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Biorxiv : the Preprint Server for Biology|July 29, 2026
A Quartet of Native Orai Channel Isoforms Orchestrates Graded NFAT Activation and TranscriptionAhmed Emam Abdelnaby, Yin-Hu Wang, J Cory Benson, et al.Biorxiv : the Preprint Server for Biology|June 5, 2026
Cell autonomous inflammation in VEXAS is mediated by cGAS-STINGSamuel J Magaziner, Jason C Collins, Brecca Miller, et al.The Journal of Allergy and Clinical Immunology|May 28, 2021
Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXASCaspar I van der Made, Judith Potjewijd, Annemiek Hoogstins, et al.Arthritis Care & Research|July 13, 2026
Development of a Disease Activity Index for the Assessment of VEXAS Syndrome (VEXAS-DAI)Kevin Byram, Heřman Mann, Danielle Hammond, et al.Proceedings of the National Academy of Sciences of the United States of America|May 22, 2023
Germline C1GALT1C1 mutation causes a multisystem chaperonopathyFlorian Erger, Rajindra P Aryal, Björn Reusch, et al.Pediatric Nephrology (Berlin, Germany)|January 10, 2024
Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tractMarcin Kołbuc, Mateusz F Kołek, Rafał Motyka, et al.Kidney International Reports|October 27, 2025
Novel RRAGD Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic PerspectivesAnastasia Adella, François Jouret, Leire Madariaga, et al.Human Mutation|July 22, 2014
Mutation of POC1B in a severe syndromic retinal ciliopathyBodo B Beck, Jennifer B Phillips, Malte P Bartram, et al.Kidney International Reports|October 18, 2023
Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria ConsortiumElisabeth L Metry, Sander F Garrelfs, Lisa J Deesker, et al.Journal of the American Society of Nephrology : JASN|July 4, 2018
Noninvasive Immunohistochemical Diagnosis and Novel MUC1 Mutations Causing Autosomal Dominant Tubulointerstitial Kidney DiseaseMartina Živná, Kendrah Kidd, Anna Přistoupilová, et al.Pageof 61