22 results on '"Gbadegesin, Rasheed A"'
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2. Diagnosis, Education, and Care of Patients with APOL1-Associated Nephropathy: A Delphi Consensus and Systematic Review
3. A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS
4. TRPC6 Enhances Angiotensin II-induced Albuminuria
5. Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome
6. Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome
7. The Natural History and Genetics of TRPC6-Associated Podocytopathy
8. Multi-Ethnic Genome-Wide Association Study (GWAS) for Idiopathic Nephrotic Syndrome Identifies Susceptibility Loci Across the Life Span, Response to Therapy, and Genetic Ancestry
9. Dietary Patterns and Kidney Function in West Africans with CKD
10. The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes
11. Large-Scale Case-Control Exome-Wide Association Study Identifies Known and Novel Susceptibility Genes for Idiopathic Nephrotic Syndrome
12. Association Between Social Vulnerability, Environmental Burden, and Kidney Outcomes Among Individuals with Glomerular Disease: Results from the Cure Glomerulopathy Network (CureGN)
13. TRPC6 Nephropathy: An International Registry of Prevalence and Outcome
14. Defects in CLVS1 Gene Increase Glycolytic Activity in Cultured Human Podocytes
15. Association of Preterm Birth with Adverse Outcomes of Glomerular Disease in Children and Adults in the CureGN Cohort
16. A Novel Frameshift Mutation in CLCN5 in a Family with Podocytopathy Phenotype
17. Food Insecurity and High Blood Pressure Among Individuals with CKD in West Africa
18. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome
19. A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS
20. Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS
21. TNXB Mutations Can Cause Vesicoureteral Reflux
22. A New Locus for Familial FSGS on Chromosome 2P
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