計畫


第 1 到 42 筆結果，共 42 筆。

啟始時間標題P-Investigator經費來源
2023Development of Absorbable Middle Ear Ventilation TubeCHEN-CHI WUNational Science and Technology Council
2023Precision medicine of childhood hearing impairmentCHEN-CHI WUNational Institutes of Health (NIH)
2023蒙古人民特發性聽損之基因研究CHEN-CHI WUNational Science and Technology Council
2022Very Low Intensity Ultrasound Facilitated Gene Therapy for Hereditary Hearing Impairment (II)CHEN-CHI WUNational Science and Technology Council
2022To Optimize the Genetic Diagnostics and High Polymer-Based Molecular Therapeutics for Hearing ImpairmentCHEN-CHI WUNational Science and Technology Council
2022Precision medicine of childhood hearing impairmentCHEN-CHI WUNational Institutes of Health (NIH)
2021To Optimize the Genetic Diagnostics and High Polymer-Based Molecular Therapeutics for Hearing ImpairmentCHEN-CHI WUNational Science and Technology Council
2021Very Low Intensity Ultrasound Facilitated Gene Therapy for Hereditary Hearing Impairment (I)CHEN-CHI WUNational Science and Technology Council
2021Development of a Novel Method, Protocol and Reagent for Rapid Newborn Genetic Screening of Hearing ImpairmentCHEN-CHI WUNational Science and Technology Council
2021Precision medicine of childhood hearing impairmentCHEN-CHI WUNational Institutes of Health (NIH)
2020Establishing Next-Generation Sequencing Database for Hereditary Hearing Impairment and Applying Artificial Intelligence to Facilitate Genetic Diagnosis and Prognosis PredictionCHEN-CHI WUNational Science and Technology Council
2020Precision medicine of childhood hearing impairmentCHEN-CHI WUNational Institutes of Health (NIH)
2019Development of a Novel Method, Protocol and Reagent for Genetic Testing of Hearing Loss Using the Next-Generation Sequencing (II)CHEN-CHI WUNational Science and Technology Council
2019Hereditary Hearing Impairment: Whole Genome Sequencing and Therapeutic Genome Editing (In Transgenic Mice)CHEN-CHI WUNational Science and Technology Council
2019Establishing Next-Generation Sequencing Database for Hereditary Hearing Impairment and Applying Artificial Intelligence to Facilitate Genetic Diagnosis and Prognosis PredictionCHEN-CHI WUNational Science and Technology Council
2018Development of a Novel Method, Protocol and Reagent for Genetic Testing of Hearing Loss Using the Next-Generation Sequencing (I)CHEN-CHI WUNational Science and Technology Council
2018Establishing Next-Generation Sequencing Database for Hereditary Hearing Impairment and Applying Artificial Intelligence to Facilitate Genetic Diagnosis and Prognosis PredictionCHEN-CHI WUNational Science and Technology Council
2018Molecular genetic studies of hereditary hearing impairmentCHEN-CHI WUNational Institutes of Health (NIH)
2017Establishing Platforms for Validating the Pathogenetic Mechasnisms of Deafness Genetic Mutations by Combining the “Talen Genomic Editing Technique” and “Zebrafish/Mouse Animal Models”CHEN-CHI WUNational Science and Technology Council
2017Molecular genetic studies of hereditary hearing impairmentCHEN-CHI WUNational Institutes of Health (NIH)
2016Genetic Epidemiological Study and Construction of the Dna Sample Bank in Mongolian Patients with Hereditary Hearing ImpairmentCHEN-CHI WUNational Science and Technology Council
2016Exploring the Pathogenetic Mechanisms of SLC26A4 Mutations with Next Generation Sequencing and Developing Novel Therapeutic StrategiesCHEN-CHI WUNational Science and Technology Council
2016Establishing Platforms for Validating the Pathogenetic Mechasnisms of Deafness Genetic Mutations by Combining the “Talen Genomic Editing Technique” and “Zebrafish/Mouse Animal Models”CHEN-CHI WUNational Science and Technology Council
2016Molecular genetic studies of hereditary hearing impairmentCHEN-CHI WUNational Health Research Institutes
2015Exploring the Pathogenetic Mechanisms of SLC26A4 Mutations with Next Generation Sequencing and Developing Novel Therapeutic StrategiesCHEN-CHI WUNational Science and Technology Council
2015Establishing Platforms for Validating the Pathogenetic Mechasnisms of Deafness Genetic Mutations by Combining the “TALEN Genomic Editing Technique” and “Zebrafish/Mouse Animal Models”CHEN-CHI WUNational Science and Technology Council
2015The Evaluation and Development of Infectious Disease Control Application by Integrating CDC and Other Governmental Health Related DatabasesCHEN-CHI WUNational Science and Technology Council
2015Molecular genetic studies of hereditary hearing impairmentCHEN-CHI WUNational Health Research Institutes
2014Exploring the Pathogenetic Mechanisms of SLC26A4 Mutations with Next Generation Sequencing and Developing Novel Therapeutic StrategiesCHEN-CHI WUNational Science and Technology Council
2014Establishing Platforms for Validating the Pathogenetic Mechasnisms of Deafness Genetic Mutations by Combining the “Talen Genomic Editing Technique” and “Zebrafish/Mouse Animal Models”CHEN-CHI WUNational Science and Technology Council
2013Using candidate gene approach and next generation sequencing to investigate age-related hearing impairment, followed by establishment of animal modelsCHEN-CHI WUNational Science and Technology Council
2012Using Candidate Gene Approach and Next Generation Sequencing to Investigate Age-Related Hearing Impairment, Followed by Establishment of Animal ModelsCHEN-CHI WUNational Science and Technology Council
2012Investigating Enlarged Vestibular Aqueduct Syndrome by Using Knock-In Mice Model with Slc26a4 Mutations: the Clarification of Pathogenetic Mechanisms and the Development of Novel Therapeutic StrategiesCHEN-CHI WUNational Science and Technology Council
2011Investigating Enlarged Vestibular Aqueduct Syndrome by Using Knock-In Mice Model with Slc26a4 Mutations: the Clarification of Pathogenetic Mechanisms and the Development of Novel Therapeutic StrategiesCHEN-CHI WUNational Science and Technology Council
2011Using Candidate Gene Approach and Next Generation Sequencing to Investigate Age-Related Hearing Impairment, Followed by Establishment of Animal ModelsCHEN-CHI WUNational Science and Technology Council
2010Development of an Efficient and Low-Cost Diagnostic Tool to Promote Genetic Examination in Taiwanese Patients with Hearing ImpairmentCHEN-CHI WUNational Science and Technology Council
2010Investigating Enlarged Vestibular Aqueduct Syndrome by Using Knock-In Mice Model with SLC26A4 Mutations: the Clarification of Pathogenetic Mechanisms and the Development of Novel Therapeutic StrategiesCHEN-CHI WUNational Science and Technology Council
2009Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients with SLC26A4 Mutations: Double-Blind Randomized Clinical Trials, Functional Genetic Studies in Cell Lines and the Establishment of Animal ModelsCHEN-CHI WUNational Science and Technology Council
2009Development of an Efficient and Low-Cost Diagnostic Tool to Promote Genetic Examination in Taiwanese Patients with Hearing ImpairmentCHEN-CHI WUNational Science and Technology Council
2008Development of an Efficient and Low-Cost Diagnostic Tool to Promote Genetic Examination in Taiwanese Patients with Hearing ImpairmentCHEN-CHI WUNational Science and Technology Council
2008Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients with SLC26A4 Mutations: Double-Blind Randomized Clinical Trials, Functional Genetic Studies in Cell Lines and the Establishment of Animal ModelsCHEN-CHI WUNational Science and Technology Council
2007Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients with SLC26A4 Mutations---Double-Blind Randomized Clinical Trials, Functional Genetic Studies in Cell Lines and the Establishment of Animal ModelsCHEN-CHI WUNational Science and Technology Council