單位人員計畫
(單位計畫)


第 1 到 176 筆結果，共 176 筆。

啟始時間標題P-Investigator經費來源
2023Study of Time since Deposition and Determination Stabilization Based on Microrna and Mrna Markers and Using Rna/Dna Co-Analysis System of Massively Parallel Sequencing for Body Fluid Linking Individual Identification to Donors in Body Fluid MixturesHSIAO-LIN HWANational Science and Technology Council
2023The Impacts of Gut Microbiome on the Therapeutic Efficacy of Immunotherapy and the Corresponding Mouse Model and Underling Mechanism Exploration in Head and Neck CancerCHI-MAW LINNational Science and Technology Council
2023Artificial Intelligence Powered Cervical Stiffness Prediction for Preterm Delivery Risk Assessment and Labor Induction OutcomesYI-YUN TAINational Science and Technology Council
2023Molecular Profiles of Primary Versus Metastatic Thyroid Cancers in TaiwanSHYANG-RONG SHIHNational Science and Technology Council
2023Genomics, Molecular Subtyping and Mechanism of Parent-Of-Origin Effects of Pheochromocytoma and Paraganglioma in TaiwanWAN-CHEN WUNational Science and Technology Council
2023Exploring the Neural Network and Strategies of Preservation in Inherited Retinal DegenerationTA-CHING CHENNational Science and Technology Council
2023Gene Editing Therapy for Acute Hepatic PorphyriasNI-CHUNG LEENational Science and Technology Council
2022Artificial Intelligence Application in Screening for Spontaneous Preterm Birth by Cervical Length and Shear-Wave ElastographyYI-YUN TAINational Science and Technology Council
2022C5a Induced Proteinuria in Murine Model-The Role of Cytokine and T Cell Part Ii: the Pathological Roles of Il-6 TransactivationI-JUNG TSAINational Science and Technology Council
2022Development of a New Panel with Multiple Single Nucleotide Polymorphism/Short Tandem Repeat Markers of Rna/Dna Using Massively Parallel Sequencing and Neural Networks for Body Fluid and Individual Identification and Linking Body Fluid to Donor in MixturesHSIAO-LIN HWANational Science and Technology Council
2022Whole Genome Sequencing and Functional Validation for Unsolved Families of Retinitis PigmentosaTA-CHING CHENNational Science and Technology Council
2022Exploring the Neural Network and Strategies of Preservation in Inherited Retinal DegenerationTA-CHING CHENNational Science and Technology Council
2022Evolution of Dopaminergic Neurons in Aromatic L-Amino Acid Decarboxylase DeficiencyNI-CHUNG LEENational Science and Technology Council
2022Functional Disturbances of Mpnst Cells Post the Treatment of CordycepinMING-JEN LEENational Science and Technology Council
2022Manipulation of Neuronal Cholesterol Fluxes in Niemann-Pick Type C Disease MiceWUH-LIANG ​​HWUNational Science and Technology Council
2022Development of Gene Editing Therapy for Pompe DiseaseYIN-HSIU CHIENNational Science and Technology Council
2022Molecular Profiles of Primary Versus Metastatic Thyroid Cancers in TaiwanSHYANG-RONG SHIHNational Science and Technology Council
2022Genomics, Molecular Subtyping and Mechanism of Parent-Of-Origin Effects of Pheochromocytoma and Paraganglioma in TaiwanWAN-CHEN WUNational Science and Technology Council
2021Whole Genome Sequencing and Functional Validation for Unsolved Families of Retinitis PigmentosaTA-CHING CHENNational Science and Technology Council
2021Building a Disease Prediction Model for Type 1 Diabetes through Multi-Omics (Continuation Plan)YI-CHING TUNGNational Science and Technology Council
2021Development of gene editing therapy for Pompe diseaseYIN-HSIU CHIENNational Science and Technology Council
2021Combine Use of Bone Ultrasound Velocity and Dried Blood Spots for Vitamin D Level to Set up a New Screening Protocol of Metabolic Bone Disease of PrematurityCHIEN-YI CHENNational Science and Technology Council
2021Evolution of Dopaminergic Neurons in Aromatic L-Amino Acid Decarboxylase DeficiencyNI-CHUNG LEENational Science and Technology Council
2021Functional Disturbances of Mpnst Cells Post the Treatment of CordycepinMING-JEN LEENational Science and Technology Council
2021Manipulation of Neuronal Cholesterol Fluxes in Niemann-Pick Type C Disease MiceWUH-LIANG ​​HWUNational Science and Technology Council
2021Integrated Genomic and Immunological Study of Autoimmune Thyroid Disease and Related-Phenotypes – Focusing on the Single-Cell RNA Sequencing ApproachPEI-LUNG CHENNational Science and Technology Council
2021開發一整套奈米孔長片段定序之標靶區域富集及錯誤校正全新方法(1/2)PEI-LUNG CHENNational Science and Technology Council
2021基因研究與次世代定序資料的判讀及分析WUH-LIANG ​​HWU
2021臺大與中研院創新性合作計畫【創新穩定蛋白之小分子並用於探討龐貝氏症的治療效果】WUH-LIANG ​​HWUHigher Education Sprout Project
2020Deciphering the Autism Spectrum Disorder beyond Genomics: Ai Learning for Whole Exome Sequencing, Metabolomics and PhenotypeSUSAN SHUR-FEN GAUNational Science and Technology Council
2020The Impact of Rett-Related Genes in Neurological Function (Third Phase)LEE-CHIN WONGNational Science and Technology Council
2020To Explore the Genetic and Environmental Factors Associated with Breast Cancer Risk in Taiwan Brca Mutation Carriers and Search for New Methods to Reduce CancerPO-HAN LINNational Science and Technology Council
2020Assay of Single Source and Mixed Touch Dna Samples Using Massive Parallel Sequencing and Data Analysis Using Deep Neural Networks for Individual IdentificationHSIAO-LIN HWANational Science and Technology Council
2020Evolution of Dopaminergic Neurons in Aromatic L-Amino Acid Decarboxylase DeficiencyNI-CHUNG LEENational Science and Technology Council
2020Functional Disturbances of Mpnst Cells Post the Treatment of CordycepinMING-JEN LEENational Science and Technology Council
2020Manipulation of Neuronal Cholesterol Fluxes in Niemann-Pick Type C Disease MiceWUH-LIANG ​​HWUNational Science and Technology Council
2020Integrated Genomic and Immunological Study of Autoimmune Thyroid Disease and Related-Phenotypes – Focusing on the Single-Cell RNA Sequencing ApproachPEI-LUNG CHENNational Science and Technology Council
2020Development of the Novel Method, Protocol and Reagent for Genotyping of the Killer Cell Immunoglobulin-Like Receptor (Kir) GenesPEI-LUNG CHENNational Science and Technology Council
2020藥物基因體資料整理計畫WUH-LIANG ​​HWU
2019Assay of Mixtures of Minor Contributors’ Degraded Dna and Major Contributors’ Nondegraded Dna Using Massive Parallel Sequencing and Data Analysis Using Deep Learning Models of Artificial Intelligence for Individual IdentificationHSIAO-LIN HWANational Science and Technology Council
2019Gene Editing Treatments for Aromatic L-Amino Acid Decarboxylase (Aadc) DeficiencyWUH-LIANG ​​HWUNational Science and Technology Council
2019Effectiveness for the Preclinical Studies Combining Chemotherapeutic Agents and Photodynamic Therapy in Mouse Models with Nf1-Associated Malignant NeurofibromaMING-JEN LEENational Science and Technology Council
2019The Impact of Rett-Related Genes in Neurological Function (Second Phase)LEE-CHIN WONGNational Science and Technology Council
2019Analysis of Mitochondrial Dna Structural Abnormality by Long-Read Next Generation SequencingNI-CHUNG LEENational Science and Technology Council
2019Integrated Genomic and Immunological Study of Autoimmune Thyroid Disease and Related-Phenotypes – Focusing on the Single-Cell RNA Sequencing ApproachPEI-LUNG CHENNational Science and Technology Council
2019Development of the Novel Method, Protocol and Reagent for Genotyping of the Human Leukocyte Antigen (HLA) Genes (II/II)PEI-LUNG CHENNational Science and Technology Council
2019Rapid Genetic Diagnosis Employing Next Generation Sequencing for Critical Illness in Infants and ChildrenWUH-LIANG ​​HWUNational Science and Technology Council
2019Graves’ disease: genomic study, immunological investigation and animal models-third yearPEI-LUNG CHENNTUH
2019高等教育深耕計畫－核心研究群計畫－以單細胞轉譯體及免疫套組研究自體免疫甲狀腺疾病PEI-LUNG CHENHigher Education Sprout Project
2019Resarch of Blood Biomarkers of Alzheimer'S Disease and Its Related Disorders - New Index and Algorithm( III )MING-JANG CHIUNational Science and Technology Council
2019纖維肌痛症調控酸的止痛作用與酸痛感的分子遺傳機制：從病患到小鼠的轉譯醫學研究PEI-LUNG CHENInstitute of Biomedical Sciences, Academia Sinica
2018Assay of Mixtures of Minor Contributors’ Degraded Dna and Major Contributors’ Nondegraded Dna Using Massive Parallel Sequencing and Data Analysis Using Deep Learning Models of Artificial Intelligence for Individual IdentificationHSIAO-LIN HWANational Science and Technology Council
2018Research on the Mechanism of Tumoricidal Effect of Nf1-Related Malignant Peripheral Nerve Sheath Tumor with Calebin-AMING-JEN LEENational Science and Technology Council
2018Using Exosome and Next Generation Sequencing to Help the Diagnosis of Thyroid Nodules Which Are Undiagnosable by the Fine Needle Aspiration Cytology ExaminationSHYANG-RONG SHIHNational Science and Technology Council
2018The Impact of Rett-Related Genes in Neurological FunctionsLEE-CHIN WONGNational Science and Technology Council
2018Gene Editing Treatments for Aromatic L-Amino Acid Decarboxylase (Aadc) DeficiencyWUH-LIANG ​​HWUNational Science and Technology Council
2018Modulation of Neuronal Activity in Aromatic L-Amino Acid Decarboxylase DeficiencyNI-CHUNG LEENational Science and Technology Council
2018Development of the Novel Method, Protocol and Reagent for Genotyping of the Human Leukocyte Antigen (HLA) Genes (I)PEI-LUNG CHENNational Science and Technology Council
2018Rapid Genetic Diagnosis Employing Next Generation Sequencing for Critical Illness in Infants and Children( II )WUH-LIANG ​​HWU
2018Graves’ disease: genomic study, immunological investigation and animal models-second yearPEI-LUNG CHENNTUH
2018Establishment of a single-cell immune repertoire platform and application to a murine model of autoimmune cholangitisPEI-LUNG CHENNTUH; National Taiwan University
2018Resarch of Blood Biomarkers of Alzheimer'S Disease and Its Related Disorders - New Index and Algorithm( II )MING-JANG CHIUNational Science and Technology Council
2017Development of a New Multiple Short Tandem Repeat and Single Nucleotide Polymorphism Loci Individual Identification Panel for Massively Parallel Sequencing to Identify Dna MixtureHSIAO-LIN HWANational Science and Technology Council
2017Explore the Utility of Minimally-Invasive Procedures and Molecular Testing?As the Diagnostic Approaches for Thyroid NodulesCHUN-NAN CHENNational Science and Technology Council
2017Research on the Mechanism of Tumoricidal Effect of Nf1-Related Malignant Peripheral Nerve Sheath Tumor with Calebin-AMING-JEN LEENational Science and Technology Council
2017Gene Editing Treatments for Aromatic L-Amino Acid Decarboxylase (Aadc) DeficiencyWUH-LIANG ​​HWUNational Science and Technology Council
2017Modulation of Neuronal Activity in Aromatic L-Amino Acid Decarboxylase DeficiencyNI-CHUNG LEENational Science and Technology Council
2017Rapid Genetic Diagnosis Employing Next Generation Sequencing for Critical Illness in Infants and Children( I )WUH-LIANG ​​HWUNational Science and Technology Council
2017Identification of novel causative genes of pheochromocytoma and paraganglioma through next-generation sequencingPEI-LUNG CHENNTUH
2017Graves’ disease: genomic study, immunological investigation and animal models-first yearPEI-LUNG CHENNTUH
2017Resarch of Blood Biomarkers of Alzheimer'S Disease and Its Related Disorders - New Index and Algorithm( I )MING-JANG CHIUNational Science and Technology Council
2016A Phase I/Ii Clinical Trial for Treatment of Aromatic L-Amino Acid Decarboxylase (Aadc) Deficiency Using Aav2-Haadc( III )WUH-LIANG ​​HWUNational Science and Technology Council
2016Genetic study and immunological analysis of Graves’ disease and antithyroid drug-induced adverse effectsPEI-LUNG CHENNational Science and Technology Council
2016Development of a New Multiple Short Tandem Repeat and Single Nucleotide Polymorphism Loci Individual Identification Panel for Massively Parallel Sequencing to Identify Dna MixtureHSIAO-LIN HWANational Science and Technology Council
2016Intervention of Ultrasound-Guided Techniques in Indeterminate Thyroid Nodules: Significance and Implication for Molecular Diagnoses and Clinical ManagementCHUN-NAN CHENNational Science and Technology Council
2016Advanced Exploration of Novel Genetic Causes of Familial Parkinson’s Disease---Next Generation Sequencing Analyses and Functional StudyCHIN-HSIEN LINNational Science and Technology Council
2016Osteonecrosis of the Jaw Induced by Oral Bisphosphonates for Osteoporosis: Pharmacogenomics Study and Prediction ModelWEI-YIH CHIUNational Science and Technology Council
2016Research on the Mechanism of Tumoricidal Effect of Nf1-Related Malignant Peripheral Nerve Sheath Tumor with Calebin-AMING-JEN LEENational Science and Technology Council
2016Genetic Study and Immunological Analysis of Graves$ Disease and Antithyroid Drug-Induced Adverse EffectsPEI-LUNG CHENNational Science and Technology Council
2016A Study on the Residual Symptoms of the Early-Treated Patients with Pompe DiseaseYIN-HSIU CHIENNational Science and Technology Council
2016Modulation of Neuronal Activity in Aromatic L-Amino Acid Decarboxylase DeficiencyNI-CHUNG LEENational Science and Technology Council
2016Prospective recruitment of a new cohort of Graves’ disease patients to study the pathophysiology of anti-thyroid drug-induced agranulocytosisPEI-LUNG CHEN
2016Genetic study of anti-thyroid drug-induced agranulocytosisPEI-LUNG CHENNational Taiwan University Hospital
2016Identification of novel genetic mechanism and novel causative genes of tuberous sclerosis complexPEI-LUNG CHENNTUH
2016Establishing a pharmacogenomics testing platform and searching for possible genetic causes of aberrant drug responsePEI-LUNG CHENNTUH; National Taiwan University
2016Anti-thyroid drug-induced agranulocytosis: investigation of disease mechanism and establishment of a prospective patient cohortPEI-LUNG CHENAcademia Sinica
2015A Phase I/II Clinical Trial for Treatment of Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency Using AAV2-HAADC (II)WUH-LIANG ​​HWUNational Science and Technology Council
2015Identification of the susceptibility genes of anti-thyroid drug-induced agranulocytosis, and establishment of humanized MHC mouse for study of immune-related diseasePEI-LUNG CHENNational Science and Technology Council
2015Individual Identification and Parentage Testing of Fragmented DNA Mixtures with Multiple Single Nucleotide Polymorphism Analysis Using Next Generation Sequencing (NGS)HSIAO-LIN HWANational Science and Technology Council
2015Advanced Exploration of Novel Genetic Causes of Familial Parkinson’s Disease---Next Generation Sequencing Analyses and Functional StudyCHIN-HSIEN LINNational Science and Technology Council
2015Investigating the Pathogenesis of Arterial Stenosis in Moyamoya DiseaseMING-JEN LEENational Science and Technology Council
2015A Study on the Residual Symptoms of the Early-Treated Patients with Pompe DiseaseYIN-HSIU CHIENNational Science and Technology Council
2015Establish of Diagnostic and Prognostic Evaluation Tools for Down SyndromeNI-CHUNG LEENational Science and Technology Council
2015Animal Model for AADC Deficiency---Go beyond the Knock-In Mice (II)NI-CHUNG LEENational Science and Technology Council
2015Establishing a next-generation sequencing (NGS)-based genetic test platform for autosomal dominant polycystic kidney disease (ADPKD) and deciphering the sequences of PKD1 pseudogenesPEI-LUNG CHENNTUH
2014A Phase I/II Clinical Trial for Treatment of Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency Using AAV2-HAADC (I)WUH-LIANG ​​HWUNational Science and Technology Council
2014Individual Identification and Parentage Testing of Fragmented DNA Mixtures with Multiple Single Nucleotide Polymorphism Analysis Using Next Generation Sequencing (NGS)HSIAO-LIN HWANational Science and Technology Council
2014Deciphering the Association between Graves$ Disease and Hla Genes---Mouse Model and Extended Human StudyTIEN-CHUN CHANGNational Science and Technology Council
2014Genetic Analysis of Moyamoya Disease (III)MING-JEN LEENational Science and Technology Council
2014Correcting a Splicing Error in L-Aromatic Amino Acid Decarboxylase (AADC) DeficiencyWUH-LIANG ​​HWUNational Science and Technology Council
2014A Study on the Residual Symptoms of the Early-Treated Patients with Pompe DiseaseYIN-HSIU CHIENNational Science and Technology Council
2014Animal Model for AADC Deficiency---Go beyond the Knock-In Mice (I)NI-CHUNG LEENational Science and Technology Council
2014Genetic study of idiopathic hypogonadotropic hypogonadism (IHH) and Kallmann syndrome (KS): using next-generation sequencing platform as a powerful approachPEI-LUNG CHENNTUH
2013Development of single nucleotide polymorphisms based forensic identification systemHSIAO-LIN HWANational Science and Technology Council
2013Genetic Analysis of Moyamoya Disease (II)MING-JEN LEENational Science and Technology Council
2013Correcting a splicing error in L-aromatic amino acid decarboxylase (AADC) deficiencyWUH-LIANG ​​HWUNational Science and Technology Council
2013A Mouse Model for Aromatic L-Amino Acid Decarboxylase Deficiency (III)NI-CHUNG LEENational Science and Technology Council
2013Next-generation sequencing for human leukocyte antigen (HLA) genotypingPEI-LUNG CHENNTUH; National Taiwan University
2013Pheochromocytoma and paraganglioma: Next-generation sequencing (NGS) for genetic diagnosis and for identification of novel causative genesPEI-LUNG CHENNTUH
2012Development of Single Nucleotide Polymorphisms Based Forensic Identification SystemHSIAO-LIN HWANational Science and Technology Council
2012Clinical Application and Pathophysiological Mechanism of Plasma S-Adenosylhomocysteine in Acute Myocardial InfarctionPO-YUAN CHANGNational Science and Technology Council
2012Correcting a Splicing Error in L-Aromatic Amino Acid Decarboxylase (Aadc) DeficiencyWUH-LIANG ​​HWUNational Science and Technology Council
2012Genetic Study of Graves Disease – an Integrated Family-Based and Case-Control StudyPEI-LUNG CHENNational Science and Technology Council
2012Genetic Analysis of Moyamoya Disease( I )MING-JEN LEENational Science and Technology Council
2012Pompe Disease: Disease and Treatment ModelsYIN-HSIU CHIENNational Science and Technology Council
2012A Mouse Model for Aromatic L-Amino Acid Decarboxylase DeficiencyNI-CHUNG LEENational Science and Technology Council
2012Comprehensive HLA genotyping to test for genetic association with type 1 diabetes mellitusPEI-LUNG CHENNTUH
2011Development of Single Nucleotide Polymorphisms Based Forensic Identification SystemHSIAO-LIN HWANational Science and Technology Council
2011Genetic Study of Graves Disease – an Integrated Family-Based and Case-Control StudyPEI-LUNG CHENNational Science and Technology Council
2011Treating Huntington's Disease with ChaperoneWUH-LIANG ​​HWUNational Science and Technology Council
2011Pompe Disease: Disease and Treatment ModelsYIN-HSIU CHIENNational Science and Technology Council
2011&Quot;Role of Pseudogene in Incontinentia Pigmenti, and Its Potential Treatment&Quot;NI-CHUNG LEENational Science and Technology Council
2011A Mouse Model for Aromatic L-Amino Acid Decarboxylase DeficiencyNI-CHUNG LEENational Science and Technology Council
2011常見新生兒先天性代謝異常疾病篩檢項目之探討YIN-HSIU CHIENHealth Promotion Administration, MOHW
2011Genetic and molecular diagnosis of pseudohypoparathyroidism and mutation analysis of GNAS1 genePEI-LUNG CHENNTUH
2010以lentivirus修飾之間質細胞治療黏多醣症第二型WUH-LIANG ​​HWUMinistry of Health and Welfare
2010Risk Factors in Fabry DiseaseWUH-LIANG ​​HWUNational Science and Technology Council
2010Pompe Disease---Disease and Treatment ModelsYIN-HSIU CHIENNational Science and Technology Council
2010Role of Pseudogene in Incontinentia Pigmenti, and Its Potential TreatmentNI-CHUNG LEENational Science and Technology Council
2010Mechanistic and Clinical Investigations of a Progressive Neurological Disorder, Normal Pressure Hydrocephalus (III)MING-JEN LEENational Science and Technology Council
2010Family-based study to test associations with Graves’ disease at four candidate regions from our pilot genome-wide association studyPEI-LUNG CHENNTUH
2009Risk Factors in Fabry DiseaseWUH-LIANG ​​HWUNational Science and Technology Council
2009Study on Factors Affecting Drug Response of Patients with Alzheimer's DiseaseMING-JANG CHIUScience and Technology Information Center, National Science Council
2009Acid Alpha Glucosidase Gene Variation and Related Genes in Individuals with Low Enzyme ActivityYIN-HSIU CHIENNational Science and Technology Council
2009Role of Pseudogene in Incontinentia Pigmenti, and Its Potential TreatmentNI-CHUNG LEENational Science and Technology Council
2009Mechanistic and Clinical Investigations of a Progressive Neurological Disorder, Normal Pressure HydrocephalusMING-JEN LEENational Science and Technology Council
2008Study on Factors Affecting Drug Response of Patients with Alzheimer's DiseaseMING-JANG CHIUScience and Technology Information Center, National Science Council
2008Study of the Mechanisms for Neuronal Apoptosis Induced by the Pink1 MutationMING-JEN LEENational Science and Technology Council
2008Risk Factors in Fabry DiseaseWUH-LIANG ​​HWUNational Science and Technology Council
2008Acid Alpha Glucosidase Gene Variation and Related Genes in Individuals with Low Enzyme ActivityYIN-HSIU CHIENNational Science and Technology Council
2008Mechanistic and Clinical Investigations of a Progressive Neurological Disorder, Normal Pressure HydrocephalusMING-JEN LEENational Science and Technology Council
2008The Investigation of the Ethical Issues in Genetic TestingWUH-LIANG ​​HWUMinistry of Health and Welfare
2007Study of the Mechanisms for Neuronal Apoptosis Induced by the PINK1 MutationMING-JEN LEENational Science and Technology Council
2007Regulation of Nitric Oxide Synthase by Tetrahydrobiopterin (III)WUH-LIANG ​​HWUNational Science and Technology Council
2007Acid Alpha Glucosidase Gene Variation and Related Genes in Individuals with Low Enzyme ActivityYIN-HSIU CHIENNational Science and Technology Council
2006Genetype and Phenotype Correlation Analysis: Medium-Chain Acyl-Coa Dehydrogenase Deficiency, Glutaric Aciduria Type I , 3-Methylcrotonyl-Coa-Carboxylase DeficiencyYIN-HSIU CHIENHealth Promotion Administration, MOHW
2006Hypoxia Inducible Factor1-Alpha Genetic Polymorphism of Obstructive Sleep ApneaHUEY-DONG WUNational Science and Technology Council
2006Study of the Mechanisms for Neuronal Apoptosis Induced by the PINK1 MutationMING-JEN LEENational Science and Technology Council
2006Regulation of Nitric Oxide Synthase by Tetrahydrobiopterin (II)WUH-LIANG ​​HWUNational Science and Technology Council
2006The Role of CD7 Surface Marker in Skin Inflammation (II)YIN-HSIU CHIENNational Science and Technology Council
2005Establish the Model for Clinical Diagnosis and Genetic Counseling for Genetic Disease: Medium Chain Acyl-Coa Dehydrogenase Deficiency; Glutaric Acidemia Type IYIN-HSIU CHIENHealth Promotion Administration, MOHW
2005Establish the Model for Clinical Diagnosis and Genetic Counseling for Genetic Disease: Medium Chain Acyl-Coa Dehydrogenase Deficiency; Glutaric Acidemia Type IYIN-HSIU CHIENHealth Promotion Administration, MOHW
2005The Association Study of Parkin Gene Polymorphism and the Role of Pathogenic DJ-1 Gene Mutations in a Cohort of Taiwanese, Ethnic Han Chinese with Parkinson's Disease (II)RUEY-MEEI WUScience and Technology Information Center, National Science Council
2005Genotyping in Taiwanese Patients with Familial and Young-Onset Amyotrophic Lateral SclerosisMING-JEN LEENational Science and Technology Council
2005Regulation of Nitric Oxide Synthase by Tetrahydrobiopterin (I)WUH-LIANG ​​HWUNational Science and Technology Council
2005The Role of CD7 Surface Marker in Skin InflammationYIN-HSIU CHIENNational Science and Technology Council
2004The Effect of High-Dose Tetrahydrobiopterin on Inflammation and the Production of Nitric Oxide and Free RadicalWUH-LIANG ​​HWUNational Science and Technology Council
2004The Ethical and Psychosocial Issues of Genetic Evaluation---Prenatal Diagnosis (III)LIAN-HUA HUANGNational Science and Technology Council
2004Study on the Mechanisms of Motor Neuron Degeneration Caused by a Novel SOD1 Mutation in a C. elegans Animal ModelMING-JEN LEENational Science and Technology Council
2003Functional Implications of Cct4 Mutations on Neuronal ApoptosisMING-JEN LEENational Science and Technology Council
2003Molecular Structural Mechanisms of GTP Cyclohydrolase I Mutations and Alternative Splicing (III)WUH-LIANG ​​HWUNational Science and Technology Council
2003Installation of an Open Service for Counseling of Genetic DiseasesYIN-HSIU CHIENMinistry of Health and Welfare
2003The Ethical and Psychosocial Issues of Genetic Evaluation---Prenatal Diagnosis (II)LIAN-HUA HUANGNational Science and Technology Council
2002Molecular Structural Mechanisms of GTP Cyclohydrolase I Mutations and Alternative Splicing (II)WUH-LIANG ​​HWUNational Science and Technology Council
2002The Ethical and Psychosocial Issues of Genetic Evaluation:Prenatal Diagnosis (I)LIAN-HUA HUANGNational Science and Technology Council
2002A Proteomic Approach to Lysosomal Storage DiseaseWUH-LIANG ​​HWUNational Science and Technology Council
2001Molecular Structural Mechanisms of GTP Cyclohydrolase I Mutations and Alternative Splicing (I)WUH-LIANG ​​HWUNational Science and Technology Council
2000GTP Cyclohydrolase I Transgenic Mice---Histochemical Localization and PhenotypeWUH-LIANG ​​HWUNational Science and Technology Council
2000A Study on the Molecular Basis of ProgeriaWUH-LIANG ​​HWUNational Science and Technology Council
1999Genetic and Biochemical Analysis of GTP Cyclohydrolase I Deficient Transgenic MiceWUH-LIANG ​​HWUNational Science and Technology Council
1998The Cost-Effectiveness Analysis of Maternal Serum Screening for Down's SyndromeHSIAO-LIN HWANational Science and Technology Council
1998Mitochondrial DNA Mutation in ProgeriaWUH-LIANG ​​HWUNational Science and Technology Council
1998A Mouse Model of GTP-Cyclohydrolase I DeficiencyWUH-LIANG ​​HWUNational Science and Technology Council
1997Analysis of Point or Small Mutations in Duchenne/Becker Muscular DystrophyTSANG-MING KONational Science and Technology Council
1997Antibody Blocking of Fibroblast Growth Factor Receptor 3WUH-LIANG ​​HWUNational Science and Technology Council
1995Differential Allelic Expression Analysis in Genetic DiseasesWUH-LIANG ​​HWUNational Science and Technology Council