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Clinical and Experimental Otorhinolaryngology
|
February 13, 2025
Screening for Hearing Impairment in Newborns Using Targeted Genomic Sequencing: A Large Pilot Cohort Study
Pei-Hsuan Lin, Yu-Ting Chiang, Cheng-Yu Tsai, et al.
In Vivo (Athens, Greece)
|
April 28, 2022
Bisdemethoxycurcumin-mediated Attenuation of Apoptosis Prevents Gentamicin-induced Ototoxicity in Mouse Cochlear UB/OC-2 Cells
Ting-Ya Kang, Chuan-Jen Hsu, Jia-Ni Lin, et al.
Stem Cell Research
|
September 8, 2022
Generation of induced pluripotent stem cells from a patient with hearing loss carrying OPA1 c.1468T>C (p.Cys490Arg) variant
Yen-Hui Chan, Chang-Han Ho, Cheng-Yu Tsai, et al.
Clinical and Experimental Otorhinolaryngology
|
February 28, 2025
Predominance of Auditory but not Vestibular Deficits in the Mouse Model of Congenital Cytomegalovirus Infection
Chi-Chieh Chang, Ying-Chang Lu, Po-Nien Tsao, et al.
Stem Cell Research
|
March 18, 2023
Generation of induced pluripotent stem cells (IBMSi027-A) from a patient with hearing loss carrying WFS1 c.2051C > T (p.Ala684Val) variant
Yen-Hui Chan, Cheng-Yu Tsai, Chang-Han Ho, et al.
Plos One
|
August 4, 2011
Establishment of a knock-in mouse model with the SLC26A4 c.919-2A>G mutation and characterization of its pathology
Ying-Chang Lu, Chen-Chi Wu, Wen-Sheng Shen, 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 Anc80L65
Chin-Ju Hu, Ying-Chang Lu, Yi-Hsiu Tsai, et al.
Genes
|
April 28, 2023
Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population
Yen-Hui Lee, Cheng-Yu Tsai, Yue-Sheng Lu, 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 phasing
Pei-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 mutation
Yen-Fu Cheng, Yen-Hui Chan, Chin-Ju Hu, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 112) with videos related to
Sort By:
Page
of 12
Clinical and Experimental Otorhinolaryngology
|
February 13, 2025
Screening for Hearing Impairment in Newborns Using Targeted Genomic Sequencing: A Large Pilot Cohort Study
Pei-Hsuan Lin, Yu-Ting Chiang, Cheng-Yu Tsai, et al.
In Vivo (Athens, Greece)
|
April 28, 2022
Bisdemethoxycurcumin-mediated Attenuation of Apoptosis Prevents Gentamicin-induced Ototoxicity in Mouse Cochlear UB/OC-2 Cells
Ting-Ya Kang, Chuan-Jen Hsu, Jia-Ni Lin, et al.
Stem Cell Research
|
September 8, 2022
Generation of induced pluripotent stem cells from a patient with hearing loss carrying OPA1 c.1468T>C (p.Cys490Arg) variant
Yen-Hui Chan, Chang-Han Ho, Cheng-Yu Tsai, et al.
Clinical and Experimental Otorhinolaryngology
|
February 28, 2025
Predominance of Auditory but not Vestibular Deficits in the Mouse Model of Congenital Cytomegalovirus Infection
Chi-Chieh Chang, Ying-Chang Lu, Po-Nien Tsao, et al.
Stem Cell Research
|
March 18, 2023
Generation of induced pluripotent stem cells (IBMSi027-A) from a patient with hearing loss carrying WFS1 c.2051C > T (p.Ala684Val) variant
Yen-Hui Chan, Cheng-Yu Tsai, Chang-Han Ho, et al.
Plos One
|
August 4, 2011
Establishment of a knock-in mouse model with the SLC26A4 c.919-2A>G mutation and characterization of its pathology
Ying-Chang Lu, Chen-Chi Wu, Wen-Sheng Shen, 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 Anc80L65
Chin-Ju Hu, Ying-Chang Lu, Yi-Hsiu Tsai, et al.
Genes
|
April 28, 2023
Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population
Yen-Hui Lee, Cheng-Yu Tsai, Yue-Sheng Lu, 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 phasing
Pei-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 mutation
Yen-Fu Cheng, Yen-Hui Chan, Chin-Ju Hu, et al.
Page
of 12