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International Journal of Pediatric Otorhinolaryngology|May 19, 2019
EYA1 mutations leads to Branchio-Oto syndrome in two Chinese Han deaf familiesPenghui Chen, Haijin Liu, Yun Lin, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|May 20, 2020
The p.R206C Mutation in MYO7A Leads to Autosomal Dominant Nonsyndromic Hearing LossJiawen Lu, Penghui Chen, Tuanjie Chen, et al.
International Journal of Pediatric Otorhinolaryngology|June 24, 2015
Mono-allelic mutations of SLC26A4 is over-presented in deaf patients with non-syndromic enlarged vestibular aqueductXiuhong Pang, Yongchuan Chai, Penghui Chen, et al.
The Journal of Reproduction and Development|February 8, 2023
Estradiol enhances T-type calcium channel activation in human myometrium telocytesLin Zhu, Tao Shangguan, Penghui Chen, et al.
Environmental Science and Pollution Research International|February 13, 2024
Synergistic effect of hydrothermal sludge and food waste in the anaerobic co-digestion process: microbial shift and dewaterabilityPenghui Chen, Enzhen Wang, Yonghui Zheng, et al.
Neurobiology of Disease|April 12, 2026
Parvalbumin neurons in inferior colliculus mediate maladaptive inhibitory compensation in age-related hearing lossYinpei Luo, Guoliang Wei, Yunxiao Lou, et al.
Frontiers in Neuroscience|June 26, 2018
Cognitive Decline, Dementia, Alzheimer's Disease and Presbycusis: Examination of the Possible Molecular MechanismYilin Shen, Bin Ye, Penghui Chen, et al.
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