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Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|November 27, 2007
[Sequence analysis of OTOF gene in a Chinese pedigree with autosomal dominant auditory neuropathy]Shuai Xu, Guangqian Xing, Xin Cao, et al.
International Journal of Audiology|November 16, 2012
Identification of two heterozygous deafness mutations in SLC26A4 (PDS) in a Chinese family with two siblingsJie Chen, Qinjun Wei, Jun Yao, et al.
Communications Biology|February 13, 2026
Abnormal iron homeostasis mediates cochlear hair cell impairment and hearing loss in Gprasp2-deficient miceYajie Lu, Fanghong Sheng, Jun Yao, et al.
JCI Insight|January 18, 2022
Mutations in OSBPL2 cause hearing loss associated with primary cilia defects via sonic hedgehog signalingHairong Shi, Hongshun Wang, Cheng Zhang, et al.
Hearing Research|September 21, 2025
OSBPL2 deficiency impaired cochlear blood-labyrinth barrier via activation of NF-κB signaling pathwayQian Yang, Tianqi Li, Yajie Lu, et al.
The Journal of Steroid Biochemistry and Molecular Biology|November 5, 2018
25-hydroxycholesterol down-regulates oxysterol binding protein like 2 (OSBPL2) via the p53/SREBF2/NFYA signaling pathwayQuan Wang, Changsong Lin, Cui Zhang, et al.
Cell Death Discovery|May 18, 2021
Oxysterol-binding protein-like 2 contributes to the developmental progression of preadipocytes by binding to β-cateninTianming Wang, Tianyu Zhang, Youzhi Tang, et al.
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