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2. Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux

3. TRPC6 Enhances Angiotensin II-induced Albuminuria

5. Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux

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. Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

9. Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS

10. Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity

11. TNXB Mutations Can Cause Vesicoureteral Reflux

12. Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis

13. A New Locus for Familial FSGS on Chromosome 2P

14. Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity.

15. Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

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