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International Journal of Molecular Sciences
|
July 29, 2025
Molecular Mechanisms of Aminoglycoside-Induced Ototoxicity in Murine Auditory Cells: Implications for Otoprotective Drug Development
Cheng-Yu Hsieh, Jia-Ni Lin, Yi-Fan Chou, et al.
Plos One
|
October 1, 2020
Altered expression of genes regulating inflammation and synaptogenesis during regrowth of afferent neurons to cochlear hair cells
Chen-Chi Wu, Aurore Brugeaud, Richard Seist, et al.
The Laryngoscope
|
March 27, 2012
Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome
Shih-Hao Wang, Chen-Chi Wu, Ying-Chang Lu, et al.
Scientific Reports
|
August 10, 2017
A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss
Yin-Hung Lin, Yi-Hsin Lin, Ying-Chang Lu, et al.
ACS Applied Materials & Interfaces
|
December 15, 2025
Multifaced Generation of MOF Coatings via Vapor-Phase Sublimation and Deposition Reactions
Shu-Man Hu, Chin-Yun Lee, Yu-Ming Chang, et al.
The Laryngoscope
|
October 17, 2025
Bilateral Sudden on Chronic Hearing Loss as an Auditory Manifestation of Mitochondrial DNA Mutations
Chin-Nung Liu, Hong-Yu Yan, Steven Chun-Kang Liao, et al.
Hearing Research
|
August 6, 2025
The impact of transcranial ultrasound on auditory brainstem responses and neuronal activation in the cochlear nucleus
Shang-Yi Hsueh, Ying-Chang Lu, Jormay Lim, et al.
Stem Cell Research
|
May 11, 2020
Establishment of an induced pluripotent stem cell (iPSC) line from a 7-year-old male patient with profound hearing loss carrying c.235delC in GJB2 gene
Chun-Ying Huang, Yi-Hsiu Tsai, Yi-Ching Tsai, et al.
Stem Cell Research
|
October 14, 2018
Generation of induced pluripotent stem cells from a patient with hearing loss carrying GJB2 p.V37I mutation
Yen-Hui Chan, Yen-Fu Cheng, You-Tzung Chen, et al.
Orphanet Journal of Rare Diseases
|
June 15, 2024
High prevalence of exon-13 variants in USH2A-related retinal dystrophies in Taiwanese population
Yu-Wei Lin, Yu-Shu Huang, Chien-Yu Lin, et al.
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Showing results (51-60 of 112) with videos related to
Sort By:
Page
of 12
International Journal of Molecular Sciences
|
July 29, 2025
Molecular Mechanisms of Aminoglycoside-Induced Ototoxicity in Murine Auditory Cells: Implications for Otoprotective Drug Development
Cheng-Yu Hsieh, Jia-Ni Lin, Yi-Fan Chou, et al.
Plos One
|
October 1, 2020
Altered expression of genes regulating inflammation and synaptogenesis during regrowth of afferent neurons to cochlear hair cells
Chen-Chi Wu, Aurore Brugeaud, Richard Seist, et al.
The Laryngoscope
|
March 27, 2012
Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome
Shih-Hao Wang, Chen-Chi Wu, Ying-Chang Lu, et al.
Scientific Reports
|
August 10, 2017
A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss
Yin-Hung Lin, Yi-Hsin Lin, Ying-Chang Lu, et al.
ACS Applied Materials & Interfaces
|
December 15, 2025
Multifaced Generation of MOF Coatings via Vapor-Phase Sublimation and Deposition Reactions
Shu-Man Hu, Chin-Yun Lee, Yu-Ming Chang, et al.
The Laryngoscope
|
October 17, 2025
Bilateral Sudden on Chronic Hearing Loss as an Auditory Manifestation of Mitochondrial DNA Mutations
Chin-Nung Liu, Hong-Yu Yan, Steven Chun-Kang Liao, et al.
Hearing Research
|
August 6, 2025
The impact of transcranial ultrasound on auditory brainstem responses and neuronal activation in the cochlear nucleus
Shang-Yi Hsueh, Ying-Chang Lu, Jormay Lim, et al.
Stem Cell Research
|
May 11, 2020
Establishment of an induced pluripotent stem cell (iPSC) line from a 7-year-old male patient with profound hearing loss carrying c.235delC in GJB2 gene
Chun-Ying Huang, Yi-Hsiu Tsai, Yi-Ching Tsai, et al.
Stem Cell Research
|
October 14, 2018
Generation of induced pluripotent stem cells from a patient with hearing loss carrying GJB2 p.V37I mutation
Yen-Hui Chan, Yen-Fu Cheng, You-Tzung Chen, et al.
Orphanet Journal of Rare Diseases
|
June 15, 2024
High prevalence of exon-13 variants in USH2A-related retinal dystrophies in Taiwanese population
Yu-Wei Lin, Yu-Shu Huang, Chien-Yu Lin, et al.
Page
of 12