Olivier Devuyst
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Biology
Olivier Devuyst's Degrees
- PhD Biomedical Sciences University of Geneva
- Masters Biochemistry University of Zurich
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(Suggest an Edit or Addition)Olivier Devuyst's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Tolvaptan in patients with autosomal dominant polycystic kidney disease. (2012) (1190)
- Evolving importance of kidney disease: from subspecialty to global health burden (2013) (909)
- Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 (2021) (811)
- Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (2012) (678)
- Autosomal-dominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. (2015) (409)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- Tolvaptan in Later‐Stage Autosomal Dominant Polycystic Kidney Disease (2017) (339)
- Factors influencing success of clinical genome sequencing across a broad spectrum of disorders (2015) (319)
- Loss of chloride channel ClC-5 impairs endocytosis by defective trafficking of megalin and cubilin in kidney proximal tubules (2003) (306)
- NHE2 and NHE3 are human and rabbit intestinal brush-border proteins. (1996) (304)
- The Current State of Peritoneal Dialysis. (2016) (299)
- Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression (2013) (298)
- Mice lacking renal chloride channel, CLC-5, are a model for Dent's disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosis. (2000) (293)
- Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease. (1999) (271)
- Genetic loci influencing kidney function and chronic kidney disease (2010) (266)
- Cubilin is essential for albumin reabsorption in the renal proximal tubule. (2010) (255)
- Mutations in SEC63 cause autosomal dominant polycystic liver disease (2004) (254)
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (252)
- Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management--A KDIGO consensus report. (2015) (234)
- The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease. (2011) (232)
- Autosomal dominant polycystic kidney disease: the changing face of clinical management (2015) (231)
- The pathophysiology of the peritoneal membrane. (2010) (223)
- CUBN is a gene locus for albuminuria. (2011) (214)
- Vascular proliferation and enhanced expression of endothelial nitric oxide synthase in human peritoneum exposed to long-term peritoneal dialysis. (2000) (207)
- Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney Disorders and European Renal Best Practice (2016) (204)
- A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin. (2003) (199)
- Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. (2017) (198)
- Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels (2019) (183)
- Uromodulin: from physiology to rare and complex kidney disorders (2017) (180)
- CNNM2, encoding a basolateral protein required for renal Mg2+ handling, is mutated in dominant hypomagnesemia. (2011) (178)
- Spectrum of mutations in Gitelman syndrome. (2011) (176)
- Regulated acid–base transport in the collecting duct (2009) (173)
- Modifier effect of ENOS in autosomal dominant polycystic kidney disease. (2002) (173)
- Rare inherited kidney diseases: challenges, opportunities, and perspectives (2014) (168)
- A role for Rhesus factor Rhcg in renal ammonium excretion and male fertility (2008) (167)
- SARS-CoV-2 causes a specific dysfunction of the kidney proximal tubule (2020) (162)
- Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood. (2011) (155)
- Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome. (2007) (150)
- Aquaporin-1 plays an essential role in water permeability and ultrafiltration during peritoneal dialysis. (2006) (150)
- A role for CFTR in human autosomal dominant polycystic kidney disease. (1996) (148)
- A New Antigen Recognized by Cytolytic T Lymphocytes on a Human Kidney Tumor Results from Reverse Strand Transcription (1999) (148)
- Dent's disease (2010) (138)
- Both the wild type and a functional isoform of CFTR are expressed in kidney. (1996) (137)
- Rationale and design of the TEMPO (Tolvaptan Efficacy and Safety in Management of Autosomal Dominant Polycystic Kidney Disease and its Outcomes) 3-4 Study. (2011) (134)
- Expression of aquaporins-1 and -2 during nephrogenesis and in autosomal dominant polycystic kidney disease. (1996) (132)
- Autophagosome-lysosome fusion triggers a lysosomal response mediated by TLR9 and controlled by OCRL (2016) (122)
- Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes (2015) (121)
- Effect of Tolvaptan in Autosomal Dominant Polycystic Kidney Disease by CKD Stage: Results from the TEMPO 3:4 Trial. (2016) (119)
- Genetic and clinical factors influence the baseline permeability of the peritoneal membrane. (2005) (118)
- Chronic uremia induces permeability changes, increased nitric oxide synthase expression, and structural modifications in the peritoneum. (2001) (115)
- Expression of PKD1 and PKD2 transcripts and proteins in human embryo and during normal kidney development. (2002) (113)
- A primary culture of mouse proximal tubular cells, established on collagen-coated membranes. (2007) (112)
- Regulation of aquaporin-1 and nitric oxide synthase isoforms in a rat model of acute peritonitis. (1999) (109)
- High citrate diet delays progression of renal insufficiency in the ClC-5 knockout mouse model of Dent's disease. (2005) (106)
- Multicenter, open-label, extension trial to evaluate the long-term efficacy and safety of early versus delayed treatment with tolvaptan in autosomal dominant polycystic kidney disease: the TEMPO 4:4 Trial (2017) (106)
- Molecular Physiology of Water Balance. (2015) (103)
- Impaired autophagy bridges lysosomal storage disease and epithelial dysfunction in the kidney (2018) (103)
- The Hypertension Pandemic: An Evolutionary Perspective. (2017) (101)
- Aortic Stiffness and Central Wave Reflections Predict Outcome in Renal Transplant Recipients (2011) (101)
- Phenotype and outcome in hereditary tubulointerstitial nephritis secondary to UMOD mutations. (2011) (101)
- Endocytosis provides a major alternative pathway for lysosomal biogenesis in kidney proximal tubular cells (2007) (98)
- Tamm-Horsfall protein or uromodulin: new ideas about an old molecule. (2005) (98)
- Cofilin Interacts with ClC-5 and Regulates Albumin Uptake in Proximal Tubule Cell Lines* (2003) (98)
- Aristolochic acid impedes endocytosis and induces DNA adducts in proximal tubule cells. (2001) (98)
- A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesis (2011) (96)
- Progression of coronary artery calcification and thoracic aorta calcification in kidney transplant recipients. (2012) (95)
- ZONAB promotes proliferation and represses differentiation of proximal tubule epithelial cells. (2010) (94)
- Fluid transport and cystogenesis in autosomal dominant polycystic kidney disease. (2011) (93)
- Comparison between siblings and twins supports a role for modifier genes in ADPKD. (2004) (93)
- Cystic fibrosis is associated with a defect in apical receptor-mediated endocytosis in mouse and human kidney. (2007) (91)
- Toward better dialysis compatibility: advances in the biochemistry and pathophysiology of the peritoneal membranes. (2002) (89)
- Genetics of hypercalciuric stone forming diseases. (2007) (89)
- Corticosteroids induce expression of aquaporin-1 and increase transcellular water transport in rat peritoneum. (2003) (88)
- A transgenic mouse model for uromodulin-associated kidney diseases shows specific tubulo-interstitial damage, urinary concentrating defect and renal failure. (2010) (88)
- Aquaporin-1 and endothelial nitric oxide synthase expression in capillary endothelia of human peritoneum. (1998) (87)
- Apical plasma membrane mispolarization of NaK-ATPase in polycystic kidney disease epithelia is associated with aberrant expression of the beta2 isoform. (2000) (87)
- Positron-emission computed tomography in cyst infection diagnosis in patients with autosomal dominant polycystic kidney disease. (2011) (86)
- Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria (2019) (86)
- Morphological and functional changes in the dialysed peritoneal cavity: impact of more biocompatible solutions. (2002) (85)
- Altered polarity and expression of H+-ATPase without ultrastructural changes in kidneys of Dent's disease patients. (2003) (85)
- Renal phenotype of the cystinosis mouse model is dependent upon genetic background. (2010) (85)
- The loss of the chloride channel, ClC-5, delays apical iodide efflux and induces a euthyroid goiter in the mouse thyroid gland. (2006) (83)
- Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis. (2014) (83)
- The 5-phosphatase OCRL in Lowe syndrome and Dent disease 2 (2017) (82)
- Gitelman’s syndrome: towards genotype-phenotype correlations? (2007) (82)
- Haematological changes and infectious complications in anorexia nervosa: a case-control study. (1993) (81)
- The serine protease hepsin mediates urinary secretion and polymerisation of Zona Pellucida domain protein uromodulin (2015) (79)
- The triggering of human peritoneal mesothelial cell apoptosis and oncosis by glucose and glycoxydation products. (2004) (78)
- Diagnosis of cyst infection in patients with autosomal dominant polycystic kidney disease: attributes and limitations of the current modalities. (2012) (77)
- Expression of aquaporin-1 in a long-term peritoneal dialysis patient with impaired transcellular water transport. (1999) (76)
- Uromodulin is expressed in the distal convoluted tubule, where it is critical for regulation of the sodium chloride cotransporter NCC. (2018) (76)
- Autosomal dominant tubulointerstitial kidney disease (2019) (75)
- Renal expression of parvalbumin is critical for NaCl handling and response to diuretics (2007) (75)
- The ClC‐5 Knockout Mouse Model of Dent's Disease Has Renal Hypercalciuria and Increased Bone Turnover (2003) (74)
- Developmental regulation of CFTR expression during human nephrogenesis. (1996) (74)
- Deterioration in renal function associated with fibrate therapy. (2001) (74)
- Determination of uromodulin in human urine: influence of storage and processing. (2014) (74)
- Interstitial Fibrosis Restricts Osmotic Water Transport in Encapsulating Peritoneal Sclerosis. (2015) (72)
- Water transport across the peritoneal membrane. (2014) (72)
- Associations of Urinary Uromodulin with Clinical Characteristics and Markers of Tubular Function in the General Population. (2016) (72)
- Soluble klotho and autosomal dominant polycystic kidney disease. (2012) (70)
- PKD1 haploinsufficiency causes a syndrome of inappropriate antidiuresis in mice. (2007) (68)
- Vacuolar H+-ATPase d2 subunit: molecular characterization, developmental regulation, and localization to specialized proton pumps in kidney and bone. (2005) (67)
- Multicenter, open-label, extension trial to evaluate the long-term efficacy and safety of early versus delayed treatment with tolvaptan in autosomal dominant polycystic kidney disease: the TEMPO 4:4 Trial. (2017) (67)
- Increased protein glycation in fructosamine 3-kinase-deficient mice. (2006) (67)
- Chloride channels in the kidney: lessons learned from knockout animals. (2002) (67)
- Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies. (2018) (64)
- Dedifferentiation and aberrations of the endolysosomal compartment characterize the early stage of nephropathic cystinosis. (2014) (64)
- Somatic uniparental isodisomy explains multifocality of glomuvenous malformations. (2013) (63)
- Diabetes-induced microvascular dysfunction in the hydronephrotic kidney: role of nitric oxide. (2001) (63)
- Urine Osmolality, Response to Tolvaptan, and Outcome in Autosomal Dominant Polycystic Kidney Disease: Results from the TEMPO 3:4 Trial. (2017) (62)
- Serum fetuin-A levels are associated with vascular calcifications and predict cardiovascular events in renal transplant recipients. (2011) (60)
- CLC-5 and KIF3B interact to facilitate CLC-5 plasma membrane expression, endocytosis, and microtubular transport: relevance to pathophysiology of Dent's disease (2009) (59)
- Mice that lack endothelial nitric oxide synthase are protected against functional and structural modifications induced by acute peritonitis. (2003) (59)
- Genetic variation of DKK3 may modify renal disease severity in ADPKD. (2010) (58)
- Observations of a large Dent disease cohort. (2016) (58)
- Anorexia nervosa: correlation between MR appearance of bone marrow and severity of disease. (1994) (58)
- Role of the monoclonal kappa chain V domain and reversibility of renal damage in a transgenic model of acquired Fanconi syndrome. (2006) (58)
- Renal transplantation in autosomal dominant polycystic kidney disease (2014) (57)
- Osmoregulation, vasopressin, and cAMP signaling in autosomal dominant polycystic kidney disease (2013) (57)
- Endocytosis of the somatostatin analogue, octreotide, by the proximal tubule-derived opossum kidney (OK) cell line. (2005) (56)
- Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1 (2015) (56)
- Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome (2017) (56)
- Architecture and function of human uromodulin filaments in urinary tract infections (2020) (56)
- Transgenic Mouse Models (2007) (54)
- Copeptin is associated with kidney length, renal function, and prevalence of simple cysts in a population-based study. (2015) (54)
- Metabolic effects of amino acid solutions infused for renal protection during therapy with radiolabelled somatostatin analogues. (2004) (53)
- Fibroblast growth factor 23 and markers of mineral metabolism in individuals with preserved renal function. (2016) (53)
- Biochemical characterization of bona fide polycystin-1 in vitro and in vivo. (2001) (53)
- Toward understanding renal Fanconi syndrome: step by step advances through experimental models. (2011) (52)
- Prevalence of Hypertension in Children with Early-Stage ADPKD. (2018) (52)
- The relation between hypomagnesaemia and vascular stiffness in renal transplant recipients. (2011) (52)
- Autosomal dominant polycystic kidney disease is associated with central and nephrogenic defects in osmoregulation. (2012) (52)
- AqF026 is a pharmacologic agonist of the water channel aquaporin-1. (2013) (51)
- Role of RhAG and AQP1 in NH3 and CO2 gas transport in red cell ghosts: a stopped-flow analysis. (2006) (51)
- Expression of CFTR in human and bovine thyroid epithelium. (1997) (50)
- The UMOD Locus: Insights into the Pathogenesis and Prognosis of Kidney Disease. (2017) (50)
- Inhibition of nitric oxide synthase reverses changes in peritoneal permeability in a rat model of acute peritonitis. (2001) (49)
- Coronary artery calcification: a strong predictor of cardiovascular events in renal transplant recipients. (2010) (49)
- Association of PKD2 (polycystin 2) mutations with left-right laterality defects. (2011) (49)
- Carbohydrate antigen 19-9 as a diagnostic marker for hepatic cyst infection in autosomal dominant polycystic kidney disease. (2010) (48)
- Critical Role of Aquaporins in Interleukin 1β (IL-1β)-induced Inflammation* (2014) (47)
- Ubiquitous and kidney-specific subunits of vacuolar H+-ATPase are differentially expressed during nephrogenesis. (2005) (47)
- Combined Structural and Functional Imaging of the Kidney Reveals Major Axial Differences in Proximal Tubule Endocytosis. (2018) (46)
- Albuminuria and tolvaptan in autosomal-dominant polycystic kidney disease: results of the TEMPO 3:4 Trial. (2016) (46)
- Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency (2020) (46)
- Clinical and Genetic Spectra of Autosomal Dominant Tubulointerstitial Kidney Disease due to Mutations in UMOD and MUC1. (2020) (45)
- CF gene and cystic fibrosis transmembrane conductance regulator expression in autosomal dominant polycystic kidney disease. (2000) (45)
- SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. (2017) (44)
- A novel renal carbonic anhydrase type III plays a role in proximal tubule dysfunction. (2008) (44)
- Modified aquaporin 5 expression and distribution in submandibular glands from NOD mice displaying autoimmune exocrinopathy. (2007) (42)
- Expression of the beta2-subunit and apical localization of Na+-K+-ATPase in metanephric kidney. (1999) (42)
- Experimental diabetes induces functional and structural changes in the peritoneum. (2002) (42)
- Impaired Lysosomal Function Underlies Monoclonal Light Chain-Associated Renal Fanconi Syndrome. (2016) (41)
- Learning Physiology From Inherited Kidney Disorders. (2019) (41)
- Plasma copeptin levels predict disease progression and tolvaptan efficacy in autosomal dominant polycystic kidney disease. (2019) (39)
- Early experience with COVID-19 in kidney transplantation (2020) (39)
- Tolvaptan and Kidney Pain in Patients With Autosomal Dominant Polycystic Kidney Disease: Secondary Analysis From a Randomized Controlled Trial (2016) (39)
- Gating defects of a novel Na+ channel mutant causing hypokalemic periodic paralysis. (2006) (39)
- A New Role for Aquaporin 7 in Insulin Secretion (2012) (38)
- Chloride Channels and Endocytosis: New Insights from Dent’s Disease and ClC-5 Knockout Mice (2005) (38)
- Implication of fibrate therapy for homocysteine (1999) (38)
- A coherent organization of differentiation proteins is required to maintain an appropriate thyroid function in the Pendred thyroid. (2010) (37)
- Creatinine rise after fibrate therapy in renal graft recipients (1993) (37)
- The rhesus protein RhCG: a new perspective in ammonium transport and distal urinary acidification. (2011) (37)
- Epigenetic control of aquaporin 1 expression by the amyloid precursor protein (2009) (37)
- Functional and molecular characterization of a peritoneal dialysis model in the C57BL/6J mouse. (2005) (37)
- Basolateral chloride transporters in autosomal dominant polycystic kidney disease (2002) (36)
- Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia. (2015) (36)
- Uromodulin: Roles in Health and Disease. (2021) (36)
- Role of caveolin-1 in thyroid phenotype, cell homeostasis, and hormone synthesis: in vivo study of caveolin-1 knockout mice. (2009) (36)
- Prevalence and Determinants of Coronary and Aortic Calcifications Assessed by Chest CT in Renal Transplant Recipients (2007) (36)
- Uromodulin and Nephron Mass. (2018) (36)
- Prognostic Enrichment Design in Clinical Trials for Autosomal Dominant Polycystic Kidney Disease: The TEMPO 3:4 Clinical Trial (2016) (36)
- Tubular Disorders of Electrolyte Regulation (2009) (36)
- L-carnitine is an osmotic agent suitable for peritoneal dialysis. (2011) (35)
- Acetazolamide Attenuates Lithium-Induced Nephrogenic Diabetes Insipidus. (2016) (35)
- Tolerability of Aquaretic-Related Symptoms Following Tolvaptan for Autosomal Dominant Polycystic Kidney Disease: Results From TEMPO 3:4 (2017) (35)
- Suppression of microRNA Activity in Kidney Collecting Ducts Induces Partial Loss of Epithelial Phenotype and Renal Fibrosis. (2017) (35)
- OCRL deficiency impairs endolysosomal function in a humanized mouse model for Lowe syndrome and Dent disease (2018) (35)
- Chloride transporters and receptor‐mediated endocytosis in the renal proximal tubule (2015) (34)
- PKD1 haploinsufficiency is associated with altered vascular reactivity and abnormal calcium signaling in the mouse aorta (2009) (34)
- Mechanisms of Crystalloid versus Colloid Osmosis across the Peritoneal Membrane. (2018) (34)
- Apolipoprotein M modulates erythrocyte efflux and tubular reabsorption of sphingosine-1-phosphate (2014) (33)
- A specific method for measurement of nitric oxide synthase enzymatic activity in peritoneal biopsies. (2000) (33)
- Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. (2017) (33)
- Central and extrapontine myelinolysis in a patient in spite of a careful correction of hyponatremia. (2001) (33)
- The Uromodulin Gene Locus Shows Evidence of Pathogen Adaptation through Human Evolution. (2016) (33)
- CFTR and defective endocytosis: new insights in the renal phenotype of cystic fibrosis (2009) (33)
- Long wavelength multiphoton excitation is advantageous for intravital kidney imaging. (2016) (33)
- A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress (2017) (33)
- Study of candidate genes affecting the progression of renal disease in autosomal dominant polycystic kidney disease type 1. (2007) (33)
- New insights in the molecular mechanisms regulating peritoneal permeability. (2002) (33)
- Nitric oxide synthase isoforms play distinct roles during acute peritonitis (2009) (32)
- Hydrochlorothiazide attenuates lithium-induced nephrogenic diabetes insipidus independently of the sodium-chloride cotransporter. (2014) (32)
- Single photon emission-computed tomography (SPECT) for functional investigation of the proximal tubule in conscious mice. (2010) (32)
- Renal handling of zinc in chronic kidney disease patients and the role of circulating zinc levels in renal function decline. (2020) (32)
- Genetic deletion of aquaporin-1 results in microcardia and low blood pressure in mouse with intact nitric oxide-dependent relaxation, but enhanced prostanoids-dependent relaxation (2014) (32)
- Parvalbumin: calcium and magnesium buffering in the distal nephron. (2012) (32)
- Haploinsufficiency of the Ammonia Transporter Rhcg Predisposes to Chronic Acidosis (2012) (31)
- Can we further enrich autosomal dominant polycystic kidney disease clinical trials for rapidly progressive patients? Application of the PROPKD score in the TEMPO trial (2017) (31)
- Proteomic and transcriptomic profiling reveal different aspects of aging in the kidney (2020) (31)
- Clinical, Genetic, and Urinary Factors Associated with Uromodulin Excretion. (2016) (31)
- Hepsin-mediated Processing of Uromodulin is Crucial for Salt-sensitivity and Thick Ascending Limb Homeostasis (2019) (30)
- Glomerular and proximal tubule cysts as early manifestations of Pkd1 deletion. (2010) (30)
- Autosomal dominant polycystic kidney disease: modifier genes and endothelial dysfunction. (2003) (29)
- Impaired osmoregulation in anorexia nervosa: a case-control study. (2004) (29)
- Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5. (2004) (29)
- Aquaporin-1 and endothelial nitric oxide synthase expression in capillary endothelia of human peritoneum. (1998) (28)
- High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults. (2019) (28)
- Targeting of sodium-glucose cotransporters with phlorizin inhibits polycystic kidney disease progression in Han:SPRD rats. (2013) (28)
- Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes. (2017) (28)
- Erratum: A role for CFTR in human autosomal dominant polycystic kidney disease (American Journal of Physiology - Cell Physiology (January 1996) 270:39 (C389-C399)) (1996) (27)
- Novel Mouse Models of Methylmalonic Aciduria Recapitulate Phenotypic Traits with a Genetic Dosage Effect* (2016) (27)
- AQUAPORIN-1: NEW DEVELOPMENTS AND PERSPECTIVES FOR PERITONEAL DIALYSIS (2010) (27)
- European ADPKD Forum multidisciplinary position statement on autosomal dominant polycystic kidney disease care (2017) (27)
- Renal cyst infection in autosomal dominant polycystic kidney disease. (2007) (26)
- A primary culture system of mouse thick ascending limb cells with preserved function and uromodulin processing (2014) (25)
- Nitric oxide is involved in interleukin-1alpha-induced cytotoxicity in polarised human thyrocytes. (2002) (25)
- [Systematically Initiating Insulin: The Staged Diabetes Management Approach] (2006) (25)
- Regulation of Macrophage Motility by the Water Channel Aquaporin-1: Crucial Role of M0/M2 Phenotype Switch (2015) (25)
- Tubular proteinuria in patients with HNF1α mutations: HNF1α drives endocytosis in the proximal tubule. (2016) (25)
- Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine (2016) (25)
- Salt wasting and blood pressure (2008) (24)
- A homozygous mutation in INVS causing juvenile nephronophthisis with abnormal reactivity of the Wnt/beta-catenin pathway. (2010) (24)
- The soluble intracellular domain of megalin does not affect renal proximal tubular function in vivo. (2010) (23)
- Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21 (2010) (23)
- Inhibition of aquaporin-1 prevents myocardial remodeling by blocking the transmembrane transport of hydrogen peroxide (2020) (23)
- A protein kinase A-independent pathway controlling aquaporin 2 trafficking as a possible cause for the syndrome of inappropriate antidiuresis associated with polycystic kidney disease 1 haploinsufficiency. (2014) (23)
- Expression patterns of the aquaporin gene family during renal development: influence of genetic variability (2009) (22)
- Aquaporin‐1 in the peritoneal membrane: implications for peritoneal dialysis and endothelial cell function (2005) (22)
- Bone marrow transplantation improves proximal tubule dysfunction in a mouse model of Dent disease. (2017) (22)
- Multicenter Study of Long-Term Safety of Tolvaptan in Later-Stage Autosomal Dominant Polycystic Kidney Disease. (2020) (22)
- Tolvaptan suppresses monocyte chemotactic protein-1 excretion in autosomal-dominant polycystic kidney disease (2016) (22)
- Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness (2021) (21)
- Resistance to Insulin in Patients with Gitelman Syndrome and a Subtle Intermediate Phenotype in Heterozygous Carriers: A Cross-Sectional Study. (2019) (21)
- The NLRP3 Inflammasome Has a Critical Role in Peritoneal Dialysis-Related Peritonitis. (2017) (21)
- Estimated 24-h urinary sodium and sodium-to-potassium ratio are predictors of kidney function decline in a population-based study. (2019) (21)
- Which type of dialysis in patients with cholesterol crystal embolism? (2002) (21)
- Water and solute transport in peritoneal dialysis: models and clinical applications. (2008) (21)
- An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis. (2021) (20)
- Localization of a Band 3‐related protein in the mitochondria‐rich cells of amphibian skin epithelium (1993) (20)
- Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome. (2008) (20)
- Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. (2022) (20)
- Digital Image Analysis of Picrosirius Red Staining: A Robust Method for Multi-Organ Fibrosis Quantification and Characterization (2020) (20)
- Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations (2020) (20)
- Inhibition of Nitric Oxide Synthase Reverses Permeability Changes in a Mouse Model of Acute Peritonitis (2005) (19)
- New autosomal recessive mutations in aquaporin‐2 causing nephrogenic diabetes insipidus through deficient targeting display normal expression in Xenopus oocytes (2010) (19)
- Decreased renal accumulation of aminoglycoside reflects defective receptor-mediated endocytosis in cystic fibrosis and Dent’s disease (2011) (19)
- Paradoxical response to furosemide in uromodulin-associated kidney disease. (2015) (19)
- A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension. (2006) (19)
- Gitelman syndrome and glomerular proteinuria: a link between loss of sodium-chloride cotransporter and podocyte dysfunction? (2014) (19)
- A population-based approach to assess the heritability and distribution of renal handling of electrolytes. (2017) (19)
- AQP1 Promoter Variant, Water Transport, and Outcomes in Peritoneal Dialysis. (2021) (19)
- Renal involvement in a patient with cobalamin A type (cblA) methylmalonic aciduria: a 42-year follow-up. (2013) (19)
- Influence of the endothelial nitric oxide synthase gene on conventional and ambulatory blood pressure: sib-pair analysis and haplotype study (2005) (18)
- The anti-oxidative role of cytoglobin in podocytes: implications for a role in chronic kidney disease. (2020) (18)
- The -174G/C variant of IL6 as risk factor for mortality and technique failure in a large cohort of peritoneal dialysis patients. (2012) (18)
- Clinical application of aquaporin research: aquaporin-1 in the peritoneal membrane (2008) (18)
- Autoantibodies against intercalated cells in Sjögren's syndrome. (2009) (18)
- Effect of N-acetyl-cysteine and hyperoxia on erythropoietin production (2011) (18)
- NRF2 regulates the glutamine transporter Slc38a3 (SNAT3) in kidney in response to metabolic acidosis (2018) (18)
- Influence of ACE (I/D) and G460W polymorphism of alpha-adducin in autosomal dominant polycystic kidney disease. (2003) (18)
- TRPV4 is associated with central rather than nephrogenic osmoregulation (2016) (18)
- The vasopressin system: new insights for patients with kidney diseases (2017) (18)
- NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality. (2017) (18)
- Clinical utility gene card for (2011) (18)
- Intrafamilial phenotype variability in nephrogenic diabetes insipidus. (2002) (18)
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- Endocytosis of radiolabelled somatostatin analogues by the OK cell line, as an in vitro model to assess their mechanism of kidney uptake (2004) (0)
- Comparative ontogeny of the chloride channel CIC-5 and the vacuolar H+-ATPase during nephrogenesis (2003) (0)
- Intravital multiphoton microscopy reveals several levels of heterogeneity in endocytic uptake by mouse renal proximal tubules " (2019) (0)
- Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine (2016) (0)
- MP120THE URINARY UROMODULLIN CREATININE RATIO IS DECREASED 6 WEEKS POST-PARTUM IN WOMEN WITH PREECLAMPSIA (2017) (0)
- WCN23-0391 THE CLINICAL CHARACTERISTICS AND KIDNEY OUTCOME IN CHINESE PATIENTS WITH TYPICAL AND ATYPICAL POLYCYSTIC KIDNEY DISEASE (2023) (0)
- Purinergic Signaling Regulates the Expression of the Sodium-chloride Cotransporter Ncc in the Distal Convoluted Tubule (2010) (0)
- Mutations in the UMOD gene lead to abnormal expression of uromodulin in familial juvenile hyperuricemic nephropathy. (2003) (0)
- PD Research Round-up: Sodium Sensing: Link to (Auto)immunity (2013) (0)
- The Aminoglycoside Clearance Is Increased in Cystic Fibrosis and Dent's Disease Models of Proximal Tubule Dysfunction (2010) (0)
- CIC-5 is an essential component of the endoytic machinery in proximal tubule cells (2002) (0)
- Acetazolamide: an improved treatment for lithium‐induced NDI? (LB726) (2014) (0)
- Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels (2019) (0)
- Towards the subcellular location of human ClC-6: development of anti-ClC-6 antibody (2005) (0)
- ClC5 knock-out induces multiple alterations in the endocytic apparatus of proximal tubular cells. (2002) (0)
- Author Correction: Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency (2020) (0)
- A mouse model of peritoneal dialysis reveals a predominant role of neuronal nitric oxide synthase in lipopolysaccharide-induced acute peritonitis. (2003) (0)
- COPEPTIN IN CKD (2014) (0)
- The adult with renal cysts (2015) (0)
- Allelic and Gene Dosage Effects Involving Uromodulin Aggregates Drive Autosomal Dominant Tubulointerstitial Kidney Disease (2022) (0)
- University of Groningen Tolvaptan and Kidney Pain in Patients With Autosomal Dominant Polycystic Kidney Disease (2018) (0)
- MP359FGF23 AND MARKERS OF MINERAL METABOLISM IN SUBJECTS WITH PRESERVED RENAL FUNCTION (2016) (0)
- Coronary calcifications predict cardiovascular events in renal transplant recipients (2008) (0)
- The determinants of the evolution of coronary and aortic calcifications in renal transplant recipients (2010) (0)
- CKD PATHOPHYSIOLOGY AND CLINICAL STUDIES (2014) (0)
- Cystic fibrosis is associated with a defect in low molecular weight protein handling in the kidney. (2005) (0)
- Impaired autophagy bridges lysosomal storage disease and epithelial dysfunction in the kidney (2018) (0)
- PIEZO2, a mechanosensor in the urinary bladder. (2021) (0)
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What Schools Are Affiliated With Olivier Devuyst?
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