Citations for
1DFNA50, MIR96
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing.
Soldà G, Robusto M, Primignani P, Castorina P, Benzoni E, Cesarani A, Ambrosetti U, Asselta R, Duga S.
Hum Mol Genet 21(3):577-85. doi: 10.1093/hmg/ddr493. Epub 2011 Oct 28. 2012
2FOXO1, MIR96
miR-96 regulates the progression of differentiation in mammalian cochlear inner and outer hair cells.
Kuhn S, Johnson SL, Furness DN, Chen J, Ingham N, Hilton JM, Steffes G, Lewis MA, Zampini V, Hackney CM, Masetto S, Holley MC, Steel KP, Marcotti W.
Proc Natl Acad Sci U S A 108(6):2355-60. Epub 2011 Jan 18. 2011
3MIR96
Unregulated miR-96 induces cell proliferation in human breast cancer by downregulating transcriptional factor FOXO3a.
Lin H, Dai T, Xiong H, Zhao X, Chen X, Yu C, Li J, Wang X, Song L.
PLoS One 5(12):e15797. 2010
4MIR96
miRNA-96 suppresses KRAS and functions as a tumor suppressor gene in pancreatic cancer.
Yu S, Lu Z, Liu C, Meng Y, Ma Y, Zhao W, Liu J, Yu J, Chen J.
Cancer Res 70(14):6015-25. Epub 2010 Jul 7. 2010
5MIR96
Expression patterns of miR-96, miR-182 and miR-183 in the development inner ear.
Sacheli R, Nguyen L, Borgs L, Vandenbosch R, Bodson M, Lefebvre P, Malgrange B.
Gene Expr Patterns 9(5):364-70. 2009
6DFNA50, MIR96
Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss.
Mencía A, Modamio-Høybjør S, Redshaw N, Morín M, Mayo-Merino F, Olavarrieta L, Aguirre LA, del Castillo I, Steel KP, Dalmay T, Moreno F, Moreno-Pelayo MA.
Nat Genet at Genet. 2009 2009