計畫


第 1 到 31 筆結果，共 31 筆。

啟始時間標題P-Investigator經費來源
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
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
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
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
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
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
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
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
2016Genetic study and immunological analysis of Graves’ disease and antithyroid drug-induced adverse effectsPEI-LUNG CHENNational Science and Technology Council
2016Genetic Study and Immunological Analysis of Graves$ Disease and Antithyroid Drug-Induced Adverse EffectsPEI-LUNG CHENNational 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
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
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
2014Genetic study of idiopathic hypogonadotropic hypogonadism (IHH) and Kallmann syndrome (KS): using next-generation sequencing platform as a powerful approachPEI-LUNG CHENNTUH
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
2012Genetic Study of Graves Disease – an Integrated Family-Based and Case-Control StudyPEI-LUNG CHENNational Science and Technology Council
2012Comprehensive HLA genotyping to test for genetic association with type 1 diabetes mellitusPEI-LUNG CHENNTUH
2011Genetic Study of Graves Disease – an Integrated Family-Based and Case-Control StudyPEI-LUNG CHENNational Science and Technology Council
2011Genetic and molecular diagnosis of pseudohypoparathyroidism and mutation analysis of GNAS1 genePEI-LUNG CHENNTUH
2010Family-based study to test associations with Graves’ disease at four candidate regions from our pilot genome-wide association studyPEI-LUNG CHENNTUH