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Editorial Board

doi : 10.1016/S0085-2538(25)00355-2

Volume 108, Issue 1, July 2025, Page A1

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Indigenous spirituality and cultural knowledges provide strength and resilience to Aboriginal people with chronic kidney disease

doi : 10.1016/j.kint.2025.02.022

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Steroidal or nonsteroidal mineralocorticoid receptor antagonists for reducing cardiovascular burden in chronic kidney disease

doi : 10.1016/j.kint.2025.03.010

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Humanizing flies with transgenic nephrin

doi : 10.1016/j.kint.2025.04.011

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To do or not to do—genetic testing for autosomal dominant polycystic kidney disease in children and adolescents

doi : 10.1016/j.kint.2025.05.001

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Fluid resuscitation in acute kidney injury: too much of a good thing

doi : 10.1016/j.kint.2024.05.034

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Fluid management in acute kidney injury should be liberal when needed

doi : 10.1016/j.kint.2025.02.003

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Fluid management in patients with acute kidney injury: a balancing act

doi : 10.1016/j.kint.2025.03.016

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Genetic studies on metabolic disorder–associated kidney diseases

doi : 10.1016/j.kint.2025.01.042

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Unlocking the full potential of human pluripotent stem cell–derived kidney organoids through bioengineering

doi : 10.1016/j.kint.2025.01.043

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Targeted delivery of IL-21 neutralizing nanotherapeutics to lymph nodes and kidney allografts attenuates B cell alloimmunity

doi : 10.1016/j.kint.2025.03.017

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Transgenic human nephrin in Drosophila nephrocytes facilitates variant analysis

doi : 10.1016/j.kint.2025.03.030

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Gene signature-guided drug screening identified narciclasine as a potential therapeutic for interstitial fibrosis of the kidney

doi : 10.1016/j.kint.2025.03.021

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Single-cell analysis of proximal tubular cells with different DNA content reveals functional heterogeneity in the acute kidney injury to chronic kidney disease transition

doi : 10.1016/j.kint.2025.03.025

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Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries

doi : 10.1016/j.kint.2025.02.026

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B cell–derived exosomal miR-483-5p and its potential role in promoting kidney function loss in IgA nephropathy

doi : 10.1016/j.kint.2025.03.019

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Efficacy and safety of finerenone in patients with an acute change in estimated glomerular filtration rate in the prespecified FIDELITY pool analysis

doi : 10.1016/j.kint.2025.03.018

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CRISPR-Cas9 mediated proteinase 3 autoantigen deletion as a treatment strategy for anti-neutrophil cytoplasmic autoantibody-associated vasculitis

doi : 10.1016/j.kint.2025.03.020

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Autosomal dominant polycystic kidney disease

doi : 10.1016/j.kint.2025.02.014

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Reevaluating principal component analysis: advocating for nonlinear and nonparametric methods in multi-omics data analysis

doi : 10.1016/j.kint.2025.03.002

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Cholesterol crystal embolism treatment: from bench to bedside

doi : 10.1016/j.kint.2025.03.012

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IgG4-related tubulointerstitial nephritis with negative contrast-enhanced computed tomography: diagnostic insights from 18F-fluorodeoxyglucose–positron emission tomography/computed tomography

doi : 10.1016/j.kint.2025.02.031

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ALECT2 amyloidosis in a patient with myeloma cast nephropathy

doi : 10.1016/j.kint.2024.12.024

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Q fever endocarditis and glomerulonephritis

doi : 10.1016/j.kint.2024.12.023

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The Case | Livedo, necrotic skin lesions, and acute kidney injury

doi : 10.1016/j.kint.2025.02.011

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