Characterization of SLC26A9 in Patients with CF-Like Lung Disease

Role of Cystic Fibrosis Transmembrane Conductance Regulator in Patients With Chronic Sinopulmonary Disease

(2012) Tanja Gonska et al.   CHEST

Functional analysis of nonsynonymous single nucleotide polymorphisms in human SLC26A9

(2012) An-Ping Chen et al.   HUMAN MUTATION

SLC26A9-mediated chloride secretion prevents mucus obstruction in airway inflammation

(2012) Pinelopi Anagnostopoulou et al.   JOURNAL OF CLINICAL INVESTIGATION

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis

(2012) Lei Sun et al.   NATURE GENETICS

Functional Interaction between CFTR and the Sodium-Phosphate Co-Transport Type 2a in Xenopus laevis Oocytes

(2012) Naziha Bakouh et al.   PLoS One

Characterization of the L683P mutation of SLC26A9 in Xenopus oocytes

(2011) Martine Avella et al.   BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS

The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation

(2011) Baptiste Rode et al.   HUMAN MOLECULAR GENETICS

Recommendations for the classification of diseases as CFTR-related disorders

(2011) C. Bombieri et al.   Journal of Cystic Fibrosis

Damage to the gastric epithelium activates cellular bicarbonate secretion via SLC26A9 Cl−/HCO3− exchange

(2010) Elise S. Demitrack et al.   AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY

Clinical Phenotype and Genotype of Children with Borderline Sweat Test and Abnormal Nasal Epithelial Chloride Transport

(2010) Isabelle Sermet-Gaudelus et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Bronchiectasis

(2010) Richard C. Boucher   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Cystic Fibrosis Transmembrane Conductance Regulator Channel Dysfunction in Non–Cystic Fibrosis Bronchiectasis

(2010) Thierry Bienvenu et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Interaction between CFTR and prestin (SLC26A5)

(2010) Kazuaki Homma et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES

SLC26A9 stimulates CFTR expression and function in human bronchial cell lines

(2010) Martine Avella et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Structure of the Cytosolic Portion of the Motor Protein Prestin and Functional Role of the STAS Domain in SLC26/SulP Anion Transporters

(2010) Elisa Pasqualetto et al.   JOURNAL OF MOLECULAR BIOLOGY

Cystic Fibrosis Transmembrane Regulator Inhibitors CFTRinh-172 and GlyH-101 Target Mitochondrial Functions, Independently of Chloride Channel Inhibition

(2010) M. Kelly et al.   JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS

Structure of a SLC26 Anion Transporter STAS Domain in Complex with Acyl Carrier Protein: Implications for E. coli YchM in Fatty Acid Metabolism

(2010) Mohan Babu et al.   STRUCTURE

Combination of ENaC and CFTR mutations may predispose to cystic fibrosis-like disease

(2009) I. Fajac et al.   EUROPEAN RESPIRATORY JOURNAL

Slc26a9 Is Inhibited by the R-region of the Cystic Fibrosis Transmembrane Conductance Regulator via the STAS Domain

(2009) Min-Hwang Chang et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

SLC26A9 is a constitutively active, CFTR-regulated anion conductance in human bronchial epithelia

(2009) Carol A. Bertrand et al.   JOURNAL OF GENERAL PHYSIOLOGY

Slc26a9—Anion Exchanger, Channel and Na+ Transporter

(2009) Min-Hwang Chang et al.   JOURNAL OF MEMBRANE BIOLOGY

Membrane topology of the cyanobacterial bicarbonate transporter, BicA, a member of the SulP (SLC26A) family

(2009) Megan C. Shelden et al.   MOLECULAR MEMBRANE BIOLOGY

Characterization of SLC26A9, Facilitation of Cl- Transport by Bicarbonate

(2008) Celine Loriol et al.   CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Regulation of CFTR Trafficking by Its R Domain

(2008) Christopher M. Lewarchik et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Deletion of the chloride transporter Slc26a9 causes loss of tubulovesicles in parietal cells and impairs acid secretion in the stomach

(2008) J. Xu et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Expression, purification and characterisation of the C-terminal STAS domain of the SLC26 anion transporter prestin

(2007) Elisa Pasqualetto et al.   PROTEIN EXPRESSION AND PURIFICATION