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Genetic Testing and Molecular Biomarkers|August 3, 2012
Mitochondrial DNA mutation screening in an ethnically diverse nonsyndromic deafness cohortRichard J Vivero, Xiaomei Ouyang, Denise Yan, et al.International Journal of Audiology|November 30, 2012
Hearing loss and PRPS1 mutations: Wide spectrum of phenotypes and potential therapyXue Zhong Liu, Dinghua Xie, Hui Jun Yuan, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 21, 2018
A Xenograft Model of Vestibular Schwannoma and Hearing LossChristine T Dinh, Olena Bracho, Christine Mei, et al.Ear and Hearing|June 7, 2005
Audiological features of GJB2 (connexin 26) deafnessXue Zhong Liu, Arti Pandya, Simon Angeli, et al.Stem Cell Research|October 10, 2020
Characterization of UMi028-A-1 stem cell line that contains a CRISPR/Cas9 induced hearing loss-associated variant (V60L (c.178G > T)) in the P2RX2 geneNicholas C Gosstola, Zaohua Huang, Xiaoying Tong, et al.Human Molecular Genetics|April 1, 2021
Generation and characterization of a P2rx2 V60L mouse model for DFNA41Xiaoya Chen, Clemer Abad, Zheng-Yi Chen, et al.Anatomical Record (Hoboken, N.J. : 2007)|July 2, 2019
The Generation of Zebrafish Mariner Model Using the CRISPR/Cas9 SystemBing Zou, Alexandra A Desmidt, Rahul Mittal, et al.Frontiers in Cell and Developmental Biology|October 5, 2020
Bromodomain Protein BRD4 Is Essential for Hair Cell Function and SurvivalAbhiraami Kannan-Sundhari, Clemer Abad, Marie E Maloof, et al.Genes|March 6, 2021
Spectrum of MYO7A Mutations in an Indigenous South African Population Further Elucidates the Nonsyndromic Autosomal Recessive Phenotype of DFNB2 to Include Both Homozygous and Compound Heterozygous MutationsRosemary Ida Kabahuma, Wolf-Dieter Schubert, Christiaan Labuschagne, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|April 22, 2021
Screening Strategies for Deafness Genes and Functional Outcomes in Cochlear Implant PatientsEric Nisenbaum, Sandra Prentiss, Denise Yan, et al.Pageof 14