14 results on '"Winn, Michelle P"'
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2. OPINION: Genetic testing in nephrotic syndrome —challenges and opportunities
3. Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis
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. Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS
8. A Mutation in the TRPC6 Cation Channel Causes Familial Focal Segmental Glomerulosclerosis
9. Approach to the evaluation of heritable diseases and update on familial focal segmental glomerulosclerosis
10. Linkage of a Gene Causing Familial Membranoproliferative Glomerulonephritis Type III to Chromosome 1
11. Not All in the Family: Mutations of Podocin in Sporadic Steroid-Resistant Nephrotic Syndrome
12. Evidence for genetic factors in the development and progression of IgA nephropathy
13. Spectrum of disease in familial focal and segmental glomerulosclerosis
14. Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis
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