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Biochemical and Biophysical Research Communications
|
September 12, 2020
Generation and pathological characterization of a transgenic mouse model carrying a missense PJVK mutation
Yen-Fu Cheng, Yi-Hsiu Tsai, Chun-Ying Huang, et al.
Plos One
|
August 4, 2011
Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center
Chen-Chi Wu, Chia-Cheng Hung, Shin-Yu Lin, et al.
Medicine
|
July 14, 2015
Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing
Chen-Chi Wu, Yin-Hung Lin, Tien-Chen Liu, et al.
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.
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.
International Journal of Molecular Medicine
|
March 29, 2022
2,3,4',5‑Tetrahydroxystilbene‑2‑O‑β‑D‑glucoside ameliorates gentamicin‑induced ototoxicity by modulating autophagy via Sesn2/AMPK/mTOR signaling
Yu-Hsuan Wen, Hui-Yi Lin, Jia-Ni Lin, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 7, 2003
Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness
Hsiao-Lin Hwa, Tsang-Ming Ko, Chuan-Jen Hsu, et al.
Molecular Genetics & Genomic Medicine
|
November 4, 2022
Identification of nine novel variants across PAX3, SOX10, EDNRB, and MITF genes in Waardenburg syndrome with next-generation sequencing
Chen-Yu Lee, Ming-Yu Lo, You-Mei Chen, et al.
The Journal of Molecular Diagnostics : JMD
|
October 1, 2018
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct
Yin-Hung Lin, Chen-Chi Wu, Yi-Hsin Lin, et al.
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Search research articles
Search
Showing results (81-90 of 132) with videos related to
Sort By:
Page
of 14
Biochemical and Biophysical Research Communications
|
September 12, 2020
Generation and pathological characterization of a transgenic mouse model carrying a missense PJVK mutation
Yen-Fu Cheng, Yi-Hsiu Tsai, Chun-Ying Huang, et al.
Plos One
|
August 4, 2011
Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center
Chen-Chi Wu, Chia-Cheng Hung, Shin-Yu Lin, et al.
Medicine
|
July 14, 2015
Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing
Chen-Chi Wu, Yin-Hung Lin, Tien-Chen Liu, et al.
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.
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.
International Journal of Molecular Medicine
|
March 29, 2022
2,3,4',5‑Tetrahydroxystilbene‑2‑O‑β‑D‑glucoside ameliorates gentamicin‑induced ototoxicity by modulating autophagy via Sesn2/AMPK/mTOR signaling
Yu-Hsuan Wen, Hui-Yi Lin, Jia-Ni Lin, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 7, 2003
Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness
Hsiao-Lin Hwa, Tsang-Ming Ko, Chuan-Jen Hsu, et al.
Molecular Genetics & Genomic Medicine
|
November 4, 2022
Identification of nine novel variants across PAX3, SOX10, EDNRB, and MITF genes in Waardenburg syndrome with next-generation sequencing
Chen-Yu Lee, Ming-Yu Lo, You-Mei Chen, et al.
The Journal of Molecular Diagnostics : JMD
|
October 1, 2018
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct
Yin-Hung Lin, Chen-Chi Wu, Yi-Hsin Lin, et al.
Page
of 14