Citations for
1FSGS5, INF2
Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease.
Challis RC, Ring T, Xu Y, Wong EK, Flossmann O, Roberts IS, Ahmed S, Wetherall M, Salkus G, Brocklebank V, Fester J, Strain L, Wilson V, Wood KM, Marchbank KJ, Santibanez-Koref M, Goodship TH, Kavanagh D.
J Am Soc Nephrol Am Soc Nephrol. 2016 Dec 14. pii: ASN.2015101189. [Epub ahead of print] 2016
2FSGS5, INF2
Familial focal segmental glomerulosclerosis: mutation in inverted formin 2 mimicking Alport syndrome.
Rood IM, Bongers EM, Lugtenberg D, Klein IH, Steenbergen EJ, Wetzels JF, Deegens JK.
Neth J Med 74(2):82-5. 2016
3FSGS5, INF2
Reduced INF2 expression in nephrotic syndrome is possibly related to clinical severity of steroid resistance in children.
Tamura H, Nakazato H, Kuraoka S, Yoneda K, Takahashi W, Endo F.
Nephrology (Carlton) 21(6):467-75. doi: 10.1111/nep.12627. 2016
4CMTDIE, FSGS5, INF2
Mutations to the formin homology 2 domain of INF2 protein have unexpected effects on actin polymerization and severing.
Ramabhadran V, Gurel PS, Higgs HN.
J Biol Chem 287(41):34234-45. doi: 10.1074/jbc.M112.365122. Epub 2012 Aug 9. 2012
5FSGS5, INF2
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.
Brown EJ, Schlöndorff JS, Becker DJ, Tsukaguchi H, Uscinski AL, Higgs HN, Henderson JM, Pollak MR.
Nat Genet 42(1):72-6. Epub 2009 Dec 20. 2010