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NDT on Twitter: "🆕Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end stage renal disease of unknown origin 📖https://t.co/su0e6JkVWP 📸Composition of kidney transplantation waitlist 📸Proposed diagnostic ...
Laminin α2-Mediated Focal Adhesion Kinase Activation Triggers Alport Glomerular Pathogenesis | PLOS ONE
DNA-Encoded Library-Derived DDR1 Inhibitor Prevents Fibrosis and Renal Function Loss in a Genetic Mouse Model of Alport Syndrome | ACS Chemical Biology
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Ultrastructural Characterization of the Glomerulopathy in Alport Mice by Helium Ion Scanning Microscopy (HIM) | Scientific Reports
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Pathogenic Variants in the Genes Affected in Alport Syndrome (COL4A3–COL4A5) and Their Association With Other Kidney Conditions: A Review - American Journal of Kidney Diseases
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The importance of clinician, patient and researcher collaborations in Alport syndrome | SpringerLink
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Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane. - Abstract - Europe PMC
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