel gating by phosphorylation and nucleotide hydrolysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Isotype-specific activation of cystic fibrosis transmembrane conductance regulator-chloride channels by cGMP-dependent protein kinase II.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Distinct and specific functions of cGMP-dependent protein kinases

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Membrane targeting of cGMP-dependent protein kinase is required for cystic fibrosis transmembrane conductance regulator Cl- channel activation

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Guanylin in the human pancreas: a novel luminocrine regulatory pathway of electrolyte secretion via cGMP and CFTR in the ductal system

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Protein kinase C regulates the magnitude and stability of CFTR currents in pancreatic duct cells

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Functional characterization of the CFTR R domain using CFTR/MDR1 hybrid and deletion constructs

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by its R domain

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

A functional R domain from cystic fibrosis transmembrane conductance regulator is predominantly unstructured in solution

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Stimulation of CFTR activity by its phosphorylated R domain.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Coupling of CFTR Cl- channel gating to an ATP hydrolysis cycle

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Control of CFTR chloride conductance by ATP levels through non-hydrolytic binding

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Association of domains within the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Channel-lining residues in the M3 membrane-spanning segment of the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Intracellular loop between transmembrane segments IV and V of cystic fibrosis transmembrane conductance regulator is involved in regulation of chloride channel conductance state

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Disease-associated mutations in the fourth cytoplasmic loop of cystic fibrosis transmembrane conductance regulator compromise biosynthetic processing and chloride channel activity.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cytoplasmic loop three of cystic fibrosis transmembrane conductance regulator contributes to regulation of chloride channel activity.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Disease-Associated Mutations in Cytoplasmic Loops 1 and 2 of Cystic Fibrosis Transmembrane Conductance Regulator Impede Processing or Opening of the Channel†

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cystic fibrosis: a disease in electrolyte transport.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

CFTR as a cAMP-dependent regulator of sodium channels

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Regulation of epithelial sodium channels by the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Wild type but not deltaF508 CFTR inhibits Na+ conductance when coexpressed in Xenopus oocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Inhibition of epithelial Na+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Role of actin in regulation of epithelial sodium channels by CFTR.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Activation of the epithelial Na+ channel (ENaC) requires CFTR Cl- channel function

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

CFTR and outward rectifying chloride channels are distinct proteins with a regulatory relationship

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Purified cystic fibrosis transmembrane conductance regulator (CFTR) does not function as an ATP channel

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cellular ATP release by the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Electrodiffusional ATP movement through the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

CFTR Cl- channel and CFTR-associated ATP channel: distinct pores regulated by common gates.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cystic fibrosis transmembrane conductance regulator mediates sulphonylurea block of the inwardly rectifying K+ channel Kir6.1.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Mechanisms of renal tubular cell hypertrophy: mitogen-induced suppression of proteolysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Inhibition of volume-regulated anion channels by expression of the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Interaction between calcium-activated chloride channels and the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

The cystic fibrosis transmembrane conductance regulator attenuates the endogenous Ca2+ activated Cl- conductance of Xenopus oocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

cAMP stimulation of CFTR-expressing Xenopus oocytes activates a chromanol-inhibitable K+ conductance.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Aquaporin 3 cloned from Xenopus laevis is regulated by the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

CFTR protein is involved in the efflux of neutral amino acids

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Defective acidification of intracellular organelles in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Functional CFTR in endosomal compartment of CFTR-expressing fibroblasts and T84 cells

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Regulation of plasma membrane recycling by CFTR.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

CFTR is involved in membrane endocytosis but not in fluid-phase and receptor-mediated endocytosis in human respiratory epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylation

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

CFTR-dependent membrane insertion is linked to stimulation of the CFTR chloride conductance.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Functional integrity of the vesicle transporting machinery is required for complete activation of cFTR expressed in xenopus laevis oocytes

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Stabilization of F-actin prevents cAMP-elicited Cl- secretion in T84 cells

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Dynamic role of microfilaments in intestinal chloride secretion

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

cAMP-independent regulation of CFTR by the actin cytoskeleton

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

The actin filament disrupter cytochalasin D activates the recombinant cystic fibrosis transmembrane conductance regulator Cl- channel in mouse 3T3 fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Protein kinase A associates with cystic fibrosis transmembrane conductance regulator via an interaction with ezrin

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

PKA holoenzyme is functionally coupled to CFTR by AKAPs

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Peptide binding consensus of the NHE-RF-PDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR)

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

PDZ domain proteins: scaffolds for signaling complexes

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

A C-terminal motif found in the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteins

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Inhibition of cystic fibrosis transmembrane conductance regulator by novel interaction with the metabolic sensor AMP-activated protein kinase

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Regulation of CFTR chloride channels by syntaxin and Munc18 isoforms

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Molecular cloning, expression analysis, and chromosomal localization of human syntaxin 8 (STX8)

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Complexity in a monogenic disease

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Conformational and temperature-sensitive stability defects of the delta F508 cystic fibrosis transmembrane conductance regulator in post-endoplasmic reticulum compartments.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Structural cues involved in endoplasmic reticulum degradation of G85E and G91R mutant cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

C-terminal truncations destabilize the cystic fibrosis transmembrane conductance regulator without impairing its biogenesis. A novel class of mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

European Epidemiologic Registry of Cystic Fibrosis (ERCF): comparison of major disease manifestations between patients with different classes of mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasis

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Delivery of purified, functional CFTR to epithelial cells in vitro using influenza hemagglutinin

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Assessment of the efficacy of in vivo CFTR protein replacement therapy in CF mice

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Gene therapy for cystic fibrosis: which postman, which box?

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

A membrane lipid imbalance plays a role in the phenotypic expression of cystic fibrosis in cftr(-/-) mice

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein

1 reference

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

7 January 2021

https://api.crossref.org/works/10.1016%2FS1569-1993%2801%2900003-0

1 reference

7 January 2021

10.1016/S1569-1993(01)00003-0

Identifiers

DOI

1 reference

1 August 2017

1 reference

PubMed ID

15463806