| 臺大學術典藏 |
2010 |
WT1 mutation in 470 adult patients with acute myeloid leukemia: Stability during disease evolution and implication of its incorporation into a survival scoring system
|
Chou W.-C.; Chen C.-Y.; Lin L.-I.; Liu C.-Y.; Huang T.-C.; Hou H.-A.; Chen Y.-C.; Tien H.-F.; Tsay W.; Wu S.-J.; Hsu S.-C.; Huang S.-Y.; Ko B.-S.; Tang J.-L.; Tseng M.-H.; Huang C.-F.; Chiang Y.-C.; Lee F.-Y.; Liu M.-C.; MING YAO |
| 臺大學術典藏 |
2010 |
WT1 mutation in 470 adult patients with acute myeloid leukemia: Stability during disease evolution and implication of its incorporation into a survival scoring system
|
HWEI-FANG TIEN; Tsay W.; Chen Y.-C.; Wu S.-J.; Hsu S.-C.; Ko B.-S.; Huang S.-Y.; Yao M.; Liu M.-C.; Hou H.-A.; Huang T.-C.; Lin L.-I.; Liu C.-Y.; Chen C.-Y.; Chou W.-C.; Tang J.-L.; Tseng M.-H.; Huang C.-F.; Chiang Y.-C.; Lee F.-Y. |
| 臺大學術典藏 |
2010 |
Induction of DNA damage-inducible gene GADD45�] contributes to sorafenib-induced apoptosis in hepatocellular carcinoma cells
|
Ou D.-L.; Shen Y.-C.; Yu S.-L.; Chen K.-F.; Yeh P.-Y.; Fan H.-H.; Feng W.-C.; Wang C.-T.; Lin L.-I.; CHIUN HSU; Cheng A.-L. |
| 臺大學術典藏 |
2009 |
Human Parvovirus B19 Infection in Patients with Coronary Atherosclerosis
|
Liu S.-C.; Tsai C.-T.; CHO-KAI WU; Yu M.-F.; Wu M.-Z.; Lin L.-I.; Wang S.-S.; Hwang J.-J.; Tseng Y.-Z.; Chiang F.-T.; Tseng C.-D. |
| 臺大學術典藏 |
2009 |
Human Parvovirus B19 Infection in Patients with Coronary Atherosclerosis
|
Tseng Y.-Z.; HWANG, JUEY-JEN; Wang S.-S.; Lin L.-I.; Wu M.-Z.; Yu M.-F.; Wu C.-K.; Tsai C.-T.; Liu S.-C.; Chiang F.-T.; Tseng C.-D. |
| 臺大學術典藏 |
2009 |
Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: Comparative analysis of 493 adult patients
|
Hou H.-A.; Chen C.-Y.; Chou W.-C.; HWEI-FANG TIEN; Huang C.-F.; Tseng M.-H.; Huang Y.-N.; Chen Y.-C.; Huang S.-Y.; Hsu S.-C.; Ko B.-S.; Wu S.-J.; Tsay W.; Yao M.; Tang J.-L.; Lin L.-I. |
| 臺大學術典藏 |
2009 |
AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: Prognostic implication and interaction with other gene alterations
|
Hsu S.-C.; Ko B.-S.; Huang S.-Y.; Yao M.; Liu M.-C.; Lee F.-Y.; Huang C.-F.; Tseng M.-H.; Chou W.-C.; Tang J.-L.; Hou H.-A.; Chen C.-Y.; Liu C.-Y.; SHANG-JU WU; Tsay W.; Chen Y.-C.; Lin L.-I.; Tien H.-F. |
| 臺大學術典藏 |
2009 |
AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: Prognostic implication and interaction with other gene alterations
|
Liu C.-Y.; Chen C.-Y.; Hou H.-A.; Tang J.-L.; Wu S.-J.; Hsu S.-C.; Ko B.-S.; Huang S.-Y.; MING YAO; Liu M.-C.; Lee F.-Y.; Huang C.-F.; Chou W.-C.; Tseng M.-H.; Tsay W.; Chen Y.-C.; Lin L.-I.; Tien H.-F. |
| 臺大學術典藏 |
2009 |
Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: Comparative analysis of 493 adult patients
|
Chen C.-Y.; Chou W.-C.; Huang Y.-N.; Chen Y.-C.; Huang S.-Y.; Hsu S.-C.; Wu S.-J.; Ko B.-S.; Tsay W.; MING YAO; Tang J.-L.; Hou H.-A.; Lin L.-I.; Tseng M.-H.; Huang C.-F.; Tien H.-F. |
| 臺大學術典藏 |
2009 |
AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: Prognostic implication and interaction with other gene alterations
|
HWEI-FANG TIEN; Lin L.-I.; Tsay W.; Chen Y.-C.; Hsu S.-C.; Wu S.-J.; Ko B.-S.; Huang S.-Y.; Yao M.; Liu M.-C.; Lee F.-Y.; Tang J.-L.; Hou H.-A.; Chen C.-Y.; Liu C.-Y.; Chou W.-C.; Tseng M.-H.; Huang C.-F. |
| 臺大學術典藏 |
2008 |
Expression of angiopoietins and vascular endothelial growth factors and their clinical significance in acute myeloid leukemia
|
HWEI-FANG TIEN; Tsay W.; Chen C.-Y.; Yao M.; Huang C.-F.; Tseng M.-H.; Tang J.-L.; Lin L.-I.; Chou W.-C.; Hou H.-A. |
| 臺大學術典藏 |
2008 |
Expression of angiopoietins and vascular endothelial growth factors and their clinical significance in acute myeloid leukemia
|
Tien H.-F.; Tsay W.; MING YAO; Chen C.-Y.; Huang C.-F.; Tseng M.-H.; Tang J.-L.; Lin L.-I.; Hou H.-A.; Chou W.-C. |
| 臺大學術典藏 |
2008 |
Characterization of acute myeloid leukemia with PTPN11 mutation: The mutation is closely associated with NPM1 mutation but inversely related to FLT3/ITD
|
HWEI-FANG TIEN; Lee F.-Y.; Liu M.-C.; Chiou R.-J.; Huang C.-F.; Tseng M.-H.; Hou H.-A.; Chou W.-C.; Lin L.-I.; Chen C.-Y.; Tang J.-L. |
| 臺大學術典藏 |
2007 |
Marrow angiogenesis-associated factors as prognostic biomarkers in patients with acute myelogenous leukaemia
|
Lee C.-Y.; HWEI-FANG TIEN; Hu C.-Y.; Chou W.-C.; Lin L.-I. |
| 臺大學術典藏 |
2007 |
Erratum: A novel fluorescence-based multiplex PCR assay for rapid simultaneous detection of CEBPA mutations and NPM mutations in patients with acute myeloid leukemias (Leukemia (2007) vol. 21 (2236) 10.1038/sj.leu.2404888)
|
HWEI-FANG TIEN; Lin D.-T.; Tang J.-L.; Chou W.-C.; Lin T.-C.; Lin L.-I. |
| 臺大學術典藏 |
2007 |
RUNX1 gene mutation in primary myelodysplastic syndrome - The mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome
|
Tien H.-F.; Tseng M.-H.; SHANG-JU WU; Chen C.-Y.; Lin L.-I.; Tang J.-L.; Ko B.-S.; Tsay W.; Chou W.-C.; Yao M. |
| 臺大學術典藏 |
2007 |
RUNX1 gene mutation in primary myelodysplastic syndrome - The mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome
|
Lin L.-I.; Tang J.-L.; Chen C.-Y.; HWEI-FANG TIEN; Tseng M.-H.; Wu S.-J.; Yao M.; Chou W.-C.; Tsay W.; Ko B.-S. |
| 臺大學術典藏 |
2007 |
RUNX1 gene mutation in primary myelodysplastic syndrome - The mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome
|
Ko B.-S.; Tang J.-L.; Chen C.-Y.; Lin L.-I.; Tsay W.; Chou W.-C.; MING YAO; Wu S.-J.; Tseng M.-H.; Tien H.-F. |
| 臺大學術典藏 |
2006 |
Chemokine receptor expression profiles in nasopharyngeal carcinoma and their association with metastasis and radiotherapy
|
Ou D.-L.;Chen C.-L.;Lin S.B.;Chih-Hung Hsu;Lin L.-I.; Ou D.-L.; Chen C.-L.; Lin S.B.; CHIH-HUNG HSU; Lin L.-I. |
| 臺大學術典藏 |
2006 |
Nucleophosmin mutations in de novo acute myeloid leukemia: The age-dependent incidences and the stability during disease evolution
|
Chou W.-C.; Tang J.-L.; Lin L.-I.; Yao M.; Tsay W.; Chen C.-Y.; Wu S.-J.; Huang C.-F.; Chiou R.-J.; Tseng M.-H.; Lin D.-T.; Lin K.-H.; Chen Y.-C.; HWEI-FANG TIEN |
| 臺大學術典藏 |
2006 |
A novel fluorescence-based multiplex PCR assay for rapid simultaneous detection of CEBPA mutations and NPM mutations in patients with acute myeloid leukemias [8]
|
Lin T.-C.; Lin L.-I.; Chou W.-C.; Tang J.-L.; Lin D.-T.; HWEI-FANG TIEN |
| 臺大學術典藏 |
2006 |
Nucleophosmin mutations in de novo acute myeloid leukemia: The age-dependent incidences and the stability during disease evolution
|
Tang J.-L.; Chou W.-C.; Tien H.-F.; Chen Y.-C.; Lin K.-H.; Lin L.-I.; MING YAO; Tsay W.; Chen C.-Y.; Wu S.-J.; Huang C.-F.; Chiou R.-J.; Tseng M.-H.; Lin D.-T. |
| 臺大學術典藏 |
2005 |
Characterization of CEBPA mutations in acute myeloid leukemia: Most patients with CEBPA mutations have biallelic mutations and show a distinct immunophenotype of the leukemic cells
|
Shen H.-L.; Yeh Y.-C.; Tang J.-L.; Tsay W.; Lin D.-T.; Chen C.-Y.; Lin L.-I.; Tien H.-F.; MING YAO; Huang S.-Y.; Su F.-H. |
| 國立臺灣大學 |
1993 |
A New Codon 31 (-C) Mutant Resulting in B-Thalassemic
|
Lin, L. I.; 林國信; Lin, K. H.; Lin, L. I.; Lin, Kuo-Sin; Lin, K. H. |
| 臺大學術典藏 |
1992 |
A novel -32 (C-A) mutant identified in amplified genomic DNA of a Chinese β-thalassemic patient [2]
|
KAI-HSIN LIN; Lin, L.-I.;Lin, K.-S.;Lin, K.-H.;Cheng, T.-Y. |
