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Angewandte Chemie (International Ed. in English)|January 10, 2018
Insights into the Desaturation of Cyclopeptin and its C3 Epimer Catalyzed by a non-Heme Iron Enzyme: Structural Characterization and Mechanism ElucidationHsuan-Jen Liao, Jikun Li, Jhih-Liang Huang, et al.
Scientific Reports|June 9, 2021
The impact of different first-line EGFR-TKIs on the clinical outcome of sequential osimertinib treatment in advanced NSCLC with secondary T790MYen-Hsiang Huang, Jeng-Sen Tseng, Kuo-Hsuan Hsu, et al.
Annals of Biomedical Engineering|August 29, 2022
Classifying Temporomandibular Disorder with Artificial Intelligent Architecture Using Magnetic Resonance ImagingZih-Kai Kao, Neng-Tai Chiu, Hung-Ta Hondar Wu, et al.
Plos One|January 22, 2021
The clinicopathological significance of SWI/SNF alterations in gastric cancer is associated with the molecular subtypesShih-Chiang Huang, Kwai-Fong Ng, Ian Yi-Feng Chang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 4, 2012
PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's diseaseChin-Song Lu, Szu-Chia Lai, Ruey-Meei Wu, et al.
Targeted Oncology|April 23, 2022
The Difference in Clinical Outcomes Between Osimertinib and Afatinib for First-Line Treatment in Patients with Advanced and Recurrent EGFR-Mutant Non-Small Cell Lung Cancer in TaiwanYen-Hsiang Huang, Kuo-Hsuan Hsu, Jeng-Sen Tseng, et al.
Urologia Internationalis|September 27, 2003
Prognostic values of p53 and HER-2/neu coexpression in invasive bladder cancer in TaiwanYuh-Shyan Tsai, Tzong-Shin Tzai, Nan-Hua Chow, et al.
Experimental Neurology|September 17, 2013
Neurovascular abnormalities in humans and mice with Huntington's diseaseChien-Yuan Lin, Yi-Hua Hsu, Ming-Huang Lin, et al.
Journal of Neurology|October 26, 2007
PINK1 mutation in Taiwanese early-onset parkinsonism : clinical, genetic, and dopamine transporter studiesYi-Hsin Weng, Yah-Huei Wu Chou, Wen-Shiang Wu, et al.
Journal of Clinical Medicine|July 9, 2022
Identification of Genetic Variations in the NAD-Related Pathways for Patients with Major Depressive Disorder: A Case-Control Study in TaiwanDaniel Tzu-Li Chen, Szu-Wei Cheng, Tiffany Chen, et al.
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