Olivier Devuyst


Ontology type: schema:Person     


Person Info

NAME

Olivier

SURNAME

Devuyst

Publications in SciGraph latest 50 shown

  • 2018-12 NRF2 regulates the glutamine transporter Slc38a3 (SNAT3) in kidney in response to metabolic acidosis in SCIENTIFIC REPORTS
  • 2018-12 Impaired autophagy bridges lysosomal storage disease and epithelial dysfunction in the kidney in NATURE COMMUNICATIONS
  • 2018-07 Copeptin and insulin resistance: effect modification by age and 11 β-HSD2 activity in a population-based study in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2018-02 Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome in GENETICS IN MEDICINE
  • 2018-01-08 Genetics of kidney diseases in 2017: Unveiling the genetic architecture of kidney disease in NATURE REVIEWS NEPHROLOGY
  • 2017-08-07 Uromodulin: from physiology to rare and complex kidney disorders in NATURE REVIEWS NEPHROLOGY
  • 2017-07-03 The 5-phosphatase OCRL in Lowe syndrome and Dent disease 2 in NATURE REVIEWS NEPHROLOGY
  • 2017-01 Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2016-09 TRPV4 is associated with central rather than nephrogenic osmoregulation in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2016-08 Autophagosome-lysosome fusion triggers a lysosomal response mediated by TLR9 and controlled by OCRL in NATURE CELL BIOLOGY
  • 2016-04 Human proximal tubule cells form functional microtissues in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2016-03 Long wavelength multiphoton excitation is advantageous for intravital kidney imaging in KIDNEY INTERNATIONAL
  • 2016 Renal Tubular Disorders of Electrolyte Regulation in Children in PEDIATRIC NEPHROLOGY
  • 2015-11 Uromodulin, kidney function, cardiovascular disease, and mortality in KIDNEY INTERNATIONAL
  • 2015-10 Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management—A KDIGO consensus report in KIDNEY INTERNATIONAL
  • 2015-08 The SAM domain of ANKS6 has different interacting partners and mutations can induce different cystic phenotypes in KIDNEY INTERNATIONAL
  • 2015-07 Factors influencing success of clinical genome sequencing across a broad spectrum of disorders in NATURE GENETICS
  • 2015-07 Autosomal-dominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference in KIDNEY INTERNATIONAL
  • 2015 Renal Tubular Disorders of Electrolyte Regulation in Children in PEDIATRIC NEPHROLOGY
  • 2014-11 P2Y2 receptor activation inhibits the expression of the sodium-chloride cotransporter NCC in distal convoluted tubule cells in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2014-08 Renal transplantation in autosomal dominant polycystic kidney disease in NATURE REVIEWS NEPHROLOGY
  • 2014-04 Water transport across the peritoneal membrane in KIDNEY INTERNATIONAL
  • 2014-02 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 in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2014-02 A primary culture system of mouse thick ascending limb cells with preserved function and uromodulin processing in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2013-12 Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression in NATURE MEDICINE
  • 2013-11 Targeting of sodium–glucose cotransporters with phlorizin inhibits polycystic kidney disease progression in Han:SPRD rats in KIDNEY INTERNATIONAL
  • 2013-08 The effect of common uromodulin variants on urinary protein level and gene transcription in KIDNEY INTERNATIONAL
  • 2013-02 Genome-wide association analyses identify 18 new loci associated with serum urate concentrations in NATURE GENETICS
  • 2012-11 Autosomal dominant polycystic kidney disease is associated with central and nephrogenic defects in osmoregulation in KIDNEY INTERNATIONAL
  • 2011-12 The inositol Inpp5k 5-phosphatase affects osmoregulation through the vasopressin-aquaporin 2 pathway in the collecting system in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2011-12 Decreased renal accumulation of aminoglycoside reflects defective receptor-mediated endocytosis in cystic fibrosis and Dent’s disease in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2011-11 Effect of N-acetyl-cysteine and hyperoxia on erythropoietin production in EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY
  • 2011-10 Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood in KIDNEY INTERNATIONAL
  • 2011-09 L-Carnitine is an osmotic agent suitable for peritoneal dialysis in KIDNEY INTERNATIONAL
  • 2011-08 Clinical utility gene card for: Gitelman syndrome in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-08 The rediscovery of uromodulin (Tamm–Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease in KIDNEY INTERNATIONAL
  • 2011-04-20 Segmental and Subcellular Distribution of CFTR in the Kidney in CYSTIC FIBROSIS
  • 2011-01 Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21 in HUMAN GENETICS
  • 2011-01 The rhesus protein RhCG: a new perspective in ammonium transport and distal urinary acidification in KIDNEY INTERNATIONAL
  • 2010-12 Dent's disease in ORPHANET JOURNAL OF RARE DISEASES
  • 2010-11-22 Oxidative Stress in the Kidney: Proximal Tubule Disorders in STUDIES ON RENAL DISORDERS
  • 2010-09 The soluble intracellular domain of megalin does not affect renal proximal tubular function in vivo in KIDNEY INTERNATIONAL
  • 2010-05 Genetic loci influencing kidney function and chronic kidney disease in NATURE GENETICS
  • 2009-10 ζ-Crystallin mediates the acid pH-induced increase of BSC1 cotransporter mRNA stability in KIDNEY INTERNATIONAL
  • 2009-08 Expression patterns of the aquaporin gene family during renal development: influence of genetic variability in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2009-07 Autoantibodies against intercalated cells in Sjögren's syndrome in KIDNEY INTERNATIONAL
  • 2009-05 Regulated acid–base transport in the collecting duct in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2009-04 CFTR and defective endocytosis: new insights in the renal phenotype of cystic fibrosis in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2009-02 PKD1 haploinsufficiency is associated with altered vascular reactivity and abnormal calcium signaling in the mouse aorta in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2009 Tubular Disorders of Electrolyte Regulation in PEDIATRIC NEPHROLOGY
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