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Editorial Board

doi : 10.1016/S0085-2538(26)00095-5

Volume 109, Issue 4, April 2026, Pages A1-A2

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Nobel prize–winning Treg cells in autoimmune kidney diseases and transplantation

doi : 10.1016/j.kint.2026.01.005

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Dynamic control of Na-Cl cotransporter by kidney-specific with-no-lysine 1 kinase: a biphasic response to K+ via condensate signaling

doi : 10.1016/j.kint.2025.09.022

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Giving monocytes their due: how CD47–SIRP-α reframes allograft rejection

doi : 10.1016/j.kint.2025.10.008

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When YAP is hyperactivated in podocytes, it persistently “yaps,� disrupting the quiescence of neighboring glomerular cells

doi : 10.1016/j.kint.2025.10.013

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The Janus face of parathyroid hormone in renal osteodystrophy

doi : 10.1016/j.kint.2026.01.008

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ALDH1A1 is a potential novel target for treatment of ADPKD

doi : 10.1016/j.kint.2026.01.011

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Predicting steroid treatment benefit in IgA nephropathy: are we ready for precision care?

doi : 10.1016/j.kint.2026.01.007

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Taking the “unknown� out of CKDu—optimizing approaches to uncover the cause(s) of epidemic-level kidney disease in low- and middle-income settings: a report from the ISN’s International Consortium of CKDu Collaborators (ISN i3C)

doi : 10.1016/j.kint.2025.12.027

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Primary hyperoxaluria(s): from trials to real-life data and pipeline therapies

doi : 10.1016/j.kint.2025.12.029

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Eligibility, timing, and organ quality: indications and outcomes of kidney transplantation in older patients

doi : 10.1016/j.kint.2025.11.026

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Targeting cellular senescence in diabetic kidney disease: potential of regenerative, cell-based therapies and other senotherapeutic approaches

doi : 10.1016/j.kint.2025.10.019

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Uremia and parathyroid hormone have distinct effects on bone protein and gene expression

doi : 10.1016/j.kint.2025.12.025

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Aldehyde dehydrogenase 1 A1 regulates the transcription of PD-L1 and its targeting with disulfiram together with PD-L1 immunotherapy synergistically delays cyst growth in ADPKD

doi : 10.1016/j.kint.2025.12.004

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Heat shock protein 70s are modifiers of endothelial function in Fabry disease

doi : 10.1016/j.kint.2026.01.004

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A secondary analysis of the TESTING trial predicted individual patient response to corticosteroid treatment in IgA nephropathy

doi : 10.1016/j.kint.2025.12.024

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Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis

doi : 10.1016/j.kint.2025.12.013

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Genotype-phenotype characteristics and disease progression of FAN1-related karyomegalic tubulointerstitial nephropathy

doi : 10.1016/j.kint.2026.01.001

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Multi-omics analyses reveal the pathogenic role of terminal ileum-derived IgA+β7+ cells in IgA nephropathy

doi : 10.1016/j.kint.2025.12.026

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Laser microdissection coupled to mass spectrometry is more sensitive than immunohistochemistry in diagnosing phospholipase A2 receptor–positive membranous nephropathy

doi : 10.1016/j.kint.2025.12.017

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Reversible cerebral lesions in adult STEC-associated hemolytic uremic syndrome

doi : 10.1016/j.kint.2025.08.047

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Amyloid light-chain amyloidosis presenting as lambda-restricted tubular amyloid casts

doi : 10.1016/j.kint.2025.08.044

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Displaced kidneys in a giant inguinoscrotal hernia: an unusual cause of hydronephrosis

doi : 10.1016/j.kint.2025.08.043

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Catheter malposition in a peritoneal dialysis patient with Chilaiditi sign

doi : 10.1016/j.kint.2025.08.046

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The Case | A young man with medullary nephrocalcinosis and chronic kidney disease

doi : 10.1016/j.kint.2025.09.007

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The Case | Severe metabolic acidosis with normal anion gap

doi : 10.1016/j.kint.2025.08.021

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