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Journal of Biomedical Science
|
August 7, 2025
Whole exome sequencing and polygenic risk assessment for kidney functions and clinical management in both hospital-based cohort and population-based Asian cohorts
Min-Rou Lin, I-Wen Wu, Wan-Hsuan Chou, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
June 12, 2013
Apoptotic toxicity of destruxin B in human non-Hodgkin lymphoma cells
Pin-Zhir Chao, Yi-Ping Chin, I-Uen Hsu, et al.
Alzheimer'S Research & Therapy
|
June 22, 2023
Acrolein adducts and responding autoantibodies correlate with metabolic disturbance in Alzheimer's disease
Monika Renuka Sanotra, Shu-Huei Kao, Ching-Kuo Lee, et al.
The Journal of Molecular Diagnostics : JMD
|
January 18, 2022
A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan
Meng-Chen Wu, Yung-Yee Chang, Min-Yu Lan, et al.
Journal of Bacteriology
|
December 9, 2008
Streptomyces telomeres contain a promoter
Yuh-ru Lin, Mi-Young Hahn, Jung-Hye Roe, et al.
Plos One
|
February 12, 2015
Huntingtin-associated protein 1 interacts with breakpoint cluster region protein to regulate neuronal differentiation
Pai-Tsang Huang, Chien-Ho Chen, I-Uen Hsu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
May 29, 2026
Population genomics and disease risk of primary cutaneous amyloidosis: A prominent genodermatosis of Southeast Asia
Hui-Ying Weng, Ding-Dar Lee, Yung-Feng Lin, et al.
Oxidative Medicine and Cellular Longevity
|
September 16, 2021
Genetic Association in the Maintenance of the Mitochondrial Microenvironment and Sperm Capacity
Hwang I S Thomas, Ying-Shiuan Chen, Ching-Han Hung, et al.
Clinical Immunology (Orlando, Fla.)
|
January 20, 2023
Lymphocyte disturbance and functional assessment of the [Asp521Asn] ZAP70 mutation
Yung-Feng Lin, Wen-I Lee, Ching-Huang Ho, et al.
Journal of Biomedical Science
|
September 27, 2021
Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48)
Huan-Yun Chen, Chia-Lang Hsu, Han-Yi Lin, et al.
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of 7
Search research articles
Search
Showing results (41-50 of 68) with videos related to
Sort By:
Page
of 7
Journal of Biomedical Science
|
August 7, 2025
Whole exome sequencing and polygenic risk assessment for kidney functions and clinical management in both hospital-based cohort and population-based Asian cohorts
Min-Rou Lin, I-Wen Wu, Wan-Hsuan Chou, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
June 12, 2013
Apoptotic toxicity of destruxin B in human non-Hodgkin lymphoma cells
Pin-Zhir Chao, Yi-Ping Chin, I-Uen Hsu, et al.
Alzheimer'S Research & Therapy
|
June 22, 2023
Acrolein adducts and responding autoantibodies correlate with metabolic disturbance in Alzheimer's disease
Monika Renuka Sanotra, Shu-Huei Kao, Ching-Kuo Lee, et al.
The Journal of Molecular Diagnostics : JMD
|
January 18, 2022
A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan
Meng-Chen Wu, Yung-Yee Chang, Min-Yu Lan, et al.
Journal of Bacteriology
|
December 9, 2008
Streptomyces telomeres contain a promoter
Yuh-ru Lin, Mi-Young Hahn, Jung-Hye Roe, et al.
Plos One
|
February 12, 2015
Huntingtin-associated protein 1 interacts with breakpoint cluster region protein to regulate neuronal differentiation
Pai-Tsang Huang, Chien-Ho Chen, I-Uen Hsu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
May 29, 2026
Population genomics and disease risk of primary cutaneous amyloidosis: A prominent genodermatosis of Southeast Asia
Hui-Ying Weng, Ding-Dar Lee, Yung-Feng Lin, et al.
Oxidative Medicine and Cellular Longevity
|
September 16, 2021
Genetic Association in the Maintenance of the Mitochondrial Microenvironment and Sperm Capacity
Hwang I S Thomas, Ying-Shiuan Chen, Ching-Han Hung, et al.
Clinical Immunology (Orlando, Fla.)
|
January 20, 2023
Lymphocyte disturbance and functional assessment of the [Asp521Asn] ZAP70 mutation
Yung-Feng Lin, Wen-I Lee, Ching-Huang Ho, et al.
Journal of Biomedical Science
|
September 27, 2021
Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48)
Huan-Yun Chen, Chia-Lang Hsu, Han-Yi Lin, et al.
Page
of 7