6.
Xia W, Yan H, Zhang Y, Wang C, Gao W, Lv C
. Congenital Human Cytomegalovirus Infection Inducing Sensorineural Hearing Loss. Front Microbiol. 2021; 12:649690.
PMC: 8079719.
DOI: 10.3389/fmicb.2021.649690.
View
7.
Okur M, Djalilian H
. Approaches to Mitigate Mitochondrial Dysfunction in Sensorineural Hearing Loss. Ann Biomed Eng. 2022; 50(12):1762-1770.
DOI: 10.1007/s10439-022-03103-y.
View
8.
Fetoni A, Paciello F, Rolesi R, Paludetti G, Troiani D
. Targeting dysregulation of redox homeostasis in noise-induced hearing loss: Oxidative stress and ROS signaling. Free Radic Biol Med. 2019; 135:46-59.
DOI: 10.1016/j.freeradbiomed.2019.02.022.
View
9.
Liu S, Li S, Zhu H, Cheng S, Zheng Q
. A mutation in the cdh23 gene causes age-related hearing loss in Cdh23(nmf308/nmf308) mice. Gene. 2012; 499(2):309-17.
PMC: 3526976.
DOI: 10.1016/j.gene.2012.01.084.
View
10.
Li X, Shi L, Wang L
. A review of the mechanisms underlying the role of the gene in hereditary deafness. Front Synaptic Neurosci. 2023; 14:1101587.
PMC: 9872657.
DOI: 10.3389/fnsyn.2022.1101587.
View
11.
Wingard J, Zhao H
. Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness. Front Cell Neurosci. 2015; 9:202.
PMC: 4448512.
DOI: 10.3389/fncel.2015.00202.
View
12.
Wang Y, Jin Y, Zhang Q, Xiong Y, Gu X, Zeng S
. Research progress in delineating the pathological mechanisms of -related hearing loss. Front Cell Neurosci. 2023; 17:1208406.
PMC: 10272732.
DOI: 10.3389/fncel.2023.1208406.
View
13.
Brandt A, Striessnig J, Moser T
. CaV1.3 channels are essential for development and presynaptic activity of cochlear inner hair cells. J Neurosci. 2003; 23(34):10832-40.
PMC: 6740966.
View
14.
Roux I, Safieddine S, Nouvian R, Grati M, Simmler M, Bahloul A
. Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell. 2006; 127(2):277-89.
DOI: 10.1016/j.cell.2006.08.040.
View
15.
Sloan-Heggen C, Bierer A, Shearer A, Kolbe D, Nishimura C, Frees K
. Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss. Hum Genet. 2016; 135(4):441-450.
PMC: 4796320.
DOI: 10.1007/s00439-016-1648-8.
View
16.
Rodriguez-Ballesteros M, Reynoso R, Olarte M, Villamar M, Morera C, Santarelli R
. A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy. Hum Mutat. 2008; 29(6):823-31.
DOI: 10.1002/humu.20708.
View
17.
Iwasa Y, Nishio S, Sugaya A, Kataoka Y, Kanda Y, Taniguchi M
. OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients. PLoS One. 2019; 14(5):e0215932.
PMC: 6522017.
DOI: 10.1371/journal.pone.0215932.
View
18.
Choi B, Ahmed Z, Bhinder M, Shahzad M, Husnain T, Riazuddin S
. Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan. Clin Genet. 2009; 75(3):237-43.
PMC: 3461579.
DOI: 10.1111/j.1399-0004.2008.01128.x.
View
19.
Delmaghani S, Del Castillo F, Michel V, Leibovici M, Aghaie A, Ron U
. Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Nat Genet. 2006; 38(7):770-8.
DOI: 10.1038/ng1829.
View
20.
Delmaghani S, Defourny J, Aghaie A, Beurg M, Dulon D, Thelen N
. Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes. Cell. 2015; 163(4):894-906.
DOI: 10.1016/j.cell.2015.10.023.
View