CD2-associated protein and the kidney

Current Opinion in Nephrology and Hypertension

Volumn 10, Issue 1, 2001, Pages 19-22

  Shaw, Andrey S ^a   Miner, Jeffrey H ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CD2 ASSOCIATED PROTEIN; CYTOPLASM PROTEIN; NEPHRIN; UNCLASSIFIED DRUG;

DISEASE ASSOCIATION; GLOMERULOPATHY; GLOMERULUS FILTRATION; HUMAN; KIDNEY FAILURE; KNOCKOUT MOUSE; NONHUMAN; PATHOGENESIS; PODOCYTE; PRIORITY JOURNAL; REVIEW;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ANIMALS; CYTOSKELETAL PROTEINS; HUMANS; KIDNEY; KIDNEY DISEASES; KIDNEY FAILURE; KIDNEY GLOMERULUS; MICE; MICE, KNOCKOUT; PROTEINS;

EID: 0035132759     PISSN: 10624821     EISSN: None     Source Type: Journal    
DOI: 10.1097/00041552-200101000-00004     Document Type: Review

References (17)

1. A novel adaptor protein orchestrates receptor patterning and cytoskeletal polarity in T-cell contacts
2. CMS: An adapter molecule involved in cytoskeletal rearrangements
3. Cloning and characterization of a novel adaptor protein, CIN85, that interacts with c-Cbl
4. Congenital nephrotic syndrome in mice lacking CD2-associated protein
5. CD2AP is expressed with nephrin in developing podocytes and is found widely in mature kidney and elsewhere
6. Structure and function of podocytes: An update
7. Porous substructure of the glomerular slit diaphragm in the rat and mouse
8. Positionally cloned gene for a novel glomerular protein-nephrin-is mutated in congenital nephrotic syndrome
9. Nephrin is specifically located at the slit diaphragm of glomerular podocytes
10. Cloning of rat nephrin: Expression in developing glomeruli and in proteinuric states
11. Nephrin localizes at the podocyte filtration slit area and is characteristically spliced in the human kidney
12. Nephrin localizes to the slit pore of the glomerular epithelial cell
13. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis
14. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
15. Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations
16. Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type
17. In vivo interaction of the adapter protein CD2AP with the type 2 polycystic kidney disease protein, polycystin-2