8 results on '"Hall, Gentzon"'
Search Results
2. The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes
3. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome
4. A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS
5. Abstract 601: A Biased AT1 Receptor Agonist Stimulates COX2 Expression In Intercalated Cells
6. Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS
7. TNXB Mutations Can Cause Vesicoureteral Reflux
8. TRPC6 Enhances Angiotensin II-induced Albuminuria
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.