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Biomedicines|August 29, 2024
Sphingolipid Metabolism Is Associated with Cardiac Dyssynchrony in Patients with Acute Myocardial InfarctionChing-Hui Huang, Chen-Ling Kuo, Yu-Shan Cheng, et al.The Kaohsiung Journal of Medical Sciences|November 1, 2019
Association of cyclophilin A level and pulse pressure in predicting recurrence of cerebral infarctionChen-Shu Chang, Chen-Ling Kuo, Ching-Shan Huang, et al.Current Protocols|August 23, 2023
A Protocol for Culture and Characterization of Human Induced Pluripotent Stem Cells After InductionYu-Shan Cheng, Miao Xu, Guibin Chen, et al.Lipids in Health and Disease|December 30, 2025
Lecithin coenzyme Q10 restores mitochondrial dynamics and alleviates hepatic dysfunction in high-fat Diet-Fed db/db miceChen-Ling Kuo, Chih-Chung Wu, Yu-Shan Cheng, et al.Stem Cell Research|May 10, 2019
Generation of an induced pluripotent stem cell line (TRNDi008-A) from a Hunter syndrome patient carrying a hemizygous 208insC mutation in the IDS geneJunjie Hong, Miao Xu, Rong Li, et al.Journal of Medical Internet Research|August 16, 2024
Short-Term Effects of an eHealth Care Experiential Learning Program Among Patients With Type 2 Diabetes: Randomized Controlled TrialYu-Shan Cheng, Cheng-Pei Lin, Lu-Yen Anny Chen, et al.Frontiers in Oncology|November 28, 2022
Terfenadine resensitizes doxorubicin activity in drug-resistant ovarian cancer cells via an inhibition of CaMKII/CREB1 mediated ABCB1 expressionWei Huang, Shu Yang, Yu-Shan Cheng, et al.Stem Cell Research|October 10, 2020
Four induced pluripotent stem cell lines (TRNDi021-C, TRNDi023-D, TRNDi024-D and TRNDi025-A) generated from fibroblasts of four healthy individualsXiaogang Xu, Manisha Pradhan, Miao Xu, et al.Stem Cell Research|June 5, 2021
Generation of Alagille syndrome derived induced pluripotent stem cell line carrying heterozygous mutation in the JAGGED-1 gene at splicing site (Chr20: 10,629,709C>A) before exon 11Wei Zhu, Yu-Shan Cheng, Miao Xu, et al.Stem Cell Research|June 5, 2021
Generation of an induced pluripotent stem cell line (TRNDi030-A) from a patient with Farber disease carrying a homozygous p. Y36C (c. 107 A>G) mutation in ASAH1Brianna M Brooks, Charles D Yeh, Jeanette Beers, et al.Pageof 5