Results 141 to 150 of about 37,354 (236)

Cell-specific delivery of GJB2 restores auditory function in mouse models of DFNB1 deafness and mediates appropriate expression in NHP cochlea. [PDF]

Nat Commun
Ivanchenko MV, Booth KTA, Karavitaki KD, Antonellis LM, Nagy MA, Peters CW, Price S, Li Y, Lytvyn A, Ward A, Griffith EC, Hrvatin S, Greenberg ME, Corey DP.   +13 more
europepmc   +1 more source

Bmi1 controls auditory sensory epithelial cell proliferation through genome-wide H3K27me3 modifications. [PDF]

Epigenetics Chromatin
Lu X, Zhang Y, Dai R, Wang K, Lan F, Yu H, Zhao L, Chai R, Sun S.   +8 more
europepmc   +1 more source

The Role of Calcium Signaling in Sensorineural Hearing Loss. [PDF]

Int J Med Sci
Hu Y, Li J, Tian L, Zhang P, Zeng X.
europepmc   +1 more source

Recent preclinical and clinical advances in gene therapy for hereditary hearing loss. [PDF]

Mol Cells
Jang SH, Song HG, Jung J, Gee HY.
europepmc   +1 more source

Planar polarized organization of mouse hair cells is established and maintained by STK32A, GPR156 and EMX2. [PDF]

J Cell Sci
Jia S, Goodrich EJ, Tarchini B, Deans MR.   +3 more
europepmc   +1 more source

Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish. [PDF]

Cells
Zhang G, Li Q, Xu Y, Zhao H, Yang C, Liu D, Gong J.   +6 more
europepmc   +1 more source

Single-cell RNA sequencing data analysis of the inner ear in gentamicin-treated mice via intraperitoneal injection. [PDF]

Open Med (Wars)
Bao X, Wang Y, Liu W, Tang H, Guo Y.
europepmc   +1 more source

Mechanistic insights into cisplatin-induced ototoxicity: the central role of transient receptor potential channels. [PDF]

Front Mol Biosci
Yu M, Li J, Zeng X.
europepmc   +1 more source

Dual-AAV mediated transfer of full-length otoferlin cDNA into auditory inner hair cells and the effects of different mutations in the OTOF gene on the protein levels and cellular distribution of otoferlin in auditory inner hair cells [PDF]

, 2022
openaire   +1 more source

Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease. [PDF]

MedComm (2020)
Parra-Perez AM, Gallego-Martinez A, Escalera-Balsera A, Robles-Bolivar P, Perez-Carpena P, Lopez-Escamez JA.   +5 more
europepmc   +1 more source