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JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
Rivista
Codice:
E094141
ISSN:
1046-6673
Dati Generali
Dati Generali
Pubblicazioni (49)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
. Bartter Syndrome due to K29E activating mutation of Ca sensing receptor gene in monozygotic twin sisters with autosomal dominant hypocalcemia
Abstract
2-Deoxy-d-Glucose Ameliorates PKD Progression
Articolo
ABCB1 Genotypes Predict Cyclosporine-Related Adverse Events and Kidney Allograft Outcome
Articolo
ACE and ADD1 polymorphisms on progression of renal damage in hypertensive patients.
Abstract
An alternative splicing of Na-H exchange isoform 1 underlies human erythrocyte Na-Li countertransport
Articolo
Arachidonic acid and its metabolites PGE 1 and 2 stimulate calcium transport in human osteoblast-like cells
Abstract
Arteriovenous fistula patency in hemodialysis patients role of adducin genes.
Abstract
Ca sensing receptor Arg990Gly polymorphism does predispose to idiopathic hypercalciuria
Abstract
Calcium excretion as a determinant of bone mineral density
Abstract
Calorie Restriction Leads to Degradation of Mutant Uromodulin and Ameliorates Inflammation and Fibrosis in UMOD-Related Kidney Disease
Articolo
Chloride fluxes activated by parathyroid hormone in human erythrocytes
Abstract
Common Variants in UMOD Associate with Urinary Uromodulin Levels: A Meta-Analysis
Articolo
Complement-Activating Anti-HLA Antibodies in Kidney Transplantation: Allograft Gene Expression Profiling and Response to Treatment
Articolo
Effect of a lanosterol synthase polymorphism affecting blood pressure and endogenous ouabain levels in two different clinical settings.
Abstract
Effects of the calcium sensing receptor promoter region polymorphisms in kidney stone disease
Abstract
Elevated endogenous ouabain and reduced wxcretion of uric acid after acute salt load in hypertensive patients.
Abstract
Endogenous ouabain a new biomarker for glomerular damage.
Abstract
Endogenous ouabain is implicated in acute kidney injury in cardiac surgery and critically ill patients.
Abstract
Endogenous ouabain levels predict survival rate in septic acute kidney injury.
Abstract
Erythrocyte voltage-dependent calcium influx is associated with cardiac disorders in hemodialyzed patients.
Abstract
Erythrocyte voltage-dependent calcium influx is associated with cardiac disorders in hemodyalized patients
Abstract
Everolimus with Reduced Calcineurin Inhibitor Exposure in Renal Transplantation
Articolo
Expression of renal aquaporins in a rat model of human sodium-sensitive hypertension
Abstract
Genes involved in blood pressure response to chronic low salt intake: identification of a new pathway.
Abstract
Genetic impact on renal function decay in radical and partial nephrectomy
Abstract
Genetic profile of ACE-inhibitor responder patients in essential hypertension
Abstract
Genetics of essential hypertension: from families to genes
Articolo
Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy
Articolo
Gitelman syndrome is caused by mutations in the human Na-Cl cotransporter gene: Molecular analysis in Italian families.
Articolo
Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppression
Articolo
Human urine-derived renal progenitors for personalized modeling of genetic kidney disorders
Articolo
Increased urinary excretion of aquaporin 2 in patients with essential hypertension: genetic association with polymorphism of the cytoskeletal protein alpha-adducin.
Abstract
Influence of calcium-sensing receptor gene on urinary calcium excretion in stone-forming patients
Articolo
Islet Transplantation Is Associated with Improvement of Renal Function among Uremic Patients with Type I Diabetes Mellitus and Kidney Transplants
Articolo
Low salt diet and diuretic effect on blood pressure and organ damage
Recensione
Network of salt-sensitive hypertension: time effect of a genetic hub.
Abstract
New candidate genes for salt sensitive hypertension.
Abstract
Ouabain as an Early Marker of AKI
Abstract
PKD1 and PKD2 gene variants in Italian patients affected by autosomal dominant polycystic kidney disease (ADPKD).
Abstract
Pharmacogenomics and pharmacogenetics of hypertension: update and perspectives - the adducin paradigm.
Recensione
Renal COP9 signalosome deficiency alters CUL3-KLHL3-WNK signaling pathway
Articolo
Risk models of acute kidney injury (AKI) in cardiac surgery.
Abstract
Rostafuroxin protects from podocyte injury and proteinuria induced by adducin genetic variants and ouabain.
Abstract
Salt Sensitivity Is Modulated by Lanosterol Synthase rs2254524 Polymorphism
Abstract
Stem cells and the kidney: A new therapeutic tool?
Articolo
The Uromodulin Gene Locus Shows Evidence of Pathogen Adaptation through Human Evolution
Articolo
UMOD gene polymorphisms affect GFR decay in ADPKD
Abstract
UNMOD gene in salt sensitivity: a new pathogenetic mechanism
Abstract
Vitamin D receptor gene polymorphism in calcium stone formers
Abstract
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