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Scientific Reports|October 27, 2016
Functional kinomics establishes a critical node of volume-sensitive cation-Cl- cotransporter regulation in the mammalian brainJinwei Zhang, Geng Gao, Gulnaz Begum, et al.Nature Medicine|July 11, 2017
Inflammation-dependent cerebrospinal fluid hypersecretion by the choroid plexus epithelium in posthemorrhagic hydrocephalusJason K Karimy, Jinwei Zhang, David B Kurland, et al.American Journal of Physiology. Cell Physiology|August 19, 2011
Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65SAndrew K Stewart, Boris E Shmukler, David H Vandorpe, et al.Brain : a Journal of Neurology|December 16, 2024
De novo variants disrupt an LDB1-regulated transcriptional network in congenital ventriculomegalyGarrett Allington, Neel H Mehta, Evan Dennis, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 22, 2020
Characteristics and Outcomes of Individuals With Pre-existing Kidney Disease and COVID-19 Admitted to Intensive Care Units in the United StatesJennifer E Flythe, Magdalene M Assimon, Matthew J Tugman, et al.American Journal of Nephrology|June 7, 2021
Plasma Mucin-1 (CA15-3) Levels in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 MutationsPetr Vylet'al, Kendrah Kidd, Hannah C Ainsworth, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 25, 2017
A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathyKarl L Skorecki, Jessica H Lee, Carl D Langefeld, et al.Blood|March 13, 2013
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1Immacolata Andolfo, Seth L Alper, Lucia De Franceschi, et al.Human Mutation|February 11, 2009
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?Byung Yoon Choi, Andrew K Stewart, Anne C Madeo, et al.Acta Neuropathologica Communications|April 24, 2025
Premature skeletal muscle aging in VPS13A deficiency relates to impaired autophagyVeronica Riccardi, Carlo Fiore Viscomi, Marco Sandri, et al.Pageof 27