Published in J Biol Chem on February 03, 2004
The mechanism of ammonia transport based on the crystal structure of AmtB of Escherichia coli. Proc Natl Acad Sci U S A (2004) 2.91
NH3 and NH4+ permeability in aquaporin-expressing Xenopus oocytes. Pflugers Arch (2005) 1.64
Human Rhesus-associated glycoprotein mediates facilitated transport of NH(3) into red blood cells. Proc Natl Acad Sci U S A (2004) 1.51
Effect of collecting duct-specific deletion of both Rh B Glycoprotein (Rhbg) and Rh C Glycoprotein (Rhcg) on renal response to metabolic acidosis. Am J Physiol Renal Physiol (2013) 1.50
Molecular mechanisms of renal ammonia transport. Annu Rev Physiol (2007) 1.43
Electroneutral ammonium transport by basolateral rhesus B glycoprotein. J Physiol (2004) 1.42
Regulated acid-base transport in the collecting duct. Pflugers Arch (2009) 1.42
Function of human Rh based on structure of RhCG at 2.1 A. Proc Natl Acad Sci U S A (2010) 1.41
Characterization of ammonia transport by the kidney Rh glycoproteins RhBG and RhCG. Am J Physiol Renal Physiol (2005) 1.39
Role of NH3 and NH4+ transporters in renal acid-base transport. Am J Physiol Renal Physiol (2010) 1.39
Different transport mechanisms in plant and human AMT/Rh-type ammonium transporters. J Gen Physiol (2006) 1.35
Collecting duct-specific Rh C glycoprotein deletion alters basal and acidosis-stimulated renal ammonia excretion. Am J Physiol Renal Physiol (2009) 1.27
Expression of the ammonia transporter, rh C glycoprotein, in normal and neoplastic human kidney. J Am Soc Nephrol (2006) 1.23
Human Rhesus B and Rhesus C glycoproteins: properties of facilitated ammonium transport in recombinant kidney cells. Biochem J (2005) 1.23
Evolutionary conservation and diversification of Rh family genes and proteins. Proc Natl Acad Sci U S A (2005) 1.20
Ammonium ion transport by the AMT/Rh homologue LeAMT1;1. Biochem J (2006) 1.20
Genome analysis and signature discovery for diving and sensory properties of the endangered Chinese alligator. Cell Res (2013) 1.18
Amt/MEP/Rh proteins conduct ammonia. Pflugers Arch (2005) 1.17
Substrate binding, deprotonation, and selectivity at the periplasmic entrance of the Escherichia coli ammonia channel AmtB. Proc Natl Acad Sci U S A (2008) 1.14
Renal ammonia metabolism and transport. Compr Physiol (2013) 1.11
Deprotonation by dehydration: the origin of ammonium sensing in the AmtB channel. PLoS Comput Biol (2006) 1.06
Expression of the gas-transporting proteins, Rh B glycoprotein and Rh C glycoprotein, in the murine lung. Am J Physiol Lung Cell Mol Physiol (2009) 1.02
Concentration-dependent effects on intracellular and surface pH of exposing Xenopus oocytes to solutions containing NH3/NH4(+). J Membr Biol (2009) 1.02
Structural involvement in substrate recognition of an essential aspartate residue conserved in Mep/Amt and Rh-type ammonium transporters. Curr Genet (2006) 1.01
Expression of the human erythroid Rh glycoprotein (RhAG) enhances both NH3 and NH4+ transport in HeLa cells. Pflugers Arch (2005) 0.99
Ammonium ion transport by the AMT/Rh homolog TaAMT1;1 is stimulated by acidic pH. Pflugers Arch (2009) 0.95
Expression of ammonia transporters, Rhbg and Rhcg, in chronic cyclosporine nephropathy in rats. Nephron Exp Nephrol (2008) 0.93
RhCG is the major putative ammonia transporter expressed in the human kidney, and RhBG is not expressed at detectable levels. Am J Physiol Renal Physiol (2009) 0.93
Functional reconstitution into liposomes of purified human RhCG ammonia channel. PLoS One (2010) 0.93
PvAMT1;1, a highly selective ammonium transporter that functions as H+/NH4(+) symporter. J Biol Chem (2011) 0.93
Overexpressing of OsAMT1-3, a High Affinity Ammonium Transporter Gene, Modifies Rice Growth and Carbon-Nitrogen Metabolic Status. Int J Mol Sci (2015) 0.93
Molecular physiology of the Rh ammonia transport proteins. Curr Opin Nephrol Hypertens (2010) 0.91
Ammonia transport in the kidney by Rhesus glycoproteins. Am J Physiol Renal Physiol (2014) 0.90
Substrate specificity of Rhbg: ammonium and methyl ammonium transport. Am J Physiol Cell Physiol (2010) 0.89
Phosphorylation and ankyrin-G binding of the C-terminal domain regulate targeting and function of the ammonium transporter RhBG. J Biol Chem (2008) 0.88
Expression of the non-erythroid Rh glycoproteins in mammalian tissues. Transfus Clin Biol (2006) 0.88
CeRh1 (rhr-1) is a dominant Rhesus gene essential for embryonic development and hypodermal function in Caenorhabditis elegans. Proc Natl Acad Sci U S A (2006) 0.88
Characteristics of mammalian Rh glycoproteins (SLC42 transporters) and their role in acid-base transport. Mol Aspects Med (2013) 0.85
Rhesus glycoprotein p2 (Rhp2) is a novel member of the Rh family of ammonia transporters highly expressed in shark kidney. J Biol Chem (2009) 0.82
Cystic fibrosis transmembrane conductance regulator in the gills of the climbing perch, Anabas testudineus, is involved in both hypoosmotic regulation during seawater acclimation and active ammonia excretion during ammonia exposure. J Comp Physiol B (2012) 0.82
Functional role of Asp160 and the deprotonation mechanism of ammonium in the Escherichia coli ammonia channel protein AmtB. J Phys Chem B (2009) 0.81
Physiological and molecular analysis of the interactive effects of feeding and high environmental ammonia on branchial ammonia excretion and Na+ uptake in freshwater rainbow trout. J Comp Physiol B (2010) 0.80
Mechanisms of ammonia and ammonium transport by rhesus-associated glycoproteins. Am J Physiol Cell Physiol (2015) 0.78
Ammonia Transporters and Their Role in Acid-Base Balance. Physiol Rev (2017) 0.77
NH4+ currents across the peribacteroid membrane of soybean. Macroscopic and microscopic properties, inhibition by Mg2+, and temperature dependence indicate a SubpicoSiemens channel finely regulated by divalent cations. Plant Physiol (2005) 0.77
Structural determinants of NH3 and NH4+ transport by mouse Rhbg, a renal Rh glycoprotein. Am J Physiol Renal Physiol (2016) 0.75
Nitrogen metabolism, acid-base regulation, and molecular responses to ammonia and acid infusions in the spiny dogfish shark (Squalus acanthias). J Comp Physiol B (2015) 0.75
Iron is a substrate of the Plasmodium falciparum chloroquine resistance transporter PfCRT in Xenopus oocytes. J Biol Chem (2017) 0.75
Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter. N Engl J Med (2002) 3.24
NHERF1 mutations and responsiveness of renal parathyroid hormone. N Engl J Med (2008) 2.70
DNA bar coding and pyrosequencing to analyze adverse events in therapeutic gene transfer. Nucleic Acids Res (2008) 2.64
In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: a pilot study. BMC Med (2007) 1.82
Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome. J Am Soc Nephrol (2002) 1.75
Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation. Pediatr Res (2002) 1.61
Association between Hsp90 and the ClC-2 chloride channel upregulates channel function. Am J Physiol Cell Physiol (2005) 1.56
Evaluation of MRP1-5 gene expression in cystic fibrosis patients homozygous for the delta F508 mutation. Pediatr Res (2003) 1.50
Distribution of ClC-2 chloride channel in rat and human epithelial tissues. Am J Physiol Cell Physiol (2002) 1.44
Analysis of human histone H2AZ deposition in vivo argues against its direct role in epigenetic templating mechanisms. Mol Cell Biol (2006) 1.27
Antibodies for CFTR studies. J Cyst Fibros (2004) 1.06
Discovery of novel potent ΔF508-CFTR correctors that target the nucleotide binding domain. EMBO Mol Med (2013) 1.04
Rescue of DeltaF508-CFTR (cystic fibrosis transmembrane conductance regulator) by curcumin: involvement of the keratin 18 network. J Pharmacol Exp Ther (2006) 1.04
Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotes. Am J Respir Crit Care Med (2005) 1.03
Neutrophil elastase degrades cystic fibrosis transmembrane conductance regulator via calpains and disables channel function in vitro and in vivo. Am J Respir Crit Care Med (2012) 1.03
Basic protocol for transepithelial nasal potential difference measurements. J Cyst Fibros (2004) 1.01
Structural involvement in substrate recognition of an essential aspartate residue conserved in Mep/Amt and Rh-type ammonium transporters. Curr Genet (2006) 1.01
Evidence for activation of endogenous transporters in Xenopus laevis oocytes expressing the Plasmodium falciparum chloroquine resistance transporter, PfCRT. J Biol Chem (2004) 1.00
Down-regulation of the anti-inflammatory protein annexin A1 in cystic fibrosis knock-out mice and patients. Mol Cell Proteomics (2005) 1.00
Cystic fibrosis enters the proteomics scene: new answers to old questions. Proteomics (2006) 1.00
LNK (SH2B3) is a key regulator of integrin signaling in endothelial cells and targets α-parvin to control cell adhesion and migration. FASEB J (2012) 1.00
Biochemical methods to assess CFTR expression and membrane localization. J Cyst Fibros (2004) 1.00
Cystic fibrosis transmembrane regulator inhibitors CFTR(inh)-172 and GlyH-101 target mitochondrial functions, independently of chloride channel inhibition. J Pharmacol Exp Ther (2010) 0.99
Expression of the human erythroid Rh glycoprotein (RhAG) enhances both NH3 and NH4+ transport in HeLa cells. Pflugers Arch (2005) 0.99
Peroxiredoxin 6 fails to limit phospholipid peroxidation in lung from Cftr-knockout mice subjected to oxidative challenge. PLoS One (2009) 0.97
Cell-specific posttranscriptional regulation of CFTR gene expression via influence of MAPK cascades on 3'UTR part of transcripts. Am J Physiol Cell Physiol (2005) 0.96
Blue native/SDS-PAGE analysis reveals reduced expression of the mClCA3 protein in cystic fibrosis knock-out mice. Mol Cell Proteomics (2005) 0.95
TGF-beta 1 downregulates CFTR expression and function in nasal polyps of non-CF patients. Am J Physiol Lung Cell Mol Physiol (2004) 0.94
Anti-Gb3 monoclonal antibody inhibits angiogenesis and tumor development. PLoS One (2012) 0.94
A neutral variant involved in a complex CFTR allele contributes to a severe cystic fibrosis phenotype. Hum Genet (2005) 0.93
Coronin-1 is associated with neutrophil survival and is cleaved during apoptosis: potential implication in neutrophils from cystic fibrosis patients. J Immunol (2009) 0.93
Lipid mapping of colonic mucosa by cluster TOF-SIMS imaging and multivariate analysis in cftr knockout mice. J Lipid Res (2010) 0.92
Global proteomic approach unmasks involvement of keratins 8 and 18 in the delivery of cystic fibrosis transmembrane conductance regulator (CFTR)/deltaF508-CFTR to the plasma membrane. Proteomics (2004) 0.90
A novel lipidomic strategy reveals plasma phospholipid signatures associated with respiratory disease severity in cystic fibrosis patients. PLoS One (2009) 0.90
Plasma lipidomics reveals potential prognostic signatures within a cohort of cystic fibrosis patients. J Lipid Res (2011) 0.90
Measurement of halide efflux from cultured and primary airway epithelial cells using fluorescence indicators. J Cyst Fibros (2004) 0.89
The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation. Hum Mol Genet (2011) 0.89
Membrane cholesterol content modulates ClC-2 gating and sensitivity to oxidative stress. J Biol Chem (2006) 0.89
Disruption of cytokeratin-8 interaction with F508del-CFTR corrects its functional defect. Hum Mol Genet (2011) 0.89
Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport. Am J Respir Crit Care Med (2010) 0.88
Control of basal CFTR gene expression by bicarbonate-sensitive adenylyl cyclase in human pulmonary cells. Cell Physiol Biochem (2008) 0.88
Distinct roles of Bcl-2 and Bcl-Xl in the apoptosis of human bone marrow mesenchymal stem cells during differentiation. PLoS One (2011) 0.88
Postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis. PLoS One (2012) 0.88
Effect of ouabain on CFTR gene expression in human Calu-3 cells. Am J Physiol Cell Physiol (2003) 0.87
Proximity ligation in situ assay for monitoring the global DNA methylation in cells. BMC Biotechnol (2011) 0.87
PfCHA is a mitochondrial divalent cation/H+ antiporter in Plasmodium falciparum. Mol Microbiol (2010) 0.87
Measurement of nasal potential difference in young children with an equivocal sweat test following newborn screening for cystic fibrosis. Thorax (2010) 0.86
Resveratrol rescues cAMP-dependent anionic transport in the cystic fibrosis pancreatic cell line CFPAC1. Br J Pharmacol (2011) 0.85
Immunohistochemistry of CFTR in native tissues and primary epithelial cell cultures. J Cyst Fibros (2004) 0.84
Intramyocardial delivery of mesenchymal stem cell-seeded hydrogel preserves cardiac function and attenuates ventricular remodeling after myocardial infarction. PLoS One (2012) 0.84
GSH monoethyl ester rescues mitochondrial defects in cystic fibrosis models. Hum Mol Genet (2011) 0.84
CFTR inhibition provokes an inflammatory response associated with an imbalance of the annexin A1 pathway. Am J Pathol (2010) 0.84
A new human NHERF1 mutation decreases renal phosphate transporter NPT2a expression by a PTH-independent mechanism. PLoS One (2012) 0.83
Eicosanoid release is increased by membrane destabilization and CFTR inhibition in Calu-3 cells. PLoS One (2009) 0.83
Inhibition of the calcium release-activated calcium (CRAC) current in Jurkat T cells by the HIV-1 envelope protein gp160. J Biol Chem (2001) 0.83
Contribution of proteomics to the study of the role of cytokeratins in disease and physiopathology. Proteomics Clin Appl (2008) 0.82
Restoration of human B-cell differentiation into NOD-SCID mice engrafted with gene-corrected CD34+ cells isolated from Artemis or RAG1-deficient patients. Mol Ther (2007) 0.82
High sensitivity identification of membrane proteins by MALDI TOF-MASS spectrometry using polystyrene beads. J Proteome Res (2007) 0.82
Lanthanum carbonate, like sevelamer-HCl, retards the progression of vascular calcification and atherosclerosis in uremic apolipoprotein E-deficient mice. Nephrol Dial Transplant (2011) 0.81
Regulation of interleukin-6 in head and neck squamous cell carcinoma is related to papillomavirus infection. J Proteome Res (2014) 0.81
Cytokines and culture medium have a major impact on human in vitro T-cell differentiation. Blood Cells Mol Dis (2011) 0.81
The Gef1 protein of Saccharomyces cerevisiae is associated with chloride channel activity. Biochem Biophys Res Commun (2002) 0.81
Effect of reactive oxygen species on NH4+ permeation in Xenopus laevis oocytes. Am J Physiol Cell Physiol (2002) 0.81
Visceral adipose tissue and leptin increase colonic epithelial tight junction permeability via a RhoA-ROCK-dependent pathway. FASEB J (2013) 0.81
A new workflow for proteomic analysis of urinary exosomes and assessment in cystinuria patients. J Proteome Res (2014) 0.81
Structural models of CFTR-AMPK and CFTR-PKA interactions: R-domain flexibility is a key factor in CFTR regulation. J Mol Model (2011) 0.79
Long-term CFTR inhibition modulates 15d-prostaglandin J2 in human pulmonary cells. Int J Biochem Cell Biol (2012) 0.79
New lipidomic approaches in cystic fibrosis. Methods Mol Biol (2011) 0.79
The functioning of mammalian ClC-2 chloride channel in Saccharomyces cerevisiae cells requires an increased level of Kha1p. Biochem J (2005) 0.79
Characterization of SLC26A9 in patients with CF-like lung disease. Hum Mutat (2013) 0.78
Quantitative differential proteomics of cystic fibrosis cell models by SILAC (stable isotope labelling in cell culture). Methods Mol Biol (2011) 0.77
Characterization of nasal potential difference in cftr knockout and F508del-CFTR mice. PLoS One (2013) 0.77
The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening. BMC Pediatr (2006) 0.77
Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype. Hum Mutat (2005) 0.77
Farnesyltransferase inhibitor R115777 protects against vascular disease in uremic mice. Atherosclerosis (2013) 0.76