Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis-Reference-Cited by-同舟云学术

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

Published:2009-12-20 Issue:1 Volume:42 Page:72-76
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Brown Elizabeth J,Schlöndorff Johannes S,Becker Daniel J,Tsukaguchi Hiroyasu,Tonna Stephen J,Uscinski Andrea L,Higgs Henry N,Henderson Joel M,Pollak Martin R

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.505.pdf

Reference22 articles.

1. Kaplan, J.M. et al. Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis. Nat. Genet. 24, 251–256 (2000).

2. Winn, M.P. et al. A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. Science 308, 1801–1804 (2005).

3. Reiser, J. et al. TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function. Nat. Genet. 37, 739–744 (2005).

4. Chhabra, E.S. & Higgs, H.N. INF2 is a WASP homology 2 motif-containing formin that severs actin filaments and accelerates both polymerization and depolymerization. J. Biol. Chem. 281, 26754–26767 (2006).

5. D'Agati, V.D., Fogo, A.B., Bruijn, J.A. & Jennette, J.C. Pathologic classification of focal segmental glomerulosclerosis: a working proposal. Am. J. Kidney Dis. 43, 368–382 (2004).

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