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Yen-Fu Cheng

Showing results (101-110 of 111) with videos related to

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International Journal of Molecular Sciences|April 3, 2021
Toward the Pathogenicity of the <i>SLC26A4</i> p.C565Y Variant Using a Genetically Driven Mouse ModelChin-Ju Hu, Ying-Chang Lu, Ting-Hua Yang, et al.
Molecular Medicine (Cambridge, Mass.)|May 9, 2025
Unraveling the complex genetic landscape of OTOF-related hearing loss: a deep dive into cryptic variants and haplotype phasingPei-Hsuan Lin, Cheng-Yu Tsai, Yu-Ting Chiang, et al.
Stem Cell Research|August 16, 2019
Generation of a human iPS cell line (CGMH.SLC26A4919-2) from a Pendred syndrome patient carrying SLC26A4 c.919-2A>G splice-site mutationYen-Fu Cheng, Yen-Hui Chan, Chin-Ju Hu, et al.
Molecular Therapy. Methods & Clinical Development|August 11, 2020
Efficient in Utero Gene Transfer to the Mammalian Inner Ears by the Synthetic Adeno-Associated Viral Vector Anc80L65Chin-Ju Hu, Ying-Chang Lu, Yi-Hsiu Tsai, et al.
Genes|October 5, 2019
Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese PopulationChen-Chi Wu, Cheng-Yu Tsai, Yi-Hsin Lin, et al.
Scientific Reports|October 26, 2021
Insights into phenotypic differences between humans and mice with p.T721M and other C-terminal variants of the SLC26A4 geneChin-Ju Hu, Ying-Chang Lu, Cheng-Yu Tsai, et al.
International Journal of Molecular Sciences|June 13, 2025
Low Efficiency of Homology-Independent Targeted Integration for CRISPR/Cas9 Correction in the Vicinity of the <i>SLC26A4</i> c.919-2A>G VariantChang-Han Ho, Cheng-Yu Tsai, Chi-Chieh Chang, et al.
Ear and Hearing|January 2, 2022
Hearing Features and Cochlear Implantation Outcomes in Patients With Pathogenic MYO15A Variants: a Multicenter Observational StudyPey-Yu Chen, Cheng-Yu Tsai, Jiunn-Liang Wu, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 16, 2021
International Survey of Operative Practices for Otologists and Neurotologists During the COVID-19 CrisisSarah E Ridge, Divya A Chari, Elliott D Kozin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2019
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert PanelJun Shen, Andrea M Oza, Ignacio Del Castillo, et al.
Pageof 12

Showing results (101-110 of 111) with videos related to

Sort By:
Pageof 12
International Journal of Molecular Sciences|April 3, 2021
Toward the Pathogenicity of the <i>SLC26A4</i> p.C565Y Variant Using a Genetically Driven Mouse ModelChin-Ju Hu, Ying-Chang Lu, Ting-Hua Yang, et al.
Molecular Medicine (Cambridge, Mass.)|May 9, 2025
Unraveling the complex genetic landscape of OTOF-related hearing loss: a deep dive into cryptic variants and haplotype phasingPei-Hsuan Lin, Cheng-Yu Tsai, Yu-Ting Chiang, et al.
Stem Cell Research|August 16, 2019
Generation of a human iPS cell line (CGMH.SLC26A4919-2) from a Pendred syndrome patient carrying SLC26A4 c.919-2A>G splice-site mutationYen-Fu Cheng, Yen-Hui Chan, Chin-Ju Hu, et al.
Molecular Therapy. Methods & Clinical Development|August 11, 2020
Efficient in Utero Gene Transfer to the Mammalian Inner Ears by the Synthetic Adeno-Associated Viral Vector Anc80L65Chin-Ju Hu, Ying-Chang Lu, Yi-Hsiu Tsai, et al.
Genes|October 5, 2019
Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese PopulationChen-Chi Wu, Cheng-Yu Tsai, Yi-Hsin Lin, et al.
Scientific Reports|October 26, 2021
Insights into phenotypic differences between humans and mice with p.T721M and other C-terminal variants of the SLC26A4 geneChin-Ju Hu, Ying-Chang Lu, Cheng-Yu Tsai, et al.
International Journal of Molecular Sciences|June 13, 2025
Low Efficiency of Homology-Independent Targeted Integration for CRISPR/Cas9 Correction in the Vicinity of the <i>SLC26A4</i> c.919-2A>G VariantChang-Han Ho, Cheng-Yu Tsai, Chi-Chieh Chang, et al.
Ear and Hearing|January 2, 2022
Hearing Features and Cochlear Implantation Outcomes in Patients With Pathogenic MYO15A Variants: a Multicenter Observational StudyPey-Yu Chen, Cheng-Yu Tsai, Jiunn-Liang Wu, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 16, 2021
International Survey of Operative Practices for Otologists and Neurotologists During the COVID-19 CrisisSarah E Ridge, Divya A Chari, Elliott D Kozin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2019
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert PanelJun Shen, Andrea M Oza, Ignacio Del Castillo, et al.
Pageof 12