(Q43670738)

25 November 2017

Cystic fibrosis: the 'bicarbonate before chloride' hypothesis (English)

1 reference

25 November 2017

0 references

Wine JJ

1

1 reference

PubMed ID

11448786

25 November 2017

language of work or name

English

0 references

publication date

1 June 2001

1 reference

25 November 2017

1 reference

25 November 2017

11

1 reference

25 November 2017

R463-6

1 reference

25 November 2017

12

1 reference

Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator

25 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

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%2FS0960-9822%2801%2900282-2

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%2FS0960-9822%2801%2900282-2

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%2FS0960-9822%2801%2900282-2

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%2FS0960-9822%2801%2900282-2

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%2FS0960-9822%2801%2900282-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

Cystic fibrosis transmembrane conductance regulator regulates luminal Cl-/HCO3- exchange in mouse submandibular and pancreatic ducts

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

Regulation of Cl-/ HCO3- exchange by cystic fibrosis transmembrane conductance regulator expressed in NIH 3T3 and HEK 293 cells

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

HCO3- transport in a mathematical model of the pancreatic ductal epithelium.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

Low sweat electrolytes in a patient with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

Defective beta adrenergic response of cystic fibrosis sweat glands in vivo and in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

Relative ion permeability of normal and cystic fibrosis nasal epithelium

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

The neglected ion: HCO3-

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

Influence of buffer capacity and pH-dependent rheological properties of respiratory mucus on health effects due to acidic pollution.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

Identification of eight mutations and three sequence variations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900282-2

7 January 2021

10.1016/S0960-9822(01)00282-2

Identifiers

DOI

1 reference

25 November 2017

1 reference

PubMed ID

11448786