(Q42472855)

1 November 2017

title

Chloride conductance of CFTR facilitates basal Cl-/HCO3- exchange in the villous epithelium of intact murine duodenum (English)

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1 November 2017

Janet E Simpson

1

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1 November 2017

Lara R Gawenis

2

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1 November 2017

Nancy M Walker

3

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1 November 2017

Kathryn T Boyle

4

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1 November 2017

Lane L Clarke

5

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1 November 2017

publication date

13 January 2005

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American Journal of Physiology - Gastrointestinal and Liver Physiology

1 November 2017

published in

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1 November 2017

volume

288

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1 November 2017

issue

6

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1 November 2017

page(s)

G1241-51

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

1 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Expression and regulation of the Na+-K+-2Cl- cotransporter NKCC1 in the normal and CFTR-deficient murine colon

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Acute regulation of the SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Abnormal Paneth cell granule dissolution and compromised resistance to bacterial colonization in the intestine of CF mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Stimulation of Cl/HCO3 exchange in rat duodenal brush border membrane vesicles by cAMP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

High intracellular pH in CFPAC: A pancreas cell line from a patient with cystic fibrosis is lowered by retrovirus-mediated CFTR gene transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

cAMP inhibition of murine intestinal Na/H exchange requires CFTR-mediated cell shrinkage of villus epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Intestinal NaCl transport in NHE2 and NHE3 knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Cystic fibrosis gene mutation reduces epithelial cell acidification and injury in acid-perfused mouse duodenum

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Anion selectivity of apical membrane conductance of Calu 3 human airway epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Down-regulated in adenoma mediates apical Cl-/HCO3- exchange in rabbit, rat, and human duodenum

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Specificity of anion exchange mediated by mouse Slc26a6

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

AE4 is a DIDS-sensitive Cl(-)/HCO(-)(3) exchanger in the basolateral membrane of the renal CCD and the SMG duct

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Gating of CFTR by the STAS domain of SLC26 transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

The down regulated in adenoma (dra) gene product binds to the second PDZ domain of the NHE3 kinase A regulatory protein (E3KARP), potentially linking intestinal Cl-/HCO3- exchange to Na+/H+ exchange

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

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%2FAJPGI.00493.2004

Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

HCO3- salvage mechanisms in the submandibular gland acinar and duct cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

The SLC26 gene family of multifunctional anion exchangers

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Colocalization of the apical Cl-/HCO3- exchanger PAT1 and gastric H-K-ATPase in stomach parietal cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

The cystic fibrosis transmembrane conductance regulator is not a base transporter in isolated duodenal epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Identification of transport abnormalities in duodenal mucosa and duodenal enterocytes from patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Control of dynamic CFTR selectivity by glutamate and ATP in epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

A functional CFTR protein is required for mouse intestinal cAMP-, cGMP- and Ca(2+)-dependent HCO3- secretion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Dynamic control of cystic fibrosis transmembrane conductance regulator Cl(-)/HCO3(-) selectivity by external Cl(-)

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

An animal model for cystic fibrosis made by gene targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Independence of apical Cl-/HCO3- exchange and anion conductance in duodenal HCO3- secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Intracellular pH measurements in Ehrlich ascites tumor cells utilizing spectroscopic probes generated in situ

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

An alternate pathway of cAMP-stimulated Cl secretion across the NKCC1-null murine duodenum

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Intracellular pH and its relationship to regulation of ion transport in normal and cystic fibrosis human nasal epithelia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Molecular characterization of the murine Slc26a6 anion exchanger: functional comparison with Slc26a1

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Identification of an apical Cl-/HCO3- exchanger in gastric surface mucous and duodenal villus cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

A mouse model for the delta F508 allele of cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

Multi-ion pore behaviour in the CFTR chloride channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPGI.00493.2004

21 January 2018

Identifiers

DOI

10.1152/AJPGI.00493.2004

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1 November 2017

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