10 results on '"Wu, Guanghong"'
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2. TRPC6 Enhances Angiotensin II-induced Albuminuria
3. The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes
4. Defects in CLVS1 Gene Increase Glycolytic Activity in Cultured Human Podocytes
5. A Novel Frameshift Mutation in CLCN5 in a Family with Podocytopathy Phenotype
6. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome
7. A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS
8. Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS
9. TNXB Mutations Can Cause Vesicoureteral Reflux
10. A New Locus for Familial FSGS on Chromosome 2P
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