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CHEN-CHI WU
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簡歷
研究成果
100
計畫
42
計畫
(Principal Investigator)
Principal Investigator
共同研究人員
顯示/隱藏過濾條件
起始日期
12
2020 - 2023
25
2010 - 2019
5
2007 - 2009
關閉過濾條件
第 1 到 42 筆結果,共 42 筆。
啟始時間
標題
P-Investigator
經費來源
2023
Development of Absorbable Middle Ear Ventilation Tube
CHEN-CHI WU
National Science and Technology Council
2023
Precision medicine of childhood hearing impairment
CHEN-CHI WU
National Institutes of Health (NIH)
2023
蒙古人民特發性聽損之基因研究
CHEN-CHI WU
National Science and Technology Council
2022
Very Low Intensity Ultrasound Facilitated Gene Therapy for Hereditary Hearing Impairment (II)
CHEN-CHI WU
National Science and Technology Council
2022
To Optimize the Genetic Diagnostics and High Polymer-Based Molecular Therapeutics for Hearing Impairment
CHEN-CHI WU
National Science and Technology Council
2022
Precision medicine of childhood hearing impairment
CHEN-CHI WU
National Institutes of Health (NIH)
2021
To Optimize the Genetic Diagnostics and High Polymer-Based Molecular Therapeutics for Hearing Impairment
CHEN-CHI WU
National Science and Technology Council
2021
Very Low Intensity Ultrasound Facilitated Gene Therapy for Hereditary Hearing Impairment (I)
CHEN-CHI WU
National Science and Technology Council
2021
Development of a Novel Method, Protocol and Reagent for Rapid Newborn Genetic Screening of Hearing Impairment
CHEN-CHI WU
National Science and Technology Council
2021
Precision medicine of childhood hearing impairment
CHEN-CHI WU
National Institutes of Health (NIH)
2020
Establishing Next-Generation Sequencing Database for Hereditary Hearing Impairment and Applying Artificial Intelligence to Facilitate Genetic Diagnosis and Prognosis Prediction
CHEN-CHI WU
National Science and Technology Council
2020
Precision medicine of childhood hearing impairment
CHEN-CHI WU
National Institutes of Health (NIH)
2019
Development of a Novel Method, Protocol and Reagent for Genetic Testing of Hearing Loss Using the Next-Generation Sequencing (II)
CHEN-CHI WU
National Science and Technology Council
2019
Hereditary Hearing Impairment: Whole Genome Sequencing and Therapeutic Genome Editing (In Transgenic Mice)
CHEN-CHI WU
National Science and Technology Council
2019
Establishing Next-Generation Sequencing Database for Hereditary Hearing Impairment and Applying Artificial Intelligence to Facilitate Genetic Diagnosis and Prognosis Prediction
CHEN-CHI WU
National Science and Technology Council
2018
Development of a Novel Method, Protocol and Reagent for Genetic Testing of Hearing Loss Using the Next-Generation Sequencing (I)
CHEN-CHI WU
National Science and Technology Council
2018
Establishing Next-Generation Sequencing Database for Hereditary Hearing Impairment and Applying Artificial Intelligence to Facilitate Genetic Diagnosis and Prognosis Prediction
CHEN-CHI WU
National Science and Technology Council
2018
Molecular genetic studies of hereditary hearing impairment
CHEN-CHI WU
National Institutes of Health (NIH)
2017
Establishing Platforms for Validating the Pathogenetic Mechasnisms of Deafness Genetic Mutations by Combining the “Talen Genomic Editing Technique” and “Zebrafish/Mouse Animal Models”
CHEN-CHI WU
National Science and Technology Council
2017
Molecular genetic studies of hereditary hearing impairment
CHEN-CHI WU
National Institutes of Health (NIH)
2016
Genetic Epidemiological Study and Construction of the Dna Sample Bank in Mongolian Patients with Hereditary Hearing Impairment
CHEN-CHI WU
National Science and Technology Council
2016
Exploring the Pathogenetic Mechanisms of SLC26A4 Mutations with Next Generation Sequencing and Developing Novel Therapeutic Strategies
CHEN-CHI WU
National Science and Technology Council
2016
Establishing Platforms for Validating the Pathogenetic Mechasnisms of Deafness Genetic Mutations by Combining the “Talen Genomic Editing Technique” and “Zebrafish/Mouse Animal Models”
CHEN-CHI WU
National Science and Technology Council
2016
Molecular genetic studies of hereditary hearing impairment
CHEN-CHI WU
National Health Research Institutes
2015
Establishing Platforms for Validating the Pathogenetic Mechasnisms of Deafness Genetic Mutations by Combining the “TALEN Genomic Editing Technique” and “Zebrafish/Mouse Animal Models”
CHEN-CHI WU
National Science and Technology Council
2015
Exploring the Pathogenetic Mechanisms of SLC26A4 Mutations with Next Generation Sequencing and Developing Novel Therapeutic Strategies
CHEN-CHI WU
National Science and Technology Council
2015
The Evaluation and Development of Infectious Disease Control Application by Integrating CDC and Other Governmental Health Related Databases
CHEN-CHI WU
National Science and Technology Council
2015
Molecular genetic studies of hereditary hearing impairment
CHEN-CHI WU
National Health Research Institutes
2014
Exploring the Pathogenetic Mechanisms of SLC26A4 Mutations with Next Generation Sequencing and Developing Novel Therapeutic Strategies
CHEN-CHI WU
National Science and Technology Council
2014
Establishing Platforms for Validating the Pathogenetic Mechasnisms of Deafness Genetic Mutations by Combining the “Talen Genomic Editing Technique” and “Zebrafish/Mouse Animal Models”
CHEN-CHI WU
National Science and Technology Council
2013
Using candidate gene approach and next generation sequencing to investigate age-related hearing impairment, followed by establishment of animal models
CHEN-CHI WU
National Science and Technology Council
2012
Using Candidate Gene Approach and Next Generation Sequencing to Investigate Age-Related Hearing Impairment, Followed by Establishment of Animal Models
CHEN-CHI WU
National Science and Technology Council
2012
Investigating Enlarged Vestibular Aqueduct Syndrome by Using Knock-In Mice Model with Slc26a4 Mutations: the Clarification of Pathogenetic Mechanisms and the Development of Novel Therapeutic Strategies
CHEN-CHI WU
National Science and Technology Council
2011
Investigating Enlarged Vestibular Aqueduct Syndrome by Using Knock-In Mice Model with Slc26a4 Mutations: the Clarification of Pathogenetic Mechanisms and the Development of Novel Therapeutic Strategies
CHEN-CHI WU
National Science and Technology Council
2011
Using Candidate Gene Approach and Next Generation Sequencing to Investigate Age-Related Hearing Impairment, Followed by Establishment of Animal Models
CHEN-CHI WU
National Science and Technology Council
2010
Development of an Efficient and Low-Cost Diagnostic Tool to Promote Genetic Examination in Taiwanese Patients with Hearing Impairment
CHEN-CHI WU
National Science and Technology Council
2010
Investigating Enlarged Vestibular Aqueduct Syndrome by Using Knock-In Mice Model with SLC26A4 Mutations: the Clarification of Pathogenetic Mechanisms and the Development of Novel Therapeutic Strategies
CHEN-CHI WU
National Science and Technology Council
2009
Development of an Efficient and Low-Cost Diagnostic Tool to Promote Genetic Examination in Taiwanese Patients with Hearing Impairment
CHEN-CHI WU
National Science and Technology Council
2009
Applying 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 Models
CHEN-CHI WU
National Science and Technology Council
2008
Development of an Efficient and Low-Cost Diagnostic Tool to Promote Genetic Examination in Taiwanese Patients with Hearing Impairment
CHEN-CHI WU
National Science and Technology Council
2008
Applying 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 Models
CHEN-CHI WU
National Science and Technology Council
2007
Applying 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 Models
CHEN-CHI WU
National Science and Technology Council
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