13 results on '"Winn, Michelle P"'
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2. Screening for NPHS2 Mutations May Help Predict FSGS Recurrence after Transplantation
3. TRPC6 Enhances Angiotensin II-induced Albuminuria
4. Linkage of a Gene Causing Familial Membranoproliferative Glomerulonephritis Type III to Chromosome 1
5. Not All in the Family: Mutations of Podocin in Sporadic Steroid-Resistant Nephrotic Syndrome
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. Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS
9. TNXB Mutations Can Cause Vesicoureteral Reflux
10. A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy
11. A New Locus for Familial FSGS on Chromosome 2P
12. 2007 Young Investigator Award: TRP'ing into a New Era for Glomerular Disease
13. Unexpected Role ofTRPC6Channel in Familial Nephrotic Syndrome: Does It Have Clinical Implications?
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