Projects
(Principal Investigator)



Results 1-39 of 39 (Search time: 0.008 seconds).

Start DateTitleP-InvestigatorFunding Organization/經費來源
2011(100CAP004-1) Exploring the Mutation of Genes Involving Epigenetic Modification in Acute Myeloid Leukemia and Its Clinical Implication (I)HWEI-FANG TIENMinistry of Science and Technology
2012(100CAP004-1) Exploring the Mutation of Genes Involving Epigenetic Modification in Acute Myeloid Leukemia and its Clinical Implication (II)HWEI-FANG TIENMinistry of Science and Technology
2003Aberrant Methylation of SOCS-1 Gene and SHP-1 Gene in Acute Myeloid Leukemia (I)HWEI-FANG TIENMinistry of Science and Technology
2004Aberrant Methylation of SOCS-1 Gene and SHP-1 Gene in Acute Myeloid Leukemia (II)HWEI-FANG TIENMinistry of Science and Technology
1997CD44 Variant Isoforms in Acute Leukemia and Its Clinical ImplicationsHWEI-FANG TIENMinistry of Science and Technology
1996Deletion of P16/sup INK4A/ and P15/sup INK4B/ in Hematologic Malignancies and Its Clinical ImplicationsHWEI-FANG TIENMinistry of Science and Technology
1997Deletion of P16/sup INK4A/ and P15/sup INK4B/ in Hematologic Malignancies and Its Clinical Implications (II)HWEI-FANG TIENMinistry of Science and Technology
2013Exploring the role of DNMT3A mutation in myelodysplastic syndrome and its clinical implicationHWEI-FANG TIENMinistry of Science and Technology
2011Exploring the Role of Dnmt3a Mutation in Myelodysplastic Syndrome and Its Clinical ImplicationHWEI-FANG TIENMinistry of Science and Technology
2009Exploring the Role of WNT Signaling Pathway in Acute Myeloid Leukemia and Its Clinical ImplicationHWEI-FANG TIENMinistry of Science and Technology
2010Exploring the Roles of Gene Aberrations, Angiogenesis and Regulatory T-Cells in the Pathogenesis of Myelodysplastic Syndrome and Their Clinical ImplicationsHWEI-FANG TIENMinistry of Science and Technology
2009Exploring the Roles of Gene Aberrations, Angiogenesis and Regulatory T-Cells in the Pathogenesis of Myelodysplastic Syndrome and Their Clinical ImplicationsHWEI-FANG TIENMinistry of Science and Technology
2008Exploring the Roles of Gene Aberrations, Angiogenesis and Regulatory T-Cells in the Pathogenesis of Myelodysplastic Syndrome and Their Clinical ImplicationsHWEI-FANG TIENMinistry of Science and Technology
2005Fluorescence in situ Hybridization and Multicolor Spectral Karyotyping in Myelodysplastic Syndrome (I)HWEI-FANG TIENMinistry of Science and Technology
1998Hypermenthylation of Multiple Tumor Suppressor Gene in Myelodysplastic SyndromeHWEI-FANG TIENMinistry of Science and Technology
1999Hypermethylation of Multiple Suppressor Gene in Myelodysplastic Syndrome(II)HWEI-FANG TIENMinistry of Science and Technology
2002Hypermetylation of Multiple Suppressor Gene p15INK4B in Acute Myeloid Leukemia and Its Aapplication in Monitoring of Minimal Residual Disease (II)HWEI-FANG TIENMinistry of Science and Technology
2013Investigating the Evolution of ASXL1 Mutation and Its Interaction with Other Gene Alterations during the Clinical Courses of Acute Myeloid Leukemia by Next Generation Sequencing (I)HWEI-FANG TIENMinistry of Science and Technology
2014Investigating the Evolution of ASXL1 Mutation and Its Interaction with Other Gene Alterations during the Clinical Courses of Acute Myeloid Leukemia by Next Generation Sequencing (II)HWEI-FANG TIENMinistry of Science and Technology
1999Kaposis Sarcoma Associated Herpes Virus (KSHV)/Human Herpes Virus Type 8 (HHV8) Infection in Patients with Multiple Myeloma and Its Clinical SignificanceHWEI-FANG TIENMinistry of Science and Technology
2003Multicolor Spectral Karyotyping in Acute Leukemia (I)HWEI-FANG TIENMinistry of Science and Technology
2004Multicolor Spectral Karyotyping in Acute Leukemia (II)HWEI-FANG TIENMinistry of Science and Technology
2007Npm Mutation in Patients with Acute Myeloid Leukemia and Its Implication in Monitoring Minimal Residual DiseaseHWEI-FANG TIENMinistry of Science and Technology
2006NPM Mutation in Patients with Acute Myeloid Leukemia and Its Implication in Monitoring Minimal Residual DiseaseHWEI-FANG TIENMinistry of Science and Technology
2010Organizing Plan of Committee Chairman in Department of Biology of National Science Council (NSC) --- Division of Internal Medicine (II)HWEI-FANG TIENMinistry of Science and Technology
2008Organizing Plan of Committee Chairman in Department of Biology of National Science Council (Nsc)---Division of Internal Medicine(II)HWEI-FANG TIENMinistry of Science and Technology
1994Phenotyping, Genotyping, and Chromosome Studies in Myelodysplastic Syndrome with Acute TransformationHWEI-FANG TIENMinistry of Science and Technology
1993Ras Mutation in Myelodysplastic Syndrome and Its Clinical Implication (I)HWEI-FANG TIENMinistry of Science and Technology
1992Rearrangements of Immunoglobulin and T-cell Receptor Genes in Acute Myeloid Leukemia and Their Correlation with Immunophenotype and Chromosome ChangesHWEI-FANG TIENMinistry of Science and Technology
1995Studies on PML/RAR Alpha Fusion Transcript in Acute Promyelocytic LeukemiaHWEI-FANG TIENMinistry of Science and Technology
1996Studies on PML/RAR Alpha Fusion Transcript in Acute Promyelocytic Leukemia (II)HWEI-FANG TIENMinistry of Science and Technology
2001Study of the Pathogenesis of Multiple Myeloma by Fluororescence in situ Hybridization and Microarray Technology (I)HWEI-FANG TIENMinistry of Science and Technology
2002Study of the Pathogenesis of Multiple Myeloma by Fluororescence in situ Hybridization and Microarray Technology (II)HWEI-FANG TIENMinistry of Science and Technology
1995Study on CD7 Positive Myeloid Cells in Fetal Liver (II)HWEI-FANG TIENMinistry of Science and Technology
1994Study on CD7 Positive Myeloid Cells in Fetal LiversHWEI-FANG TIENMinistry of Science and Technology
1994Study on CD7 Positive Myeloid Cells in Fetal LiversHWEI-FANG TIENMinistry of Science and Technology
2007The Role of Haploinsufficiency of NPM and AML1 Genes in the Pathogenesis of Human Myelodysplastic SyndromeHWEI-FANG TIENMinistry of Science and Technology
2019探討 ASXL1 蛋白轉譯後修飾作用在血液腫瘤之致病機制(2/3)HWEI-FANG TIENMinistry of Science and Technology
2019骨髓化生不良症候群在疾病進展時基因突變的演化及其臨床應用(3/3)HWEI-FANG TIENMinistry of Science and Technology