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Translational Psychiatry
|
September 26, 2022
Involvement of a BH3-only apoptosis sensitizer gene Blm-s in hippocampus-mediated mood control
Pei-Hsin Huang, Tsung-Ying Yang, Chia-Wei Yeh, et al.
Scientific Reports
|
July 27, 2017
Genetic loci associated with an earlier age at onset in multiplex schizophrenia
Annemarie L Woolston, Po-Chang Hsiao, Po-Hsiu Kuo, et al.
Scientific Reports
|
November 10, 2017
ADAM9 promotes lung cancer progression through vascular remodeling by VEGFA, ANGPT2, and PLAT
Chen-Yuan Lin, Chia-Fong Cho, Shih-Ting Bai, et al.
Communications Biology
|
September 10, 2021
Differential whole-genome doubling and homologous recombination deficiencies across breast cancer subtypes from the Taiwanese population
Chia-Hsin Wu, Chia-Shan Hsieh, Yo-Cheng Chang, et al.
Oncogenesis
|
December 7, 2018
The extracellular SEMA domain attenuates intracellular apoptotic signaling of semaphorin 6A in lung cancer cells
Cheng-Ying Shen, Ya-Chu Chang, Li-Han Chen, et al.
Scientific Reports
|
October 24, 2014
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
Jyh-Ming Jimmy Juang, Tzu-Pin Lu, Liang-Chuan Lai, et al.
Scientific Reports
|
January 28, 2014
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in Brugada syndrome
Jyh-Ming Jimmy Juang, Tzu-Pin Lu, Liang-Chuan Lai, et al.
Resuscitation Plus
|
December 16, 2025
Vasopressin, steroids, and epinephrine in out-of-hospital cardiac arrest - a protocol for a randomized controlled trial (OHCA REVIVES trial)
Ying-Chih Ko, Yu-You Lin, Wen-Shuo Yang, et al.
Journal of Advanced Research
|
May 24, 2021
Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine
Jyh-Ming Jimmy Juang, Tzu-Pin Lu, Ming-Wei Su, et al.
Ebiomedicine
|
July 10, 2020
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
Jyh-Ming Jimmy Juang, Anna Binda, Shyh-Jye Lee, et al.
Page
of 18
Search research articles
Search
Showing results (161-170 of 178) with videos related to
Sort By:
Page
of 18
Translational Psychiatry
|
September 26, 2022
Involvement of a BH3-only apoptosis sensitizer gene Blm-s in hippocampus-mediated mood control
Pei-Hsin Huang, Tsung-Ying Yang, Chia-Wei Yeh, et al.
Scientific Reports
|
July 27, 2017
Genetic loci associated with an earlier age at onset in multiplex schizophrenia
Annemarie L Woolston, Po-Chang Hsiao, Po-Hsiu Kuo, et al.
Scientific Reports
|
November 10, 2017
ADAM9 promotes lung cancer progression through vascular remodeling by VEGFA, ANGPT2, and PLAT
Chen-Yuan Lin, Chia-Fong Cho, Shih-Ting Bai, et al.
Communications Biology
|
September 10, 2021
Differential whole-genome doubling and homologous recombination deficiencies across breast cancer subtypes from the Taiwanese population
Chia-Hsin Wu, Chia-Shan Hsieh, Yo-Cheng Chang, et al.
Oncogenesis
|
December 7, 2018
The extracellular SEMA domain attenuates intracellular apoptotic signaling of semaphorin 6A in lung cancer cells
Cheng-Ying Shen, Ya-Chu Chang, Li-Han Chen, et al.
Scientific Reports
|
October 24, 2014
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
Jyh-Ming Jimmy Juang, Tzu-Pin Lu, Liang-Chuan Lai, et al.
Scientific Reports
|
January 28, 2014
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in Brugada syndrome
Jyh-Ming Jimmy Juang, Tzu-Pin Lu, Liang-Chuan Lai, et al.
Resuscitation Plus
|
December 16, 2025
Vasopressin, steroids, and epinephrine in out-of-hospital cardiac arrest - a protocol for a randomized controlled trial (OHCA REVIVES trial)
Ying-Chih Ko, Yu-You Lin, Wen-Shuo Yang, et al.
Journal of Advanced Research
|
May 24, 2021
Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine
Jyh-Ming Jimmy Juang, Tzu-Pin Lu, Ming-Wei Su, et al.
Ebiomedicine
|
July 10, 2020
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
Jyh-Ming Jimmy Juang, Anna Binda, Shyh-Jye Lee, et al.
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of 18