27 results on '"Winn, Michelle P"'
Search Results
2. Gq signaling causes glomerular injury by activating TRPC6
3. Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomeruosclerosis
4. TORCing up the Importance of Calcium Signaling
5. Screening for NPHS2 Mutations May Help Predict FSGS Recurrence after Transplantation
6. TRPC6 Enhances Angiotensin II-induced Albuminuria
7. Approach to the evaluation of heritable diseases and update on familial focal segmental glomerulosclerosis
8. Evidence for genetic factors in the development and progression of IgA nephropathy
9. Spectrum of disease in familial focal and segmental glomerulosclerosis
10. Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis
11. Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation
12. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome
13. A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS
14. Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis
15. Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS
16. Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity
17. TNXB Mutations Can Cause Vesicoureteral Reflux
18. A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy
19. Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis
20. Hepatorenal Correction in Murine Glycogen Storage Disease Type I With a Double-stranded Adeno-associated Virus Vector
21. A New Locus for Familial FSGS on Chromosome 2P
22. 2007 Young Investigator Award: TRP'ing into a New Era for Glomerular Disease
23. TRPC6 and FSGS: The latest TRP channelopathy
24. Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity.
25. Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity
26. TRPC1 Channels Are Critical for Hypertrophic Signaling in the Heart.
27. Gq signaling causes glomerular injury by activating TRPC6.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.