CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS)-Reference-Cited by-同舟云学术

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CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS)

Published:2009-01-07 Issue:6 Volume:24 Page:1858-1864
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

Gigante M.,Pontrelli P.,Montemurno E.,Roca L.,Aucella F.,Penza R.,Caridi G.,Ranieri E.,Ghiggeri G. M.,Gesualdo L.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/24/6/1858/7631370/gfn712.pdf

Reference17 articles.

1. A Novel Adaptor Protein Orchestrates Receptor Patterning and Cytoskeletal Polarity in T-Cell Contacts

2. CD2AP Localizes to the Slit Diaphragm and Binds to Nephrin via a Novel C-Terminal Domain

3. Podocin, a raft-associated component of the glomerular slit diaphragm, interacts with CD2AP and nephrin

4. Congenital Nephrotic Syndrome in Mice Lacking CD2-Associated Protein

5. CD2-Associated Protein Haploinsufficiency Is Linked to Glomerular Disease Susceptibility

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