Not all in the family: Mutations of podocin in sporadic steroid-resistant nephrotic syndrome

Journal of the American Society of Nephrology

Volumn 13, Issue 2, 2002, Pages 577-579

  Winn, Michelle P ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PODOCIN; PROTEIN; STEROID; UNCLASSIFIED DRUG;

AUTOSOMAL RECESSIVE DISORDER; EDITORIAL; FAMILIAL DISEASE; GLOMERULUS FILTRATION; HUMAN; MUTATION; NEPHROTIC SYNDROME; PRIORITY JOURNAL;

EID: 0036158076     PISSN: 10466673     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Editorial

References (28)

1. Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis
2. A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13
3. Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis
4. Diffuse mesangial sclerosis: A unique type of congenital and infantile nephrotic syndrome
5. Spectrum of disease in familial focal and segmental glomerulosclerosis (FFSGS)
6. Management of congenital nephrotic syndrome of the Finnish type
7. Nephrin is specifically located at the slit diaphragm of glomerular podocytes
8. Congenital nephrotic syndrome in mice lacking CD2-associated protein
9. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
10. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis
11. Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis
12. Model organisms: New insights into ion channel and transporter function. Stomatin homologues interact in Caenorhabditis elegans
13. A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31
14. Novel mutations in NPHS2 are detected in familial as well as sporadic steroid-resistant nephrotic syndrome
15. Focal segmental glomerulosclerosis: Unremitting proteinuria of long duration as a possible etiology?
16. Interstitial nephritis induced by protein-overload proteinuria
17. Predictive value of repeat renal biopsies in children with nephrotic syndrome
18. Clinical and genetic evaluation of familial steroid-responsive nephrotic syndrome in childhood
19. Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19
20. Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites
21. Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type
22. Congenital nephrotic syndrome of the Finnish type: Linkage to the locus in a non-Finnish population
23. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome
24. Positionally cloned gene for a novel glomerular protein-nephrin-is mutated in congenital nephrotic syndrome
25. Focal glomerulosclerosis associated with Charcot-Marie-Tooth disease
26. Focal sclerosing glomerulonephritis in a child with Laurence-Moon-Biedl syndrome
27. Clinical spectrum of Denys-Drash and Frasier syndrome
28. Unraveling the mechanisms of glomerular ultrafiltration: Nephrin, a key component of the slit diaphragm