10 results on '"Homstad, Alison"'
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2. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome
3. A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS
4. Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis
5. Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS
6. Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity
7. TNXB Mutations Can Cause Vesicoureteral Reflux
8. Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis
9. A New Locus for Familial FSGS on Chromosome 2P
10. Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity.
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