[1] Marcolla A, Bouchetemble P, Lerosey Y, Marie JP, Dehesdin D. Genetic deafness. Ann Otolaryngol Chir Cervicofac, 2006, 123(3): 143-147.[2] Dror AA, Avraham KB. Hearing impairment: a panoply of genes and functions. Neuron, 2010, 68(2): 293-308.[3] Sprinzl GM, Wolf-Magele A, Schnabl J, Koci V. The active middle ear implant for the rehabilitation of sen-sorineural, mixed and conductive hearing losses. Laryngorhinootologie, 2011, 90(9): 560-572.[4] Friedman LM, Dror AA, Avraham KB. Mouse models to study inner ear development and hereditary hearing loss. Int J Dev Biol, 2007, 51(6-7): 609-631.[5] Friedman LM, Dror AA, Mor E, Tenne T, Toren G, Satoh T, Biesemeier DJ, Shomron N, Fekete DM, Hornstein E, Avraham KB. MicroRNAs are essential for development and function of inner ear hair cells in vertebrates. Proc Natl Acad Sci USA, 2009, 106(19): 7915-7920.[6] Friedman RC, Farh KKH, Burge CB, Bartel DP. Most mammalian mRNAs are conserved targets of microRNAs. Genome Res, 2009, 19(1): 92-105.[7] O'Day E, Lal A. MicroRNAs and their target gene networks in breast cancer. Breast Cancer Res, 2010, 12(2): 201.[8] Landgraf P, Rusu M, Sheridan R, Sewer A, Iovino N, Aravin A, Pfeffer S, Rice A, Kamphorst AO, Landthaler M, Lin C, Socci ND, Hermida L, Fulci V, Chiaretti S, Foà R, Tuschl T. A mammalian microRNA expression atlas based on small RNA library sequencing. Cell, 2007, 129(7): 1401-1414.[9] Weston MD, Pierce ML, Rocha-Sanchez S, Beisel KW, Soukup GA. MicroRNA gene expression in the mouse inner ear. Brain Res, 2006, 1111(1): 95-104.[10] Xu SB, Witmer PD, Lumayag S, Kovacs B, Valle D. MicroRNA (miRNA) transcriptome of mouse retina and identification of a sensory organ-specific miRNA cluster. J Biol Chem, 2007, 282(34): 25053-25066.[11] Sacheli R, Nguyen L, Borgs L, Vandenbosch R, Bodson M, Lefebvre P, Malgrange B. Expression patterns of miR-96, miR-182 and miR-183 in the developing inner ear. Gene Expr Patterns, 2009, 9(5): 364-370.[12] Li HQ, Kloosterman W, Fekete DM. MicroRNA-183 family members regulate sensorineural fates in the inner ear. J Neurosci, 2010, 30(9): 3254-3263.[13] Pierce ML, Weston MD, Fritzsch B, Gabel HW, Ruvkun G, Soukup GA. MicroRNA-183 family conservation and cili-ated neurosensory organ expression. Evol Dev, 2008, 10(1): 106-113.[14] Lewis MA, Quint E, Glazier AM, Fuchs H, De Angelis MH, Langford C, van Dongen S, Abreu-Goodger C, Pii-pari M, Redshaw N, Dalmay T, Moreno-Pelayo MA, En-right AJ, Steel KP. An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice. Nat Genet, 2009, 41(5): 614-618.[15] 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. Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss. Nat Genet, 2009, 41(5): 609-613.[16] Soukup GA, Fritzsch B, Pierce ML, Weston MD, Jahan I, McManus MT, Harfe BD. Residual microRNA expression dictates the extent of inner ear development in conditional Dicer knockout mice. Dev Biol, 2009, 328(2): 328-341.[17] Gehring M, Reik W, Henikoff S. DNA demethylation by DNA repair. Trends Genet, 2009, 25(2): 82-90.[18] Richards AJ, McNinch A, Martin H, Oakhill K, Rai H, Waller S, Treacy B, Whittaker J, Meredith S, Poulson A, Snead MP. Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1. Hum Mutat, 2010, 31(6): E1461-E1471.[19] Hoornaert KP, Vereecke I, Dewinter C, Rosenberg T, Beemer FA, Leroy JG, Bendix L, Björck E, Bonduelle M, Boute O, Cormier-Daire V, De Die-Smulders C, Mortier GR. Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series o |