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Frontiers in Molecular Neuroscience|January 21, 2025
Modeling of auditory neuropathy spectrum disorders associated with the TEME43 variant reveals impaired gap junction function of iPSC-derived glia-like support cellsXiaoming Kang, Lu Ma, Jie Wen, et al.Scientific Reports|July 31, 2025
Full length transcriptomic profiling reveals insights into the white coat phenotype in Waardenburg syndrome mice harboring the Mitf R324del mutationWei Gong, Lu Ma, Zhili Feng, et al.Plos One|September 14, 2023
Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing lossXianlin Liu, Jie Wen, Xuezhong Liu, et al.Clinical and Experimental Otorhinolaryngology|October 11, 2023
A Novel EYA1 Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical ApplicationAnhai Chen, Jie Ling, Xin Peng, et al.Scientific Reports|October 23, 2012
Visualizing the chemistry and structure dynamics in lithium-ion batteries by in-situ neutron diffractionXun-Li Wang, Ke An, Lu Cai, et al.Pageof 3