H
Hui-Hua Hsiao
Researcher at Kaohsiung Medical University
Publications - 87
Citations - 827
Hui-Hua Hsiao is an academic researcher from Kaohsiung Medical University. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 13, co-authored 70 publications receiving 658 citations.
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Journal ArticleDOI
MALAT1 long non-coding RNA is overexpressed in multiple myeloma and may serve as a marker to predict disease progression.
Shih-Feng Cho,Yuli Christine Chang,Chao-Sung Chang,Sheng-Fung Lin,Yi-Chang Liu,Hui-Hua Hsiao,Jan-Gowth Chang,Ta-Chih Liu +7 more
TL;DR: MALAT1 was overexpressed in patients with myeloma and may play a role in its pathogenesis and in addition, MALAT1 may serve as a molecular predictor of early progression.
Journal ArticleDOI
Altered Expression of Circadian Clock Genes in Human Chronic Myeloid Leukemia
Ming-Yu Yang,Wen-Chi Yang,Pai-Mei Lin,Jui-Feng Hsu,Hui-Hua Hsiao,Yi-Chang Liu,Hui-Jen Tsai,Chao-Sung Chang,Sheng-Fung Lin +8 more
TL;DR: Comparisons were made between the expression profiles of 9 circadian clock genes from peripheral blood mononuclear cells (PBMCs) and polymorphonuclear Cells (PMNs) and patients with chronic myeloid leukemia to indicate a possible association of the disrupted daily patterns of circadian clock gene expression with the pathogenesis of CML.
Journal ArticleDOI
Deregulated expression of circadian clock genes in gastric cancer.
Ming-Luen Hu,Kun-Tu Yeh,Pai-Mei Lin,Cheng-Ming Hsu,Hui-Hua Hsiao,Yi-Chang Liu,Hugo You-Hsien Lin,Sheng-Fung Lin,Ming-Yu Yang +8 more
TL;DR: The results suggest deregulated expressions of circadian clock genes exist in GC and circadian rhythm disturbance may be associated with the development of GC.
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The association of JAK2V617F mutation and leukocytosis with thrombotic events in essential thrombocythemia.
Hui-Hua Hsiao,Ming-Yu Yang,Yi-Chang Liu,Ching-Ping Lee,Wen-Chi Yang,Ta-Chih Liu,Chao-Sung Chang,Sheng-Fung Lin +7 more
TL;DR: The JAK2V617F mutation was noted in a certain population of ET patients and correlated with leukocytosis, high hemoglobin level, and thrombosis and can affect not only the diagnosis, but also the management ofET patients.
Journal ArticleDOI
Dihydropyrimidine dehydrogenase pharmacogenetics in the Taiwanese population
Hui-Hua Hsiao,Ming-Yu Yang,Jan-Gowth Chang,Yi-Chang Liu,Ta-Chih Liu,Chao-Sung Chang,Tyen-Po Chen,Sheng-Fung Lin +7 more
TL;DR: Results indicate that examination of these mutations is insufficient to provide a high-value prediction of the 5-FU pharmacogenetic syndrome in Taiwanese, and the 1627A>G (DPYD*5) mutation might be a polymorphism in the DPD gene.