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Frontiers in Molecular Biosciences|August 8, 2022
NPC1 Deficiency Contributes to Autophagy-Dependent Ferritinophagy in HEI-OC1 Auditory CellsLihong Liang, Hongshun Wang, Jun Yao, et al.Biochemical and Biophysical Research Communications|October 21, 2019
Comparative transcriptome analysis of auditory OC-1 cells and zebrafish inner ear tissues in the absence of human OSBPL2 orthologuesHairong Shi, Hongshun Wang, Jun Yao, et al.Journal of Translational Medicine|July 6, 2013
Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of ChinaQinjun Wei, Shuai Wang, Jun Yao, et al.Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|January 24, 2009
[Sequence analysis of DFNB59 gene in a Chinese family with dominantly inherited auditory neuropathy]Shuai Xu, Zhibin Chen, Yajie Lu, et al.International Journal of Molecular Medicine|December 17, 2013
A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a familyQinjun Wei, Youguo Liu, Shuai Wang, et al.Annals of Medicine|April 20, 2026
Placental transport dysfunction in omega-3 and omega-6 fatty acid in patients with gestational diabetes mellitusWei Long, Fang Guo, Jun Yao, et al.Biochemical and Biophysical Research Communications|June 20, 2006
Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicityGuangqian Xing, Zhibin Chen, Qinjun Wei, et al.Biochemical and Biophysical Research Communications|May 3, 2006
Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese familyGuangqian Xing, Zhibin Chen, Qinjun Wei, et al.Journal of Medical Genetics|January 19, 2017
GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing lossGuangqian Xing, Jun Yao, Chunyu Liu, et al.Journal of Translational Medicine|November 13, 2014
Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing lossQinjun Wei, Hongmei Zhu, Xuli Qian, et al.Pageof 5