“Biomarking” the transition from genetic risk to kidney disease
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference9 articles.
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2. Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene;Tzur;Hum Genet,2010
3. APOL1 nephropathy: a population genetics and evolutionary medicine detective story;Kruzel-Davila;Semin Nephrol,2017
4. Freedman BI, Kistler AL, Skewes-Cox P, et al. JC polyoma viruria associates with protection from chronic kidney disease independently from apolipoprotein L1 genotype in African Americans [e-pub ahead of print]. Nephrol Dial Transplant. https://doi.org/10.1093/ndt/gfx368.
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2. A quenching electrochemiluminescence immunosensor based on a novel Ag@Ce2Sn2O7 luminophore for the detection of neuron-specific enolase;Sensors and Actuators B: Chemical;2023-01
3. A Quenced Electrochemiluminesence Immunosensor Based on a Novel Ag@Ce2sn2o7 Luminophore for the Detection of Neuron-Specific Enolase;SSRN Electronic Journal;2022
4. JC Viruria Is Associated With Reduced Risk of Diabetic Kidney Disease;The Journal of Clinical Endocrinology & Metabolism;2019-01-30
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